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Dr. Kwame Anyane-Yeboa, MBBS
Director, NewYork-Presbyterian/Columbia University Irving Medical Center (New York, NY)
Bachelor of Medicine and Surgery, University of Ghana Medical School
Dr. Kwame Anyane-Yeboa has years of experience in the field of Pediatrics and Medical Genetics. He earned his MBBS from the University of Ghana Medical School. After completing his residency in Pediatrics at NYC Health + Hospitals/Harlem, he went on to complete his fellowship in Clinical Genetics at NewYork-Presbyterian/Columbia University Irving Medical Center. Today, he is board certified in Pediatrics and Clinical Genetics. Formerly, he served as a Professor of Pediatrics at the Columbia University Vagelos College of Physicians and Surgeons. Most recently, he served as a Clinical Assistant Professor (Voluntary) of Pediatrics and Genetics at the University of Rochester School of Medicine and Dentistry and as a Physician with UR Medicine.
a*********@g*****.com
(914) ***-****
Yorktown Heights, New York
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Expert Witness Activity
Plaintiff Cases
Defense Cases
15
Expert Challenges
9
Deposition Transcripts
Publications
111
Media & News
199
Social Media Mentions
16
Radar found 21 records
Case Name | Role | Filed Date |
|---|---|---|
Yu Yun Dong v. Reginald Ruiz MD, et al. | Expert Witness | 2009-01-01 |
Marijohnne Upshur v. Staten Island Medical Center | Expert Witness | 2004-09-28 |
Amani Royal, et al. v. Marti Gilbert, et al. | Expert Witness | 2004-09-22 |
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Institution | Degree Type |
|---|---|
University of Ghana Medical School | Bachelor of Medicine and Surgery |
Title | Employer |
|---|---|
Director | NewYork-Presbyterian/Columbia University Irving Medical Center (New York, NY) |
Director | NewYork-Presbyterian/Columbia University Irving Medical Center (New York, NY) |
— | NewYork-Presbyterian/Columbia University Irving Medical Center (New York, NY) |
Radar found 111 records
Title | Type |
|---|---|
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals | Journal Article |
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms | Journal Article |
Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders | Journal Article |
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Radar found 199 records
Title | Description |
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