Publications
Download CSV
Download XLSX
Download TXT
Tables
2024 (576)
2023 (879)
2022 (829)
2021 (892)
2020 (640)
2019 (727)
2018 (651)
2017 (681)
2016 (664)
2015 (429)
2014 (376)
2013 (319)
2012 (245)
2011 (163)
2010 (139)
All (8210)
Infrastructure Units
Infrastructure Units list
Infrastructure Units table
Researchers
Subset
Documentation
About
Contact
Software
Login
Mahajan A
JSON
CSV
XLSX
TXT
Family name
Mahajan
Given name
Anubha
Initials
A
ORCID
ORCID
0000-0001-5585-3420
Affiliations
Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
9 publications
PubMed
DOI
Crossref
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus.
Mathieson I
,
Day FR
, Barban N, ...,
Mills MC
,
Perry JRB
Nat Hum Behav
-
(-) - [2023-03-02; online 2023-03-02]
NGI SNP genotyping [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
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
Predicting and elucidating the etiology of fatty liver disease: A machine learning modeling and validation study in the IMI DIRECT cohorts.
Atabaki-Pasdar N
,
Ohlsson M
,
Viñuela A
, ..., Pavo I,
Franks PW
PLoS Med.
17
(6) e1003149 [2020-06-00; online 2020-06-19]
Affinity Proteomics Stockholm [Collaborative]
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]
PubMed
DOI
Crossref
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Bentley AR
, Sung YJ, Brown MR, ...,
Rotimi CN
,
Cupples LA
Nat. Genet.
51
(4) 636-648 [2019-04-00; online 2019-03-29]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Multi-ethnic genome-wide association study for atrial fibrillation.
Roselli C
,
Chaffin MD
, Weng LC, ..., Lunetta KL,
Ellinor PT
Nat. Genet.
50
(9) 1225-1233 [2018-06-11; online 2018-06-11]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
SciLifeLab Data Centre
Publications
9.5.1