Evidence map›Paper›PMID 30297428›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Genetic variation in the

Eric Jorgenson, Navneet Matharu, Melody R Palmer, Jie Yin, Jun Shan, Thomas J Hoffmann, Khanh K Thai, Xujia Zhou, James M Hotaling, Gail P Jarvik and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% of its field
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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Genetic factors associated with erectile dysfunction- mendelian randomisation analysis.American journal of clinical and experimental urology · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Genetics · 2019
    Review
  16. Some concerns regarding the association of rs17185536 in SIM1 with erectile dysfunction.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Review
  18. Genetic variant rs17185536 regulatesProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Reply to Liu et al.: Tissue specificity ofProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

Eric JorgensonDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612; eric.jorgenson@kp.org Stephen.vandeneeden@kp.org.ORCID 0000-0002-5829-8191
Navneet MatharuDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158.
Melody R PalmerDivision of Medical Genetics, University of Washington School of Medicine, Seattle, WA 98195.
Jie YinDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612.
Jun ShanDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612.
Thomas J HoffmannInstitute for Human Genetics, University of California, San Francisco, CA 94158.
Khanh K ThaiDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612.
Xujia ZhouDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158.
James M HotalingDepartment of Surgery (Urology), University of Utah School of Medicine, Salt Lake City, UT 84132.
Gail P JarvikDivision of Medical Genetics, University of Washington School of Medicine, Seattle, WA 98195.
Nadav AhituvDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, CA 94158.
Hunter WessellsDeparment of Urology, University of Washington School of Medicine, Seattle, WA 98195.
Stephen K Van Den EedenDivision of Research, Kaiser Permanente Northern California, Oakland, CA 94612; eric.jorgenson@kp.org Stephen.vandeneeden@kp.org.
Kaiser Permanente · USUniversity of California, San Francisco · USUniversity of Washington Medical Center · USUniversity of Utah · USUniversity of Washington · US

Funding

A Resource for Genetic Epidemiology Research in Adult Health and AgingRC2AG036607 · NIA · KAISER FOUNDATION RESEARCH INSTITUTE · PI RISCH, NEIL J., SCHAEFER, CATHERINE ANN · 2009 to 2010
$24.8M
Non-coding/epigenetic regulationP01HD084387 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI Nadav Ahituv, LILIANNA SOLNICAKREZEL · 2016 to 2026
$14.2M
Massively parallel reporter assays and genome editing of ENCODE predicted regulatory elementsUM1HG009408 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AHITUV, NADAV, SHENDURE, JAY ASHOK · 2017 to 2021
$7.6M
Massively parallel dissection of psychiatric regulatory networksR01MH109907 · NIMH · J. DAVID GLADSTONE INSTITUTES · PI AHITUV, NADAV, POLLARD, KATHERINE S. · 2016 to 2020
$3.4M
The Role of Refractive Error in the Etiology of GlaucomaR01EY027004 · NEI · KAISER FOUNDATION RESEARCH INSTITUTE · PI CHOQUET, HELENE · 2017 to 2020
$1.6M
Airway Epithelial Reprogramming in AsthmaR01HL138424 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ERLE, DAVID J · 2017 to 2018
$1.3M
Identification & functional characterization of SIM1 obesity-associated variantsR01DK090382 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AHITUV, NADAV, VAISSE, CHRISTIAN · 2012 to 2015
$1.3M
Susceptibility Genes for Erectile DysfunctionR01DK104764 · NIDDK · UNIVERSITY OF WASHINGTON · PI HOTALING, JAMES, VAN DEN EEDEN, STEPHEN K. · 2016 to 2019
$768k
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NEI NIH HHS R01 EY027004NHGRI NIH HHS UM1 HG009408NHLBI NIH HHS R01 HL138424NIA NIH HHS RC2 AG036607NICHD NIH HHS P01 HD084387NIDDK NIH HHS R01 DK090382NIDDK NIH HHS R01 DK104764NIMH NIH HHS R01 MH109907
6 · The paper itself

Abstract

Erectile dysfunction affects millions of men worldwide. Twin studies support the role of genetic risk factors underlying erectile dysfunction, but no specific genetic variants have been identified. We conducted a large-scale genome-wide association study of erectile dysfunction in 36,649 men in the multiethnic Kaiser Permanente Northern California Genetic Epidemiology Research in Adult Health and Aging cohort. We also undertook replication analyses in 222,358 men from the UK Biobank. In the discovery cohort, we identified a single locus (rs17185536-T) on chromosome 6 near the single-minded family basic helix-loop-helix transcription factor 1 (

Indexed as

AgedAllelesBody Mass IndexCase-Control StudiesChromosomes, Human, Pair 6Cohort StudiesErectile DysfunctionGenetic Predisposition to DiseaseGenetic VariationHumansLeptinMaleMelanocortinsMiddle AgedPromoter Regions, GeneticLeptinMelanocortinserectile dysfunctiongeneticgenome-wide associationmelanocortinSIM1

Identifiers

PMID30297428
PMCPMC6205494
OpenAlexW2894899887

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.