Evidence map›Paper›PMID 42718649›Full record

ArticleGenetics in medicine open2026

Assessment of local provider engagement of an in-home collaborative model for remote genetic services.

Daniel Chavez-Yenter, Kevin Oeffinger, Brian Egleston, Elisabeth McCarty Wood, Sarah Howe, Sarah Brown, Janice Christiansen, Cara Cacioppo, Michelle Weinberg, Elena Elkin and 7 more

Abstract read
In one paragraph

Article in Genetics in medicine open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Daniel Chavez-YenterDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Kevin OeffingerDepartment of Medicine, Duke University, Durham, NC.
Brian EglestonSchool of Public Health, Columbia University, New York, NY.
Elisabeth McCarty WoodDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Sarah HoweDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Sarah BrownDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Janice ChristiansenDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Cara CacioppoDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Michelle WeinbergDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Elena ElkinSchool of Public Health, Columbia University, New York, NY.
Linda FleisherFox Chase Cancer Center, Temple University, Philadephia, PA.
Rajia MimDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Santina HernandezDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Demetrios OfidisDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Dominique FetzerDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.
Tara O HendersonDepartment of Pediatrics, Lurie Children's Hospital, Chicago, IL.
Angela BradburyDivision of Hematology-Oncology, Perelman School of Medicine, University of Pennsylvania, Philadephia, PA.

Funding

Improving Delivery of Genetic Services to High Risk Childhood Cancer Survivors: A Randomized Study of Remote Genetic Services Versus Usual CareR01CA237369 · NCI · UNIVERSITY OF CHICAGO · PI BRADBURY, ANGELA R., HENDERSON, TARA OLIVE · 2020 to 2024
$3.4M
Investigating Medically Underserved Populations’ attitudes, perceptions, and use of genomic testingK00HG012487 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI Daniel Chavez-Yenter · 2024 to 2026
$304k
NCI NIH HHS R01 CA237369NHGRI NIH HHS K00 HG012487
6 · The paper itself

Abstract

Purpose: Clinical genetic testing demand has increased in the era of precision medicine. However, the availability of cancer genetic services remains limited in the United States, prompting a rise in telehealth delivery. Through our Telegenetics program, we seek to promote genetic service delivery across the United States, and here, we assess engagement through registrations with local providers using a service delivery model. Methods: This report describes the Penn Telegenetics Program experience across 4 research and clinical activities using an in-home collaborative local provider model. We report the clinical procedures and our initial experience implementing this model across these 4 research and clinical activities in the Penn Telegenetics Program. We present descriptive findings of the registrations and, in cases of refusals, the rationale provided. Results: From 2018 to 2025, 473 providers (89.4%) successfully registered. Providers were predominantly MD/DO licensed (85.0%). Family medicine was the most frequent specialty (54.3%), followed by internal medicine (20.9%) and clinical oncology (11.8%). Most providers were in suburban locations by zip codes (56.2%); 20.1% were in rural zip codes. Only 56 providers declined collaboration (10.6%); the most common reasons reported were preferring local genetic services (22.5%) and not being comfortable as the ordering provider (22.5%). Conclusion: Our data demonstrate that most local providers are willing to collaborate with a centralized telegenetics program. Still, subsequent engagement from local providers in follow-up questions or other referrals remains a missed opportunity to improve telegenetics access. Refining procedures to increase collaborative care and engagement may provide opportunities to increase access to cancer genetic testing.

Indexed as

Genetic testingGermline testingHereditary cancerPrimary careTelehealth

Identifiers

PMID42718649
PMCPMC13553557

What OpenQuestion holds

Textmetadata
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.