Allissa Dillman
Allissa Dillman
NLM, National Center for Biotechnology Information
Verified email at nih.gov
Title
Cited by
Cited by
Year
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
IPDG Consortium
The Lancet 377 (9766), 641-649, 2011
8672011
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
JR Gibbs, MP Van Der Brug, DG Hernandez, BJ Traynor, MA Nalls, SL Lai, ...
PLoS genetics 6 (5), e1000952, 2010
7912010
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivičres, ...
Nature 520 (7546), 224-229, 2015
6562015
Genetic variability in the regulation of gene expression in ten regions of the human brain
A Ramasamy, D Trabzuni, S Guelfi, V Varghese, C Smith, R Walker, T De, ...
Nature neuroscience 17 (10), 1418-1428, 2014
5472014
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699-705, 2011
4522011
The transcriptional landscape of age in human peripheral blood
MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ...
Nature communications 6 (1), 1-14, 2015
3472015
Genome-wide association study of obsessive-compulsive disorder
SE Stewart, D Yu, JM Scharf, BM Neale, JA Fagerness, CA Mathews, ...
Molecular psychiatry 18 (7), 788-798, 2013
3092013
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
3002014
Loss of VPS13C function in autosomal-recessive Parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
2422016
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
2122017
Novel genetic loci associated with hippocampal volume
DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ...
Nature communications 8 (1), 1-12, 2017
1942017
Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
Human molecular genetics 21 (22), 4996-5009, 2012
1872012
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ...
Nature neuroscience 19 (3), 420-431, 2016
1812016
A two-stage meta-analysis identifies several new loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium (IPDGC), ...
PLoS genetics 7 (6), e1002142, 2011
1812011
Novel genetic loci underlying human intracranial volume identified through genome-wide association
HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Renterķa, ...
Nature neuroscience 19 (12), 1569-1582, 2016
1682016
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies
D Trabzuni, S Wray, J Vandrovcova, A Ramasamy, R Walker, C Smith, ...
Human molecular genetics 21 (18), 4094-4103, 2012
1642012
Acetylation of cytidine in mRNA promotes translation efficiency
D Arango, D Sturgill, N Alhusaini, AA Dillman, TJ Sweet, G Hanson, ...
Cell 175 (7), 1872-1886. e24, 2018
1612018
Genomic biomarkers and cellular pathways of ischemic stroke by RNA gene expression profiling
TL Barr, Y Conley, J Ding, A Dillman, S Warach, A Singleton, M Matarin
Neurology 75 (11), 1009-1014, 2010
1582010
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma
MM Carrasquillo, AM Nicholson, NC Finch, JR Gibbs, M Baker, ...
The American Journal of Human Genetics 87 (6), 890-897, 2010
1352010
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain
DG Hernandez, MA Nalls, M Moore, S Chong, A Dillman, D Trabzuni, ...
Neurobiology of disease 47 (1), 20-28, 2012
1272012
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