Profile

Stephanie E. Wallace, MD

Stephanie E. Wallace, MD

Genetics

On staff since September 2005

Children's Title: Associate Clinical Director, Medical Genetics

Stephanie E. Wallace, MD, is attending physician at Seattle Childrens Hospital and assistant professor in the Department of Pediatrics at the University of Washington School of Medicine. Dr. Wallace is board certified in Pediatrics and Clinical Genetics.

Her clinical work is performed primarily through the Medical Genetics Clinic at Childrens. She also sees patients in genetics clinics in Bellingham, Yakima and Wenatchee, Wash., and in the State of Alaska outreach clinic. She leads the Neurofibromatosis Clinic and participates in the Skeletal Dysplasia Clinic at Childrens and provides an adult cancer genetics clinic at Tacoma General Hospital. Areas of interest include skeletal dysplasias and cancer genetics.

Overview

Board Certification(s)

Pediatrics
Clinical Genetics (MD)

Medical/Professional School

UCLA David Geffen School of Medicine, Los Angeles

Residency

Combined Pediatrics-Medical Genetics, Cedars-Sinai Medical Center, Los Angeles

Clinical Interests

Long term management of genetic disorders; skeletal dysplasias

Awards and Honors

Award Name Award Description Awarded By Award Date
Western Society of Pediatric Research Travel Award 2004
Paul Rubenstein, MD Award for Excellence in Clinical Research 2002
Magna cum laude, University of Washington 1995
Howard Hughes Research Scholarship, University of Washington 1994
Phi Beta Kappa, University of Washington 1992
The major goal is to introduce novel experimental standards that are realistic known complex protein samples, uniquely based on the diverse proteins.

Publications

  • Stephanie E. Wallace, MD
    Clinical Features in a 4 year old male with trisomy 8p23.3p11.1
  • Bachmann-Gagescu R, Mefford HC, Cowan C, Glew GM, Hing AV, Wallace S, Bader PI, Hamati A, Reitnauer PJ, Smith R, Stockton DW, Muhle H, Helbig I, Eichler EE, Ballif BC, Rosenfeld J, Tsuchiya KD
    Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity.
    Genetics in medicine : official journal of the American College of Medical Genetics , 2010 Oct. : 12(10)641-7
  • Stephanie E. Wallace, MD
    Recurrence of a 1 Mb 9q34.3 subtelomeric deletion in siblings detected by oligonucleotide array
  • Stephanie E. Wallace, MD
    Macrocephaly, conductive hearing loss, atrial septal defect, and congenital radial head dislocation in a father and two sons
  • Stephanie E. Wallace, MD
    FOXL2 copy number changes in the molecular pathogenesis of BPES: Unique cohort of 17 deletions
    Human Mutation , 2010 : 31((5))E1332-E1347
  • Stephanie E. Wallace, MD
    Distal Phalanx and Nail Hypoplasia Associated with Osteopetrosis: Report of an Affected Mother and Son
  • Wallace SE, Lachman RS, Mekikian PB, Bui KK, Wilcox WR
    Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): report of a four-generation pedigree, identification of a mutation in TGFB1, and review.
    American journal of medical genetics. Part A , 2004 Sept. 1 : 129A(3)235-47
  • Stephanie E. Wallace, MD
    Progressive Diaphyseal Dysplasia (Camurati-Engelmann Disease): Report of a Four-Generation Pedigree, Review of the Literature, and Identification of a Mutation in TGFB1
  • Stephanie E. Wallace, MD
    Marked Phenotype Variability in Progressive Diaphyseal Dysplasia (Camurati-Engelmann Disease): Report of a Four-Generation Pedigree, Identification of a Mutation in TGFBI, and Review
    American Journal of Medical Genetics , 2004 : 129A(3)235-247
  • Stephanie E. Wallace, MD
    Progressive Diaphyseal Dysplasia (Camurati-Engelmann Disease): Report of a 6 Generation Pedigree with Remarkable Variation in Expressivity and a Review of the Literature
  • Stephanie E. Wallace, MD
    Update on Camurati-Engelmann Disease
  • Stephanie E. Wallace, MD
    Clinical Features of Camurati-Engelmann Disease
  • Stephanie E. Wallace, MD
    Camurati-Engelmann Disease
    GeneReviews at GeneTests: Medical Genetics Information Resource [database online] Available at http://www.genetests.org , 1997 - 2010
  • Stephanie E. Wallace, MD
    Possible Roles of the Nucleus Prepositus Hypoglossi in Smooth-Pursuit Eye Movements
    BIOS , 1996 : 66203-211
  • Wallace SE, Wilcox WR, Pagon RA, Bird TD, Dolan CR, Stephens K
    Camurati-Engelmann Disease
  • Stephanie E. Wallace, MD
    Identification of a recurrent microdeletion of 3q13.2q13.31 associated with hypotonia and developmental delay