CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism

IGSF10mutations dysregulate gonadotropin‐releasing hormone neuronal migration resulting in delayed puberty

(2016) Sasha R Howard et al.   EMBO Molecular Medicine

CCDC141 Mutation Identified in Anosmic Hypogonadotropic Hypogonadism (Kallmann Syndrome) Alters GnRH Neuronal Migration

(2016) B. Ian Hutchins et al.   ENDOCRINOLOGY

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

(2015) Jessica X. Chong et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Shared Genetic Basis for Self-Limited Delayed Puberty and Idiopathic Hypogonadotropic Hypogonadism

(2015) Jia Zhu et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mutations in FEZF1 Cause Kallmann Syndrome

(2014) L. Damla Kotan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Reversal and Relapse of Hypogonadotropic Hypogonadism: Resilience and Fragility of the Reproductive Neuroendocrine System

(2013) Valerie F. Sidhoum et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Calcium Release-Dependent Actin Flow in the Leading Process Mediates Axophilic Migration

(2013) B. I. Hutchins et al.   JOURNAL OF NEUROSCIENCE

wANNOVAR: annotating genetic variants for personal genomes via the web

(2012) Xiao Chang et al.   JOURNAL OF MEDICAL GENETICS

CAMDI, a Novel Disrupted in Schizophrenia 1 (DISC1)-binding Protein, Is Required for Radial Migration

(2010) Toshifumi Fukuda et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

TAC3/TACR3Mutations Reveal Preferential Activation of Gonadotropin-Releasing Hormone Release by Neurokinin B in Neonatal Life Followed by Reversal in Adulthood

(2010) Elena Gianetti et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

From Nose to Brain: Development of Gonadotrophin-Releasing Hormone -1 Neurones

(2010) S. Wray   JOURNAL OF NEUROENDOCRINOLOGY

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency

(2010) G. P. Sykiotis et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: The pitfalls of homozygosity mapping

(2009) Liat Benayoun et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

(2009) Julie Sarfati et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Fezf1is required for penetration of the basal lamina by olfactory axons to promote olfactory development

(2009) Yasuhito Watanabe et al.   JOURNAL OF COMPARATIVE NEUROLOGY