DeemaAljeaidMDFAAP, FACMG

PubMed

• 1 citations
  Comparison of Evolution of Aortic Root Dilation and Ghent Criteria in Preadolescents and Adolescents with and without Marfan Syndrome
  Danielle Monteil, Amy R. Shikany, Deema Aljeaid, Ashley Parrott, Justin T. Tretter, Jeanne James, Lisa J. Martin, K. Nicole Weaver> ;The Journal of Pediatrics. 2020 Jun 1
• 38 citations
  Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
  Pamela Magini, Daphne J. Smits, Laura Vandervore, Rachel Schot, Marta Columbaro, Esmee Kasteleijn, Mees van der Ent, Flavia Palombo, Maarten H. Lequin, Marjolein H G D...> ;American Journal of Human Genetics. 2019 Oct 3
• 7 citations
  A novel pathogenic variant in OFD1 results in X-linked Joubert syndrome with orofaciodigital features and pituitary aplasia
  Deema Aljeaid, Rachel C. Lombardo, David P. Witte, Robert J. Hopkin> ;American Journal of Medical Genetics. Part A. 2019 Jun 1
• 8 citations
  Prevalence of pathogenic and likely pathogenic variants in the RASopathy genes in patients who have had panel testing for cardiomyopathy.
  Deema Aljeaid, Ana Isabel Sánchez, Emily Wakefield, Sarah E. Chadwell, Nicole Moore, Carlos E. Prada, Wenying Zhang> ;American Journal of Medical Genetics. Part A. 2019 Apr 1
• 9 citations
  Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations
  Katheryn Grand, Christina X Gonzalez-Gandolfi, Amanda M. Ackermann, Deema Aljeaid, Emma Bedoukian, Lynne M. Bird, Diva D. De León, Jullianne Diaz, Robert J. Hopkin, Se...> ;American Journal of Medical Genetics. Part A. 2019 Apr 1
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