For researchers

Is your paper here?

2,661 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.

24 matches for Witte JS, showing the first 20.

Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts
Nature communications · 2020 · PMID 32887889 · open access
12 pages+
rs34563311 rs5995881 rs9273501 rs2856437 rs4785767 rs73169065
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs963800 rs73909841 rs10788167 rs3787099 rs371707439 rs12701838
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10180829 rs10071837 rs4899520 rs75823898 rs112226333 rs2553033
Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia
American journal of human genetics · 2021 · PMID 34469753
12 pages+
rs116141391 rs12219294 rs141800474 rs141951483 rs149524498 rs28724235
Genetically adjusted PSA levels for prostate cancer screening
Nature medicine · 2023 · PMID 37264206 · open access
12 pages+
rs7219536 rs7129424 rs80122351 rs9933507 rs10193919 rs11709611
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs10886810 rs1037137 rs11892008 rs6151589 rs4713343 rs78416326
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups
Nature genetics · 2025 · PMID 39930085 · open access
12 pages+
rs113697264 rs1203008 rs56404456 rs12107722 rs8012109 rs28435470
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
11 pages
rs62105306 rs17057164 rs149352150 rs56330886 rs112778462 rs378854
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Breast and Prostate Cancer Cohort Consortium (BPC3) · PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25217961 · open access
10 pages
rs1041449 rs17599629 rs9287719 rs56232506 rs17694493 rs76934034
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
rs55726902 rs7130753 rs17607589 rs11236814 rs11204896 rs35469349
Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry
PLoS genetics · 2011 · PMID 21998595 · open access
7 pages
rs2351491 rs9470004 rs6440003 rs11658329 rs2854160 rs1787200
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 pages
rs7559046 rs7521390 rs73739621 rs2918302 rs3017289 rs61907712
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 of prostate-specific antigen levels identifies novel loci independent of prostate cancer
Nature communications · 2017 · PMID 28139693 · open access
5 pages
rs11084596 rs16980679 rs4378355 rs8023057 Prostate-Specific Antigen (PSA) Levels
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Cancer discovery · 2015 · PMID 26034056
3 pages
rs116041037 rs72725879 rs10896449
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Nature genetics · 2022 · PMID 35915169
3 pages
rs11607355 rs2413932 rs12348845
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin
MetGen Investigators · DPP Investigators and 1 more consortia
Nature genetics · 2016 · PMID 27500523 · open access
2 pages
rs8192675 Type 2 Diabetes
Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry
PRACTICAL/ELLIPSE Consortium
Journal of the National Cancer Institute · 2017 · PMID 29117387 · open access
2 pages
rs75823044 rs78554043
Genome-wide meta-analyses of smoking behaviors in African Americans
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
rs2036527

Showing 20 of 24 · 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.