Nouf S. Al‐Numair - Concepedia

Author

Nouf S. Al‐Numair

King Faisal Specialist Hospital & Research Centre ORCID

Also Known As

Nouf Al-Numair, Nouf Alnumair, Nouf S Al-Numair, Nouf S. Al-Numair, Nouf S. Al‐Numair, Nouf S. Al‑Numair, Nouf S. Al-Numair

Publications

506

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre Alfaisal University King Saud University University College London King Abdulaziz City for Science and Technology

About

Nouf S. Al‐Numair is an author at King Faisal Specialist Hospital & Research Centre specializing in genetic epidemiology, genetics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	41
2	Health Sciences	1	1	37
3	Public Health	1	1	37
4	Clinical Nutrition	1	1	37
5	Epidemiology	1	1	37

Nouf S. Al‐Numair

Publications

388

Citations

H-Index

Page 1

	Year	Citations
Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency Anas M. Alazami, Maryam Al-Helale, Safa Alhissi, Frontiers in Immunology	2018	66
The SAAP pipeline and database: tools to analyze the impact and predict the pathogenicity of mutations Nouf S. Al‐Numair, Andrew C.R. Martin BMC Genomics	2013	56
Iron Deficiency and Iron Deficiency Anemia Are Common Epidemiological Conditions in Saudi Arabia: Report of the National Epidemiological Survey Tarek Owaidah, Nouf S. Al‐Numair, Ayman Alsuliman, Anemia AnemiaNutritionWorld Health OrganizationNutritional RequirementPediatric Hematology	2020	37
Potential role of Toll-like receptor 2 expression and polymorphisms in colon cancer susceptibility in the Saudi Arabian population Abdelhabib Semlali, Narasimha Reddy Parine, Nouf S. Al‐Numair, OncoTargets and Therapy	2018	32
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families Mohamed H. Al‐Hamed, Nada Alsahan, Sarah J. Rice, Pediatric Nephrology Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic Disease	2019	31
Identification of <i>TMC1</i> as a relatively common cause for nonsyndromic hearing loss in the Saudi population Khushnooda Ramzan, Mohammed Al‐Owain, Nouf S. Al‐Numair, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2019	28
Novel sequence variants in the TLR6 gene associated with advanced breast cancer risk in the Saudi Arabian population Abdelhabib Semlali, Mikhlid H. Almutairi, Mahmoud Rouabhia, PLoS ONE	2018	26
Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease Faiqa Imtiaz, Abeer Al‐Mostafa, Rabab Allam, Molecular Genetics and Metabolism Reports	2017	24
Protective effect of Cardiospermum halicacabum leaf extract on glycoprotein components on STZ–induced hyperglycemic rats Chinnadurai Veeramani, Khalid S. Al‐Numair, Mohammed A. Alsaif, Asian Pacific Journal of Tropical Medicine	2012	19
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss Khushnooda Ramzan, Nouf S. Al‐Numair, Sarah Al‐Ageel, Genes	2020	19

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