Evidence map›Paper›PMID 37117326›Full record

ArticleEuropean journal of human genetics : EJHG2023

Underrepresentation of racial and ethnic minorities in cascade testing for hereditary cancer syndromes.

Muhammad Danyal Ahsan, Emily M Webster, Natalie T Nguyen, Murtaza Qazi, Sarah R Levi, Lisa C Diamond, Ravi N Sharaf, Melissa K Frey

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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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

8 authors.

Muhammad Danyal AhsanWeill Cornell Medicine, New York, NY, USA. mua2023@qatar-med.cornell.edu.ORCID 0000-0001-8633-8931
Emily M WebsterWeill Cornell Medicine, New York, NY, USA.
Natalie T NguyenWeill Cornell Medicine, New York, NY, USA.ORCID 0000-0002-3433-4282
Murtaza QaziWeill Cornell Medicine, New York, NY, USA.
Sarah R LeviWeill Cornell Medicine, New York, NY, USA.
Lisa C DiamondMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Ravi N SharafWeill Cornell Medicine, New York, NY, USA.
Melissa K FreyWeill Cornell Medicine, New York, NY, USA.

Funding

Disparities in COVID Disease Severity and Outcomes in New York CityUL1TR002384 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JULIANNE L IMPERATO-MCGINLEY · 2017 to 2026
$86.2M
Institutional Career Development CoreKL2TR002385 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI YUAN-SHAN ZHU · 2017 to 2026
$13.3M
Implementing Universal Lynch Syndrome Screening across Multiple Healthcare Systems: Identifying Strategies to Facilitate and Maintain Programs in Different Organizational ContextsR01CA211723 · NCI · GEISINGER CLINIC · PI RAHM, ALANNA K · 2017 to 2021
$3.7M
Gene Dependent Cancer Risk and Optimal Cancer Prevention Strategies in Lynch SyndromeK07CA216326 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI SHARAF, RAVI · 2018 to 2021
$675k
NCATS NIH HHS KL2 TR002385NCATS NIH HHS UL1 TR002384NCI NIH HHS K07 CA216326NCI NIH HHS R01 CA211723
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Ethnic and Racial MinoritiesNeoplastic Syndromes, HereditaryEthnicityHumansMinority GroupsRacial Groups

Identifiers

PMID37117326
PMCPMC10325970

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.