For researchers

Is your paper here?

2,673 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.

54 matches for Holm H, showing the first 20.

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
rs138587317 rs62193080 rs9467148 rs141828605 rs773257111 rs73005873
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Alcohol Genome-wide Association (AlcGen) Consortium · Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and 5 more consortia
Nature genetics · 2011 · PMID 22001757
10 pages
rs13030978 rs7267979 rs6834314 rs2954021 rs1976403 rs1883415
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
rs6561599 rs381949 rs10054105 rs200476 rs72878024 rs8853
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs17287293 rs11118555 rs13030174 rs826838 rs11578508 rs4140885
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
rs5931180 rs12382607 rs4328011 rs139036121 rs5933079 rs181497961
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 pages
rs12526453 rs17114036 rs3798220 rs3825807 rs1231206 rs12936587
Sequence variants associating with urinary biomarkers
Human molecular genetics · 2019 · PMID 30476138 · open access
7 pages
rs760545501 rs141627694 rs752992795 rs763092306 rs551225 rs201938902
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Nature communications · 2019 · PMID 31053729 · open access
7 pages
rs10917168 rs9341808 rs1159421 rs1507462 rs72834687 rs12507427
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Communications biology · 2021 · PMID 34108613 · open access
7 pages
rs118174674 rs55635402 rs13147559 rs12784122 rs139123090 rs141952919
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs762517 rs12012576 rs139120857 rs5942972 rs7063103 rs62603531
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
LifeLines Cohort Study · EchoGen consortium and 6 more consortia
Nature genetics · 2011 · PMID 21909110 · open access
6 pages
rs2071518 rs11222084 rs13082711 rs11191593 rs319690 rs1327235
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
Nature communications · 2016 · PMID 26838040 · open access
6 pages
rs150956780 rs116841148 rs11559024 rs2930191 rs4072797 rs17412833
Identification of sequence variants influencing immunoglobulin levels
Nature genetics · 2017 · PMID 28628107
6 pages
rs11651596 rs2133037 rs112763553 rs2239701 rs35043490 rs72704050
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs10896090 rs10035291 rs111444407 rs10950456 rs57957974 rs17183814
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
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
Genome biology · 2018 · PMID 30012220 · open access
4 pages
rs11588271 rs116202356 rs3746435 rs11848785
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
Nature genetics · 2023 · PMID 37932435 · open access
4 pages
rs61914392 rs17099617 rs73217448 rs60147627
Discovery of common variants associated with low TSH levels and thyroid cancer risk
Nature genetics · 2012 · PMID 22267200
3 pages
rs2439302 rs116909374 Thyroid Cancer

Showing 20 of 54 · page 2 of 3

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.