Charis Eng, MD, PhD, 1962-2024, In Memoriam

passed away on August 13, 2024, after a courageous battle with metastatic breast cancer.Charis's inf luence was profound in so many ways, including numerous contributions to cancer genetics/genomics by performing at the highest levels of research, building specialty clinics for patients in clinical genetics and cancer, and finally in training the next generation of researchers and clinicians.Her imprint on Human Molecular Genetics was essential.Charis's groundbreaking discovery of PTEN germline mutations in Cowden syndrome patients revolutionized the clinical genetic management of these patients.The condition, now known as PTEN hamartoma tumor syndrome (PHTS), is associated with a high incidence of breast, thyroid, and other cancers and is the most common genetic cause of autism spectrum disorder.Dr Eng led a renowned multidisciplinary PHTS clinic that drew patients from around the world.Her prolific research, with over 400 peerreviewed publications, has left an indelible mark on the field.

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Publication Details

Journal
Human Molecular Genetics
Published
2024-09-23
DOI
https://doi.org/10.1093/hmg/ddae140
Primary Topic
History of Medical Practice
Type
article
Field-Weighted Citation Impact
0.00

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article

Charis Eng, MD, PhD, 1962-2024, In Memoriam

Kay E. Davies, Anthony Wynshaw‐Boris
Human Molecular Genetics
History of Medical Practice
article

Charis Eng, MD, PhD, 1962-2024, In Memoriam

Kay E. Davies, Anthony Wynshaw‐Boris
article en

Abstract

passed away on August 13, 2024, after a courageous battle with metastatic breast cancer.Charis's inf luence was profound in so many ways, including numerous contributions to cancer genetics/genomics by performing at the highest levels of research, building specialty clinics for patients in clinical genetics and cancer, and finally in training the next generation of researchers and clinicians.Her imprint on Human Molecular Genetics was essential.Charis's groundbreaking discovery of PTEN germline mutations in Cowden syndrome patients revolutionized the clinical genetic management of these patients.The condition, now known as PTEN hamartoma tumor syndrome (PHTS), is associated with a high incidence of breast, thyroid, and other cancers and is the most common genetic cause of autism spectrum disorder.Dr Eng led a renowned multidisciplinary PHTS clinic that drew patients from around the world.Her prolific research, with over 400 peerreviewed publications, has left an indelible mark on the field.

Human Molecular GeneticsVol. 33(22)
University of Oxford (GB), Pediatrics and Genetics (US), Case Western Reserve University (US)
Cleveland Clinic, Case Western Reserve University, Case Comprehensive Cancer Center, Case Western Reserve University
Openalex Percentile: Top 75%
History of Medical Practice
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