Louanne Hudgins
Academic Appointments
- Professor - Med Center Line, Pediatrics - Medical Genetics
- Member, Child Health Research Institute
- Professor - Med Center Line (By courtesy), Obstetrics & Gynecology
Key Documents
Contact Information
-
Clinical Offices
Medical Genetics 730 Welch Road, 2nd Floor Palo Alto, CA 94304 Tel Work (650) 721-5804 Fax (650) 498-4555Practices at Stanford Hospital and Clinics and Lucile Packard Children's Hospital
- Academic Offices
Personal Information EmailNot for medical emergencies or patient use
Professional Overview
Clinical Focus
- Clinical Genetics
- Perinatal Genetics
Honors and Awards
- Mosbacher Family Distinguished Packard Fellow, Stanford University School of Medicine, Department of Pediatrics (2008-present)
Professional Education
| Fellowship: | University of Connecticut CT (1990) |
| Board Certification: | Clinical Genetics, American Board of Medical Genetics (1993) |
| Residency: | University of Connecticut CT (1987) |
| Medical Education: | University of Kansas Medical KS (1984) |
| Internship: | University of Connecticut-School of Medicine CT (1985) |
Scientific Focus
Current Research Interests
I am interested in prenatal genetic screening and diagnosis.
Publications
- Best ethical practices for clinicians and laboratories in the provision of noninvasive prenatal testing. Prenat Diagn. 2013: 1-6
- Expanding the phenotype of cardiovascular malformations in Adams-Oliver syndrome. Am J Med Genet A. 2013; (6): 1386-9
- Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen. Hum Mol Genet. 2013; (1): 1-17
- NIPT in a Clinical Setting: An analysis of Uptake in the First Months of Clinical Availability. J Genet Couns. 2013
- The Decision to Continue a Pregnancy Affected by Down Syndrome: Timing of Decision and Satisfaction with Receiving a Prenatal Diagnosis. J Genet Couns. 2013
- Variables influencing pregnancy termination following prenatal diagnosis of fetal chromosome abnormalities. J Genet Couns. 2013; (2): 238-48
Help