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Home › Researcher directory › Eissa Faqeih

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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Research areas

  • Genomics and Rare Diseases
  • Metabolism and Genetic Disorders
  • Genetics and Neurodevelopmental Disorders
  • Connective tissue disorders research
  • Genetic and Kidney Cyst Diseases

Publications (3)

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

Bibliographic data from OpenAlex (open database).

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