Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty
Tansit Saengkaew(Prince of Songkla University), Sasha Howard(Queen Mary University of London), Leo Dunkel(Kuopio University Hospital), Claudia Cabrera(Queen Mary University of London), Katia Mariniello(Queen Mary University of London), Alessia David(Imperial College London), Leonardo Guasti(Queen Mary University of London), Alessandra Mancini(Brigham and Women's Hospital), Michael R. Barnes(Munich Cluster for Systems Neurology), Gerard Ruiz‐Babot(Harvard Stem Cell Institute)
Cited by 8
Related Papers
Examination of US Puberty-Timing Data from 1940 to 1994 for Secular Trends: Panel Findings
|PEDIATRICS|2008|670
Disruption of the neurexin 1 gene is associated with schizophrenia
|Human Molecular Genetics|2008|485
Rituximab versus tocilizumab in rheumatoid arthritis: synovial biopsy-based biomarker analysis of the phase 4 R4RA randomized trial
|Nature Medicine|2022|277
Evidence for a Continuum of Genetic, Phenotypic, and Biochemical Abnormalities in Children with Growth Hormone Insensitivity
|Endocrine Reviews|2011|202
Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci
|The American Journal of Human Genetics|2014|165