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STEPHANIE SHERMAN

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Medicine
DivisionMedicine-General Med/Ben Taub
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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. Chernus JM, Allen EG, Zeng Z, Hoffman ER, Hassold TJ, Feingold E, Sherman SL. A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. PLoS Genet. 2019 12; 15(12):e1008414. PMID: 31830031.
      View in: PubMed
    2. Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, Wood BL, Carroll WL, Raetz EA, Feingold E, Devidas M, Barcellos LF, Hansen HM, Morimoto L, Kang AY, Smirnov I, Healy J, Laverdière C, Sinnett D, Taub JW, Birch JM, Thompson P, Spector LG, Pombo-de-Oliveira MS, DeWan AT, Mullighan CG, Hunger SP, Pui CH, Loh ML, Zwick ME, Metayer C, Ma X, Mueller BA, Sherman SL, Wiemels JL, Relling MV, Yang JJ, Lupo PJ, Rabin KR. Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome. Blood. 2019 10 10; 134(15):1227-1237. PMID: 31350265.
      View in: PubMed
    3. 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.
      View in: PubMed
    4. Rosser TC, Edgin JO, Capone GT, Hamilton DR, Allen EG, Dooley KJ, Anand P, Strang JF, Armour AC, Frank-Crawford MA, Channell MM, Pierpont EI, Feingold E, Maslen CL, Reeves RH, Sherman SL. Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project. Am J Intellect Dev Disabil. 2018 11; 123(6):514-528. PMID: 30421968.
      View in: PubMed
    5. 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.
      View in: PubMed
    6. Begum F, Chowdhury R, Cheung VG, Sherman SL, Feingold E. Genome-Wide Association Study of Meiotic Recombination Phenotypes. G3 (Bethesda). 2016 12 07; 6(12):3995-4007. PMID: 27733454.
      View in: PubMed
    7. Oliver TR, Middlebrooks C, Harden A, Scott N, Johnson B, Jones J, Walker C, Wilkerson C, Saffold SH, Akinseye A, Smith T, Feingold E, Sherman SL. Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin. J Down Syndr Chromosom Abnorm. 2016 Dec; 2(2). PMID: 28702511.
      View in: PubMed
    8. Begum F, Sharker MH, Sherman SL, Tseng GC, Feingold E. Regionally Smoothed Meta-Analysis Methods for GWAS Datasets. Genet Epidemiol. 2016 Feb; 40(2):154-60. PMID: 26707090.
      View in: PubMed
    9. Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. G3 (Bethesda). 2015 Jul 20; 5(10):1961-71. PMID: 26194203.
      View in: PubMed
    10. Ramachandran D, Mulle JG, Locke AE, Bean LJ, Rosser TC, Bose P, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Sherman SL, Zwick ME. Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects. Genet Med. 2015 Jul; 17(7):554-60. PMID: 25341113.
      View in: PubMed
    11. 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.
      View in: PubMed
    12. 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.
      View in: PubMed
    13. 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.
      View in: PubMed
    14. 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.
      View in: PubMed
    15. Ackerman C, Locke AE, Feingold E, Reshey B, Espana K, Thusberg J, Mooney S, Bean LJ, Dooley KJ, Cua CL, Reeves RH, Sherman SL, Maslen CL. An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. Am J Hum Genet. 2012 Oct 05; 91(4):646-59. PMID: 23040494.
      View in: PubMed
    16. Li H, Cherry S, Klinedinst D, DeLeon V, Redig J, Reshey B, Chin MT, Sherman SL, Maslen CL, Reeves RH. Genetic modifiers predisposing to congenital heart disease in the sensitized Down syndrome population. Circ Cardiovasc Genet. 2012 Jun; 5(3):301-8. PMID: 22523272.
      View in: PubMed
    17. 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.
      View in: PubMed
    18. 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.
      View in: PubMed
    19. Cheung VG, Sherman SL, Feingold E. Genetics. Genetic control of hotspots. Science. 2010 Feb 12; 327(5967):791-2. PMID: 20150474.
      View in: PubMed
    20. 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.
      View in: PubMed
    21. Chowdhury R, Bois PR, Feingold E, Sherman SL, Cheung VG. Genetic analysis of variation in human meiotic recombination. PLoS Genet. 2009 Sep; 5(9):e1000648. PMID: 19763160.
      View in: PubMed
    22. 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.
      View in: PubMed
    23. Arnold S, Pelet A, Amiel J, Borrego S, Hofstra R, Tam P, Ceccherini I, Lyonnet S, Sherman S, Chakravarti A. Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association. Hum Mutat. 2009 May; 30(5):771-5. PMID: 19306335.
      View in: PubMed
    24. 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.
      View in: PubMed
    25. 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.
      View in: PubMed
    26. Duffy KJ, Littrell J, Locke A, Sherman SL, Olivier M. A novel procedure for genotyping of single nucleotide polymorphisms in trisomy with genomic DNA and the invader assay. Nucleic Acids Res. 2008 Dec; 36(22):e145. PMID: 18940863.
      View in: PubMed
    27. Lin Y, Tseng GC, Cheong SY, Bean LJ, Sherman SL, Feingold E. Smarter clustering methods for SNP genotype calling. Bioinformatics. 2008 Dec 01; 24(23):2665-71. PMID: 18826959.
      View in: PubMed
    28. Oliver TR, Feingold E, Yu K, Cheung V, Tinker S, Yadav-Shah M, Masse N, Sherman SL. New insights into human nondisjunction of chromosome 21 in oocytes. PLoS Genet. 2008 Mar 14; 4(3):e1000033. PMID: 18369452.
      View in: PubMed
    29. Prandini P, Deutsch S, Lyle R, Gagnebin M, Delucinge Vivier C, Delorenzi M, Gehrig C, Descombes P, Sherman S, Dagna Bricarelli F, Baldo C, Novelli A, Dallapiccola B, Antonarakis SE. Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance. Am J Hum Genet. 2007 Aug; 81(2):252-63. PMID: 17668376.
      View in: PubMed
    30. 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.
      View in: PubMed
    31. 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.
      View in: PubMed
    32. 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.
      View in: PubMed
    33. 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.
      View in: PubMed
    34. Christianson RE, Sherman SL, Torfs CP. Maternal meiosis II nondisjunction in trisomy 21 is associated with maternal low socioeconomic status. Genet Med. 2004 Nov-Dec; 6(6):487-94. PMID: 15545744.
      View in: PubMed
    35. Kong A, Barnard J, Gudbjartsson DF, Thorleifsson G, Jonsdottir G, Sigurdardottir S, Richardsson B, Jonsdottir J, Thorgeirsson T, Frigge ML, Lamb NE, Sherman S, Gulcher JR, Stefansson K. Recombination rate and reproductive success in humans. Nat Genet. 2004 Nov; 36(11):1203-6. PMID: 15467721.
      View in: PubMed
    36. Xu Z, Kerstann KF, Sherman SL, Chakravarti A, Feingold E. A trisomic transmission disequilibrium test. Genet Epidemiol. 2004 Feb; 26(2):125-31. PMID: 14748012.
      View in: PubMed
    37. Laurent AM, Li M, Sherman S, Roizès G, Buard J. Recombination across the centromere of disjoined and non-disjoined chromosome 21. Hum Mol Genet. 2003 Sep 01; 12(17):2229-39. PMID: 12915463.
      View in: PubMed
    38. Nolin SL, Brown WT, Glicksman A, Houck GE, Gargano AD, Sullivan A, Biancalana V, Bröndum-Nielsen K, Hjalgrim H, Holinski-Feder E, Kooy F, Longshore J, Macpherson J, Mandel JL, Matthijs G, Rousseau F, Steinbach P, Väisänen ML, von Koskull H, Sherman SL. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles. Am J Hum Genet. 2003 Feb; 72(2):454-64. PMID: 12529854.
      View in: PubMed
    39. Berend SA, Page SL, Atkinson W, McCaskill C, Lamb NE, Sherman SL, Shaffer LG. Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction. Am J Hum Genet. 2003 Feb; 72(2):488-95. PMID: 12506337.
      View in: PubMed
    40. 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.
      View in: PubMed
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