IGNATIAVAN DEN VEYVERIGNATIA VAN DEN VEYVER0.000000000000000.000000000000001989VAN DEN VEYVER, IGNATIAProfessorprns:coAuthorOfcoauthor ofprns:endDateend dateFaculty Rankprns:fullNamefull nameprns:grantAwardedBygrant awarded byprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:physicalNeighborOfphysical neighborprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:principalInvestigatorNameprincipal investigator nameprns:publicationDatepublication dateprns:similarTosimilar toprns:sortOrdersort orderprns:startDatestart dateprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:addressStatestate or provinceAgreementvivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionGrantvivo:hasMemberRolemember ofvivo:hasResearchArearesearch areasvivo:hasResearcherRoleresearch activitiesvivo:hrJobTitleHR job titleInformation Resourcevivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressMember Rolevivo:memberRoleOfmember role ofvivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titleResearcher Rolevivo:researcherRoleOfresearcher role ofRolevivo:roleContributesTocontributes tovivo:sponsorAwardIdsponsor award idrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst nameGroupfoaf:lastNamelast nameOrganizationPerson25376457Aghajanova L, Mahadevan S, Altm?e S, Stavreus-Evers A, Regan L, Sebire N, Dixon P, Fisher RA, Van den Veyver IBHuman reproduction (Oxford, England)No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility. Hum Reprod. 2015 Jan; 30(1):232-8.Hum Reprod2014-11-05T00:00:002014No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.25464842Ross J, Busch J, Mintz E, Ng D, Stanley A, Brafman D, Sutton VR, Van den Veyver I, Willert KCell reportsA rare human syndrome provides genetic evidence that WNT signaling is required for reprogramming of fibroblasts to induced pluripotent stem cells. Cell Rep. 2014 Dec 11; 9(5):1770-1780.Cell Rep2014-11-20T00:00:002014A rare human syndrome provides genetic evidence that WNT signaling is required for reprogramming of fibroblasts to induced pluripotent stem cells.Authorship 820566Authorship 861681Authorship 1035015Authorship 1104703Authorship 1106478Authorship 1136251Authorship 1136629Authorship 1159135Authorship 1202771Authorship 224201Authorship 1611285Authorship 162656625492685Murry JB, Santos XM, Wang X, Wan YW, Van den Veyver IB, Dietrich JEFertility and sterilityA genome-wide screen for copy number alterations in an adolescent pilot cohort with m?llerian anomalies. Fertil Steril. 2015 Feb; 103(2):487-93.Fertil Steril2014-12-06T00:00:002014A genome-wide screen for copy number alterations in an adolescent pilot cohort with m?llerian anomalies.25715356Yagel S, Cohen SM, Benacerraf BR, Cuckle H, Kagan KO, Van den Veyver I, Wapner R, Lee WJournal of ultrasound in medicine : official journal of the American Institute of Ultrasound in MedicineNoninvasive prenatal testing and fetal sonographic screening: roundtable discussion. J Ultrasound Med. 2015 Mar; 34(3):363-9.J Ultrasound Med2015-03-01T00:00:002015Noninvasive prenatal testing and fetal sonographic screening: roundtable discussion.Authorship 284528Authorship 3391211Authorship 372711Authorship 406811Authorship 4243910Authorship 573407Authorship 576286Authorship 577106Authorship 620061Authorship 661876Authorship 692091Authorship 69702Authorship 720822Authorship 731763Authorship 783461Authorship 842075Authorship 9520753275983van Dam PA, Van Goethem ML, Kersschot E, Vervliet J, Van den Veyver IB, De Schepper A, Buytaert PRadiologyPalpable solid breast masses: retrospective single- and multimodality evaluation of 201 lesions. Radiology. 1988 Feb; 166(2):435-9.Radiology1988-02-01T00:00:001988Palpable solid breast masses: retrospective single- and multimodality evaluation of 201 lesions.7856682Van den Veyver IB, Chong SS, Cota J, Bennett PR, Fisk NM, Handyside AH, Cartron JP, Le Van Kim C, Colin Y, Snabes MCAmerican journal of obstetrics and gynecologySingle-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn. Am J Obstet Gynecol. 1995 Feb; 172(2 Pt 1):533-40.Am J Obstet Gynecol1995-02-01T00:00:001995Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn.8141206Van den Veyver IB, Chong SS, Kristjansson K, Snabes MC, Moise KJ, Hughes MRAmerican journal of obstetrics and gynecologyMolecular analysis of human platelet antigen system 1 antigen on single cells can be applied to preimplantation genetic diagnosis for prevention of alloimmune thrombocytopenia. Am J Obstet Gynecol. 1994 Mar; 170(3):807-12.Am J Obstet Gynecol1994-03-01T00:00:001994Molecular analysis of human platelet antigen system 1 antigen on single cells can be applied to preimplantation genetic diagnosis for prevention of alloimmune thrombocytopenia.8942854Van den Veyver IB, Moise KJObstetrics and gynecologyFetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunization. Obstet Gynecol. 1996 Dec; 88(6):1061-7.Obstet Gynecol1996-12-01T00:00:001996Fetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunization.7982337Kramer WB, Van den Veyver IB, Kirshon BClinics in perinatologyTreatment of polyhydramnios with indomethacin. Clin Perinatol. 1994 Sep; 21(3):615-30.Clin Perinatol1994-09-01T00:00:001994Treatment of polyhydramnios with indomethacin.9722948Van den Veyver IB, Cormier TA, Jurecic V, Baldini A, Zoghbi HYGenomicsCharacterization and physical mapping in human and mouse of a novel RING finger gene in Xp22. Genomics. 1998 Jul 15; 51(2):251-61.Genomics1998-07-15T00:00:001998Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22.1250 MOURSUND STREETHouston, 77030TX8355924Van den Veyver IB, Moise KJObstetrical & gynecological surveyProstaglandin synthetase inhibitors in pregnancy. Obstet Gynecol Surv. 1993 Jul; 48(7):493-502.Obstet Gynecol Surv1993-07-01T00:00:001993Prostaglandin synthetase inhibitors in pregnancy.8377971Van den Veyver IB, Moise KJ, Ou CN, Carpenter RJObstetrics and gynecologyThe effect of gestational age and fetal indomethacin levels on the incidence of constriction of the fetal ductus arteriosus. Obstet Gynecol. 1993 Oct; 82(4 Pt 1):500-3.Obstet Gynecol1993-10-01T00:00:001993The effect of gestational age and fetal indomethacin levels on the incidence of constriction of the fetal ductus arteriosus.9551303Van den Veyver IB, Roa BBCurrent opinion in obstetrics & gynecologyApplied molecular genetic techniques for prenatal diagnosis. Curr Opin Obstet Gynecol. 1998 Apr; 10(2):97-103.Curr Opin Obstet Gynecol1998-04-01T00:00:001998Applied molecular genetic techniques for prenatal diagnosis.10508514Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HYNature geneticsRett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet. 1999 Oct; 23(2):185-8.Nat Genet1999-10-01T00:00:001999Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.8598966Van Den Veyver IB, Subramanian SB, Hudson KM, Werch J, Moise KJ, Hughes MRObstetrics and gynecologyPrenatal diagnosis of the RhD fetal blood type on amniotic fluid by polymerase chain reaction. Obstet Gynecol. 1996 Mar; 87(3):419-22.Obstet Gynecol1996-03-01T00:00:001996Prenatal diagnosis of the RhD fetal blood type on amniotic fluid by polymerase chain reaction.Authorship 2973508Authorship 297450410826991Van den Veyver IB, Zoghbi HYCurrent opinion in genetics & developmentMethyl-CpG-binding protein 2 mutations in Rett syndrome. Curr Opin Genet Dev. 2000 Jun; 10(3):275-9.Curr Opin Genet Dev2000-06-01T00:00:002000Methyl-CpG-binding protein 2 mutations in Rett syndrome.Authorship 2985363Authorship 298657126237491Westerfield L, Darilek S, van den Veyver IBJournal of clinical medicineCounseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis. J Clin Med. 2014 Sep 12; 3(3):1018-32.J Clin Med2014-09-12T00:00:002014Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis.26253094van den Veyver IB, Eng CMCold Spring Harbor perspectives in medicineGenome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders. Cold Spring Harb Perspect Med. 2015 Aug 07; 5(10).Cold Spring Harb Perspect Med2015-08-07T00:00:002015Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.26275793Westerfield LE, Stover SR, Mathur VS, Nassef SA, Carter TG, Yang Y, Eng CM, Van den Veyver IBPrenatal diagnosisReproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice. Prenat Diagn. 2015 Oct; 35(10):1022-9.Prenat Diagn2015-09-04T00:00:002015Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.26287960Richards EG, Sangi-Haghpeykar H, McGuire AL, Van den Veyver IB, Fruhman GPrenatal diagnosisPregnant patients' risk perception of prenatal test results with uncertain fetal clinical significance: ultrasound versus advanced genetic testing. Prenat Diagn. 2015 Dec; 35(12):1213-7.Prenat Diagn2015-09-18T00:00:002015Pregnant patients' risk perception of prenatal test results with uncertain fetal clinical significance: ultrasound versus advanced genetic testing.10395802Prakash SK, Van den Veyver IB, Franco B, Volta M, Ballabio A, Zoghbi HYGenomicsCharacterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3. Genomics. 1999 Jul 01; 59(1):77-84.Genomics1999-07-01T00:00:001999Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3.11738862Van den Veyver IB, Zoghbi HYBrain & developmentMutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome. Brain Dev. 2001 Dec; 23 Suppl 1:S147-51.Brain Dev2001-12-01T00:00:002001Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome.10739772Zhang W, Amir R, Stockton DW, Van Den Veyver IB, Bacino CA, Zoghbi HYAmerican journal of human geneticsTerminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter. Am J Hum Genet. 2000 Apr; 66(4):1461-4.Am J Hum Genet2000-03-17T00:00:002000Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter.9674913Van den Veyver IB, Subramanian S, Zoghbi HYAmerican journal of medical geneticsGenomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome. Am J Med Genet. 1998 Jun 30; 78(2):179-81.Am J Med Genet1998-06-30T00:00:001998Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome.10072436Moglabey YB, Kircheisen R, Seoud M, El Mogharbel N, Van den Veyver I, Slim RHuman molecular geneticsGenetic mapping of a maternal locus responsible for familial hydatidiform moles. Hum Mol Genet. 1999 Apr; 8(4):667-71.Hum Mol Genet1999-04-01T00:00:001999Genetic mapping of a maternal locus responsible for familial hydatidiform moles.LAURENWESTERFIELDLAUREN WESTERFIELD11442WESTERFIELD, LAURENAssistant Professor10805343Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ, Philippi A, Timar L, Percy AK, Motil KJ, Lichtarge O, Smith EO, Glaze DG, Zoghbi HYAnnals of neurologyInfluence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann Neurol. 2000 May; 47(5):670-9.Ann Neurol2000-05-01T00:00:002000Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes.74Professor10Assistant Professor54Instructor21Chair14Associate Professor42Director46Distinguished Emeritus Professor88Senior Faculty15689438Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IBJournal of medical geneticsMutations in exon 1 of MECP2 are a rare cause of Rett syndrome. J Med Genet. 2005 Feb; 42(2):e15.J Med Genet2005-02-01T00:00:002005Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.SARAARIANSARA ARIAN11715ARIAN, SARASenior Faculty12900577Van den Veyver IBCytogenetic and genome researchMicrophthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders? Cytogenet Genome Res. 2002; 99(1-4):289-96.Cytogenet Genome Res2002-01-01T00:00:002002Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?12112732Van den Veyver IB, Zoghbi HYMental retardation and developmental disabilities research reviewsGenetic basis of Rett syndrome. Ment Retard Dev Disabil Res Rev. 2002; 8(2):82-6.Ment Retard Dev Disabil Res Rev2002-01-01T00:00:002002Genetic basis of Rett syndrome.13129680Saxena A, Frank D, Panichkul P, Van den Veyver IB, Tycko B, Thaker HPlacentaThe product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole. Placenta. 2003 Sep-Oct; 24(8-9):835-42.Placenta2003-09-01T00:00:002003The product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole.16540529Van den Veyver IB, Al-Hussaini TKHuman reproduction updateBiparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring. Hum Reprod Update. 2006 May-Jun; 12(3):233-42.Hum Reprod Update2006-03-15T00:00:002006Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring.14536082Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RRMolecular cellA mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. Mol Cell. 2003 Aug; 12(2):425-35.Mol Cell2003-08-01T00:00:002003A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos.14550593Al-Hussaini TK, Abd el-Aal DM, Van den Veyver IBInternational journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and ObstetricsRecurrent pregnancy loss due to familial and non-familial habitual molar pregnancy. Int J Gynaecol Obstet. 2003 Nov; 83(2):179-86.Int J Gynaecol Obstet2003-11-01T00:00:002003Recurrent pregnancy loss due to familial and non-familial habitual molar pregnancy.Authorship 326724527368744Normand E, Qdaisat S, Bi W, Shaw C, Van den Veyver I, Beaudet A, Breman APrenatal diagnosisComparison of three whole genome amplification methods for detection of genomic aberrations in single cells. Prenat Diagn. 2016 Sep; 36(9):823-30.Prenat Diagn2016-07-30T00:00:002016Comparison of three whole genome amplification methods for detection of genomic aberrations in single cells.15475242Yu L, Liu C, Bennett K, Wu YZ, Dai Z, Vandeusen J, Opavsky R, Raval A, Trikha P, Rodriguez B, Becknell B, Mao C, Lee S, Davuluri RV, Leone G, Van den Veyver IB, Caligiuri MA, Plass CGenomicsA NotI-EcoRV promoter library for studies of genetic and epigenetic alterations in mouse models of human malignancies. Genomics. 2004 Oct; 84(4):647-60.Genomics2004-10-01T00:00:002004A NotI-EcoRV promoter library for studies of genetic and epigenetic alterations in mouse models of human malignancies.14738943Van den Veyver IB, Panichkul PP, Antalffy BA, Sun Y, Hunter JV, Armstrong DDPediatric neurologyPresence of filamin in the astrocytic inclusions of Aicardi syndrome. Pediatr Neurol. 2004 Jan; 30(1):7-15.Pediatr Neurol2004-01-01T00:00:002004Presence of filamin in the astrocytic inclusions of Aicardi syndrome.19784914Kolomeyevskaya N, Blazo M, Van den Veyver I, Strehlow S, Aagaard-Tillery KMAmerican journal of perinatologyPheochromocytoma and Von Hippel-Lindau in pregnancy. Am J Perinatol. 2010 Mar; 27(3):257-63.Am J Perinatol2009-09-26T00:00:002009Pheochromocytoma and Von Hippel-Lindau in pregnancy.Authorship 3281201827616633Breman AM, Chow JC, U'Ren L, Normand EA, Qdaisat S, Zhao L, Henke DM, Chen R, Shaw CA, Jackson L, Yang Y, Vossaert L, Needham RH, Chang EJ, Campton D, Werbin JL, Seubert RC, Van den Veyver IB, Stilwell JL, Kaldjian EP, Beaudet ALPrenatal diagnosisEvidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing. Prenat Diagn. 2016 Nov; 36(11):1009-1019.Prenat Diagn2016-10-02T00:00:002016Evidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing.17546030Wang X, Reid Sutton V, Omar Peraza-Llanes J, Yu Z, Rosetta R, Kou YC, Eble TN, Patel A, Thaller C, Fang P, Van den Veyver IBNature geneticsMutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia. Nat Genet. 2007 Jul; 39(7):836-8.Nat Genet2007-06-03T00:00:002007Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia.16859563Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IBBMC medical geneticsExpression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med Genet. 2006 Jul 21; 7:61.BMC Med Genet2006-07-21T00:00:002006Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients.17621479Glasmacher MA, Sutton VR, Hopkins B, Eble T, Lewis RA, Park Parsons D, Van den Veyver IBJournal of child neurologyPhenotype and management of Aicardi syndrome: new findings from a survey of 69 children. J Child Neurol. 2007 Feb; 22(2):176-84.J Child Neurol2007-02-01T00:00:002007Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children.1988328Van den Veyver IB, Schatteman E, Vanderheyden JS, Van Wiemeersch J, Meulyzer PEuropean journal of obstetrics, gynecology, and reproductive biologyAntenatal fetal death in twin pregnancies: a dangerous condition mainly for the surviving co-twin; a report of four cases. Eur J Obstet Gynecol Reprod Biol. 1991 Jan 04; 38(1):69-73.Eur J Obstet Gynecol Reprod Biol1991-01-04T00:00:001991Antenatal fetal death in twin pregnancies: a dangerous condition mainly for the surviving co-twin; a report of four cases.18039680Kou YC, Shao L, Peng HH, Rosetta R, del Gaudio D, Wagner AF, Al-Hussaini TK, Van den Veyver IBMolecular human reproductionA recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles. Mol Hum Reprod. 2008 Jan; 14(1):33-40.Mol Hum Reprod2007-11-26T00:00:002007A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.18925666Hopkins B, Sutton VR, Lewis RA, Van den Veyver I, Clark GAmerican journal of medical genetics. Part ANeuroimaging aspects of Aicardi syndrome. Am J Med Genet A. 2008 Nov 15; 146A(22):2871-8.Am J Med Genet A2008-11-15T00:00:002008Neuroimaging aspects of Aicardi syndrome.19116729Eble TN, Sutton VR, Sangi-Haghpeykar H, Wang X, Jin W, Lewis RA, Fang P, Van den Veyver IBHuman geneticsNon-random X chromosome inactivation in Aicardi syndrome. Hum Genet. 2009 Mar; 125(2):211-6.Hum Genet2009-01-01T00:00:002009Non-random X chromosome inactivation in Aicardi syndrome.Authorship 6528731Authorship 6537184Authorship 6541535Authorship 654628627761919K?lvraa S, Singh R, Normand EA, Qdaisat S, van den Veyver IB, Jackson L, Hatt L, Schelde P, Uldbjerg N, Vestergaard EM, Zhao L, Chen R, Shaw CA, Breman AM, Beaudet ALPrenatal diagnosisGenome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women. Prenat Diagn. 2016 Dec; 36(12):1127-1134.Prenat Diagn2016-11-18T00:00:002016Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women.27853526Van den Veyver IBF1000ResearchRecent advances in prenatal genetic screening and testing. F1000Res. 2016; 5:2591.F1000Res2016-10-28T00:00:002016Recent advances in prenatal genetic screening and testing.27925703Mack LM, Lee W, Mastrobattista JM, Belfort MA, Van den Veyver IB, Shamshirsaz AA, Ruano R, Sanz Cortes M, Espinoza A, Thiam Diouf A, Espinoza JJournal of ultrasound in medicine : official journal of the American Institute of Ultrasound in MedicineAre First Trimester Nuchal Septations Independent Risk Factors for Chromosomal Anomalies? J Ultrasound Med. 2017 Jan; 36(1):155-161.J Ultrasound Med2016-11-28T00:00:002016Are First Trimester Nuchal Septations Independent Risk Factors for Chromosomal Anomalies?28099477Crossland RF, Balasa A, Ramakrishnan R, Mahadevan SK, Fiorotto ML, Van den Veyver IBPloS oneChronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring. PLoS One. 2017; 12(1):e0170127.PLoS One2017-01-18T00:00:002017Chronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring.19760649Wang X, Sutton VR, Eble TN, Lewis RA, Gunaratne P, Patel A, Van den Veyver IBAmerican journal of medical genetics. Part AA genome-wide screen for copy number alterations in Aicardi syndrome. Am J Med Genet A. 2009 Oct; 149A(10):2113-21.Am J Med Genet A2009-10-01T00:00:002009A genome-wide screen for copy number alterations in Aicardi syndrome.20171603Olivarez SA, Maheshwari B, McCarthy M, Zacharias N, van den Veyver I, Casturi L, Sangi-Haghpeykar H, Aagaard-Tillery KAmerican journal of obstetrics and gynecologyProspective trial on obstructive sleep apnea in pregnancy and fetal heart rate monitoring. Am J Obstet Gynecol. 2010 Jun; 202(6):552.e1-7.Am J Obstet Gynecol2010-02-20T00:00:002010Prospective trial on obstructive sleep apnea in pregnancy and fetal heart rate monitoring.20854095Fernandes PH, Wen S, Sutton VR, Ward PA, Van den Veyver IB, Fang PGenetic testing and molecular biomarkersPORCN mutations and variants identified in patients with focal dermal hypoplasia through diagnostic gene sequencing. Genet Test Mol Biomarkers. 2010 Oct; 14(5):709-13.Genet Test Mol Biomarkers2010-09-20T00:00:002010PORCN mutations and variants identified in patients with focal dermal hypoplasia through diagnostic gene sequencing.20458665Mendez-Figueroa H, Lamance K, Sutton VR, Aagaard-Tillery K, Van den Veyver IAmerican journal of perinatologyManagement of ornithine transcarbamylase deficiency in pregnancy. Am J Perinatol. 2010 Nov; 27(10):775-84.Am J Perinatol2010-05-10T00:00:002010Management of ornithine transcarbamylase deficiency in pregnancy.21686566Scott RW, Pivnick EK, Dowell SH, Eubanks JW, Huang EY, Van den Veyver IB, Wang XBMJ case reportsGoltz syndrome: report of two severe cases. BMJ Case Rep. 2009; 2009.BMJ Case Rep2009-03-17T00:00:002009Goltz syndrome: report of two severe cases.22013202Balasa A, Sanchez-Valle A, Sadikovic B, Sangi-Haghpeykar H, Bravo J, Chen L, Liu W, Wen S, Fiorotto ML, Veyver IBThe Journal of nutritionChronic maternal protein deprivation in mice is associated with overexpression of the cohesin-mediator complex in liver of their offspring. J Nutr. 2011 Dec; 141(12):2106-12.J Nutr2011-10-19T00:00:002011Chronic maternal protein deprivation in mice is associated with overexpression of the cohesin-mediator complex in liver of their offspring.2365122Van den Veyver I, Vanderheyden J, Krauss E, Jankie SEuropean journal of obstetrics, gynecology, and reproductive biologyAseptic necrosis of the femoral head associated with pregnancy; a case report. Eur J Obstet Gynecol Reprod Biol. 1990 Jul-Aug; 36(1-2):167-73.Eur J Obstet Gynecol Reprod Biol1990-07-01T00:00:001990Aseptic necrosis of the femoral head associated with pregnancy; a case report.22412863Liu W, Shaver TM, Balasa A, Ljungberg MC, Wang X, Wen S, Nguyen H, Van den Veyver IBPloS oneDeletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome). PLoS One. 2012; 7(3):e32331.PLoS One2012-03-06T00:00:002012Deletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome).22467161Willis AS, van den Veyver I, Eng CMPrenatal diagnosisMultiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis. Prenat Diagn. 2012 Apr; 32(4):315-20.Prenat Diagn2012-04-01T00:00:002012Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis.22467166Breman A, Pursley AN, Hixson P, Bi W, Ward P, Bacino CA, Shaw C, Lupski JR, Beaudet A, Patel A, Cheung SW, Van den Veyver IPrenatal diagnosisPrenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature. Prenat Diagn. 2012 Apr; 32(4):351-61.Prenat Diagn2012-04-01T00:00:002012Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.22470934Bi W, Breman A, Shaw CA, Stankiewicz P, Gambin T, Lu X, Cheung SW, Jackson LG, Lupski JR, Van den Veyver IB, Beaudet ALPrenatal diagnosisDetection of =1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays. Prenat Diagn. 2012 Jan; 32(1):10-20.Prenat Diagn2012-01-01T00:00:002012Detection of =1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays.22719832Aagaard K, Riehle K, Ma J, Segata N, Mistretta TA, Coarfa C, Raza S, Rosenbaum S, Van den Veyver I, Milosavljevic A, Gevers D, Huttenhower C, Petrosino J, Versalovic JPloS oneA metagenomic approach to characterization of the vaginal microbiome signature in pregnancy. PLoS One. 2012; 7(6):e36466.PLoS One2012-06-13T00:00:002012A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy.IMENCHAKCHOUKIMEN CHAKCHOUK12817CHAKCHOUK, IMENInstructor21745012Strassberg M, Fruhman G, Van den Veyver IBExpert review of molecular diagnosticsCopy-number changes in prenatal diagnosis. Expert Rev Mol Diagn. 2011 Jul; 11(6):579-92.Expert Rev Mol Diagn2011-07-01T00:00:002011Copy-number changes in prenatal diagnosis.22681940Fruhman G, Eble TN, Gambhir N, Sutton VR, Van den Veyver IB, Lewis RAJournal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and StrabismusOphthalmologic findings in Aicardi syndrome. J AAPOS. 2012 Jun; 16(3):238-41.J AAPOS2012-06-01T00:00:002012Ophthalmologic findings in Aicardi syndrome.28317850Mahadevan S, Sathappan V, Utama B, Lorenzo I, Kaskar K, Van den Veyver IBScientific reportsMaternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming. Sci Rep. 2017 03 20; 7:44667.Sci Rep2017-03-20T00:00:002017Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming.Authorship 868504628361097Wong BK, Sutton VR, Lewis RA, Van den Veyver IBMolecular genetics & genomic medicineIndependent variant analysis of TEAD1 and OCEL1 in 38 Aicardi syndrome patients. Mol Genet Genomic Med. 2017 Mar; 5(2):117-121.Mol Genet Genomic Med2017-01-25T00:00:002017Independent variant analysis of TEAD1 and OCEL1 in 38 Aicardi syndrome patients.Authorship 8686774Authorship 868902428384392McClatchey T, Lay E, Strassberg M, Van den Veyver IBPrenatal diagnosisMissed opportunities: unidentified genetic risk factors in prenatal care. Prenat Diagn. 2018 01; 38(1):75-79.Prenat Diagn2017-04-24T00:00:002017Missed opportunities: unidentified genetic risk factors in prenatal care.28422141Mahadevan S, Sathappan V, Utama B, Lorenzo I, Kaskar K, Van den Veyver IBScientific reportsErratum: Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming. Sci Rep. 2017 04 19; 7:46434.Sci Rep2017-04-19T00:00:002017Erratum: Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming.Authorship 10203916Authorship 8694046Authorship 10218237794512Montgomery LD, Belfort MA, Saade GR, Baker BW, Pokorny W, Minifee P, Langston C, Jevon G, Van den Veyver I, Robie DFetal diagnosis and therapyIatrogenic gastroschisis decreases pulmonary hypoplasia in an ovine congenital diaphragmatic hernia model. Fetal Diagn Ther. 1995 Mar-Apr; 10(2):119-26.Fetal Diagn Ther1995-03-01T00:00:001995Iatrogenic gastroschisis decreases pulmonary hypoplasia in an ovine congenital diaphragmatic hernia model.8136827Kristjansson K, Chong SS, Van den Veyver IB, Subramanian S, Snabes MC, Hughes MRNature geneticsPreimplantation single cell analyses of dystrophin gene deletions using whole genome amplification. Nat Genet. 1994 Jan; 6(1):19-23.Nat Genet1994-01-01T00:00:001994Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification.8291550Van den Veyver IB, Macha ME, McCaskill C, Carpenter RJ, Shaffer LGAmerican journal of medical geneticsPrenatal diagnosis and clinical findings in a case of hexasomy 12p. Am J Med Genet. 1993 Dec 01; 47(8):1171-4.Am J Med Genet1993-12-01T00:00:001993Prenatal diagnosis and clinical findings in a case of hexasomy 12p.9562961Van den Veyver IB, Ni J, Bowles N, Carpenter RJ, Weiner CP, Yankowitz J, Moise KJ, Henderson J, Towbin JAMolecular genetics and metabolismDetection of intrauterine viral infection using the polymerase chain reaction. Mol Genet Metab. 1998 Feb; 63(2):85-95.Mol Genet Metab1998-02-01T00:00:001998Detection of intrauterine viral infection using the polymerase chain reaction.10592422Van Den Veyver IB, Yankowitz J, Subramanian SB, Dorman KF, Moise KJGynecologic and obstetric investigationDiscordance between fetal RhD typing using molecular methods and neonatal typing with serology. Gynecol Obstet Invest. 1999; 48(4):229-31.Gynecol Obstet Invest1999-01-01T00:00:001999Discordance between fetal RhD typing using molecular methods and neonatal typing with serology.Authorship 873137928626639Madan S, Liu W, Lu JT, Sutton VR, Toth B, Joe P, Waterson JR, Gibbs RA, Van den Veyver IB, Lammer EJ, Campeau PM, Lee BHMolecular genetics and metabolism reportsA non-mosaic PORCN mutation in a male with severe congenital anomalies overlapping focal dermal hypoplasia. Mol Genet Metab Rep. 2017 Sep; 12:57-61.Mol Genet Metab Rep2017-06-07T00:00:002017A non-mosaic PORCN mutation in a male with severe congenital anomalies overlapping focal dermal hypoplasia.10982966Bacino CA, Stockton DW, Sierra RA, Heilstedt HA, Lewandowski R, Van den Veyver IBAmerican journal of medical geneticsTerminal osseous dysplasia and pigmentary defects: clinical characterization of a novel male lethal X-linked syndrome. Am J Med Genet. 2000 Sep 11; 94(2):102-12.Am J Med Genet2000-09-11T00:00:002000Terminal osseous dysplasia and pigmentary defects: clinical characterization of a novel male lethal X-linked syndrome.Authorship 874714328654730Best S, Wou K, Vora N, Van der Veyver IB, Wapner R, Chitty LSPrenatal diagnosisPromises, pitfalls and practicalities of prenatal whole exome sequencing. Prenat Diagn. 2018 01; 38(1):10-19.Prenat Diagn2017-07-25T00:00:002017Promises, pitfalls and practicalities of prenatal whole exome sequencing.11668396Cormier TA, Prakash SK, Magner DB, Zoghbi HY, Van den Veyver IBMammalian genome : official journal of the International Mammalian Genome SocietyAnalysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice. Mamm Genome. 2001 Oct; 12(10):796-8.Mamm Genome2001-10-01T00:00:002001Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice.Authorship 104196515979551Panichkul PC, Al-Hussaini TK, Sierra R, Kashork CD, Popek EJ, Stockton DW, Van den Veyver IBJournal of the Society for Gynecologic InvestigationRecurrent biparental hydatidiform mole: additional evidence for a 1.1-Mb locus in 19q13.4 and candidate gene analysis. J Soc Gynecol Investig. 2005 Jul; 12(5):376-83.J Soc Gynecol Investig2005-07-01T00:00:002005Recurrent biparental hydatidiform mole: additional evidence for a 1.1-Mb locus in 19q13.4 and candidate gene analysis.16007484Prakash SK, Gibson CW, Wright JT, Boyd C, Cormier T, Sierra R, Li Y, Abrams WR, Aragon MA, Yuan ZA, van den Veyver IBCalcified tissue internationalTooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus. Calcif Tissue Int. 2005 Jul; 77(1):23-9.Calcif Tissue Int2005-07-14T00:00:002005Tooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus.16158440Sutton VR, Hopkins BJ, Eble TN, Gambhir N, Lewis RA, Van den Veyver IBAmerican journal of medical genetics. Part AFacial and physical features of Aicardi syndrome: infants to teenagers. Am J Med Genet A. 2005 Oct 15; 138A(3):254-8.Am J Med Genet A2005-10-15T00:00:002005Facial and physical features of Aicardi syndrome: infants to teenagers.16225835Amir RE, Sutton VR, Van den Veyver IBJournal of child neurologyNewborn screening and prenatal diagnosis for Rett syndrome: implications for therapy. J Child Neurol. 2005 Sep; 20(9):779-83.J Child Neurol2005-09-01T00:00:002005Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.16601480Van den Veyver IB, Beaudet ALCurrent opinion in obstetrics & gynecologyComparative genomic hybridization and prenatal diagnosis. Curr Opin Obstet Gynecol. 2006 Apr; 18(2):185-91.Curr Opin Obstet Gynecol2006-04-01T00:00:002006Comparative genomic hybridization and prenatal diagnosis.17108764Sahoo T, Cheung SW, Ward P, Darilek S, Patel A, del Gaudio D, Kang SH, Lalani SR, Li J, McAdoo S, Burke A, Shaw CA, Stankiewicz P, Chinault AC, Van den Veyver IB, Roa BB, Beaudet AL, Eng CMGenetics in medicine : official journal of the American College of Medical GeneticsPrenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med. 2006 Nov; 8(11):719-27.Genet Med2006-11-01T00:00:002006Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.19012303Van den Veyver IB, Patel A, Shaw CA, Pursley AN, Kang SH, Simovich MJ, Ward PA, Darilek S, Johnson A, Neill SE, Bi W, White LD, Eng CM, Lupski JR, Cheung SW, Beaudet ALPrenatal diagnosisClinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn. 2009 Jan; 29(1):29-39.Prenat Diagn2009-01-01T00:00:002009Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.Authorship 877676820494259Fruhman G, Van den Veyver IBObstetrics and gynecology clinics of North AmericaApplications of array comparative genomic hybridization in obstetrics. Obstet Gynecol Clin North Am. 2010 Mar; 37(1):71-85, Table of Contents.Obstet Gynecol Clin North Am2010-03-01T00:00:002010Applications of array comparative genomic hybridization in obstetrics.20583181Brunetti-Pierri N, Lachman R, Lee K, Leal SM, Piccolo P, Van Den Veyver IB, Bacino CAAmerican journal of medical genetics. Part ATerminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region. Am J Med Genet A. 2010 Jul; 152A(7):1825-31.Am J Med Genet A2010-07-01T00:00:002010Terminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region.21732394Harris RA, Ferrari F, Ben-Shachar S, Wang X, Saade G, Van Den Veyver I, Facchinetti F, Aagaard-Tillery KPrenatal diagnosisGenome-wide array-based copy number profiling in human placentas from unexplained stillbirths. Prenat Diagn. 2011 Oct; 31(10):932-44.Prenat Diagn2011-07-05T00:00:002011Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths.29032050Petersen AK, Cheung SW, Smith JL, Bi W, Ward PA, Peacock S, Braxton A, Van Den Veyver IB, Breman AMAmerican journal of obstetrics and gynecologyPositive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory. Am J Obstet Gynecol. 2017 12; 217(6):691.e1-691.e6.Am J Obstet Gynecol2017-10-13T00:00:002017Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.Authorship 880553329395096Normand EA, Alaimo JT, Van den Veyver IBFertility and sterilityExome and genome sequencing in reproductive medicine. Fertil Steril. 2018 02; 109(2):213-220.Fertil Steril2018-02-01T00:00:002018Exome and genome sequencing in reproductive medicine.true1ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessortrue1Assistant ProfessorAssistant Professor2ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessorD030342Disorders1434420.721733Genetic Diseases, InbornD011296Procedures1865790.71561Prenatal DiagnosisD011247Physiology141775950.38582PregnancyD005817OccupationsProcedures1613770.821794Genetic CounselingAuthorship 1048149Authorship 9312085Authorship 93340022Authorship 9342953Authorship 9374776Authorship 9392646Authorship 9394132730266093Normand EA, Braxton A, Nassef S, Ward PA, Vetrini F, He W, Patel V, Qu C, Westerfield LE, Stover S, Dharmadhikari AV, Muzny DM, Gibbs RA, Dai H, Meng L, Wang X, Xiao R, Liu P, Bi W, Xia F, Walkiewicz M, Van den Veyver IB, Eng CM, Yang YGenome medicineClinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder. Genome Med. 2018 09 28; 10(1):74.Genome Med2018-09-28T00:00:002018Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.30016362Crossland RF, Balasa A, Ramakrishnan R, Mahadevan SK, Fiorotto ML, Van den Veyver IBPloS oneCorrection: Chronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring. PLoS One. 2018; 13(7):e0201079.PLoS One2018-07-17T00:00:002018Correction: Chronic Maternal Low-Protein Diet in Mice Affects Anxiety, Night-Time Energy Expenditure and Sleep Patterns, but Not Circadian Rhythm in Male Offspring.30094853Gu S, Jernegan M, Van den Veyver IB, Peacock S, Smith J, Breman APrenatal diagnosisChromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions. Prenat Diagn. 2018 10; 38(11):858-865.Prenat Diagn2018-09-05T00:00:002018Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions.30731021Larsen D, Ma J, Strassberg M, Ramakrishnan R, Van den Veyver IBPrenatal diagnosisThe uptake of pan-ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling. Prenat Diagn. 2019 03; 39(4):319-323.Prenat Diagn2019-03-01T00:00:002019The uptake of pan-ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling.30388401Nguyen NMP, Ge ZJ, Reddy R, Fahiminiya S, Sauthier P, Bagga R, Sahin FI, Mahadevan S, Osmond M, Breguet M, Rahimi K, Lapensee L, Hovanes K, Srinivasan R, Van den Veyver IB, Sahoo T, Ao A, Majewski J, Taketo T, Slim RAmerican journal of human geneticsCausative Mutations and Mechanism of Androgenetic Hydatidiform Moles. Am J Hum Genet. 2018 11 01; 103(5):740-751.Am J Hum Genet2018-11-01T00:00:002018Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.30692697Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, Breman A, Xia F, Yang Y, Purgason A, Pourpak A, Chen Z, Wang X, Wang Y, Kulkarni S, Choy KW, Wapner RJ, Van den Veyver IB, Beaudet A, Parmar S, Wong LJ, Eng CMNature medicineNon-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nat Med. 2019 03; 25(3):439-447.Nat Med2019-01-28T00:00:002019Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.Authorship 1049558D025063Disorders1694170.801676Chromosome Disorders2024-05-31NIHVAN DEN VEYVER, IGNATIA B2018-08-15Characterization of the role of maternal effect gene Nlrp2 in reproductionR01HD0927462010-11-30NIHVAN DEN VEYVER, IGNATIA B2004-12-06Genetic Studies in Gestational Trophoblastic DiseaseR01HD0459702007-02-28NIHVAN DEN VEYVER, IGNATIA B2003-06-02Do Diet and DNA Methylation Affect Fetal Programming?R21ES0123202009-02-28NIHVAN DEN VEYVER, IGNATIA B2007-03-01New strategies to identify the gene mutated in Aicardi syndromeR21HD0518052007-05-31NIHZOGHBI, HUDA Y2001-07-23Pathophysiology of Rett Syndrome /MECP2 MutationsP01HD0403012021-02-28NIHVAN DEN VEYVER, IGNATIA B2015-03-01The Role of NLRP7 and KHDC3L in Germline Imprinting and Embryonic ReprogrammingR01HD0794422023-08-31NIHCHUNG, WENDY K;CLIFTON, REBECCA GERSNOVIEZ;VAN DEN VEYVER, IGNATIA B;WAPNER, RONALD2007-06-08Prenatal Genetic Diagnosis by Genomic Sequencing: A Prospective EvaluationR01HD0556512011-05-31NIHVAN DEN VEYVER, IGNATIA B2008-06-24The role of NLRP7 and related genes in hydatidiform moles and reproductive failurR21HD0580812014-12-30NIHZOGHBI, HUDA Y1988-08-01Baylor Intellectual and Developmental Disabilities Research CenterP30HD0240642002-02-28NIHVAN DEN VEYVER, IGNATIA B1997-03-06FUNCTIONAL ANALYSIS OF CANDIDATE GENES FOR MLS SYNDROMEK08HD0011712020-06-30NIHVAN DEN VEYVER, IGNATIA B2010-07-01Training Program in Translational Biology and Molecular MedicineT32GM088129Co-Principal InvestigatorPrincipal InvestigatorPrincipal InvestigatorCo-Principal InvestigatorPrincipal InvestigatorCo-Principal InvestigatorPrincipal InvestigatorPrincipal InvestigatorPrincipal InvestigatorPrincipal InvestigatorPrincipal InvestigatorDepartment of MedicineDepartment of Obstetrics & GynecologyGraduate School of Biomedical SciencesDepartment of Molecular & Human GeneticsGraduate Sch of Biomedical SciencesMedicine-General MedicineMolecular & Human GeneticsObstet & Gyne: Maternal & Fetal MedObstet & Gyne: Reprod GeneticsObstetrics and GynecologyBaylor College of MedicineMICHAELBELFORTMICHAEL BELFORT0.000000000000000.000000000000001955BELFORT, MICHAELProfessor111groups7.888370.00075148521research areas2.727710.0083324176coauthor of142.80921.450260similar to11138selected publicationsCATHERINEEPPESCATHERINE EPPES0.000000000000000.000000000000004464EPPES, CATHERINEAssociate ProfessorJAMESLUPSKIJAMES LUPSKI29.71073630000000-95.396604500000003140LUPSKI, JAMESProfessorWESLEYLEEWESLEY LEE0.000000000000000.000000000000003977LEE, WESLEYProfessorKIRANTAM TAMKIRAN TAM TAM0.000000000000000.000000000000003960TAM TAM, KIRANAssistant ProfessorMILDREDRAMIREZMILDRED RAMIREZ0.000000000000000.000000000000004069RAMIREZ, MILDREDProfessorSAU WAICHEUNGSAU WAI CHEUNG29.69822590000000-95.35731940000000499CHEUNG, SAU WAIProfessorAuthorship 9426152730787481Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, Breman A, Xia F, Yang Y, Purgason A, Pourpak A, Chen Z, Wang X, Wang Y, Kulkarni S, Choy KW, Wapner RJ, Van den Veyver IB, Beaudet A, Parmar S, Wong LJ, Eng CMNature medicinePublisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nat Med. 2019 Apr; 25(4):701-702.Nat Med2019-04-01T00:00:002019Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.RICHARDGIBBSRICHARD GIBBS0.000000000000000.000000000000003131GIBBS, RICHARDDistinguished Service ProfessorLAURENCEMCCULLOUGHLAURENCE MCCULLOUGH29.71073630000000-95.396604500000003238MCCULLOUGH, LAURENCEDistinguished Emeritus ProfessorVERNONSUTTONVERNON SUTTON29.70508570000000-95.401808700000003508SUTTON, VERNONProfessorAuthorship 9432911830357877Vossaert L, Wang Q, Salman R, Zhuo X, Qu C, Henke D, Seubert R, Chow J, U'ren L, Enright B, Stilwell J, Kaldjian E, Yang Y, Shaw C, Levy B, Wapner R, Breman A, Van den Veyver I, Beaudet APrenatal diagnosisReliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing. Prenat Diagn. 2018 12; 38(13):1069-1078.Prenat Diagn2018-11-19T00:00:002018Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing.31256877Paine I, Posey JE, Grochowski CM, Jhangiani SN, Rosenheck S, Kleyner R, Marmorale T, Yoon M, Wang K, Robison R, Cappuccio G, Pinelli M, Magli A, Coban Akdemir Z, Hui J, Yeung WL, Wong BKY, Ortega L, Bekheirnia MR, Bierhals T, Hempel M, Johannsen J, Santer R, Aktas D, Alikasifoglu M, Bozdogan S, Aydin H, Karaca E, Bayram Y, Ityel H, Dorschner M, White JJ, Wilichowski E, Wortmann SB, Casella EB, Kitajima JP, Kok F, Monteiro F, Muzny DM, Bamshad M, Gibbs RA, Sutton VR, University of Washington Center for Mendelian Genomics, Baylor-Hopkins Center for Mendelian Genomics, Van Esch H, Brunetti-Pierri N, Hildebrandt F, Brautbar A, Van den Veyver IB, Glass I, Lessel D, Lyon GJ, Lupski JRAmerican journal of human geneticsParalog Studies Augment Gene Discovery: DDX and DHX Genes. Am J Hum Genet. 2019 08 01; 105(2):302-316.Am J Hum Genet2019-06-27T00:00:002019Paralog Studies Augment Gene Discovery: DDX and DHX Genes.Authorship 95135045Authorship 1118382Authorship 952856131353536Van den Veyver IBPrenatal diagnosisPrenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review. Prenat Diagn. 2019 08; 39(9):666-678.Prenat Diagn2019-07-28T00:00:002019Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review.Dr. Shaulsky's GroupMembertrue1ProfessorProfessorZAHRAANVARZAHRA ANVAR15071ANVAR, ZAHRAInstructorAuthorship 960694931703095Wong BKY, Murry JB, Ramakrishnan R, He F, Balasa A, Stinnett GR, Pedersen SE, Pautler RG, Van den Veyver IBPloS oneMaternal stress in Shank3ex4-9 mice increases pup-directed care and alters brain white matter in male offspring. PLoS One. 2019; 14(11):e0224876.PLoS One2019-11-08T00:00:002019Maternal stress in Shank3ex4-9 mice increases pup-directed care and alters brain white matter in male offspring.Authorship 961418231754893Sabbagh R, Van den Veyver IBHuman geneticsThe current and future impact of genome-wide sequencing on fetal precision medicine. Hum Genet. 2020 Sep; 139(9):1121-1130.Hum Genet2019-11-21T00:00:002019The current and future impact of genome-wide sequencing on fetal precision medicine.Authorship 9619301631785788Vossaert L, Wang Q, Salman R, McCombs AK, Patel V, Qu C, Mancini MA, Edwards DP, Malovannaya A, Liu P, Shaw CA, Levy B, Wapner RJ, Bi W, Breman AM, Van den Veyver IB, Beaudet ALAmerican journal of human geneticsValidation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis. Am J Hum Genet. 2019 12 05; 105(6):1262-1273.Am J Hum Genet2019-11-27T00:00:002019Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis.Authorship 1295928Authorship 12959311Authorship 129594324105752Mahadevan S, Wen S, Balasa A, Fruhman G, Mateus J, Wagner A, Al-Hussaini T, Van den Veyver IBPrenatal diagnosisNo evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles. Prenat Diagn. 2013 Dec; 33(13):1242-7.Prenat Diagn2013-10-04T00:00:002013No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles.24105472Mahadevan S, Wen S, Wan YW, Peng HH, Otta S, Liu Z, Iacovino M, Mahen EM, Kyba M, Sadikovic B, Van den Veyver IBHuman molecular geneticsNLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation. Hum Mol Genet. 2014 Feb 01; 23(3):706-16.Hum Mol Genet2013-09-18T00:00:002013NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation.24214820Bui TH, Raymond FL, Van den Veyver IBPrenatal diagnosisCurrent controversies in prenatal diagnosis 2: should incidental findings arising from prenatal testing always be reported to patients? Prenat Diagn. 2014 Jan; 34(1):12-7.Prenat Diagn2013-12-05T00:00:002013Current controversies in prenatal diagnosis 2: should incidental findings arising from prenatal testing always be reported to patients?Authorship 978438332091628Amor DJ, Chitty LS, Van den Veyver IBPrenatal diagnosisCurrent controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing. Prenat Diagn. 2020 12; 40(12):1508-1514.Prenat Diagn2020-04-17T00:00:002020Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing.Authorship 987455732297346Arian SE, Erfani H, Westerfield LE, Buffie A, Nassef S, Gibbons WE, Van den Veyver IBPrenatal diagnosisPrenatal testing in pregnancies conceived by in vitro fertilization with pre-implantation genetic testing. Prenat Diagn. 2020 06; 40(7):846-851.Prenat Diagn2020-05-20T00:00:002020Prenatal testing in pregnancies conceived by in vitro fertilization with pre-implantation genetic testing.Authorship 990191732452065Panchalee T, Vossaert L, Wang Q, Crovetti BR, McCombs AK, Wapner RJ, Van den Veyver IB, Beaudet ALPrenatal diagnosisThe effect of maternal body mass index and gestational age on circulating trophoblast yield in cell-based noninvasive prenatal testing. Prenat Diagn. 2020 10; 40(11):1383-1389.Prenat Diagn2020-08-05T00:00:002020The effect of maternal body mass index and gestational age on circulating trophoblast yield in cell-based noninvasive prenatal testing.2025-06-30NIHSMITH, CAROLYN LOUISE;VAN DEN VEYVER, IGNATIA B2020-07-01The Clinical Translational Research Certificate of Added Qualification ProgramT32GM136554Principal InvestigatorAuthorship 10033341133090377Arian S, Rubin J, Chakchouk I, Sharif M, Mahadevan SK, Erfani H, Shelly K, Liao L, Lorenzo I, Ramakrishnan R, Van den Veyver IBReproductive sciences (Thousand Oaks, Calif.)Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect. Reprod Sci. 2021 07; 28(7):1850-1865.Reprod Sci2020-10-22T00:00:002020Reproductive Outcomes from Maternal Loss of Nlrp2 Are Not Improved by IVF or Embryo Transfer Consistent with Oocyte-Specific Defect.Authorship 1160024Authorship 1016382633857205Zhuo X, Wang Q, Vossaert L, Salman R, Kim A, Van den Veyver I, Breman A, Beaudet APloS oneUse of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT. PLoS One. 2021; 16(4):e0249695.PLoS One2021-04-15T00:00:002021Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT.Authorship 1018270433974713Vossaert L, Chakchouk I, Zemet R, Van den Veyver IBPrenatal diagnosisOverview and recent developments in cell-based noninvasive prenatal testing. Prenat Diagn. 2021 Sep; 41(10):1202-1214.Prenat Diagn2021-05-18T00:00:002021Overview and recent developments in cell-based noninvasive prenatal testing.Authorship 1018900134008861Van den Veyver IBPrenatal diagnosisImproving the prenatal diagnosis of Beckwith-Wiedemann syndrome. Prenat Diagn. 2021 06; 41(7):795-797.Prenat Diagn2021-05-25T00:00:002021Improving the prenatal diagnosis of Beckwith-Wiedemann syndrome.Authorship 1028459634440388Anvar Z, Chakchouk I, Demond H, Sharif M, Kelsey G, Van den Veyver IBGenesDNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting. Genes (Basel). 2021 08 06; 12(8).Genes (Basel)2021-08-06T00:00:002021DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting.true1Distinguished Service ProfessorDistinguished Service Professortrue1Associate ProfessorAssociate Professortrue1InstructorInstructortrue1InstructorInstructorAuthorship 10435552Authorship 10446031135394072Zemet R, Van den Veyver IB, Stankiewicz PPrenatal diagnosisParental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges. Prenat Diagn. 2022 06; 42(7):811-821.Prenat Diagn2022-04-14T00:00:002022Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges.35476893Kernie CG, Wynn J, Rosenbaum A, de Voest J, Galloway S, Giordano J, Stover S, Westerfield L, Gilmore K, Wapner RJ, Van den Veyver IB, Vora NL, Clifton RG, Caughey AB, Chung WKPrenatal diagnosisInformation is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies. Prenat Diagn. 2022 06; 42(7):947-954.Prenat Diagn2022-05-04T00:00:002022Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies.Authorship 135490222467159Shaffer LG, Van den Veyver IBPrenatal diagnosisNew technologies for the assessment of chromosomes in prenatal diagnosis. Prenat Diagn. 2012 Apr; 32(4):307-8.Prenat Diagn2012-04-01T00:00:002012New technologies for the assessment of chromosomes in prenatal diagnosis.Authorship 10461411Authorship 1046142135583085Van den Veyver IB, Chandler N, Wilkins-Haug LE, Wapner RJ, Chitty LS, ISPD Board of DirectorsPrenatal diagnosisInternational Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis. Prenat Diagn. 2022 05; 42(6):796-803.Prenat Diagn2022-05-01T00:00:002022International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis.35583086Van den Veyver IBPrenatal diagnosisPrenatal exomes and genomes - so much new and so much more to learn. Prenat Diagn. 2022 05; 42(6):659-661.Prenat Diagn2022-05-01T00:00:002022Prenatal exomes and genomes - so much new and so much more to learn.Authorship 10464481235604365Pereira S, Carmi S, Altarescu G, Austin J, Barlevy D, Hershlag A, Juengst E, Kostick-Quenet K, Kovanci E, Lathi RB, Mukherjee M, Van den Veyver I, Zuk O, L?zaro-Mu?oz G, Lencz THuman reproduction (Oxford, England)Polygenic embryo screening: four clinical considerations warrant further attention. Hum Reprod. 2022 06 30; 37(7):1375-1378.Hum Reprod2022-06-30T00:00:002022Polygenic embryo screening: four clinical considerations warrant further attention.Authorship 1049477735765264Crovetti B, Maktabi MA, Erfani H, Panchalee T, Wang Q, Vossaert L, Van den Veyver IPrenatal diagnosisCirculating trophoblast numbers as a potential marker for pregnancy complications. Prenat Diagn. 2022 08; 42(9):1182-1189.Prenat Diagn2022-07-02T00:00:002022Circulating trophoblast numbers as a potential marker for pregnancy complications.Authorship 1050063435799470Johnson K, Erfani H, Maktabi MA, Van den Veyver I, Nassef SJournal of genetic counselingLack of consensus among healthcare professionals at a large academic medical center on the use of exome sequencing for prenatal diagnosis. J Genet Couns. 2022 12; 31(6):1330-1340.J Genet Couns2022-07-07T00:00:002022Lack of consensus among healthcare professionals at a large academic medical center on the use of exome sequencing for prenatal diagnosis.true1Senior FacultySenior Facultytrue1Assistant ProfessorAssistant ProfessorAuthorship 10628256Authorship 105849512Authorship 105641612Authorship 10552751Authorship 10546503Authorship 10568278Authorship 1055430236647833Sharif M, Detti L, Van den Veyver IBThe Journal of clinical investigationTake your mother's ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport. J Clin Invest. 2023 01 17; 133(2).J Clin Invest2023-01-17T00:00:002023Take your mother's ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport.36610024Zemet R, Krispin E, Johnson RM, Kumar NR, Westerfield LE, Stover S, Mann DG, Castillo J, Castillo HA, Nassr AA, Sanz Cortes M, Donepudi R, Espinoza J, Whitehead WE, Belfort MA, Shamshirsaz AA, Van den Veyver IBUltrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and GynecologyImplication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect. Ultrasound Obstet Gynecol. 2023 Jun; 61(6):719-727.Ultrasound Obstet Gynecol2023-06-01T00:00:002023Implication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect.36403095Brar BK, Thompson MG, Vora NL, Gilmore K, Blakemore K, Miller KA, Giordano J, Dufke A, Wong B, Stover S, Lianoglou B, Van den Veyver I, Dempsey E, Rosner M, Chong K, Chitayat D, Sparks TN, Norton ME, Wapner R, Baranano K, Jelin AC, Fetal Sequencing ConsortiumPrenatal diagnosisPrenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series. Prenat Diagn. 2022 12; 42(13):1686-1693.Prenat Diagn2022-11-28T00:00:002022Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.36281059Chitty LS, Van den Veyver IBPrenatal diagnosisFacilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis. Prenat Diagn. 2022 11; 42(12):1479-1480.Prenat Diagn2022-11-03T00:00:002022Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis.36221164Van den Veyver IB, Yaron Y, Deans ZCPrenatal diagnosisInternational Society for Prenatal Diagnosis 2022 debate 3-Fetal genome sequencing should be offered to all pregnant patients. Prenat Diagn. 2023 04; 43(4):428-434.Prenat Diagn2022-10-21T00:00:002022International Society for Prenatal Diagnosis 2022 debate 3-Fetal genome sequencing should be offered to all pregnant patients.36229886Cacheiro P, Westerberg CH, Mager J, Dickinson ME, Nutter LMJ, Mu?oz-Fuentes V, Hsu CW, Van den Veyver IB, Flenniken AM, McKerlie C, Murray SA, Teboul L, Heaney JD, Lloyd KCK, Lanoue L, Braun RE, White JK, Creighton AK, Laurin V, Guo R, Qu D, Wells S, Cleak J, Bunton-Stasyshyn R, Stewart M, Harrisson J, Mason J, Haseli Mashhadi H, Parkinson H, Mallon AM, International Mouse Phenotyping Consortium, Genomics England Research Consortium, Smedley DGenome medicineMendelian gene identification through mouse embryo viability screening. Genome Med. 2022 10 13; 14(1):119.Genome Med2022-10-13T00:00:002022Mendelian gene identification through mouse embryo viability screening.35943975Madala D, Maktabi MA, Sabbagh R, Erfani H, Moon A, Van den Veyver IBPrenatal diagnosisLower fetal fraction in clinical cell-free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy. Prenat Diagn. 2022 09; 42(10):1253-1261.Prenat Diagn2022-08-22T00:00:002022Lower fetal fraction in clinical cell-free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy.Authorship 10632042336726284Bedei I, Gehrke T, Gloning KP, Meyer-Wittkopf M, Willner D, Krapp M, Scharf A, Degenhardt J, Heling KS, Kozlowski P, Trautmann K, Jahns KM, Geipel A, Baum?ller JE, Wilhelm L, Gottschalk I, Schr?er A, Graf A, Wolter A, Schenk J, Weber A, Van den Veyver IB, Axt-Fliedner RPrenatal diagnosisMulticenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants. Prenat Diagn. 2023 02; 43(2):192-206.Prenat Diagn2023-02-09T00:00:002023Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variants.Authorship 1064675736846174Sakyu T, Stover SR, Wang Y, Ward P, Gandhi M, Braun MC, Van den Veyver IB, Bi WClinical case reportsCompound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios. Clin Case Rep. 2023 Feb; 11(2):e6692.Clin Case Rep2023-02-23T00:00:002023Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios.Authorship 1067046936976514Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Nasiotis ET, Su L, Liu Z, Wan YW, Van den Veyver IBReproductive sciences (Thousand Oaks, Calif.)Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B. Reprod Sci. 2023 09; 30(9):2780-2793.Reprod Sci2023-03-28T00:00:002023Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B.Authorship 10684772037124138Jolly A, Du H, Borel C, Chen N, Zhao S, Grochowski CM, Duan R, Fatih JM, Dawood M, Salvi S, Jhangiani SN, Muzny DM, Koch A, Rouskas K, Glentis S, Deligeoroglou E, Bacopoulou F, Wise CA, Dietrich JE, Van den Veyver IB, Dimas AS, Brucker S, Sutton VR, Gibbs RA, Antonarakis SE, Wu N, Coban-Akdemir ZH, Zhu L, Posey JE, Lupski JRHGG advancesRare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-K?ster-Hauser syndrome. HGG Adv. 2023 07 13; 4(3):100188.HGG Adv2023-03-29T00:00:002023Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-K?ster-Hauser syndrome.Authorship 10775033Authorship 1077332937650673Maktabi MA, Vossaert L, Van den Veyver IBClinical obstetrics and gynecologyCell-based Noninvasive Prenatal Testing (cbNIPT)-A Review on the Current Developments and Future Prospects. Clin Obstet Gynecol. 2023 09 01; 66(3):636-648.Clin Obstet Gynecol2023-07-17T00:00:002023Cell-based Noninvasive Prenatal Testing (cbNIPT)-A Review on the Current Developments and Future Prospects.37658178Anvar Z, Chakchouk I, Sharif M, Mahadevan S, Su L, Anikar S, Naini FA, Utama AB, Van den Veyver IBReproductive sciences (Thousand Oaks, Calif.)Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 Signaling. Reprod Sci. 2024 Jan; 31(1):173-189.Reprod Sci2023-09-01T00:00:002023Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 Signaling.Authorship 201782Authorship 1501711true1Distinguished Emeritus ProfessorDistinguished Emeritus ProfessorAuthorship 184058Authorship 187801Authorship 1087671338260283Cacheiro P, Lawson S, Van den Veyver IB, Marengo G, Zocche D, Murray SA, Duyzend M, Robinson PN, Smedley DmedRxiv : the preprint server for health sciencesLethal phenotypes in Mendelian disorders. medRxiv. 2024 Jan 13.medRxiv2024-01-13T00:00:002024Lethal phenotypes in Mendelian disorders.Authorship 190841Authorship 194994Authorship 209411Authorship 19123Authorship 237271Authorship 267261Authorship 377815Authorship 270786Authorship 381019Authorship 1434962Authorship 1434973Authorship 143498624849140Gregg AR, Van den Veyver IB, Gross SJ, Madankumar R, Rink BD, Norton MEAnnual review of genomics and human geneticsNoninvasive prenatal screening by next-generation sequencing. Annu Rev Genomics Hum Genet. 2014; 15:327-47.Annu Rev Genomics Hum Genet2014-05-14T00:00:002014Noninvasive prenatal screening by next-generation sequencing.3338608Gerris J, Van Nueten J, Van Camp C, Gentens P, Van de Vijver I, Van Camp KEuropean journal of obstetrics, gynecology, and reproductive biologyClinical aspects in the surgical treatment of varicocele in subfertile men. II. The role of the epididymal factor. Eur J Obstet Gynecol Reprod Biol. 1988 Jan; 27(1):43-51.Eur J Obstet Gynecol Reprod Biol1988-01-01T00:00:001988Clinical aspects in the surgical treatment of varicocele in subfertile men. II. The role of the epididymal factor.Authorship 521915Authorship 382767Authorship 453137Authorship 480884Authorship 682601Authorship 504761Authorship 7222715Authorship 7686412Authorship 775455Authorship 798392Authorship 585551Authorship 602821Authorship 15080610Authorship 151988324989832Chandrasekharan S, McGuire AL, Van den Veyver IBPrenatal diagnosisDo recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care? Prenat Diagn. 2014 Oct; 34(10):921-6.Prenat Diagn2014-07-31T00:00:002014Do recent US Supreme Court rulings on patenting of genes and genetic diagnostics affect the practice of genetic screening and diagnosis in prenatal and reproductive care?25044986Emrick LT, Murphy L, Shamshirsaz AA, Ruano R, Cassady CI, Liu L, Chang F, Sutton VR, Li M, Van den Veyver IBAmerican journal of medical genetics. Part APrenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes. Am J Med Genet A. 2014 Oct; 164A(10):2633-7.Am J Med Genet A2014-07-14T00:00:002014Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes.Authorship 621851Authorship 652731Authorship 955521Authorship 679523Authorship 724092Authorship 776191Authorship 1550988Authorship 1551808