Rehan S Shaikh

Rehan S Shaikh

UNVERIFIED PROFILE

Are you Rehan S Shaikh?   Register this Author

Register author
Rehan S Shaikh

Rehan S Shaikh

Publications by authors named "Rehan S Shaikh"

Are you Rehan S Shaikh?   Register this Author

15Publications

363Reads

14Profile Views

A simple method for preparing ultra-light graphene aerogel for rapid removal of U(VI) from aqueous solution.

Environ Pollut 2019 Aug 9;251:547-554. Epub 2019 May 9.

Key Laboratory of Photovoltaic and Energy Conservation Materials, Institute of Plasma Physics, Chinese Academy of Sciences, P.O. Box 1126, Hefei, 230031, Anhui, PR China; NAAM Research Group, Faculty of Science, King Abdulaziz University, Jeddah, 21589, Saudi Arabia. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.envpol.2019.05.011DOI Listing
August 2019

FUT2 Variants Confer Susceptibility to Familial Otitis Media.

Am J Hum Genet 2018 11 25;103(5):679-690. Epub 2018 Oct 25.

Department of Otorhinolaryngology, Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, MD 21201, USA.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S00029297183032
Publisher Site
http://dx.doi.org/10.1016/j.ajhg.2018.09.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6217759PMC
November 2018

Molecular detection of Ehrlichia canis in dogs from three districts in Punjab (Pakistan).

Vet Med Sci 2018 05 7;4(2):126-132. Epub 2018 Feb 7.

Institute of Pure and Applied Biology, Zoology Division, Bahauddin Zakariya University, Multan, Pakistan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/vms3.94DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979635PMC
May 2018

Identification and clinical characterization of Hermansky-Pudlak syndrome alleles in the Pakistani population.

Pigment Cell Melanoma Res 2016 Mar 18;29(2):231-5. Epub 2015 Dec 18.

Department of Otorhinolaryngology Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1111/pcmr.12438
Publisher Site
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062593PMC
http://dx.doi.org/10.1111/pcmr.12438DOI Listing
March 2016

Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy.

Eur J Hum Genet 2015 Apr 23;23(4):473-80. Epub 2014 Jul 23.

1] Institute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, Pakistan [2] Department of Otorhinolaryngology Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/ejhg.2014.136DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666578PMC
April 2015

Association of XRCC1, XRCC3, and XPD genetic polymorphism with an increased risk of hepatocellular carcinoma because of the hepatitis B and C virus.

Eur J Gastroenterol Hepatol 2013 Feb;25(2):166-79

Institute of Molecular Biology & Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MEG.0b013e328359a775DOI Listing
February 2013

Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.

Hum Mutat 2008 Apr;29(4):502-11

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.20677DOI Listing
April 2008

A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.

Hum Genet 2005 Jan 6;116(1-2):17-22. Epub 2004 Nov 6.

National Centre of Excellence in Molecular Biology, University of the Punjab, 87-West Canal Bank Road, Thokar Niaz Baig, Lahore 53700, Pakistan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-004-1205-8DOI Listing
January 2005