Publications by authors named "Ali Muhammad Waryah"

10Publications

MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study.

Authors:
Feriha Fatima Khidri Yar Muhammad Waryah Faiza Kamran Ali Hina Shaikh Ikram Din Ujjan Ali Muhammad Waryah

BMC Med Genet 2019 10 23;20(1):163. Epub 2019 Oct 23.

Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.

View Article and Find Full Text PDF
October 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.

View Article and Find Full Text PDF
July 2019

Two novel variants in gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients.

Authors:
Yar Muhammad Waryah Muhammad Iqbal Shakeel Ahmed Sheikh Muhammad Azhar Baig Ashok Kumar Narsani Muhammad Atif Munir Ahmad Bhinder Attiq Ur Rahman Azam Iqbal Memon Muhammad Suleman Pirzado Ali Muhammad Waryah

Int J Ophthalmol 2019 18;12(1):8-15. Epub 2019 Jan 18.

Molecular Biology and Genetics Department, Liaquat University of Medical and Health Sciences, Jamshoro, Sindh 76090, Pakistan.

View Article and Find Full Text PDF
January 2019

Discriminating power of rapidly mutating Y-STRs in deep rooted endogamous pedigrees from Sindhi population of Pakistan.

Authors:
Allah Rakha Yu Na Oh Hwan Young Lee Safdar Hussain Ali Muhammad Waryah Atif Adnan Kyoung-Jin Shin

Leg Med (Tokyo) 2018 Sep 4;34:17-20. Epub 2018 Aug 4.

Department of Forensic Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

View Article and Find Full Text PDF
September 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.

View Article and Find Full Text PDF
June 2018

IL28B rs12980275 polymorphism shows association with response to treatment in Pakistani patients with chronic hepatitis C.

Authors:
Naila Shaikh Ali Muhammad Waryah Bikha Ram Devrajani Muhammad Irfan Rajput Atif Sitwat Hayat Samiullah Shaikh

J Med Virol 2015 May 4;87(5):814-20. Epub 2015 Feb 4.

Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro; Department of Pathology, Liaquat University of Medical and Health Sciences, Jamshoro.

View Article and Find Full Text PDF
May 2015

Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.

Authors:
Shakeel Ahmed Sheikh Ali Muhammad Waryah Ashok Kumar Narsani Hina Shaikh Imtiaz Ahmed Gilal Khairuddin Shah Muhammad Qasim Azam Iqbal Memon Pitambar Kewalramani Naila Shaikh

Mol Vis 2014 7;20:991-1001. Epub 2014 Jul 7.

Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan ; Department of Pathology, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.

View Article and Find Full Text PDF
September 2014

The novel heterozygous Thr377Arg MYOC mutation causes severe Juvenile Open Angle Glaucoma in a large Pakistani family.

Authors:
Ali Muhammad Waryah Ashok Kumar Narsani Shakeel Ahmad Sheikh Hina Shaikh Muhammad Yaqoob Shahani

Gene 2013 Oct 23;528(2):356-9. Epub 2013 Jul 23.

Molecular Biology & Genetics Department, Medical Research Center, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan.

View Article and Find Full Text PDF
October 2013

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

Authors:
Zafar Iqbal Geert Vandeweyer Monique van der Voet Ali Muhammad Waryah Muhammad Yasir Zahoor Judith A Besseling Laura Tomas Roca Anneke T Vulto-van Silfhout Bonnie Nijhof Jamie M Kramer Nathalie Van der Aa Muhammad Ansar Hilde Peeters Céline Helsmoortel Christian Gilissen Lisenka E L M Vissers Joris A Veltman Arjan P M de Brouwer R Frank Kooy Sheikh Riazuddin Annette Schenck Hans van Bokhoven Liesbeth Rooms

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.

View Article and Find Full Text PDF
May 2013

Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.

Authors:
Nevra Nal Zubair M Ahmed Engin Erkal Ozgül M Alper Güven Lüleci Oktay Dinç Ali Muhammad Waryah Quratul Ain Saba Tasneem Tayyab Husnain Parna Chattaraj Saima Riazuddin Erich Boger Manju Ghosh Madhulika Kabra Sheikh Riazuddin Robert J Morell Thomas B Friedman

Hum Mutat 2007 Oct;28(10):1014-9

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville 20850, Maryland, USA.

View Article and Find Full Text PDF
October 2007