For researchers

Is your paper here?

3,082 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.

25 matches for Ni B, showing the first 20.

Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Breast and Ovarian Cancer Susceptibility Collaboration · Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and 3 more consortia
Nature genetics · 2013 · PMID 23535729
12 pages+
rs16857609 rs6762644 rs9790517 rs6828523 rs204247 rs720475
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
rs2274465 rs6747380 rs6758290 rs4369815 rs17236969 rs17233066
Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs117618124 rs7529522 rs113577745 rs206966 rs10510097 rs60954078
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs12144319 rs145364999 rs116353863 rs117079142 rs11884596 rs12708491
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
12 pages+
rs74685827 rs60755019 rs3848143 rs10947943 rs6489896 rs7908662
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs280097 rs7810512 rs2516452 rs9614460 rs1554865 rs966816
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs12887451 rs12118203 rs11754000 rs11263445 rs17180949 rs3852525
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology and Hemostasis Working Group and 1 more consortia
Nature communications · 2024 · PMID 38789417 · open access
12 pages+
rs35510081 rs62139251 rs2572 rs9939870 rs56099285 rs10954213
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
11 pages
rs150293538 rs320203 rs1879586 rs7207826 rs11651755 rs688187
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
8 pages
rs72905558 rs3129813 rs78062588 rs9258381 rs6457312 rs239933
APOE-stratified genome-wide association analyses provide insights into the genetic etiology of Alzheimers's disease
Nature genetics · 2026 · PMID 42736378 · open access
8 pages
rs75763893 rs17208902 rs113221226 rs9268888 rs10131116 rs77892656
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
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
6 pages
rs7222250 rs60882887 rs9901834 rs12470785 rs79183898 rs736596
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
5 pages
rs11065822 rs17743054 rs7760611 rs1375631 rs13256025
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Nature communications · 2015 · PMID 26151821
4 pages
rs11190164 rs35360328 rs812481 rs73208120
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
rs7561528 rs9349407 Alzheimer's Disease
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus
Nature communications · 2014 · PMID 24920014 · open access
2 pages
rs2069757 Hodgkin Lymphoma

Showing 20 of 25 · page 1 of 2

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.