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One or more keywords matched the following properties of Waggoner, Darrel J.
PropertyValue
keywords Clinical and Medical Genetics
overview I am a clinical geneticist and 50% of my effort is devoted to patient activity. I participate in a general genetics clinic one full day where with a team of genetic counselors and fellows we see a wide range of both adult and pediatric patients for evaluation, diagnosis, counseling and treatment for genetic disorders. In addition I am involved in several multidisciplinary clinics including Marfan and Craniofacial clinic. I am also involved in education throughout the university specifically in the medical school. I am interested in developing new and unique curriculum for integrating genetics into the four years of the medical school training and residency programs. I am the Program Director for the Genetics Laboratory Training Program in molecular and cytogenetics and soon to be Laboratory Genetics and Genomics program. I am also interested in developing curriculum to facilitate the training of clinical genetics professionals on new technology. Specifically I have been involved in developing tools that help counselors and clinicians to interpret new genetic technology such as microarray and Next Generation sequencing results for panels and exome sequencing. Since I am mostly involved in the clinical aspects of the Department of Human Genetics my research is collaborative where I provide a clinical perspective for others research programs. My goal is to provide clinical correlation for the basic science research projects in the department. I have been involved in projects looking at telomere genotype/phenotype correlations, Soto syndrome, and chromosome abnormalities. I have recently been involved in a project with Dr.Carole Ober studying different clinic phenotypes in the Hutterite populations.
preferred title Clinical Professor
One or more keywords matched the following items that are connected to Waggoner, Darrel J.
Item TypeName
Concept Clinical Competence
Concept Genetics, Medical
Academic Article TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome.
Academic Article NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory.
Academic Article Integration of internet-based genetic databases into the medical school pre-clinical and clinical curriculum.
Academic Article Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
Academic Article Internet resources in medical genetics.
Academic Article Internet resources in medical genetics.
Academic Article Recommendations for the integration of genomics into clinical practice.
Academic Article Medical genetics and genomics education: how do we define success? Where do we focus our resources?
Academic Article Professional medical education and genomics.
Academic Article Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 9 affected individuals.
Academic Article Correction: "Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals".
Academic Article Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Academic Article Training the next generation of genomic medicine providers: trends in medical education and national assessment.
Academic Article The relationship between performance on the medical genetics and genomics in-training and certifying examinations.
Search Criteria
  • Clinical
  • Medical Genetics