Takip et
Nada AL TASSAN
Nada AL TASSAN
Senior Scientist, King Faisal Specialist Hospital and Research Center
kfshrc.edu.sa üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
N Al-Tassan, NH Chmiel, J Maynard, N Fleming, AL Livingston, ...
Nature genetics 30 (2), 227-232, 2002
16772002
Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature
J Morales, L Al-Sharif, DS Khalil, JMA Shinwari, P Bavi, RA Al-Mahrouqi, ...
The American Journal of Human Genetics 85 (5), 558-568, 2009
2492009
Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.
Mol Psychiatry 22 (4), 615-624, 2017
2222017
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
PJ Law, M Timofeeva, C Fernandez-Rozadilla, P Broderick, J Studd, ...
Nature communications 10 (1), 2154, 2019
2052019
Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes
FA Costa-Barbosa, R Balasubramanian, KW Keefe, ND Shaw, ...
The Journal of Clinical Endocrinology & Metabolism 98 (5), E943-E953, 2013
1862013
Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q
H Lamlum, N Al Tassan, E Jaeger, I Frayling, O Sieber, FB Reza, M Eckert, ...
Human Molecular Genetics 9 (15), 2215-2221, 2000
1672000
Expanding the genetic heterogeneity of intellectual disability
S Anazi, S Maddirevula, V Salpietro, YT Asi, S Alsahli, A Alhashem, ...
Human genetics 136, 1419-1429, 2017
1502017
Characterizing the morbid genome of ciliopathies
R Shaheen, K Szymanska, B Basu, N Patel, N Ewida, E Faqeih, ...
Genome biology 17, 1-11, 2016
1502016
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer
NA Al-Tassan, N Whiffin, FJ Hosking, C Palles, SM Farrington, ...
Scientific reports 5 (1), 10442, 2015
1412015
Comprehensive gene panels provide advantages over clinical exome sequencing for Mendelian diseases
Saudi Mendeliome Group falkuaya@ kfshrc. edu. sa
Genome biology 16, 1-14, 2015
1382015
Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis
SM Wakil, DM Monies, M Abouelhoda, N Al‐Tassan, H Al‐Dusery, ...
Arthritis & rheumatology 67 (1), 288-295, 2015
1302015
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases
H Al-Mousa, M Abouelhoda, DM Monies, N Al-Tassan, A Al-Ghonaium, ...
Journal of Allergy and Clinical Immunology 137 (6), 1780-1787, 2016
1292016
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies
N Patel, MA Aldahmesh, H Alkuraya, S Anazi, H Alsharif, AO Khan, ...
Genetics in Medicine 18 (6), 554-562, 2016
1072016
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
M Abouelhoda, T Sobahy, M El-Kalioby, N Patel, H Shamseldin, D Monies, ...
Genetics in Medicine 18 (12), 1244-1249, 2016
1012016
Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis
S May-Wilson, A Sud, PJ Law, K Palin, S Tuupanen, A Gylfe, ...
European Journal of Cancer 84, 228-238, 2017
1002017
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families
B Al-Mubarak, M Abouelhoda, A Omar, H AlDhalaan, M Aldosari, ...
Scientific reports 7 (1), 5679, 2017
952017
Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer
H Rodriguez‐Broadbent, PJ Law, A Sud, K Palin, S Tuupanen, A Gylfe, ...
International journal of cancer 140 (12), 2701-2708, 2017
852017
9 Interleukin 17A and F and Asthma in Saudi Arabia: Gene Polymorphisms and Protein Levels
MD Bazzi, MA Sultan, N Al Tassan, M Alanazi, A Al-Amri, MS Al-Hajjaj, ...
Journal of Investigational Allergology and Clinical Immunology 21 (7), 551, 2011
772011
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency
R Balasubramanian, JH Choi, L Francescatto, J Willer, ER Horton, ...
Proceedings of the National Academy of Sciences 111 (50), 17953-17958, 2014
742014
Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer
D Jarvis, JS Mitchell, PJ Law, K Palin, S Tuupanen, A Gylfe, UA Hänninen, ...
British journal of cancer 115 (2), 266-272, 2016
712016
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20