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Erin L Youngs

TitleProf,Clin Asst
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentDept of Pediatrics
AddressOUCPB 12909
1200 Childrens Ave
Oklahoma City OK 73104
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Butler MG, Youngs EL, Roberts JL, Hellings JA. Assessment and treatment in autism spectrum disorders: a focus on genetics and psychiatry. Autism Res Treat. 2012; 2012:242537. PMID: 22934170.
      Citations: 7     
    2. Youngs EL, Henkhaus RS, Hellings JA, Butler MG. 12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes. Clin Dysmorphol. 2012 Apr; 21(2):93-96. PMID: 22127048.
      Citations: 4     Fields:    Translation:HumansCells
    3. Youngs EL, Dasouki M, Butler MG. 14q32 deletion syndrome: a clinical report. Clin Dysmorphol. 2012 Jan; 21(1):42-44. PMID: 22143351.
      Citations:    Fields:    Translation:HumansCells
    4. Youngs EL, Henkhaus R, Hellings JA, Butler MG. IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features. Eur J Med Genet. 2012 Jan; 55(1):32-6. PMID: 21933724.
      Citations: 12     Fields:    Translation:HumansCells
    5. Youngs EL, Hellings JA, Butler MG. A clinical report and further delineation of the 14q32 deletion syndrome. Clin Dysmorphol. 2011 Jul; 20(3):143-147. PMID: 21358539.
      Citations: 4     Fields:    Translation:HumansCells
    6. Youngs EL, Hellings JA, Butler MG. ANKRD11 gene deletion in a 17-year-old male. Clin Dysmorphol. 2011 Jul; 20(3):170-171. PMID: 21527850.
      Citations: 14     Fields:    Translation:HumansCells
    7. Dasouki MJ, Youngs EL, Hovanes K. Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature. Curr Genomics. 2011 May; 12(3):190-203. PMID: 22043167.
      Citations: 14     
    8. Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Hum Genet. 2011 Oct; 130(4):517-28. PMID: 21359847.
      Citations: 111     Fields:    Translation:HumansCells
    9. Youngs EL, McCord T, Hellings JA, Spinner NB, Schneider A, Butler MG. An 18-year follow-up report on an infant with a duplication of 9q34. Am J Med Genet A. 2010 Jan; 152A(1):230-3. PMID: 20034079.
      Citations: 4     Fields:    Translation:HumansCells
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