For researchers

Is your paper here?

2,662 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.

22 matches for Kranzler HR, 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+
rs1724429 rs10783446 rs7552830 rs75199129 rs13024996 rs13077520
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+
rs11581459 rs11191487 rs9375328 rs11012750 rs12632110 rs1385108
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+
rs2336147 rs10866641 rs67712855 rs748455 rs78308718 rs6875495
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+
rs4285945 rs1002202 rs6588376 rs4890356 rs7086061 rs7329873
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+
rs10865093 rs7431106 rs61946067 rs28986300 rs16948230 rs6801151
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
rs3935942 rs1626329 rs6059896 rs168144 rs74816838 rs3810367
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder
Molecular psychiatry · 2022 · PMID 35181757 · open access
7 pages
rs55770986 rs12699336 rs10105545 rs11949077 rs10235664 rs931774
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
rs28470433 rs13130101 rs13146907 rs144228648 rs147759217 rs565298761
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
rs540606 rs1229978 rs11075992 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
4 pages
rs12497569 rs11570190 rs10835372 rs62461186
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
rs3778151 rs112068658
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
A regulatory variant of CHRM3 is associated with cannabis-induced hallucinations in European Americans
Translational psychiatry · 2019 · PMID 31740666 · open access
1 page
rs115455482
Systematic review and meta-analysis of the moderating effect of rs1799971 in OPRM1, the mu-opioid receptor gene, on response to naltrexone treatment of alcohol use disorder
Addiction (Abingdon, England) · 2020 · PMID 31961981
1 page
Opioid Receptor Sensitivity (OPRM1)

Showing 20 of 22 · 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.