For researchers

Is your paper here?

2,663 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.

73 matches for Sulem P, showing the first 20.

Deciphering the genetics and mechanisms of predisposition to multiple myeloma
Nature communications · 2024 · PMID 39103364 · open access
9 pages
rs9386514 rs9856633 rs7621631 rs75341503 rs5995688 rs6546615
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
rs1635501 rs10183486 rs2153157 rs12294104 rs10852344 rs12461110
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs4328011 rs139036121 rs5933079 rs181497961 rs111410539 rs5933443
Genome-wide meta-analysis identifies genetic drivers of bile acid metabolism in intrahepatic cholestasis of pregnancy
FinnGen · Estonian Biobank research team and 1 more consortia
Nature communications · 2026 · PMID 42178310 · open access
8 pages
rs6733156 rs4148211 rs2788095 rs4805129 rs58238559 rs10773287
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
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Communications biology · 2021 · PMID 34108613 · open access
7 pages
rs141952919 rs74543584 rs118174674 rs55635402 rs13147559 rs12784122
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
7 pages
rs9980363 rs1945016 rs17649684 rs13128363 rs11749692 rs955007
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
PLoS genetics · 2013 · PMID 23754956 · open access
6 pages
rs1131603 rs41281112 rs2270655 rs2336573 rs3742801 rs7788053
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
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
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
rs72704050 rs11651596 rs2133037 rs112763553 rs2239701
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 insight into sick sinus syndrome
DBDS Genomic Consortium
European heart journal · 2021 · PMID 33580673 · open access
5 pages
rs7689774 rs11554495 rs12932445 rs35813871 Sick Sinus Syndrome
Genetic correction of PSA values using sequence variants associated with PSA levels
Science translational medicine · 2010 · PMID 21160077
4 pages
rs401681 rs17632542 rs10788160 rs11067228
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
rs61914392 rs17099617 rs73217448 rs60147627
The genetic architecture of fibromyalgia across 2.5 million individuals
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
rs62194170 rs2734833 rs34683740 Fibromyalgia

Showing 20 of 73 · 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.