William Crowley

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Davis EE, Balasubramanian R, Kupchinsky ZA, et al. (2020) TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci. Human Molecular Genetics
Shirazi TN, Self H, Dawood K, et al. (2020) Pubertal timing predicts adult psychosexuality: Evidence from typically developing adults and adults with isolated GnRH deficiency. Psychoneuroendocrinology. 119: 104733
Delaney A, Volochayev R, Meader B, et al. (2019) SUN-219 Human Congenital Arhinia Is Associated with GnRH Deficiency and Primary Testicular Defects Journal of the Endocrine Society. 3
Cox KH, Oliveira LMB, Plummer L, et al. (2017) Modeling Mutant/Wild-type Interactions to Ascertain Pathogenicity of PROKR2 Missense Variants in Patients with Isolated GnRH Deficiency. Human Molecular Genetics
Stamou MI, Cox KH, Crowley WF. (2016) 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
Stamou MI, Cox KH, Crowley WF. (2015) 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
Caronia LM, Martin C, Welt CK, et al. (2011) A genetic basis for functional hypothalamic amenorrhea. The New England Journal of Medicine. 364: 215-25
Sykiotis GP, Plummer L, Hughes VA, et al. (2010) Oligogenic basis of isolated gonadotropin-releasing hormone deficiency. Proceedings of the National Academy of Sciences of the United States of America. 107: 15140-4
Balasubramanian R, Dwyer A, Seminara SB, et al. (2010) Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons. Neuroendocrinology. 92: 81-99
Sykiotis GP, Pitteloud N, Seminara SB, et al. (2010) Deciphering genetic disease in the genomic era: the model of GnRH deficiency. Science Translational Medicine. 2: 32rv2