Hadia Hijazi - Concepedia

Author

Hadia Hijazi

King Faisal Specialist Hospital & Research Centre ORCID

Also Known As

Elvin Hsu, H Hijazi, H. Hijazi, Hadia Hijazi

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre Alfaisal University King Saud University Baylor College of Medicine King Khalid University Hospital

About

Hadia Hijazi is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	403
2	Social Sciences	2	2	49
3	Public Health	1	1	20
4	Cell Biology	1	1	35
5	Immunology	1	1	35

Hadia Hijazi

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin, Cell Reports	2014	465
TLE6 mutation causes the earliest known human embryonic lethality Anas M. Alazami, Salma Awad, Serdar Coşkun, Genome biology	2015	216
Mutation in <i>ADAT3</i>, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus Anas M. Alazami, Hadia Hijazi, Mohammed S. Al‐Dosari, Journal of Medical Genetics	2013	129
Mutations in LRPAP1 Are Associated with Severe Myopia in Humans Mohammed A. Aldahmesh, Arif O. Khan, Hisham Alkuraya, The American Journal of Human Genetics OphthalmologySevere MyopiaGenetic DisorderGeneticsPathology	2013	128
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in <i>MYO18B</i> Anas M. Alazami, Amal Y. Kentab, Eissa Faqeih, Journal of Medical Genetics	2015	79
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease Angad Jolly, Yavuz Bayram, Serap Turan, The Journal of Clinical Endocrinology & Metabolism	2019	75
Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes Mohammed A. Aldahmesh, Arif O. Khan, Jawahir Y. Mohamed, Genetics in Medicine MedicineGeneticsPathogenesisGenomic AnalysisPathology	2012	60
Molecular characterization of Joubert syndrome in Saudi Arabia Anas M. Alazami, Muneera Alshammari, Mustafa A. Salih, Human Mutation Mendelian DisorderJoubert SyndromeSaudi ArabiaGeneticsInherited Metabolic Disease	2012	59
Distinct patterns of complex rearrangements and a mutational signature of microhomeology are frequently observed in PLP1 copy number gain structural variants Vahid Bahrambeigi, Xiaofei Song, Karen Sperle, Genome Medicine	2019	36
Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders Tadahiro Mitani, Jaya Punetha, İbrahim Akalın, The American Journal of Human Genetics Tubgcp2 Cause MicrocephalyAllelic VariantLissencephaly Spectrum DisordersBi-allelic Pathogenic VariantsDisease Mechanism	2019	35

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