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Identification of the genetic basis of novel PIDs. The advent of whole genome and exome sequencing has facilitated discovery of novel genetic causes underlying PIDs. The Geha lab utilizes functional immunologic assays as well as whole genome/exome sequencing to identify the causative mutation(s) for patients with uncharacterized PIDs. Biochemical and molecular assays as well as mouse models are then used to investigate the pathogenic effect of the mutation and to study gene function in depth. Dr. Geha chairs the International Consortium for Primary Immunodeficiency diseases, an international network of medical and research centers in many countries including Greece, Kuwait, Saudi Arabia, Morocco, UAE, Turkey, Egypt, and Lebanon. This collaboration enables the exchange of expertise in primary immunodeficiency research among all members. These studies are critical not only for the diagnosis of patients with rare PIDs, but also for advancing our understanding of normal immune function. They have resulted in the recent discovery of several new genes that cause PIDS.
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Brian Woods,Brenna LaBere, Anne Chu,Wayne Bainter,Barbara Yang,Mrinmoy Das,Patrick Schlievert,Wanda Phipatanakul, JuanManuel LeyvaCastillo,Janet Chou,Raif Geha
Journal of Allergy and Clinical Immunologyno. 2 (2024): AB255
Mrinmoy Das,Brian Woods,Maheshwor Timilshina,Juan Manuel Leyva-Castillo,Simon P. Hogan,Fred D. Finkelman,Frank Brombacher, Patrick & Shirley Schlievert,Raif Geha
Journal of Allergy and Clinical Immunologyno. 2 (2024): AB74
Journal of Allergy and Clinical Immunology (2024)
Journal of Investigative Dermatology (2024)
Journal of Allergy and Clinical Immunologyno. 4 (2023): 907-915
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Journal of drugs in dermatology : JDDno. 10 (2023): 1001-1006
Erin Janssen,Mohammad F Alosaimi,Anas M Alazami, Abdullah Alsuliman,Ayodele Alaiya,Bandar Al-Saud,Hamoud Al-Mousa, Tariq Jassim Al-Zaid,Emma Smith,Craig D Platt,Hibah Alruwaili,Sarah Albanyan,
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