Mohamed El-Kalioby
Researcher · Biochemistry, Genetics and Molecular Biology
Source-listed associations: King Faisal Specialist Hospital & Research Centre
Saudi Arabia
Mohamed El-Kalioby has indexed research in Biochemistry, Genetics and Molecular Biology. Research topics in the source record include Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetic Associations and Epidemiology.
Read biography ↓Biography, research & contributions
Mohamed El-Kalioby has indexed research in Biochemistry, Genetics and Molecular Biology. Research topics in the source record include Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetic Associations and Epidemiology.
Research and publications
The selected publications below appear in both the public ORCID record and the OpenAlex author record. The list is a subset of the researcher’s work.
Institutional record
OpenAlex lists King Faisal Specialist Hospital & Research Centre among its last-known institutional associations. These records do not confirm a current appointment.
Identity and source coverage
The public ORCID name and at least one education or employment institution were matched with the OpenAlex record on 2026-10-03. Publication identifiers were also compared between the two sources. Positions, education, honors and portrait are included only when separately documented.
At a glance
- Full name
- Mohamed El-Kalioby
- Alternative names
- El-Kalioby, Mohamed M. El‐Kalioby Mohamed El-Kalioby Mohamed ElKalioby Mohamed Elkalioby Mohamed M. ElKalioby Mohammed El-Kalioby
- Fields
- Biochemistry, Genetics and Molecular Biology
- ORCID
- 0000-0001-7655-4198
- OpenAlex ID
- A5022862119
Research interests
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Genetic and Kidney Cyst Diseases
- Muscle Physiology and Disorders
Research topics
Education
Not yet documented in this profile.
Selected research & further reading
A curated reading list, not a ranking by citation count. References use DOI metadata, matching public scholarly records or authoritative lecture sources.
- Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population ↗2019 · The American Journal of Human GeneticsDOI: 10.1016/j.ajhg.2019.04.011
- Characterizing the morbid genome of ciliopathies ↗2016 · Genome biologyDOI: 10.1186/s13059-016-1099-5
- Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases ↗2016 · Journal of Allergy and Clinical ImmunologyDOI: 10.1016/j.jaci.2015.12.1310
- Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden ↗2016 · Genetics in MedicineDOI: 10.1038/gim.2016.37
- Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families ↗2017 · Scientific ReportsDOI: 10.1038/s41598-017-06033-1
Citation & publication trends
Annual source counts; separate scales. OpenAlex coverage may be incomplete for historical researchers.
View exact annual counts
| Year | Publications | Citations |
|---|---|---|
| 2010 | 2 | 8 |
| 2012 | 1 | 27 |
| 2013 | 2 | 11 |
| 2015 | 1 | 6 |
| 2016 | 43 | 620 |
| 2017 | 2 | 430 |
| 2018 | 1 | 2 |
| 2019 | 2 | 340 |
| 2022 | 1 | 31 |
| 2024 | 2 | 24 |
Source: OpenAlex · Retrieved 2026-10-03T06:41:07+00:00. Metrics are database-specific and are not a scientific ranking.
Most-cited linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population ↗2019-05-23 · The American Journal of Human Genetics293OpenAlex citations
- Characterizing the morbid genome of ciliopathies ↗2016-11-28 · Genome biology173OpenAlex citations
- Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases ↗2016-02-24 · Journal of Allergy and Clinical Immunology118OpenAlex citations
- Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden ↗2016-04-28 · Genetics in Medicine113OpenAlex citations
- 106OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population ↗2019-10-01 · The American Journal of Human Genetics
- Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population ↗2019-05-23 · The American Journal of Human Genetics
- Exploiting In-memory Systems for Genomic Data Analysis ↗2018-01-01 · Lecture notes in computer science
Journals published in
- BioMed Research International
- BMC Bioinformatics
- Genetics in Medicine
- Genome Biology
- Human Genomics
- Journal of Allergy and Clinical Immunology
- Journal of Medical Genetics
- PLoS ONE
- Scientific Reports
Related publishers
Institutions
Current verified institution
No verified record links added yet.
Previous institutions
No verified record links added yet.
Awards & honors
Not yet documented in this profile.
Career timeline
Not yet documented in this profile.
Co-authors
No verified record links added yet.
Education & career institution links
No verified record links added yet.
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Sign in to claim this profileSources & data information
Editorial review: Pending review · Last data update: 2026-10-03T08:22:07+00:00
Automated identity and publication-source comparison: 2026-10-03T08:19:03+00:00. This is separate from manual editorial review and profile ownership.
Unknown values are left blank. Linked publications may be a subset of total works. Identity verification, data retrieval and profile ownership are separate checks.