Publications by authors named "Muhammad Yasir Zahoor"

15Publications

Population demographic history and population structure for Pakistani Nili-Ravi breeding bulls based on SNP genotyping to identify genomic regions associated with male effects for milk yield and body weight.

Authors:

Saher Islam Umesh K Reddy Purushothaman Natarajan Venkata Lakshmi Abburi Amna Arshad Bajwa Muhammad Imran Muhammad Yasir Zahoor Muhammad Abdullah Aamir Mehmood Bukhari Sajid Iqbal Kamran Ashraf Asif Nadeem Habibur Rehman Imran Rashid Wasim Shehzad

PLoS One 2020 24;15(11):e0242500. Epub 2020 Nov 24.

Institute of Biochemistry and Biotechnology, University of Veterinary and Animal Sciences, Lahore, Pakistan.

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January 2021

Mutational spectrum of gene in Pakistani Niemann-Pick disease patients.

Authors:

Huma Arshad Cheema Iqra Ghulam Rasool Muhammad Nadeem Anjum Muhammad Yasir Zahoor

Pak J Med Sci 2020 Mar-Apr;36(3):479-484

Dr. Muhammad Yasir Zahoor, PhD. Institute of Biochemistry & Biotechnology, University of Veterinary & Animal Sciences, Lahore, Pakistan.

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April 2020

Genetic Analysis of Tyrosinemia Type 1 and Fructose-1, 6 Bisphosphatase Deficiency Affected in Pakistani Cohorts.

Authors:

Muhammad Yasir Zahoor Huma Arshad Cheema Sadaqat Ijaz Zafar Fayyaz

Fetal Pediatr Pathol 2020 Oct 4;39(5):430-440. Epub 2019 Oct 4.

Department of Pediatric Gastroenterology and Hepatology, Children's Hospital and Institute of Child Health, Lahore, Pakistan.

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October 2020

Mapping of IDUA gene variants in Pakistani patients with mucopolysaccharidosis type 1.

Authors:

Muhammad Yasir Zahoor Huma Arshad Cheema Sadaqat Ijaz Muhammad Nadeem Anjum Khushnooda Ramzan Munir Ahmad Bhinder

J Pediatr Endocrinol Metab 2019 Nov;32(11):1221-1227

Department of Human Genetics and Molecular Biology, University of Health Sciences, Lahore, Pakistan.

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November 2019

Consanguinity: A blessing or menace at population level?

Authors:

Munir Ahmad Bhinder Haleema Sadia Nasir Mahmood Muhammad Qasim Zawar Hussain Muhammad Mudassar Rashid Muhammad Yasir Zahoor Rashid Bhatti Wasim Shehzad Ali Muhammad Waryah Shah Jahan

Ann Hum Genet 2019 07 19;83(4):214-219. Epub 2019 Mar 19.

University of Health Sciences, Lahore, 54600, Pakistan.

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July 2019

Seroprevalence of Bluetongue virus in small and large ruminants in Punjab province, Pakistan.

Authors:

Tayyebah Sohail Tahir Yaqub Tariq Abbas Masood Rabbani Jawad Nazir Syeda Marriam Maqbool Saima Yaqub Momena Habib Aziz Ul-Rahman Nadia Mukhtar Muhammad Shahbaz Muhammad Yasir Zahoor Muhammad Zubair Shabbir

Acta Trop 2019 Jan 24;189:22-29. Epub 2018 Sep 24.

University of Veterinary and Animal Sciences, Lahore 54600, Pakistan. Electronic address:

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January 2019

Cloning and Expression of NS3 Gene of Pakistani Isolate Type 2 Dengue Virus.

Authors:

Farkhanda Yasmin Tahir Yaqub Muhammad Idrees Wasim Shahzad Abu Saeed Hashmi Kiran Aqil Nadia Mukhtar Muhammad Yasir Zahoor Naeem Akhtar Sajid Umar

J Vet Res 2018 Mar 30;62(1):17-26. Epub 2018 Mar 30.

Pir Mehr Ali Shah Arid Agriculture University, 46000, Rawalpindi, Pakistan.

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March 2018

SE33 locus as a reliable genetic marker for forensic DNA analysis systems

Authors:

Munir Ahmad Bhinder Muhammad Yasir Zahoor Haleema Sadia Muhammad Qasim Rukhsana Perveen Ghulam Murtaza Anjum Muhammad Iqbal Najeeb Ullah Wasim Shehzad Muhammad Tariq Ali Muhammad Waryah

Turk J Med Sci 2018 Jun 14;48(3):611-614. Epub 2018 Jun 14.

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June 2018

Genetic analysis of fructose-1,6-bisphosphatase (FBPase) deficiency in nine consanguineous Pakistani families.

Authors:

Sadaqat Ijaz Muhammad Yasir Zahoor Muhammad Imran Khushnooda Ramzan Munir Ahmad Bhinder Hussain Shakeel Muhammad Iqbal Asim Aslam Wasim Shehzad Huma Arshad Cheema Habib Rehman

J Pediatr Endocrinol Metab 2017 Oct;30(11):1203-1210

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October 2017

Junctional Epidermolysis Bullosa (Non-Herlitz Type).

Authors:

Munir Ahmad Bhinder Muhammad Waqar Arshad Muhammad Yasir Zahoor Wasim Shehzad Muhammad Tariq Muhammad Imran Shabbir

J Coll Physicians Surg Pak 2017 May;27(5):308-310

Department of Bioinformatics and Biotechnology, International Islamic University, Islamabad. Pakistan.

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May 2017

Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutation.

Authors:

Sadaqat Ijaz Muhammad Yasir Zahoor Muhammad Imran Sibtain Afzal Munir A Bhinder Ihsan Ullah Huma Arshad Cheema Khushnooda Ramzan Wasim Shehzad

J Pediatr Endocrinol Metab 2016 Mar;29(3):327-32

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March 2016

Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration.

Authors:

Zafar Iqbal Lucia Püttmann Luciana Musante Attia Razzaq Muhammad Yasir Zahoor Hao Hu Thomas F Wienker Masoud Garshasbi Zohreh Fattahi Christian Gilissen Lisenka E L M Vissers Arjan P M de Brouwer Joris A Veltman Rolph Pfundt Hossein Najmabadi Hans-Hilger Ropers Sheikh Riazuddin Kimia Kahrizi Hans van Bokhoven

Eur J Hum Genet 2016 Mar 15;24(3):392-9. Epub 2015 Jul 15.

Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

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March 2016

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.

Hum Mol Genet 2013 May 5;22(10):1960-70. Epub 2013 Feb 5.

Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Donders Institute for Brain, Cognitionand Behaviour, Radboud University Medical Centre, Nijmegen, TheNetherlands.

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May 2013

A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype.

Authors:

Zafar Iqbal Mohsin Shahzad Lisenka E L M Vissers Monique van Scherpenzeel Christian Gilissen Attia Razzaq Muhammad Yasir Zahoor Shaheen N Khan Tjitske Kleefstra Joris A Veltman Arjan P M de Brouwer Dirk J Lefeber Hans van Bokhoven Sheikh Riazuddin

Eur J Hum Genet 2013 Aug 19;21(8):844-9. Epub 2012 Dec 19.

Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.

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August 2013

Targeted next generation sequencing reveals a novel intragenic deletion of the TPO gene in a family with intellectual disability.

Authors:

Zafar Iqbal Kornelia Neveling Attia Razzaq Mohsin Shahzad Muhammad Yasir Zahoor Muhammad Qasim Christian Gilissen Nienke Wieskamp Michael P Kwint Sabine Gijsen Arjan P M de Brouwer Joris A Veltman Sheikh Riazuddin Hans van Bokhoven

Arch Med Res 2012 May 3;43(4):312-6. Epub 2012 Mar 3.

Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, The Netherlands.

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May 2012