Lawrence C. Layman

Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Hyung‐Goo Kim, Ingo Kurth, Fei Lan et al. · The American Journal of Human Genetics · 2008 · 332 citations · Full text

Medicine, Endocrinology, Genetics +15

Liquid Chromatography–Tandem Mass Spectrometry Analysis of Human Adrenal Vein 19-Carbon Steroids Before and After ACTH Stimulation

Juilee Rege, Yasuhiro Nakamura, Fumitoshi Satoh et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 233 citations · Full text

Life Sciences, Biochemistry, Endocrinology +17

WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Hyung‐Goo Kim, Jang-Won Ahn, Ingo Kurth et al. · The American Journal of Human Genetics · 2010 · 196 citations · Full text

Life Sciences, Endocrinology, Genetics +11

FSHβ Gene Mutations in a Female with Partial Breast Development and a Male Sibling with Normal Puberty and Azoospermia

Lawrence C. Layman, Adriana Lofrano Alves Porto, Jun Xie et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 128 citations · Full text

Medicine, Endocrinology, Genetics +17

Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism

Balasubramanian Bhagavath, Robert H. Podolsky, Metin Özata et al. · Fertility and Sterility · 2006 · 111 citations

Medicine, Endocrinology, Molecular Medicine +14