Raheel Qamar

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maleeha azamCOMSATS Institute of Information TechnologyVerified email at comsats.edu.pk
Rob CollinAssociate Professor, RadboudumcVerified email at radboudumc.nl
Dr. Muhammad AjmalRadboud University Medical Centre NijmegenVerified email at gen.umcn.nl
aisha mohyuddinShifa College of Medicine, Islamabad, PakistanVerified email at shifacollege.edu
Atika MansoorVerified email at ibge.edu.pk
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
waqas ahmedCOMSATS institute of information TechnologyVerified email at uoh.edu.pk
Alamdar Hussain BalochKarolinska Institutet, MedH, Cell and Gene Therapy Group, Stockholm, SwedenVerified email at ki.se
Matthew HurlesSenior Group Leader in Human Genetics, Wellcome Trust Sanger InstituteVerified email at sanger.ac.uk
Azeem Mehmood ButtTranslational Genomics Lab, Dept of Biosciences, COMSATS University Islamabad (CUI), IslamabadVerified email at comsats.edu.pk
saima siddiqiIBGEVerified email at ibge.edu.pk
Nadira Yusupovna YuldashevaSenior Scientific Officer, University of LeedsVerified email at leeds.ac.uk
R. Spencer WellsThe Insitome InstituteVerified email at insito.me
Michael HammerARL Division of Biotechnology, University of ArizonaVerified email at email.arizona.edu
Pakeeza Arzoo ShaiqAssistant Professor, University Institute of Biochemistry and Biotechnology, PMAS-AAURVerified email at uaar.edu.pk
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

Raheel Qamar

Head of S&T Sector, ICESCO,Tenured Professor of Biochemistry & Molecular Biology, Ex-Rector COMSATS

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	604	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	284	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	240	2000
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	191	2014
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	188	2001
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	122	2016
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	110	2018
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	104	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	93	2010
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	83	2010
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	82	2009
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	78	2017
ABCA4 midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease R Sangermano, M Khan, SS Cornelis, V Richelle, S Albert, A Garanto, ... Genome research 28 (1), 100-110, 2018	76	2018
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	69	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
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	62	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	61	2008
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), 1-10, 2010	57	2010
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	56	2014
CLRN1 mutations cause nonsyndromic retinitis pigmentosa MI Khan, FFJ Kersten, M Azam, RWJ Collin, A Hussain, STA Shah, ... Ophthalmology, 2011	55	2011

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