Abdul Nasir

ResearcherID ResearcherID Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 30

Top Venues

Genes

PloS one

Journal of human genetics

Artificial cells, nanomedicine, and biotechnology

Abdul Wali Khan University

Ajou University Department of Molecular Science and Technology (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Abdul Wali Khan University Jun 01 2015 - Apr 19 2016

Pakistan

Research Associate and Demonstrator :: Computational Medicinal Chemistry Lab Department of Biochemistry, Abdul Wali Khan University Mardan, Pakistan

Quaid-i-Azam University Sep 05 2013 - Feb 13 2015

Pakistan

Research Assistant :: Faculty of Biological Sciences, Department of Biochemistry

Abdul Wali Khan University Oct 02 2011 - Sep 15 2013

Pakistan

Research Assistant :: Department of Biochemistry,

Education History

Ajou University Department of Molecular Science and Technology Sep 02 2016

South Korea

PHD :: Department of Molecular Science and Technology

Abdul Wali Khan University - Jul 15 2013

Pakistan

MSC :: Department of biochemistry

Abdul Wali Khan University May 08 2009 - Jul 14 2011

Pakistan

BSC :: Department of Chemistry

Publications

Ayesha Raza, Tayyab Ali, Muhammad Naeem, Muhammad Asim, Fatma Hussain, Zhiye Li, Abdul Nasir
Biochemical characterization of bioinspired nanosuspensions from Swertia chirayita extract and their therapeutic effects through nanotechnology approach. PloS one 19 (2) (2024)
Ayesha Raza, Tayyab Ali, Muhammad Naeem, Muhammad Asim, Fatma Hussain, Zhiye Li, Abdul Nasir
Biochemical characterization of bioinspired nanosuspensions from Swertia chirayita extract and their therapeutic effects through nanotechnology approach. PloS one 19 (2) (2024)
Ayesha Raza, Tayyab Ali, Muhammad Naeem, Muhammad Asim, Fatma Hussain, Zhiye Li, Abdul Nasir
Biochemical characterization of bioinspired nanosuspensions from Swertia chirayita extract and their therapeutic effects through nanotechnology approach. PloS one 19 (2) (2024)
Ayesha Raza, Tayyab Ali, Muhammad Naeem, Muhammad Asim, Fatma Hussain, Zhiye Li, Abdul Nasir
Biochemical characterization of bioinspired nanosuspensions from Swertia chirayita extract and their therapeutic effects through nanotechnology approach. PloS one 19 (2) (2024)
Abdul Nasir, Mujeeb Ur Rehman, Tamreez Khan, Mansoor Husn, Manzar Khan, Ahmad Khan, Abdifatah Mohamed Nuh, Wei Jiang, Hafiz Muhammad Umer Farooqi, Qain Bai
Advances in nanotechnology-assisted photodynamic therapy for neurological disorders: a comprehensive review. Artificial cells, nanomedicine, and biotechnology 52 (1) (2024)
Abdul Nasir, Mujeeb Ur Rehman, Tamreez Khan, Mansoor Husn, Manzar Khan, Ahmad Khan, Abdifatah Mohamed Nuh, Wei Jiang, Hafiz Muhammad Umer Farooqi, Qain Bai
Advances in nanotechnology-assisted photodynamic therapy for neurological disorders: a comprehensive review. Artificial cells, nanomedicine, and biotechnology 52 (1) (2024)
Abdul Nasir, De-Liang Li, Bing Rong Liu
Author response to: Comment on: Endoscopic retrograde appendicitis therapy or antibiotics for uncomplicated appendicitis. The British journal of surgery (2023)
Khurram Liaqat, Thashi Bharadwaj, Khadim Shah, Abdul Nasir, Anushree Acharya, Saadullah Khan, Irfan Ullah, Isabelle Schrauwen, Wasim Ahmad, Suzanne M Leal
Nonsense variant in a consanguineous family expands the phenotype of KPTN gene-related syndrome to include hearing impairment. Clinical genetics (2023)
Khurram Liaqat, Shabir Hussain, Anushree Acharya, Abdul Nasir, Thashi Bharadwaj, Muhammad Ansar, Sulman Basit, Isabelle Schrauwen, Wasim Ahmad, Suzanne M Leal
Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family. Genes 13 (4) (2022)
Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam-Tingang, Kevin Kum Esoh, Kalinka Popel, Noluthando Manyisa, Mario Jonas, Carmen deKock, Victoria Nembaware, Diana M Cornejo Sanchez, Thashi Bharadwaj, Abdul Nasir, Jenna L Everard, Magda K Kadlubowska, Liz M Nouel-Saied, Anushree Acharya, Osbourne Quaye, Geoffrey K Amedofu, Gordon Akanzuwine Awandare, Suzanne M Leal
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes. Communications biology 5 (1) (2022)
Fozia Fozia, Rubina Nazli, Sher Alam Khan, Ahmed Bari, Abdul Nasir, Riaz Ullah, Hafiz Majid Mahmood, Muhammad Sohaib, Abdulrahman Alobaid, Siddique Akber Ansari, Sulman Basit, Saadullah Khan
Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis. Genes 12 (3) (2021)
Anushree Acharya, Syed Irfan Raza, Muhammad Zeeshan Anwar, Thashi Bharadwaj, Khurram Liaqat, Muhammad Akram Shahzad Khokhar, Jenna L Everard, Abdul Nasir, null null, Deborah A Nickerson, Michael J Bamshad, Muhammad Ansar, Isabelle Schrauwen, Wasim Ahmad, Regie Lyn P Santos-Cortez
Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13. Journal of human genetics 66 (10) (2021)
Ghazanfar Ali, Sadia Sadia, Jia Nee Foo, Abdul Nasir, Chu-Hua Chang, Elaine GuoYan Chew, Zahid Latif, Zahid Azeem, Syeda Ain-Ul-Batool, Syed Akif Raza Kazmi, Naheed Bashir Awan, Abdul Hameed Khan, Fazal-Ur- Rehman, Madiha Khalid, Abdul Wali, Samina Sarwar, Wasim Akhtar, Ansar Ahmed Abbasi, Rameez Nisar
Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome. BioMed research international 2021 (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Suzanne M Leal, Ambroise Wonkam
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. Experimental biology and medicine (Maywood, N.J.) 246 (13) (2021)
Khurram Liaqat, Shabir Hussain, Muhammad Bilal, Abdul Nasir, Anushree Acharya, Raja Hussain Ali, Shoaib Nawaz, Muhammad Umair, Isabelle Schrauwen, Wasim Ahmad, Suzanne M Leal
Correction: Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment. Journal of human genetics (2021)
Amjad Ali, Atif Ali Khan Khalil, Fazli Khuda, Nausheen Nazir, Riaz Ullah, Ahmed Bari, Adnan Haider, Syed Babar Jamal, Sareer Ahmad, Zahid Khan, Syed Muhammad Mukarram Shah, Syed Wadood Ali Shah, Abdul Nasir, Abid Ali, Mohammad Zahoor, Samin Jan
Phytochemical and Biological Screening of Leaf, Bark and Fruit Extracts from Ilex dipyrena Wall. Life (Basel, Switzerland) 11 (8) (2021)
Thashi Bharadwaj, Isabelle Schrauwen, Sakina Rehman, Khurram Liaqat, Anushree Acharya, Arnaud P J Giese, Liz M Nouel-Saied, Abdul Nasir, Jenna L Everard, Lana M Pollock, Shaoyuan Zhu, Michael J Bamshad, Deborah A Nickerson, Raja Hussain Ali, Asmat Ullah, Abdul Wali, Ghazanfar Ali, Regie Lyn P Santos-Cortez, Zubair M Ahmed, Brian M McDermott, Muhammad Ansar, Saima Riazuddin, Wasim Ahmad, Regie Lyn P Santos-Cortez
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment. European journal of human genetics : EJHG (2021)
Abdulaziz Asiri, Deemah Alwadaani, Muhammad Umair, Kheloud M Alhamoudi, Mohammed H Almuhanna, Abdul Nasir, Bahauddeen M Alrfaei, Abeer Al Tuwaijri, Tlili Barhoumi, Yusra Alyafee, Bader Almuzzaini, Mohammed Aldrees, Mariam Ballow, Latifah Alayyar, Abdulkareem AlAbdulrahman, Yazeid Alhaidan, Nahlah Al Ghasham, Sulaiman Al-Ajaji, Mohammad Alsalamah, Wafa Al Suwairi, Majid Alfadhel
Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Phenotypic Spectrum. Genes 12 (2) (2021)
Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo-Ngongang, Kalinka Popel, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Edmond Wonkam-Tingang, Carmen de Kock, Collet Dandara, Suzanne M Leal, Ambroise Wonkam
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes 12 (11) (2021)
Ashfaq Ur Rehman, Guodong Zhen, Bozitao Zhong, Duan Ni, Jiayi Li, Abdul Nasir, Moustafa T Gabr, Humaira Rafiq, Abdul Wadood, Shaoyong Lu, Jian Zhang, Hai-Feng Chen
Mechanism of zinc ejection by disulfiram in nonstructural protein 5A. Physical chemistry chemical physics : PCCP 23 (21) (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Samuel Mawuli Adadey, Shaheen Mowla, Suzanne M Leal, Ambroise Wonkam
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment. Genes 11 (11) (2020)
Sulaiman Shams, Nazia Imran, Sahib Gul Afridi, Muhammad Ayaz, Atif Ali Khan Khalil, Abdul Nasir
In vitro differentiation effect of CCL4-induced liver injured mice serum on bone marrow-derived mesenchymal stem cells toward hepatocytes like cells. Cell and tissue banking 22 (2) (2020)
Abdul Nasir, Mushtaq Khan, Zainab Rehman, Atif Ali Khan Khalil, Saira Farman, Naeema Begum, Muhammad Irfan, Wasim Sajjad, Zahida Parveen
Evaluation of Alpha-Amylase Inhibitory, Antioxidant, and Antimicrobial Potential and Phytochemical Contents of Polygonum hydropiper L. Plants (Basel, Switzerland) 9 (7) (2020)
Isabelle Schrauwen, Khurram Liaqat, Isabelle Schatteman, Thashi Bharadwaj, Abdul Nasir, Anushree Acharya, Wasim Ahmad, Guy Van Camp, Suzanne M Leal
Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment. Genes 11 (6) (2020)
Isabelle Schrauwen, Béla I Melegh, Imen Chakchouk, Anushree Acharya, Abdul Nasir, Alexis Poston, Diana M Cornejo-Sanchez, Zsolt Szabo, Tamás Karosi, Judit Bene, Béla Melegh, Suzanne M Leal
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. European journal of human genetics : EJHG 27 (6) (2019)
Muhammad Shakil, Gaurav V Harlalka, Shamshad Ali, Siying Lin, Ilaria D'Atri, Shabbir Hussain, Abdul Nasir, Muhammad Aiman Shahzad, Muhammad Ikram Ullah, Jay E Self, Emma L Baple, Andrew H Crosby, Saqib Mahmood
Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families. Eye (London, England) 33 (8) (2019)
Khurram Liaqat, Shabir Hussain, Muhammad Bilal, Abdul Nasir, Anushree Acharya, Raja Hussain Ali, Shoaib Nawaz, Muhammad Umair, Isabelle Schrauwen, Wasim Ahmad, Suzanne M Leal
Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment. Journal of human genetics 65 (2) (2019)
Farooq Ahmad, Abdul Nasir, Holger Thiele, Muhammad Umair, Guntram Borck, Wasim Ahmad
A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndrome. Annals of human genetics 82 (4) (2018)
Khurram Liaqat, Isabelle Schrauwen, Syed Irfan Raza, Kwanghyuk Lee, Shabir Hussain, Imen Chakchouk, Abdul Nasir, Anushree Acharya, Izoduwa Abbe, Muhammad Umair, Muhammad Ansar, Irfan Ullah, Khadim Shah, null null, Michael J Bamshad, Deborah A Nickerson, Wasim Ahmad, Suzanne M Leal
Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance. Journal of human genetics 64 (2) (2018)
Ye Seop Park, Un Jong Choi, Nguyen Hoai Nam, Sang Jin Choi, Abdul Nasir, Sun-Gu Lee, Kyung Jin Kim, Gyoo Yeol Jung, Sangdun Choi, Jeung Yeop Shim, Sunghoon Park, Tae Hyeon Yoo
Engineering an aldehyde dehydrogenase toward its substrates, 3-hydroxypropanal and NAD+, for enhancing the production of 3-hydroxypropionic acid. Scientific reports 7 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Abdul Nasir