Sulman Basit
Taibah University
H-index: 27
Asia-Saudi Arabia
Top articles of Sulman Basit
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
A retrospective case-control study for Clinical Validation of mutated ZNF208 as a novel biomarker of fatal blast crisis in Chronic Myeloid Leukemia | medRxiv | Nawaf Alanzazi Amer Mahmood Masood A Shammas Salman Basit Aamer Aleem | 2024 |
Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women | Biomedicines | Ahmed M Almatrafi Ali M Hibshi Sulman Basit | 2024/4/3 |
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia | The Journal of Gene Medicine | Warda Akbar Asmat Ullah Nighat Haider Sufyan Suleman Fati Ullah Khan | 2024/1 |
Loss-of-function variant in spermidine/spermine N1-acetyl transferase like 1 (SATL1) gene as an underlying cause of autism spectrum disorder | Scientific Reports | Abdulfatah M Alayoubi Muhammad Iqbal Hassan Aman Jamil A Hashmi Laila Alayadhi | 2024/3/8 |
Identification of Novel and Recurrent Variants in BTD, GBE1, AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia | Frontiers in Genetics | Kevin T Booth Yoel Hirsch Anna C Vardaro Josef Ekstein Devorah Yefet | 2021/10/18 |
Clinical Validation Of ANKRD36 Mutations As A Novel Biomarker For Monitoring Early Progression and Timely Clinical Interventions In Blast Crisis CML | Nawaf Al-anazi Muhammad Absar Abdulaziz Siyal Salman Basit Masood Shammas | 2024/1/3 | |
Clinical heterogeneity of epilepsy and mutation spectrum of voltage-gated sodium channel genes | Mohammad Uzair Ali Mir Sulman Basit Hammad Qaiser Deeba Noreen Baig | 2024/1/2 | |
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family | Clinical and Experimental Dermatology | Xing Xiong Syed Ashraf Uddin Sobia Munir Nicole Cesarato Holger Thiele | 2023/4 |
Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency | Medicina | Ahmed M Almatrafi Ali M Hibshi Sulman Basit | 2023/2/27 |
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia | Medicina | Asmat Ullah Abid Ali Shah Fibhaa Syed Arif Mahmood Hassan Ur Rehman | 2023/2/16 |
Discovery of Mutated MUC3A Gene As a Novel Transcription Factor Exclusively Associated with Accelerated Phase Chronic Myeloid Leukemia: Hunt for Common Biomarker of Fatal CML … | Blood | Sameen Shahid Muhammad Sabar Abid Jamil Muhammad Abbas Khokar Muhammad Absar | 2023/11/28 |
Association between 17q21 variants and asthma predisposition in Pashtun population from Pakistan | Journal of Asthma | Sibtain Afzal Khushnooda Ramzan Sajjad Ullah Arshad Jamal Sulman Basit | 2023/1/2 |
Homozygous Duplication in the CHRNE in a Family with Congenital Myasthenic Syndrome 4C: 18-Year Follow Up | Biomedicines | Ahmad M Almatrafi Majed M Alluqmani Sulman Basit | 2023/11/6 |
Investigations on Clinical Validation of mutated ANKRD36 as a Novel Molecular Biomarker for Monitoring Early Progression and Timely Therapeutic Interventions in Blast Crisis CML | medRxiv | Nawaf Alanzazi Muhammad Absar Masood A Shammas Sulman Basit Abdulaziz Siyal | 2023 |
Polymorphisms in the Drug Transporter Gene ABCB1 Are Associated with Drug Response in Saudi Epileptic Pediatric Patients | Biomedicines | Rania Magadmi Reem Alyoubi Tahani Moshrif Duaa Bakhshwin Bandar A Suliman | 2023/9/11 |
Phenotype expansion for atypical Gaucher disease due to homozygous missense PSAP variant in a large consanguineous Pakistani family | Genes | Suzanne M. Leal Khurram Liaqat Shabir Hussain Anushree Acharya Abdul Nasir Thashi Bharadwaj | 2022/4/9 |
A novel nonsense variant in EXOC8 underlies a neurodevelopmental disorder | neurogenetics | Asmat Ullah Jai Krishin Nighat Haider Brekhna Aurangzeb Abdullah | 2022/7 |
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3) | Genes | Adil U Rehman Malaika Hamid Sher Alam Khan Muhammad Eisa Wasim Ullah | 2022/12/6 |
A homozygous missense variant in the MLC1 gene underlies megalencephalic leukoencephalopathy with subcortical cysts in large kindred: Heterozygous carriers … | American Journal of Medical Genetics Part A | Syeda Ain ul Batool Ahmad Almatrafi Fatima Fadhli Majed Alluqmani Sadia | 2022/4 |
Ultrastructure abnormalities of collagen and elastin in Arab patients with arterial tortuosity syndrome | Journal of Cutaneous Pathology | Muhammad Faiyaz‐Ul‐Haque Mohammed Mubarak Atqah AbdulWahab Ammar C AlRikabi Abbas H Alsaeed | 2022/7 |
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