Hakon Hakonarson
Hakon Hakonarson
Director, Center for Applied Genomics, CHOP, UPENN
Verified email at email.chop.edu - Homepage
Title
Cited by
Cited by
Year
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
K Wang, M Li, H Hakonarson
Nucleic acids research 38 (16), e164-e164, 2010
86092010
Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease
L Jostins, S Ripke, RK Weersma, RH Duerr, DP McGovern, KY Hui, ...
Nature 491 (7422), 119-124, 2012
39932012
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
31182013
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
A Franke, DPB McGovern, JC Barrett, K Wang, GL Radford-Smith, ...
Nature genetics 42 (12), 1118-1125, 2010
26972010
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
S Sawcer, G Hellenthal, M Pirinen, CCA Spencer, NA Patsopoulos, ...
Nature 476 (7359), 214, 2011
24512011
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
20122010
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ...
Nature genetics 43 (5), 436-441, 2011
17292011
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
K Wang, M Li, D Hadley, R Liu, J Glessner, SFA Grant, H Hakonarson, ...
Genome research 17 (11), 1665-1674, 2007
17102007
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
GB Ehret, PB Munroe, KM Rice, M Bochud, AD Johnson, DI Chasman, ...
Nature 478 (7367), 103-109, 2011
16192011
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
CA Anderson, G Boucher, CW Lees, A Franke, M D'Amato, KD Taylor, ...
Nature genetics 43 (3), 246-252, 2011
14352011
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ...
Nature 459 (7246), 569-573, 2009
14112009
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984-995, 2013
13362013
Identification of ALK as a major familial neuroblastoma predisposition gene
YP Mossť, M Laudenslager, L Longo, KA Cole, A Wood, EF Attiyeh, ...
Nature 455 (7215), 930-935, 2008
13232008
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke
A Helgadottir, A Manolescu, G Thorleifsson, S Gretarsdottir, H Jonsdottir, ...
Nature genetics 36 (3), 233-239, 2004
11452004
Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants
Myocardial Infarction Genetics Consortium
Nature genetics 41 (3), 334, 2009
11422009
An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data
TD Satterthwaite, MA Elliott, RT Gerraty, K Ruparel, J Loughead, ...
Neuroimage 64, 240-256, 2013
11252013
Sex differences in the structural connectome of the human brain
M Ingalhalikar, A Smith, D Parker, TD Satterthwaite, MA Elliott, K Ruparel, ...
Proceedings of the National Academy of Sciences 111 (2), 823-828, 2014
10732014
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
10242018
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
10232019
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
10162009
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