Naomi Yachelevich, MD

  • Specialty: Pediatrics
  • Languages: English, Hebrew
  • Phone: 646-754-2222

About Me

Conditions and Treatments

genetic counseling, birthmark, lysosomal storage disease, neurofibromatosis, multiple pterygium syndrome, kabuki syndrome, intellectual disability, connective tissue disease, ear malformation, movement disorders, congenital heart defect, growth disorders, autism, cleft palate, vascular malformation, normal pressure hydrocephalus (nph), genetic skin diseases, kidney malformation, arthrogryposis, cystic fibrosis, inborn scoliosis, achondroplasia, short stature, multiple endocrine neoplasia, epilepsy, hand deformities, muscular dystrophy, coarctation, congenital hydrocephalus, pseudoachondroplasia, marfan syndrome, limb abnormalities, craniosynostosis
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Credentials

Positions

  • Assistant Professor, Department of Pediatrics

Board Certifications

    2011
  • American Board of Medical Genetics - Clinical Genetics
    2008
  • American Board of Pediatrics - Pediatrics

Education and Training

  • 2010
  • Residency, Montefiore Medical Center, Genetics
  • Other Credentials
  • from

Departments

Locations and Appointments

55 Insurance Plans Accepted
  • Aetna HMO
  • Aetna Medicare
  • Aetna POS
  • Aetna PPO/EPO
  • Cigna EPO/POS
  • Cigna PPO
  • ElderPlan
  • Empire Blue Cross Blue Shield EPO
  • Empire Blue Cross Blue Shield HMO
  • Empire Blue Cross Blue Shield Healthy NY
  • Empire Blue Cross Blue Shield Indemnity
  • Empire Blue Cross Blue Shield MediBlue
  • Empire Blue Cross Blue Shield POS
  • Empire Blue Cross Blue Shield PPO
  • Empire Blue Cross Blue Shield Pathways, Enhanced
  • GHI CBP
  • HIP Access I
  • HIP Access II
  • HIP Child Health
  • HIP EPO/PPO
  • HIP Family Health
  • HIP HMO
  • HIP Medicaid
  • HIP Medicare
  • HIP POS
  • HealthPlus Child Health (Amerigroup)
  • HealthPlus Family Health (Amerigroup)
  • HealthPlus Medicaid (Amerigroup)
  • HealthRepublic
  • HealthSmart (WTC)
  • Humana Medicare
  • Local 1199 PPO
  • MagnaCare PPO
  • Medicare
  • MultiPlan/PHCS PPO
  • NY Medicaid
  • NYS Empire Plan
  • Oscar
  • Oxford Exchange
  • Oxford Freedom
  • Oxford Liberty
  • Oxford Medicare
  • United Exchange- Compass
  • UnitedHealthcare Community & State Plan
  • UnitedHealthcare EPO
  • UnitedHealthcare HMO
  • UnitedHealthcare Medicare
  • UnitedHealthcare POS
  • UnitedHealthcare PPO
  • UnitedHealthcare Top Tier
  • Visiting Nurse Service (VNS) Medicare
  • WellCare Child Health
  • WellCare Family Health
  • WellCare Medicaid
  • WellCare Medicare
*Insurance listed above may not be accepted at all office locations. Please confirm prior to each visit. The information presented here may not be complete or may have been changed.

NYU Pediatric Genetics Associates
145 East 32nd Street, 14th Floor
New York, NY 10016

Contact

Phone: 646-754-2222

Welcome back!

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Publications

  • Corrigendum: Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability

    Tatton-Brown, Katrina; Seal, Sheila; Ruark, Elise; Harmer, Jenny; Ramsay, Emma; Del Vecchio Duarte, Silvana; Zachariou, Anna; Hanks, Sandra; O'Brien, Eleanor; Aksglaede, Lise; Baralle, Diana; Dabir, Tabib; Gener, Blanca; Goudie, David; Homfray, Tessa; Kumar, Ajith; Pilz, Daniela T; Selicorni, Angelo; Temple, I Karen; Van Maldergem, Lionel; Yachelevich, Naomi; van Montfort, Robert; Rahman, Nazneen 2014 May; 657-657, Nature genetics — id: 1018642, year: 2014, page: 657, stat: Journal Article
  • Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability

    Tatton-Brown, Katrina; Seal, Sheila; Ruark, Elise; Harmer, Jenny; Ramsay, Emma; Del Vecchio Duarte, Silvana; Zachariou, Anna; Hanks, Sandra; O'Brien, Eleanor; Aksglaede, Lise; Baralle, Diana; Dabir, Tabib; Gener, Blanca; Goudie, David; Homfray, Tessa; Kumar, Ajith; Pilz, Daniela T; Selicorni, Angelo; Temple, I Karen; Van Maldergem, Lionel; Yachelevich, Naomi; van Montfort, Robert; Rahman, Nazneen 2014 Apr; 385-388, Nature genetics — id: 898912, year: 2014, page: 385, stat: Journal Article
  • Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: a case series

    Yachelevich, Naomi; Gittler, Julia Klein; Klugman, Susan; Feldman, Barbara; Martin, Joanna; Brooks, Susan Sklower; Dobkin, Carl; Nolin, Sarah L 2011 Apr; 870-874, American journal of medical genetics. Pt A — id: 170692, year: 2011, page: 870, stat: Case Reports; Journal Article
Read All Publications (5)