For researchers

Is your paper here?

3,098 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.

25 matches for Stein J, showing the first 20.

Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
12 pages+
rs10217651 rs35200015 rs3133370 rs2410767 rs10439607 rs2206656
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+
rs79478621 rs80249955 rs9390172 rs8134737 rs10995239 rs1545660
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
rs16885613 rs4980383 rs10995187 rs10087804 rs9397436 rs3819405
The X chromosome's influences on the human brain
Science advances · 2025 · PMID 39854466 · open access
12 pages+
rs146210600 rs2743914 rs3105280 rs5934135 rs142344396 rs5924922
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
11 pages
rs1879586 rs7207826 rs11651755 rs688187 rs7902587 rs9886651
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 pages
rs12752552 rs3751667 rs11233250 rs2235573 rs4252707 rs12076373
Discovery of 42 genome-wide significant loci associated with dyslexia
23andMe Research Team · Quantitative Trait Working Group of the GenLang Consortium
Nature genetics · 2022 · PMID 36266505 · open access
10 pages
rs72916919 rs3735260 rs13097431 rs4845687 rs7625418 rs72841395
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
8 pages
rs17114036 rs12526453 rs2306374 rs12936587 rs3798220 rs3825807
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 1 more consortia
Nature genetics · 2019 · PMID 30478444
8 pages
rs11591402 rs1427829 rs3001723 rs1592757 rs4275621 rs2243517
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
8 pages
rs111444407 rs10950456 rs57957974 rs17183814 rs10896090 rs10035291
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Cancer research · 2024 · PMID 38832928
8 pages
rs7580240 rs77825513 rs10890841 rs3745191 rs6663303 rs6547894
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21
GliomaScan consortium
Scientific reports · 2018 · PMID 29743610 · open access
4 pages
rs2297440 rs634537 rs55705857 Glioma
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Schizophrenia Working Group of the Psychiatric Genomics Consortium · Bipolar Disorder Working Group of the Psychiatric Genomics Consortium and 3 more consortia
Biological psychiatry · 2022 · PMID 34099189
4 pages
rs793571 rs28473013 rs3145 rs431414
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk
Nature communications · 2020 · PMID 33037222 · open access
3 pages
rs10995181 rs4849864 rs6001984
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
Communications biology · 2021 · PMID 34620984 · open access
3 pages
rs7130190 rs7541515 rs139734888
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse
European heart journal · 2022 · PMID 35245370
3 pages
rs112258894 rs12406058 rs34871776
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
2 pages
rs17178006 rs6581612
Genetic variants associated with longitudinal changes in brain structure across the lifespan
IMAGEN Consortium
Nature neuroscience · 2022 · PMID 35383335 · open access
2 pages
rs72772746 rs1425034

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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.