Sulman Basit

Citeret af

	Alle	Siden 2020
Henvisninger	3573	2117
h-index	29	20
i10-indeks	72	50

480

240

120

360

201020112012201320142015201620172018201920202021202220232024202536 35 77 98 145 184 175 174 212 271 346 378 397 453 476 65

Offentlig adgang

Se alle

19 artikler

3 artikler

tilgængelige

ikke tilgængelige

Baseret på krav i forbindelse med finansiering

Medforfattere

Khushnooda RamzanScientistVerificeret mail på kfshrc.edu.sa
Muhammad AnsarDepartment of Biochemistry, Quaid-i-Azam UniversityVerificeret mail på qau.edu.pk
Saad Ullah KhanAssociate Prof. Kohat Uni of Science & Technology Kohat,Verificeret mail på kust.edu.pk
Dr. Sibtain AfzalSenior LecturerVerificeret mail på alfaisal.edu
Ali GhazanfarUniversity of Azad Jammu and Kashmir, Quaid-i-Azam University, King Saud University Saudi ArabiaVerificeret mail på 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, KSAVerificeret mail på ksau-hs.edu.sa
Amer MahmoodStem Cell Unit, Department of Anatomy, College of Medicine, King Saud UniversityVerificeret mail på ksu.edu.sa
Ahmed M AlmatrafiAssociate Professor of Medical Molecular Genetics, Taibah universityVerificeret mail på taibahu.edu.sa
Naveed WasifUniversity Hopistal, Schleswig-Holstein, Campus Kiel, GermanyVerificeret mail på uksh.de
Asmat UllahAarhus University DenmarkVerificeret mail på bs.qau.edu.pk
Muhammad UmairPI-Team Leader-Scientist at King Abdullah International Medical Research Center (KAIMRC)Verificeret mail på ngha.med.sa
Kwanghyuk LeeBaylor College of MedicineVerificeret mail på bcm.edu
Dr. Musharraf JelaniAssociate Professor Centre for Omic Sciences, Islamia College PeshawarVerificeret mail på icp.edu.pk
Khalid I. KhoshhalPrince Mohammed Bin Abdulaziz Hospital, Ministry of National Guard-Health Affairs, AlmadinahVerificeret mail på ngha.med.sa
Essa AlharbyCenter for Genetics and Inherited Diseases, Taibah UniversityVerificeret mail på taibahu.edu.sa
Regie Santos-CortezAssociate Professor, Otolaryngology-Head and Neck SurgeryVerificeret mail på cuanschutz.edu
Noor MuhammadProfessor in Department of Biotechnology and Genetic Engineering, Kohat University ofVerificeret mail på kust.edu.pk
Muhammad AyubInstitute of Biochemistry, University of Balochistan, Quetta, PakistanVerificeret mail på um.uob.edu.pk
muhammad jaseem khanKhyber medical university PeshawarVerificeret mail på kmu.edu.pk
Mahmood RasoolProfessor, CEGMR, King AbdulAziz UniversityVerificeret mail på kau.edu.sa

Følg

Sulman Basit

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

Verificeret mail på taibahu.edu.sa

Genetics Mutation Linkage analysis Whole genome SNP genotyping Exome Sequencing


Titel Sortér efter henvisninger Sortér efter årstal Sortér efter titel	Citeret af Citeret af	År
Genetic basis of polycystic ovary syndrome (PCOS): current perspectives MJ Khan, A Ullah, S Basit The application of clinical genetics, 249-260, 2019	394	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	266	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	237	2015
Vitamin D in health and disease: a literature review S Basit British journal of biomedical science 70 (4), 161-172, 2013	232	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	130	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	115	2017
Genetics of clubfoot; recent progress and future perspectives S Basit, KI Khoshhal European Journal of Medical Genetics 61 (2), 107-113, 2018	102	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
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	47	2011
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	46	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
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	42	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	34	2012
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family MJ Khan, N Pollock, H Jiang, C Castro, R Nazli, J Ahmed, S Basit, ... Scientific Reports 8 (1), 16280, 2018	33	2018

Systemet kan ikke foretage handlingen nu. Prøv igen senere.

Artikler 1–20

Henvisninger pr. år

Dublerede henvisninger

Flettede henvisninger

Tilføj medforfattereMedforfattere

Følg

Citeret af

Medforfattere