Reversal and Relapse of Hypogonadotropic Hypogonadism: Resilience and Fragility of the Reproductive Neuroendocrine System von Sidhoum, Valerie F, Chan, Yee-Ming, Lippincott, Margaret F, Balasubramanian, Ravikumar, Quinton, Richard, Plummer, Lacey, Dwyer, Andrew, Pitteloud, Nelly, Hayes, Frances J, Hall, Janet E, Martin, Kathryn A, Boepple, Paul A, Seminara, Stephanie B

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Low Perinatal Androgens Predict Recalled Childhood Gender Nonconformity in Men von Shirazi, Talia N., Self, Heather, Rosenfield, Kevin A., Dawood, Khytam, Welling, Lisa L. M., Cárdenas, Rodrigo, Bailey, J. Michael, Balasubramanian, Ravikumar, Delaney, Angela, Breedlove, S. Marc, Puts, David A.

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Behind the scenes: epigenetic mechanisms rule the roost in pubertal timing von Balasubramanian, Ravikumar

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Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency von Balasubramanian, Ravikumar, Choi, Jin-Ho, Francescatto, Ludmila, Willer, Jason, Horton, Edward R., Asimacopoulos, Eleni P., Stankovic, Konstantina M., Plummer, Lacey, Buck, Cassandra L., Quinton, Richard, Nebesio, Todd D., Mericq, Veronica, Merino, Paulina M., Meyer, Brian F., Monies, Dorota, Gusella, James F., Tassan, Nada Al, Katsanis, Nicholas, Crowley, William F.

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Phenotypic continuum between Waardenburg syndrome and idiopathic hypogonadotropic hypogonadism in humans with SOX10 variants von Rojas, Rebecca A., Kutateladze, Anna A., Plummer, Lacey, Stamou, Maria, Keefe, David L., Salnikov, Kathryn B., Delaney, Angela, Hall, Janet E., Sadreyev, Ruslan, Ji, Fei, Fliers, Eric, Gambosova, Katarina, Quinton, Richard, Merino, Paulina M., Mericq, Veronica, Seminara, Stephanie B., Crowley, William F., Balasubramanian, Ravikumar

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The Role of the Prokineticin 2 Pathway in Human Reproduction: Evidence from the Study of Human and Murine Gene Mutations von Martin, Cecilia, Balasubramanian, Ravikumar, Dwyer, Andrew A, Au, Margaret G, Sidis, Yisrael, Kaiser, Ursula B, Seminara, Stephanie B, Pitteloud, Nelly, Zhou, Qun-Yong, Crowley, William F

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POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression von Cho, Hyun-Ju, Gurbuz, Fatih, Stamou, Maria, Kotan, Leman Damla, Farmer, Stephen Matthew, Can, Sule, Tompkins, Miranda Faith, Mammadova, Jamala, Altincik, S Ayca, Gokce, Cumali, Catli, Gonul, Bugrul, Fuat, Bartlett, Keenan, Turan, Ihsan, Balasubramanian, Ravikumar, Yuksel, Bilgin, Seminara, Stephanie B, Wray, Susan, Topaloglu, A Kemal

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Reversible hypogonadotropic hypogonadism in men with the fertile eunuch/Pasqualini syndrome: A single-center natural history study von Dwyer, Andrew A, Stamou, Maria, McDonald, Isabella R, Anghel, Ella, Cox, Kimberly H, Salnikov, Kathryn B, Plummer, Lacey, Seminara, Stephanie B, Balasubramanian, Ravikumar

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Expanding the Spectrum of Founder Mutations Causing Isolated Gonadotropin-Releasing Hormone Deficiency von Choi, Jin-Ho, Balasubramanian, Ravikumar, Lee, Phil H, Shaw, Natalie D, Hall, Janet E, Plummer, Lacey, Buck, Cassandra L, Kottler, Marie-Laure, Jarzabek, Katarzyna, Wołczynski, Sławomir, Quinton, Richard, Latronico, Ana Claudia, Dode, Catherine, Ogata, Tsutomu, Kim, Hyung-Goo, Layman, Lawrence C, Gusella, James F, Crowley, William F

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Human GnRH Deficiency: A Unique Disease Model to Unravel the Ontogeny of GnRH Neurons von Balasubramanian, Ravikumar, Dwyer, Andrew, Seminara, Stephanie B., Pitteloud, Nelly, Kaiser, Ursula B., Crowley, Jr, William F.

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Signaling role of prokineticin 2 on the estrous cycle of female mice von Xiao, Ling, Zhang, Chengkang, Li, Xiaohan, Gong, Shiaoching, Hu, Renming, Balasubramanian, Ravikumar, Crowley W, Jr, William F, Hastings, Michael H, Zhou, Qun-Yong

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Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanisms von Cassin, Jessica, Stamou, Maria I, Keefe, Kimberly W, Sung, Kaitlin E, Bojo, Celine C, Tonsfeldt, Karen J, Rojas, Rebecca A, Ferreira Lopes, Vanessa, Plummer, Lacey, Salnikov, Kathryn B, Keefe, Jr, David L, Ozata, Metin, Genel, Myron, Georgopoulos, Neoklis A, Hall, Janet E, Crowley, Jr, William F, Seminara, Stephanie B, Mellon, Pamela L, Balasubramanian, Ravikumar

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Pioglitazone Decreases Fasting and Postprandial Endogenous Glucose Production in Proportion to Decrease in Hepatic Triglyceride Content von RAVIKUMAR, Balasubramanian, GERRARD, Jean, DALLA MAN, Chiara, FIRBANK, Michael J, LANE, Annette, ENGLISH, Philip T, COBELLI, Claudio, TAYLOR, Roy

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The puzzles of the prokineticin 2 pathway in human reproduction von Balasubramanian, Ravikumar, Plummer, Lacey, Sidis, Yisrael, Pitteloud, Nelly, Martin, Cecilia, Zhou, Qun-Yong, Crowley, William F.

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Hypothalamic Ceramides and the Ovarian Sympathetic System: At the Crossroads of Obesity and Puberty von Stamou, Maria I., Balasubramanian, Ravikumar

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A prevalent variant in PPP1R3A impairs glycogen synthesis and reduces muscle glycogen content in humans and mice von Savage, David B, Zhai, Lanmin, Ravikumar, Balasubramanian, Choi, Cheol Soo, Snaar, Johanna E, McGuire, Amanda C, Wou, Sung-Eun, Medina-Gomez, Gemma, Kim, Sheene, Bock, Cheryl B, Segvich, Dyann M, Solanky, Bhavana, Deelchand, Dinesh, Vidal-Puig, Antonio, Wareham, Nicholas J, Shulman, Gerald I, Karpe, Fredrik, Taylor, Roy, Pederson, Bartholomew A, Roach, Peter J, O'Rahilly, Stephen, DePaoli-Roach, Anna A

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Lack of a genetic risk continuum between pubertal timing in the general population and idiopathic hypogonadotropic hypogonadism von Plummer, Lacey, Balasubramanian, Ravikumar, Stamou, Maria, Campbell, Mark, Dewan, Pranav, Bryant, Nora, Salnikov, Kathryn, Lippincott, Margaret, Seminara, Stephanie

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How human genetic context can inform pathogenicity classification: FGFR1 variation in idiopathic hypogonadotropic hypogonadism von Xu, Wanxue, Plummer, Lacey, Seminara, Stephanie B., Balasubramanian, Ravikumar, Lippincott, Margaret F.

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Requiem for International Medical Graduates von Natarajan, Arun, Ravikumar, Balasubramanian

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Kisspeptin Overcomes GnRH Neuronal Suppression Secondary to Hyperprolactinemia in Humans von Hoskova, Katerina, Kayton Bryant, Nora, Chen, Margaret E, Nachtigall, Lisa B, Lippincott, Margaret F, Balasubramanian, Ravikumar, Seminara, Stephanie B

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