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.

21 matches for Williams F, showing the first 20.

Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
American journal of human genetics · 2018 · PMID 29304378
12 pages+
rs71569047 rs10450586 rs34406563 rs7112229 rs11606709 rs4647728
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
rs72622585 rs13148153 rs4660885 rs61734651 rs11881070 rs11152089
A genome-wide association study in 10,000 individuals links plasma N-glycome to liver disease and anti-inflammatory proteins
Nature communications · 2025 · PMID 40593539 · open access
12 pages+
rs311432 rs12341905 rs2745851 rs17630758 rs4074453 rs10903118
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 and 3 more consortia
Annals of neurology · 2013 · PMID 23381943 · open access
11 pages
rs2022309 rs10922162 rs3211770 rs1318606 rs555212 rs10982156
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
rs434943 rs2106854 rs7968440 rs1938492 rs1019670 rs4817986
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
rs7953528 rs163879 rs1864325 rs344081 rs3905706 rs1566045
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment
PLoS genetics · 2014 · PMID 24945404 · open access
7 pages
rs2450083 rs3920498 rs7776725 rs17536328 rs2235529 rs798943
Genome-wide association study identifies eight loci associated with blood pressure
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
rs12946454 rs1530440 rs16948048 rs17367504
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Genetic Factors for Osteoporosis (GEFOS) Consortium
Nature genetics · 2009 · PMID 19801982 · open access
4 pages
rs7524102 rs7932354 rs11898505 Spine Bone Mineral Density
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Human molecular genetics · 2014 · PMID 24430505
4 pages
rs3020331 rs2982552 rs10416265 rs7902708
Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019 · PMID 30320955 · open access
4 pages
rs1243579 rs10743612 rs73197346 rs17725170
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
Genome-wide meta-analysis identifies new susceptibility loci for migraine
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
rs11759769 rs12134493 rs4379368
Genetic Variants Associated with Circulating Parathyroid Hormone
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
rs4443100 rs35194449 rs4074995
Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals
CHARGE Musculoskeletal Working Group
Pain · 2019 · PMID 30747904
3 pages
rs72666766 rs1865442 rs2672596
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects
Annals of the rheumatic diseases · 2013 · PMID 22993228 · open access
2 pages
rs2187689 rs926849
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2
Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) Consortium Neurology Working Group · CARDIoGRAM Consortium and 1 more consortia
Arteriosclerosis, thrombosis, and vascular biology · 2014 · PMID 24578379
2 pages
rs9399599 rs3136739
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing
Human molecular genetics · 2014 · PMID 25060954 · open access
1 page
rs681524
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
PLoS genetics · 2018 · PMID 30261039 · open access
1 page
rs12310519
Defining the genetic control of human blood plasma N-glycome using genome-wide association study
Human molecular genetics · 2019 · PMID 31163085
1 page
rs7255720

Showing 20 of 21 · 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.