Recent advances and future directions for the pharmacogenetic basis of anti-VEGF treatment response in neovascular age-related macular degeneration

por Riaz, Moeen, Baird, Paul N.
Publicado 2017

The genetic spectrum of familial hypercholesterolemia in Pakistan

por Ahmed, Waqas, Whittall, Ros, Riaz, Moeen, Ajmal, Muhammad, Sadeque, Ahmed, Ayub, Humaira, Qamar, Raheel, Humphries, Steve E.
Publicado 2013

Genetic discrimination by Australian insurance companies: a survey of consumer experiences

por Tiller, Jane, Morris, Susan, Rice, Toni, Barter, Krystal, Riaz, Moeen, Keogh, Louise, Delatycki, Martin B., Otlowski, Margaret, Lacaze, Paul
Publicado 2019

A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease

por Waheed, Nadia K., Qavi, Ahmed H., Malik, Sarah N., Maria, Maleeha, Riaz, Moeen, Cremers, Frans P. M., Azam, Maleeha, Qamar, Raheel
Publicado 2012

A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells

por Riaz, Moeen, Mattisson, Jonas, Polekhina, Galina, Bakshi, Andrew, Halvardson, Jonatan, Danielsson, Marcus, Ameur, Adam, McNeil, John, Forsberg, Lars A., Lacaze, Paul
Publicado 2021

Genomic Risk Score for Advanced Osteoarthritis in Older Adults

por Lacaze, Paul, Wang, Yuanyuan, Polekhina, Galina, Bakshi, Andrew, Riaz, Moeen, Owen, Alice, Franks, Angus, Abidi, Jawad, Tiller, Jane, McNeil, John, Cicuttini, Flavia
Publicado 2022

XRCC1 and XPD DNA repair gene polymorphisms: A potential risk factor for glaucoma in the Pakistani population

por Yousaf, Sajeela, Khan, Muhammad Imran, Micheal, Shazia, Akhtar, Farah, Ali, Syeda Hafiza Benish, Riaz, Moeen, Ali, Mahmood, Lall, Pramila, Waheed, Nadia Khalida, den Hollander, Anneke I., Ahmed, Asifa, Qamar, Raheel
Publicado 2011

Exome Sequencing Identifies Three Novel Candidate Genes Implicated in Intellectual Disability

por Agha, Zehra, Iqbal, Zafar, Azam, Maleeha, Ayub, Humaira, Vissers, Lisenka E. L. M., Gilissen, Christian, Ali, Syeda Hafiza Benish, Riaz, Moeen, Veltman, Joris A., Pfundt, Rolph, van Bokhoven, Hans, Qamar, Raheel
Publicado 2014

Role of ACE and PAI-1 Polymorphisms in the Development and Progression of Diabetic Retinopathy

por Saleem, Saba, Azam, Aisha, Maqsood, Sundus Ijaz, Muslim, Irfan, Bashir, Shaheena, Fazal, Nosheen, Riaz, Moeen, Ali, Syeda Hafiza Benish, Niazi, Muhammad Khizar, Ishaq, Mazhar, Waheed, Nadia Khalida, Qamar, Raheel, Azam, Maleeha
Publicado 2015

Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis

por Zhang, Lei, Bao, Yining, Riaz, Moeen, Tiller, Jane, Liew, Danny, Zhuang, Xun, Amor, David J., Huq, Aamira, Petelin, Lara, Nelson, Mark, James, Paul A., Winship, Ingrid, McNeil, John J., Lacaze, Paul
Publicado 2019

Correction: Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis

por Zhang, Lei, Bao, Yining, Riaz, Moeen, Tiller, Jane, Liew, Danny, Zhuang, Xun, Amor, David J., Huq, Aamira, Petelin, Lara, Nelson, Mark, James, Paul A., Winship, Ingrid, McNeil, John J., Lacaze, Paul
Publicado 2019

Using whole-genome sequencing to characterize clinically significant blood groups among healthy older Australians

por Jadhao, Sudhir, Davison, Candice, Roulis, Eileen V., Lee, Simon, Lacaze, Paul, Riaz, Moeen, McNeil, John J., Thomas, David M., Pecheniuk, Natalie M., Hyland, Catherine A., Flower, Robert L., Nagaraj, Shivashankar H.
Publicado 2022

Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent

por Lacaze, Paul, Sebra, Robert, Riaz, Moeen, Ingles, Jodie, Tiller, Jane, Thompson, Bryony A., James, Paul A., Fatkin, Diane, Semsarian, Christopher, Reid, Christopher M., Tonkin, Andrew M., Winship, Ingrid, Schadt, Eric, McNeil, John J.
Publicado 2021

Protective lipid-lowering variants in healthy older individuals without coronary heart disease

por Lacaze, Paul, Riaz, Moeen, Sebra, Robert, Hooper, Amanda J, Pang, Jing, Tiller, Jane, Polekhina, Galina, Tonkin, Andrew, Reid, Chris, Zoungas, Sophia, Murray, Anne M, Nicholls, Stephen, Watts, Gerald, Schadt, Eric, McNeil, John J
Publicado 2021

Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome

por Ajmal, Muhammad, Khan, Muhammad Imran, Neveling, Kornelia, Tayyab, Ali, Jaffar, Sulman, Sadeque, Ahmed, Ayub, Humaira, Abbasi, Nasir Mahmood, Riaz, Moeen, Micheal, Shazia, Gilissen, Christian, Ali, Syeda Hafiza Benish, Azam, Maleeha, Collin, Rob W. J., Cremers, Frans P. M., Qamar, Raheel
Publicado 2013

Polygenic score modifies risk for Alzheimer's disease in APOE ε4 homozygotes at phenotypic extremes

por Huq, Aamira J., Fulton‐Howard, Brian, Riaz, Moeen, Laws, Simon, Sebra, Robert, Ryan, Joanne, Renton, Alan E., Goate, Alison M., Masters, Colin L., Storey, Elsdon, Shah, Raj C., Murray, Anne, McNeil, John, Winship, Ingrid, James, Paul A., Lacaze, Paul
Publicado 2021

Effect of APOE and a polygenic risk score on incident dementia and cognitive decline in a healthy older population

por Riaz, Moeen, Huq, Aamira, Ryan, Joanne, Orchard, Suzanne G, Tiller, Jane, Lockery, Jessica, Woods, Robyn L., Wolfe, Rory, Renton, Alan E., Goate, Alison M., Sebra, Robert, Schadt, Eric, Brodtmann, Amy, Shah, Raj C., Storey, Elsdon, Murray, Anne M, McNeil, John J., Lacaze, Paul
Publicado 2021

A Polygenic Risk Score Predicts Incident Prostate Cancer Risk in Older Men but Does Not Select for Clinically Significant Disease

por Bakshi, Andrew, Riaz, Moeen, Orchard, Suzanne G., Carr, Prudence R., Joshi, Amit D., Cao, Yin, Rebello, Richard, Nguyen-Dumont, Tú, Southey, Melissa C., Millar, Jeremy L., Gately, Lucy, Gibbs, Peter, Ford, Leslie G., Parnes, Howard L., Chan, Andrew T., McNeil, John J., Lacaze, Paul
Publicado 2021

Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer

por Nguyen-Dumont, Tú, Dowty, James G., MacInnis, Robert J., Steen, Jason A., Riaz, Moeen, Dugué, Pierre-Antoine, Renault, Anne-Laure, Hammet, Fleur, Mahmoodi, Maryam, Theys, Derrick, Tsimiklis, Helen, Severi, Gianluca, Bolton, Damien, Lacaze, Paul, Sebra, Robert, Schadt, Eric, McNeil, John, Giles, Graham G., Milne, Roger L., Southey, Melissa C.
Publicado 2021

GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration

por Riaz, Moeen, Lorés-Motta, Laura, Richardson, Andrea J., Lu, Yi, Montgomery, Grant, Omar, Amer, Koenekoop, Robert K., Chen, John, Muether, Philipp, Altay, Lebriz, Schick, Tina, Fauser, Sascha, Smailhodzic, Dzenita, van Asten, Freekje, de Jong, Eiko K., Hoyng, Carel B., Burdon, Kathryn P., MacGregor, Stuart, Guymer, Robyn H., den Hollander, Anneke I., Baird, Paul N.
Publicado 2016