Articles with public access mandates - Joseph D BuxbaumLearn more
Available somewhere: 331
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
Mandates: US National Institutes of Health, Danish Council for Independent Research …
Most genetic risk for autism resides with common variation
T Gaugler, L Klei, SJ Sanders, CA Bodea, AP Goldberg, AB Lee, ...
Nature genetics 46 (8), 881-885, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
V Trubetskoy, AF Pardiñas, T Qi, G Panagiotaropoulou, S Awasthi, ...
Nature 604 (7906), 502-508, 2022
Mandates: Fundação de Amparo à Pesquisa do Estado de São Paulo, US National Institutes …
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
Mandates: US National Institutes of Health, Autism Speaks Inc, USA
A framework for the interpretation of de novo mutation in human disease
KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ...
Nature genetics 46 (9), 944-950, 2014
Mandates: US National Institutes of Health, Autism Speaks Inc, USA
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Gene expression elucidates functional impact of polygenic risk for schizophrenia
M Fromer, P Roussos, SK Sieberts, JS Johnson, DH Kavanagh, ...
Nature neuroscience 19 (11), 1442-1453, 2016
Mandates: US National Institutes of Health, US Department of Veterans Affairs
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
Mandates: US National Institutes of Health, Swedish Research Council, UK Medical …
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27-35, 2017
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
Mandates: US Department of Defense, US National Institutes of Health, US Department of …
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
Mandates: US National Institutes of Health, Health Research Board, Ireland, UK Medical …
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution
JJ Smith, S Kuraku, C Holt, T Sauka-Spengler, N Jiang, MS Campbell, ...
Nature genetics 45 (4), 415-421, 2013
Mandates: US National Institutes of Health, Canadian Institutes of Health Research, UK …
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
Mandates: US National Institutes of Health, Australian Research Council, National …
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
O Bozdagi, T Sakurai, D Papapetrou, X Wang, DL Dickstein, N Takahashi, ...
Molecular autism 1, 1-15, 2010
Mandates: US National Institutes of Health
A spectral approach integrating functional genomic annotations for coding and noncoding variants
I Ionita-Laza, K McCallum, B Xu, JD Buxbaum
Nature genetics 48 (2), 214-220, 2016
Mandates: US National Institutes of Health
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
Mandates: US National Institutes of Health
Association of genetic and environmental factors with autism in a 5-country cohort
D Bai, BHK Yip, GC Windham, A Sourander, R Francis, R Yoffe, ...
JAMA psychiatry 76 (10), 1035-1043, 2019
Mandates: US National Institutes of Health, National Health and Medical Research …
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
Mandates: US National Institutes of Health, National Health and Medical Research …
Publication and funding information is determined automatically by a computer program