Brahim Tabarki

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 8

Top Venues

Neurogenetics

Neurology. Genetics

Archives of disease in childhood. Education and practice edition

American journal of medical genetics. Part A

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

Publications

Wejdan Hakami, Farah Thabet, Amal Alhashem, Abdulaziz Alghamdi, Saad Alshahwan, Fowzan S Alkuraya, Brahim Tabarki
Bi-allelic variants in HCRT cause autosomal recessive narcolepsy. Neurogenetics 25 (2) (2024)
Rawan Alsafh, Amal M Alhashem, Aly Elsyed, Zafer Yüksel, Kalthoum Graiess-Tlili, Khalid Hundallah, Farah Thabet, Brahim Tabarki
Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly. Neurology. Genetics 10 (4) (2024)
Rawan Alsafh, Amal M Alhashem, Aly Elsyed, Zafer Yüksel, Kalthoum Graiess-Tlili, Khalid Hundallah, Farah Thabet, Brahim Tabarki
Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly. Neurology. Genetics 10 (4) (2024)
Wejdan Hakami, Farah Thabet, Amal Alhashem, Abdulaziz Alghamdi, Saad Alshahwan, Fowzan S Alkuraya, Brahim Tabarki
Bi-allelic variants in HCRT cause autosomal recessive narcolepsy. Neurogenetics (2024)
Wejdan Hakami, Farah Thabet, Amal Alhashem, Abdulaziz Alghamdi, Saad Alshahwan, Fowzan S Alkuraya, Brahim Tabarki
Bi-allelic variants in HCRT cause autosomal recessive narcolepsy. Neurogenetics 25 (2) (2024)
Bashaer Albulushi, Farah Thabet, Saad Alshahwan, Yasser Elborai, Nawaf Alkhayat, Mohamed Alshahrani, Brahim Tabarki
Problem-solving in clinical practice: breathing difficulty and muscle weakness following allogeneic haematopoietic stem cell transplantation. Archives of disease in childhood. Education and practice edition 106 (2) (2020)
Zafer Yüksel, Florian Vogel, Amal M Alhashem, Talal S A Alanzi, Brahim Tabarki, Kapil Kampe, Krishna K Kandaswamy, Martin Werber, Aida M Bertoli-Avella, Christian Beetz, Arndt Rolfs, Peter Bauer
A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia. Clinical genetics 95 (5) (2019)
Sarah Alsubhi, Amal Alhashem, Eissa Faqeih, Majid Alfadhel, Abdullah Alfaifi, Waleed Altuwaijri, Saud Alsahli, Hesham Aldhalaan, Fowzan Sami Alkuraya, Khalid Hundallah, Adel Mahmoud, Ali Alasmari, Fuad Al Mutairi, Hanem Abduraouf, Layan AlRasheed, Saad Alshahwan, Brahim Tabarki
Congenital disorders of glycosylation: The Saudi experience. American journal of medical genetics. Part A 173 (10) (2017)

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Publication Activity (10 Years)

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Brahim Tabarki