| Year |
Citation |
Score |
| 2020 |
Davis EE, Balasubramanian R, Kupchinsky ZA, Keefe DL, Plummer L, Khan K, Meczekalski B, Heath KE, Lopez-Gonzalez V, Ballesta-Martinez MJ, Margabanthu G, Price S, Greening J, Brauner R, Valenzuela I, ... ... Crowley WF, et al. TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci. Human Molecular Genetics. PMID 32620954 DOI: 10.1093/hmg/ddaa120 |
0.303 |
|
| 2020 |
Shirazi TN, Self H, Dawood K, Cárdenas R, Welling LLM, Rosenfield KA, Ortiz TL, Carré JM, Balasubramanian R, Delaney A, Crowley W, Breedlove SM, Puts DA. Pubertal timing predicts adult psychosexuality: Evidence from typically developing adults and adults with isolated GnRH deficiency. Psychoneuroendocrinology. 119: 104733. PMID 32563936 DOI: 10.1016/J.Psyneuen.2020.104733 |
0.341 |
|
| 2019 |
Delaney A, Volochayev R, Meader B, Lee J, Almpani N, Noukelak G, Brooks B, Henkind J, Chalmers L, Law J, Williamson K, Jacobsen C, Buitrago TP, Silva OP, Chie-Hee C, ... ... Crowley W, et al. SUN-219 Human Congenital Arhinia Is Associated with GnRH Deficiency and Primary Testicular Defects Journal of the Endocrine Society. 3. DOI: 10.1210/Js.2019-Sun-219 |
0.316 |
|
| 2017 |
Cox KH, Oliveira LMB, Plummer L, Corbin B, Gardella T, Balasubramanian R, Crowley WF. Modeling Mutant/Wild-type Interactions to Ascertain Pathogenicity of PROKR2 Missense Variants in Patients with Isolated GnRH Deficiency. Human Molecular Genetics. PMID 29161432 DOI: 10.1093/hmg/ddx404 |
0.532 |
|
| 2016 |
Stamou MI, Cox KH, Crowley WF. Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era. Endocrine Reviews. 2016: 4-22. PMID 27454361 DOI: 10.1210/er.2015-1045.2016.1.test |
0.308 |
|
| 2015 |
Stamou MI, Cox KH, Crowley WF. Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era. Endocrine Reviews. er20151045. PMID 26394276 DOI: 10.1210/er.2015-1045 |
0.549 |
|
| 2011 |
Caronia LM, Martin C, Welt CK, Sykiotis GP, Quinton R, Thambundit A, Avbelj M, Dhruvakumar S, Plummer L, Hughes VA, Seminara SB, Boepple PA, Sidis Y, Crowley WF, Martin KA, et al. A genetic basis for functional hypothalamic amenorrhea. The New England Journal of Medicine. 364: 215-25. PMID 21247312 DOI: 10.1056/NEJMoa0911064 |
0.304 |
|
| 2010 |
Sykiotis GP, Plummer L, Hughes VA, Au M, Durrani S, Nayak-Young S, Dwyer AA, Quinton R, Hall JE, Gusella JF, Seminara SB, Crowley WF, Pitteloud N. Oligogenic basis of isolated gonadotropin-releasing hormone deficiency. Proceedings of the National Academy of Sciences of the United States of America. 107: 15140-4. PMID 20696889 DOI: 10.1073/pnas.1009622107 |
0.304 |
|
| 2010 |
Balasubramanian R, Dwyer A, Seminara SB, Pitteloud N, Kaiser UB, Crowley WF. Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons. Neuroendocrinology. 92: 81-99. PMID 20606386 DOI: 10.1159/000314193 |
0.326 |
|
| 2010 |
Sykiotis GP, Pitteloud N, Seminara SB, Kaiser UB, Crowley WF. Deciphering genetic disease in the genomic era: the model of GnRH deficiency. Science Translational Medicine. 2: 32rv2. PMID 20484732 DOI: 10.1126/Scitranslmed.3000288 |
0.324 |
|
| 2007 |
Pitteloud N, Quinton R, Pearce S, Raivio T, Acierno J, Dwyer A, Plummer L, Hughes V, Seminara S, Cheng YZ, Li WP, Maccoll G, Eliseenkova AV, Olsen SK, Ibrahimi OA, ... ... Crowley W, et al. Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism Journal of Clinical Investigation. 117: 457-463. PMID 17235395 DOI: 10.1172/Jci29884 |
0.375 |
|
| 2004 |
Gottsch ML, Cunningham MJ, Smith JT, Popa SM, Acohido BV, Crowley WF, Seminara S, Clifton DK, Steiner RA. A role for kisspeptins in the regulation of gonadotropin secretion in the mouse. Endocrinology. 145: 4073-7. PMID 15217982 DOI: 10.1210/En.2004-0431 |
0.429 |
|
| 2003 |
Seminara SB, Messager S, Chatzidaki EE, Thresher RR, Acierno JS, Shagoury JK, Bo-Abbas Y, Kuohung W, Schwinof KM, Hendrick AG, Zahn D, Dixon J, Kaiser UB, Slaugenhaupt SA, Gusella JF, ... ... Crowley WF, et al. The GPR54 gene as a regulator of puberty. The New England Journal of Medicine. 349: 1614-27. PMID 14573733 DOI: 10.1056/Nejmoa035322 |
0.318 |
|
| 2001 |
Seminara SB, Oliveira LM, Beranova M, Hayes FJ, Crowley WF. Genetics of hypogonadotropic hypogonadism. Journal of Endocrinological Investigation. 23: 560-5. PMID 11079449 DOI: 10.1007/BF03343776 |
0.321 |
|
| 1996 |
Habiby RL, Boepple P, Nachtigall L, Sluss PM, Crowley WF, Jameson JL. Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: Evidence that DAX-1 mutations lead to combined hypothalamic and pituitary defects in gonadotropin production Journal of Clinical Investigation. 98: 1055-1062. PMID 8770879 DOI: 10.1172/JCI118866 |
0.302 |
|
| 1992 |
Weiss J, Adams E, Whitcomb RW, Crowley WF, Jameson JL. Normal sequence of the gonadotropin-releasing hormone gene in patients with idiopathic hypogonadotropic hypogonadism. Biology of Reproduction. 45: 743-7. PMID 1756212 DOI: 10.1095/biolreprod45.5.743 |
0.303 |
|
| 1991 |
Crowley W, Whitcomb R. Gonadotropin-releasing hormone deficiency in men: Diagnosis and treatment with exogenous gonadotropin-releasing hormone International Journal of Gynecology & Obstetrics. 36: 85-85. DOI: 10.1016/0020-7292(91)90214-P |
0.343 |
|
| 1989 |
Weiss J, Crowley WF, Jameson JL. Normal structure of the gonadotropin-releasing hormone (GnRH) gene in patients with GnRH deficiency and idiopathic hypogonadotropic hypogonadism. The Journal of Clinical Endocrinology and Metabolism. 69: 299-303. PMID 2546961 DOI: 10.1210/jcem-69-2-299 |
0.305 |
|
| 1984 |
Spratt D, Crowley W, Butler J, Badger T. Plasma luteinizing hormone releasing hormone (LHRH) patterns and luteiniz-ing hormone (LH) responses following intravenous (IV) and subcutaneous (SC) injections in men Journal of Steroid Biochemistry. 20: 1407. DOI: 10.1016/0022-4731(84)90498-9 |
0.346 |
|
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