Publications
Download CSV
Download XLSX
Download TXT
Tables
2024 (841)
2023 (887)
2022 (831)
2021 (892)
2020 (640)
2019 (727)
2018 (651)
2017 (681)
2016 (664)
2015 (429)
2014 (376)
2013 (319)
2012 (244)
2011 (163)
2010 (139)
2000 (2)
1977 (2)
All (8488)
Infrastructure Units
Infrastructure Units list
Infrastructure Units table
Researchers
Subset
Documentation
About
Contact
Software
Login
Milani L
JSON
CSV
XLSX
TXT
Family name
Milani
Given name
Lili
Initials
L
ORCID
ORCID
0000-0002-5323-3102
Affiliations
Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, 51010, Estonia.
10 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
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
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
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
de Las Fuentes L
, Sung YJ, Noordam R, ..., Rao DC, Fornage M
Mol. Psychiatry
26
(6) 2111-2125 [2021-06-00; online 2020-05-05]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
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
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
Interferon signature in patients with STAT1 gain-of-function mutation is epigenetically determined.
Kaleviste E, Saare M, Leahy TR, ...,
Peterson P
,
Kisand K
Eur. J. Immunol.
49
(5) 790-800 [2019-05-00; online 2019-03-07]
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
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Marshall CR, Howrigan DP, Merico D, ...,
Sebat J
, CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium
Nat. Genet.
49
(1) 27-35 [2017-01-00; online 2016-11-21]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
SciLifeLab Data Centre
Publications
9.5.1