Advances in Risk Prediction of Type 2 Diabetes: Integrating Genetic Scores With Framingham Risk Models

Por Keating, Brendan J.
Publicado no Diabetes (2015)

Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations

Por Li, Yun R, Keating, Brendan J
Publicado no Genome Med (2014)

Machine learning derived risk prediction of anorexia nervosa

Por Guo, Yiran, Wei, Zhi, Keating, Brendan J., Hakonarson, Hakon
Publicado no BMC Med Genomics (2016)

Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantation

Por Li, Yun R, Levine, John E, Hakonarson, Hakon, Keating, Brendan J
Publicado em 2014

Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes

Por Almoguera, Berta, Vazquez, Lyam, Connolly, John J., Bradfield, Jonathan, Sleiman, Patrick, Keating, Brendan, Hakonarson, Hakon
Publicado em 2014

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

Por Guo, Yiran, Lanktree, Matthew B., Taylor, Kira C., Hakonarson, Hakon, Lange, Leslie A., Keating, Brendan J.
Publicado em 2013

An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6

Por Fairfax, Benjamin P., Vannberg, Fredrik O., Radhakrishnan, Jayachandran, Hakonarson, Hakon, Keating, Brendan J., Hill, Adrian V.S., Knight, Julian C.
Publicado em 2010

Fatty-Acid Binding Protein 4 Gene Polymorphisms and Plasma Levels in Children with Obstructive Sleep Apnea

Por Bhushan, Bharat, Khalyfa, Abdelnaby, Spruyt, Karen, Kheirandish-Gozal, Leila, Capdevila, Oscar Sans, Bhattacharjee, Rakesh, Kim, Jinkwan, Keating, Brendan, Hakonarson, Hakon, Gozal, David
Publicado em 2011

Genetic variance in Nitric Oxide Synthase and Endothelin Genes among children with and without Endothelial Dysfunction

Por Chatsuriyawong, Siriporn, Gozal, David, Kheirandish-Gozal, Leila, Bhattacharjee, Rakesh, Khalyfa, Ahamed A, Wang, Yang, Hakonarson, Hakon, Keating, Brendan, Sukhumsirichart, Wasana, Khalyfa, Abdelnaby
Publicado em 2013

IBC CARe Microarray Allelic Population Prevalences in an American Indian Population

Por Best, Lyle G., Anderson, Cindy M., Saxena, Richa, Almoguera, Berta, Chandrupatla, Hareesh, Martin, Candelaria, Falcon, Gilbert, Keplin, Kylie, Pearson, Nichole, Keating, Brendan J.
Publicado em 2013

Identification of Common Genetic Variation That Modulates Alternative Splicing

Por Hull, Jeremy, Campino, Susana, Rowlands, Kate, Chan, Man-Suen, Copley, Richard R, Taylor, Martin S, Rockett, Kirk, Elvidge, Gareth, Keating, Brendan, Knight, Julian, Kwiatkowski, Dominic
Publicado em 2007

Whole-genome sequencing in an autism multiplex family

Por Shi, Lingling, Zhang, Xu, Golhar, Ryan, Otieno, Frederick G, He, Mingze, Hou, Cuiping, Kim, Cecilia, Keating, Brendan, Lyon, Gholson J, Wang, Kai, Hakonarson, Hakon
Publicado em 2013

Elevated Fibroblast Growth Factor 23 Concentration: Prediction of Mortality among Chronic Kidney Disease Patients

Por Chathoth, Shahanas, Al-Mueilo, Samir, Cyrus, Cyril, Vatte, Chittibabu, Al-Nafaie, Awatif, Al-Ali, Rudaynah, Keating, Brendan J., Al-Muhanna, Fahad, Al Ali, Amein
Publicado no Cardiorenal Med (2015)

Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk

Por Tragante, Vinicius, Asselbergs, Folkert W., Swerdlow, Daniel I., Palmer, Tom M., Moore, Jason H., de Bakker, Paul I. W., Keating, Brendan J., Holmes, Michael V.
Publicado no Hum Genet (2016)

Subclinical Atherosclerosis and Increased Risk of Hearing Impairment

Por Fischer, Mary E, Schubert, Carla R, Nondahl, David M, Dalton, Dayna S, Huang, Guan-Hua, Keating, Brendan J, Klein, Barbara EK, Klein, Ronald, Tweed, Ted S, Cruickshanks, Karen J.
Publicado no Atherosclerosis (2014)

Intensity of Salt Taste and Prevalence of Hypertension Are Not Related in the Beaver Dam Offspring Study

Por Fischer, Mary E, Cruickshanks, Karen J, Pinto, Alex, Schubert, Carla R, Klein, Barbara E K, Klein, Ronald, Nieto, F Javier, Pankow, James S, Snyder, Derek J, Keating, Brendan J
Publicado em 2012

Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia

Por Spracklen, Cassandra N., Saftlas, Audrey F., Triche, Elizabeth W., Bjonnes, Andrew, Keating, Brendan, Saxena, Richa, Breheny, Patrick J., Dewan, Andrew T., Robinson, Jennifer G., Hoh, Josephine, Ryckman, Kelli K.
Publicado no Am J Hypertens (2015)

The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians

Por Cyrus, Cyril, Vatte, Chittibabu, Al-Nafie, Awatif, Chathoth, Shahanas, Al-Ali, Rudaynah, Al-Shehri, Abdullah, Akhtar, Mohammed Shakil, Almansori, Mohammed, Al-Muhanna, Fahad, Keating, Brendan, Al-Ali, Amein
Publicado no Hum Genomics (2016)

Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia

Por Smith, Caitlin J., Saftlas, Audrey F., Spracklen, Cassandra N., Triche, Elizabeth W., Bjonnes, Andrew, Keating, Brendan, Saxena, Richa, Breheny, Patrick J., Dewan, Andrew T., Robinson, Jennifer G., Hoh, Josephine, Ryckman, Kelli K.
Publicado no Am J Hypertens (2016)

Whole Exome Sequencing Identifies the Genetic Basis of Late-Onset Leigh Syndrome in a Patient with MRI but Little Biochemical Evidence of a Mitochondrial Disorder

Por Nafisinia, Michael, Guo, Yiran, Dang, Xiao, Li, Jiankang, Chen, Yulan, Zhang, Jianguo, Lake, Nicole J., Gold, Wendy A., Riley, Lisa G., Thorburn, David R., Keating, Brendan, Xu, Xun, Hakonarson, Hakon, Christodoulou, John
Publicado no JIMD Rep (2016)