Sulman Basit (S Basit)

Loop profile ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 59

Top Venues

Medicina (Kaunas, Lithuania)

Genes

Journal of clinical medicine

Biomedicines

Taibah University

Quaid-i-Azam University (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Taibah University Jun 16 2013

Saudi Arabia

Assistant Professor :: Center for Genetics and Inherited Diseases

King Saud University Sep 17 2011 - Sep 11 2012

Saudi Arabia

Post Doctoral Fellow :: Pathology

Education History

Quaid-i-Azam University Mar 16 2008 - Oct 19 2012

Pakistan

PHD :: Biochemistry

University of Arid Agriculture Jun 02 2003 - Aug 17 2005

Pakistan

MSC :: Biochemistry

Publications

Muhammad Latif, Jamil Amjad Hashmi, Abdulfatah M Alayoubi, Arusha Ayub, Sulman Basit
Identification of Novel and Recurrent Variants in BTD , GBE1 , AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia. Journal of clinical medicine 13 (5) (2024)
Ahmed M Almatrafi, Abdulfatah M Alayoubi, Majed M Alluqmani, Jamil A Hashmi, Sulman Basit
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia. Journal of clinical medicine 13 (14) (2024)
Ahmed M Almatrafi, Abdulfatah M Alayoubi, Majed M Alluqmani, Jamil A Hashmi, Sulman Basit
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia. Journal of clinical medicine 13 (14) (2024)
Ahmed M Almatrafi, Abdulfatah M Alayoubi, Majed M Alluqmani, Jamil A Hashmi, Sulman Basit
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia. Journal of clinical medicine 13 (14) (2024)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women. Biomedicines 12 (4) (2024)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women. Biomedicines 12 (4) (2024)
Muhammad Latif, Jamil Amjad Hashmi, Abdulfatah M Alayoubi, Arusha Ayub, Sulman Basit
Identification of Novel and Recurrent Variants in BTD , GBE1 , AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia. Journal of clinical medicine 13 (5) (2024)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Warda Akbar, Asmat Ullah, Nighat Haider, Sufyan Suleman, Fati Ullah Khan, Abid Ali Shah, Muhammad Atif Sikandar, Sulman Basit, Wasim Ahmad
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia. The journal of gene medicine (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency. Medicina (Kaunas, Lithuania) 59 (3) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency. Medicina (Kaunas, Lithuania) 59 (3) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Ahmed M Almatrafi, Majed M Alluqmani, Sulman Basit
Homozygous Duplication in the CHRNE in a Family with Congenital Myasthenic Syndrome 4C: 18-Year Follow Up. Biomedicines 11 (11) (2023)
Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency. Medicina (Kaunas, Lithuania) 59 (3) (2023)
Rania M Magadmi, Reem Alyoubi, Tahani Moshrif, Duaa Bakhshwin, Bandar A Suliman, Fatemah Kamel, Maha Jamal, Abdulhadi S Burzangi, Sulman Basit
Polymorphisms in the Drug Transporter Gene ABCB1 Are Associated with Drug Response in Saudi Epileptic Pediatric Patients. Biomedicines 11 (9) (2023)
Syeda Farwa Naqvi, Rana Muhammad Kamran Shabbir, Aslıhan Tolun, Sulman Basit, Sajid Malik
A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family. Genetic testing and molecular biomarkers 26 (1) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Muhammad Faiyaz-Ul-Haque, Mohammed Mubarak, Atqah AbdulWahab, Ammar C AlRikabi, Abbas H Alsaeed, Maram Al-Otaiby, Zafar Nawaz, Syed H E Zaidi, Sulman Basit
Ultrastructure abnormalities of collagen and elastin in Arab patients with arterial tortuosity syndrome. Journal of cutaneous pathology 49 (7) (2022)
Anam Simaab, Jai Krishin, Sultan Rashid Alaradi, Nighat Haider, Muqadar Shah, Asmat Ullah, Abdullah Abdullah, Wasim Ahmad, Torben Hansen, Sulman Basit
Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Asmat Ullah, Jai Krishin, Nighat Haider, Brekhna Aurangzeb, null Abdullah, Sufyan Suleman, Wasim Ahmad, Torben Hansen, Sulman Basit
A novel nonsense variant in EXOC8 underlies a neurodevelopmental disorder. Neurogenetics 23 (3) (2022)
Anam Simaab, Jai Krishin, Sultan Rashid Alaradi, Nighat Haider, Muqadar Shah, Asmat Ullah, Abdullah Abdullah, Wasim Ahmad, Torben Hansen, Sulman Basit
Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Anam Simaab, Jai Krishin, Sultan Rashid Alaradi, Nighat Haider, Muqadar Shah, Asmat Ullah, Abdullah Abdullah, Wasim Ahmad, Torben Hansen, Sulman Basit
Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Asmat Ullah, Abid Ali Shah, Majed Alluqmani, Nighat Haider, Hasan Aman, Fatima Alfadhli, Ahmed M Almatrafi, Alia M Albalawi, Jai Krishin, Fati Ullah Khan, Bilal Ali Anjam, null Abdullah, Elionora Peña Lozano, Abdus Samad, Wasim Ahmad, Torben Hansen, Kun Xia, Sulman Basit
Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 82 (8) (2022)
Anam Simaab, Jai Krishin, Sultan Rashid Alaradi, Nighat Haider, Muqadar Shah, Asmat Ullah, Abdullah Abdullah, Wasim Ahmad, Torben Hansen, Sulman Basit
Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Anam Simaab, Jai Krishin, Sultan Rashid Alaradi, Nighat Haider, Muqadar Shah, Asmat Ullah, Abdullah Abdullah, Wasim Ahmad, Torben Hansen, Sulman Basit
Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome. Medicina (Kaunas, Lithuania) 58 (12) (2022)
Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family ( ARMC3 ). Genes 13 (12) (2022)
Khurram Liaqat, Shabir Hussain, Anushree Acharya, Abdul Nasir, Thashi Bharadwaj, Muhammad Ansar, Sulman Basit, Isabelle Schrauwen, Wasim Ahmad, Suzanne M Leal
Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family. Genes 13 (4) (2022)
Rubab Raza, Asmat Ullah, Nighat Haider, Jai Krishin, Muqadar Shah, Fati Ullah Khan, null Abdullah, Torben Hansen, Syed Irfan Raza, Wasim Ahmad, Sulman Basit
Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis. Clinical and experimental dermatology (2022)
Fozia Fozia, Rubina Nazli, Sher Alam Khan, Ahmed Bari, Abdul Nasir, Riaz Ullah, Hafiz Majid Mahmood, Muhammad Sohaib, Abdulrahman Alobaid, Siddique Akber Ansari, Sulman Basit, Saadullah Khan
Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis. Genes 12 (3) (2021)
Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao, Sadia Kanwal, Asma Gul, Sulman Basit
An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation. American journal of medical genetics. Part A 185 (10) (2021)
Maan Abdullah Albarry, Muhammad Latif, Ahdab Qasem Alreheli, Mohammed A Awadh, Ahmad M Almatrafi, Alia M Albalawi, Sulman Basit
Frameshift variant in MITF gene in a large family with Waardenburg syndrome type II and a co-segregation of a C2orf74 variant. PloS one 16 (2) (2021)
Samuel M Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Thashi Bharadwaj, Kevin Kum Esoh, Sulman Basit, Anushree Acharya, Liz M Nouel-Saied, Khurram Liaqat, Edmond Wonkam-Tingang, Shaheen Mowla, Gordon A Awandare, Wasim Ahmad, Regie Lyn P Santos-Cortez, Ambroise Wonkam
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of human genetics 66 (12) (2021)
Syeda Ain Ul Batool, Ahmad Almatrafi, Fatima Fadhli, Majed Alluqmani, null Sadia, Ghazanfar Ali, Sulman Basit
A homozygous missense variant in the MLC1 gene underlies megalencephalic leukoencephalopathy with subcortical cysts in large kindred: Heterozygous carriers show seizure and mild motor function deterioration. American journal of medical genetics. Part A 188 (4) (2021)
Zafar Iqbal, Muhammad Absar, Tanveer Akhtar, Aamer Aleem, Abid Jameel, Sulman Basit, Anhar Ullah, Sibtain Afzal, Khushnooda Ramzan, Mahmood Rasool, Sajjad Karim, Zeenat Mirza, Mudassar Iqbal, Maryam AlMajed, Buthinah AlShehab, Sarah AlMukhaylid, Nouf AlMutairi, Nawaf Al-Anazi, Muhammad Farooq Sabar, Muhammad Arshad, Muhammad Asif, Masood Shammas, Amer Mahmood
Integrated Genomic Analysis Identifies ANKRD36 Gene as a Novel and Common Biomarker of Disease Progression in Chronic Myeloid Leukemia. Biology 10 (11) (2021)
Ahmad Almatrafi, Muhammad Umair, Amr Eldardear, Majid Al-Luqmani, Jamil A Hashmi, Alia M Albalawi, Majid Alfadhel, Khushnooda Ramzan, Sulman Basit
A homozygous missense variant in the homeobox domain of the NKX6-2 results in progressive spastic ataxia type 8 associated with lower limb weakness and neurological manifestations. The journal of gene medicine 22 (8) (2020)
Ayesha Zaka, Shaheen Shahzad, Hadi Zahid Rao, Yasmin Hashim, Sulman Basit
A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis-2 with impaired intellectual development. American journal of medical genetics. Part A 185 (2) (2020)
Sulman Basit, Howaida Mohammed Al-Edressi, Mona Hamza Sairafi, Jamil Amjad Hashmi, Essa Alharby, Ramzia Safar, Khushnooda Ramzan
Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome. Journal of nephrology 33 (4) (2020)
Ghulam M Khan, Noor Hassan, Niamatullah Khan, Muhammad Humayun, Kafaitullah Khan, Samira Khaliq, Fazal U Rehman, Sheikh Ahmed, Khadim Shah, Sher A Khan, Noor Muhammad, Abdul Wali, Saadullah Khan, Sulman Basit, Muhammad Ayub
Biallelic mutations in the LPAR6 gene causing autosomal recessive wooly hair/hypotrichosis phenotype in five Pakistani families. International journal of dermatology 58 (8) (2019)
Ali A Assiry, Alia M Albalawi, Muhammad S Zafar, Siraj D Khan, Anhar Ullah, Ahmed Almatrafi, Khushnooda Ramzan, Sulman Basit
KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption. Scientific reports 9 (1) (2019)
Maryam Yousaf, Asmat Ullah, Zahid Azeem, Ayesha Isani Majeed, Muhammad Iqbal Memon, Tahseen Ghous, Sulman Basit, Wasim Ahmad
Novel heterozygous sequence variant in the GLI1 underlies postaxial polydactyly. Congenital anomalies 60 (4) (2019)
Muhammad Umair, Naveed Wasif, Alia M Albalawi, Khushnooda Ramzan, Majid Alfadhel, Wasim Ahmad, Sulman Basit
Exome sequencing revealed a novel loss-of-function variant in the GLI3 transcriptional activator 2 domain underlies nonsyndromic postaxial polydactyly. Molecular genetics & genomic medicine 7 (7) (2019)
Muhammad Jaseem Khan, Anwar Ullah, Sulman Basit
Genetic Basis of Polycystic Ovary Syndrome (PCOS): Current Perspectives. The application of clinical genetics 12 (2019)
K Shah, A Jan, F Ahmad, Sulman Basit, K Ramzan, Wasim Ahmad
Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene. Clinical and experimental dermatology 45 (2) (2019)
Alia M Albalawi, Jamil A Hashmi, Fatima Alfadhli, Ahmed M Almatrafi, Khushnooda Ramzan, Sulman Basit
Missense Mutations in the CTSC Gene in Saudi Families Segregating Papillon-Lefèvre Syndrome. Annals of dermatology 32 (1) (2019)
Ambreen Ijaz, Sulman Basit, Ajab Gul, Lilas Batool, Abrar Hussain, Sibtain Afzal, Khushnooda Ramzan, Jamil Ahmad, Abdul Wali
XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect. Congenital anomalies 59 (1) (2018)
Muhammad Umair, A Ullah, S Abbas, Wasim Ahmad, Sulman Basit, W Ahmad
First direct evidence of involvement of a homozygous loss-of-function variant in the EPS15L1 gene underlying split-hand/split-foot malformation. Clinical genetics 93 (3) (2018)
Khurram Liaqat, Ilene Chiu, Kwanghyuk Lee, Imen Chakchouk, Paula B Andrade-Elizondo, Regie Lyn P Santos-Cortez, Shabir Hussain, Shoaib Nawaz, Muhammad Ansar, Muhammad Nasim Khan, Sulman Basit, Isabelle Schrauwen, Wasim Ahmad, Suzanne M Leal
Novel missense and 3'-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. Journal of human genetics 63 (11) (2018)
Muhammad Latif, Zaman Ashraf, Sulman Basit, Abdul Ghaffar, Muhammad Sohail Zafar, Aamer Saeed, Sultan Ayoub Meo
Latest perspectives of orally bioavailable 2,4-diarylaminopyrimidine analogues (DAAPalogues) as anaplastic lymphoma kinase inhibitors: discovery and clinical developments. RSC advances 8 (30) (2018)
Khalid M Alharbi, Abdelhadi H Al-Mazroea, Atiyeh M Abdallah, Yousef Almohammadi, S Justin Carlus, Sulman Basit
Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients. Pediatric cardiology 39 (8) (2018)
E Alharby, A M Albalawi, A Nasir, S A Alhijji, A Mahmood, K Ramzan, F Abdusamad, A Aljohani, O Abdelsalam, A Eldardear, Sulman Basit
A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia. Clinical genetics 92 (6) (2017)
Sulman Basit, Essa Alharby, Alia M Albalawi, Khalid I Khoshhal
Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2. Congenital anomalies 58 (2) (2017)
Sulman Basit, Alia M Albalawi, Essa Alharby, Khalid I Khoshhal
Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip. BMC medical genetics 18 (1) (2017)
Jamil Amjad Hashmi, Maan Abdullah Albarry, Ahmed M Almatrafi, Alia M Albalawi, Amer Mahmood, Sulman Basit
Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. Congenital anomalies 58 (1) (2017)

Sulman Basit.css-eqlu8i{font-size:small;padding-left:4px;} (S Basit)

Publication Activity (10 Years)

Top Topics

Top Venues

Sulman Basit (S Basit)