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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
98452010
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
43762012
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
34632013
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
28372010
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
26242011
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
21002010
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
20592013
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
18632011
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
17902007
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
15172011
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
14562009
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
14182008
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
13142019
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
12722013
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
12232019
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
12122014
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ...
Nature genetics 41 (3), 334-341, 2009
12032009
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
11562004
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
11212013
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
10492009
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