Aarno Palotie
Aarno Palotie
FIMM, Broad Institute, UCLA, University of Helsinki, Sanger Institute
Verified email at helsinki.fi
TitleCited byYear
Executive summary: heart disease and stroke statistics—2013 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, WB Borden, ...
Circulation 127 (1), 143-152, 2013
127462013
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
66782010
Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285, 2016
53422016
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421, 2014
36032014
Heart disease and stroke statistics-2018 update: a report from the American Heart Association.
EJ Benjamin, SS Virani, CW Callaway, AM Chamberlain, AR Chang, ...
Circulation 137 (12), e67, 2018
24832018
Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
22432010
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
19022011
In vivo amplification of the androgen receptor gene and progression of human prostate cancer
T Visakorpi, E Hyytinen, P Koivisto, M Tanner, R Keinšnen, C Palmberg, ...
Nature genetics 9 (4), 401, 1995
15661995
Discovery and refinement of loci associated with lipid levels
CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, ...
Nature genetics 45 (11), 1274, 2013
14292013
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
T Jonsson, JK Atwal, S Steinberg, J Snaedal, PV Jonsson, S Bjornsson, ...
Nature 488 (7409), 96, 2012
13402012
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ...
Nature 515 (7526), 209, 2014
13092014
De novo mutations in schizophrenia implicate synaptic networks
M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ...
Nature 506 (7487), 179, 2014
10922014
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, 2013
10332013
TET1 and hydroxymethylcytosine in transcription and DNA methylation fidelity
K Williams, J Christensen, MT Pedersen, JV Johansen, PAC Cloos, ...
Nature 473 (7347), 343, 2011
8442011
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature genetics 48 (10), 1279, 2016
8212016
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
N Craddock, ME Hurles, N Cardin, RD Pearson, V Plagnol, S Robson, ...
Nature 464 (7289), 713, 2010
7752010
Carbonic anhydrase IX is an independent predictor of survival in advanced renal clear cell carcinoma: implications for prognosis and therapy
MHT Bui, D Seligson, K Han, AJ Pantuck, FJ Dorey, Y Huang, S Horvath, ...
Clinical cancer research 9 (2), 802-811, 2003
7362003
Genome-wide association study identifies 74 loci associated with educational attainment
A Okbay, JP Beauchamp, MA Fontana, JJ Lee, TH Pers, CA Rietveld, ...
Nature 533 (7604), 539, 2016
6832016
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
CA Rietveld, SE Medland, J Derringer, J Yang, T Esko, NW Martin, ...
science 340 (6139), 1467-1471, 2013
6292013
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, 2014
5902014
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