Nada A Al-Tassan

Nada A Al-Tassan

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Nada A Al-Tassan

Nada A Al-Tassan

Publications by authors named "Nada A Al-Tassan"

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22Publications

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Estimating transfection efficiency in differentiated and undifferentiated neural cells.

BMC Res Notes 2019 Apr 15;12(1):225. Epub 2019 Apr 15.

Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, 11211, Saudi Arabia.

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http://dx.doi.org/10.1186/s13104-019-4249-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466792PMC
April 2019

Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder.

Psychiatr Genet 2017 08;27(4):131-138

aBehavioral Genetics Unit, Department of Genetics bDepartment of Psychiatry, King Faisal Specialist Hospital & Research Center cThe National Center for Genomic Technology, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia dDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan, USA.

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http://dx.doi.org/10.1097/YPG.0000000000000173DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495552PMC
August 2017

Exotropic Duane syndrome with synergistic divergence and no mutations in COL25A1.

J AAPOS 2016 12 20;20(6):542-544.e2. Epub 2016 Sep 20.

King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.jaapos.2016.05.019DOI Listing
December 2016

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.

BMC Res Notes 2016 Jun 7;9:295. Epub 2016 Jun 7.

Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.

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http://dx.doi.org/10.1186/s13104-016-2102-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897907PMC
June 2016

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

Authors:
Timothy H T Cheng Deborah Thompson Jodie Painter Tracy O'Mara Maggie Gorman Lynn Martin Claire Palles Angela Jones Daniel D Buchanan Aung Ko Win John Hopper Mark Jenkins Noralane M Lindor Polly A Newcomb Steve Gallinger David Conti Fred Schumacher Graham Casey Graham G Giles Paul Pharoah Julian Peto Angela Cox Anthony Swerdlow Fergus Couch Julie M Cunningham Ellen L Goode Stacey J Winham Diether Lambrechts Peter Fasching Barbara Burwinkel Hermann Brenner Hiltrud Brauch Jenny Chang-Claude Helga B Salvesen Vessela Kristensen Hatef Darabi Jingmei Li Tao Liu Annika Lindblom Per Hall Magdalena Echeverry de Polanco Monica Sans Angel Carracedo Sergi Castellvi-Bel Augusto Rojas-Martinez Samuel Aguiar Jnr Manuel R Teixeira Alison M Dunning Joe Dennis Geoffrey Otton Tony Proietto Elizabeth Holliday John Attia Katie Ashton Rodney J Scott Mark McEvoy Sean C Dowdy Brooke L Fridley Henrica M J Werner Jone Trovik Tormund S Njolstad Emma Tham Miriam Mints Ingo Runnebaum Peter Hillemanns Thilo Dörk Frederic Amant Stefanie Schrauwen Alexander Hein Matthias W Beckmann Arif Ekici Kamila Czene Alfons Meindl Manjeet K Bolla Kyriaki Michailidou Jonathan P Tyrer Qin Wang Shahana Ahmed Catherine S Healey Mitul Shah Daniela Annibali Jeroen Depreeuw Nada A Al-Tassan Rebecca Harris Brian F Meyer Nicola Whiffin Fay J Hosking Ben Kinnersley Susan M Farrington Maria Timofeeva Albert Tenesa Harry Campbell Robert W Haile Shirley Hodgson Luis Carvajal-Carmona Jeremy P Cheadle Douglas Easton Malcolm Dunlop Richard Houlston Amanda Spurdle Ian Tomlinson

Sci Rep 2015 12 1;5:17369. Epub 2015 Dec 1.

Molecular and Population Genetics Laboratory, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.

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http://dx.doi.org/10.1038/srep17369DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664893PMC
December 2015

Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome.

Mol Vis 2011 20;17:1997-2002. Epub 2011 Jul 20.

Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154136PMC
December 2011

The optic nerve head in congenital fibrosis of the extraocular muscles.

Ophthalmic Genet 2011 Sep 31;32(3):175-80. Epub 2011 Mar 31.

Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.3109/13816810.2011.567318DOI Listing
September 2011

Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia.

BMC Med Genet 2011 Feb 16;12:27. Epub 2011 Feb 16.

Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riaydh, Saudi Arabia.

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http://dx.doi.org/10.1186/1471-2350-12-27DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048493PMC
February 2011

Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles.

Ophthalmology 2010 Jan 5;117(1):154-8. Epub 2009 Nov 5.

Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia; Department of Genetics, Research Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.ophtha.2009.06.029DOI Listing
January 2010

Congential fibrosis of the extraocular muscles type I (CFEOM1) on the Arabian Peninsula.

Ophthalmic Genet 2008 Mar;29(1):25-8

Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, KSA.

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http://dx.doi.org/10.1080/13816810701850058DOI Listing
March 2008

Screening for hOGG1 S326C variant in normal Saudi population.

Saudi Med J 2007 May;28(5):802-3

Department of Biochemistry, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.

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May 2007