Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer
Rodriguez‐Broadbent, Henry, Law, Philip J., Sud, Amit, Palin, Kimmo, Tuupanen, Sari, Gylfe, Alexandra, Hänninen, Ulrika A., Cajuso, Tatiana, Tanskanen, Tomas, Kondelin, Johanna, Kaasinen, Eevi, Sarin, Antti‐Pekka, Ripatti, Samuli, Eriksson, Johan G., Rissanen, Harri, Knekt, Paul, Pukkala, Eero, Jousilahti, Pekka, Salomaa, Veikko, Palotie, Aarno, Renkonen‐Sinisalo, Laura, Lepistö, Anna, Böhm, Jan, Mecklin, Jukka‐Pekka, Al‐Tassan, Nada A., Palles, Claire, Martin, Lynn, Barclay, Ella, Farrington, Susan M., Timofeeva, Maria N., Meyer, Brian F., Wakil, Salma M., Campbell, Harry, Smith, Christopher G., Idziaszczyk, Shelley, Maughan, Timothy S., Kaplan, Richard, Kerr, Rachel, Kerr, David, Passarelli, Michael N., Figueiredo, Jane C., Buchanan, Daniel D., Win, Aung K., Hopper, John L., Jenkins, Mark A., Lindor, Noralane M., Newcomb, Polly A., Gallinger, Steven, Conti, David, Schumacher, Fred, Casey, Graham, Aaltonen, Lauri A., Cheadle, Jeremy P., Tomlinson, Ian P., Dunlop, Malcolm G., Houlston, Richard S.
Published in International journal of cancer (15.06.2017)
Published in International journal of cancer (15.06.2017)
Get full text
Journal Article
Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand‐foot syndrome
Watts, Katie, Wills, Christopher, Madi, Ayman, Palles, Claire, Maughan, Timothy S., Kaplan, Richard, Al‐Tassan, Nada A., Kerr, Rachel, Kerr, David J., Houlston, Richard S., Escott‐Price, Valentina, Cheadle, Jeremy P.
Published in International journal of cancer (15.09.2022)
Published in International journal of cancer (15.09.2022)
Get full text
Journal Article
Genome‐wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer
Watts, Katie, Wills, Christopher, Madi, Ayman, Palles, Claire, Maughan, Timothy S., Kaplan, Richard, Al‐Tassan, Nada A., Kerr, Rachel, Kerr, David, Gray, Victoria, West, Hannah, Houlston, Richard S., Escott‐Price, Valentina, Cheadle, Jeremy P.
Published in International journal of cancer (01.11.2021)
Published in International journal of cancer (01.11.2021)
Get full text
Journal Article
Germline variation in RASAL2 may predict survival in patients with RAS‐activated colorectal cancer
Wills, Christopher, Watts, Katie, Maughan, Timothy S., Fisher, David, Al‐Tassan, Nada A., Houlston, Richard S., Escott‐Price, Valentina, Cheadle, Jeremy P.
Published in Genes chromosomes & cancer (01.06.2023)
Published in Genes chromosomes & cancer (01.06.2023)
Get full text
Journal Article
Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder
Shinwari, Jameela M.A., Khan, Arif, Awad, Salma, Shinwari, Zakia, Alaiya, Ayodele, Alanazi, Mohamad, Tahir, Asma, Poizat, Coralie, Al Tassan, Nada
Published in American journal of human genetics (08.01.2015)
Published in American journal of human genetics (08.01.2015)
Get full text
Journal Article
Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature
Morales, Jose, Al-Sharif, Latifa, Khalil, Dania S., Shinwari, Jameela M.A., Bavi, Prashant, Al-Mahrouqi, Rahima A., Al-Rajhi, Ali, Alkuraya, Fowzan S., Meyer, Brian F., Al Tassan, Nada
Published in American journal of human genetics (13.11.2009)
Published in American journal of human genetics (13.11.2009)
Get full text
Journal Article
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency
Balasubramanian, Ravikumar, Choi, Jin-Ho, Francescatto, Ludmila, Willer, Jason, Horton, Edward R., Asimacopoulos, Eleni P., Stankovic, Konstantina M., Plummer, Lacey, Buck, Cassandra L., Quinton, Richard, Nebesio, Todd D., Mericq, Veronica, Merino, Paulina M., Meyer, Brian F., Monies, Dorota, Gusella, James F., Tassan, Nada Al, Katsanis, Nicholas, Crowley, William F.
Published in Proceedings of the National Academy of Sciences - PNAS (16.12.2014)
Published in Proceedings of the National Academy of Sciences - PNAS (16.12.2014)
Get full text
Journal Article
Parkinson's Disease in Saudi Patients: A Genetic Study
Al-Mubarak, Bashayer R, Bohlega, Saeed A, Alkhairallah, Thamer S, Magrashi, Amna I, AlTurki, Maha I, Khalil, Dania S, AlAbdulaziz, Basma S, Abou Al-Shaar, Hussam, Mustafa, Abeer E, Alyemni, Eman A, Alsaffar, Bashayer A, Tahir, Asma I, Al Tassan, Nada A
Published in PloS one (14.08.2015)
Published in PloS one (14.08.2015)
Get full text
Journal Article
A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders
El Bitar, Fadia, Al Sudairy, Nourah, Qadi, Najeeb, Al Rajeh, Saad, Alghamdi, Fatimah, Al Amari, Hala, Al Dawsari, Ghadeer, Alsubaie, Sahar, Al Sudairi, Mishael, Abdulaziz, Sara, Al Tassan, Nada
Published in Current Alzheimer research (01.01.2020)
Published in Current Alzheimer research (01.01.2020)
Get more information
Journal Article
Molecular classification of blood and bleeding disorder genes
Baz, Batoul, Abouelhoda, Mohamed, Owaidah, Tarek, Dasouki, Majed, Monies, Dorota, Al Tassan, Nada
Published in Npj genomic medicine (16.07.2021)
Published in Npj genomic medicine (16.07.2021)
Get full text
Journal Article
Exotropic Duane syndrome with synergistic divergence and no mutations in COL25A1
Khan, Arif O., MD, Shinwari, Jameela M., Bsc, Al-Tassan, Nada A., PhD
Published in Journal of AAPOS (01.12.2016)
Published in Journal of AAPOS (01.12.2016)
Get full text
Journal Article
Estimating transfection efficiency in differentiated and undifferentiated neural cells
Alabdullah, Abeer A, Al-Abdulaziz, Basma, Alsalem, Hanan, Magrashi, Amna, Pulicat, Subramanian M, Almzroua, Amer A, Almohanna, Falah, Assiri, Abdullah Mohamed, Al Tassan, Nada A, Al-Mubarak, Bashayer R
Published in BMC research notes (15.04.2019)
Published in BMC research notes (15.04.2019)
Get full text
Journal Article
A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24
Wakil, Salma M., Muiya, Nzioka P., Tahir, Asma I., al-Najai, Mohammed, Baz, Batoul, Andres, Editha, Mazhar, Nejat, al-Tassan, Nada, Alshahid, Maie, Meyer, Brian F., Dzimiri, Nduna
Published in Disease markers (01.01.2014)
Published in Disease markers (01.01.2014)
Get full text
Journal Article
Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients
Owaidah, Tarek, Saleh, Mahasen, Baz, Batoul, Abdulaziz, Basma, Alzahrani, Hazza, Tarawah, Ahmed, Almusa, Abdulrahman, AlNounou, Randa, AbaAlkhail, Hala, Al-Numair, Nouf, Altahan, Rahaf, Abouelhoda, Mohammed, Alamoudi, Thamer, Monies, Dorota, Jabaan, Amjad, Al Tassan, Nada
Published in Npj genomic medicine (14.02.2019)
Published in Npj genomic medicine (14.02.2019)
Get full text
Journal Article
Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection
Mustafa, Abeer, Faquih, Tariq, Baz, Batoul, Kattan, Rana, Al-Issa, Abdulelah, Tahir, Asma, Imtiaz, Faiqa, Ramzan, Khushnooda, Al-Sayed, Moeenaldeen, Alowain, Mohammed, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Abouelhoda, Mohamed, Al-Mubarak, Bashayer, Al Tassan, Nada
Published in Genes (22.05.2018)
Published in Genes (22.05.2018)
Get full text
Journal Article
DNA Repair Genes XRCC1, XRCC3, XPD, and OGG1 Polymorphisms among the Central Region Population of Saudi Arabia
Alanazi, Mohammad, Pathan, Akbar Ali Khan, Ajaj, Sana Abdulla, Khan, Wajahatullah, Shaik, Jilani P, Al Tassan, Nada, Parine, Narasimha Reddy
Published in Biological research (2013)
Published in Biological research (2013)
Get full text
Journal Article
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
Bohlega, Saeed A, Al-Mubarak, Bashayer R, Alyemni, Eman A, Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer E, Khalil, Dania S, Al Haibi, Sara, Abou Al-Shaar, Hussam, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma I, Al Tassan, Nada A
Published in BMC research notes (07.06.2016)
Published in BMC research notes (07.06.2016)
Get full text
Journal Article
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden
Abouelhoda, Mohamed, Sobahy, Turki, El-Kalioby, Mohamed, Patel, Nisha, Shamseldin, Hanan, Monies, Dorota, Al-Tassan, Nada, Ramzan, Khushnooda, Imtiaz, Faiqa, Shaheen, Ranad, Alkuraya, Fowzan S.
Published in Genetics in medicine (01.12.2016)
Published in Genetics in medicine (01.12.2016)
Get full text
Journal Article
Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis
Wakil, Salma M., Monies, Dorota M., Abouelhoda, Mohamed, Al‐Tassan, Nada, Al‐Dusery, Haya, Naim, Ewa A., Al‐Younes, Banan, Shinwari, Jameela, Al‐Mohanna, Futwan A., Meyer, Brian F., Al‐Mayouf, Sulaiman
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.01.2015)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.01.2015)
Get full text
Journal Article