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Nature Neuroscience|March 18, 2018
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.
Nature|October 9, 2009
Finding the missing heritability of complex diseasesTeri A Manolio, Francis S Collins, Nancy J Cox, et al.
The New England Journal of Medicine|March 25, 2011
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in EuropeansMark McCormack, Ana Alfirevic, Stephane Bourgeois, et al.
American Journal of Human Genetics|September 26, 2017
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with SeizuresCandace T Myers, Nicholas Stong, Emily I Mountier, et al.
Orphanet Journal of Rare Diseases|September 28, 2015
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patientsEleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Autoantibodies neutralizing type I IFNs in 40% of patients with WNV encephalitis in seven new cohortsAdrian Gervais, Francesca Trespidi, Alessandro Ferrari, et al.
Journal of Human Immunity|March 16, 2026
Autoantibodies neutralizing type I IFNs in 40% of patients with WNV encephalitis in seven new cohortsAdrian Gervais, Francesca Trespidi, Alessandro Ferrari, et al.
BMC Bioinformatics|August 15, 2025
HIV-phyloTSI: subtype-independent estimation of time since HIV-1 infection for cross-sectional measures of population incidence using deep sequence dataTanya Golubchik, Lucie Abeler-Dörner, Matthew Hall, et al.
Trials|July 6, 2021
Hormonal intervention for the treatment of veterans with COVID-19 requiring hospitalization (HITCH): a multicenter, phase 2 randomized controlled trial of best supportive care vs best supportive care plus degarelix: study protocol for a randomized controlled trialNicholas G Nickols, Matthew B Goetz, Christopher J Graber, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyErin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, et al.
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