Stephanie L. Sherman
Stephanie L. Sherman
Professor of Human Genetics, Emory University School of Medicine
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FMR1 and the fragile X syndrome: human genome epidemiology review
DC Crawford, JM Acuņa, SL Sherman
Genetics in Medicine 3 (5), 359-371, 2001
Further segregation analysis of the fragile X syndrome with special reference to transmitting males
SL Sherman, PA Jacobs, NE Morton, U Froster-Iskenius, ...
Human genetics 69 (4), 289-299, 1985
Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity
ID Waldman, DC Rowe, A Abramowitz, ST Kozel, JH Mohr, SL Sherman, ...
The American Journal of Human Genetics 63 (6), 1767-1776, 1998
Population‐based study of congenital heart defects in Down syndrome
SB Freeman, LF Taft, KJ Dooley, K Allran, SL Sherman, TJ Hassold, ...
American journal of medical genetics 80 (3), 213-217, 1998
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
CA Hobbs, SL Sherman, P Yi, SE Hopkins, CP Torfs, RJ Hine, M Pogribna, ...
The American Journal of Human Genetics 67 (3), 623-630, 2000
Premature ovarian failure in the fragile X syndrome
SL Sherman
American journal of medical genetics 97 (3), 189-194, 2000
Epidemiology of Down syndrome
SL Sherman, EG Allen, LH Bean, SB Freeman
Mental retardation and developmental disabilities research reviews 13 (3 …, 2007
The marker (X) syndrome: a cytogenetic and genetic analysis
SL Sherman, NE Morton, PA Jacobs, G Turner
Annals of human genetics 48 (1), 21-37, 1984
Association of FMR1 repeat size with ovarian dysfunction
AK Sullivan, M Marcus, MP Epstein, EG Allen, AE Anido, JJ Paquin, ...
Human Reproduction 20 (2), 402-412, 2005
The FMR1 premutation and reproduction
MD Wittenberger, RJ Hagerman, SL Sherman, A McConkie-Rosell, ...
Fertility and sterility 87 (3), 456-465, 2007
Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II
NE Lamb, SB Freeman, A Savage-Austin, D Pettay, L Taft, J Hersey, Y Gu, ...
Nature genetics 14 (4), 400-405, 1996
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles
SL Nolin, WT Brown, A Glicksman, GE Houck Jr, AD Gargano, A Sullivan, ...
The American Journal of Human Genetics 72 (2), 454-464, 2003
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA
B Coffee, K Keith, I Albizua, T Malone, J Mowrey, SL Sherman, ST Warren
The American Journal of Human Genetics 85 (4), 503-514, 2009
Fragile X syndrome: diagnostic and carrier testing
S Sherman, BA Pletcher, DA Driscoll
Genetics in Medicine 7 (8), 584-587, 2005
Dopamine DRD4 receptor polymorphism and attention deficit hyperactivity disorder
DC Rowe, C Stever, LN Giedinghagen, JMC Gard, HH Cleveland, ...
Molecular psychiatry 3 (5), 419-426, 1998
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project
SB Freeman, LH Bean, EG Allen, SW Tinker, AE Locke, C Druschel, ...
Genetics in Medicine 10 (3), 173-180, 2008
E (2009)
ST Allen
Citizen Journalism: Global Perspec, 1973
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21
NE Lamb, E Feingold, A Savage, D Avramopoulos, S Freeman, Y Gu, ...
Human molecular genetics 6 (9), 1391-1399, 1997
Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.
T Hassold, M Merrill, K Adkins, S Freeman, S Sherman
American journal of human genetics 57 (4), 867, 1995
Recombination and nondisjunction in humans and flies
KE Koehler, RS Hawley, S Sherman, T Hassold
Human molecular genetics 5 (Supplement_1), 1495-1504, 1996
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