Detalhe da pesquisa
1.
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 575(7783): E4, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31686056
2.
Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 572(7769): 323-328, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31367044
3.
Bayesian model comparison for rare-variant association studies.
Am J Hum Genet
; 108(12): 2354-2367, 2021 12 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34822764
4.
linemodels: clustering effects based on linear relationships.
Bioinformatics
; 39(3)2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36864614
5.
Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.
Ann Neurol
; 94(4): 713-726, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37486023
6.
Changes in the fine-scale genetic structure of Finland through the 20th century.
PLoS Genet
; 17(3): e1009347, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33661898
7.
Exploring machine learning strategies for predicting cardiovascular disease risk factors from multi-omic data.
BMC Med Inform Decis Mak
; 24(1): 116, 2024 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38698395
8.
Longitudinal multi-omics study reveals common etiology underlying association between plasma proteome and BMI trajectories in adolescent and young adult twins.
BMC Med
; 21(1): 508, 2023 12 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38129841
9.
Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools.
Brain
; 145(1): 142-153, 2022 03 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34273149
10.
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland.
Am J Hum Genet
; 104(6): 1169-1181, 2019 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31155286
11.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Mol Psychiatry
; 26(6): 2212-2223, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32157176
12.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Cephalalgia
; 42(7): 631-644, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35166138
13.
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.
Cephalalgia
; 42(4-5): 345-356, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34648375
14.
The budding and depth of invasion model in oral cancer: A systematic review and meta-analysis.
Oral Dis
; 28(2): 275-283, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33031610
15.
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 15(5): e1008190, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31145742
16.
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.
Am J Hum Genet
; 102(5): 760-775, 2018 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29706349
17.
Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in MUC5B mutation carriers.
Ann Rheum Dis
; 80(12): 1530-1536, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34344703
18.
Clinical significance of tumor-stroma ratio in head and neck cancer: a systematic review and meta-analysis.
BMC Cancer
; 21(1): 480, 2021 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33931044
19.
First genome-wide association study on rocuronium dose requirements shows association with SLCO1A2.
Br J Anaesth
; 126(5): 949-957, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33676726
20.
The fine-scale genetic structure of the British population.
Nature
; 519(7543): 309-314, 2015 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25788095