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American Journal of Human Genetics|April 6, 2019
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research ResultsYvonne Bombard, Kyle B Brothers, Sara Fitzgerald-Butt, et al.
The Oncologist|April 6, 2022
"Game Changer": Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome ManagementSalma Shickh, Leslie E Oldfield, Marc Clausen, et al.
Pediatrics|August 4, 2016
Parent Experience With False-Positive Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
American Journal of Human Genetics|October 6, 2023
Current and new frontiers in hereditary cancer surveillance: Opportunities for liquid biopsyKirsten M Farncombe, Derek Wong, Maia L Norman, et al.
The Journal of Pediatrics|March 11, 2017
Psychosocial Response to Uncertain Newborn Screening Results for Cystic FibrosisRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 16, 2024
Offering complex genomic screening in acute pediatric settings: Family decision-making and outcomesMelissa Martyn, Ling Lee, Alli Jan, et al.
BMJ Open|June 3, 2023
Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocolSophie E Bouffler, Ling Lee, Fiona Lynch, et al.
The American Journal of Surgical Pathology|August 25, 2009
Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panelJinru Shia, Laura H Tang, Efsevia Vakiani, et al.
European Journal of Human Genetics : EJHG|June 1, 2024
Benign splenic lesions in BAP1-tumor predisposition syndrome: a case seriesJoao Miranda, Priya Dave, Yelena Kemel, et al.
Human Mutation|October 2, 2009
Functional redundancy of exon 12 of BRCA2 revealed by a comprehensive analysis of the c.6853A>G (p.I2285V) variantLili Li, Kajal Biswas, Laura Anne Habib, et al.
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