CV | Zohor Asaad Omer Azher | Umm Al-Qura University

Qualifications

الماجستير

2015

الأحياء العامة

جامعة مونبيليية | فرنسا

البكالوريوس

1429

الجراحة العامة

جامعة ام القرى | المملكة العربية السعودية

الزماله

2017

علم الوراثة

جامعة مونبيليية | فرنسا

الزماله

2017

علم الوراثة

جامعة مونبيليية | فرنسا

Scientific Research

Familial novel androgen receptor gene variant associated with bilateral cryptorchidism and severe male infertility: A case report

2025

مقال في مجلة | ِElsevier | Urology Case Reports

Descriptive epidemiology of female breast cancer around the world: incidence, mortality, and sociodemographic risks and disparities

2025

مقال في مجلة | Taylor and Francis | International Journal of Environmental Health Research

Mutational spectrum and profle of breast and ovarian cancer patients in Saudi Arabia’s western region: single center experience

2025

مقال في مجلة | «حقهرلثق | Discover Oncology

Adult genomic medicine: lessons from a multisite study of 2700 patients

2025

مقال في مجلة | BMC | Genome Medicine

Ameliorative Effect of N-Acetylcysteine Against 5- Fluorouracil-Induced Cardiotoxicity via Targeting TLR4/NF-κB and Nrf2/HO-1 Pathways

2026

مقال في مجلة | MDPI | Medicina

Biallelic Variants in DNAH12 Gene Linked to Male infertility:Two New Cases and Literature Review

2025

مقال في مجلة | MDPI | Uro

Autism Spectrum Disorder: A Review of Genomic Risk Factors, Diagnostic and Pharmacotherapeutic Strategies

2025

مقال في مجلة | UQU | Saudi Toxicology Journal

Translocation t(Y;16) in a male pateint with non-obstructive azoospermia

2024

ورقة مؤتمر | saudi Urological association | 35th saudi Urological association

Transplantation of hyaluronic acid and menstrual blood-derived stem cells accelerated wound healing in a diabetic rat model

2024

مقال في مجلة | ScienceDirect | Tissue and Cell

أكثر

Impact of rs599839 Polymorphism on Coronary Artery Disease Risk in Saudi Diabetic Patients

2024

مقال في مجلة | Wiley | Disease Markers

أكثر

Influence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome

2024

مقال في مجلة | ScienceDirect | Journal of Stroke and Cerebrovascular Diseases

أكثر

Partial trisomy 19p: Case report and a literature review”

2024

ورقة مؤتمر | European Human Genetics Conference 2023 | European Human Genetics Conference 2023

Mosaic mutation in androgen receptor gene in a patient with partial androgen insensitivity syndrome

2023

ورقة مؤتمر | European Human Genetics Conference 2022 | European Human Genetics Conference 2022

Heterozygous mutation in SCRIB gene in adult patient with myelomeningocele and primary infertility

2583

ورقة مؤتمر | European Human Genetics Virtual Conference 2021 | European Human Genetics Virtual Conference 2021

Phenotypic variability to medication management: an update on fragile X syndrome.

2584

مقال في مجلة | BMC | Human Genomics

أكثر

Sequence Variants in PSMB8/PSMB9 Immunoproteasome Genes and Risk of Urothelial Bladder Carcinoma

2584

مقال في مجلة | SPRINGERNATURE | CUREUS JOURNAL OF MEDICAL SCIENCE

أكثر

Reciprocal Translocation T(Y;16) in a Male Patient With Non-obstructive Azoospermia: A Case Report and Literature Review

2583

مقال في مجلة | SPRINGERNATURE | CUREUS JOURNAL OF MEDICAL SCIENCE

أكثر

Androgen Receptor Gene Mosaicism in Partial Androgen Insensitivity Syndrome Patient Detected

2584

مقال في مجلة | Hilaris | Clinical Case Reports

أكثر

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients

2018

مقال في مجلة | Springer Nature | Springer Nature

Achievements

المشاركة في الحملة التوعوية للفحص المبكر لحديثي الولادة للحد من الاعاقة

Committee

لجنة وحدة المناهج

2023 – 2024

منسقة مقرر التطور الجيني والسرطان

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CV

Qualifications

الماجستير

البكالوريوس

الزماله

الزماله

Scientific Research

Familial novel androgen receptor gene variant associated with bilateral cryptorchidism and severe male infertility: A case report

Descriptive epidemiology of female breast cancer around the world: incidence, mortality, and sociodemographic risks and disparities

Mutational spectrum and profle of breast and ovarian cancer patients in Saudi Arabia’s western region: single center experience

Adult genomic medicine: lessons from a multisite study of 2700 patients

Ameliorative Effect of N-Acetylcysteine Against 5- Fluorouracil-Induced Cardiotoxicity via Targeting TLR4/NF-κB and Nrf2/HO-1 Pathways

Biallelic Variants in DNAH12 Gene Linked to Male infertility:Two New Cases and Literature Review

Autism Spectrum Disorder: A Review of Genomic Risk Factors, Diagnostic and Pharmacotherapeutic Strategies

Translocation t(Y;16) in a male pateint with non-obstructive azoospermia

Transplantation of hyaluronic acid and menstrual blood-derived stem cells accelerated wound healing in a diabetic rat model

Impact of rs599839 Polymorphism on Coronary Artery Disease Risk in Saudi Diabetic Patients

Influence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome

Partial trisomy 19p: Case report and a literature review”

Mosaic mutation in androgen receptor gene in a patient with partial androgen insensitivity syndrome

Heterozygous mutation in SCRIB gene in adult patient with myelomeningocele and primary infertility

Phenotypic variability to medication management: an update on fragile X syndrome.

Sequence Variants in PSMB8/PSMB9 Immunoproteasome Genes and Risk of Urothelial Bladder Carcinoma

Reciprocal Translocation T(Y;16) in a Male Patient With Non-obstructive Azoospermia: A Case Report and Literature Review

Androgen Receptor Gene Mosaicism in Partial Androgen Insensitivity Syndrome Patient Detected

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients

Achievements

المشاركة في الحملة التوعوية للفحص المبكر لحديثي الولادة للحد من الاعاقة

Committee

لجنة وحدة المناهج

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