Research Interests

Papers共 147 篇Author StatisticsCo-AuthorSimilar Experts

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A CLASP1 variant suggests a phenotypic relation with lissencephaly in humans
Rawan Alsafeh,Amal AlHashem, Aly Elsayed,Zafer Yüksel, Kalthoum Graies-Tlili,Farah Thabet,Brahim Tabarki
biorxiv（2024）
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Mutations in the Ciliary Transport Gene IFT140 Cause Syndromic Congenital Retinal Dystrophy
Enam Danish,Amal Alhashem, Nada Naaman, Faeeqah Almhmoudi, Aziza Mushiba, Abdulrahman Almatrafi, Abdulaziz Raggam, Raghad Bukhari
Journal of American Association for Pediatric Ophthalmology and Strabismuspp.104007, (2024)
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Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly
Rawan Alsafh,Amal Alhashem, Aly Elsyed, Zafer Yüksel, Kalthoum Graiess-Tlili,Khalid Hundallah,Farah Thabet,Brahim Tabarki
Neurology. Geneticsno. 4 (2024): e200172-e200172
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ACLASP1variant suggests a phenotypic relation with lissencephaly in humans
Rawan Alsafeh,Amal AlHashem, Aly Elsayed, Zafer Yüksel, Kalthoum Graies-Tlili,Farah Thabet,Brahim Tabarki
crossref（2024）
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Author Statistics

#Papers: 148

#Citation: 3658

H-Index: 33

G-Index: 58

Sociability: 7

Diversity: 0

Activity: 3

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