| Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study—preliminary data DJ Allingham‐Hawkins, R Babul‐Hirji, D Chitayat, JJA Holden, KT Yang, ... American journal of medical genetics 83 (4), 322-325, 1999 | 582 | 1999 |
| 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 | 467 | 2003 |
| Familial transmission of the FMR1 CGG repeat. SL Nolin, FA Lewis 3rd, LL Ye, GE Houck Jr, AE Glicksman, P Limprasert, ... American journal of human genetics 59 (6), 1252, 1996 | 259 | 1996 |
| Mosaicism in fragile X affected males SL Nolin, A Glicksman, GE Houck Jr, WT Brown, CS Dobkin American journal of medical genetics 51 (4), 509-512, 1994 | 173 | 1994 |
| Mosaicism in fragile X affected males SL Nolin, A Glicksman, GE Houck Jr, WT Brown, CS Dobkin American journal of medical genetics 51 (4), 509-512, 1994 | 173 | 1994 |
| Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers SL Nolin, A Glicksman, N Ersalesi, C Dobkin, WT Brown, RU Cao, E Blatt, ... Genetics in Medicine 17 (5), 358-364, 2015 | 142 | 2015 |
| Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles SL Nolin, S Sah, A Glicksman, SL Sherman, E Allen, E Berry‐Kravis, ... American Journal of Medical Genetics Part A 161 (4), 771-778, 2013 | 136 | 2013 |
| Fragile X analysis of 1112 prenatal samples from 1991 to 2010 SL Nolin, A Glicksman, X Ding, N Ersalesi, WT Brown, SL Sherman, ... Prenatal diagnosis 31 (10), 925-931, 2011 | 116 | 2011 |
| The fragile X mental retardation protein FMRP binds elongation factor 1A mRNA and negatively regulates its translation in vivo YJ Sung, N Dolzhanskaya, SL Nolin, T Brown, JR Currie, RB Denman Journal of Biological Chemistry 278 (18), 15669-15678, 2003 | 110 | 2003 |
| Prenatal diagnosis and carrier screening for fragile X by PCR WT Brown, S Nolin, G Houck Jr, X Ding, A Glicksman, SY Li, ... American journal of medical genetics 64 (1), 191-195, 1996 | 82 | 1996 |
| Examination of factors associated with instability of the FMR1 CGG repeat AE Ashley-Koch, H Robinson, AE Glicksman, SL Nolin, CE Schwartz, ... The American Journal of Human Genetics 63 (3), 776-785, 1998 | 73 | 1998 |
| Mosaicism for the FMR1 gene influences adaptive skills development in fragile X‐affected males IL Cohen, SL Nolin, V Sudhalter, XH Ding, CS Dobkin, WT Brown American journal of medical genetics 64 (2), 365-369, 1996 | 68 | 1996 |
| Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population DC Crawford, CE Schwartz, KL Meadows, JL Newman, LF Taft, C Gunter, ... The American Journal of Human Genetics 66 (2), 480-493, 2000 | 65 | 2000 |
| Neutrophil interaction with influenza-infected epithelial cells DR Ratcliffe, SL Nolin, EB Cramer | 63 | 1988 |
| Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles SL Nolin, A Glicksman, N Tortora, E Allen, J Macpherson, M Mila, ... American Journal of Medical Genetics Part A 179 (7), 1148-1156, 2019 | 60 | 2019 |
| Fragile X screening by quantification of FMRP in dried blood spots by a Luminex immunoassay G LaFauci, T Adayev, R Kascsak, R Kascsak, S Nolin, P Mehta, WT Brown, ... The Journal of Molecular Diagnostics 15 (4), 508-517, 2013 | 55 | 2013 |
| Tissue differences in fragile X mosaics: mosaicism in blood cells may differ greatly from skin CS Dobkin, SL Nolin, I Cohen, V Sudhalter, MG Bialer, XH Ding, ... American journal of medical genetics 64 (2), 296-301, 1996 | 54 | 1996 |
| The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective GJ Latham, J Coppinger, AG Hadd, SL Nolin Frontiers in Genetics 5, 244, 2014 | 53 | 2014 |
| Reverse mutations in the fragile X syndrome WT Brown, GE Houck Jr, X Ding, N Zhong, S Nolin, A Glicksman, ... American journal of medical genetics 64 (2), 287-292, 1996 | 48 | 1996 |
| Fragile X founder effects and new mutations in Finland N Zhong, E Kajanoja, B Smits, J Pietrofesa, D Curley, D Wang, W Ju, ... American journal of medical genetics 64 (1), 226-233, 1996 | 46 | 1996 |
