Sarah Scollon

Assistant Professsor/Genetic Counselor

Baylor College of Medicine

United States

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About

Dr. Sarah Scollon is an Assistant Professor and Genetic Counselor at Baylor College of Medicine in the United States. Her research primarily focuses on cancer surveillance and genetic testing in pediatric populations, particularly in relation to syndromes like Neurofibromatosis and hereditary predisposition to various cancers. Recent publications include works on pediatric cancer surveillance recommendations and family-based approaches to cascade genetic testing.

Articles (13)

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2025

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2022

Collaborators (9)

William Foulkes

Full Professor

McGill University

CANADA

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Anne Slavotinek

UNITED STATES

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Frank Lin

Baylor College of Medicine Department of Pediatrics

UNITED STATES

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Laura Hendon

Associate Professor, Certified Genetic Counselor

University of Mississippi Medical Center

UNITED STATES

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Gregory Cooper

HudsonAlpha Institute for Biotechnology

UNITED STATES

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Gail Tomlinson

Professor

The University of Texas Health Science Center at Houston

UNITED STATES

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Bradford Powell

University of North Carolina

UNITED STATES

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Jack Brzezinski

Associate Professor

University of Washington

UNITED STATES

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Donald Parsons

Professor

Baylor College of Medicine

UNITED STATES

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Sarah Scollon

Research Interests

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About

Articles (13)

Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2-, SMARCB1-, and LZTR1-Related Schwannomatosis

A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic

Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes

Update on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies

Update on Genetic Counselor Practice and Recommendations for Pediatric Cancer Predisposition Evaluation and Surveillance

Satisfaction with mode of delivery of genomic sequencing results in a diverse national sample of research participants through the Clinical Sequencing Evidence-Generating Research Consortium

Neuroblastoma Predisposition and Surveillance—An Update from the 2023 AACR Childhood Cancer Predisposition Workshop

Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors

Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research.

Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) study

Clinical and molecular features of pediatric cancer patients with Lynch syndrome.

Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.

FOCAD Indel in a Family With Juvenile Polyposis Syndrome.

Collaborators (9)

William Foulkes

Anne Slavotinek

Frank Lin

Laura Hendon

Gregory Cooper

Gail Tomlinson

Bradford Powell

Jack Brzezinski

Donald Parsons

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