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.

17 matches for Franke B.

Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs56044892 rs12410444 rs12754946 rs1008078 rs17372140 rs78365243
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
12 pages+
rs1861979 rs57246240 rs12218858 rs1419859 rs17178139 rs77956314
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+
rs76470478 rs2301718 rs56007616 rs61508189 rs1080066 rs73313052
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs9505301 rs2410767 rs10439607 rs10217651 rs35200015 rs3133370
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
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality
ADHD Group of the Psychiatric Genomics Consortium, International Cannabis Consortium
Molecular psychiatry · 2020 · PMID 30610198
5 pages
rs113551349 rs797267 rs56319043 rs2782639 ADHD (Attention Deficit Hyperactivity Disorder)
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
4 pages
rs76857496 rs6537401 rs114142727 rs2311059
Many sequence variants affecting diversity of adult human height
Nature genetics · 2008 · PMID 18391951
3 pages
rs12198986 rs6830062 rs3748069
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
Common variants in DGKK are strongly associated with risk of hypospadias
Nature genetics · 2011 · PMID 21113153
2 pages
rs1934179 Hypospadias
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
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption
Human molecular genetics · 2011 · PMID 21357676
1 page
rs6968865
Identification of common variants associated with human hippocampal and intracranial volumes
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
rs10784502
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis
PGC ADHD Working Group · PGC Bipolar Disorder Working Group
Biological psychiatry · 2017 · PMID 27890468
1 page
rs7089973
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
23andMe Research Team · Psychiatric Genomics Consortium: ADHD Subgroup and 1 more consortia
Biological psychiatry · 2018 · PMID 29325848 · open access
1 page
rs8039398
Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time
Translational psychiatry · 2018 · PMID 30287865 · open access
1 page
rs62182100
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature communications · 2021 · PMID 33495439 · open access
1 page
rs7118422

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.