For researchers

Is your paper here?

2,673 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

83 matches for Ikram MA, showing the first 20.

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
Nature genetics · 2017 · PMID 28530673 · open access
5 pages
rs7646501 rs10191758 rs12744310 rs12928404 rs36093924
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
23andMe Research Team
Human molecular genetics · 2018 · PMID 29659830 · open access
5 pages
rs4927012 rs12474669 rs847158 rs10790969 rs1080014
Novel genetic loci affecting facial shape variation in humans
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
rs8077906 rs12504954 rs79732694 rs56049331 rs34032897
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
rs1740397 rs3809761 rs13297008 rs62330021 rs9971729
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs72934589 rs76110445 rs12415501 rs60401382 Cardioembolic Stroke
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
rs2107595 rs879324 rs13407662 Ischaemic Stroke
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
rs7214628 rs7894407 rs72848980 rs7909791
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair
Human molecular genetics · 2018 · PMID 29220522 · open access
4 pages
rs11585357 rs11170678 rs143290289 rs310642
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
4 pages
rs9308788 rs141962517 rs75535814 rs113809930
Genome-wide meta-analysis identifies new susceptibility loci for migraine
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
rs11759769 rs12134493 rs4379368
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature communications · 2017 · PMID 29030599 · open access
3 pages
rs34831921 rs55730499 Human Lifespan and Longevity
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages
Brain communications · 2020 · PMID 33345186 · open access
3 pages
rs75945125 rs71329093 rs2242882
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs112407396 rs72485816 rs6011998
Genome-wide gene-sleep interaction study identifies novel lipid loci in 732,564 participants
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
rs150607032 rs190975828 rs192018195
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
2 pages
rs2287921 rs17421627
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
rs9399599 rs3136739
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
rs9902453 rs7800944
Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity
Blood · 2015 · PMID 25934476
2 pages
rs3118667 rs41314453

Showing 20 of 83 · page 3 of 5

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.