Stephanie L. Sherman
Stephanie L. Sherman
Professor of Human Genetics, Emory University School of Medicine
Geverifieerd e-mailadres voor emory.edu - Homepage
TitelGeciteerd doorJaar
FMR1 and the fragile X syndrome: Human genome epidemiology review
DC Crawford, JM Acuņa, SL Sherman
Genetics in medicine 3 (5), 359, 2001
6172001
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
5991985
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
5601998
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
4632000
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
4521998
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
4411984
Premature ovarian failure in the fragile X syndrome
SL Sherman
American journal of medical genetics 97 (3), 189-194, 2000
4342000
Epidemiology of Down syndrome
SL Sherman, EG Allen, LH Bean, SB Freeman
Mental retardation and developmental disabilities research reviews 13 (3 …, 2007
4022007
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
3862005
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, 1996
3841996
The FMR1 premutation and reproduction
MD Wittenberger, RJ Hagerman, SL Sherman, A McConkie-Rosell, ...
Fertility and sterility 87 (3), 456-465, 2007
3772007
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
3602003
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
3392009
Fragile X syndrome: diagnostic and carrier testing
S Sherman, BA Pletcher, DA Driscoll
Genetics in Medicine 7 (8), 584, 2005
2862005
Dopamine DRD4 receptor polymorphism and attention deficit hyperactivity disorder
DC Rowe, C Stever, LN Giedinghagen, JMC Gard, HH Cleveland, ...
Molecular psychiatry 3 (5), 419, 1998
2651998
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, 2008
2382008
E (2009)
MB Allen, M McGregor
Cash Income from agriculture, 283-423, 2007
228*2007
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
2251997
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
2231995
Trisomy 21: association between reduced recombination and nondisjunction
SL Sherman, N Takaesu, SB Freeman, M Grantham, C Phillips, ...
American journal of human genetics 49 (3), 608, 1991
2221991
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Artikelen 1–20