For researchers

Is your paper here?

2,690 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.

17 matches for Boland A.

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
10 pages
rs3848143 rs10947943 rs62374257 rs3851179 rs6605556 rs7767350
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden
ILCCO consortium
Journal of the National Cancer Institute · 2022 · PMID 35511172 · open access
7 pages
rs6457312 rs239933 rs11571815 rs72905558 rs3129813 rs78062588
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Nature communications · 2017 · PMID 28598434 · open access
6 pages
rs4381241 rs67311347 rs11813268 rs74911261 rs4903064 Renal Cell Carcinoma
Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes
Blood · 2025 · PMID 40811855
5 pages
rs113846542 rs45562031 rs145765113 rs3744462 rs148611543
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Nature genetics · 2014 · PMID 25305756 · open access
4 pages
rs17019602 rs6677604 rs2412971 IgA Nephropathy
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
EADB consortium · GR@ACE study group
Acta neuropathologica · 2022 · PMID 36066633 · open access
3 pages
rs4686570 rs9877502 rs10937450
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Nature · 2008 · PMID 18385738
2 pages
rs8034191 Lung Cancer
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection
Swiss Hepatitis C Cohort Study Group, International Hepatitis C Genetics Consortium · French ANRS HC EP 26 Genoscan Study Group
Gastroenterology · 2012 · PMID 22841784
2 pages
rs16851720 rs4374383
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
European heart journal · 2021 · PMID 33677556
2 pages
rs62232870 Dilated Cardiomyopathy
Genome-wide association study of HPV seropositivity
Human molecular genetics · 2011 · PMID 21896673
1 page
rs9357152
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528
A GWAS in uveal melanoma identifies risk polymorphisms in the <i>CLPTM1L</i> locus
NPJ genomic medicine · 2017 · PMID 28781888 · open access
1 page
rs452932
Sex specific associations in genome wide association analysis of renal cell carcinoma
European journal of human genetics : EJHG · 2019 · PMID 31231134
1 page
rs78971134
Family-based genome-wide association study of leprosy in Vietnam
PLoS pathogens · 2020 · PMID 32421744 · open access
1 page
rs114598080
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Nature communications · 2023 · PMID 37286573 · open access
1 page
rs10737681
Genome-wide association study of early-onset and late-onset postpartum depression: the IGEDEPP prospective study
IGEDEPP Group
European psychiatry : the journal of the Association of European Psychiatrists · 2024 · PMID 38555957 · open access
1 page
rs6028719

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.