For researchers

Is your paper here?

2,677 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.

215 matches for Ng K, showing the first 20.

Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature human behaviour · 2021 · PMID 34211149 · open access
12 pages+
rs34804222 rs6797231 rs9538248 rs183103 rs9964201 rs2849767
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
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+
rs2003892 rs56299595 rs7212325 rs11183212 rs577703186 rs184980867
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs68002929 rs12541 rs61833239 rs13016542 rs11711948 rs9674103
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots
Nature communications · 2022 · PMID 35773277 · open access
12 pages+
rs4872393 rs72810972 rs11057402 rs6903044 rs35641603 rs55744247
Dyslipidaemia-Genotype Interactions with Nutrient Intake and Cerebro-Cardiovascular Disease
Biomedicines · 2022 · PMID 35884923 · open access
12 pages+
rs79829439 rs11066525 rs79035076 rs12229054 rs200435297 rs12447640
Common and ethnic-specific genetic determinants of hemoglobin concentration between Taiwanese Han Chinese and European Whites: findings from comparative two-stage genome-wide association studies
The Journal of nutritional biochemistry · 2023 · PMID 35964923
12 pages+
rs2799079 rs3129012 rs10489609 rs4464148 rs16907334 rs1040360
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs4483592 rs1947066 rs144839021 rs1625595 rs197439 rs68049022
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+
rs17599910 rs2116498 rs2288183 rs2306376 rs2393595 rs6934083
Lifestage Sex-Specific Genetic Effects on Metabolic Disorders in an Adult Population in Korea: The Korean Genome and Epidemiology Study
International journal of molecular sciences · 2022 · PMID 36233190 · open access
12 pages+
rs17410996 rs75326924 rs6467314 rs4821130 rs10422861 rs2494746
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs1868781 rs2049866 rs217286 rs2992070 rs73109704 rs7762246
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs6434979 rs4236382 rs10751097 rs10978941 rs62042090 rs17686932
Genomics and phenomics of body mass index reveals a complex disease network
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
12 pages+
rs4601464 rs827156 rs12146571 rs12990777 rs13249124 rs146171187
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Nature genetics · 2023 · PMID 36635386
12 pages+
rs3740065 rs11893247 rs1473206 rs10888445 rs3828671 rs9469582
The Genetic Determinants of Aortic Distention
Journal of the American College of Cardiology · 2023 · PMID 37019578
12 pages+
rs35247409 rs408067 rs2445361 rs147121076 rs62053262 rs1570350
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Nature communications · 2023 · PMID 37120605 · open access
12 pages+
rs7759971 rs7848647 rs1181388 rs28862935 rs2637678 rs412175
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
NHLBI Trans-Omics for Precision Medicine (TOPMed)
Nature communications · 2023 · PMID 37253714 · open access
12 pages+
rs3108963 rs2631359 rs78250434 rs1343904 rs879333 rs34595355
Comprehensive genetic study of the insulin resistance marker TG:HDL-C in the UK Biobank
Nature genetics · 2024 · PMID 38200128
12 pages+
rs34934360 rs12927305 rs111831594 rs7966846 rs79859462 rs7298135
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs28475375 rs61748094 rs75640507 rs17489568 rs208311 rs6697896
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
DBDS Genomic Consortium · Regeneron Genetics Center and 3 more consortia
Nature genetics · 2024 · PMID 38632349 · open access
12 pages+
rs554146 rs10517369 rs11815438 rs113469203 rs7280197 rs12552930

Showing 20 of 215 · page 3 of 11

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.