| Profound obesity associated with a balanced translocation that disrupts the SIM1 gene JL Holder Jr, NF Butte, AR Zinn Human molecular genetics 9 (1), 101-108, 2000 | 471 | 2000 |
| Oxytocin Deficiency Mediates Hyperphagic Obesity of Sim1 Haploinsufficient Mice BM Kublaoui, T Gemelli, KP Tolson, Y Wang, AR Zinn Molecular endocrinology 22 (7), 1723-1734, 2008 | 263 | 2008 |
| Phenotypes associated with SHOX deficiency JL Ross, C Scott Jr, P Marttila, K Kowal, A Nass, P Papenhausen, ... The Journal of Clinical Endocrinology & Metabolism 86 (12), 5674-5680, 2001 | 261 | 2001 |
| Evidence for a Turner syndrome locus or loci at Xp11. 2-p22. 1 AR Zinn, VS Tonk, Z Chen, WL Flejter, HA Gardner, R Guerra, H Kushner, ... The American Journal of Human Genetics 63 (6), 1757-1766, 1998 | 242 | 1998 |
| Turner syndrome: the case of the missing sex chromosome AR Zinn, DC Page, EMC Fisher Trends in Genetics 9 (3), 90-93, 1993 | 220 | 1993 |
| Cognitive and motor development during childhood in boys with Klinefelter syndrome JL Ross, DP Roeltgen, G Stefanatos, R Benecke, MPD Zeger, H Kushner, ... American Journal of Medical Genetics Part A 146 (6), 708-719, 2008 | 210 | 2008 |
| Behavioral and social phenotypes in boys with 47, XYY syndrome or 47, XXY Klinefelter syndrome JL Ross, DP Roeltgen, H Kushner, AR Zinn, A Reiss, MZ Bardsley, ... Pediatrics 129 (4), 769-778, 2012 | 205 | 2012 |
| Neurodevelopmental and psychosocial aspects of Turner syndrome J Ross, A Zinn, E McCauley Mental retardation and developmental disabilities research reviews 6 (2 …, 2000 | 188 | 2000 |
| Transposition of an intron in yeast mitochondria requires a protein encoded by that intron IG Macreadie, RM Scott, AR Zinn, RA Butow Cell 41 (2), 395-402, 1985 | 186 | 1985 |
| Turner syndrome and haploinsufficiency AR Zinn, JL Ross Current opinion in genetics & development 8 (3), 322-327, 1998 | 167 | 1998 |
| Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and oxytocin expression KP Tolson, T Gemelli, L Gautron, JK Elmquist, AR Zinn, BM Kublaoui Journal of Neuroscience 30 (10), 3803-3812, 2010 | 166 | 2010 |
| Early androgen deficiency in infants and young boys with 47, XXY Klinefelter syndrome JL Ross, C Samango-Sprouse, N Lahlou, K Kowal, FF Elder, A Zinn Hormone Research in Paediatrics 64 (1), 39-45, 2005 | 166 | 2005 |
| Cognition and the sex chromosomes: studies in Turner syndrome J Ross, D Roeltgen, A Zinn Hormone Research in Paediatrics 65 (1), 47-56, 2006 | 162 | 2006 |
| Androgen Receptor CAGn Repeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome AR Zinn, P Ramos, FF Elder, K Kowal, C Samango-Sprouse, JL Ross The Journal of Clinical Endocrinology & Metabolism 90 (9), 5041-5046, 2005 | 162 | 2005 |
| Sex-chromosome dosage effects on gene expression in humans A Raznahan, NN Parikshak, V Chandran, JD Blumenthal, LS Clasen, ... Proceedings of the National Academy of Sciences 115 (28), 7398-7403, 2018 | 157 | 2018 |
| DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA: DNA synthesis P Starokadomskyy, T Gemelli, JJ Rios, C Xing, RC Wang, H Li, ... Nature immunology 17 (5), 495-504, 2016 | 146 | 2016 |
| An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47, XYY syndrome or 47, XXY Klinefelter syndrome JL Ross, MPD Zeger, H Kushner, AR Zinn, DP Roeltgen Developmental disabilities research reviews 15 (4), 309-317, 2009 | 144 | 2009 |
| Persistent cognitive deficits in adult women with Turner syndrome JL Ross, GA Stefanatos, H Kushner, A Zinn, C Bondy, D Roeltgen Neurology 58 (2), 218-225, 2002 | 144 | 2002 |
| Sim1 Haploinsufficiency Impairs Melanocortin-Mediated Anorexia and Activation of Paraventricular Nucleus Neurons BM Kublaoui, JL Holder Jr, T Gemelli, AR Zinn Molecular Endocrinology 20 (10), 2483-2492, 2006 | 141 | 2006 |
| Functional equivalence of human X–and Y–encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome M Watanabe, AR Zinn, DC Page, T Nishimoto Nature genetics 4 (3), 268-271, 1993 | 141 | 1993 |
