For researchers

Is your paper here?

3,055 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.

19 matches for Schofield P.

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs117431198 rs9966005 rs62037363 rs5758605 rs75477016 rs77418166
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
12 pages+
rs2410767 rs10439607 rs10217651 rs35200015 rs3133370 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+
rs40115 rs76398229 rs1080066 rs73313052 rs9375477 rs117461235
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs11249945 rs17205972 rs7596872 rs55940034 rs2303655 rs55897749
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs5758064 rs61554907 rs6865469 rs7199910 rs12289486 rs62581014
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Molecular psychiatry · 2022 · PMID 35974141 · open access
11 pages
rs347713 rs1386320 rs9528370 rs11148561 rs11711421 rs797311
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
rs11624408 rs111444407 rs10950456 rs57957974 rs17183814 rs10896090
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors
VA Million Veteran Program (MVP) · MVP Suicide Exemplar Workgroup and 6 more consortia
The American journal of psychiatry · 2023 · PMID 37777856
7 pages
rs7649709 rs62404522 rs9525171 rs850261 rs17485141 rs2284000
Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study
International Consortium on Lithium Genetics (ConLi+Gen)
JAMA psychiatry · 2018 · PMID 29121268
5 pages
rs324899 rs6942227 rs209474 rs6728642 rs66486766
Genome-wide association study reveals two new risk loci for bipolar disorder
Nature communications · 2014 · PMID 24618891
4 pages
rs12290811 rs17826816 rs12202969 rs6550435
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Stroke · 2020 · PMID 32517579
4 pages
rs2598420 rs3758575 rs72934760 rs2665962
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
rs431414 rs793571 rs28473013 rs3145
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Bipolar Disorder Genome Study (BiGS) Consortium
American journal of human genetics · 2011 · PMID 21353194
2 pages
rs1064395 Bipolar Disorder
Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium
Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Biological psychiatry · 2015 · PMID 25648963
2 pages
rs13360092 rs11074779
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study
Lancet (London, England) · 2016 · PMID 26806518 · open access
2 pages
rs74795342 rs78015114
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Human molecular genetics · 2016 · PMID 27329760
2 pages
rs2517959 rs4236274
Genetic variants associated with longitudinal changes in brain structure across the lifespan
IMAGEN Consortium
Nature neuroscience · 2022 · PMID 35383335 · open access
2 pages
rs1425034 rs72772746
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Nature communications · 2018 · PMID 30258056 · open access
1 page
rs34113929
Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium · Bipolar Disorder Working Group of the Psychiatric Genomics Consortium and 4 more consortia
Biological psychiatry · 2022 · PMID 34861974 · open access
1 page
rs71557378

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.