팔로우
Priit Palta
Priit Palta
Estonian Genome Centre, Institute of Genomics, University of Tartu
ut.ee의 이메일 확인됨 - 홈페이지
제목
인용
인용
연도
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
19742023
De novo mutations in schizophrenia implicate synaptic networks
M Fromer, AJ Pocklington, DH Kavanagh, HJ Williams, S Dwyer, ...
Nature 506 (7487), 179-184, 2014
18592014
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
14882018
Detection and interpretation of shared genetic influences on 42 human traits
JK Pickrell, T Berisa, JZ Liu, L Ségurel, JY Tung, DA Hinds
Nature genetics 48 (7), 709-717, 2016
12462016
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
7992016
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium
Science (New York, NY) 360 (6395), 2018
7032018
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
6262010
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
4872013
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
4772014
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
4672010
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
4412022
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
3852020
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
2832022
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
2342017
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
1652019
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
1422021
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
1392020
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
1362015
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
1162012
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
1082018
현재 시스템이 작동되지 않습니다. 나중에 다시 시도해 주세요.
학술자료 1–20