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STEPHANIE SHERMAN

TitleAssociate Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Medicine
Address1504 TAUB LOOP
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    Collapse Biography 
    Collapse education and training
    Harvard College, Cambridge, MAAB05/2005History of Science
    University of Michigan Medical School, Ann Arbor, MIMD05/2011Medicine
    Massachussetts General Hospital, Boston, MA06/2014Internal Medicine Residency
    Collapse awards and honors
    2021John P. McGovern Outstanding Teacher Award - Clinical Teaching, Baylor College of Medicine
    2018 - 2021Graduating Class Teaching Award, Baylor College of Medicine
    2021Women of Excellence Award, Baylor College of Medicine
    2019Baylor Housestaff Teaching Faculty Award - VA Hospital, Baylor College of Medicine IM Residency
    2019White Coat Ceremony Speaker, Baylor College of Medicine
    2018Early Career Faculty Award for Excellence in Patient Care, Baylor College of Medicine
    2018Baylor Housestaff Teaching Faculty Award - Ben Taub Hospital, Baylor College of Medicine IM Residency
    2018Internal Medicine Core Clerkship Best Teaching Attending, Baylor College of Medicine
    2017Baylor Housestaff Teaching Faculty Award - Ben Taub Hospital, Baylor College of Medicine IM Residency
    2017Internal Medicine Core Clerkship Best Teaching Attending, Baylor College of Medicine
    2015Harris Health Hero Award, Ben Taub General Hospital

    Collapse Featured Content 
    Collapse Twitter

    Collapse Bibliographic 
    Collapse selected publications
    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.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Feldman ER, Li Y, Cutler DJ, Rosser TC, Wechsler SB, Sanclemente L, Rachubinski AL, Elliott N, Vyas P, Roberts I, Rabin KR, Wagner M, Gelb BD, Espinosa JM, Lupo PJ, de Smith AJ, Sherman SL, Leslie-Clarkson EJ. Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS. Genet Epidemiol. 2025 Jun; 49(4):e70010. PMID: 40407036.
      Citations:    Fields:    
    2. Feldman ER, Li Y, Cutler DJ, Rosser TC, Wechsler SB, Sanclemente L, Rachubinski AL, Elliott N, Vyas P, Roberts I, Rabin KR, Wagner M, Gelb BD, Espinosa JM, Lupo PJ, de Smith AJ, Sherman SL, Leslie EJ. Genome-wide association studies of Down syndrome associated congenital heart defects. medRxiv. 2024 Sep 06. PMID: 39281767; PMCID: PMC11398599.
      Citations:    
    3. Jamison T, Sargsyan Z, Ayyala U, Sherman S, Kaplan H. A Mini Chalk Talk Workshop for Fourth-Year Medical Students: Facilitating the Transition From Student to Resident Educator. MedEdPORTAL. 2024; 20:11404. PMID: 38957529; PMCID: PMC11219125.
      Citations:    Fields:    Translation:Humans
    4. Sargsyan Z, Sherman S. Upright Positioning to Maintain Quantitative Measurement of Higher Right Atrial Pressures. J Am Soc Echocardiogr. 2023 05; 36(5):565-566. PMID: 36773818.
      Citations:    Fields:    Translation:Humans
    5. Harrison D, Pahwa A, Muradali K, Misra A, Sherman S. Things 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. PMID: 36739110.
      Citations:    Fields:    
    6. Rendon DR, Shiau J, Sherman SV. Lobar Pneumonia Presenting as Fever, Headaches, and a Negative Chest Radiograph. Am J Med. 2023 04; 136(4):e65-e66. PMID: 36649839.
      Citations: 1     Fields:    Translation:Humans
    7. Rezigh AB, Rezigh A, Kanjee Z, Sargsyan Z, Sherman S, Kumfer AM. Outside looking in. J Hosp Med. 2023 07; 18(7):633-637. PMID: 36451344.
      Citations:    Fields:    
    8. Poteet B, Ali N, Bellcross C, Sherman SL, Espinel W, Hipp H, Allen EG. The diagnostic experience of women with fragile X-associated primary ovarian insufficiency (FXPOI). J Assist Reprod Genet. 2023 Jan; 40(1):179-190. PMID: 36447079; PMCID: PMC9840735.
      Citations:    Fields:    
    9. Kusnoor AV, Balchandani R, Pillow MT, Sherman S, Ismail N. Near-peers effectively teach clinical documentation skills to early medical students. BMC Med Educ. 2022 Oct 08; 22(1):712. PMID: 36209076; PMCID: PMC9548193.
      Citations:    Fields:    Translation:Humans
    10. Albizua 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 EG. Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Mol Genet Genomic Med. 2022 08; 10(8):e2001. PMID: 35852003; PMCID: PMC9356544.
      Citations:    
    11. Kong 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 P. Identification 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. PMID: 35617426; PMCID: PMC9295734.
      Citations:    Fields:    Translation:HumansAnimals
    12. Thapi S, Tsega S, Zhao C, Olson APJ, Sherman SV. Dyspneic and dizzy. J Hosp Med. 2022 08; 17(8):657-660. PMID: 35535933.
      Citations:    
    13. H?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 A. COVID-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). PMID: 35455279; PMCID: PMC9030605.
      Citations:    
    14. Phadke VK, Jagannath AD, Patel AA, Sherman SV. Over the Threshold: an Exercise in Clinical Reasoning. J Gen Intern Med. 2022 04; 37(5):1290-1294. PMID: 35075534; PMCID: PMC8971242.
      Citations:    
    15. Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Hunter JE, Shelly KE, Sherman SL. Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation. Front Psychiatry. 2021; 12:715922. PMID: 34658954; PMCID: PMC8517131.
      Citations:    
    16. Trevino 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 ME. Author 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. PMID: 34285246; PMCID: PMC8292424.
      Citations:    Fields:    
    17. Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Nolin SL, Glicksman A, Tortora N, McKinnon B, Shelly KE, Sherman SL. Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size. Genet Med. 2021 09; 23(9):1648-1655. PMID: 33927378; PMCID: PMC8460441.
      Citations:    
    18. Walsh MB, Charen K, Shubeck L, McConkie-Rosell A, Ali N, Bellcross C, Sherman SL. Men with an FMR1 premutation and their health education needs. J Genet Couns. 2021 08; 30(4):1156-1167. PMID: 33788978; PMCID: PMC8363520.
      Citations:    
    19. H?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 Initiative. Medical 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. PMID: 33644721; PMCID: PMC7897934.
      Citations:    
    20. Trevino 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 ME. Identifying 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. PMID: 33093519; PMCID: PMC7582922.
      Citations: 4     Fields:    Translation:Humans
    21. Oakman N, Lim J, Bui C, Kaplan H, Sherman S. 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. PMID: 33456146; PMCID: PMC7785196.
      Citations:    
    22. Guo Z, Cui Y, Shi X, Birchler JA, Albizua I, Sherman SL, Qin ZS, Ji T. An 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. PMID: 33575620; PMCID: PMC7671412.
      Citations:    
    23. Sherman S, Kumar S, Lim J, Sargsyan Z, Ratan B, Turner T. Measuring teacher identity during the transition from medical school to residency. Proc (Bayl Univ Med Cent). 2020 Jul 23; 33(4):566-571. PMID: 33100530; PMCID: PMC7549982.
      Citations:    
    24. Albizua I, Chopra P, Allen EG, He W, Amin AS, Sherman SL. Study of telomere length in men who carry a fragile X premutation or full mutation allele. Hum Genet. 2020 Dec; 139(12):1531-1539. PMID: 32533363; PMCID: PMC8494119.
      Citations:    
    25. Albizua I, Chopra P, Sherman SL, Gambello MJ, Warren ST. Analysis 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. PMID: 31813999.
      Citations:    
    26. Allen EG, Charen K, Hipp HS, Shubeck L, Amin A, He W, Hunter JE, Sherman SL. Clustering of comorbid conditions among women who carry an FMR1 premutation. Genet Med. 2020 04; 22(4):758-766. PMID: 31896764; PMCID: PMC7118023.
      Citations:    
    27. Keen C, Hunter JE, Allen EG, Rocheleau C, Waters M, Sherman SL. The 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. PMID: 31519426.
      Citations:    Fields:    Translation:HumansCellsPHPublic Health
    28. Gilbertson KE, Jackson HL, Dziuban EJ, Sherman SL, Berry-Kravis EM, Erickson CA, Valdez R. Preventive care services and health behaviors in children with fragile X syndrome. Disabil Health J. 2019 10; 12(4):564-573. PMID: 31118158; PMCID: PMC6778488.
      Citations:    
    29. Allen EG, Glicksman A, Tortora N, Charen K, He W, Amin A, Hipp H, Shubeck L, Nolin SL, Sherman SL. FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation. Front Genet. 2018; 9:292. PMID: 30123240; PMCID: PMC6086008.
      Citations:    
    30. Sherman SL, Rao DC, Keats BJ, Yee S, Spence MA, Hassold TJ, Chakravarti A, Elston RC, Crolla JA, Ennis S, Risch N. Newton E. Morton (1929-2018). Am J Hum Genet. 2018 Jun 07; 102(6):1011-1017. PMID: 33220219; PMCID: PMC8175862.
      Citations:    
    31. Rambo-Martin BL, Mulle JG, Cutler DJ, Bean LJH, Rosser TC, Dooley KJ, Cua C, Capone G, Maslen CL, Reeves RH, Sherman SL, Zwick ME. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda). 2018 01 04; 8(1):105-111. PMID: 29141989; PMCID: PMC5765339.
      Citations: 3     Fields:    Translation:HumansCells
    32. Fischer ST, Lili LN, Li S, Tran VT, Stewart KB, Schwartz CE, Jones DP, Sherman SL, Fridovich-Keil JL. Low-level maternal exposure to nicotine associates with significant metabolic perturbations in second-trimester amniotic fluid. Environ Int. 2017 10; 107:227-234. PMID: 28759762; PMCID: PMC5569895.
      Citations:    
    33. Reines V, Charen K, Rosser T, Eisen A, Sherman SL, Visootsak J. Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome. J Genet Couns. 2017 Dec; 26(6):1333-1340. PMID: 28536925.
      Citations:    
    34. . Cases from Baylor College of Medicine. ACP Hospitalist. 2017. View Publication.
    35. Hipp HS, Charen KH, Spencer JB, Allen EG, Sherman SL. Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI). Menopause. 2016 09; 23(9):993-9. PMID: 27552334; PMCID: PMC4998843.
      Citations:    
    36. SHERMAN S. In: Miller C, ed. Clinical Decision Support: Hospital Medicine. Decision Support in Medicine. Cerebellar Degeneration. 2016. View Publication.
    37. SHERMAN S. In: Miller C, ed. Clinical Decision Support: Hospital Medicine. Decision Support in Medicine. Eosinophilic Pneumonia. 2016. View Publication.
    38. Espinel W, Charen K, Huddleston L, Visootsak J, Sherman S. Improving Health Education for Women Who Carry an FMR1 Premutation. J Genet Couns. 2016 Apr; 25(2):228-38. PMID: 26174939; PMCID: PMC4831205.
      Citations:    
    39. . Cases from Massachusetts General Hospital. ACP Hospitalist. 2015. View Publication.
    40. Sherman SL, Curnow EC, Easley CA, Jin P, Hukema RK, Tejada MI, Willemsen R, Usdin K. Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI). J Neurodev Disord. 2014; 6(1):26. PMID: 25147583; PMCID: PMC4139715.
      Citations:    
    41. Allen EG, Grus WE, Narayan S, Espinel W, Sherman SL. Approaches 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. PMID: 25147555; PMCID: PMC4124461.
      Citations:    
    42. Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL. An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. PLoS One. 2014; 9(6):e99560. PMID: 24926858; PMCID: PMC4057233.
      Citations: 7     Fields:    Translation:HumansCells
    43. SHERMAN S, Chong C. In: Kiefer MM, Chong CR, eds. Pocket Primary Care: A Massachusetts General Hospital Handbook. Anemia. 2014.
    44. Middlebrooks CD, Mukhopadhyay N, Tinker SW, Allen EG, Bean LJ, Begum F, Chowdhury R, Cheung V, Doheny K, Adams M, Feingold E, Sherman SL. Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Hum Mol Genet. 2014 Jan 15; 23(2):408-17. PMID: 24014426; PMCID: PMC3869361.
      Citations: 5     Fields:    Translation:HumansCells
    45. Hunter 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 SL. The 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. PMID: 23558253; PMCID: PMC4122862.
      Citations: 2     Fields:    Translation:HumansCells
    46. Hollis 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 LJ. Preconception 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. PMID: 23401135; PMCID: PMC3607196.
      Citations:    
    47. Juncos JL, Lazarus JT, Rohr J, Allen EG, Shubeck L, Hamilton D, Novak G, Sherman SL. Olfactory dysfunction in fragile X tremor ataxia syndrome. Mov Disord. 2012 Oct; 27(12):1556-9. PMID: 23079771; PMCID: PMC3696490.
      Citations:    
    48. Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SL. Depression 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. PMID: 22573456; PMCID: PMC3696495.
      Citations:    
    49. Hunter JE, Sherman S, Grigsby J, Kogan C, Cornish K. Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology. 2012 Mar; 26(2):156-64. PMID: 22251309; PMCID: PMC3295926.
      Citations:    
    50. Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SL. Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Hum Genet. 2012 Jul; 131(7):1039-46. PMID: 22160426; PMCID: PMC3925977.
      Citations: 15     Fields:    Translation:HumansCells
    51. Visootsak J, Charen K, Rohr J, Allen E, Sherman S. Diagnosis of fragile X syndrome: a qualitative study of African American families. J Genet Couns. 2012 Dec; 21(6):845-53. PMID: 22134579; PMCID: PMC3508319.
      Citations:    
    52. Hunter JE, Epstein MP, Tinker SW, Abramowitz A, Sherman SL. The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance. Behav Genet. 2012 May; 42(3):415-22. PMID: 22101959; PMCID: PMC3696489.
      Citations:    
    53. Juncos JL, Lazarus JT, Graves-Allen E, Shubeck L, Rusin M, Novak G, Hamilton D, Rohr J, Sherman SL. New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS). Neurogenetics. 2011 May; 12(2):123-35. PMID: 21279400; PMCID: PMC3766636.
      Citations:    
    54. Locke 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 LJ. Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genet Epidemiol. 2010 Sep; 34(6):613-23. PMID: 20718043; PMCID: PMC3378053.
      Citations: 30     Fields:    Translation:HumansCells
    55. Peprah EK, Allen EG, Williams SM, Woodard LM, Sherman SL. Genetic 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. PMID: 20597902; PMCID: PMC4149914.
      Citations:    
    56. Peprah E, He W, Allen E, Oliver T, Boyne A, Sherman SL. Examination of FMR1 transcript and protein levels among 74 premutation carriers. J Hum Genet. 2010 Jan; 55(1):66-8. PMID: 19927162; PMCID: PMC4122982.
      Citations:    
    57. Epstein MP, Hunter JE, Allen EG, Sherman SL, Lin X, Boehnke M. A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes. Stat Biosci. 2009 Nov; 1(2):181-198. PMID: 20436936; PMCID: PMC2860148.
      Citations:    
    58. Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren ST. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet. 2009 Oct; 85(4):503-14. PMID: 19804849; PMCID: PMC2756550.
      Citations: 127     Fields:    Translation:HumansCellsPHPublic Health
    59. Oliver TR, Bhise A, Feingold E, Tinker S, Masse N, Sherman SL. Investigation of factors associated with paternal nondisjunction of chromosome 21. Am J Med Genet A. 2009 Aug; 149A(8):1685-90. PMID: 19606484; PMCID: PMC4111419.
      Citations:    
    60. Hunter JE, Abramowitz A, Rusin M, Sherman SL. Is 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. PMID: 19265746; PMCID: PMC2652667.
      Citations:    
    61. Allen EG, Freeman SB, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL. Maternal 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. PMID: 19050929; PMCID: PMC2833410.
      Citations: 31     Fields:    Translation:Humans
    62. Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL. No 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. PMID: 19026394; PMCID: PMC2668066.
      Citations: 37     Fields:    Translation:HumansCells
    63. Hunter JE, Epstein MP, Tinker SW, Charen KH, Sherman SL. Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. Genet Epidemiol. 2008 Sep; 32(6):553-9. PMID: 18357616; PMCID: PMC2881575.
      Citations: 15     Fields:    Translation:HumansCells
    64. Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL. Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers. Behav Genet. 2008 Sep; 38(5):493-502. PMID: 18535897; PMCID: PMC3696488.
      Citations:    
    65. De Caro JJ, Dominguez C, Sherman SL. Reproductive 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. PMID: 18574214.
      Citations:    
    66. Anido A, Carlson LM, Sherman SL. Attitudes toward fragile X mutation carrier testing from women identified in a general population survey. J Genet Couns. 2007 Feb; 16(1):97-104. PMID: 17295053.
      Citations:    
    67. Freeman SB, Allen EG, Oxford-Wright CL, Tinker SW, Druschel C, Hobbs CA, O'Leary LA, Romitti PA, Royle MH, Torfs CP, Sherman SL. The National Down Syndrome Project: design and implementation. Public Health Rep. 2007 Jan-Feb; 122(1):62-72. PMID: 17236610; PMCID: PMC1802119.
      Citations: 27     Fields:    Translation:HumansCells
    68. Sherman SL, Allen EG, Bean LH, Freeman SB. Epidemiology of Down syndrome. Ment Retard Dev Disabil Res Rev. 2007; 13(3):221-7. PMID: 17910090.
      Citations: 71     Fields:    Translation:HumansAnimalsCells
    69. Anido A, Carlson LM, Taft L, Sherman SL. Women's attitudes toward testing for fragile X carrier status: a qualitative analysis. J Genet Couns. 2005 Aug; 14(4):295-306. PMID: 16047092.
      Citations:    
    70. Allen EG, Sherman S, Abramowitz A, Leslie M, Novak G, Rusin M, Scott E, Letz R. Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance. Behav Genet. 2005 Jul; 35(4):435-45. PMID: 15971024.
      Citations:    
    71. Small CM, Marcus M, Sherman SL, Sullivan AK, Manatunga AK, Feigelson HS. CYP17 genotype predicts serum hormone levels among pre-menopausal women. Hum Reprod. 2005 Aug; 20(8):2162-7. PMID: 15878919.
      Citations:    
    72. Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SL. Association between maternal age and meiotic recombination for trisomy 21. Am J Hum Genet. 2005 Jan; 76(1):91-9. PMID: 15551222; PMCID: PMC1196437.
      Citations: 27     Fields:    Translation:HumansCells
    73. Kerstann KF, Feingold E, Freeman SB, Bean LJ, Pyatt R, Tinker S, Jewel AH, Capone G, Sherman SL. Linkage 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. PMID: 15389927.
      Citations: 8     Fields:    Translation:Humans
    74. Allen EG, He W, Yadav-Shah M, Sherman SL. A study of the distributional characteristics of FMR1 transcript levels in 238 individuals. Hum Genet. 2004 Apr; 114(5):439-47. PMID: 14758538.
      Citations: 67     Fields:    Translation:HumansCells
    75. Hertzberg VS, Stern BJ, Sherman S. Analytic strategies for stroke genetics. J Stroke Cerebrovasc Dis. 2002 Sep-Oct; 11(5):272-8. PMID: 17903885.
      Citations:    
    76. Crawford DC, Meadows KL, Newman JL, Taft LF, Scott E, Leslie M, Shubek L, Holmgreen P, Yeargin-Allsopp M, Boyle C, Sherman SL. Prevalence of the fragile X syndrome in African-Americans. Am J Med Genet. 2002 Jul 01; 110(3):226-33. PMID: 12116230.
      Citations: 51     Fields:    Translation:HumansCells
    77. Sullivan AK, Crawford DC, Scott EH, Leslie ML, Sherman SL. Paternally 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. PMID: 11992259; PMCID: PMC379140.
      Citations: 24     Fields:    Translation:HumansCells
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