Richard J. Sherins

CARE Fertility — United States

Medicine · Health Sciences

57h-index10.4kcitations154works0.02yr avg
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Research Topics

Sperm and Testicular Function(53), Hypothalamic control of reproductive hormones(39), Hormonal and reproductive studies(38), Sexual Differentiation and Disorders(30), Reproductive Biology and Fertility(28)

Publications154 total

In Memoriam: C. Wayne Bardin, 1934–2019
Endocrinology·2020Open Access
In Memoriam: C. Wayne Bardin, MD (1934 – 2019)
Andrology·2020Open Access
<i>In Memoriam</i>: C. Wayne Bardin, 1934-2019
The Journal of Clinical Endocrinology & Metabolism·2020Open Access
In Memoriam: C. Wayne Bardin, 1934–2019
Endocrine Reviews·2020Open Access
In Memoriam: C. Wayne Bardin, 1934-2019
Journal of the Endocrine Society·2020Open Access
Successful Fertility Restoration after Allogenic Hematopoietic Stem Cell Transplantation
Endocrine Practice·2014· 17 citedOpen Access
POTE protein, a cancer-testis antigen, is highly expressed in spermatids in human testis and is associated with apoptotic cells
Biochemical and Biophysical Research Communications·2012· 16 cited
The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome
Fertility and Sterility·2011· 104 citedOpen Access
Table of Contents
Fertility and Sterility·2011Open Access
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome
Fertility and Sterility·2011· 65 cited
WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
The American Journal of Human Genetics·2010· 192 citedOpen Access
C. Alvin Paulsen, M.D., 1924–2008
Fertility and Sterility·2010Open Access
Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
The American Journal of Human Genetics·2008· 331 citedOpen Access
The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
Molecular Human Reproduction·2008· 73 citedOpen Access
KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans
Molecular Human Reproduction·2007· 39 cited
Eugenia Rosemberg Endowment Fund
Journal of Andrology·2006
Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism
Fertility and Sterility·2006· 111 cited
REPRODUCTIVE ENDOCRINOLOGY Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism
2006
The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism
Fertility and Sterility·2005· 57 citedOpen Access
Analysis of the <i>PROP1</i> gene in a large cohort of patients with idiopathic hypogonadotropic hypogonadism
Clinical Endocrinology·2003· 7 cited
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Frequent Co-authors

David Bick(8), Lawrence C. Layman(6), D. Lynn Loriaux(4), Hyung‐Goo Kim(3), Metin Özata(3), Roger Lester(3), Allen S. Burris(3), Stephen J. Winters(3), Gary D. Hodgen(3), Richard V. Clark(3), David Vantman(3), Thaddeus Mann(2), Ingo Kurth(2), Irene Meliciani(2), Wolfgang Wenzel(2), Georg Rosenberger(2), Mustafa Tekin(2), James F. Gusella(2), David H. Van Thiel(2), Anita S. Kulharya(2)