Evidence map›Paper›PMID 36395242›Full record

ArticleScience (New York, N.Y.)2022

Cross-trait assortative mating is widespread and inflates genetic correlation estimates.

Richard Border, Georgios Athanasiadis, Alfonso Buil, Andrew J Schork, Na Cai, Alexander I Young, Thomas Werge, Jonathan Flint, Kenneth S Kendler, Sriram Sankararaman and 2 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

123 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  7. Genetic architectures of brain-related traits are shaped by strong selective constraints.Proceedings of the National Academy of Sciences of the United States of America · 2026
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63 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Richard BorderDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-6293-2968
Georgios AthanasiadisInstitute of Biological Psychiatry, Mental Health Center Sct Hans, Copenhagen University Hospital-Mental Health Services CPH, 2100 Copenhagen, Denmark.ORCID 0000-0002-2927-4035
Alfonso BuilInstitute of Biological Psychiatry, Mental Health Center Sct Hans, Copenhagen University Hospital-Mental Health Services CPH, 2100 Copenhagen, Denmark.ORCID 0000-0002-1863-164X
Andrew J SchorkInstitute of Biological Psychiatry, Mental Health Center Sct Hans, Copenhagen University Hospital-Mental Health Services CPH, 2100 Copenhagen, Denmark.ORCID 0000-0003-4164-9335
Na CaiHelmholtz Pioneer Campus, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0001-7496-2075
Alexander I YoungAnderson School of Management, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0001-9930-989X
Thomas WergeInstitute of Biological Psychiatry, Mental Health Center Sct Hans, Copenhagen University Hospital-Mental Health Services CPH, 2100 Copenhagen, Denmark.ORCID 0000-0003-1829-0766
Jonathan FlintCenter for Neurobehavioral Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-9427-4429
Kenneth S KendlerDepartment of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.ORCID 0000-0001-8689-6570
Sriram SankararamanDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0003-1586-9641
Andy W DahlSection of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, IL 60637, USA.ORCID 0000-0001-6520-4766
Noah A ZaitlenDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-3553-3670

Funding

Polygenic Risk Scores for Diverse Populations - Bridging Research and Clinical CareR01HL151152 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Christy Leigh Avery, Jennifer Below · 2020 to 2026
$12.3M
Identifying the genetic causes of depression in a deeply phenotyped population from South KoreaU01MH126798 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHN, YONG MIN, FLINT, JONATHAN · 2021 to 2025
$8.9M
Methods for Genome-wide Association Studies in Admixed PopulationsR01HG006399 · NHGRI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI PRICE, ALKES L · 2011 to 2024
$6.3M
Training Grant in Neurobehavioral GeneticsT32NS048004 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BEARDEN, CARRIE E, OPHOFF, ROEL A · 2004 to 2025
$5.8M
Optimizing imputation for diverse populations in a distributed frameworkU01HG009080 · NHGRI · STANFORD UNIVERSITY · PI KENNY, EIMEAR ELIZABETH · 2016 to 2020
$5.2M
SINGLE-CELL MULTI-OMIC APPROACHES TO MECHANISTICALLY CHARACTERIZE PSYCHIATRIC DISORDER RISK LOCI IN THE HUMAN BRAINR01MH125252 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUO, CHONGYUAN · 2021 to 2025
$3.7M
Improved methods for inference of genotype-specific response to environmental toxinsR01ES029929 · NIEHS · PRINCETON UNIVERSITY · PI AYROLES, JULIEN, CLARK, ANDREW G · 2019 to 2023
$3.6M
(PQ3) A functional genomic approach to identification and interpretation of germline-tumor genetic interactionsR01CA227237 · NCI · DANA-FARBER CANCER INST · PI GUSEV, ALEXANDER, ZAITLEN, NOAH A · 2018 to 2022
$3.5M
(8) Genetics of Immune Related Adverse Events and Response to ImmunotherapyR01CA227466 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZIV, ELAD · 2018 to 2023
$3.3M
Genomic Approaches to Population Health in Multi-Ethnic Hospital SystemsR01HG011345 · NHGRI · UNIVERSITY OF COLORADO DENVER · PI ARBOLEDA, VALERIE A, GIGNOUX, CHRISTOPHER R · 2020 to 2023
$3.1M
Epigenomics of asthma risk factors and clinical subtypes in minority childrenR01HL155024 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BORRELL, LUISA N, ZAITLEN, NOAH A · 2021 to 2024
$2.9M
Genome-Wide Analyses of Health and Well-Being PhenotypesR01AG042568 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BENJAMIN, DANIEL J · 2015 to 2021
$2.8M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NCI NIH HHS R01 CA227237NCI NIH HHS R01 CA227466NHGRI NIH HHS R01 HG006399NHGRI NIH HHS R01 HG011345NHGRI NIH HHS U01 HG009080NHLBI NIH HHS R01 HL151152NHLBI NIH HHS R01 HL155024NIA NIH HHS R01 AG042568NIA NIH HHS R24 AG065184NIEHS NIH HHS R01 ES029929NIGMS NIH HHS R01 GM142112NIGMS NIH HHS R35 GM125055NIGMS NIH HHS R35 GM133531NIMH NIH HHS R01 MH122688NIMH NIH HHS R01 MH125252NIMH NIH HHS R01 MH130581NIMH NIH HHS U01 MH126798NINDS NIH HHS T32 NS048004Wellcome Trust
6 · The paper itself

Abstract

The observation of genetic correlations between disparate human traits has been interpreted as evidence of widespread pleiotropy. Here, we introduce cross-trait assortative mating (xAM) as an alternative explanation. We observe that xAM affects many phenotypes and that phenotypic cross-mate correlation estimates are strongly associated with genetic correlation estimates (

Indexed as

Genome-Wide Association StudyMultifactorial InheritanceCell CommunicationHumansPhenotype

Identifiers

PMID36395242
PMCPMC9901291

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.