Sulman Basit

Citované v

	Všetky	Od 2019
Citácie	3181	2011
h-index	29	20
i10-index	65	52

440

220

110

330

20102011201220132014201520162017201820192020202120222023202436 33 76 99 146 185 173 175 210 270 345 372 406 422 181

Verejný prístup

všetky položky

18 článkov

2 články

dostupné

nedostupné

Na základe mandátov na financovanie

Spoluautori

Khushnooda RamzanScientistOverená e-mailová adresa na: kfshrc.edu.sa
Muhammad AnsarDepartment of Biochemistry, Quaid-i-Azam UniversityOverená e-mailová adresa na: qau.edu.pk
Saad Ullah KhanAssociate Prof. Kohat Uni of Science & Technology Kohat,Overená e-mailová adresa na: kust.edu.pk
Dr. Sibtain AfzalSenior LecturerOverená e-mailová adresa na: alfaisal.edu
Ali GhazanfarUniversity of Azad Jammu and Kashmir, Quaid-i-Azam University, King Saud University Saudi ArabiaOverená e-mailová adresa na: ajku.edu.pk
Dr Zafar Iqbal MPhil PhD PDrCAMS-Al Ahsa, King Saud Bin Abdulaziz University for Health Sciences, KAMC, NGHA, KSAOverená e-mailová adresa na: ksau-hs.edu.sa
Naveed WasifUniversity Hopistal, Schleswig-Holstein, Campus Kiel, GermanyOverená e-mailová adresa na: uksh.de
Asmat UllahBroad Institute of Harvard and MITOverená e-mailová adresa na: bs.qau.edu.pk
Muhammad AyubInstitute of Biochemistry, University of Balochistan, Quetta, PakistanOverená e-mailová adresa na: um.uob.edu.pk
Syed Kamran Ul Hassan NaqviCOMSATS University Islamabad, PakistanOverená e-mailová adresa na: comsats.edu.pk
Ahmed M AlmatrafiAssociate Professor of Medical Molecular Genetics, Taibah universityOverená e-mailová adresa na: taibahu.edu.sa
Muhammad UmairPI-Team Leader-Scientist at King Abdullah International Medical Research Center (KAIMRC)Overená e-mailová adresa na: ngha.med.sa
Muhammad AbsarResearch ScientistOverená e-mailová adresa na: ngha.med.sa
Kwanghyuk LeeBaylor College of MedicineOverená e-mailová adresa na: bcm.edu
Dr. Musharraf JelaniAssociate Professor Centre for Omic Sciences, Islamia College PeshawarOverená e-mailová adresa na: icp.edu.pk
Khalid I. KhoshhalPrince Mohammed Bin Abdulaziz Hospital, Ministry of National Guard-Health Affairs, AlmadinahOverená e-mailová adresa na: ngha.med.sa
Amer MahmoodKing Saud UniversityOverená e-mailová adresa na: ksu.edu.sa
Essa AlharbyCenter for Genetics and Inherited Diseases, Taibah UniversityOverená e-mailová adresa na: taibahu.edu.sa
Regie Santos-CortezAssociate Professor, Otolaryngology-Head and Neck SurgeryOverená e-mailová adresa na: cuanschutz.edu
Noor MuhammadProfessor in Department of Biotechnology and Genetic Engineering, Kohat University ofOverená e-mailová adresa na: kust.edu.pk

Sledovať

Sulman Basit

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

Overená e-mailová adresa na: taibahu.edu.sa

Genetics Mutation Linkage analysis Whole genome SNP genotyping Exome Sequencing


Názov Zoradiť podľa citácií Zoradiť podľa roka Zoradiť podľa názvu	Citované v Citované v	Rok
Genetic basis of polycystic ovary syndrome (PCOS): current perspectives MJ Khan, A Ullah, S Basit The application of clinical genetics, 249-260, 2019	285	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	257	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	217	2015
Vitamin D in health and disease: a literature review S Basit British journal of biomedical science 70 (4), 161-172, 2013	211	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	119	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	102	2017
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	95	2009
Genetics of clubfoot; recent progress and future perspectives S Basit, KI Khoshhal European Journal of Medical Genetics 61 (2), 107-113, 2018	90	2018
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	74	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	59	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	54	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	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	43	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	39	2017
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	38	2011
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	35	2016
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	34	2013
Mutation Analysis of the ASPM Gene in 18 Pakistani Families With Autosomal Recessive Primary Microcephaly R Kousar, H Nawaz, M Khurshid, G Ali, SU Khan, H Mir, M Ayub, A Wali, ... Journal of child neurology 25 (6), 715-720, 2010	34	2010
High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families LY AlAyadhi, JA Hashmi, M Iqbal, AM Albalawi, MI Samman, NE Elamin, ... Neuroscience 339, 561-570, 2016	32	2016

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