Monogenic leptin deficiency in early childhood obesity

Severe early onset obesity due to a novel missense mutation in exon 3 of leptin gene in an infant from Northwest India

(2018) Devi Dayal et al.   Journal of Clinical Research in Pediatric Endocrinology

VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions

(2017) Peter J. Freeman et al.   HUMAN MUTATION

Genetics of non-syndromic childhood obesity and the use of high-throughput DNA sequencing technologies

(2017) Ana Carolina Proença da Fonseca et al.   JOURNAL OF DIABETES AND ITS COMPLICATIONS

Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants

(2017) Clara Serra-Juhé et al.   PLoS Genetics

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

(2016) Johan T. den Dunnen et al.   HUMAN MUTATION

Rare Genetic Forms of Obesity: Clinical Approach and Current Treatments in 2016

(2016) Hélène Huvenne et al.   Obesity Facts

20 YEARS OF LEPTIN: Human disorders of leptin action

(2014) I Sadaf Farooqi et al.   JOURNAL OF ENDOCRINOLOGY

One hundred years of congenital adrenal hyperplasia in Sweden: a retrospective, population-based cohort study

(2013) Sebastian Gidlöf et al.   Lancet Diabetes & Endocrinology

Ten years of leptin replacement therapy

(2011) G. Paz-Filho et al.   Obesity Reviews

Genomic insights into early-onset obesity

(2010) Hélène Choquet et al.   Genome Medicine

Lessons from Extreme Human Obesity: Monogenic Disorders

(2008) Sayali A. Ranadive et al.   ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA

The role of peptide YY in appetite regulation and obesity

(2008) Efthimia Karra et al.   JOURNAL OF PHYSIOLOGY-LONDON

Mutations in ligands and receptors of the leptin–melanocortin pathway that lead to obesity

(2008) I Sadaf Farooqi et al.   Nature clinical practice. Endocrinology & metabolism