Hamad Alzaidan - Concepedia

Author

Hamad Alzaidan

King Faisal Specialist Hospital & Research Centre

Also Known As

Fuad Al Mutairi, H Al-Zaidan, H Al‐Zaidan, H. AlZaidan, H.I. Alzaidan, Hamad Al-Zaidan, Hamad AlZaidan, Hamad Alzaidan, Hamad Al‐Zaidan, Hamad I. Alzaidan

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre Alfaisal University King Saud University Riyadh Armed Forces Hospital King Saud bin Abdulaziz University for Health Sciences

About

Hamad Alzaidan 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	15	17	1.1K
2	Public Health	2	2	25
3	Engineering	1	1	28
4	Natural Sciences	1	1	63
5	Biostatistics	1	1	10

Hamad Alzaidan

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Human Genetics	2017	296
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, The American Journal of Human Genetics SequencingNext-generation SequencingGeneticsPathologyOmics	2019	276
Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet, The American Journal of Human Genetics Cognitive DelayMendelian DisorderSpeech ImpairmentGenetic DisorderNalcn Cause	2013	119
Autozygome and high throughput confirmation of disease genes candidacy Sateesh Maddirevula, Fatema Alzahrani, Mohammed Al‐Owain, Genetics in Medicine	2018	112
Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue Anas M. Alazami, Sarah M. Al-Qattan, Eissa Faqeih, Human Genetics Mendelian DisorderClinical Genetic DisordersGenetic DisorderGeneticsConnective Tissue	2016	111
Expanded Newborn Screening Program in Saudi Arabia: Incidence of screened disorders Majid Alfadhel, Ali Al Othaim, Saif Al Saif, Journal of Paediatrics and Child Health	2017	111
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Genetics in Medicine Ocular DiseaseRetinaOphthalmologyGeneticsLocus Heterogeneity	2015	109
Identification of novel loci for pediatric cholestatic liver disease defined by KIF12, PPM1F, USP53, LSR, and WDR83OS pathogenic variants Sateesh Maddirevula, Hamoud Alhebbi, Awad Alqahtani, Genetics in Medicine HepatologyBiliary TractMedicineLiver PhysiologyGenetics	2018	109
The morbid genome of ciliopathies: an update Hanan E. Shamseldin, Ranad Shaheen, Nour Ewida, Genetics in Medicine Genetic DisorderMedicineGeneticsPathologyGenome Analysis	2020	103
Map of autosomal recessive genetic disorders in Saudi Arabia: Concepts and future directions Mohammed Al‐Owain, Hamad Alzaidan, Zuhair N. Al‐Hassnan American Journal of Medical Genetics Part A	2012	101

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