Läll K - Search Results

1

Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome.

Alver M, Mancini V, Läll K, Schneider M, Romano L; Estonian Biobank Research Team; Mägi R, Dermitzakis ET, Eliez S, Reymond A. Alver M, et al. Among authors: lall k. Mol Psychiatry. 2022 Oct;27(10):4191-4200. doi: 10.1038/s41380-022-01674-9. Epub 2022 Jun 29. Mol Psychiatry. 2022. PMID: 35768638 Free PMC article.

2

Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores.

Läll K, Mägi R, Morris A, Metspalu A, Fischer K. Läll K, et al. Genet Med. 2017 Mar;19(3):322-329. doi: 10.1038/gim.2016.103. Epub 2016 Aug 11. Genet Med. 2017. PMID: 27513194 Free PMC article.

3

Genetic variants linked to education predict longevity.

Marioni RE, Ritchie SJ, Joshi PK, Hagenaars SP, Okbay A, Fischer K, Adams MJ, Hill WD, Davies G; Social Science Genetic Association Consortium; Nagy R, Amador C, Läll K, Metspalu A, Liewald DC, Campbell A, Wilson JF, Hayward C, Esko T, Porteous DJ, Gale CR, Deary IJ. Marioni RE, et al. Among authors: lall k. Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):13366-13371. doi: 10.1073/pnas.1605334113. Epub 2016 Oct 31. Proc Natl Acad Sci U S A. 2016. PMID: 27799538 Free PMC article.

4

Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia.

Alver M, Palover M, Saar A, Läll K, Zekavat SM, Tõnisson N, Leitsalu L, Reigo A, Nikopensius T, Ainla T, Kals M, Mägi R, Gabriel SB, Eha J, Lander ES, Irs A, Philippakis A, Marandi T, Natarajan P, Metspalu A, Kathiresan S, Esko T. Alver M, et al. Among authors: lall k. Genet Med. 2019 May;21(5):1173-1180. doi: 10.1038/s41436-018-0311-2. Epub 2018 Oct 1. Genet Med. 2019. PMID: 30270359 Free PMC article.

5

Estimating the performance of three cardiovascular disease risk scores: the Estonian Biobank cohort study.

Saar A, Läll K, Alver M, Marandi T, Ainla T, Eha J, Metspalu A, Fischer K. Saar A, et al. Among authors: lall k. J Epidemiol Community Health. 2019 Mar;73(3):272-277. doi: 10.1136/jech-2017-209965. Epub 2019 Jan 11. J Epidemiol Community Health. 2019. PMID: 30635435

6

Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.

Timmers PR, Mounier N, Lall K, Fischer K, Ning Z, Feng X, Bretherick AD, Clark DW; eQTLGen Consortium; Shen X, Esko T, Kutalik Z, Wilson JF, Joshi PK. Timmers PR, et al. Among authors: lall k. Elife. 2019 Jan 15;8:e39856. doi: 10.7554/eLife.39856. Elife. 2019. PMID: 30642433 Free PMC article.

7

Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification.

Läll K, Lepamets M, Palover M, Esko T, Metspalu A, Tõnisson N, Padrik P, Mägi R, Fischer K. Läll K, et al. BMC Cancer. 2019 Jun 10;19(1):557. doi: 10.1186/s12885-019-5783-1. BMC Cancer. 2019. PMID: 31182048 Free PMC article.

8

Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort study.

Tillmann T, Läll K, Dukes O, Veronesi G, Pikhart H, Peasey A, Kubinova R, Kozela M, Pajak A, Nikitin Y, Malyutina S, Metspalu A, Esko T, Fischer K, Kivimäki M, Bobak M. Tillmann T, et al. Among authors: lall k. Eur Heart J. 2020 Sep 14;41(35):3325-3333. doi: 10.1093/eurheartj/ehaa571. Eur Heart J. 2020. PMID: 33011775 Free PMC article.

9

Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease.

Gola D, Erdmann J, Läll K, Mägi R, Müller-Myhsok B, Schunkert H, König IR. Gola D, et al. Among authors: lall k. Circ Genom Precis Med. 2020 Dec;13(6):e002932. doi: 10.1161/CIRCGEN.120.002932. Epub 2020 Nov 10. Circ Genom Precis Med. 2020. PMID: 33170024

10

Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis.

Ojavee SE, Kousathanas A, Trejo Banos D, Orliac EJ, Patxot M, Läll K, Mägi R, Fischer K, Kutalik Z, Robinson MR. Ojavee SE, et al. Among authors: lall k. Nat Commun. 2021 Apr 20;12(1):2337. doi: 10.1038/s41467-021-22538-w. Nat Commun. 2021. PMID: 33879782 Free PMC article.

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