For researchers

Is your paper here?

2,665 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.

23 matches for Lam M, showing the first 20.

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
rs2952156 rs17806299 rs4988958 rs2596464 rs6893213 rs1663687
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs28433345 rs10798879 rs71324996 rs8070135 rs151231 rs954734
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs6668048 rs17836155 rs2485371 rs11932971 rs13381096 rs2450333
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
rs12646523 rs1464015 rs13187428 rs1143770 rs11708774 rs17287504
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs2358483 rs149142 rs78155705 rs62005276 rs639016 rs34322452
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs11680723 rs12498839 rs10873538 rs7803571 rs4936215 rs3016384
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs290490 rs3742636 rs74387263 rs10758321 rs11023938 rs116257126
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes
Genes · 2022 · PMID 36292730 · open access
4 pages
rs4902684 rs4809370 rs10814274 rs73050128
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Veterans Affairs Million Veteran Program
Nature genetics · 2023 · PMID 37985822 · open access
4 pages
rs12497569 rs11570190 rs10835372 rs62461186
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
rs7561528 rs9349407 Alzheimer's Disease
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants
EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
The Journal of allergy and clinical immunology · 2014 · PMID 24315451
3 pages
rs3751972 rs2016444 rs12500579
Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of <i>FADS1</i> variants to arachidonic acid, a critical infant micronutrient
Journal of medical genetics · 2018 · PMID 29514873 · open access
3 pages
rs7198595 rs12583793 rs12535041
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
Communications biology · 2022 · PMID 35393509 · open access
2 pages
rs2980766 rs13039863
Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin
International Headache Genetics Consortium (IHGC)
Human genetics · 2023 · PMID 36808568 · open access
2 pages
rs28728306 rs10906203
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs1898895 rs111486601
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
DIAGRAM · MuTHER
Nature genetics · 2011 · PMID 21874001
1 page
rs4812829
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium
Annals of neurology · 2013 · PMID 23225573
1 page
rs10136766

Showing 20 of 23 · 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.