• |
  • |
  • |
  • |
Donate

AUCD Experts

Kathleen Angkustsiri, MD

Login to Update Your Profile
Contact Information:
916-703-0278
Leadership:
Primary Activity Coordinators:
Clinical Services
Discipline Coordinators:
Pediatrics
Project/Program/Clinic Contacts:
Healthy Minds Clinic (22q)
Discipline(s):
Medicine-Pediatrics
Human Development/Child Development
Medicine-Developmental-Behavioral Pediatrics
AUCD Council Membership:
No Council Membership
Vita/Bio:

Kathleen Angkustsiri
2825 50th Street. Sacramento, CA 95817.
EDUCATION
Fellowship, Developmental-Behavioral Pediatrics, June 2009
University of California, Davis, Medical Center, M.I.N.D. Institute, Sacramento, CA

Pediatric Residency, June 2006
Children's Hospital and Research Center at Oakland, Oakland, CA

Doctor of Medicine, May 2003
New York University School of Medicine, New York, NY

Bachelor of Arts; Major: Psychology. Minor: Human Biology, June 1998
Stanford University, Stanford, CA

LICENSURE AND CERTIFICATION
Licensed to practice medicine in the state of California
Board Certified, American Board of Pediatrics, January 2007

PUBLICATIONS AND PRESENTATIONS
Publications:
• Hansen RL, Ozonoff S, Krakowiak P, Angkustsiri K, Jones C, Deprey LJ, Le DN, Croen LA, Hertz-Picciotto I. Regression in Autism: Prevalence and Associated Factors in the CHARGE Study. Ambul Pediatr 2008;8(1):25-31.
• Angkustsiri K, Wirojanan J, Deprey LJ, Gane LW, Hagerman RJ. Fragile X Syndrome with Anxiety Disorder and Exceptional Verbal Intelligence. Am J Med Gen A 2008;146A(3)376-379.
• Wirojanan J, Kraff J, Hawkins DS, Laird C, Gane LS, Angkustsiri K, Tassone F, Hagerman RJ. Two Boys with fragile X Syndrome and Hepatic Tumors. J Pediatric Hematology and Oncology 2008;30(3):239-41.
• Wirojanan J, Angkustsiri K, Tassone F, Hagerman RJ. A Girl with Fragile X Premutation from Sperm Donation. Am J Med Gen A 2008;146(7):888-92.
• Perry R, Gilbert EM, Angkustsiri K. Jensen PS. Are Stimulants Overprescribed? [Comment: Letter] Journal of the American Academy of Child & Adolescent Psychiatry. 2000; 39(3):269-271.
• Coleman AE, Angkustsiri K, Janz S. Use of B1-repeat-supplemented Cot-1 DNA to enhance background suppression in FISH. [Technical Tips] Elsevier Trends Journals Technical Tips Online. 1999;1:72:T01769. http://tto.trends.com

Presentations:
• Chromosome 22q11.2 Deletion Syndrome Family Meeting, Sacramento, CA
Chromosome 22q.11 Deletion Syndrome: Medical and Behavioral Issues
• 2008 Western Society for Pediatric Research Regional Meeting, Carmel, CA
Dysmorphology and Autism.
• 2007 Western Society for Pediatric Research Regional Meeting, Carmel, CA
Gastrointestinal Symptoms and Seizures in Autistic Regression.
• 2007 California Children's Services-High Risk Infant Follow-up Annual Meeting, Sacramento, CA
Common Developmental Assessment Tools

PROFESSIONAL AFFILIATIONS
Society of Developmental and Behavioral Pediatrics, American Academy of Pediatrics, Western Society for Pediatric Research, American Society of Human Genetics

HONORS AND AWARDS
2007 WSPR Carmel Scholar Award, 2008 WSPR Mead Johnson Travel Award, 2004 Outstanding Housestaff Clinician Award, 2003 NYU School of Medicine President's Service Award, 1998 Psi Chi (National Psychology Honor Society)

 

 

Service:
Linked Projects

3a-3 Chromosome 22q11.2 Deletion Syndrome Healthy Minds Clinic
3a-3 Chromosome 22q11.2 Deletion Syndrome Healthy Minds Clinic
3a-3 Chromosome 22q11.2 Deletion Syndrome Healthy Minds Clinic
3a-3 Chromosome 22q11.2 Deletion Syndrome Healthy Minds Clinic
3a-3 Chromosome 22q11.2 Deletion Syndrome Healthy Minds Clinic
Linked Products

Journal: Atypical presentation of Angelman syndrome with intact expressive language due to low-level mosaicism.
Journal: Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS
Journal: Association of Breastfeeding Duration with Neurodevelopmental Outcomes in an Enriched Familial Likelihood Cohort for Autism Spectrum Disorder.
Conf Pres: Meta-analysis of the Modified Checklist for Autism in Toddlers, Revised/Follow-up for Screening for Autism Spectrum Disorder.
Journal: Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome.