Sulman Basit

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Khushnooda RamzanScientistAdresse e-mail validée de kfshrc.edu.sa
Muhammad AnsarDepartment of Biochemistry, Quaid-i-Azam UniversityAdresse e-mail validée de qau.edu.pk
Saad Ullah KhanAssociate Prof. Kohat Uni of Science & Technology Kohat,Adresse e-mail validée de kust.edu.pk
Dr. Sibtain AfzalSenior LecturerAdresse e-mail validée de alfaisal.edu
Ali GhazanfarUniversity of Azad Jammu and Kashmir, Quaid-i-Azam University, King Saud University Saudi ArabiaAdresse e-mail validée de ajku.edu.pk
Prof. Dr. Zafar Iqbal, M.Phil. Ph.D. P.Dr.Genomic & Experimental Medicine / QAAA Unit, CAMS-Al Ahsa, KSAU-HS, KAMC, NGHA, KSAAdresse e-mail validée de ksau-hs.edu.sa
Ahmed M AlmatrafiAssociate Professor of Medical Molecular Genetics, Taibah universityAdresse e-mail validée de taibahu.edu.sa
Amer MahmoodStem Cell Unit, Department of Anatomy, College of Medicine, King Saud UniversityAdresse e-mail validée de ksu.edu.sa
Naveed WasifUniversity Hopistal, Schleswig-Holstein, Campus Kiel, GermanyAdresse e-mail validée de uksh.de
Asmat UllahAarhus University DenmarkAdresse e-mail validée de bs.qau.edu.pk
Muhammad UmairPI-Team Leader-Scientist at King Abdullah International Medical Research Center (KAIMRC)Adresse e-mail validée de ngha.med.sa
Kwanghyuk LeeBaylor College of MedicineAdresse e-mail validée de bcm.edu
Dr. Musharraf JelaniAssociate Professor Centre for Omic Sciences, Islamia College PeshawarAdresse e-mail validée de icp.edu.pk
Khalid I. KhoshhalPrince Mohammed Bin Abdulaziz Hospital, Ministry of National Guard-Health Affairs, AlmadinahAdresse e-mail validée de ngha.med.sa
Essa AlharbyCenter for Genetics and Inherited Diseases, Taibah UniversityAdresse e-mail validée de taibahu.edu.sa
Regie Santos-CortezAssociate Professor, Otolaryngology-Head and Neck SurgeryAdresse e-mail validée de cuanschutz.edu
Noor MuhammadProfessor in Department of Biotechnology and Genetic Engineering, Kohat University ofAdresse e-mail validée de kust.edu.pk
Muhammad AyubInstitute of Biochemistry, University of Balochistan, Quetta, PakistanAdresse e-mail validée de um.uob.edu.pk
muhammad jaseem khanKhyber medical university PeshawarAdresse e-mail validée de kmu.edu.pk
Mahmood RasoolProfessor, CEGMR, King AbdulAziz UniversityAdresse e-mail validée de kau.edu.sa

Suivre

Sulman Basit

Assistant Professor at the Department of Biochemistry and Molecular Medicine, College of Medicine

Adresse e-mail validée de taibahu.edu.sa

Genetics Mutation Linkage analysis Whole genome SNP genotyping Exome Sequencing


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Genetic basis of polycystic ovary syndrome (PCOS): current perspectives MJ Khan, A Ullah, S Basit The application of clinical genetics, 249-260, 2019	389	2019
Alterations of the CIB2 calcium-and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48 S Riazuddin, IA Belyantseva, APJ Giese, K Lee, AA Indzhykulian, ... Nature genetics 44 (11), 1265-1271, 2012	268	2012
Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability S AlAsiri, S Basit, MA Wood-Trageser, SA Yatsenko, EP Jeffries, U Surti, ... The Journal of clinical investigation 125 (1), 258-262, 2015	236	2015
Vitamin D in health and disease: a literature review S Basit British journal of biomedical science 70 (4), 161-172, 2013	230	2013
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42 G Borck, AU Rehman, K Lee, HM Pogoda, N Kakar, S Von Ameln, ... The American Journal of Human Genetics 88 (2), 127-137, 2011	131	2011
Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89 RLP Santos-Cortez, K Lee, Z Azeem, PJ Antonellis, LM Pollock, S Khan, ... The American Journal of Human Genetics 93 (1), 132-140, 2013	127	2013
First macrocyclic 3rd-generation ALK inhibitor for treatment of ALK/ROS1 cancer: Clinical and designing strategy update of lorlatinib S Basit, Z Ashraf, K Lee, M Latif European Journal of Medicinal Chemistry 134, 348-356, 2017	112	2017
Genetics of clubfoot; recent progress and future perspectives S Basit, KI Khoshhal European Journal of Medical Genetics 61 (2), 107-113, 2018	103	2018
A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles M Ayub, S Basit, M Jelani, FU Rehman, M Iqbal, M Yasinzai, W Ahmad The American Journal of Human Genetics 85 (4), 515-520, 2009	97	2009
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment M Schraders, K Lee, J Oostrik, PLM Huygen, G Ali, LH Hoefsloot, ... The American Journal of Human Genetics 86 (2), 138-147, 2010	77	2010
CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly S Basit, KM Al-Harbi, SAM Alhijji, AM Albalawi, E Alharby, A Eldardear, ... Human genetics 135, 1199-1207, 2016	65	2016
A novel homozygous missense mutation in WNT10B in familial split‐hand/foot malformation S Khan, S Basit, FK Zimri, N Ali, G Ali, M Ansar, W Ahmad Clinical genetics 82 (1), 48-55, 2012	58	2012
Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly R Kousar, MJ Hassan, B Khan, S Basit, S Mahmood, A Mir, W Ahmad, ... BMC neurology 11, 1-6, 2011	47	2011
A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani … S Basit, SKH Naqvi, N Wasif, G Ali, M Ansar, W Ahmad BMC medical genetics 9, 1-6, 2008	44	2008
Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families N Wasif, SKH Naqvi, S Basit, N Ali, M Ansar, W Ahmad Human genetics 129, 419-424, 2011	43	2011
Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip S Basit, AM Albalawi, E Alharby, KI Khoshhal BMC Medical Genetics 18, 1-10, 2017	41	2017
Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families M Umair, A Hassan, A Jan, F Ahmad, M Imran, MI Samman, S Basit, ... Journal of human genetics 61 (3), 207-213, 2016	39	2016
Pakistan genetic mutation database (PGMD); a centralized Pakistani mutome data source I Qasim, B Ahmad, MA Khan, N Khan, N Muhammad, S Basit, S Khan European journal of medical genetics 61 (4), 204-208, 2018	35	2018
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13. 3–q21. 2 and screening of the candidate genes S Basit, S Kamran-ul-Hassan Naqvi, M Ansar, W Ahmad Human genetics 131, 415-422, 2012	35	2012
A novel WDR62 mutation causes primary microcephaly in a Pakistani family MM Memon, SI Raza, S Basit, R Kousar, W Ahmad, M Ansar Molecular biology reports 40, 591-595, 2013	33	2013

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