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Plos One|February 6, 2013
Age- and sex-related variations in platelet count in Italy: a proposal of reference ranges based on 40987 subjects' dataGinevra Biino, Iolanda Santimone, Cosetta Minelli, et al.Plos One|November 16, 2016
Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum HepcidinTessel E Galesloot, Niek Verweij, Michela Traglia, et al.Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.Nature Communications|June 24, 2017
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populationsYali Xue, Massimo Mezzavilla, Marc Haber, et al.American Journal of Human Genetics|February 18, 2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephalyMaila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna, et al.Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.Genes|December 23, 2022
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis SusceptibilityFederica Esposito, Ana Maria Osiceanu, Melissa Sorosina, et al.Journal of the American Society of Nephrology : JASN|March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysisMatthias Olden, Tanguy Corre, Caroline Hayward, et al.Brain : a Journal of Neurology|January 12, 2017
COL6A5 variants in familial neuropathic chronic itchFilippo Martinelli-Boneschi, Marina Colombi, Marco Castori, et al.Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.Pageof 12