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Structure: Internal structure identifier : 469696

Common variants at 12q14 and 12q24 are associated with hippocampal volume.

Joshua C Bis , Charles Decarli , Albert Vernon Smith , Fedde van Der Lijn , Fabrice Crivello , et al.
Nature Genetics, 2012, 44 (5), pp.545-551. ⟨10.1038/ng.2237⟩
Journal articles 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 , Lu Qi , Soren Brage , Stephen J. Sharp , Emily Sonestedt , et al.
PLoS Medicine, 2011, 8 (11), pp.e1001116. ⟨10.1371/journal.pmed.1001116⟩
Journal articles inserm-00702827v1
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Analysis of shared heritability in common disorders of the brain

Verneri Anttila , Brenda Sullivan , Hilary Finucane , Walter Walters , Jose Bras , et al.
Science, 2018, 360 (6395), eaap8757. ⟨10.1126/science.aap8757⟩
Journal articles 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 , Cláudio Pereira Figueira , Gisele R Santos , Kristel Lourdault , Michael Matthias , et al.
Infection and Immunity, 2016, 84 (7), pp.2105-2115. ⟨10.1128/IAI.00094-16⟩
Journal articles pasteur-02548670v1
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The Transcription Factor Encyclopedia.

Dimas Yusuf , Stefanie Butland , Magdalena Swanson , Eugene Bolotin , Amy Ticoll , et al.
Genome Biology, 2012, 13 (3), pp.R24. ⟨10.1186/gb-2012-13-3-r24⟩
Journal articles inserm-00716041v1

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

Karin R Engelhardt , Michael E Gertz , Sevgi Keles , Alejandro A Schäffer , Elena C Sigmund , et al.
Journal of Allergy and Clinical Immunology: In Practice, 2015, 136 (2), pp.402-12. ⟨10.1016/j.jaci.2014.12.1945⟩
Journal articles pasteur-01375035v1

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

Karin R. Engelhardt , Sean Mcghee , Sabine Winkler , Atfa Sassi , Cristina Woellner , et al.
Journal of Allergy and Clinical Immunology, 2009, 124 (6), pp.1289-1302. ⟨10.1016/j.jaci.2009.10.038⟩
Journal articles pasteur-01375326v1
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Novel genetic loci associated with hippocampal volume

Derrek P. Hibar , Hieab H. H. Adams , Neda Jahanshad , Ganesh Chauhan , Jason L. Stein , et al.
Nature Communications, 2017, 8, pp.13624. ⟨10.1038/ncomms13624⟩
Journal articles hal-01488337v1
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What Makes a Bacterial Species Pathogenic?:Comparative Genomic Analysis of the Genus Leptospira.

Derrick E Fouts , Michael A Matthias , Haritha Adhikarla , Ben Adler , Luciane Amorim-Santos , et al.
PLoS Neglected Tropical Diseases, 2016, 10 (2), pp.e0004403. ⟨10.1371/journal.pntd.0004403⟩
Journal articles pasteur-01436457v1

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.

Simon von Ameln , Geng Wang , Redouane Boulouiz , Mark A Rutherford , Geoffrey M Smith , et al.
American Journal of Human Genetics, 2012, 91 (5), pp.919-27. ⟨10.1016/j.ajhg.2012.09.002⟩
Journal articles pasteur-00796959v1
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Meta‐analysis of genome‐wide DNA methylation and integrative omics of age in human skeletal muscle

Sarah Voisin , Macsue Jacques , Shanie Landen , Nicholas R. Harvey , Larisa M. Haupt , et al.
Journal of Cachexia, Sarcopenia and Muscle, 2021, 12 (4), pp.1064-1078. ⟨10.1002/jcsm.12741⟩
Journal articles 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 , Sven van Der Lee , Adam Naj , Céline Bellenguez , Nandini Badarinarayan , et al.
Nature Genetics, 2017, 49 (9), pp.1373-1384. ⟨10.1038/ng.3916⟩
Journal articles inserm-02466466v1