Raheel Qamar

Cited by

	All	Since 2015
Citations	4135	2209
h-index	34	25
i10-index	77	60

460

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199920002001200220032004200520062007200820092010201120122013201420152016201720182019202014 32 64 85 109 91 79 94 120 108 99 136 176 182 196 243 314 318 371 399 452 348

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
Azeem Mehmood ButtTranslational Genomics Lab, Dept of Biosciences, COMSATS University Islamabad (CUI), IslamabadVerified email at comsats.edu.pk
Nadira Yusupovna YuldashevaSenior Scientific Officer, University of LeedsVerified email at leeds.ac.uk
R. Spencer WellsThe Insitome InstituteVerified 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
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
Mark G ThomasProfessor of Evolutionary Genetics, University College LondonVerified email at ucl.ac.uk

Raheel Qamar

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

Verified email at comsats.edu.pk

Molecular Genetics


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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	571	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	278	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	237	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	185	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	173	2014
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), 556-562, 2016	95	2016
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	89	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), 973-984, 2018	85	2018
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	76	2009
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	74	2016
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	73	2010
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	64	1998
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	58	2000
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	57	2008
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci T Aung, M Ozaki, MC Lee, U Schlötzer-Schrehardt, G Thorleifsson, ... Nature genetics 49 (7), 993-1004, 2017	56	2017
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	56	2000
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	53	2014
CLRN1 mutations cause nonsyndromic retinitis pigmentosa MI Khan, FFJ Kersten, M Azam, RWJ Collin, A Hussain, STA Shah, ... Ophthalmology, 2011	53	2011
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	52	2002

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