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GTR Home > Laboratories > Quest Diagnostics Nichols Institute Chantilly

Quest Diagnostics Nichols Institute Chantilly

GTR Lab ID: 500061, Last updated:2024-01-08

Personnel

  • Director: Debra Boles, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Colyn Cain, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Nicole Christacos, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Julie Cox, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Christine Curtis, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Haiying Meng, PhD, MD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Navnit Mitter, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Malini Sathanoori, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Steven Schonberg, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Director: Sunita Singh, PhD, MD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
  • Courtney Banner, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 866-GENEINFO
  • Meredith Masiello, MS, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 866-GENEINFO
  • Lisa Pike-Buchanan, MSc, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 866-GENEINFO
  • Bonnie Epstein, MS, Genetic Counselor
    Phone: 866-436-3463
  • Amanda Hahn, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 866-436-3463

Conditions and tests

  • 4p partial monosomy syndrome1 test
  • 5p partial monosomy syndrome1 test
  • Abacavir hypersensitivity1 test
  • Advanced maternal age gravida3 tests
  • Autism spectrum disorder5 tests
  • Bloom syndrome2 tests
  • Cognitive impairment5 tests
  • Congenital chromosomal disease2 tests
  • DiGeorge syndrome1 test
  • Dysmorphic features5 tests
  • Fanconi anemia complementation group A2 tests
  • Fanconi anemia complementation group B2 tests
  • Fanconi anemia complementation group C2 tests
  • Fanconi anemia complementation group D12 tests
  • Fanconi anemia complementation group D22 tests
  • Fanconi anemia complementation group E2 tests
  • Fanconi anemia complementation group F2 tests
  • Fanconi anemia complementation group G2 tests
  • Fanconi anemia complementation group I2 tests
  • Fanconi anemia complementation group J2 tests
  • Fanconi anemia complementation group L2 tests
  • Fanconi anemia complementation group N2 tests
  • Fanconi anemia complementation group O2 tests
  • Fanconi anemia complementation group P2 tests
  • Fanconi anemia, complementation group M2 tests
  • Global developmental delay5 tests
  • Hypogonadotropic hypogonadism 1 with or without anosmia1 test
  • Infertility disorder3 tests
  • Klinefelter syndrome3 tests
  • Known OR suspected fetal abnormality affecting management of mother3 tests
  • Maternal care for suspected chromosomal abnormality in fetus3 tests
  • Miller Dieker syndrome1 test
  • Miscarriage1 test
  • Multiple congenital anomalies5 tests
  • Prader-Willi syndrome1 test
  • Pregnancy loss, recurrent, susceptibility to, 13 tests
  • Smith-Magenis syndrome1 test
  • Turner syndrome3 tests
  • Velocardiofacial syndrome1 test
  • Williams syndrome1 test
  • X-linked ichthyosis with steryl-sulfatase deficiency1 test

List of services

  • Maternal cell contamination study (MCC): Order Code: 10262

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 49D0221801, Expiration date: 2025-02-08
  • CAP, Number: 1361101, Expiration date: 2025-04-22

Licenses

  • CA - California Department of Public Health CDPH, Number: COS00800071, Expiration date: 2024-03-27
  • NY - New York State Department of Health NYSDOH, Number: PFI: 3745, Expiration date: 2024-06-30

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.