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Priit Palta
Priit Palta
Estonian Genome Centre, Institute of Genomics, University of Tartu
在 ut.ee 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
De novo mutations in schizophrenia implicate synaptic networks
M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ...
Nature 506 (7487), 179-184, 2014
18122014
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
14042018
FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
12912023
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
7562016
A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2
RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ...
Nature 463 (7281), 671-675, 2010
6042010
Genome-wide meta-analysis identifies new susceptibility loci for migraine
V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ...
Nature genetics 45 (8), 912-917, 2013
4712013
Distribution and medical impact of loss-of-function variants in the Finnish founder population
ET Lim, P Würtz, AS Havulinna, P Palta, T Tukiainen, K Rehnström, ...
PLoS genetics 10 (7), e1004494, 2014
4622014
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
4592010
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
medrxiv, 2022.03. 03.22271360, 2022
4122022
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers
N Mars, JT Koskela, P Ripatti, TTJ Kiiskinen, AS Havulinna, JV Lindbohm, ...
Nature medicine 26 (4), 549-557, 2020
3432020
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ...
Cell Genomics 2 (10), 2022
2252022
Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel
M Mitt, M Kals, K Pärn, SB Gabriel, ES Lander, A Palotie, S Ripatti, ...
European Journal of Human Genetics 25 (7), 869-876, 2017
2112017
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
R Tabassum, JT Rämö, P Ripatti, JT Koskela, M Kurki, J Karjalainen, ...
Nature communications 10 (1), 4329, 2019
1522019
Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants
R Malik, T Freilinger, BS Winsvold, V Anttila, J Vander Heiden, M Traylor, ...
Neurology 84 (21), 2132-2145, 2015
1322015
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health
S Strausz, S Ruotsalainen, HM Ollila, J Karjalainen, T Kiiskinen, M Reeve, ...
European Respiratory Journal 57 (5), 2021
1232021
The role of polygenic risk and susceptibility genes in breast cancer over the course of life
N Mars, E Widén, S Kerminen, T Meretoja, M Pirinen, ...
Nature communications 11 (1), 6383, 2020
1162020
A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip® for methylome profiling
C Clark, P Palta, CJ Joyce, C Scott, E Grundberg, P Deloukas, A Palotie, ...
PloS one 7 (11), e50233, 2012
1152012
Common variant burden contributes to the familial aggregation of migraine in 1,589 families
P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ...
Neuron 98 (4), 743-753. e4, 2018
982018
Polygenic hyperlipidemias and coronary artery disease risk
P Ripatti, JT Rämö, NJ Mars, Y Fu, J Lin, S Söderlund, C Benner, ...
Circulation: Genomic and Precision Medicine 13 (4), e002725, 2020
922020
The GENCODE exome: sequencing the complete human exome
AJ Coffey, F Kokocinski, MS Calafato, CE Scott, P Palta, E Drury, ...
European journal of human genetics 19 (7), 827-831, 2011
872011
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