Articles with public access mandates - Joseph D Buxbaum - German Research FoundationLearn more
NoteFor this mandate, articles should be available from specific locations.
Available based on mandate: 27
Review
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ...
PLoS genetics 18 (11), e1010367, 2022
Review
Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis
E Velthorst, S Froudist-Walsh, E Stahl, D Ruderfer, I Ivanov, J Buxbaum, ...
Translational psychiatry 8 (1), 204, 2018
Review
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD
L Pavinato, A Delle Vedove, D Carli, M Ferrero, S Carestiato, JL Howe, ...
Brain 146 (2), 534-548, 2023
Review
StandardRat: A multi-center consensus protocol to enhance functional connectivity specificity in the rat brain
J Grandjean, G Desrosiers-Gregoire, C Anckaerts, D Angeles-Valdez, ...
bioRxiv, 2022.04. 27.489658, 2022
Review
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome
P Jain, T Miller-Fleming, A Topaloudi, D Yu, P Drineas, M Georgitsi, ...
Translational psychiatry 13 (1), 69, 2023
Review
Genome-wide Association Study identifies two novel loci for Gilles de la Tourette Syndrome
F Tsetsos, A Topaloudi, P Jain, Z Yang, D Yu, P Kolovos, Z Tumer, ...
medRxiv, 2021.12. 11.21267560, 2021
Review
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics …
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
bioRxiv, 040493, 2016
Publication and funding information is determined automatically by a computer program