For researchers

Is your paper here?

2,665 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.

66 matches for Marchand L, showing the first 20.

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
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
rs3850699 rs1894292 rs2273669 rs1270884 rs11650494 rs1218582
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
Identification of nine new susceptibility loci for endometrial cancer
Nature communications · 2018 · PMID 30093612 · open access
6 pages
rs113998067 rs1740828 rs9668337 rs10850382 rs7981863 Endometrial Cancer
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of medicine · 2021 · PMID 32889700
6 pages
rs465498 rs1200399 rs2517873 rs4573350 rs1264308 rs17038564
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
rs7884019 rs56210063 rs78532451 rs1867073 rs7622417 rs2715879
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Nature genetics · 2014 · PMID 25086665 · open access
5 pages
rs9581943 rs2736098 rs6971499 rs7190458 Pancreatic Cancer
Two susceptibility loci identified for prostate cancer aggressiveness
African Ancestry Prostate Cancer GWAS Consortium
Nature communications · 2015 · PMID 25939597 · open access
5 pages
rs71277158 rs7929962 rs17023900 rs35148638 rs16901979
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
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
5 pages
rs7222250 rs60882887 rs12470785 rs79183898 rs736596
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs71467682 rs75031349 rs137884934 rs682888 rs10901793
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Nature communications · 2015 · PMID 26151821
4 pages
rs11190164 rs35360328 rs812481 rs73208120
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Nature communications · 2018 · PMID 29422604 · open access
4 pages
rs13303010 rs1517037 rs4795218 rs2941471
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
rs10094872 rs35226131 Pancreatic Cancer
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
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
Genome-wide association studies and Mendelian randomization analyses provide insights into the causes of early-onset colorectal cancer
Colorectal Transdisciplinary (CORECT) Study, the Colon Cancer Family Registry (CCFR), Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO)
Annals of oncology : official journal of the European Society for Medical Oncology · 2024 · PMID 38408508 · open access
3 pages
rs10808556 rs12427378 rs2427291
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Nature · 2007 · PMID 17632545
2 pages
rs2903692 rs2647044
Genome-wide association study identifies new prostate cancer susceptibility loci
Human molecular genetics · 2011 · PMID 21743057
2 pages
rs651164 rs902774

Showing 20 of 66 · page 2 of 4

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.