Stephanie L. Sherman
Stephanie L. Sherman
Professor of Human Genetics, Emory University School of Medicine
Bestätigte E-Mail-Adresse bei - Startseite
Zitiert von
Zitiert von
An international terminology for grazing lands and grazing animals
VG Allen, C Batello, EJ Berretta, J Hodgson, M Kothmann, X Li, J McIvor, ...
Grass and forage science 66 (1), 2, 2011
FMR1 and the fragile X syndrome: human genome epidemiology review
DC Crawford, JM Acuña, 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, 289-299, 1985
Epidemiology of Down syndrome
SL Sherman, EG Allen, LH Bean, SB Freeman
Mental retardation and developmental disabilities research reviews 13 (3 …, 2007
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
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
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
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
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
Down syndrome
SE Antonarakis, BG Skotko, MS Rafii, A Strydom, SE Pape, DW Bianchi, ...
Nature Reviews Disease Primers 6 (1), 9, 2020
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
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
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
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
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