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Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Joshua C Bis
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Charles Decarli
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Albert Vernon Smith
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Fedde van Der Lijn
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Fabrice Crivello
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hal-01157821v1
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Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children.
Tuomas O. Kilpeläinen
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Lu Qi
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Soren Brage
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Stephen J. Sharp
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Emily Sonestedt
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inserm-00702827v1
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Analysis of shared heritability in common disorders of the brain
Verneri Anttila
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Brenda Sullivan
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Hilary Finucane
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Walter Walters
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Jose Bras
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cea-01870483v1
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Real-Time PCR Reveals Rapid Dissemination of Leptospira interrogans after Intraperitoneal and Conjunctival Inoculation of Hamsters
Elsio A. Jr Wunder
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Cláudio Pereira Figueira
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Gisele R Santos
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Kristel Lourdault
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Michael Matthias
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pasteur-02548670v1
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The Transcription Factor Encyclopedia.
Dimas Yusuf
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Stefanie Butland
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Magdalena Swanson
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Eugene Bolotin
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Amy Ticoll
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inserm-00716041v1
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The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
Karin R Engelhardt
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Michael E Gertz
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Sevgi Keles
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Alejandro A Schäffer
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Elena C Sigmund
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pasteur-01375035v1
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Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
Karin R. Engelhardt
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Sean Mcghee
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Sabine Winkler
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Atfa Sassi
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Cristina Woellner
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pasteur-01375326v1
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Novel genetic loci associated with hippocampal volume
Derrek P. Hibar
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Hieab H. H. Adams
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Neda Jahanshad
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Ganesh Chauhan
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Jason L. Stein
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hal-01488337v1
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What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira.
Derrick E Fouts
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Michael A Matthias
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Haritha Adhikarla
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Ben Adler
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Luciane Amorim-Santos
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pasteur-01436457v1
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A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.
Simon von Ameln
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Geng Wang
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Redouane Boulouiz
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Mark A Rutherford
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Geoffrey M Smith
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pasteur-00796959v1
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Meta‐analysis of genome‐wide DNA methylation and integrative omics of age in human skeletal muscle
Sarah Voisin
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Macsue Jacques
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Shanie Landen
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Nicholas R. Harvey
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Larisa M. Haupt
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hal-03278982v1
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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Rebecca Sims
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Sven van Der Lee
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Adam Naj
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Céline Bellenguez
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Nandini Badarinarayan
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inserm-02466466v1
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