Presentation

Academic

  • Genetics Update for Pediatricians: New Therapies and Old Diagnoses in 2021. AAP Chapter 2 invited lecture, delivered on 8/18/2021 (08/2021)
  • Poster presented at the American College of medical Genetics annual conference 2021. (eP243). A low penetrance, late-truncating SALL1 variant is associated with mild phenotype of Townes-Brock syndrome in heterozygotes. Ramanathan S, Shallow N, Trapane P, Clark RD. (07/2022)

Poster

  • Clark R, Niemann B, Mandapati R. "Timothy Syndrome: A Calcium Channelopathy Assoicated with Long QT Syndrome, Hypoglycemia and Syndactyly." 27th Annual David W. Smith Workshop on Malformations and Morphogenesis. Lake Arrowhead, California (09/2006)
  • Ragoussisl, I, Mirzal G, Schimmenti L, Clark R, . "Molecular Characterization of a Case with CHARGE syndrome like phenotype and partial 6p trisomy." American Society of Human Genetics. New Orleans, Louisana (10/2006)
  • Sapp J, Clark R, Turner J, vandeKamp J, van Dijk F, Lowry B, Biesecker. "A Newly Recognized Overgrowth Syndrome Distinct from Proteus Syndrome." American Society of Human Genetics Annual Meeting . New Orleans, LA (10/2006)
  • Curry C, Tsang M, Friez M, Clark R, Brooks A. "Goldberg-Shprintzen Syndrome Due to a Homozygous Deletion in KIAA1279: Clinical Findings and Prenatal Diagnosis in an At Risk Family." Western Society for Pediatric Research. Monterey, California (02/2007)
  • Clark R, Morris C, Pani Am Hobart H, Rios C, Kimberley K, Gregg R. "Complex Chromosome Abnormalities Identified Utilizing High Resolution Chromosome Analysis, FISH, and SNP Microarrays in an Infant with Phenotypic Features of Williams Syndrome and Cri du Chat Syndrome." Annual Clinical Genetics Meeting. Nashville, Tennessee (03/2007)
  • Rogers, C, Jones KL, Graham J, Moeschler J, Clark R. "Clinical Features in Patients with Opitz-Kaveggia (FG) Syndrome and a Recurrent Mutation." European Conference of Human Genetics. Nice, France (06/2007)
  • Poster presented at the American College of Medical Genetics annual conference 2020.  TESC Gene loss causes seizures, intellectual disability and hippocampal volume loss in a patient with chromoanasynthesis-derived chromosome 12q24.22-23 deletion (03/2020)
  • Poster presentation at the American Academy of Medical Genetics annual conference 2021 (eP244)Xp21 deletion syndrome in a female with intellectual disability. Ramanathan S, Liu T, Clark RD. (03/2021)
  • Poster accepted for presentation at David W. Smith Workshop on Morphogenesis and Malfomations 2022 Norfolk, VA. Hypoglossia After Fetal Alcohol Exposure: Evidence for transient ciliopathy as a mechanism for alcohol-related birth defects. RD Clark, S Ramanathan (06/2022)

Other

  • Robin Clark. "Professional Women." AAUW Math Science Conference. University of Redlands Redlands, CA (03/2007)