For researchers

Is your paper here?

2,660 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.

14 matches for Ruth KS.

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
rs12142240 rs2236918 rs704795 rs930036 rs6856693 rs11738223
Genome-wide associations for birth weight and correlations with adult disease
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
rs35261542 rs28510415 rs700059 rs3753639 rs62466330 rs6016377
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
PloS one · 2017 · PMID 28957414 · open access
12 pages+
rs67183237 rs7735282 rs143845082 rs10479001 rs149535568 rs174559
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs9891146 rs13447324 rs5758651 rs34149579 rs12236219 rs284860
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms
Nature communications · 2019 · PMID 30696823 · open access
12 pages+
rs1931814 rs62124718 rs11165655 rs12051 rs1449403 rs12871550
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs4719648 rs61885091 rs11055030 rs2306547 rs2647873 rs6575803
Using human genetics to understand the disease impacts of testosterone in men and women
Endometrial Cancer Association Consortium
Nature medicine · 2020 · PMID 32042192 · open access
12 pages+
rs204995 rs11155076 rs4919686 rs168189 rs4828043 rs6997799
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci
PLoS genetics · 2016 · PMID 27494321 · open access
5 pages
rs77641763 rs9961653 rs75804782 rs11162296 rs17190618
Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes
European journal of human genetics : EJHG · 2016 · PMID 26014426 · open access
3 pages
rs117145500 rs11031005 rs1641549
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Age at Menarche
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
rs2971669
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour
Nature communications · 2019 · PMID 30952852 · open access
1 page
rs8045740

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.