For researchers

Is your paper here?

2,657 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.

29 matches for Masson G, showing the first 20.

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
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
Nature communications · 2018 · PMID 30194396 · open access
12 pages+
rs754058883 rs779929745 rs772494879 rs760402913 rs149787529 rs183241934
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Communications biology · 2020 · PMID 32327693 · open access
12 pages+
rs754689812 rs4842 rs77262773 rs3749971 rs33932084 rs200484
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Nature · 2020 · PMID 32581359
12 pages+
rs7218886 rs654537 rs1050976 rs2069556 rs6535628 rs11079788
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
11 pages
rs41282145 rs17300770 rs9621 rs138587317 rs62193080 rs9467148
Physical and neurobehavioral determinants of reproductive onset and success
Nature genetics · 2016 · PMID 27089180
10 pages
rs1040124 rs12522910 rs4840367 rs658385 rs2248699 rs538498277
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Nature communications · 2018 · PMID 30410027 · open access
9 pages
rs381949 rs10054105 rs200476 rs72878024 rs8853 rs1638703
New basal cell carcinoma susceptibility loci
Nature communications · 2015 · PMID 25855136 · open access
7 pages
rs7538876 rs801114 rs11170164 rs78378222 rs57244888 rs28727938
Sequence variants associating with urinary biomarkers
Human molecular genetics · 2019 · PMID 30476138 · open access
7 pages
rs141627694 rs752992795 rs763092306 rs551225 rs201938902 rs780518365
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Nature communications · 2019 · PMID 31053729 · open access
7 pages
rs72834687 rs12507427 rs9830173 rs10917168 rs9341808 rs1159421
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
PLoS genetics · 2013 · PMID 23754956 · open access
6 pages
rs7788053 rs1131603 rs41281112 rs2270655 rs2336573 rs3742801
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
Nature communications · 2016 · PMID 26838040 · open access
6 pages
rs11559024 rs2930191 rs4072797 rs17412833 rs150956780 rs116841148
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Nature communications · 2020 · PMID 31959851 · open access
6 pages
rs2230624 rs12700186 rs3853750 rs60156285 rs2180769 rs2228079
Identification of sequence variants influencing immunoglobulin levels
Nature genetics · 2017 · PMID 28628107
5 pages
rs2239701 rs72704050 rs11651596 rs2133037 rs112763553
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
Nature genetics · 2018 · PMID 30374069
5 pages
rs4733724 rs10896015 rs7222178 rs11764536 rs10948172
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Nature genetics · 2019 · PMID 30643255
5 pages
rs34210653 rs17718444 rs6543124 rs1050152 Chronic Rhinosinusitis and the Bitter Taste Receptor
Genetic correction of PSA values using sequence variants associated with PSA levels
Science translational medicine · 2010 · PMID 21160077
4 pages
rs401681 rs17632542 rs10788160 rs11067228
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
3 pages
rs10261758 rs1538981 rs7320598
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia

Showing 20 of 29 · 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.