STEPHANIESHERMANSTEPHANIE SHERMAN10953SHERMAN, STEPHANIEAssociate Professorplugins:TwitterTwitterprns:awardConferredByaward conferred byprns:coAuthorOfcoauthor ofprns:endDateend dateFaculty Rankprns:fullNamefull nameprns: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:pluginSearchableDataProfilesRNS Plugin Searchable Dataprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:similarTosimilar toprns:sortOrdersort orderprns:startDatestart dateprns:trainingAtOrganizationeducational organizationprns:trainingLocationtraining locationprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:addressStatestate or provincevivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipvivo:awardOrHonorawards and honorsAward or Honor Receiptvivo:degreeEarneddegree earnedDepartmentDivisionvivo:educationalTrainingeducation and trainingEducational Trainingvivo:hasResearchArearesearch areasvivo:hrJobTitleHR job titleInformation Resourcevivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressvivo:majorFieldmajor field of degreevivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonZAVENSARGSYANZAVEN SARGSYAN8299SARGSYAN, ZAVENAssociate Professor1504 TAUB LOOPHouston, 77030TX8.474160.0052188240research areas1.175530.055016814coauthor of115.2448.6682260similar to1174selected publications74Professor10Assistant Professor14Associate Professor6Adjunct ProfessorMedicine-Epidemiology & Populat SciCHRISAMOSCHRIS AMOS13498AMOS, CHRISProfessortrue1Associate ProfessorAssociate Professortrue1ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessortrue1ProfessorProfessorD051860Chemicals & Drugs341260.914115Fragile X Mental Retardation ProteinD005600Disorders311500.883693Fragile X SyndromeD004314Disorders1412230.795523Down SyndromeD002891Anatomy571040.934833Chromosomes, Human, Pair 21D009630DisordersPhysiology8170.986827Nondisjunction, GeneticDepartment of MedicineDepartment of NeurologyDepartment of PediatricsDepartment of Molecular & Human GeneticsMedicine-Athero & LipoproteinsMedicine-CardiologyMedicine-General Med/Ben TaubMedicine-General MedicineMolecular & Human GeneticsNeurologyPediatrics-Academic GeneralBaylor College of MedicineARUNIMAMISRAARUNIMA MISRA29.70508570000000-95.40180870000000132MISRA, ARUNIMAAssociate ProfessorTERITURNERTERI TURNER0.000000000000000.000000000000001963TURNER, TERIProfessorJOSEPHJANKOVICJOSEPH JANKOVIC0.000000000000000.000000000000002398JANKOVIC, JOSEPHProfessorERICBOERWINKLEERIC BOERWINKLE0.000000000000000.000000000000002653BOERWINKLE, ERICAdjunct ProfessorJAMESLUPSKIJAMES LUPSKI29.71073630000000-95.396604500000003140LUPSKI, JAMESProfessorDAVIDNELSONDAVID NELSON29.71073630000000-95.396604500000003130NELSON, DAVIDProfessortrue1ProfessorProfessorJONATHANLIMJONATHAN LIM14704LIM, JONATHANAssistant Professortrue1Adjunct ProfessorAdjunct ProfessorAuthorship 9810045Authorship 9810945Authorship 9811929Authorship 98131011Authorship 9814391Authorship 98162810Authorship 9816409Authorship 9817746Authorship 9818726Authorship 98216612Authorship 98255910Authorship 98258213Authorship 98276212Authorship 98388811Authorship 98414214Authorship 9849121211992259Sullivan AK, Crawford DC, Scott EH, Leslie ML, Sherman SLAmerican journal of human geneticsPaternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range. Am J Hum Genet. 2002 Jun; 70(6):1532-44.Am J Hum Genet2002-05-03T00:00:002002Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range.15551222Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SLAmerican journal of human geneticsAssociation between maternal age and meiotic recombination for trisomy 21. Am J Hum Genet. 2005 Jan; 76(1):91-9.Am J Hum Genet2004-11-18T00:00:002004Association between maternal age and meiotic recombination for trisomy 21.15389927Kerstann KF, Feingold E, Freeman SB, Bean LJ, Pyatt R, Tinker S, Jewel AH, Capone G, Sherman SLGenetic epidemiologyLinkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome. Genet Epidemiol. 2004 Nov; 27(3):240-51.Genet Epidemiol2004-11-01T00:00:002004Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome.17236610Freeman SB, Allen EG, Oxford-Wright CL, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SLPublic health reports (Washington, D.C. : 1974)The National Down Syndrome Project: design and implementation. Public Health Rep. 2007 Jan-Feb; 122(1):62-72.Public Health Rep2007-01-01T00:00:002007The National Down Syndrome Project: design and implementation.17910090Sherman SL, Allen EG, Bean LH, Freeman SBMental retardation and developmental disabilities research reviewsEpidemiology of Down syndrome. Ment Retard Dev Disabil Res Rev. 2007; 13(3):221-7.Ment Retard Dev Disabil Res Rev2007-01-01T00:00:002007Epidemiology of Down syndrome.18357616Hunter JE, Epstein MP, Tinker SW, Charen KH, Sherman SLGenetic epidemiologyFragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. Genet Epidemiol. 2008 Sep; 32(6):553-9.Genet Epidemiol2008-09-01T00:00:002008Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.19050929Allen EG, Freeman SB, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SLHuman geneticsMaternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects. Hum Genet. 2009 Feb; 125(1):41-52.Hum Genet2008-12-03T00:00:002008Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects.19026394Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SLAmerican journal of human geneticsNo evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50. Am J Hum Genet. 2008 Dec; 83(6):692-702.Am J Hum Genet2008-11-20T00:00:002008No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50.19804849Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren STAmerican journal of human geneticsIncidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet. 2009 Oct; 85(4):503-14.Am J Hum Genet2009-10-01T00:00:002009Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.19606484Oliver TR, Bhise A, Feingold E, Tinker S, Masse N, Sherman SLAmerican journal of medical genetics. Part AInvestigation of factors associated with paternal nondisjunction of chromosome 21. Am J Med Genet A. 2009 Aug; 149A(8):1685-90.Am J Med Genet A2009-08-01T00:00:002009Investigation of factors associated with paternal nondisjunction of chromosome 21.20718043Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG, Freeman SB, Torfs CP, Cua CL, Epstein MP, Wu MC, Lin X, Capone G, Sherman SL, Bean LJGenetic epidemiologyVariation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genet Epidemiol. 2010 Sep; 34(6):613-23.Genet Epidemiol2010-09-01T00:00:002010Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.22160426Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SLHuman geneticsAltered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Hum Genet. 2012 Jul; 131(7):1039-46.Hum Genet2011-12-09T00:00:002011Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.23558253Hunter JE, Allen EG, Shin M, Bean LJ, Correa A, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SLGenetics in medicine : official journal of the American College of Medical GeneticsThe association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project. Genet Med. 2013 Sep; 15(9):698-705.Genet Med2013-04-04T00:00:002013The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project.23401135Hollis ND, Allen EG, Oliver TR, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Freeman SB, Sherman SL, Bean LJAmerican journal of medical genetics. Part APreconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project. Am J Med Genet A. 2013 Mar; 161A(3):438-44.Am J Med Genet A2013-02-07T00:00:002013Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: a report from the National Down Syndrome Project.24014426Middlebrooks CD, Mukhopadhyay N, Tinker SW, Allen EG, Bean LJ, Begum F, Chowdhury R, Cheung V, Doheny K, Adams M, Feingold E, Sherman SLHuman molecular geneticsEvidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Hum Mol Genet. 2014 Jan 15; 23(2):408-17.Hum Mol Genet2013-09-06T00:00:002013Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.24926858Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SLPloS oneAn examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. PLoS One. 2014; 9(6):e99560.PLoS One2014-06-13T00:00:002014An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.29141989Rambo-Martin BL, Mulle JG, Cutler DJ, Bean LJH, Rosser TC, Dooley KJ, Cua C, Capone G, Maslen CL, Reeves RH, Sherman SL, Zwick MEG3 (Bethesda, Md.)Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda). 2018 01 04; 8(1):105-111.G3 (Bethesda)2018-01-04T00:00:002018Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.Authorship 986891631519426Keen C, Hunter JE, Allen EG, Rocheleau C, Waters M, Sherman SLInternational journal of hygiene and environmental healthThe association between maternal occupation and down syndrome: A report from the national Down syndrome project. Int J Hyg Environ Health. 2020 01; 223(1):207-213.Int J Hyg Environ Health2019-09-10T00:00:002019The association between maternal occupation and down syndrome: A report from the national Down syndrome project.true1Assistant ProfessorAssistant ProfessorALECREZIGHALEC REZIGH15997REZIGH, ALECAssistant Professor33093519Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, Goldmuntz E, Gruber PJ, O'Brien JE, Bittel DC, Wadhwa L, Cua CL, Moskowitz IP, Mulle JG, Epstein MP, Sherman SL, Zwick MEScientific reportsIdentifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Sci Rep. 2020 10 22; 10(1):18051.Sci Rep2020-10-22T00:00:002020Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.33100530Sherman S, Kumar S, Lim J, Sargsyan Z, Ratan B, Turner TProceedings (Baylor University. Medical Center)Measuring teacher identity during the transition from medical school to residency. Proc (Bayl Univ Med Cent). 2020 Jul 23; 33(4):566-571.Proc (Bayl Univ Med Cent)2020-07-23T00:00:002020Measuring teacher identity during the transition from medical school to residency.33456146Oakman N, Lim J, Bui C, Kaplan H, Sherman SProceedings (Baylor University. Medical Center)When patients die: patient memorials and group reflection in an internal medicine residency program. Proc (Bayl Univ Med Cent). 2020 Sep 28; 34(1):56-58.Proc (Bayl Univ Med Cent)2020-09-28T00:00:002020When patients die: patient memorials and group reflection in an internal medicine residency program.true1Assistant ProfessorAssistant ProfessorAuthorship 10223241Authorship 10223255Authorship 1022326Authorship 1022327Authorship 1022328Authorship 1022329Authorship 102233005/2005Harvard CollegeCambridge, MAHarvard College, History of ScienceABHistory of Science05/2011University of Michigan Medical SchoolAnn Arbor, MIUniversity of Michigan Medical School, MedicineMDMedicine06/2014Massachussetts General HospitalBoston, MAMassachussetts General Hospital, Internal Medicine ResidencyInternal Medicine ResidencyBaylor College of Medicine2021John P. McGovern Outstanding Teacher Award - Clinical TeachingBaylor College of Medicine20212018Graduating Class Teaching AwardBaylor College of Medicine2021Women of Excellence AwardBaylor College of Medicine IM Residency2019Baylor Housestaff Teaching Faculty Award - VA HospitalBaylor College of Medicine2019White Coat Ceremony SpeakerBaylor College of Medicine2018Early Career Faculty Award for Excellence in Patient CareBaylor College of Medicine IM Residency2018Baylor Housestaff Teaching Faculty Award - Ben Taub HospitalBaylor College of Medicine2018Internal Medicine Core Clerkship Best Teaching AttendingBaylor College of Medicine IM Residency2017Baylor Housestaff Teaching Faculty Award - Ben Taub HospitalBaylor College of Medicine2017Internal Medicine Core Clerkship Best Teaching AttendingBen Taub General Hospital2015Harris Health Hero AwardTwitter Tweets Harvard TweetsStephanie V. Sherman MD, Zaven Sargsyan MD, Krishna Sajja MD, Lubna Khawaja MD, Priti Dangayach MDACP HospitalistCases from Baylor College of Medicine. ACP Hospitalist. 2017.2017-01-16T00:00:002017Cases from Baylor College of MedicineAmulya Nagarur MD, Janae Heath MD, Michael Roberts MD, Stephanie Sherman MD, Adam Lurie MD, Emily Hughes MDACP HospitalistCases from Massachusetts General Hospital. ACP Hospitalist. 2015.2015-05-01T00:00:002015Cases from Massachusetts General HospitalSherman S.Cerebellar Degeneration.In: Miller C, ed. Clinical Decision Support: Hospital Medicine. Decision Support in Medicine. Cerebellar Degeneration. 2016.2016-06-01T00:00:002016In: Miller C, ed. Clinical Decision Support: Hospital Medicine. Decision Support in MedicineSherman S.Eosinophilic Pneumonia.In: Miller C, ed. Clinical Decision Support: Hospital Medicine. Decision Support in Medicine. Eosinophilic Pneumonia. 2016.2016-06-01T00:00:002016In: Miller C, ed. Clinical Decision Support: Hospital Medicine. Decision Support in MedicineSherman S, Chong C.Anemia.In: Kiefer MM, Chong CR, eds. Pocket Primary Care: A Massachusetts General Hospital Handbook. Anemia. 2014.2014-06-01T00:00:002014In: Kiefer MM, Chong CR, eds. Pocket Primary Care: A Massachusetts General Hospital Handbook34285246Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, Goldmuntz E, Gruber PJ, O'Brien JE, Bittel DC, Wadhwa L, Cua CL, Moskowitz IP, Mulle JG, Epstein MP, Sherman SL, Zwick MEScientific reportsAuthor Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Sci Rep. 2021 Jul 20; 11(1):15164.Sci Rep2021-07-20T00:00:002021Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.35617426Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, Juncos J, Nelson DL, Epstein MP, Cutler DJ, Todd PK, Sherman SL, Warren ST, Jin PProceedings of the National Academy of Sciences of the United States of AmericaIdentification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proc Natl Acad Sci U S A. 2022 05 31; 119(22):e2118124119.Proc Natl Acad Sci U S A2022-05-26T00:00:002022Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.34658954Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Hunter JE, Shelly KE, Sherman SLFrontiers in psychiatryPredictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation. Front Psychiatry. 2021; 12:715922.Front Psychiatry2021-10-01T00:00:002021Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation.33927378Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Nolin SL, Glicksman A, Tortora N, McKinnon B, Shelly KE, Sherman SLGenetics in medicine : official journal of the American College of Medical GeneticsRefining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size. Genet Med. 2021 09; 23(9):1648-1655.Genet Med2021-04-29T00:00:002021Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size.Authorship 1060420536451344Rezigh AB, Rezigh A, Kanjee Z, Sargsyan Z, Sherman S, Kumfer AMJournal of hospital medicineOutside looking in. J Hosp Med. 2023 07; 18(7):633-637.J Hosp Med2022-11-30T00:00:002022Outside looking in.36209076Kusnoor AV, Balchandani R, Pillow MT, Sherman S, Ismail NBMC medical educationNear-peers effectively teach clinical documentation skills to early medical students. BMC Med Educ. 2022 Oct 08; 22(1):712.BMC Med Educ2022-10-08T00:00:002022Near-peers effectively teach clinical documentation skills to early medical students.36739110Harrison D, Misra A, Pahwa A, Muradali K, Sherman SJournal of hospital medicineThings We Do for No Reason?: Routinely obtaining repeat transthoracic echocardiography for acute decompensation of known chronic heart failure. J Hosp Med. 2023 10; 18(10):934-937.J Hosp Med2023-02-04T00:00:002023Things We Do for No Reason?: Routinely obtaining repeat transthoracic echocardiography for acute decompensation of known chronic heart failure.Authorship 1063895236773818Sargsyan Z, Sherman SJournal of the American Society of Echocardiography : official publication of the American Society of EchocardiographyUpright Positioning to Maintain Quantitative Measurement of Higher Right Atrial Pressures. J Am Soc Echocardiogr. 2023 05; 36(5):565-566.J Am Soc Echocardiogr2023-02-10T00:00:002023Upright Positioning to Maintain Quantitative Measurement of Higher Right Atrial Pressures.true1Associate ProfessorAssociate ProfessorAuthorship 10714645Authorship 10714653Authorship 10714664Authorship 10714675Authorship 1071468435535933Thapi S, Tsega S, Zhao C, Olson APJ, Sherman SVJournal of hospital medicineDyspneic and dizzy. J Hosp Med. 2022 08; 17(8):657-660.J Hosp Med2022-03-30T00:00:002022Dyspneic and dizzy.35075534Phadke VK, Jagannath AD, Patel AA, Sherman SVJournal of general internal medicineOver the Threshold: an Exercise in Clinical Reasoning. J Gen Intern Med. 2022 04; 37(5):1290-1294.J Gen Intern Med2022-01-24T00:00:002022Over the Threshold: an Exercise in Clinical Reasoning.36649839Rendon DR, Shiau J, Sherman SVThe American journal of medicineLobar Pneumonia Presenting as Fever, Headaches, and a Negative Chest Radiograph. Am J Med. 2023 04; 136(4):e65-e66.Am J Med2023-01-14T00:00:002023Lobar Pneumonia Presenting as Fever, Headaches, and a Negative Chest Radiograph.Authorship 10718979Authorship 10718056Authorship 10717895Authorship 107184012Authorship 107181010Authorship 107189011Authorship 10718311Authorship 10719163Authorship 107192710Authorship 10718776Authorship 10718715Authorship 10719258Authorship 107189321Authorship 10717849Authorship 10718664Authorship 10718943Authorship 10719135Authorship 10718554Authorship 10718703Authorship 10718814Authorship 10719395Authorship 10718183Authorship 10718575Authorship 10718654Authorship 10719184Authorship 10718457Authorship 10718158Authorship 107180225Authorship 10718632Authorship 10718285Authorship 10719243Authorship 10718531Authorship 10718305Authorship 107182023Authorship 10719104Authorship 10718276Authorship 100336725Authorship 107194012Authorship 10718485Authorship 10718522Authorship 10719238Authorship 107179321Authorship 10719361430123240Allen EG, Glicksman A, Tortora N, Charen K, He W, Amin A, Hipp H, Shubeck L, Nolin SL, Sherman SLFrontiers in geneticsFXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation. Front Genet. 2018; 9:292.Front Genet2018-08-03T00:00:002018FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation.35455279H?ls A, Feany PT, Zisman SI, Costa ACS, Dierssen M, Balogh R, Bargagna S, Baumer NT, Brand?o AC, Carfi A, Chicoine BA, Ghosh S, Lakhanpaul M, Levin J, Lunsky Y, Manso C, Okun E, Real de Asua D, Rebillat AS, Rohrer TR, Sgandurra G, Valentini D, Sherman SL, Strydom AVaccinesCOVID-19 Vaccination of Individuals with Down Syndrome-Data from the Trisomy 21 Research Society Survey on Safety, Efficacy, and Factors Associated with the Decision to Be Vaccinated. Vaccines (Basel). 2022 Mar 29; 10(4).Vaccines (Basel)2022-03-29T00:00:002022COVID-19 Vaccination of Individuals with Down Syndrome-Data from the Trisomy 21 Research Society Survey on Safety, Efficacy, and Factors Associated with the Decision to Be Vaccinated.26174939Espinel W, Charen K, Huddleston L, Visootsak J, Sherman SJournal of genetic counselingImproving Health Education for Women Who Carry an FMR1 Premutation. J Genet Couns. 2016 Apr; 25(2):228-38.J Genet Couns2015-07-16T00:00:002015Improving Health Education for Women Who Carry an FMR1 Premutation.25147555Allen EG, Grus WE, Narayan S, Espinel W, Sherman SLFrontiers in geneticsApproaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary study. Front Genet. 2014; 5:260.Front Genet2014-08-07T00:00:002014Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary study.33220219Sherman SL, Rao DC, Keats BJ, Yee S, Spence MA, Hassold TJ, Chakravarti A, Elston RC, Crolla JA, Ennis S, Risch NAmerican journal of human geneticsNewton E. Morton (1929-2018). Am J Hum Genet. 2018 Jun 07; 102(6):1011-1017.Am J Hum Genet2018-06-07T00:00:002018Newton E. Morton (1929-2018).22251309Hunter JE, Sherman S, Grigsby J, Kogan C, Cornish KNeuropsychologyCapturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology. 2012 Mar; 26(2):156-64.Neuropsychology2012-01-16T00:00:002012Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts.19927162Peprah E, He W, Allen E, Oliver T, Boyne A, Sherman SLJournal of human geneticsExamination of FMR1 transcript and protein levels among 74 premutation carriers. J Hum Genet. 2010 Jan; 55(1):66-8.J Hum Genet2009-11-20T00:00:002009Examination of FMR1 transcript and protein levels among 74 premutation carriers.31118158Gilbertson KE, Jackson HL, Dziuban EJ, Sherman SL, Berry-Kravis EM, Erickson CA, Valdez RDisability and health journalPreventive care services and health behaviors in children with fragile X syndrome. Disabil Health J. 2019 10; 12(4):564-573.Disabil Health J2019-05-03T00:00:002019Preventive care services and health behaviors in children with fragile X syndrome.28759762Fischer ST, Lili LN, Li S, Tran VT, Stewart KB, Schwartz CE, Jones DP, Sherman SL, Fridovich-Keil JLEnvironment internationalLow-level maternal exposure to nicotine associates with significant metabolic perturbations in second-trimester amniotic fluid. Environ Int. 2017 10; 107:227-234.Environ Int2017-07-30T00:00:002017Low-level maternal exposure to nicotine associates with significant metabolic perturbations in second-trimester amniotic fluid.35852003Albizua I, Charen K, Shubeck L, Talboy A, Berry-Kravis E, Kaufmann WE, Stallworth JL, Drazba KT, Erickson CA, Sweeney JA, Tartaglia N, Warren SF, Hagerman R, Sherman SL, Warren ST, Jin P, Allen EGMolecular genetics & genomic medicineDescriptive analysis of seizures and comorbidities associated with fragile X syndrome. Mol Genet Genomic Med. 2022 08; 10(8):e2001.Mol Genet Genomic Med2022-07-18T00:00:002022Descriptive analysis of seizures and comorbidities associated with fragile X syndrome.22573456Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SLAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric GeneticsDepression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms. Am J Med Genet B Neuropsychiatr Genet. 2012 Jul; 159B(5):549-59.Am J Med Genet B Neuropsychiatr Genet2012-05-09T00:00:002012Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.15971024Allen EG, Sherman S, Abramowitz A, Leslie M, Novak G, Rusin M, Scott E, Letz RBehavior geneticsExamination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance. Behav Genet. 2005 Jul; 35(4):435-45.Behav Genet2005-07-01T00:00:002005Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance.16047092Anido A, Carlson LM, Taft L, Sherman SLJournal of genetic counselingWomen's attitudes toward testing for fragile X carrier status: a qualitative analysis. J Genet Couns. 2005 Aug; 14(4):295-306.J Genet Couns2005-08-01T00:00:002005Women's attitudes toward testing for fragile X carrier status: a qualitative analysis.31813999Albizua I, Chopra P, Sherman SL, Gambello MJ, Warren STHuman molecular geneticsAnalysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes. Hum Mol Genet. 2020 01 15; 29(2):238-247.Hum Mol Genet2020-01-15T00:00:002020Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes.23079771Juncos JL, Lazarus JT, Rohr J, Allen EG, Shubeck L, Hamilton D, Novak G, Sherman SLMovement disorders : official journal of the Movement Disorder SocietyOlfactory dysfunction in fragile X tremor ataxia syndrome. Mov Disord. 2012 Oct; 27(12):1556-9.Mov Disord2012-09-24T00:00:002012Olfactory dysfunction in fragile X tremor ataxia syndrome.17295053Anido A, Carlson LM, Sherman SLJournal of genetic counselingAttitudes toward fragile X mutation carrier testing from women identified in a general population survey. J Genet Couns. 2007 Feb; 16(1):97-104.J Genet Couns2007-02-13T00:00:002007Attitudes toward fragile X mutation carrier testing from women identified in a general population survey.25147583Sherman SL, Curnow EC, Easley CA, Jin P, Hukema RK, Tejada MI, Willemsen R, Usdin KJournal of neurodevelopmental disordersUse of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI). J Neurodev Disord. 2014; 6(1):26.J Neurodev Disord2014-08-13T00:00:002014Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI).22134579Visootsak J, Charen K, Rohr J, Allen E, Sherman SJournal of genetic counselingDiagnosis of fragile X syndrome: a qualitative study of African American families. J Genet Couns. 2012 Dec; 21(6):845-53.J Genet Couns2011-12-02T00:00:002011Diagnosis of fragile X syndrome: a qualitative study of African American families.28536925Reines V, Charen K, Rosser T, Eisen A, Sherman SL, Visootsak JJournal of genetic counselingParental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome. J Genet Couns. 2017 Dec; 26(6):1333-1340.J Genet Couns2017-05-24T00:00:002017Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome.20436936Epstein MP, Hunter JE, Allen EG, Sherman SL, Lin X, Boehnke MStatistics in biosciencesA Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes. Stat Biosci. 2009 Nov; 1(2):181-198.Stat Biosci2009-11-01T00:00:002009A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes.12116230Crawford DC, Meadows KL, Newman JL, Taft LF, Scott E, Leslie M, Shubek L, Holmgreen P, Yeargin-Allsopp M, Boyle C, Sherman SLAmerican journal of medical geneticsPrevalence of the fragile X syndrome in African-Americans. Am J Med Genet. 2002 Jul 01; 110(3):226-33.Am J Med Genet2002-07-01T00:00:002002Prevalence of the fragile X syndrome in African-Americans.33644721H?ls A, Costa ACS, Dierssen M, Baksh RA, Bargagna S, Baumer NT, Brand?o AC, Carfi A, Carmona-Iragui M, Chicoine BA, Ghosh S, Lakhanpaul M, Manso C, Mayer MA, Ortega MDC, de Asua DR, Rebillat AS, Russell LA, Sgandurra G, Valentini D, Sherman SL, Strydom A, T21RS COVID-19 InitiativeEClinicalMedicineMedical vulnerability of individuals with Down syndrome to severe COVID-19-data from the Trisomy 21 Research Society and the UK ISARIC4C survey. EClinicalMedicine. 2021 Mar; 33:100769.EClinicalMedicine2021-02-22T00:00:002021Medical vulnerability of individuals with Down syndrome to severe COVID-19-data from the Trisomy 21 Research Society and the UK ISARIC4C survey.21279400Juncos JL, Lazarus JT, Graves-Allen E, Shubeck L, Rusin M, Novak G, Hamilton D, Rohr J, Sherman SLNeurogeneticsNew clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS). Neurogenetics. 2011 May; 12(2):123-35.Neurogenetics2011-01-29T00:00:002011New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS).20597902Peprah EK, Allen EG, Williams SM, Woodard LM, Sherman SLAnnals of human geneticsGenetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population. Ann Hum Genet. 2010 Jul; 74(4):316-25.Ann Hum Genet2010-07-01T00:00:002010Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.14758538Allen EG, He W, Yadav-Shah M, Sherman SLHuman geneticsA study of the distributional characteristics of FMR1 transcript levels in 238 individuals. Hum Genet. 2004 Apr; 114(5):439-47.Hum Genet2004-02-03T00:00:002004A study of the distributional characteristics of FMR1 transcript levels in 238 individuals.27552334Hipp HS, Charen KH, Spencer JB, Allen EG, Sherman SLMenopause (New York, N.Y.)Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI). Menopause. 2016 09; 23(9):993-9.Menopause2016-09-01T00:00:002016Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).32533363Albizua I, Chopra P, Allen EG, He W, Amin AS, Sherman SLHuman geneticsStudy of telomere length in men who carry a fragile X premutation or full mutation allele. Hum Genet. 2020 Dec; 139(12):1531-1539.Hum Genet2020-06-12T00:00:002020Study of telomere length in men who carry a fragile X premutation or full mutation allele.33575620Guo Z, Cui Y, Shi X, Birchler JA, Albizua I, Sherman SL, Qin ZS, Ji TNAR genomics and bioinformaticsAn empirical bayesian approach for testing gene expression fold change and its application in detecting global dosage effects. NAR Genom Bioinform. 2020 Sep; 2(3):lqaa072.NAR Genom Bioinform2020-09-18T00:00:002020An empirical bayesian approach for testing gene expression fold change and its application in detecting global dosage effects.22101959Hunter JE, Epstein MP, Tinker SW, Abramowitz A, Sherman SLBehavior geneticsThe FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance. Behav Genet. 2012 May; 42(3):415-22.Behav Genet2011-11-19T00:00:002011The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance.17903885Hertzberg VS, Stern BJ, Sherman SJournal of stroke and cerebrovascular diseases : the official journal of National Stroke AssociationAnalytic strategies for stroke genetics. J Stroke Cerebrovasc Dis. 2002 Sep-Oct; 11(5):272-8.J Stroke Cerebrovasc Dis2002-09-01T00:00:002002Analytic strategies for stroke genetics.31896764Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Hunter JE, Sherman SLGenetics in medicine : official journal of the American College of Medical GeneticsClustering of comorbid conditions among women who carry an FMR1 premutation. Genet Med. 2020 04; 22(4):758-766.Genet Med2020-01-03T00:00:002020Clustering of comorbid conditions among women who carry an FMR1 premutation.33788978Walsh MB, Charen K, Shubeck L, McConkie-Rosell A, Ali N, Bellcross C, Sherman SLJournal of genetic counselingMen with an FMR1 premutation and their health education needs. J Genet Couns. 2021 08; 30(4):1156-1167.J Genet Couns2021-03-31T00:00:002021Men with an FMR1 premutation and their health education needs.19265746Hunter JE, Abramowitz A, Rusin M, Sherman SLGenetics in medicine : official journal of the American College of Medical GeneticsIs there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature. Genet Med. 2009 Feb; 11(2):79-89.Genet Med2009-02-01T00:00:002009Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature.36447079Poteet B, Ali N, Bellcross C, Sherman SL, Espinel W, Hipp H, Allen EGJournal of assisted reproduction and geneticsThe diagnostic experience of women with fragile X-associated primary ovarian insufficiency (FXPOI). J Assist Reprod Genet. 2023 Jan; 40(1):179-190.J Assist Reprod Genet2022-11-30T00:00:002022The diagnostic experience of women with fragile X-associated primary ovarian insufficiency (FXPOI).15878919Small CM, Marcus M, Sherman SL, Sullivan AK, Manatunga AK, Feigelson HSHuman reproduction (Oxford, England)CYP17 genotype predicts serum hormone levels among pre-menopausal women. Hum Reprod. 2005 Aug; 20(8):2162-7.Hum Reprod2005-05-05T00:00:002005CYP17 genotype predicts serum hormone levels among pre-menopausal women.18574214De Caro JJ, Dominguez C, Sherman SLAnnals of the New York Academy of SciencesReproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency. Ann N Y Acad Sci. 2008; 1135:99-111.Ann N Y Acad Sci2008-01-01T00:00:002008Reproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency.18535897Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SLBehavior geneticsInvestigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers. Behav Genet. 2008 Sep; 38(5):493-502.Behav Genet2008-06-06T00:00:002008Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers.true1Associate ProfessorAssociate Professor