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.

12 matches for Kember RL.

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
Nature neuroscience · 2020 · PMID 32451486 · open access
12 pages+
rs7552830 rs75199129 rs13024996 rs13077520 rs13288470 rs61741649
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals
VA Million Veteran Program
Nature communications · 2020 · PMID 33082346 · open access
12 pages+
rs9375328 rs11012750 rs12632110 rs1385108 rs455650 rs28717373
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · open access
12 pages+
rs34803973 rs34943930 rs1949434 rs2017923 rs61960827 rs9812906
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs114876144 rs145437104 rs3134988 rs7575245 rs269781 rs4741016
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs11570441 rs11656344 rs11030613 rs11769128 rs11955611 rs11991223
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
rs74816838 rs3810367 rs201082887 rs2763195 rs3935942 rs1626329
Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample
The American journal of psychiatry · 2023 · PMID 37282553
7 pages
rs13130101 rs13146907 rs144228648 rs147759217 rs565298761 rs75438204
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
Regeneron Genetics Center · VA Million Veterans Program and 1 more consortia
Nature genetics · 2022 · PMID 35637384
6 pages
rs9510086 rs11848552 rs17661264 rs2463481 rs2224770 rs337086
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
rs78532451 rs1867073 rs7622417 rs2715879 rs7884019 rs56210063
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
Nature communications · 2019 · PMID 30940813 · open access
4 pages
rs540606 rs1229978 rs11075992 Alcohol Use Disorder
Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction
Million Veteran Program
Nature neuroscience · 2022 · PMID 36171425
2 pages
rs3778151 rs112068658

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.