Evidence map›Paper›PMID 37917228›Full record

ReviewBehavior genetics2024

South Asia: The Missing Diverse in Diversity.

Deepika R Dokuru, Tanya B Horwitz, Samantha M Freis, Michael C Stallings, Marissa A Ehringer

Open access · greenAbstract readReview
In one paragraph

Review in Behavior genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
23.5field-weighted citation impact, top 1% 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

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

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Diabetes and Foot Health Among South Asian People Seeking Asylum in the United Kingdom: A Theory-Informed Scoping Review.Health expectations : an international journal of public participation in health care and health policy · 2026
    Article
  10. The case for an integrated biobanking initiative in South Asia.The Lancet regional health. Southeast Asia · 2026
    Review
  11. Observational
  12. Article
  13. Article
  14. Patterns of lipid profile and genetic variations in South Asians.Cardiovascular diabetology. Endocrinology reports · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Deepika R DokuruInstitute for Behavioral Genetics, University of Colorado Boulder, 1480 30 St, Boulder, CO, 80303, USA. deepika.dokuru@colorado.edu.ORCID 0000-0003-2603-6725
Tanya B HorwitzInstitute for Behavioral Genetics, University of Colorado Boulder, 1480 30 St, Boulder, CO, 80303, USA.ORCID 0000-0001-8031-3944
Samantha M FreisInstitute for Behavioral Genetics, University of Colorado Boulder, 1480 30 St, Boulder, CO, 80303, USA.ORCID 0000-0001-8664-1877
Michael C StallingsInstitute for Behavioral Genetics, University of Colorado Boulder, 1480 30 St, Boulder, CO, 80303, USA.ORCID 0000-0002-8231-9159
Marissa A EhringerInstitute for Behavioral Genetics, University of Colorado Boulder, 1480 30 St, Boulder, CO, 80303, USA.ORCID 0000-0003-0388-7375
University of Colorado Boulder · US

Funding

Colorado Adoption/Twin Study of Lifespan behavioral development & cognitive aging (CATSLife2)R01AG046938 · NIA · UNIVERSITY OF COLORADO · PI REYNOLDS, CHANDRA A, WADSWORTH, SALLY J · 2015 to 2024
$18.5M
Research Training: Mental Health Behavior GeneticsT32MH016880 · NIMH · UNIVERSITY OF COLORADO AT BOULDER · PI Naomi P. Friedman, Matthew Charles Keller · 1985 to 2026
$5.3M
Research Training-Genetics of Substance AbuseT32DA017637 · NIDA · UNIVERSITY OF COLORADO AT BOULDER · PI STITZEL, JERRY A · 2004 to 2023
$5.3M
Adult Progression of Adolescent Onset Substance Use Disorder in a High Risk SampleR01DA053693 · NIDA · UNIVERSITY OF COLORADO DENVER · PI Christian J Hopfer, Michael Craig Stallings · 2022 to 2026
$3.2M
Identification of genes and genetic networks contributing to opioid use disorder traits in the Hybrid Rat Diversity PanelU01DA051937 · NIDA · UNIVERSITY OF COLORADO · PI BACHTELL, RYAN K, EHRINGER, MARISSA A · 2020 to 2024
$2.3M
NIA NIH HHS AG046938NIA NIH HHS R01 AG046938NIDA NIH HHS DA053693NIDA NIH HHS R01 DA053693NIDA NIH HHS T32 DA017637NIDA NIH HHS T32DA017637NIDA NIH HHS U01 DA051937NIH HHS DA051937NIMH NIH HHS MH016880NIMH NIH HHS T32 MH016880
6 · The paper itself

Abstract

South Asia, making up around 25% of the world's population, encompasses a wide range of individuals with tremendous genetic and environmental diversity. This region, which spans eight countries, is home to over 4500 anthropologically defined groups that speak numerous languages and have an array of religious beliefs and cultures, making it one of the most diverse places in the world. Much of the region's rich genetic diversity and structure is the result of a complex combination of population history, migration patterns, and endogamous practices. Despite the overwhelming size and diversity, South Asians have often been underrepresented in genetic research, making up less than 2% of the participants in genetic studies. This has led to a lack of population specific understanding of genetic disease risks. We aim to raise awareness about underlying genetic diversity in this ancestry group, call attention to the lack of representation of the group, and to highlight strategies for future studies in South Asians.

Indexed as

Asian PeopleBiomedical ResearchCultural DiversityAsia, SouthernHumansDiversityEquityInclusionSouth Asian

Identifiers

PMID37917228
PMCPMC11129896
OpenAlexW4388217991

What OpenQuestion holds

Textmetadata
LicenceTDM
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.