| European consensus statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment U Boehm, PM Bouloux, MT Dattani, N De Roux, C Dodé, L Dunkel, ... Nature Reviews Endocrinology 11 (9), 547-564, 2015 | 845 | 2015 |
| Increasing insulin resistance is associated with a decrease in Leydig cell testosterone secretion in men N Pitteloud, M Hardin, AA Dwyer, E Valassi, M Yialamas, D Elahi, ... The Journal of Clinical Endocrinology & Metabolism 90 (5), 2636-2641, 2005 | 646 | 2005 |
| Relationship between testosterone levels, insulin sensitivity, and mitochondrial function in men N Pitteloud, VK Mootha, AA Dwyer, M Hardin, H Lee, KF Eriksson, ... Diabetes care 28 (7), 1636-1642, 2005 | 568 | 2005 |
| Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice J Falardeau, WCJ Chung, A Beenken, T Raivio, L Plummer, Y Sidis, ... The Journal of clinical investigation 118 (8), 2822-2831, 2008 | 474 | 2008 |
| Reversal of idiopathic hypogonadotropic hypogonadism T Raivio, J Falardeau, A Dwyer, R Quinton, FJ Hayes, VA Hughes, ... New England Journal of Medicine 357 (9), 863-873, 2007 | 465 | 2007 |
| Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism N Pitteloud, R Quinton, S Pearce, T Raivio, J Acierno, A Dwyer, ... The Journal of clinical investigation 117 (2), 457-463, 2007 | 428 | 2007 |
| Oligogenic basis of isolated gonadotropin-releasing hormone deficiency GP Sykiotis, L Plummer, VA Hughes, M Au, S Durrani, S Nayak-Young, ... Proceedings of the National Academy of Sciences 107 (34), 15140-15144, 2010 | 381 | 2010 |
| TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in … E Gianetti, C Tusset, SD Noel, MG Au, AA Dwyer, VA Hughes, AP Abreu, ... The Journal of Clinical Endocrinology & Metabolism 95 (6), 2857-2867, 2010 | 315 | 2010 |
| Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism H Miraoui, AA Dwyer, GP Sykiotis, L Plummer, W Chung, B Feng, ... The American Journal of Human Genetics 92 (5), 725-743, 2013 | 305 | 2013 |
| Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism N Pitteloud, JS Acierno Jr, A Meysing, AV Eliseenkova, J Ma, OA Ibrahimi, ... Proceedings of the National Academy of Sciences 103 (16), 6281-6286, 2006 | 297 | 2006 |
| Mutations in Prokineticin 2 and Prokineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum LW Cole, Y Sidis, CK Zhang, R Quinton, L Plummer, D Pignatelli, ... The Journal of Clinical Endocrinology & Metabolism 93 (9), 3551-3559, 2008 | 282 | 2008 |
| Acute sex steroid withdrawal reduces insulin sensitivity in healthy men with idiopathic hypogonadotropic hypogonadism MA Yialamas, AA Dwyer, E Hanley, H Lee, N Pitteloud, FJ Hayes The Journal of Clinical Endocrinology & Metabolism 92 (11), 4254-4259, 2007 | 281 | 2007 |
| Predictors of outcome of long-term GnRH therapy in men with idiopathic hypogonadotropic hypogonadism N Pitteloud, FJ Hayes, A Dwyer, PA Boepple, H Lee, WF Crowley Jr The Journal of Clinical Endocrinology & Metabolism 87 (9), 4128-4136, 2002 | 277 | 2002 |
| Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitination DH Margolin, M Kousi, YM Chan, ET Lim, JD Schmahmann, ... New England Journal of Medicine 368 (21), 1992-2003, 2013 | 245 | 2013 |
| Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes N Pitteloud, A Meysing, R Quinton, JS Acierno Jr, AA Dwyer, L Plummer, ... Molecular and cellular endocrinology 254, 60-69, 2006 | 231 | 2006 |
| Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene N Pitteloud, JS Acierno Jr, AU Meysing, AA Dwyer, FJ Hayes, ... The Journal of Clinical Endocrinology & Metabolism 90 (3), 1317-1322, 2005 | 203 | 2005 |
| Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory AL Mitchell, A Dwyer, N Pitteloud, R Quinton Trends in Endocrinology & Metabolism 22 (7), 249-258, 2011 | 189 | 2011 |
| Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes FA Costa-Barbosa, R Balasubramanian, KW Keefe, ND Shaw, ... The Journal of Clinical Endocrinology & Metabolism 98 (5), E943-E953, 2013 | 186 | 2013 |
| Inhibition of luteinizing hormone secretion by testosterone in men requires aromatization for its pituitary but not its hypothalamic effects: evidence from the tandem study of … N Pitteloud, AA Dwyer, S DeCruz, H Lee, PA Boepple, WF Crowley Jr, ... The Journal of Clinical Endocrinology & Metabolism 93 (3), 784-791, 2008 | 178 | 2008 |
| Skeletal muscle mitochondria in the elderly: effects of physical fitness and exercise training NT Broskey, C Greggio, A Boss, M Boutant, A Dwyer, L Schlueter, D Hans, ... The Journal of Clinical Endocrinology & Metabolism 99 (5), 1852-1861, 2014 | 177 | 2014 |
