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Stephanie E. Wallace, MD

Stephanie E. Wallace, MD

Genetics, Skeletal Dysplasia

On staff since September 2005

Children's Title: Associate Clinical Director, Medical Genetics

Stephanie E. Wallace, MD, is attending physician at Seattle Children's 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 Children's and provides an adult cancer genetics clinic at Tacoma General Hospital. Areas of interest include skeletal dysplasias and cancer genetics.

Recommendations

  • Honey-Marie Lake Stevens, WA 01.05.15

    Dr. Stephanie Wallace was amazing at our appointment. She took the time to be thurough and not rushed. Answered all our questions and gave us all the information we needed. She was genuinely concerned with the wellbeing of my baby. She was very approachable and her bedside manner was engaging.

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

  • Rojnueangnit K, Xie J, Gomes A, Sharp A, Callens T, Chen Y, Liu Y, Cochran M, Abbott MA, Atkin J, Babovic-Vuksanovic D, Barnett CP, Crenshaw M, Bartholomew DW, Basel L, Bellus G, Ben-Shachar S, Bialer MG, Bick D, Blumberg B, Cortes F, David KL, Destree A, Duat-Rodriguez A, Earl D, Escobar L, Eswara M, Ezquieta B, Frayling IM, Frydman M, Gardner K, Gripp KW, Hernández-Chico C, Heyrman K, Ibrahim J, Janssens S, Keena BA, Llano-Rivas I, Leppig K, McDonald M, Misra VK, Mulbury J, Narayanan V, Orenstein N, Galvin-Parton P, Pedro H, Pivnick EK, Powell CM, Randolph L, Raskin S, Rosell J, Rubin K, Seashore M, Schaaf CP, Scheuerle A, Schultz M, Schorry E, Schnur R, Siqveland E, Tkachuk A, Tonsgard J, Upadhyaya M, Verma IC, Wallace S, Williams C, Zackai E, Zonana J, Lazaro C, Claes K, Korf B, Martin Y, Legius E, Messiaen L
    High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation.
    26178382 Human mutation , 2015 Nov. - 2015 Nov. : 36(11)1052-63
  • Wallace SE, Conta JH, Winder TL, Willer T, Eskuri JM, Haas R, Patterson K, Campbell KP, Moore SA, Gospe SM Jr
    A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations.
    24491487 Neuromuscular disorders : NMD , 2014 Apr, - 2014 Apr, : 24(4)312-20 PMCID: PMC3959257
  • 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.
    20808231 Genetics in medicine : official journal of the American College of Medical Genetics , 2010 Oct. : 12(10)641-7
  • Earl D, Wallace S, Tsuchiya K
    Recurrence of a 1 Mb 9q34.3 subtelomeric deletion in siblings detected by oligonucleotide array
  • Wallace SE, Earl DE, White K, Goldberg, MJ
    Macrocephaly, conductive hearing loss, atrial septal defect, and congenital radial head dislocation in a father and two sons
  • D'haene B, Nevado J, Pugeat M, Pierquin G, Lowry RB, Reardon W, Delicado A, Garcia-Minaur S, Palomares M, Courtens W, Stefanova M, Wallace S, Watkins W, Shelling AN, Wiezorek D, Veitia RA, De Paepe A, Lapunzina P, De Baere E
    FOXL2 copy number changes in the molecular pathogenesis of BPES: Unique cohort of 17 deletions
    Human Mutation , 2010 : 31((5))E1332-E1347
  • Wallace SE, Goldberg MJ, Done S
    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.
    15326622 American journal of medical genetics. Part A , 2004 Sept. 1 : 129A(3)235-47
  • Wallace SE, Lachman RS, Mekikian PB, Bui KK, Wilcox WR
    Progressive Diaphyseal Dysplasia (Camurati-Engelmann Disease): Report of a Four-Generation Pedigree, Review of the Literature, and Identification of a Mutation in TGFB1
  • Wallace SE, Lachman RS, Mekikian PB, Bui KK, Wilcox WR
    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
  • Wallace SE, Salazar D, Cormier-Daire V, Lachman RS, Wilcox WR
    Progressive Diaphyseal Dysplasia (Camurati-Engelmann Disease): Report of a 6 Generation Pedigree with Remarkable Variation in Expressivity and a Review of the Literature
  • Wallace SE, Lachman RS, Wilcox WR
    Update on Camurati-Engelmann Disease
  • Wallace SE, Lachman RS, Wilcox WR
    Clinical Features of Camurati-Engelmann Disease
  • Wallace SE, Wilcox WR
    Camurati-Engelmann Disease
    GeneReviews at GeneTests: Medical Genetics Information Resource [database online] Available at http://www.genetests.org , 1997 - 2010
  • Stephanie E. Wallace, MD, Lambert S and Kaneko CRS
    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
    20301335
  • Ravnan JB, Rosenfeld JA, Neill NJ, Bialer MG, Moore C, Wheeler P, Wallace SE, Hannibal MC, Murray MF, Giovanni MA, Schultz RA, Ballif BC, Shaffer LG
    Identification of a recurrent microdeletion of 3q13.2q13.31 associated with hypotonia and developmental delay

Presentations

Presentations Title Event Location Date
Cystic Fibrosis Clinical Testing - The Good, the Bad, and the Confusing AACC/Seattle Childrens Hospital Webinar Series Seattle, WA Nov. 2013
Introduction to Dysmorphology, Common Syndromes A to Z North Pacific Pediatric Society 179th Scientific Conference Cle Elum, WA Aug. 2009
Cancer Genetics Alaska Native Medical Center Grand Rounds Anchorage, AK March 2009
Neurofibromatosis Tanana Valley Clinic Grand Rounds Fairbanks, AK Nov. 2008
Genetics Tutorial Bothell High School Science Olympiad Team Bothell, WA April 2007 - May 2007
Update on Cancer Genetics Evaluation and Testing Allenmore Hospital Tumor Board Tacoma, WA Feb. 2007
Introduction to Cancer Genetics Tacoma General Hospital Tumor Board Tacoma, WA July 2006
Breast Cancer Genetics Tacoma General Hospital Breast Tumor Board Tacoma, WA July 2006
Neurofibromatoses Madrona Medical Center Noon Conference Bellingham, WA May 2006
Update on Camurati-Engelmann Disease UCLA Intercampus Medical Genetics Annual Fellowship Retreat Los Angeles, CA May 2000
Clinical Features of Camurati-Engelmann Disease UCLA Intercampus Medical Genetics Annual Fellowship Retreat Los Angeles, CA May 1999

Research Funding

Grant Title Grantor Amount Award Date
Academic Enrichment Fund "Effect of active utilization management on the value and cost of genetic testing" 2012 - 2014