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Gieger C
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Family name
Gieger
Given name
Christian
Initials
C
ORCID
ORCID
0000-0001-6986-9554
Affiliations
Research Unit Molecular Epidemiology, Helmholtz Center Munich - German Research Center for Environmental Health, Neuherberg, Germany.
9 publications
PubMed
DOI
Crossref
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.
Williamson A
, Norris DM, Yin X, ...,
Fazakerley DJ
,
Langenberg C
Nat. Genet.
55
(6) 973-983 [2023-06-00; online 2023-06-08]
NGI SNP genotyping [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
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
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
Epigenome-wide association study of serum urate reveals insights into urate co-regulation and the SLC2A9 locus.
Tin A
,
Schlosser P
, Matias-Garcia PR, ...,
Teumer A
,
Köttgen A
Nat Commun
12
(1) 7173 [2021-12-09; online 2021-12-09]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Meta-analyses identify DNA methylation associated with kidney function and damage.
Schlosser P
,
Tin A
, Matias-Garcia PR, ...,
Köttgen A
,
Teumer A
Nat Commun
12
(1) 7174 [2021-12-09; online 2021-12-09]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
Grosche S, Marenholz I, Esparza-Gordillo J, ..., Xu C, Lee Y
Nat Commun
12
(1) 6618 [2021-11-16; online 2021-11-16]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Ferreira MA
, Vonk JM, Baurecht H, ...,
Koppelman GH
,
Paternoster L
Nat. Genet.
49
(12) 1752-1757 [2017-12-00; online 2017-10-30]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
SciLifeLab Data Centre
Publications
9.5.1