Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome by Kim, Hyung-Goo, Kurth, Ingo, Lan, Fei, Meliciani, Irene, Wenzel, Wolfgang, Eom, Soo Hyun, Kang, Gil Bu, Rosenberger, Georg, Tekin, Mustafa, Ozata, Metin, Bick, David P., Sherins, Richard J., Walker, Steven L., Shi, Yang, Gusella, James F., Layman, Lawrence C.

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WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome by Kim, Hyung-Goo, Ahn, Jang-Won, Kurth, Ingo, Ullmann, Reinhard, Kim, Hyun-Taek, Kulharya, Anita, Ha, Kyung-Soo, Itokawa, Yasuhide, Meliciani, Irene, Wenzel, Wolfgang, Lee, Deresa, Rosenberger, Georg, Ozata, Metin, Bick, David P., Sherins, Richard J., Nagase, Takahiro, Tekin, Mustafa, Kim, Soo-Hyun, Kim, Cheol-Hee, Ropers, Hans-Hilger, Gusella, James F., Kalscheuer, Vera, Choi, Cheol Yong, Layman, Lawrence C.

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POTE protein, a cancer-testis antigen, is highly expressed in spermatids in human testis and is associated with apoptotic cells by Bera, Tapan K., Walker, Dawn A., Sherins, Richard J., Pastan, Ira

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In Memoriam: C. Wayne Bardin, MD (1934 – 2019) by Sherins, Richard J., Santen, Richard J., Sitruk‐Ware, Regine, O’Malley, Bert, Bouchard, Philippe

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The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome by Pedersen-White, Jennifer R., Chorich, Lynn P., Bick, David P., Sherins, Richard J., Layman, Lawrence C.

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KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans by Bhagavath, Balasubramanian, Xu, Ning, Ozata, Metin, Rosenfield, Robert L., Bick, David P., Sherins, Richard J., Layman, Lawrence C.

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Analysis of the PROP1 gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadism by K. Park, John, Ozata, Metin, Chorich, Lynn P., Cheng, Lili, Bick, David P., Sherins, Richard J., Ozdemir, I. C., Bolu, Erol, Cogan, Joy D., Phillips III, John A., Layman, Lawrence C.

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Mutational Analysis of DAX1 in Patients with Hypogonadotropic Hypogonadism or Pubertal Delay1 by Achermann, John C, Gu, Wen-Xia, Kotlar, Tom J, Meeks, Joshua J, Sabacan, Leah P, Seminara, Stephanie B, Habiby, Reema L, Hindmarsh, Peter C, Bick, David P, Sherins, Richard J, Crowley Jr, William F, Layman, Lawrence C, Jameson, J. Larry

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Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay by ACHERMANN, J. C, GU, W.-X, CROWLEY, W. F, LAYMAN, L. C, JAMESON, J. L, KOTLAR, T. J, MEEKS, J. J, SABACAN, L. P, SEMINARA, S. B, HABIBY, R. L, HINDMARSH, P. C, BICK, D. P, SHERINS, R. J

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Recent Advances in Reproductive Genetic Technologies by Levinson, Gene, Coulam, Carolyn B., Spence, W. Christine, Sherins, Richard J., Schulman, Joseph D.

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Ultrastructural and biochemical analysis of sperm flagella from an infertile man with a rod-dominant retinal degeneration by Gentleman, Susan, Kaiser-Kupfer, Muriel I, Sherins, Richard J, Caruso, Rafael, Robison, W.Gerald, Lloyd-Muhammad, Rhea A, Crawford, Mary A, Pikus, Anita, Chader, Gerald J

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Mutations in CHD7, Encoding a Chronatin-Remodeling Protein. Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome by Kim, Hyung-Goo, Kurth, Ingo, Lan, Fei, Meliciani, Irene, Wenzel, Wolfgang, Eom, Soo Hyun, Kang, Gil Bu, Rosenberger, Georg, Tekin, Mustafa, Ozata, Metin, Bick, David P, Sherins, Richard J, Walker, Steven L, Shi, Yang, Gusella, James F, Layman, Lawrence C

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Genetics and human conception: DNA-based X-enriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked disease by Levinson, Gene, Keyvanfar, Keyvan, Wu, Joy C., Fugger, Edward F., Fields, Rita A., Harton, Gary L., Palmer, Frances T., Sisson, Michael E., Starr, Karin M., Dennison-Lagos, Lisa, Calvo, Lucrecia, Sherins, Richard J., Bick, David, Schulman, Joseph D., Black, Susan H.

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Andrology: Characterization and frequency distribution of sperm acrosome reaction among normal and infertile men by Calvo, Lucrecia, Dennison-Lagos, Lisa, Banks, Steven M., Sherins, Richard J.

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Andrology: Acrosome reaction inducibility predicts fertilization success at in-vitro fertilization by Calvo, Lucrecia, Dennison-Lagos, Lisa, Banks, Steven M., Dorfmann, Andrew, Thorsell, Lilli P., Bustillo, Maria, Schulman, Joseph D., Sherins, Richard J.

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Clinical Use and Misuse of Automated Semen Analysis by SHERINS, RICHARD J.

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Autoreproduction by hermaphrodites by Schulman, Joseph D., Sherins, Richard J.

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Chemical composition and protein source in the capacitation medium significantly affect the ability of human spermatozoa to undergo follicular fluid induced acrosome reaction by Calvo, Lucrecia, Dennison-Lagos, Lisa, Banks, Steven M., Fugger, Edward F., Sherins, Richard J.

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Hirsutism and Virilization by Sherins, Richard J., Horton, Richard

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DNA-based X-enriched sperm separation as an adjunct to preimplantation genetic testing for the prevention of X-linked disease by Levinson, Gene, Keyvanfar, Keyvan, Wu, Joy C., Fugger, Edward F., Fields, Rita A., Harton, Gary L., Palmer, Frances T., Sisson, Michael E., Starr, Karin M., Dennison-Lagos, Lisa, Calvo, Lucrecia, Sherins, Richard J., Bick, David, Schulman, Joseph D., Black, Susan H.

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