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IGNATIA BARBARA VAN DEN VEYVER

TitleProfessor
InstitutionBaylor College of Medicine
DepartmentDepartment of Obstetrics & Gynecology
DivisionObstet & Gyne: Maternal & Fetal Med
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    Other Positions
    TitleProfessor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Molecular & Human Genetics
    DivisionMolecular & Human Genetics


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    P30HD024064     (ZOGHBI, HUDA Y)Aug 1, 1988 - Jun 30, 2014
    NIH/NICHD
    Baylor Intellectual and Developmental Disabilities Research Center
    Role: Co-Principal Investigator

    K08HD001171     (VAN DEN VEYVER, IGNATIA B)Mar 6, 1997 - Feb 28, 2002
    NIH/NICHD
    FUNCTIONAL ANALYSIS OF CANDIDATE GENES FOR MLS SYNDROME
    Role: Principal Investigator

    P01HD040301     (ZOGHBI, HUDA Y)Jul 23, 2001 - May 31, 2007
    NIH/NICHD
    Pathophysiology of Rett Syndrome /MECP2 Mutations
    Role: Co-Principal Investigator

    R21ES012320     (VAN DEN VEYVER, IGNATIA B)Jun 2, 2003 - Feb 28, 2007
    NIH/NIEHS
    Do Diet and DNA Methylation Affect Fetal Programming?
    Role: Principal Investigator

    R01HD045970     (VAN DEN VEYVER, IGNATIA B)Dec 6, 2004 - Nov 30, 2010
    NIH/NICHD
    Genetic Studies in Gestational Trophoblastic Disease
    Role: Principal Investigator

    R21HD051805     (VAN DEN VEYVER, IGNATIA B)Mar 1, 2007 - Feb 28, 2009
    NIH/NICHD
    New strategies to identify the gene mutated in Aicardi syndrome
    Role: Principal Investigator

    R01HD055651     (WAPNER, RONALD)Jun 8, 2007 - Aug 31, 2023
    NIH/NICHD
    Prenatal Genetic Diagnosis by Genomic Sequencing: A Prospective Evaluation
    Role: Co-Principal Investigator

    R21HD058081     (VAN DEN VEYVER, IGNATIA B)Jun 24, 2008 - May 31, 2011
    NIH/NICHD
    The role of NLRP7 and related genes in hydatidiform moles and reproductive failur
    Role: Principal Investigator

    T32GM088129     (VAN DEN VEYVER, IGNATIA B)Jul 1, 2010 - Jun 30, 2020
    NIH/NIGMS
    Training Program in Translational Biology and Molecular Medicine
    Role: Principal Investigator

    R01HD079442     (VAN DEN VEYVER, IGNATIA B)Mar 1, 2015 - Feb 29, 2020
    NIH/NICHD
    The Role of NLRP7 and KHDC3L in Germline Imprinting and Embryonic Reprogramming
    Role: Principal Investigator

    R01HD092746     (VAN DEN VEYVER, IGNATIA B)Aug 15, 2018 - May 31, 2023
    NIH/NICHD
    Characterization of the role of maternal effect gene Nlrp2 in reproduction
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Van den Veyver IB. Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review. Prenat Diagn. 2019 Aug; 39(9):666-678. PMID: 31353536.
      View in: PubMed
    2. Paine 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, Van Esch H, Brunetti-Pierri N, Hildebrandt F, Brautbar A, Van den Veyver IB, Glass I, Lessel D, Lyon GJ, Lupski JR. Paralog Studies Augment Gene Discovery: DDX and DHX Genes. Am J Hum Genet. 2019 Aug 01; 105(2):302-316. PMID: 31256877.
      View in: PubMed
    3. Zhang 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 CM. Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nat Med. 2019 Apr; 25(4):701-702. PMID: 30787481.
      View in: PubMed
    4. Larsen D, Ma J, Strassberg M, Ramakrishnan R, Van den Veyver IB. The 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. PMID: 30731021.
      View in: PubMed
    5. Zhang 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 CM. Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nat Med. 2019 03; 25(3):439-447. PMID: 30692697.
      View in: PubMed
    6. Vossaert 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 A. Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing. Prenat Diagn. 2018 12; 38(13):1069-1078. PMID: 30357877.
      View in: PubMed
    7. Nguyen 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 R. Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles. Am J Hum Genet. 2018 11 01; 103(5):740-751. PMID: 30388401.
      View in: PubMed
    8. Normand 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 Y. Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder. Genome Med. 2018 09 28; 10(1):74. PMID: 30266093.
      View in: PubMed
    9. Gu S, Jernegan M, Van den Veyver IB, Peacock S, Smith J, Breman A. Chromosomal 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. PMID: 30094853.
      View in: PubMed
    10. Crossland RF, Balasa A, Ramakrishnan R, Mahadevan SK, Fiorotto ML, Van den Veyver IB. Correction: 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. PMID: 30016362.
      View in: PubMed
    11. Normand EA, Alaimo JT, Van den Veyver IB. Exome and genome sequencing in reproductive medicine. Fertil Steril. 2018 02; 109(2):213-220. PMID: 29395096.
      View in: PubMed
    12. Petersen AK, Cheung SW, Smith JL, Bi W, Ward PA, Peacock S, Braxton A, Van Den Veyver IB, Breman AM. Positive 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. PMID: 29032050.
      View in: PubMed
    13. Best S, Wou K, Vora N, Van der Veyver IB, Wapner R, Chitty LS. Promises, pitfalls and practicalities of prenatal whole exome sequencing. Prenat Diagn. 2018 01; 38(1):10-19. PMID: 28654730.
      View in: PubMed
    14. Madan S, Liu W, Lu JT, Sutton VR, Toth B, Joe P, Waterson JR, Gibbs RA, Van den Veyver IB, Lammer EJ, Campeau PM, Lee BH. A non-mosaic PORCN mutation in a male with severe congenital anomalies overlapping focal dermal hypoplasia. Mol Genet Metab Rep. 2017 Sep; 12:57-61. PMID: 28626639.
      View in: PubMed
    15. McClatchey T, Lay E, Strassberg M, Van den Veyver IB. Missed opportunities: unidentified genetic risk factors in prenatal care. Prenat Diagn. 2018 01; 38(1):75-79. PMID: 28384392.
      View in: PubMed
    16. Mahadevan S, Sathappan V, Utama B, Lorenzo I, Kaskar K, Van den Veyver IB. Erratum: Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming. Sci Rep. 2017 04 19; 7:46434. PMID: 28422141.
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    17. Mahadevan S, Sathappan V, Utama B, Lorenzo I, Kaskar K, Van den Veyver IB. Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming. Sci Rep. 2017 03 20; 7:44667. PMID: 28317850.
      View in: PubMed
    18. Wong BK, Sutton VR, Lewis RA, Van den Veyver IB. Independent variant analysis of TEAD1 and OCEL1 in 38 Aicardi syndrome patients. Mol Genet Genomic Med. 2017 Mar; 5(2):117-121. PMID: 28361097.
      View in: PubMed
    19. Crossland RF, Balasa A, Ramakrishnan R, Mahadevan SK, Fiorotto ML, Van den Veyver IB. 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. 2017; 12(1):e0170127. PMID: 28099477.
      View in: PubMed
    20. Mack LM, Lee W, Mastrobattista JM, Belfort MA, Van den Veyver IB, Shamshirsaz AA, Ruano R, Sanz Cortes M, Espinoza A, Thiam Diouf A, Espinoza J. Are First Trimester Nuchal Septations Independent Risk Factors for Chromosomal Anomalies? J Ultrasound Med. 2017 Jan; 36(1):155-161. PMID: 27925703.
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    21. Kølvraa 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 AL. Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women. Prenat Diagn. 2016 Dec; 36(12):1127-1134. PMID: 27761919.
      View in: PubMed
    22. Van den Veyver IB. Recent advances in prenatal genetic screening and testing. F1000Res. 2016; 5:2591. PMID: 27853526.
      View in: PubMed
    23. Breman 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 AL. Evidence for feasibility of fetal trophoblastic cell-based noninvasive prenatal testing. Prenat Diagn. 2016 Nov; 36(11):1009-1019. PMID: 27616633.
      View in: PubMed
    24. Normand E, Qdaisat S, Bi W, Shaw C, Van den Veyver I, Beaudet A, Breman A. Comparison of three whole genome amplification methods for detection of genomic aberrations in single cells. Prenat Diagn. 2016 Sep; 36(9):823-30. PMID: 27368744.
      View in: PubMed
    25. Richards EG, Sangi-Haghpeykar H, McGuire AL, Van den Veyver IB, Fruhman G. Pregnant 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. PMID: 26287960.
      View in: PubMed
    26. Westerfield LE, Stover SR, Mathur VS, Nassef SA, Carter TG, Yang Y, Eng CM, Van den Veyver IB. Reproductive 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. PMID: 26275793.
      View in: PubMed
    27. van den Veyver IB, Eng CM. Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders. Cold Spring Harb Perspect Med. 2015 Aug 07; 5(10). PMID: 26253094.
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    28. Yagel S, Cohen SM, Benacerraf BR, Cuckle H, Kagan KO, Van den Veyver I, Wapner R, Lee W. Noninvasive prenatal testing and fetal sonographic screening: roundtable discussion. J Ultrasound Med. 2015 Mar; 34(3):363-9. PMID: 25715356.
      View in: PubMed
    29. Murry JB, Santos XM, Wang X, Wan YW, Van den Veyver IB, Dietrich JE. A genome-wide screen for copy number alterations in an adolescent pilot cohort with müllerian anomalies. Fertil Steril. 2015 Feb; 103(2):487-93. PMID: 25492685.
      View in: PubMed
    30. Ross J, Busch J, Mintz E, Ng D, Stanley A, Brafman D, Sutton VR, Van den Veyver I, Willert K. A 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. PMID: 25464842.
      View in: PubMed
    31. Westerfield L, Darilek S, van den Veyver IB. Counseling 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. PMID: 26237491.
      View in: PubMed
    32. Chandrasekharan S, McGuire AL, Van den Veyver IB. Do 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. PMID: 24989832.
      View in: PubMed
    33. Emrick LT, Murphy L, Shamshirsaz AA, Ruano R, Cassady CI, Liu L, Chang F, Sutton VR, Li M, Van den Veyver IB. Prenatal 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. PMID: 25044986.
      View in: PubMed
    34. Gregg AR, Van den Veyver IB, Gross SJ, Madankumar R, Rink BD, Norton ME. Noninvasive prenatal screening by next-generation sequencing. Annu Rev Genomics Hum Genet. 2014; 15:327-47. PMID: 24849140.
      View in: PubMed
    35. Bui TH, Raymond FL, Van den Veyver IB. Current 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. PMID: 24214820.
      View in: PubMed
    36. Mahadevan S, Wen S, Balasa A, Fruhman G, Mateus J, Wagner A, Al-Hussaini T, Van den Veyver IB. No evidence for mutations in NLRP7 and KHDC3L in women with androgenetic hydatidiform moles. Prenat Diagn. 2013 Dec; 33(13):1242-7. PMID: 24105752.
      View in: PubMed
    37. Mahadevan S, Wen S, Wan YW, Peng HH, Otta S, Liu Z, Iacovino M, Mahen EM, Kyba M, Sadikovic B, Van den Veyver IB. NLRP7 affects trophoblast lineage differentiation, binds to overexpressed YY1 and alters CpG methylation. Hum Mol Genet. 2014 Feb 01; 23(3):706-16. PMID: 24105472.
      View in: PubMed
    38. Aagaard 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 J. A metagenomic approach to characterization of the vaginal microbiome signature in pregnancy. PLoS One. 2012; 7(6):e36466. PMID: 22719832.
      View in: PubMed
    39. Fruhman G, Eble TN, Gambhir N, Sutton VR, Van den Veyver IB, Lewis RA. Ophthalmologic findings in Aicardi syndrome. J AAPOS. 2012 Jun; 16(3):238-41. PMID: 22681940.
      View in: PubMed
    40. Breman A, Pursley AN, Hixson P, Bi W, Ward P, Bacino CA, Shaw C, Lupski JR, Beaudet A, Patel A, Cheung SW, Van den Veyver I. Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature. Prenat Diagn. 2012 Apr; 32(4):351-61. PMID: 22467166.
      View in: PubMed
    41. Willis AS, van den Veyver I, Eng CM. Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis. Prenat Diagn. 2012 Apr; 32(4):315-20. PMID: 22467161.
      View in: PubMed
    42. Shaffer LG, Van den Veyver IB. New technologies for the assessment of chromosomes in prenatal diagnosis. Prenat Diagn. 2012 Apr; 32(4):307-8. PMID: 22467159.
      View in: PubMed
    43. Liu W, Shaver TM, Balasa A, Ljungberg MC, Wang X, Wen S, Nguyen H, Van den Veyver IB. Deletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome). PLoS One. 2012; 7(3):e32331. PMID: 22412863.
      View in: PubMed
    44. Bi W, Breman A, Shaw CA, Stankiewicz P, Gambin T, Lu X, Cheung SW, Jackson LG, Lupski JR, Van den Veyver IB, Beaudet AL. Detection of =1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays. Prenat Diagn. 2012 Jan; 32(1):10-20. PMID: 22470934.
      View in: PubMed
    45. Balasa A, Sanchez-Valle A, Sadikovic B, Sangi-Haghpeykar H, Bravo J, Chen L, Liu W, Wen S, Fiorotto ML, Veyver IB. Chronic 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. PMID: 22013202.
      View in: PubMed
    46. Harris RA, Ferrari F, Ben-Shachar S, Wang X, Saade G, Van Den Veyver I, Facchinetti F, Aagaard-Tillery K. Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths. Prenat Diagn. 2011 Oct; 31(10):932-44. PMID: 21732394.
      View in: PubMed
    47. Strassberg M, Fruhman G, Van den Veyver IB. Copy-number changes in prenatal diagnosis. Expert Rev Mol Diagn. 2011 Jul; 11(6):579-92. PMID: 21745012.
      View in: PubMed
    48. Fernandes PH, Wen S, Sutton VR, Ward PA, Van den Veyver IB, Fang P. PORCN mutations and variants identified in patients with focal dermal hypoplasia through diagnostic gene sequencing. Genet Test Mol Biomarkers. 2010 Oct; 14(5):709-13. PMID: 20854095.
      View in: PubMed
    49. Brunetti-Pierri N, Lachman R, Lee K, Leal SM, Piccolo P, Van Den Veyver IB, Bacino CA. Terminal 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. PMID: 20583181.
      View in: PubMed
    50. Mendez-Figueroa H, Lamance K, Sutton VR, Aagaard-Tillery K, Van den Veyver I. Management of ornithine transcarbamylase deficiency in pregnancy. Am J Perinatol. 2010 Nov; 27(10):775-84. PMID: 20458665.
      View in: PubMed
    51. Fruhman G, Van den Veyver IB. Applications of array comparative genomic hybridization in obstetrics. Obstet Gynecol Clin North Am. 2010 Mar; 37(1):71-85, Table of Contents. PMID: 20494259.
      View in: PubMed
    52. Olivarez SA, Maheshwari B, McCarthy M, Zacharias N, van den Veyver I, Casturi L, Sangi-Haghpeykar H, Aagaard-Tillery K. Prospective trial on obstructive sleep apnea in pregnancy and fetal heart rate monitoring. Am J Obstet Gynecol. 2010 Jun; 202(6):552.e1-7. PMID: 20171603.
      View in: PubMed
    53. Wang X, Sutton VR, Eble TN, Lewis RA, Gunaratne P, Patel A, Van den Veyver IB. A genome-wide screen for copy number alterations in Aicardi syndrome. Am J Med Genet A. 2009 Oct; 149A(10):2113-21. PMID: 19760649.
      View in: PubMed
    54. Kolomeyevskaya N, Blazo M, Van den Veyver I, Strehlow S, Aagaard-Tillery KM. Pheochromocytoma and Von Hippel-Lindau in pregnancy. Am J Perinatol. 2010 Mar; 27(3):257-63. PMID: 19784914.
      View in: PubMed
    55. Scott RW, Pivnick EK, Dowell SH, Eubanks JW, Huang EY, Van den Veyver IB, Wang X. Goltz syndrome: report of two severe cases. BMJ Case Rep. 2009; 2009. PMID: 21686566.
      View in: PubMed
    56. Eble TN, Sutton VR, Sangi-Haghpeykar H, Wang X, Jin W, Lewis RA, Fang P, Van den Veyver IB. Non-random X chromosome inactivation in Aicardi syndrome. Hum Genet. 2009 Mar; 125(2):211-6. PMID: 19116729.
      View in: PubMed
    57. Van 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 AL. Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn. 2009 Jan; 29(1):29-39. PMID: 19012303.
      View in: PubMed
    58. Hopkins B, Sutton VR, Lewis RA, Van den Veyver I, Clark G. Neuroimaging aspects of Aicardi syndrome. Am J Med Genet A. 2008 Nov 15; 146A(22):2871-8. PMID: 18925666.
      View in: PubMed
    59. Kou YC, Shao L, Peng HH, Rosetta R, del Gaudio D, Wagner AF, Al-Hussaini TK, Van den Veyver IB. A 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. PMID: 18039680.
      View in: PubMed
    60. Wang 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 IB. Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia. Nat Genet. 2007 Jul; 39(7):836-8. PMID: 17546030.
      View in: PubMed
    61. Glasmacher MA, Sutton VR, Hopkins B, Eble T, Lewis RA, Park Parsons D, Van den Veyver IB. Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children. J Child Neurol. 2007 Feb; 22(2):176-84. PMID: 17621479.
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    62. Sahoo 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 CM. Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med. 2006 Nov; 8(11):719-27. PMID: 17108764.
      View in: PubMed
    63. Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med Genet. 2006 Jul 21; 7:61. PMID: 16859563.
      View in: PubMed
    64. Van den Veyver IB, Beaudet AL. Comparative genomic hybridization and prenatal diagnosis. Curr Opin Obstet Gynecol. 2006 Apr; 18(2):185-91. PMID: 16601480.
      View in: PubMed
    65. Van den Veyver IB, Al-Hussaini TK. Biparental hydatidiform moles: a maternal effect mutation affecting imprinting in the offspring. Hum Reprod Update. 2006 May-Jun; 12(3):233-42. PMID: 16540529.
      View in: PubMed
    66. Sutton VR, Hopkins BJ, Eble TN, Gambhir N, Lewis RA, Van den Veyver IB. Facial and physical features of Aicardi syndrome: infants to teenagers. Am J Med Genet A. 2005 Oct 15; 138A(3):254-8. PMID: 16158440.
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    67. Amir RE, Sutton VR, Van den Veyver IB. Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy. J Child Neurol. 2005 Sep; 20(9):779-83. PMID: 16225835.
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    68. Prakash SK, Gibson CW, Wright JT, Boyd C, Cormier T, Sierra R, Li Y, Abrams WR, Aragon MA, Yuan ZA, van den Veyver IB. Tooth enamel defects in mice with a deletion at the Arhgap 6/Amel X locus. Calcif Tissue Int. 2005 Jul; 77(1):23-9. PMID: 16007484.
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    69. Panichkul PC, Al-Hussaini TK, Sierra R, Kashork CD, Popek EJ, Stockton DW, Van den Veyver IB. Recurrent 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. PMID: 15979551.
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    70. Amir RE, Fang P, Yu Z, Glaze DG, Percy AK, Zoghbi HY, Roa BB, Van den Veyver IB. Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. J Med Genet. 2005 Feb; 42(2):e15. PMID: 15689438.
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    71. Yu 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 C. A NotI-EcoRV promoter library for studies of genetic and epigenetic alterations in mouse models of human malignancies. Genomics. 2004 Oct; 84(4):647-60. PMID: 15475242.
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    72. Van den Veyver IB, Panichkul PP, Antalffy BA, Sun Y, Hunter JV, Armstrong DD. Presence of filamin in the astrocytic inclusions of Aicardi syndrome. Pediatr Neurol. 2004 Jan; 30(1):7-15. PMID: 14738943.
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    73. Al-Hussaini TK, Abd el-Aal DM, Van den Veyver IB. Recurrent pregnancy loss due to familial and non-familial habitual molar pregnancy. Int J Gynaecol Obstet. 2003 Nov; 83(2):179-86. PMID: 14550593.
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    74. Saxena A, Frank D, Panichkul P, Van den Veyver IB, Tycko B, Thaker H. The 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. PMID: 13129680.
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    75. Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR. A 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. PMID: 14536082.
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    76. Prakash SK, Cormier TA, McCall AE, Garcia JJ, Sierra R, Haupt B, Zoghbi HY, Van Den Veyver IB. Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome. Hum Mol Genet. 2002 Dec 01; 11(25):3237-48. PMID: 12444108.
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    77. Van den Veyver IB. Genetic effects of methylation diets. Annu Rev Nutr. 2002; 22:255-82. PMID: 12055346.
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    78. Van den Veyver IB. Microphthalmia 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. PMID: 12900577.
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    79. Van den Veyver IB, Zoghbi HY. Genetic basis of Rett syndrome. Ment Retard Dev Disabil Res Rev. 2002; 8(2):82-6. PMID: 12112732.
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    80. Van den Veyver IB, Zoghbi HY. Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome. Brain Dev. 2001 Dec; 23 Suppl 1:S147-51. PMID: 11738862.
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    81. Cormier TA, Prakash SK, Magner DB, Zoghbi HY, Van den Veyver IB. Analysis 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. PMID: 11668396.
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    82. Van den Veyver IB, Norman B, Tran CQ, Bourjac J, Slim R. The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies. J Soc Gynecol Investig. 2001 Sep-Oct; 8(5):305-13. PMID: 11677152.
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    83. Van den Veyver IB. Skewed X inactivation in X-linked disorders. Semin Reprod Med. 2001 Jun; 19(2):183-91. PMID: 11480916.
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    84. Bacino CA, Stockton DW, Sierra RA, Heilstedt HA, Lewandowski R, Van den Veyver IB. Terminal 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. PMID: 10982966.
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    85. Van den Veyver IB, Zoghbi HY. Methyl-CpG-binding protein 2 mutations in Rett syndrome. Curr Opin Genet Dev. 2000 Jun; 10(3):275-9. PMID: 10826991.
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    86. Amir 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 HY. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann Neurol. 2000 May; 47(5):670-9. PMID: 10805343.
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    87. Zhang W, Amir R, Stockton DW, Van Den Veyver IB, Bacino CA, Zoghbi HY. Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter. Am J Hum Genet. 2000 Apr; 66(4):1461-4. PMID: 10739772.
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    88. Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet. 1999 Oct; 23(2):185-8. PMID: 10508514.
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    89. Prakash SK, Van den Veyver IB, Franco B, Volta M, Ballabio A, Zoghbi HY. Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3. Genomics. 1999 Jul 01; 59(1):77-84. PMID: 10395802.
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    90. Moglabey YB, Kircheisen R, Seoud M, El Mogharbel N, Van den Veyver I, Slim R. Genetic mapping of a maternal locus responsible for familial hydatidiform moles. Hum Mol Genet. 1999 Apr; 8(4):667-71. PMID: 10072436.
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    91. Van Den Veyver IB, Yankowitz J, Subramanian SB, Dorman KF, Moise KJ. Discordance between fetal RhD typing using molecular methods and neonatal typing with serology. Gynecol Obstet Invest. 1999; 48(4):229-31. PMID: 10592422.
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    92. Van den Veyver IB, Cormier TA, Jurecic V, Baldini A, Zoghbi HY. Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22. Genomics. 1998 Jul 15; 51(2):251-61. PMID: 9722948.
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    93. Van den Veyver IB, Subramanian S, Zoghbi HY. Genomic 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. PMID: 9674913.
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    94. Van den Veyver IB, Roa BB. Applied molecular genetic techniques for prenatal diagnosis. Curr Opin Obstet Gynecol. 1998 Apr; 10(2):97-103. PMID: 9551303.
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    95. Van den Veyver IB, Ni J, Bowles N, Carpenter RJ, Weiner CP, Yankowitz J, Moise KJ, Henderson J, Towbin JA. Detection of intrauterine viral infection using the polymerase chain reaction. Mol Genet Metab. 1998 Feb; 63(2):85-95. PMID: 9562961.
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    96. Van den Veyver IB, Moise KJ. Fetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunization. Obstet Gynecol. 1996 Dec; 88(6):1061-7. PMID: 8942854.
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    97. Van Den Veyver IB, Subramanian SB, Hudson KM, Werch J, Moise KJ, Hughes MR. Prenatal diagnosis of the RhD fetal blood type on amniotic fluid by polymerase chain reaction. Obstet Gynecol. 1996 Mar; 87(3):419-22. PMID: 8598966.
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    98. Montgomery LD, Belfort MA, Saade GR, Baker BW, Pokorny W, Minifee P, Langston C, Jevon G, Van den Veyver I, Robie D, et al. Iatrogenic gastroschisis decreases pulmonary hypoplasia in an ovine congenital diaphragmatic hernia model. Fetal Diagn Ther. 1995 Mar-Apr; 10(2):119-26. PMID: 7794512.
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    99. Van den Veyver IB, Chong SS, Cota J, Bennett PR, Fisk NM, Handyside AH, Cartron JP, Le Van Kim C, Colin Y, Snabes MC, et al. Single-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. PMID: 7856682.
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    100. Kramer WB, Van den Veyver IB, Kirshon B. Treatment of polyhydramnios with indomethacin. Clin Perinatol. 1994 Sep; 21(3):615-30. PMID: 7982337.
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    101. Van den Veyver IB, Chong SS, Kristjansson K, Snabes MC, Moise KJ, Hughes MR. Molecular 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. PMID: 8141206.
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    102. Kristjansson K, Chong SS, Van den Veyver IB, Subramanian S, Snabes MC, Hughes MR. Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification. Nat Genet. 1994 Jan; 6(1):19-23. PMID: 8136827.
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    103. Van den Veyver IB, Macha ME, McCaskill C, Carpenter RJ, Shaffer LG. Prenatal diagnosis and clinical findings in a case of hexasomy 12p. Am J Med Genet. 1993 Dec 01; 47(8):1171-4. PMID: 8291550.
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    104. Van den Veyver IB, Moise KJ, Ou CN, Carpenter RJ. The 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. PMID: 8377971.
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    105. Van den Veyver IB, Moise KJ. Prostaglandin synthetase inhibitors in pregnancy. Obstet Gynecol Surv. 1993 Jul; 48(7):493-502. PMID: 8355924.
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    106. Van den Veyver IB, Schatteman E, Vanderheyden JS, Van Wiemeersch J, Meulyzer P. Antenatal 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. PMID: 1988328.
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    107. Van den Veyver I, Vanderheyden J, Krauss E, Jankie S. Aseptic 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. PMID: 2365122.
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    108. van Dam PA, Van Goethem ML, Kersschot E, Vervliet J, Van den Veyver IB, De Schepper A, Buytaert P. Palpable solid breast masses: retrospective single- and multimodality evaluation of 201 lesions. Radiology. 1988 Feb; 166(2):435-9. PMID: 3275983.
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    109. Gerris J, Van Nueten J, Van Camp C, Gentens P, Van de Vijver I, Van Camp K. Clinical 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. PMID: 3338608.
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