Author

Moran Snir

Observed name: M. Snir

Observed institution: Invitae (United States)

ORCID: 0009-0006-3919-9506

Observed ORCID: 0009-0006-3919-9506

OpenAlex ID: A5085842867

Hereditary Cancer Risk Using a Genetic Chatbot Before Routine Care Visits

2021 · Shivani Nazareth, Laura Hayward, et al. · Obstetrics and Gynecology · 89

Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis

2021 · Gemme Campbell-Salome, Laney K. Jones, et al. · Circulation Genomic and Precision Medicine · 57

Democratizing genomics: Leveraging software to make genetics an integral part of routine care

2020 · Moran Snir, Shivani Nazareth, et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 48

Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hypercholesterolemia.

2021 · Gemme Campbell-Salome, Laney K Jones, et al. · PubMed Central · 31

Development and pilot testing of AYA-RISE, a risk information and screening education intervention for adolescents and young adults with cancer risk syndromes

2026 · Junne Kamihara, Lauren Fisher, et al. · Familial Cancer · 3

PDF

Developing and Assessing a Scalable Digital Health Tool for Pretest Genetic Education in Patients With Early-Onset Colorectal Cancer: Mixed Methods Design

2025 · Jessica N Rivera Rivera, Moran Snir, et al. · JMIR Cancer · 3

PDF

P517: Patient and clinician perspectives on a digital health platform for the longitudinal management of genetic cancer predisposition

2024 · Huma Rana, Tara Schmidlen, et al. · Genetics in Medicine Open · 2

PDF

Chatbot Intervention and Cancer Risk Knowledge in Adolescents and Young Adults With Cancer Predisposition

2026 · Junne Kamihara, Angel M. Cronin, et al. · JAMA Network Open

PDF

Implementing Timely Germline Genetic Testing for Patients With Pancreatic Cancer Using a Genetics Copilot for Point-of-Care Education and Health Assessment

2026 · Sophie Moravec, Laura V. Barton, et al. · JCO Precision Oncology

Development and Pilot Evaluation of REFLECT: A Digital Health Application Supporting Fertility and Genetic Decision-Making in Adolescent and Young Adult Oncology

2026 · Sarita Pathak Desai, Lindsay Fuzzell, et al. · Journal of Adolescent and Young Adult Oncology

Abstract PS3-02-28: Emergency Department Breast Cancer Screening Pilot: Improving Access to Screening and Diagnosis for Underserved Populations

2026 · A. Maheswaran, C. Mauntel-Medici, et al. · Clinical Cancer Research

Facilitating And Scaling Patient Engagement With Digital Patient Tools And The HCMA Nest Portal

2026 · Tara Schmidlen, Laura Hayward, et al. · Journal of Cardiac Failure

P539: Closing the GAPS in hereditary cancer: An EMR-integrated genetic copilot for guideline adherence, prevention, and surveillance

2026 · Huma Rana, Franciluz Lizardo-Bueno, et al. · Genetics in Medicine Open

P533: Evaluating a digital patient navigator for genetics result management within a population genomic screening program

2026 · Adam Buchanan, Emilie Simmons, et al. · Genetics in Medicine Open

PDF

O32: BeginNGS: Updates on advancing newborn screening by genome sequencing trial with federated learning models

2026 · Rebecca Reimers, Meredith Wright, et al. · Genetics in Medicine Open

PDF

Abstract 4369297: Digital Patient Navigator Facilitates And Scales Patient Engagement with the Hypertrophic Cardiomyopathy Association

2025 · Tara Schmidlen, Laura Hayward, et al. · Circulation

Abstract P1-01-11: Use of a Digital Navigator to Deliver Patient-Centered Genetic Services in Mammography

2025 · Tara Schmidlen, Emilie Simmons, et al. · Clinical Cancer Research

Use Of A Digital Care Navigator To Facilitate And Scale Patient Engagement With The Hypertrophic Cardiomyopathy Association

2025 · Tara Schmidlen, Laura Hayward, et al. · Journal of Cardiac Failure

P623: BeginNGS: Nest digital genetics navigator facilitates scale while preserving participant experience and education

2025 · Brandan Schultz, Rebecca Reimers, et al. · Genetics in Medicine Open

PDF

Abstract LB145: Implementing timely germline genetic testing for patients with pancreatic cancer via a point-of-care digital education and health assessment tool

2024 · Jennifer B. Permuth, Sophie Moravec, et al. · Cancer Research

P552: Bringing equitable access to cancer genetic services: Implementing and adapting a digital hereditary cancer screening tool at an FQHC

2024 · Vivian Pan, Tara Schmidlen, et al. · Genetics in Medicine Open

P396: The need for a longitudinal digital health platform to implement large scale genomic programs

2023 · Holly LaDuca, Moran Snir, et al. · Genetics in Medicine Open

Works count: 22

Citation count: 233

H-index: 4

I10-index: 4