Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism von Miraoui, Hichem, Dwyer, Andrew A., Sykiotis, Gerasimos P., Plummer, Lacey, Chung, Wilson, Feng, Bihua, Beenken, Andrew, Clarke, Jeff, Pers, Tune H., Dworzynski, Piotr, Keefe, Kimberley, Niedziela, Marek, Raivio, Taneli, Crowley, William F., Seminara, Stephanie B., Quinton, Richard, Hughes, Virginia A., Kumanov, Philip, Young, Jacques, Yialamas, Maria A., Hall, Janet E., Van Vliet, Guy, Chanoine, Jean-Pierre, Rubenstein, John, Mohammadi, Moosa, Tsai, Pei-San, Sidis, Yisrael, Lage, Kasper, Pitteloud, Nelly

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Oligogenic basis of isolated gonadotropin-releasing hormone deficiency von Sykiotis, Gerasimos P., Plummer, Lacey, Hughes, Virginia A., Au, Margaret, Durrani, Sadia, Nayak-Young, Sadhana, Dwyer, Andrew A., Quinton, Richard, Hall, Janet E., Gusella, James F., Seminara, Stephanie B., Crowley, William F., Pitteloud, Nelly, Donahoe, Patricia K.

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Muscle fiber size and function in elderly humans: a longitudinal study von Frontera, Walter R, Reid, Kieran F, Phillips, Edward M, Krivickas, Lisa S, Hughes, Virginia A, Roubenoff, Ronenn, Fielding, Roger A

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Epigenetics: The sins of the father von Hughes, Virginia

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THE SINS OF THE FATHER von Hughes, Virginia

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Reversal of Idiopathic Hypogonadotropic Hypogonadism von Raivio, Taneli, Falardeau, John, Dwyer, Andrew, Quinton, Richard, Hayes, Frances J, Hughes, Virginia A, Cole, Lindsay W, Pearce, Simon H, Lee, Hang, Boepple, Paul, Crowley, William F, Pitteloud, Nelly

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Microglia: The constant gardeners von Hughes, Virginia

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TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood von Gianetti, Elena, Tusset, Cintia, Noel, Sekoni D., Au, Margaret G., Dwyer, Andrew A., Hughes, Virginia A., Abreu, Ana Paula, Carroll, Jessica, Trarbach, Ericka, Silveira, Leticia F. G., Costa, Elaine M. F., de Mendonça, Berenice Bilharinho, de Castro, Margaret, Lofrano, Adriana, Hall, Janet E., Bolu, Erol, Ozata, Metin, Quinton, Richard, Amory, John K., Stewart, Susan E., Arlt, Wiebke, Cole, Trevor R., Crowley, William F., Kaiser, Ursula B., Latronico, Ana Claudia, Seminara, Stephanie B.

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Longitudinal changes in body composition in older men and women: role of body weight change and physical activity von Hughes, Virginia A, Frontera, Walter R, Roubenoff, Ronenn, Evans, William J, Fiatarone Singh, Maria A

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THE CONSTANT GARDENERS von Hughes, Virginia

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Anthropometric assessment of 10-y changes in body composition in the elderly von Hughes, V.A, Roubenoff, R, Wood, M, Frontera, W.R, Evans, W.J, Singh, M.A.F

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A Genetic Basis for Functional Hypothalamic Amenorrhea von Caronia, Lisa M, Martin, Kathryn A, Martin, Cecilia, Welt, Corrine K, Sykiotis, Gerasimos P, Quinton, Richard, Thambundit, Apisadaporn, Avbelj, Magdalena, Dhruvakumar, Sadhana, Plummer, Lacey, Hughes, Virginia A, Seminara, Stephanie B, Boepple, Paul A, Sidis, Yisrael, Crowley, William F, Hall, Janet E, Pitteloud, Nelly

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Angiogenic sprouting into neural tissue requires Gpr124, an orphan G protein-coupled receptor von Anderson, Keith D, Pan, Li, Yang, Xiao-man, Hughes, Virginia C, Walls, Johnathon R, Dominguez, Melissa G, Simmons, Mary V, Burfeind, Patricia, Xue, Yingzi, Wei, Yi, Macdonald, Lynn E, Thurston, Gavin, Daly, Christopher, Lin, Hsin Chieh, Economides, Aris N, Valenzuela, David M, Murphy, Andrew J, Yancopoulos, George D, Gale, Nicholas W

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The big fat truth von Hughes, Virginia

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Aging of skeletal muscle: a 12-yr longitudinal study von Frontera, Walter R, Hughes, Virginia A, Fielding, Roger A, Fiatarone, Maria A, Evans, William J, Roubenoff, Ronenn

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Haploinsufficiency of Delta-Like 4 Ligand Results in Embryonic Lethality Due to Major Defects in Arterial and Vascular Development von Gale, Nicholas W., Dominguez, Melissa G., Noguera, Irene, Pan, Li, Hughes, Virginia, Valenzuela, David M., Murphy, Andrew J., Adams, Niels C., Lin, Hsin Chieh, Holash, Jocelyn, Thurston, Gavin, Yancopoulos, George D.

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Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism von Tornberg, Janne, Sykiotis, Gerasimos P, Keefe, Kimberly, Plummer, Lacey, Hoang, Xuan, Hall, Janet E, Quinton, Richard, Seminara, Stephanie B, Hughes, Virginia, Van Vliet, Guy, Van Uum, Stan, Crowley, William F, Habuchi, Hiroko, Kimata, Koji, Pitteloud, Nelly, Bülow, Hannes E

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Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice von Falardeau, John, Chung, Wilson C J, Beenken, Andrew, Raivio, Taneli, Plummer, Lacey, Sidis, Yisrael, Jacobson-Dickman, Elka E, Eliseenkova, Anna V, Ma, Jinghong, Dwyer, Andrew, Quinton, Richard, Na, Sandra, Hall, Janet E, Huot, Celine, Alois, Natalie, Pearce, Simon H S, Cole, Lindsay W, Hughes, Virginia, Mohammadi, Moosa, Tsai, Pei, Pitteloud, Nelly

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Olfactory Phenotypic Spectrum in Idiopathic Hypogonadotropic Hypogonadism: Pathophysiological and Genetic Implications von Lewkowitz-Shpuntoff, Hilana M, Hughes, Virginia A, Plummer, Lacey, Au, Margaret G, Doty, Richard L, Seminara, Stephanie B, Chan, Yee-Ming, Pitteloud, Nelly, Crowley, William F, Balasubramanian, Ravikumar

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HEAD CASE von Hughes, Virginia

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