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Sarah Scollon

Baylor College of Medicine(US)

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89

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2.8K

Citations

26

h-index

38

i10-index

Sarah Scollon is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Genomics and Rare Diseases & BRCA gene mutations in cancer & Cancer Genomics and Diagnostics. The author has an h-index of 26, co-authored 76 publications.

ORCID: 0000-0003-2017-0245

Research Topics

Genomics and Rare Diseases BRCA gene mutations in cancer Cancer Genomics and Diagnostics Neuroblastoma Research and Treatments Childhood Cancer Survivors' Quality of Life

Papers by this author

works

Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients

2014 · Genome Medicine · 72 citations

https://doi.org/10.1186/s13073-014-0069-3

Sarah Scollon Katie Bergstrom Robin A. Kerstein Tao Wang

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

2024 · Clinical Cancer Research · 22 citations

https://doi.org/10.1158/1078-0432.ccr-24-1611

Melissa R. Perrino Anirban Das Sarah Scollon Sarah G. Mitchell

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

2022 · Genome Medicine · 17 citations

https://doi.org/10.1186/s13073-022-01139-2

Kevin M. Bowling Michelle L. Thompson Melissa Kelly Sarah Scollon

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

2024 · Clinical Cancer Research · 4 citations

https://doi.org/10.1158/1078-0432.ccr-24-2171

Orli Michaeli Sun Young Kim Sarah G. Mitchell Marjolijn C.J. Jongmans

Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndrome

2025 · Cancer Genetics · 2 citations

https://doi.org/10.1016/j.cancergen.2025.01.009

Lauren Desrosiers John H. Lee Izabela Tarasiewicz Andrea Gilbert

Additional file 1 of Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing

2022 · Figshare · 0 citations

https://doi.org/10.6084/m9.figshare.21621843

Kevin M. Bowling Michelle L. Thompson Melissa Kelly Sarah Scollon

Research topics

topics

Genomics and Rare Diseases

BRCA gene mutations in cancer

Cancer Genomics and Diagnostics

Neuroblastoma Research and Treatments

Childhood Cancer Survivors' Quality of Life

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