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OMIM - Multisystem Complex Disorders
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Synaptopathies: diseases of the synaptome.
Autosomal recessive mutations in the development of Parkinson's disease.
Preimplantation genetic diagnosis (PGD) for a treatable disorder: Gaucher disease type 1 as a model.
Interpretation of genomic variants using a unified biological network approach.
The HLA genomic loci map: expression, interaction, diversity and disease.
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Delineation of Novel Monogenic Disorders in the United Arab Emirates Population
Bipolar Transcranial Alternating Current Stimulation (tACS)
Exome and Genome Analysis to Elucidate Genetic Etiologies and Population Characteristics in the Plai…
Genetic and Metabolic Disease in Children
Discovering the Gene(s) Causing Developmental Dysplasia of the Hip (DDH)
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