NaomiYachelevichMD
Medical Genetics • New York, NYClinical Genetics
Assistant Professor, Pediatrics, New York University School of Medicine
Overview of Dr. Yachelevich
Dr. Naomi Yachelevich is a medical geneticist in New York, NY and is affiliated with multiple hospitals in the area, including New York-Presbyterian Hospital, NewYork-Presbyterian/Columbia University Irving Medical Center, NYU Langone Hospitals, Mount Sinai Beth Israel, NYC Health + Hospitals / Bellevue, and NewYork-Presbyterian/Lawrence Hospital. She received her medical degree from Ben Gurion University of the Negev and has been in practice 18 years. She is one of 7 doctors at NYU Langone Hospitals and one of 4 doctors at Mount Sinai Beth Israel who specialize in Medical Genetics. She has more than 10 publications and over 500 citings.
Office
21 W 86th St
New York, NY 10024Fax+1 212-305-9058
Education & Training
Montefiore Medical Center/Albert Einstein College of MedicineResidency, Medical Genetics and Genomics, 2008 - 2010
New York-Presbyterian Brooklyn Methodist HospitalResidency, Pediatrics, 2005 - 2008
Ben Gurion University of the NegevClass of 1999
Certifications & Licensure
NY State Medical License 2008 - 2026- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- CMS Meaningful Use Stage 1 Certification EpicCare Ambulatory EMR, Epic Systems Corporation, 2013
Publications & Presentations
PubMed
- 1 citationsGenotype - phenotype correlation in an adolescent girl with pathogenic variant in PPARƴ gene causing severe hypertriglyceridemia and early onset type 2 diabetes.Ana Gutierrez Alvarez, Naomi Yachelevich, Brenda Kohn, Preneet Cheema Brar
Annals of Pediatric Endocrinology & Metabolism. 2021-10-14 - 16 citationsHeterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability,speech delay, and dysmorphismMaya Chopra, Meriel McEntagart, Jill Clayton-Smith, Konrad Platzer, Anju Shukla
American Journal of Human Genetics. 2021-06-03 - 6 citationsTranscriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis.Odelia Chorin, Naomi Yachelevich, Khaled Mohamed, Ilana Moscatelli, John Pappas
Molecular Genetics & Genomic Medicine. 2020-07-21
