Muscle fiber size and function in elderly humans: a longitudinal study

Por Frontera, Walter R., Reid, Kieran F., Phillips, Edward M., Krivickas, Lisa S., Hughes, Virginia A., Roubenoff, Ronenn, Fielding, Roger A.
Publicado em 2008

Olfactory Phenotypic Spectrum in Idiopathic Hypogonadotropic Hypogonadism: Pathophysiological and Genetic Implications

Por 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
Publicado em 2012

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency

Por 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
Publicado em 2010

Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

Por Pitteloud, Nelly, Acierno, James S., Meysing, Astrid, Eliseenkova, Anna V., Ma, Jinghong, Ibrahimi, Omar A., Metzger, Daniel L., Hayes, Frances J., Dwyer, Andrew A., Hughes, Virginia A., Yialamas, Maria, Hall, Janet E., Grant, Ellen, Mohammadi, Moosa, Crowley, William F.
Publicado em 2006

Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

Por Raivio, Taneli, Sidis, Yisrael, Plummer, Lacey, Chen, Huaibin, Ma, Jinghong, Mukherjee, Abir, Jacobson-Dickman, Elka, Quinton, Richard, Van Vliet, Guy, Lavoie, Helene, Hughes, Virginia A., Dwyer, Andrew, Hayes, Frances J., Xu, Shuyun, Sparks, Susan, Kaiser, Ursula B., Mohammadi, Moosa, Pitteloud, Nelly
Publicado em 2009

Expanding the Phenotype and Genotype of Female GnRH Deficiency

Por Shaw, Natalie D., Seminara, Stephanie B., Welt, Corrine K., Au, Margaret G., Plummer, Lacey, Hughes, Virginia A., Dwyer, Andrew A., Martin, Kathryn A., Quinton, Richard, Mericq, Veronica, Merino, Paulina M., Gusella, James F., Crowley, William F., Pitteloud, Nelly, Hall, Janet E.
Publicado em 2011

Frequency of Impaired Fibroblast Growth Factor Receptor 1 Signaling as a Cause of Normosmic Idiopathic Hypogonadotropic Hypogonadism

Por Raivio, Taneli, Sidis, Yisrael, Plummer, Lacey, Chen, Huaibin, Ma, Jinghong, Mukherjee, Abir, Jacobson-Dickman, Elka, Quinton, Richard, Van Vliet, Guy, Lavoie, Helene, Hughes, Virginia A., Dwyer, Andrew, Hayes, Frances J., Xu, Shuyun, Sparks, Susan, Kaiser, Ursula B., Mohammadi, Moosa, Pitteloud, Nelly
Publicado no Mol Endocrinol (2009)

A Genetic Basis for Functional Hypothalamic Amenorrhea

Por Caronia, Lisa M., 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., Martin, Kathryn A., Hall, Janet E., Pitteloud, Nelly
Publicado em 2011

Mutations in Prokineticin 2 and Prokineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum

Por Cole, Lindsay W., Sidis, Yisrael, Zhang, ChengKang, Quinton, Richard, Plummer, Lacey, Pignatelli, Duarte, Hughes, Virginia A., Dwyer, Andrew A., Raivio, Taneli, Hayes, Frances J., Seminara, Stephanie B., Huot, Celine, Alos, Nathalie, Speiser, Phyllis, Takeshita, Akira, VanVliet, Guy, Pearce, Simon, Crowley, William F., Zhou, Qun-Yong, Pitteloud, Nelly
Publicado em 2008

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism

Por 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
Publicado em 2013

TAC3/TACR3 Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

Por 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.
Publicado em 2010