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Mahajan A
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CSV
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TXT
Family name
Mahajan
Given name
Anubha
Initials
A
ORCID
ORCID
0000-0001-5585-3420
Affiliations
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
32 publications
PubMed
DOI
Crossref
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Shrine N
,
Guyatt AL
, Erzurumluoglu AM, ...,
Tobin MD
,
Wain LV
Nat. Genet.
56
(5) 1032-1033 [2024-05-00; online 2024-04-20]
PubMed
DOI
Crossref
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Suzuki K,
Hatzikotoulas K
, Southam L, ...,
Morris AP
,
Zeggini E
Nature
627
(8003) 347-357 [2024-03-00; online 2024-02-19]
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
7
(5) 790-801 [2023-05-00; online 2023-03-02]
PubMed
DOI
Crossref
Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression.
Mattis KK
,
Krentz NAJ
,
Metzendorf C
, ...,
den Hoed M
,
Gloyn AL
Diabetologia
66
(4) 674-694 [2023-04-00; online 2023-01-12]
DOI
Crossref
Loss of RREB1 in pancreatic beta cells reduces cellular insulin content and affects endocrine cell gene expression
Mattis KK,
Krentz NA
,
Metzendorf C
, ...,
den Hoed M
,
Gloyn AL
-
-
(-) - [2022-06-05; online 2022-06-05]
PubMed
DOI
Crossref
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.
Mahajan A
, Spracklen CN,
Zhang W
, ..., McCarthy MI,
Morris AP
Nat. Genet.
54
(5) 560-572 [2022-05-00; online 2022-05-12]
DOI
Crossref
Genetic analysis of blood molecular phenotypes reveals regulatory networks affecting complex traits: a DIRECT study
Viñuela A
,
Brown AA
, Fernandez J, ...,
Pearson ER
,
Dermitzakis ET
-
-
(-) - [2021-03-29; online 2021-03-29]
PubMed
DOI
Crossref
Processes Underlying Glycemic Deterioration in Type 2 Diabetes: An IMI DIRECT Study.
Bizzotto R
, Jennison C,
Jones AG
, ...,
Mari A
, IMI DIRECT consortium
Diabetes Care
44
(2) 511-518 [2021-02-00; online 2020-12-15]
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]
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]
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]
PubMed
DOI
Crossref
Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank: A Mendelian randomization study.
Wainberg M
,
Mahajan A
,
Kundaje A
, ...,
Sinnott-Armstrong N
, Rivas MA
PLoS Med.
16
(12) e1002982 [2019-12-00; online 2019-12-10]
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]
PubMed
DOI
Crossref
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
Tin A
,
Marten J
, Halperin Kuhns VL, ...,
Vitart V
,
Köttgen A
Nat. Genet.
51
(10) 1459-1474 [2019-10-00; online 2019-10-02]
PubMed
DOI
Crossref
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Teumer A
,
Li Y
, Ghasemi S, ...,
Pattaro C
,
Köttgen A
Nat Commun
10
(1) 4130 [2019-09-11; online 2019-09-11]
PubMed
DOI
Crossref
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Shrine N
,
Guyatt AL
, Erzurumluoglu AM, ...,
Tobin MD
,
Wain LV
Nat. Genet.
51
(6) 1067 [2019-06-00; online 2019-05-22]
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]
PubMed
DOI
Crossref
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Shrine N
,
Guyatt AL
, Erzurumluoglu AM, ...,
Wain LV
, Understanding Society Scientific Group
Nat. Genet.
51
(3) 481-493 [2019-03-00; online 2019-02-25]
PubMed
DOI
Crossref
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Justice AE, Karaderi T, Highland HM, ..., T2D-Genes Consortium , MAGIC Investigators
Nat. Genet.
51
(3) 452-469 [2019-03-00; online 2019-02-18]
PubMed
DOI
Crossref
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.
Morris AP
, Le TH, Wu H, ...,
Humphreys BD
, Franceschini N
Nat Commun
10
(1) 29 [2019-01-03; online 2019-01-03]
PubMed
DOI
Crossref
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Evangelou E
, Warren HR, Mosen-Ansorena D, ...,
Elliott P
,
Caulfield MJ
Nat. Genet.
50
(12) 1755 [2018-12-00; online 2018-11-16]
PubMed
DOI
Crossref
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Mahajan A
, Taliun D, Thurner M, ...,
Boehnke M
,
McCarthy MI
Nat. Genet.
50
(11) 1505-1513 [2018-11-00; online 2018-10-08]
PubMed
DOI
Crossref
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Evangelou E
, Warren HR, Mosen-Ansorena D, ...,
Caulfield MJ
, Million Veteran Program
Nat. Genet.
50
(10) 1412-1425 [2018-10-00; online 2018-09-17]
DOI
Crossref
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE
, Latourelle JC,
Wain LV
, ...,
Tobin MD
,
London SJ
Wellcome Open Res
3
(-) 4 [2018-06-21; online 2018-06-21]
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]
PubMed
DOI
Crossref
Habitual coffee consumption and cognitive function: a Mendelian randomization meta-analysis in up to 415,530 participants.
Zhou A, Taylor AE, Karhunen V, ..., Llewellyn DJ, Hyppönen E
Sci Rep
8
(1) 7526 [2018-05-14; online 2018-05-14]
DOI
Crossref
Discovery of biomarkers for glycaemic deterioration before and after the onset of type 2 diabetes: an overview of the data from the epidemiological studies within the IMI DIRECT Consortium
Koivula RW
, Forgie IM, Kurbasic A, ..., Pearson E,
Franks PW
-
-
(-) - [2018-04-16; online 2018-04-16]
PubMed
DOI
Crossref
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Mahajan A
, Wessel J, Willems SM, ..., Rotter JI,
McCarthy MI
Nat. Genet.
50
(4) 559-571 [2018-04-00; online 2018-04-09]
DOI
Crossref
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE
, Latourelle JC,
Wain LV
, ...,
Tobin MD
,
London SJ
Wellcome Open Res
3
(-) 4 [2018-01-12; online 2018-01-12]
PubMed
DOI
Crossref
Meta-analysis of exome array data identifies six novel genetic loci for lung function.
Jackson VE
, Latourelle JC,
Wain LV
, ..., Tobin MD,
London SJ
Wellcome Open Res
3
(-) 4 [2018-01-12; online 2018-01-12]
DOI
Crossref
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Mahajan A
, Taliun D, Thurner M, ..., Boehnke M,
McCarthy MI
-
-
(-) - [2018-01-09; online 2018-01-09]
DOI
Crossref
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Mahajan A
, Wessel J, Willems SM, ..., Rotter JI, McCarthy MI
-
-
(-) - [2017-05-31; online 2017-05-31]
SciLifeLab Data Centre
Publications
9.5.1