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Epilepsia|January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies, Costin Leu, Carolien G F de Kovel, et al.
Gastrointestinal Endoscopy|February 14, 2016
EUS Needle Identification Comparison and Evaluation study (with videos)Shou-Jiang Tang, Andreas S Vilmann, Adrian Saftoiu, et al.
Brain : a Journal of Neurology|September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, et al.
NPJ Parkinson'S Disease|April 20, 2026
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Nicole Kuznetsov, et al.
Human Molecular Genetics|September 6, 2012
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32, , Michael Steffens, et al.
The British Journal of Social Psychology|March 4, 2025
Examining the connection between position-based power and social status across 70 culturesArkadiusz Wasiel, Maciej R Górski, Michael Harris Bond, et al.
American Journal of Human Genetics|November 19, 2025
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disabilityAriane Kröll-Hermi, Corinne Stoetzel, Christelle Etard, et al.
Neuropathology and Applied Neurobiology|August 13, 2021
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsiesAndre Altmann, Mina Ryten, Martina Di Nunzio, et al.
American Journal of Human Genetics|September 6, 2020
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract MalformationsDervla M Connaughton, Rufeng Dai, Danielle J Owen, et al.
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