Shilpa Chetty, MD

Perinatologist and Medical Geneticist

Dr. Shilpa P. Chetty is an obstetrician and gynecologist who specializes in high-risk pregnancy and perinatal genetics. She has a special interest in prenatal diagnosis, fetal anomalies and the management of pregnancy complicated by medical and genetic disorders.

Chetty completed a medical degree at Loma Linda University, School of Medicine, followed by an internship and residency in obstetrics and gynecology at Washington Hospital Center in Washington, D.C. Subsequently, she completed a fellowship in Clinical Genetics at the National Institutes of Health in Bethesda, Maryland, followed by an additional fellowship in maternal-fetal medicine at Stanford University. She is board certified in both obstetrics and gynecology and medical genetics.

Clinics

Fetal Treatment Center
1855 Fourth St., Second Floor, Room A-2432
San Francisco, CA 94158
Phone: (800) 793-3887
Fax: (415) 502-0660

Hours: Monday to Friday
8 a.m. - 5 p.m.

Prenatal Diagnostic Center
1825 Fourth St., Third Floor
San Francisco, CA 94158
Phone: (415) 476-4080
Fax: (415) 353-4077

Hours: Monday to Friday
8 a.m. – 5 p.m.

Board Certification

Clinical Genetics, American Board of Medical Genetics

Academic Title

Assistant Professor

More about Shilpa Chetty

Education

Loma Linda University Schoool of Medicine 2004

Residencies

Washington Hospital, Obstetrics and Gynecology 2008

Fellowships

Stanford University, Maternal-Fetal Medicine
National Institutes of Health, Clinical Genetics 2010

Selected Research and Publications

  1. Chetty S, Norton ME. Obstetric care in women with genetic disorders. Best Pract Res Clin Obstet Gynaecol. 2017 Jul; 42:86-99.
  2. Qi Z, Madaan S, Chetty S, Yu J, Wiita AP. False negative fetal cell free DNA screening for microdeletion syndromes in the presence of an unbalanced translocation involving monosomy 4p. Prenat Diagn. 2017 04; 37(4):420-422.
  3. Chen S, Chetty S, Lowenthal A, Evans JM, Vu C, Stauffer KJ, Lyell D, Selamet Tierney ES. Feasibility of neonatal pulse wave velocity and association with maternal hemoglobin A1c. Neonatology. 2015; 107(1):20-6.
  4. Yeaton-Massey A, Loring M, Chetty S, Druzin M. Uterine rupture after uterine artery embolization for symptomatic leiomyomas. Obstet Gynecol. 2014 Feb; 123(2 Pt 2 Suppl 2):418-20.
  5. Chetty S, Garabedian MJ, Norton ME. Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening. Prenat Diagn. 2013 Jun; 33(6):542-6.
  6. Chetty SP, Shaffer BL, Norton ME. Management of pregnancy in women with genetic disorders: Part 2: Inborn errors of metabolism, cystic fibrosis, neurofibromatosis type 1, and Turner syndrome in pregnancy. Obstet Gynecol Surv. 2011 Dec; 66(12):765-76.
  7. Chetty SP, Shaffer BL, Norton ME. Management of pregnancy in women with genetic disorders, Part 1: Disorders of the connective tissue, muscle, vascular, and skeletal systems. Obstet Gynecol Surv. 2011 Nov; 66(11):699-709.
  8. Chetty-John S, Piwnica-Worms K, Bryant J, Bernardini I, Fischer RE, Heller T, Gahl WA, Gunay-Aygun M. Fibrocystic disease of liver and pancreas; under-recognized features of the X-linked ciliopathy oral-facial-digital syndrome type 1 (OFD I). Am J Med Genet A. 2010 Oct; 152A(10):2640-5.
  9. Chetty-John S, Zhang J, Chen Z, Albert P, Sun L, Klebanoff M, Grewal U. Long-term physical and neurologic development in newborn infants with isolated single umbilical artery. Am J Obstet Gynecol. 2010 Oct; 203(4):368.e1-7.
  10. Sunde J, Chetty-John S, Shlobin OA, Boice CR. Epstein-Barr virus-associated uterine leiomyosarcoma in an adult lung transplant patient. Obstet Gynecol. 2010 Feb; 115(2 Pt 2):434-6.

Publications are derived from MEDLINE/PubMed and provided by UCSF Profiles, a service of the Clinical & Translational Science Institute (CTSI) at UCSF. Researchers can make corrections and additions to their publications by logging on to UCSF Profiles.