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Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment
Author / Creator:Adadey, Samuel M. ; Schrauwen, Isabelle ; Aboagye, Elvis Twumasi ; Bharadwaj, Thashi ; Esoh, Kevin K. ; Basit, Sulman ; Acharya, Anushree ; Nouel-Saied, Liz M. ; Liaqat, Khurram ; Wonkam-Tingang, Edmond ; Mowla, Shaheen ; Awandare, Gordon A. ; Ahmad, Wasim ; Leal, Suzanne M. ; Wonkam, Ambroise
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2021-12, Vol.66 (12), p.1169-1175
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Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13
Author / Creator:Acharya, Anushree ; Raza, Syed Irfan ; Anwar, Muhammad Zeeshan ; Bharadwaj, Thashi ; Liaqat, Khurram ; Khokhar, Muhammad Akram Shahzad ; Everard, Jenna L. ; Nasir, Abdul ; Nickerson, Deborah A. ; Bamshad, Michael J. ; Ansar, Muhammad ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2021-10, Vol.66 (10), p.1009-1018
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Synthesis and Characterization of Electrical and Thermal Conductive Vinyltriethoxysilane Functionalized Graphene Oxide/Poly (Methyl Methacrylate) Nanocomposite Films
Author / Creator:Fazil, Srosh ; Liaqat, Khurram ; Rehman, Wajid ; Abdellatif, Magda H.
Publisher:Switzerland: MDPI AG
Journal title:Membranes (Basel), 2023-06, Vol.13 (6), p.609
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Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
Author / Creator:Liaqat, Khurram ; Hussain, Shabir ; Bilal, Muhammad ; Nasir, Abdul ; Acharya, Anushree ; Ali, Raja Hussain ; Nawaz, Shoaib ; Umair, Muhammad ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-01, Vol.65 (2), p.187-192
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ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment
Author / Creator:Bharadwaj, Thashi ; Schrauwen, Isabelle ; Rehman, Sakina ; Liaqat, Khurram ; Acharya, Anushree ; Giese, Arnaud P. J. ; Nouel-Saied, Liz M. ; Nasir, Abdul ; Everard, Jenna L. ; Pollock, Lana M. ; Zhu, Shaoyuan ; Bamshad, Michael J. ; Nickerson, Deborah A. ; Ali, Raja Hussain ; Ullah, Asmat ; Wali, Abdul ; Ali, Ghazanfar ; Santos-Cortez, Regie Lyn P. ; Ahmed, Zubair M. ; McDermott, Brian M. ; Ansar, Muhammad ; Riazuddin, Saima ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2022-01, Vol.30 (1), p.22-33
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Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
Author / Creator:Liaqat, Khurram ; Hussain, Shabir ; Bilal, Muhammad ; Nasir, Abdul ; Acharya, Anushree ; Ali, Raja Hussain ; Nawaz, Shoaib ; Umair, Muhammad ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2022-03, Vol.67 (3), p.181-181
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Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance
Author / Creator:Liaqat, Khurram ; Schrauwen, Isabelle ; Raza, Syed Irfan ; Lee, Kwanghyuk ; Hussain, Shabir ; Chakchouk, Imen ; Nasir, Abdul ; Acharya, Anushree ; Abbe, Izoduwa ; Umair, Muhammad ; Ansar, Muhammad ; Ullah, Irfan ; Shah, Khadim ; Bamshad, Michael J. ; Nickerson, Deborah A. ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2019-02, Vol.64 (2), p.153-160
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Sulfonated Polyimide Membranes Derived from a Novel Sulfonated Diamine with Pendant Benzenesulfonic Acid for Fuel Cells
Author / Creator:Liaqat, Khurram ; Fazil, Srosh ; Rehman, Wajid ; Saeed, Shaukat ; Menaa, Farid ; Shah, Syed Asim Hussain ; Nawaz, Muhammad ; Alharbi, Walaa Naji ; Menaa, Bouzid ; Farooq, Muhammad
Publisher:Basel: MDPI AG
Journal title:Energies (Basel), 2021-10, Vol.14 (19), p.6050
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Correction: Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13
Author / Creator:Acharya, Anushree ; Raza, Syed Irfan ; Anwar, Muhammad Zeeshan ; Bharadwaj, Thashi ; Liaqat, Khurram ; Khokhar, Muhammad Akram Shahzad ; Everard, Jenna L. ; Nasir, Abdul ; Nickerson, Deborah A. ; Bamshad, Michael J. ; Ansar, Muhammad ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:London: Nature Publishing Group
Journal title:Journal of human genetics, 2021-10, Vol.66 (10), p.1019-1019
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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
Author / Creator:Schrauwen, Isabelle ; Chakchouk, Imen ; Acharya, Anushree ; Liaqat, Khurram ; Irfanullah ; Nickerson, Deborah A. ; Bamshad, Michael J. ; Shah, Khadim ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2018-07, Vol.19 (1), p.122-122, Article 122
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Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment
Author / Creator:Liaqat, Khurram ; Chiu, Ilene ; Lee, Kwanghyuk ; Chakchouk, Imen ; Andrade-Elizondo, Paula B. ; Santos-Cortez, Regie Lyn P. ; Hussain, Shabir ; Nawaz, Shoaib ; Ansar, Muhammad ; Khan, Muhammad Nasim ; Basit, Sulman ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2018-11, Vol.63 (11), p.1099-1107
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Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly
Author / Creator:Bilal, Muhammad ; Khan, Hammal ; Khan, Muhammad Javed ; Haack, Tobias B. ; Buchert, Rebecca ; Liaqat, Khurram ; Ullah, Kifayat ; Ahmed, Sohail ; Bharadwaj, Thashi ; Acharya, Anushree ; Peralta, Susana ; Najumuddin ; Ali, Hamid ; Hasni, Muhammad Sharif ; Schrauwen, Isabelle ; Ullah, Asmat ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2023-11, Vol.31 (11), p.1270-1274
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Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment
Author / Creator:Schrauwen, Isabelle ; Liaqat, Khurram ; Schatteman, Isabelle ; Bharadwaj, Thashi ; Nasir, Abdul ; Acharya, Anushree ; Ahmad, Wasim ; Van Camp, Guy ; Leal, Suzanne M.
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2020-06, Vol.11 (6), p.687
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ArticlesPeer ReviewedFull Text
Chemically tethered functionalized graphene oxide based novel sulfonated polyimide composite for polymer electrolyte membrane
Author / Creator:Rehman, Wajid ; Liaqat, Khurram ; Fazil, Srosh ; Saeed, Shaukat ; Waseem, Muhammad ; Shakeel, Muhammad ; Mir, Sadullah ; Bibi, Iram ; Guo, Cun-Yue
Publisher:Dordrecht: Springer Netherlands
Journal title:Journal of polymer research, 2019-03, Vol.26 (3), Article 82
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A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment
Author / Creator:Schrauwen, Isabelle ; Chakchouk, Imen ; Liaqat, Khurram ; Jan, Abid ; Nasir, Abdul ; Hussain, Shabir ; Nickerson, Deborah A. ; Bamshad, Michael J. ; Ullah, Asmat ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2018-07, Vol.137 (6-7), p.471-478
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Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family
Author / Creator:Liaqat, Khurram ; Hussain, Shabir ; Acharya, Anushree ; Nasir, Abdul ; Bharadwaj, Thashi ; Ansar, Muhammad ; Basit, Sulman ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2022-04, Vol.13 (4), p.662
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Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly
Author / Creator:Ullah, Irfan ; Kakar, Naseebullah ; Schrauwen, Isabelle ; Hussain, Shabir ; Chakchouk, Imen ; Liaqat, Khurram ; Acharya, Anushree ; Wasif, Naveed ; Santos-Cortez, Regie Lyn P. ; Khan, Saadullah ; Aziz, Abdul ; Lee, Kwanghyuk ; Couthouis, Julien ; Horn, Denise ; Kragesteen, Bjørt K. ; Spielmann, Malte ; Thiele, Holger ; Nickerson, Deborah A. ; Bamshad, Michael J. ; Gitler, Aaron D. ; Ahmad, Jamil ; Ansar, Muhammad ; Borck, Guntram ; Ahmad, Wasim ; Leal, Suzanne M.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2019-06, Vol.138 (6), p.593-600
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ArticlesPeer ReviewedFull Text
Novel missense and 3’-UTR splice site variants in LHFPL5 cause autosomal recessive non-syndromic hearing impairment
Author / Creator:Liaqat, Khurram ; Chiu, Ilene ; Lee, Kwanghyuk ; Chakchouk, Imen ; Andrade-Elizondo, Paula B. ; Santos-Cortez, Regie Lyn P. ; Hussain, Shabir ; Nawaz, Shoaib ; Ansar, Muhammad ; Khan, Muhammad Nasim ; Basit, Sulman ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M.
Journal title:Journal of human genetics, 2018-09, Vol.63 (11), p.1099-1107
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Spectrophotometric determination of uranium with arsenazo-III in the presence of N-cetyl-N,N,N-tri-methylammonium bromide as surfactant
Author / Creator:Khan, Muhammad Haleem ; Bukhari, Syed Manzoor Hussain ; Ali, Akbar ; Liaqat, Khurram ; Fazal, Srosh
Publisher:Dordrecht: Springer Netherlands
Journal title:Journal of radioanalytical and nuclear chemistry, 2011-07, Vol.289 (1), p.113-119
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Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family
Author / Creator:Liaqat, Khurram ; Hussain, Shabir ; Acharya, Anushree ; Nasir, Abdul ; Bharadwaj, Thashi ; Ansar, Muhammad ; Basit, Sulman ; Schrauwen, Isabelle ; Ahmad, Wasim ; Leal, Suzanne M
Journal title:Genes, 2022, Vol.13 (4)
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Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

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Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13

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Synthesis and Characterization of Electrical and Thermal Conductive Vinyltriethoxysilane Functionalized Graphene Oxide/Poly (Methyl Methacrylate) Nanocomposite Films

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Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment

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ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment

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Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment

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Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance

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Sulfonated Polyimide Membranes Derived from a Novel Sulfonated Diamine with Pendant Benzenesulfonic Acid for Fuel Cells

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Correction: Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

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Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment

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Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly

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Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

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Chemically tethered functionalized graphene oxide based novel sulfonated polyimide composite for polymer electrolyte membrane

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A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment

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Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family

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Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly

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Novel missense and 3’-UTR splice site variants in LHFPL5 cause autosomal recessive non-syndromic hearing impairment

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Spectrophotometric determination of uranium with arsenazo-III in the presence of N-cetyl-N,N,N-tri-methylammonium bromide as surfactant

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Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family

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