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Eissa Faqeih
Affiliation : King Fahd Medical City
- 3Publications (affiliation in Saudi Arabia)
- 187Total publications
- 7709Citations
- 51h-index
Research profile
Eissa Faqeih has 3 indexed publications (2017–2023). Their work appears mainly in “Nature Communications”, “Nature Genetics” and “Pediatric Neurology”. Their most cited article, “Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration” (2018), has been cited 86 times. Their work is co-authored with at least 12 researchers, including institutions in Egypt, Tunisia, Canada, United States.
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Create my free profile Add my publicationsResearch areas
- Genomics and Rare Diseases
- Metabolism and Genetic Disorders
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
Publications (3)
- Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families
- Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration
- Phenotypic and Molecular Spectrum of Aicardi-Goutières Syndrome: A Study of 24 Patients
Publication venues
- Nature Communications × 1
- Nature Genetics × 1
- Pediatric Neurology × 1
Publications per year
- 20231
- 20181
- 20171
Collaborations
Partner institutions : King Faisal Specialist Hospital & Research Centre · Riyadh Armed Forces Hospital · King Abdulaziz Medical City · National Guard Health Affairs · King Saud University
Co-authors’ countries : Egypt · Tunisia · Canada · United States
Co-authors
- Mohammed A. Al‐Owain
- Fowzan Sami Alkuraya
- Majid Alfadhel
- Fuad Al Mutairi
- Firdous Abdulwahab
- Mohammed Abouelhoda
- Muneera J. Alshammari
- Sami H. Wali
- Fatema Alzahrani
- Aisha Almulhim
- Halima Hamid
- Ali M. AlAsmari
Bibliographic data from OpenAlex (open database).
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