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 | 1122 | 2011 |
FMR1 and the fragile X syndrome: human genome epidemiology review DC Crawford, JM Acuņa, SL Sherman Genetics in medicine 3 (5), 359-371, 2001 | 849 | 2001 |
Down syndrome SE Antonarakis, BG Skotko, MS Rafii, A Strydom, SE Pape, DW Bianchi, ... Nature Reviews Disease Primers 6 (1), 9, 2020 | 731 | 2020 |
Epidemiology of Down syndrome SL Sherman, EG Allen, LH Bean, SB Freeman Mental retardation and developmental disabilities research reviews 13 (3 …, 2007 | 689 | 2007 |
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 | 677 | 1985 |
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 | 661 | 1998 |
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 | 640 | 1998 |
Premature ovarian failure in the fragile X syndrome SL Sherman American journal of medical genetics 97 (3), 189-194, 2000 | 577 | 2000 |
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 | 570 | 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 | 520 | 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 | 519 | 2009 |
The FMR1 premutation and reproduction MD Wittenberger, RJ Hagerman, SL Sherman, A McConkie-Rosell, ... Fertility and sterility 87 (3), 456-465, 2007 | 493 | 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 | 472 | 1984 |
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 | 471 | 2003 |
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 | 466 | 1996 |
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 | 396 | 2008 |
Fragile X syndrome: diagnostic and carrier testing S Sherman, BA Pletcher, DA Driscoll Genetics in medicine 7 (8), 584-587, 2005 | 367 | 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 | 313 | 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 | 309 | 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 | 283 | 1996 |