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.

24 matches for Kranzler H, showing the first 20.

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
Nature neuroscience · 2020 · PMID 32451486 · open access
12 pages+
rs7552830 rs75199129 rs13024996 rs13077520 rs13288470 rs61741649
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals
VA Million Veteran Program
Nature communications · 2020 · PMID 33082346 · open access
12 pages+
rs1385108 rs455650 rs28717373 rs2565060 rs6438208 rs12545053
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+
rs78308718 rs6875495 rs55706012 rs6993953 rs11137399 rs4748468
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · open access
12 pages+
rs7923245 rs1193232 rs12914773 rs34096939 rs7144274 rs7545279
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs6801151 rs78201023 rs7243332 rs6032660 rs10487459 rs175086
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
12 pages+
rs1275923 rs371071053 rs74315329 rs6762719 rs115378818 rs3015326
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
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
rs74816838 rs3810367 rs201082887 rs2763195 rs3935942 rs1626329
Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample
The American journal of psychiatry · 2023 · PMID 37282553
7 pages
rs13146907 rs144228648 rs147759217 rs565298761 rs75438204 rs28470433
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder
Molecular psychiatry · 2022 · PMID 35181757 · open access
6 pages
rs10105545 rs10235664 rs931774 rs145108206 rs55770986 rs12699336
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations
Nature communications · 2019 · PMID 30940813 · open access
4 pages
rs1229978 rs11075992 rs540606 Alcohol Use Disorder
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
3 pages
rs12497569 rs11570190 rs10835372
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks
JAMA psychiatry · 2016 · PMID 27028160
2 pages
rs77378271 rs146091982
Genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1
Molecular psychiatry · 2017 · PMID 28115739
2 pages
rs73568641 Opioid Receptor Sensitivity (OPRM1)
Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression
JAMA psychiatry · 2017 · PMID 29071344
2 pages
rs139438618 Major Depression and Alcohol Dependence (Comorbid)
Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction
Million Veteran Program
Nature neuroscience · 2022 · PMID 36171425
2 pages
rs112068658 rs3778151
Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci
Molecular psychiatry · 2014 · PMID 24166409
1 page
rs2066702
Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans
Biological psychiatry · 2015 · PMID 25555482
1 page
rs144667340
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020 · PMID 31294817
1 page
rs16969968
Genome-wide scan identifies opioid overdose risk locus close to MCOLN1
Addiction biology · 2020 · PMID 31362332
1 page
rs115208233

Showing 20 of 24 · 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.