Clinical characteristics, risk factors, and rate of severity of a nationwide COVID-19 Saudi cohort

Authors: Al-Numair, Nouf S., Alyounes, Banan, Al-Saud, Haya, Halwani, Rabih, Al-Muhsen, Saleh

Source: In Saudi Journal of Biological Sciences July 2022 29(7)

The protective effects of the methylenetetrahydrofolate reductase rs1801131 variant among Saudi smokers

Authors: Almutairi, Mikhlid H., Al-Numair, Nouf S., Parine, Narasimha Reddy, Almutairi, Bader O., Alrefaei, Abdulwahed F., Rouabhia, Mahmoud, Semlali, Abdelhabib

Source: In Saudi Journal of Biological Sciences July 2021 28(7):3972-3980

A novel homozygous SCN5A variant detected in sick sinus syndrome

Authors: Alkorashy, Maarab, Al‐Ghamdi, Bandar, Tulbah, Sahar, Al‐Numair, Nouf S., Alhadeq, Faten, A Takroni, Saud, Al‐Hassnan, Zuhair N.

Source: Pacing and clinical electrophysiology. 44(2):380-384

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100114874852.0x000001&indx=1&recIds=ETOCvdc_100114874852.0x000001

A homozygous loss-of-function mutation in GP1BB causing variable clinical phenotypes in a family with Bernard–Soulier syndrome

Authors: Al-Numair, Nouf, Ramzan, Khushnooda, Alquait, Laila, Alshehri, Meshal, Imtiaz, Faiqa, Owaidah, Tarek

Source: Blood coagulation and fibrinolysis. 32(5):352-355

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100122529566.0x000001&indx=1&recIds=ETOCvdc_100122529566.0x000001

Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population

Authors: Ramzan, Khushnooda, Al‐Owain, Mohammed, Al‐Numair, Nouf S., Afzal, Sibtain, Al‐Ageel, Sarah, Al‐Amer, Sultan, Al‐Baik, Lina, Al‐Otaibi, Ghoson F., Hashem, Amal, Al‐Mashharawi, Eman, Basit, Sulman, Al‐Mazroea, Abdal H., Softah, Ameen, Sogaty, Sameera, Imtiaz, Faiqa

Source: American journal of medical genetics.Part B.Neuropsychiatric genetics. 183(3):172-180

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100102869343.0x000001&indx=1&recIds=ETOCvdc_100102869343.0x000001

Evidence for an autosomal recessive pattern of inheritance in Keratitis-ichthyosis-deafness (KID) syndrome: Exome sequencing reveals a novel homozygous GJB2 mutation

Authors: Ramzan, Khushnooda, Huma, Rozeena, Al-Numair, Nouf S., Imtiaz, Faiqa, Al-Sayed, Moeenaldeen

Source: In Meta Gene February 2019 19:15-22

Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients

Authors: Owaidah, Tarek, Saleh, Mahasen, Baz, Batoul, Abdulaziz, Basma, Alzahrani, Hazza, Tarawah, Ahmed, Almusa, Abdulrahman, AlNounou, Randa, AbaAlkhail, Hala, Al-Numair, Nouf, Altahan, Rahaf, Abouelhoda, Mohammed, Alamoudi, Thamer, Monies, Dorota, Jabaan, Amjad, Al Tassan, Nada

Source: Npj genomic medicine. 4:1-7

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100128893760.0x000001&indx=1&recIds=ETOCvdc_100128893760.0x000001

Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families

Authors: Al-Hamed, Mohamed H., Alsahan, Nada, Rice, Sarah J., Edwards, Noel, Nooreddeen, Eman, Alotaibi, Maha, Kurdi, Wesam, Alnemer, Maha, Altaleb, Naderah, Ali, Wafa, Al-Numair, Nouf, Almejaish, Najd, Sayer, John A., Imtiaz, Faiqa

Source: Pediatric nephrology. 34(9):1615-1623

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100125313084.0x000001&indx=1&recIds=ETOCvdc_100125313084.0x000001

Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease

Authors: Imtiaz, Faiqa, Al-Mostafa, Abeer, Allam, Rabab, Ramzan, Khushnooda, Al-Tassan, Nada, Tahir, Asma I., Al-Numair, Nouf S., Al-Hamed, Mohamed H., Al-Hassnan, Zuhair, Al-Owain, Mohammad, Al-Zaidan, Hamad, Al-Amoudi, Mohammad, Qari, Alya, Balobaid, Ameera, Al-Sayed, Moeenaldeen

Source: In Molecular Genetics and Metabolism Reports June 2017 11:17-23

Correlation between genetic variation in thymine DNA glycosylase and smoking behavior

Authors: Almutairi, Mikhlid, Rouabhia, Mahmoud, Sahab Almutairi, Mohammed, Al-Zahrani, Mohammed, Al-Numair, Nouf S., Mohammad Alhadeq, Abdullah, Reddy Parine, Narasimha, Semlali, Abdelhabib

Source: Gene. 766

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100123102435.0x000001&indx=1&recIds=ETOCvdc_100123102435.0x000001

Clinical, Endocrine, and Molecular Genetic Analysis of a Large Cohort of Saudi Arabian Patients with Laron Syndrome

Authors: Al-Ashwal, Abdullah A., Al-Sagheir, Afaf, Ramzan, Khushnooda, Al-Owain, Mohammed, Allam, Rabab, Qari, Alya, Al-Numair, Nouf S., Imtiaz, Faiqa

Source: Hormone research in pædiatrics. 88(2):119-126

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100084696881.0x000001&indx=1&recIds=ETOCvdc_100084696881.0x000001

Iron Deficiency and Iron Deficiency Anemia Are Common Epidemiological Conditions in Saudi Arabia: Report of the National Epidemiological Survey.

Authors: Owaidah, Tarek¹ (AUTHOR), Al-Numair, Nouf² (AUTHOR), Al-Suliman, Ayman² (AUTHOR), Zolaly, Mohammed³ (AUTHOR), Hasanato, Rana⁴ (AUTHOR), Al Zahrani, Faisal⁵ (AUTHOR), Albalawi, Mohameed⁶ (AUTHOR), Bashawri, Layla⁵ (AUTHOR), Siddiqui, Khawar⁷ (AUTHOR), Alalaf, Faisal⁸ (AUTHOR), Almomen, Abdulkareem⁴ (AUTHOR), Sajid, Muhammad Raihan⁹ (AUTHOR)

Source: Anemia (20901267). 12/29/2020, p1-8. 8p.

Subject Terms: *IRON deficiency anemia, *IRON deficiency, *MALNUTRITION, *SAUDI Arabians, *SICKLE cell trait, *BLOOD testing

Geographic Terms: SAUDI Arabia, MIDDLE East

Protective effect of Cardiospermum halicacabum leaf extract on glycoprotein components on STZ–induced hyperglycemic rats

Authors: Veeramani, Chinnadurai, Al-Numair, Khalid S, Alsaif, Mohammed A, Chandramohan, Govindasamy, Al-Numair, Nouf S, Pugalendi, Kodukkur Viswanathan

Source: In Asian Pacific Journal of Tropical Medicine December 2012 5(12):939-944

The role of BRCA1/2 in hereditary and familial breast and ovarian cancers

Authors: Hawsawi, Yousef M., Al‐Numair, Nouf S., Sobahy, Turki M., Al‐Ajmi, Areej M., Al‐Harbi, Raneem M., Baghdadi, Mohammed A., Oyouni, Atif A., Alamer, Osama M.

Source: Molecular genetics & genomic medicine. 7(9)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100090975205.0x000001&indx=1&recIds=ETOCvdc_100090975205.0x000001

Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A>G) Causing a Pathogenic Variant of the Factor 8 Gene.

Authors: Owaidah, Tarek, Bakr, Salwa, Al-Numair, Nouf, AbaAlkhail, Hala, Alzahrani, Hazzaa, Saleh, Mahasen, Khogeer, Haitham, Tarawah, Ahmed, Akkad, Hadeel, Al-Allaf, Faisal

Source: Clinical & Applied Thrombosis/Hemostasis; Jan-Dec2023, Vol. 29, p1-8, 8p

Subject Terms: DELETION mutation, GENETIC databases, MEDICAL screening, BLOOD coagulation factor VIII, GENETIC engineering, HEMOPHILIA

Company/Entity: WORLD Health Organization

Prevalence of bleeding symptoms among young adults in Saudi Arabia, a national survey

Authors: AlSaleh, Khalid A., Al-Numair, Nouf S., Alsuaiman, Ayman, Zolaly, Mohammed, Khojah, Osamah T., AlZahrani, Faisal M., Siddiqui, Khawar, Al-Allaf, Faisal A., AlMomen, Abdulkareem, Sajid, Raihan, Owaidah, Tarek M.

Source: Medicine. 100(43):e27513-e27513

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100177710380.0x000001&indx=1&recIds=ETOCvdc_100177710380.0x000001

Camels' biological fluids contained nanobodies: promising avenue in cancer therapy.

Authors: Al-Numair, Nouf S.^1,2 (AUTHOR), Theyab, Abdulrahman^3,4 (AUTHOR), Alzahrani, Faisal^5,6 (AUTHOR), Shams, Anwar M.⁷ (AUTHOR), Al-Anazi, Ibrahim O.⁸ (AUTHOR), Oyouni, Atif Abdulwahab A.^9,10 (AUTHOR), Al-Amer, Osama M.¹¹ (AUTHOR), Mavromatis, Charalampos¹² (AUTHOR), Saadeldin, Islam M.¹³ (AUTHOR), Abdali, Wed A.⁹ (AUTHOR), Hawsawi, Yousef M.^{2,3,4,5,6,7,8,9,10,11,12,13,14} (AUTHOR) hyousef@kfshrc.edu.sa

Source: Cancer Cell International. 9/7/2022, Vol. 22 Issue 1, p1-18. 18p.

Subject Terms: *IMMUNOGLOBULINS, *CAMELS, *CANCER treatment, *FLUIDS, *CAUSES of death

PHENOTYPE/ GENOTYPE SCREENING PATTERN OF HEMOPHILIA A AND B IN SAUDI ARAB

Authors: Owaidah, Tarek, Bakr, Salwa, AbaAlkhail, Hala, Alzahrani, Hazza, Saleh, Mahasen, Almusa, Abdulrahman, Al-Numair, Nouf, Khogeer, Haitham, Al-Allaf, Faisal

Source: In Hematology, Transfusion and Cell Therapy October 2022 44 Supplement 1:S28-S29

Correction: Camels' biological fluids contained nanobodies: promising avenue in cancer therapy.

Authors: Al‑Numair, Nouf S.^1,2 (AUTHOR), Theyab, Abdulrahman^3,4 (AUTHOR), Alzahrani, Faisal^5,6 (AUTHOR), Shams, Anwar M.⁷ (AUTHOR), Al‑Anazi, Ibrahim O.⁸ (AUTHOR), Oyouni, Atif Abdulwahab A.^9,10 (AUTHOR), Al‑Amer, Osama M.¹¹ (AUTHOR), Mavromatis, Charalampos¹² (AUTHOR), Saadeldin, Islam M.¹³ (AUTHOR), Abdali, Wed A.⁹ (AUTHOR), Hawsawi, Yousef M.^2,14 (AUTHOR) hyousef@kfshrc.edu.sa

Source: Cancer Cell International. 3/30/2023, Vol. 23 Issue 1, p1-1. 1p.

Subject Terms: *IMMUNOGLOBULINS, *CANCER treatment, *CAMELS, *FLUIDS, *CANCER cells

The SAAP pipeline and database: tools to analyze he impact and predict the pathogenicity of mutations.

Authors: Al-Numair, Nouf S.¹, Martin, Andrew C. R.¹ andrew@bioinf.org.uk

Source: BMC Genomics. 2013, Vol. 14 Issue Suppl 3, p1-11. 11p. 3 Diagrams, 3 Charts, 5 Graphs.

Subject Terms: *PROTEIN structure, *PHENOTYPES, *MUTANT proteins, *PROLINE, *GLYCINE, *MACHINE learning