MANAGEMENT OF ENDOCRINE DISEASE: Reversible hypogonadotropic hypogonadism: Table 1

Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the “-Omics” Era

(2015) M. I. Stamou et al.   ENDOCRINE REVIEWS

Epigenetic regulation of female puberty

(2015) Alejandro Lomniczi et al.   FRONTIERS IN NEUROENDOCRINOLOGY

Evaluation of 451 Danish Boys With Delayed Puberty: Diagnostic Use of a New Puberty Nomogram and Effects of Oral Testosterone Therapy

(2015) Jacob Gerner Lawaetz et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Shared genetic aetiology of puberty timing between sexes and with health-related outcomes

(2015) Felix R. Day et al.   Nature Communications

Mutations in FEZF1 Cause Kallmann Syndrome

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

TRANSITION IN ENDOCRINOLOGY: Induction of puberty

(2014) Leo Dunkel et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Role of gonadotropin-releasing hormone receptor mutations in patients with a wide spectrum of pubertal delay

(2014) Daiane Beneduzzi et al.   FERTILITY AND STERILITY

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

(2014) John R. B. Perry et al.   NATURE

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

(2013) Hichem Miraoui et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

(2013) Veronique Pingault et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Reversal of isolated hypogonadotropic hypogonadism: long-term integrity of hypothalamo-pituitary-testicular axis in two men is dependent on intermittent androgen exposure

(2013) Anjali Santhakumar et al.   CLINICAL ENDOCRINOLOGY

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

Opposite-sex housing reactivates the declining GnRH system in aged transgenic male mice with FGF signaling deficiency

(2012) Johanna R. Rochester et al.   AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM

A homozygous R262Q mutation in the gonadotropin-releasing hormone receptor presenting as reversal of hypogonadotropic hypogonadism and late-onset hypogonadism

(2012) Johanna Tommiska et al.   CLINICAL ENDOCRINOLOGY

PROKR2 and PROK2 mutations cause isolated congenital anosmia without gonadotropic deficiency

(2012) Antoine Moya-Plana et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

(2012) Jacques Young et al.   HUMAN REPRODUCTION

InactivatingKISS1Mutation and Hypogonadotropic Hypogonadism

(2012) A. Kemal Topaloglu et al.   NEW ENGLAND JOURNAL OF MEDICINE

Delayed Puberty

(2012) Mark R. Palmert et al.   NEW ENGLAND JOURNAL OF MEDICINE

Reversible Congenital Hypogonadotropic Hypogonadism in Patients with CHD7, FGFR1 or GNRHR Mutations

(2012) Eeva-Maria Laitinen et al.   PLoS One

SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome

(2012) Naresh Kumar Hanchate et al.   PLoS Genetics

GnRH-Deficient Phenotypes in Humans and Mice with Heterozygous Variants inKISS1/Kiss1

(2011) Yee-Ming Chan et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Genetic counseling for isolated GnRH deficiency

(2011) Margaret G. Au et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

A Genetic Basis for Functional Hypothalamic Amenorrhea

(2011) Lisa M. Caronia et al.   NEW ENGLAND JOURNAL OF MEDICINE

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

(2011) J. Tornberg et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

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

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

(2009) Taneli Raivio et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Isolated Familial Hypogonadotropic Hypogonadism and aGNRH1Mutation

(2009) Jérôme Bouligand et al.   NEW ENGLAND JOURNAL OF MEDICINE

The Fetal Hypothalamus Has the Potential to Generate Cells with a Gonadotropin Releasing Hormone (GnRH) Phenotype

(2009) Roberto Salvi et al.   PLoS One

GNRH1mutations in patients with idiopathic hypogonadotropic hypogonadism

(2009) Yee-Ming Chan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: Case Report

(2008) A. A. Sinisi et al.   HUMAN REPRODUCTION

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

(2008) Lindsay W. Cole et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Gonadotropin-Releasing Hormone Neuron Requirements for Puberty, Ovulation, and Fertility

(2007) Allan E. Herbison et al.   ENDOCRINOLOGY