Nada Al-Tassan

Nada Al-Tassan

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Nada Al-Tassan

Nada Al-Tassan

Publications by authors named "Nada Al-Tassan"

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58Publications

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Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

Nat Commun 2019 05 14;10(1):2154. Epub 2019 May 14.

Colon Cancer Genetics Group, Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, EH4 2XU, UK.

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http://www.nature.com/articles/s41467-019-09775-w
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http://dx.doi.org/10.1038/s41467-019-09775-wDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6517433PMC
May 2019

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

Genetic Study of Alzheimer's Disease in Saudi Population.

J Alzheimers Dis 2019 ;67(1):231-242

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia.

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http://dx.doi.org/10.3233/JAD-180415DOI Listing
January 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

Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden.

Genet Med 2016 12 28;18(12):1244-1249. Epub 2016 Apr 28.

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

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http://dx.doi.org/10.1038/gim.2016.37DOI Listing
December 2016

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

Homozygosity analysis in subjects with autistic spectrum disorder.

Mol Med Rep 2015 Aug 22;12(2):2307-12. Epub 2015 Apr 22.

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/10.3892/mmr.2015.3663DOI Listing
August 2015

A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24.

Dis Markers 2014 26;2014:291419. Epub 2014 Jun 26.

Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia ; Cardiovascular and Pharmacogenomics Unit, MBC-03-05, Genetics Department, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1155/2014/291419DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4098619PMC
April 2015

Screening for Mutations in ABCC8 and KCNJ11 Genes in Saudi Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI) Patients.

Genes (Basel) 2015 Apr 13;6(2):206-15. Epub 2015 Apr 13.

College of Medicine, Alfaisal University, P.O. Box 50297, Riyadh 11533, Saudi Arabia.

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http://dx.doi.org/10.3390/genes6020206DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488661PMC
April 2015

ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population.

Eur J Med Genet 2014 May-Jun;57(6):253-8. Epub 2014 Apr 21.

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

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http://dx.doi.org/10.1016/j.ejmg.2014.04.004DOI Listing
February 2015

Association of a mutation in LACC1 with a monogenic form of systemic juvenile idiopathic arthritis.

Arthritis Rheumatol 2015 Jan;67(1):288-95

King Faisal Specialist Hospital and Research Centre, and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/art.38877DOI Listing
January 2015

Recessive mutations in COL25A1 are a cause of congenital cranial dysinnervation disorder.

Am J Hum Genet 2015 Jan 11;96(1):147-52. Epub 2014 Dec 11.

Department of Genetics, Research Center, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.11.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289688PMC
January 2015

DNA Repair Genes XRCC1, XRCC3, XPD, and OGG1 Polymorphisms among the Central Region Population of Saudi Arabia.

Biol Res 2013 ;46(2):161-7

Genome Research Chair, Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.4067/S0716-97602013000200007DOI Listing
October 2014

A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits.

Gene 2014 Jul 28;544(2):152-8. Epub 2014 Apr 28.

Genetics Department, King Faisal Specialist Hospital and Research Centre, P. O. Box 3354, Riyadh 11211, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2014.04.064DOI Listing
July 2014

A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders.

Hum Genomics 2013 Dec 12;7:25. Epub 2013 Dec 12.

Genetics Department, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1186/1479-7364-7-25DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899629PMC
December 2013

Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes.

J Clin Endocrinol Metab 2013 May 26;98(5):E943-53. Epub 2013 Mar 26.

Harvard Reproductive Endocrine Sciences Center and the Reproductive Endocrine Unit of the Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.

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http://dx.doi.org/10.1210/jc.2012-4116DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644607PMC
May 2013

A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia.

Hum Mutat 2012 Feb 8;33(2):351-4. Epub 2011 Dec 8.

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

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http://dx.doi.org/10.1002/humu.21650DOI Listing
February 2012

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

Prolonged pursuit by optokinetic drum testing in asymptomatic female carriers of novel FRMD7 splice mutation c.1050 +5 G>A.

Arch Ophthalmol 2011 Jul;129(7):936-40

Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh 11462, Saudi Arabia.

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http://dx.doi.org/10.1001/archophthalmol.2011.166DOI Listing
July 2011

Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3).

Mol Vis 2011 Apr 19;17:971-6. Epub 2011 Apr 19.

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

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084218PMC
April 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

Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.

Mol Vis 2011 Jan 20;17:218-24. Epub 2011 Jan 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/PMC3025099PMC
January 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

Synergistic divergence: a distinct ocular motility dysinnervation pattern.

Invest Ophthalmol Vis Sci 2009 Nov 2;50(11):5213-6. Epub 2009 Jul 2.

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

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http://dx.doi.org/10.1167/iovs.08-2928DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787189PMC
November 2009

Bilateral synergistic convergence associated with homozygous ROB03 mutation (p.Pro771Leu).

Ophthalmology 2008 Dec;115(12):2262-5

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

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http://dx.doi.org/10.1016/j.ophtha.2008.08.010DOI Listing
December 2008

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

Inherited variants in MYH are unlikely to contribute to the risk of lung carcinoma.

Hum Genet 2004 Jan 25;114(2):207-10. Epub 2003 Oct 25.

Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, Wales, UK.

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http://link.springer.com/10.1007/s00439-003-1033-2
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http://dx.doi.org/10.1007/s00439-003-1033-2DOI Listing
January 2004

Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.

Nat Genet 2002 Feb 30;30(2):227-32. Epub 2002 Jan 30.

Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff, CF14 4XN, UK.

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http://www.nature.com/articles/ng828
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http://dx.doi.org/10.1038/ng828DOI Listing
February 2002

Different combinations of biallelic APC mutation confer different growth advantages in colorectal tumours.

Cancer Res 2002 Jan;62(2):363-6

Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff CF14 4XN, United Kingdom.

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January 2002