Articles with public access mandates - David Wesley CraigLearn more
Not available anywhere: 5
Review
Deep sequencing of sncRNAs reveals hallmarks and regulatory modules of the transcriptome during Parkinson’s disease progression
F Kern, T Fehlmann, I Violich, E Alsop, E Hutchins, M Kahraman, ...
Nature Aging 1 (3), 309-322, 2021
Mandates: Michael J Fox Foundation
Review
BDNF expression in lymphoblastoid cell lines carrying BDNF SNPs associated with bipolar disorder
Y Gao, M Galante, J El-Mallakh, JI Nurnberger Jr, NA Delamere, Z Lei, ...
Psychiatric genetics 22 (5), 253-255, 2012
Mandates: US National Institutes of Health
Review
A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the …
C Balak, N Belnap, K Ramsey, S Joss, K Devriendt, M Naymik, W Jepsen, ...
American Journal of Medical Genetics Part A 176 (7), 1549-1558, 2018
Mandates: Wellcome Trust
Review
Death‐associated protein kinase 1 variation and Parkinson’s disease
JC Dachsel, C Wider, C Vilariño‐Güell, JO Aasly, A Rajput, AH Rajput, ...
European Journal of Neurology 18 (8), 1090-1093, 2011
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
Review
705. Using iPS Derived Neurons and GWAS Together to Identify Genes for Lithium Response
J Kelsoe, M McCarthy, C Nievergelt, P Shilling, J Nurnberger, E Gershon, ...
Biological Psychiatry 81 (10), S285-S286, 2017
Mandates: US National Institutes of Health
Available somewhere: 147
Review
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Review
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Mandates: Swiss National Science Foundation, US National Institutes of Health, Howard …
Review
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Mandates: Swiss National Science Foundation, US National Institutes of Health, Howard …
Review
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
Cross-Disorder Group of the Psychiatric Genomics Consortium
The Lancet 381 (9875), 1371-1379, 2013
Mandates: US National Institutes of Health, UK Medical Research Council
Review
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Mandates: US National Institutes of Health, Australian Research Council, National …
Review
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
Mandates: US National Institutes of Health, UK Medical Research Council, Parkinson's …
Review
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays
N Homer, S Szelinger, M Redman, D Duggan, W Tembe, J Muehling, ...
PLoS genetics 4 (8), e1000167, 2008
Mandates: US National Institutes of Health
Review
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Nature genetics 43 (10), 977-983, 2011
Mandates: US National Institutes of Health
Review
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
Mandates: Swiss National Science Foundation, US National Institutes of Health …
Review
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
Mandates: US National Institutes of Health, German Research Foundation
Review
Germline mutations in HOXB13 and prostate-cancer risk
CM Ewing, AM Ray, EM Lange, KA Zuhlke, CM Robbins, WD Tembe, ...
New England Journal of Medicine 366 (2), 141-149, 2012
Mandates: US National Institutes of Health
Review
Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing
RJ Leary, M Sausen, I Kinde, N Papadopoulos, JD Carpten, D Craig, ...
Science translational medicine 4 (162), 162ra154-162ra154, 2012
Mandates: US National Institutes of Health
Review
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
Mandates: US National Institutes of Health, Howard Hughes Medical Institute
Review
Translating RNA sequencing into clinical diagnostics: opportunities and challenges
SA Byron, KR Van Keuren-Jensen, DM Engelthaler, JD Carpten, ...
Nature Reviews Genetics 17 (5), 257-271, 2016
Mandates: US National Institutes of Health
Review
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
Mandates: US National Institutes of Health
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