Publications
Download CSV
Download XLSX
Download TXT
Tables
2024 (239)
2023 (884)
2022 (828)
2021 (891)
2020 (640)
2019 (727)
2018 (651)
2017 (681)
2016 (664)
2015 (429)
2014 (376)
2013 (319)
2012 (245)
2011 (163)
2010 (139)
All (7876)
Infrastructure Units
Infrastructure Units list
Infrastructure Units table
Researchers
Subset
Documentation
About
Contact
Software
Login
Salomaa V
JSON
CSV
XLSX
TXT
Family name
Salomaa
Given name
Veikko
Initials
V
ORCID
ORCID
0000-0001-7563-5324
Affiliations
Finnish Institute for Health and Welfare, Helsinki, Finland.
10 publications
PubMed
DOI
Crossref
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.
Shrine N
, Izquierdo AG,
Chen J
, ...,
Hall IP
,
Tobin MD
Nat. Genet.
55
(3) 410-422 [2023-03-00; online 2023-03-13]
NGI SNP genotyping [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Stroke genetics informs drug discovery and risk prediction across ancestries.
Mishra A
, Malik R,
Hachiya T
, ...,
Dichgans M
, Debette S
Nature
611
(7934) 115-123 [2022-11-00; online 2022-09-30]
NGI SNP genotyping [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Winkler TW
,
Rasheed H
,
Teumer A
, ...,
Pattaro C
,
Heid IM
Commun Biol
5
(1) 580 [2022-06-13; online 2022-06-13]
NGI SNP genotyping [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
The power of genetic diversity in genome-wide association studies of lipids.
Graham SE
,
Clarke SL
,
Wu KH
, ...,
Sun YV
,
Willer CJ
Nature
600
(7890) 675-679 [2021-12-00; online 2021-12-09]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Lagou V, Mägi R,
Hottenga JJ
, ..., Prokopenko I, Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nat Commun
12
(1) 24 [2021-01-05; online 2021-01-05]
NGI Stockholm (Genomics Applications) [Service]
NGI Stockholm (Genomics Production) [Service]
NGI Uppsala (SNP&SEQ Technology Platform)
National Genomics Infrastructure
PubMed
DOI
Crossref
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus.
van Zuydam NR
,
Ladenvall C
,
Voight BF
, ...,
Palmer CNA
, SUMMIT Steering Committee; CARDIOGRAMplusC4D Steering Committee*
Circ Genom Precis Med
13
(6) e002769 [2020-12-00; online 2020-08-13]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Ntalla I,
Weng LC
, Cartwright JH, ...,
Lubitz SA
,
Munroe PB
Nat Commun
11
(1) 2542 [2020-05-21; online 2020-05-21]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Shah S
,
Henry A
,
Roselli C
, ..., Swerdlow DI,
Lumbers RT
Nat Commun
11
(1) 163 [2020-01-09; online 2020-01-09]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Associations of autozygosity with a broad range of human phenotypes.
Clark DW
,
Okada Y
,
Moore KHS
, ..., Kubo M,
Wilson JF
Nat Commun
10
(1) 4957 [2019-10-31; online 2019-10-31]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Wuttke M
,
Li Y
,
Li M
, ...,
Köttgen A
,
Pattaro C
Nat. Genet.
51
(6) 957-972 [2019-06-00; online 2019-05-31]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
SciLifeLab Data Centre
Publications
9.5.0