Raheel Qamar - Google Scholar Citations

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	All	Since 2014
Citations	3669	2015
h-index	32	23
i10-index	72	61

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Co-authors

aisha mohyuddinShifa College of Medicine, Islamabad, PakistanVerified email at shifacollege.edu
Atika MansoorVerified email at ibge.edu.pk
Dr. Muhammad AjmalRadboud University Medical Centre NijmegenVerified email at gen.umcn.nl
Benish AliCOMSATS Institute of Information Technology, Islamabad, PakistanVerified email at comsats.edu.pk
Nadia K WaheedTufts University School of Medicine, Boston Image Reading CenterVerified email at tuftsmedicalcenter.org
Ahmed SadequeDepartment of Crop Sciences, UIUCVerified email at illinois.edu
Matthew HurlesSenior Group Leader in Human Genetics, Wellcome Trust Sanger InstituteVerified email at sanger.ac.uk
habib bokhari, habib bukhariCOMSATSVerified email at comsats.edu.pk
Michael HammerARL Division of Biotechnology, University of ArizonaVerified email at email.arizona.edu
Nadira Yusupovna YuldashevaSenior Scientific Officer, University of LeedsVerified email at leeds.ac.uk
R. Spencer WellsInsitome, University of Texas at AustinVerified email at insito.me
Andrea NovellettoProfessor of Genetics, University "Tor Vergata", Rome, ItalyVerified email at bio.uniroma2.it
Agnar HelgasondeCODE Genetics and University of IcelandVerified email at hi.is
Giovanni Destro BisolUniversity of Rome "La Sapienza" and Istituto Italiano di AntropologiaVerified email at uniroma1.it
Azeem Mehmood ButtTranslational Genomics Lab, Dept of Biosciences, COMSATS University Islamabad (CUI), IslamabadVerified email at comsats.edu.pk
Bertorelle GiorgioAssociate Professor in Genetics, University of FerraraVerified email at unife.it
Fabrício R SantosUniversidade Federal de Minas GeraisVerified email at icb.ufmg.br
Fulvio CrucianiSapienza Università di Roma, Dipartimento di Biologia e Biotecnologie "Charles Darwin"Verified email at uniroma1.it
Kumarasamy ThangarajCentre for Cellular and Molecular BiologyVerified email at ccmb.res.in
De Baere ElfrideProfessor, Center for Medical Genetics, Ghent University, BelgiumVerified email at ugent.be

Raheel Qamar

Tenured Professor of Biochemistry & Molecular Biology, Rector COMSATS University Islamabad

Verified email at comsats.edu.pk

Molecular Genetics


Title	Cited by	Year
The genetic legacy of the Mongols T Zerjal, Y Xue, G Bertorelle, RS Wells, W Bao, S Zhu, R Qamar, Q Ayub, ... The American Journal of Human Genetics 72 (3), 717-721, 2003	529	2003
Y-chromosomal DNA variation in Pakistan R Qamar, Q Ayub, A Mohyuddin, A Helgason, K Mazhar, A Mansoor, ... The American Journal of Human Genetics 70 (5), 1107-1124, 2002	265	2002
Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information Q Ayub, A Mohyuddin, R Qamar, K Mazhar, T Zerjal, SQ Mehdi, ... Nucleic acids research 28 (2), e8-e8, 2000	229	2000
Y-chromosome lineages trace diffusion of people and languages in southwestern Asia L Quintana-Murci, C Krausz, T Zerjal, SH Sayar, MF Hammer, SQ Mehdi, ... The American Journal of Human Genetics 68 (2), 537-542, 2001	180	2001
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements F Wang, H Wang, HF Tuan, DH Nguyen, V Sun, V Keser, SJ Bowne, ... Human Genetics 133 (3), 331-345, 2014	142	2014
Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa D Bandah-Rozenfeld, RWJ Collin, E Banin, L Ingeborgh van den Born, ... The American Journal of Human Genetics 87 (2), 199-208, 2010	77	2010
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma CC Khor, T Do, H Jia, M Nakano, R George, K Abu-Amero, R Duvesh, ... Nature genetics 48 (5), 556, 2016	72	2016
MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma S Micheal, R Qamar, F Akhtar, MI Khan, WA Khan, A Ahmed Molecular vision 15, 2268, 2009	67	2009
Differential structuring of human populations for homologous X and Y microsatellite loci R Scozzari, F Cruciani, P Malaspina, P Santolamazza, BM Ciminelli, ... The American Journal of Human Genetics 61 (3), 719-733, 1997	66	1997
Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution P Malaspina, F Cruciani, BM Ciminelli, L Terrenato, P Santolamazza, ... The American Journal of Human Genetics 63 (3), 847-860, 1998	65	1998
Association of eNOS and HSP70 gene polymorphisms with glaucoma in Pakistani cohorts H Ayub, MI Khan, S Micheal, F Akhtar, M Ajmal, S Shafique, SHB Ali, ... Molecular vision 16, 18, 2010	64	2010
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families R Harripaul, N Vasli, A Mikhailov, MA Rafiq, K Mittal, C Windpassinger, ... Molecular psychiatry 23 (4), 973, 2018	55	2018
C677T polymorphism in the methylenetetrahydrofolate reductase gene is associated with primary closed angle glaucoma S Michael, R Qamar, F Akhtar, WA Khan, A Ahmed Molecular vision 14, 661, 2008	54	2008
P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patients S Khaliq, A Hameed, T Khaliq, Q Ayub, R Qamar, A Mohyuddin, K Mazhar, ... Genetic testing 4 (1), 23-29, 2000	53	2000
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome FR Santos, A Pandya, M Kayser, RJ Mitchell, A Liu, L Singh, ... Human molecular genetics 9 (3), 421-430, 2000	53	2000
Evolution of codon usage in Zika virus genomes is host and vector specific AM Butt, I Nasrullah, R Qamar, Y Tong Emerging microbes & infections 5 (1), 1-14, 2016	51	2016
HLA polymorphism in six ethnic groups from Pakistan A Mohyuddin, Q Ayub, S Khaliq, A Mansoor, K Mazhar, S Rehman, ... Tissue antigens 59 (6), 492-501, 2002	50	2002
CLRN1 mutations cause nonsyndromic retinitis pigmentosa MI Khan, FFJ Kersten, M Azam, RWJ Collin, A Hussain, STA Shah, ... Ophthalmology, 2011	49	2011
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families S Shafique, S Siddiqi, M Schraders, J Oostrik, H Ayub, A Bilal, M Ajmal, ... PloS one 9 (6), e100146, 2014	47	2014
POLYAR, a new computer program for prediction of poly (A) sites in human sequences MN Akhtar, SA Bukhari, Z Fazal, R Qamar, IA Shahmuradov BMC genomics 11 (1), 646, 2010	46	2010

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