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1
2023
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1
Mutshaba Bashir,Wajeeha Mateen,Sadia Khurshid''A common missense variant rs874881 of PADI4 gene and rheumatoid arthritis: Genetic association study and in-silico analysis.'',Gene,2023.
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2
2022
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2
Saima Ghafoor,Muhammad Arshad Rafiq,Syed Tahir Abbas Shah''KIF1A novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with Hereditary Sensory and Autonomic Neuropathy Type IIC.'',International Journal of Neuroscience,2022.
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3
2022
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3
Aisha Nasir Hashmi, Raees Ahmed Dharejo,Usama Bin Zubair''Association of Dopamine ß-Hydroxylase Polymorphism rs1611115 And Serum Levels with Psychiatric Disorders in Pakistani Population.'',International Journal of Neuroscience,2022.
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4
2022
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4
Liaqat,Muhammad,Zheng''Responses of Enterococcus faecalis resistance and cytolysin up-regulation to nutrients in constructed mesocosms'',Journal of King Saud University - Science,2022.
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5
2020
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5
Muhammad,Sidra,Ummara''Genetic Association of Vanin 1 Gene Polymorphism With Myocardial Infarction'',Journal of the American College of Cardiology,2020.
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6
2020
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6
Netasha,Andrew,Delnaz''Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population'',Acta Diabetologica,2020.
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7
2019
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7
Moeen,Jane,Muhammad''Implementation of public health genomics in Pakistan'',European Journal of Human Genetics,2019.
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8
2019
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8
Nneoma,Elijah,Maryam''Prevalence of human T-lymphotropic virus 1/2 in Nigeria's capital territory and meta-analysis of Nigerian studies'',SAGE Open Medicine,2019.
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9
2018
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9
Muhammad,Abdul,Muhammad''Decreased Serum PON1 Arylesterase Activity in Familial Hypercholesterolemia Patients with Mutated LDLR Gene'',Genetics and Molecular Biology,2018.
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10
2017
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10
Frans,Stephanie,Nathalie''In silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Stargardt Disease and Cone-Rod Dystrophy Cases'',Investigative Ophthalmology & Visual Science,2017.
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11
2017
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11
Stephanie,Nathalie,Jana'' In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy Cases'',HUMAN MUTATION,2017.
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12
2017
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12
Liaqat,Mohsan,Yasir''Molecular Mechanism of Quorum-Sensing in Enterococcus faecalis: Its Role in Virulence and Therapeutic Approaches'',INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,2017.
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13
2016
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13
Maleeha,Miriam,Muhammad''Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum'',SCIENTIFIC REPORTS,2016.
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14
2016
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14
Galuh,Mette,Muhammad''Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark'',EUROPEAN JOURNAL OF HUMAN GENETICS,2016.
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15
2016
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15
Liaqat,Yan-Qiu,Jie''Nutrient-induced antibiotic resistance in Enterococcus faecalis in the eutrophic environment'',JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE,2016.
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16
2015
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16
Maleeha,Muhammad,Maleeha''Homozygosity Mapping and Targeted Sanger Sequencing Reveal Genetic Defects Underlying Inherited Retinal Disease in Families from Pakistan'',PLoS ONE,2015.
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17
2014
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17
Muhammad,Muhammad,Kornelia''Hypomorphic variants in the splice factor genes DHX38 and SNRNP200 are associated with autosomal recessive retinitis pigmentosa'',European Society of Human Genetics,2014.
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18
2014
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18
Frans ,Johan,Muhammad''Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases.'',Human Mutation,2014.
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19
2014
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19
Muhammad,Muhammad,Kornelia''A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma'',Journal of Medical Genetics,2014.
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20
2014
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20
Muhammad,Maleeha,Muhammad''The molecular basis of retinal dystrophies in Pakistan'',Genes,2014.
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21
2014
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21
Sobia,Saima,Margit''Genetic Spectrum of Autosomal Recessive NonSyndromic Hearing Loss in Pakistani Families'',PLoS ONE,2014.
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22
2013
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22
Muhammad,Muhammad,Kornelia''Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome. '',Molecular Vision,2013.
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23
2013
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23
Waqas,Ros,Moeen''The genetic spectrum of familial hypercholesterolemia in Pakistan. '',Clinica Chimica Acta,2013.
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24
2013
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24
Muhammad,Muhammad ,Shazia''Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan. '',Clinical Genetics,2013.
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25
2013
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25
Muhammad,Maleeha,Muhammad''Overview of genetic causes and identification of novel loci for retinal dystrophies in Pakistan'',Investigative Ophthalmology & Visual Science,2013.
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26
2013
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26
Frans,Johan,Muhammad''Towards Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases'',Investigative Ophthalmology & Visual Science,2013.
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27
2012
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27
Muhammad,Muhammad,Kornelia''Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families. '',Molecular Vision,2012.
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28
2012
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28
Muhammad,Muhammad,Shazia''Identification of recurrent and novel mutations in TULP1 in Pakistani families with early onset retinitis pigmentosa. '',Molecular Vision,2012.
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29
2012
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29
Waqas,Muhammad,Ahmed''Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients. '',Molecular Biology Reports,2012.
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30
2012
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30
Rubab,Farah,Muhammad''Prevalence of Hepatitis C Virus in Urban Ghettos of Twin Cities. '',Pakistan Journal of Zoology,2012.
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31
2011
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31
Muhammad,Waqas,Naveed''First report of a nonsense triple nucleotide polymorphism (TNP) in the low density lipoprotein receptor gene in familial hypercholesterolemia. '',Genetic Testing and Molecular Biomarkers,2011.
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32
2011
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32
Maleeha,Rob,Ayesha''The genetic basis of retinitis pigmentosa in Pakistan.'',Archives of Ophthalmology,2011.
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33
2011
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33
Waqas,Meera,Imran''Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction'',Molecular Biology Reports,2011.
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34
2010
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34
Muhammad,Waqas,Ahmed''Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia. '',Molecular Biology Reports,2010.
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35
2010
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35
Humaira,Muhammad,Shazia''Association of eNOS and HSP70gene polymorphisms with glaucoma in Pakistani cohorts. '',Molecular Vision,2010.
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36
2009
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36
Maleeha,Rob,Muhammad''A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family. '',Molecular Vision,2009.
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