waqas ahmed

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Raheel QamarHead of S&T Sector, ICESCO,Tenured Professor of Biochemistry & Molecular Biology, Ex-Rector COMSATSDirección de correo verificada de comsats.edu.pk
Dr. Muhammad AjmalCOMSATS University IslamabadDirección de correo verificada de comsats.edu.pk
maleeha azamCOMSATS Institute of Information TechnologyDirección de correo verificada de comsats.edu.pk
Ahmed SadequeDepartment of Crop Sciences, UIUCDirección de correo verificada de illinois.edu
Dr. Benish AliCOMSATS University Islamabad, Islamabad, PakistanDirección de correo verificada de comsats.edu.pk
Rob CollinAssociate Professor, RadboudumcDirección de correo verificada de radboudumc.nl
Nadia K WaheedTufts University School of Medicine, Boston Image Reading CenterDirección de correo verificada de tuftsmedicalcenter.org
Habib Bokhari, Habib Bukhari, SH Bok...Vice Chancellor, Kohsar University MurreeDirección de correo verificada de comsats.edu.pk
Alamdar Hussain BalochKarolinska Institutet, MedH, Cell and Gene Therapy Group, Stockholm, SwedenDirección de correo verificada de ki.se
maleeha mariaUniversity of Eastern Finland, Kuopio, FinlandDirección de correo verificada de uef.fi

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waqas ahmed

COMSATS institute of information Technology and The university of Haripur

Dirección de correo verificada de uoh.edu.pk

Molecular Biology


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
Association of ANRIL polymorphism (rs1333049: C> G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia W Ahmed, IS Ali, M Riaz, A Younas, A Sadeque, AK Niazi, SH Niazi, ... Gene 515 (2), 416-420, 2013	48	2013
Clinical utility of a coronary heart disease risk prediction gene score in UK healthy middle aged men and in the Pakistani population KE Beaney, JA Cooper, S Ullah Shahid, W Ahmed, R Qamar, F Drenos, ... PloS one 10 (7), e0130754, 2015	36	2015
Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosa M Ajmal, MI Khan, S Micheal, W Ahmed, A Shah, H Venselaar, H Bokhari, ... Molecular vision 18, 1226, 2012	34	2012
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan M Maria, M Ajmal, M Azam, NK Waheed, SN Siddiqui, B Mustafa, H Ayub, ... PLoS One 10 (3), e0119806, 2015	32	2015
Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction W Ahmed, M Malik, I Saeed, AA Khan, A Sadeque, U Kaleem, N Ahmed, ... Molecular biology reports 38, 2541-2548, 2011	30	2011
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families M Ajmal, MI Khan, K Neveling, YM Khan, SHB Ali, W Ahmed, MS Iqbal, ... Molecular Vision 18, 1558, 2012	22	2012
The genetic spectrum of familial hypercholesterolemia in Pakistan W Ahmed, R Whittall, M Riaz, M Ajmal, A Sadeque, H Ayub, R Qamar, ... Clinica Chimica Acta 421, 219-225, 2013	21	2013
Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia M Ajmal, W Ahmed, A Sadeque, SHB Ali, SH Bokhari, N Ahmed, R Qamar Molecular biology reports 37, 3869-3875, 2010	17	2010
Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients W Ahmed, M Ajmal, A Sadeque, RA Whittall, S Rafiq, W Putt, A Khawaja, ... Molecular biology reports 39, 7365-7372, 2012	8	2012
A novel pathogenic nonsense triple-nucleotide mutation in the low-density lipoprotein receptor gene and its clinical correlation with familial hypercholesterolemia M Ajmal, W Ahmed, N Akhtar, A Sadeque, A Khalid, SH Benish Ali, ... Genetic testing and molecular biomarkers 15 (9), 601-606, 2011	7	2011
Seroprevalence of Bordetella pertussis antibodies to pertussis toxin among healthy children MA Syed, W Ahmed, A Naeem, H Bokhari J Coll Physicians Surg Pak 22 (10), 677-8, 2012	6	2012
ANRIL polymorphism rs1333049, a novel genetic predictor for diabetic retinopathy complication A Siddiqui, S Hussain, A Azam, I Muslim, SI Maqsood, W Ahmed, ... meta gene 14, 33, 2017	2	2017

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