Mohammed Almannai (M Almannai)

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 4

Top Topics

Dna Methylation

Gene Expression

Duchenne Muscular Dystrophy

Top Venues

Clinical genetics

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Mohammed Almannai, Azza Salah, Ayman W. El-Hattab
Mitochondrial Membranes and Mitochondrial Genome: Interactions and Clinical Syndromes. Membranes 12 (6) (2022)
Mohammed Almannai, Osama Obaid, Eissa Faqeih, Ali Alasmari, Manar M Samman, Hailey Pinz, Stephen R Braddock, Fowzan Sami Alkuraya
Further delineation of METTL23-associated intellectual disability. American journal of medical genetics. Part A 182 (4) (2020)
E A Faqeih, Mohammed Almannai, M M Saleh, A H AlWadei, M M Samman, Fowzan Sami Alkuraya
Phenotypic characterization of KCTD3-related developmental epileptic encephalopathy. Clinical genetics 93 (5) (2018)
Mohammed Almannai, A Alasmari, A Alqasmi, E Faqeih, F Al Mutairi, M Alotaibi, M M Samman, W Eyaid, Y I Aljadhai, H E Shamseldin, W Craigen, Fowzan Sami Alkuraya
Expanding the phenotype of SLC25A42-associated mitochondrial encephalomyopathy. Clinical genetics 93 (5) (2018)