NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD
Snoek, Rozemarijn, van Setten, Jessica, Keating, Brendan J, Israni, Ajay K, Jacobson, Pamala A, Oetting, William S, Matas, Arthur J, Mannon, Roslyn B, Zhang, Zhongyang, Zhang, Weijia, Hao, Ke, Murphy, Barbara, Reindl-Schwaighofer, Roman, Heinzl, Andreas, Oberbauer, Rainer, Viklicky, Ondrej, Conlon, Peter J, Stapleton, Caragh P, Bakker, Stephan J L, Snieder, Harold, Peters, Edith D J, van der Zwaag, Bert, Knoers, Nine V A M, de Borst, Martin H, van Eerde, Albertien M
Published in Journal of the American Society of Nephrology (01.06.2018)
Published in Journal of the American Society of Nephrology (01.06.2018)
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Tacrolimus troughs and genetic determinants of metabolism in kidney transplant recipients: A comparison of four ancestry groups
Mohamed, Moataz E., Schladt, David P., Guan, Weihua, Wu, Baolin, Setten, Jessica, Keating, Brendan J., Iklé, David, Remmel, Rory P., Dorr, Casey R., Mannon, Roslyn B., Matas, Arthur J., Israni, Ajay K., Oetting, William S., Jacobson, Pamala A., Cecka, J. Michael, Connett, John, Cosio, Fernando G., Gaston, Robert, Gourishankar, Sita, Grande, Joseph P., Hunsicker, Lawrence, Kasiske, Bertram, Rush, David
Published in American journal of transplantation (01.10.2019)
Published in American journal of transplantation (01.10.2019)
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Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia
Menezes, Minal J, Guo, Yiran, Zhang, Jianguo, Riley, Lisa G, Cooper, Sandra T, Thorburn, David R, Li, Jiankang, Dong, Daoyuan, Li, Zhijun, Glessner, Joseph, Davis, Ryan L, Sue, Carolyn M, Alexander, Stephen I, Arbuckle, Susan, Kirwan, Paul, Keating, Brendan J, Xu, Xun, Hakonarson, Hakon, Christodoulou, John
Published in Human molecular genetics (15.04.2015)
Published in Human molecular genetics (15.04.2015)
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Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts
Al-Ali, Amein K., Al-Rubaish, Abdullah M., Alali, Rudaynah A., Almansori, Mohammed S., Al-Jumaan, Mohammed A., Alshehri, Abdullah M., Al-Madan, Mohammed S., Vatte, ChittiBabu, Cherlin, Tess, Young, Sylvia, Verma, Shefali S., Morahan, Grant, Koeleman, Bobby P. C., Keating, Brendan J.
Published in Scientific reports (10.12.2023)
Published in Scientific reports (10.12.2023)
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Gut microbiota analyses of inflammatory bowel diseases from a representative Saudi population
Alsulaiman, Raed M, Al-Quorain, Abdulaziz A, Al-Muhanna, Fahad A, Piotrowski, Stanley, Kurdi, Ezzeddin A, Vatte, Chittibabu, Alquorain, Ahmed A, Alfaraj, Noorah H, Alrezuk, Abdulaziz M, Robinson, Fred, Dowdell, Alexa K, Alamri, Turki A, Hamilton, Lauren, Lad, Hetal, Gao, Hui, Gandla, Divya, Keating, Brendan J, Meng, Ryan, Piening, Brian, Al-Ali, Amein K
Published in BMC gastroenterology (28.07.2023)
Published in BMC gastroenterology (28.07.2023)
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Current and Future Approaches for Monitoring Responses to Anti-complement Therapeutics
Mohebnasab, Maedeh, Eriksson, Oskar, Persson, Barbro, Sandholm, Kerstin, Mohlin, Camilla, Huber-Lang, Markus, Keating, Brendan J, Ekdahl, Kristina N, Nilsson, Bo
Published in Frontiers in immunology (08.11.2019)
Published in Frontiers in immunology (08.11.2019)
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Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci
Al Anazi, Abdulrahman H, Ammar, Ahmed S, Al-Hajj, Mahmoud, Cyrus, Cyril, Aljaafari, Danah, Khoda, Iname, Abdelfatah, Ahmed K, Alsulaiman, Abdullah A, Alanazi, Firas, Alanazi, Rawan, Gandla, Divya, Lad, Hetal, Barayan, Samar, Keating, Brendan J, Al-Ali, Amein K
Published in Human genomics (20.12.2022)
Published in Human genomics (20.12.2022)
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Gut microbiota analyses of Saudi populations for type 2 diabetes-related phenotypes reveals significant association
Al-Muhanna, Fahad A, Dowdell, Alexa K, Al Eleq, Abdulmohsen H, Albaker, Waleed I, Brooks, Andrew W, Al-Sultan, Ali I, Al-Rubaish, Abdullah M, Alkharsah, Khaled R, Sulaiman, Raed M, Al-Quorain, Abdulaziz A, Cyrus, Cyril, Alali, Rudaynah A, Vatte, Chittibabu, Robinson, Fred L, Zhou, Xin, Snyder, Michael P, Almuhanna, Afnan F, Keating, Brendan J, Piening, Brian D, Al-Ali, Amein K
Published in BMC microbiology (13.12.2022)
Published in BMC microbiology (13.12.2022)
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Oral microbiota analyses of paediatric Saudi population reveals signatures of dental caries
Alyousef, Yousef M, Piotrowski, Stanley, Alonaizan, Faisal A, Alsulaiman, Ahmed, Alali, Ali A, Almasood, Naif N, Vatte, Chittibabu, Hamilton, Lauren, Gandla, Divya, Lad, Hetal, Robinson, Fred L, Cyrus, Cyril, Meng, Ryan C, Dowdell, Alexa, Piening, Brian, Keating, Brendan J, Al-Ali, Amein K
Published in BMC oral health (27.11.2023)
Published in BMC oral health (27.11.2023)
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LoFTK: a framework for fully automated calculation of predicted Loss-of-Function variants and genes
Alasiri, Abdulrahman, Karczewski, Konrad J, Cole, Brian, Loza, Bao-Li, Moore, Jason H, van der Laan, Sander W, Asselbergs, Folkert W, Keating, Brendan J, van Setten, Jessica
Published in BioData mining (02.02.2023)
Published in BioData mining (02.02.2023)
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Genome-Wide Study Updates in the International Genetics and Translational Research in Transplantation Network (iGeneTRAiN)
Fishman, Claire E, Mohebnasab, Maede, van Setten, Jessica, Zanoni, Francesca, Wang, Chen, Deaglio, Silvia, Amoroso, Antonio, Callans, Lauren, van Gelder, Teun, Lee, Sangho, Kiryluk, Krzysztof, Lanktree, Matthew B, Keating, Brendan J
Published in Frontiers in genetics (15.11.2019)
Published in Frontiers in genetics (15.11.2019)
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Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls
Abumadini, Mahdi S, Al Ghamdi, Kholoud S, Alqahtani, Abdullah H, Almedallah, Dana K, Callans, Lauren, Jarad, Jumanah A, Cyrus, Cyril, Koeleman, Bobby P C, Keating, Brendan J, Pankratz, Nathan, Al-Ali, Amein K
Published in Frontiers in molecular neuroscience (10.02.2023)
Published in Frontiers in molecular neuroscience (10.02.2023)
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Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium
XIAOFENG ZHU, YOUNG, J. H, MORRISON, Alanna, NEWTON-CHEH, Christopher, KIANG LIU, GANESH, Santhi K, KUTLAR, Abdullah, VASAN, Ramachandran S, DREISBACH, Albert, WYATT, Sharon, POLAK, Joseph, PALMAS, Walter, FOX, Ervin, MUSANI, Solomon, TAYLOR, Herman, FABSITZ, Richard, TOWNSEND, Raymond R, DRIES, Daniel, GLESSNER, Joseph, CHIANG, Charleston W. K, MOSLEY, Thomas, KARDIA, Sharon, CURB, David, KEATING, Brendan J, HIRSCHHORN, Joel N, ROTIMI, Charles, REINER, Alexander, EATON, Charles, ROTTER, Jerome I, COOPER, Richard S, REDLINE, Susan, CHAKRAVARTI, Aravinda, LEVY, Daniel, FRANCESCHINI, Nora, SUNJUNG KANG, TAYO, Bamidele, ADEYEMO, Adebowale, SUN, Yun V, YALI LI
Published in Human molecular genetics (01.06.2011)
Published in Human molecular genetics (01.06.2011)
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Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study
Raffield, Laura M, Ellis, Jaclyn, Olson, Nels C, Duan, Qing, Li, Jin, Durda, Peter, Pankratz, Nathan, Keating, Brendan J, Wassel, Christina L, Cushman, Mary, Wilson, James G, Gross, Myron D, Tracy, Russell P, Rich, Stephen S, Reiner, Alex P, Li, Yun, Willis, Monte S, Lange, Ethan M, Lange, Leslie A
Published in Journal of human genetics (01.03.2018)
Published in Journal of human genetics (01.03.2018)
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Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration[S]
Lanktree, Matthew B., Elbers, Clara C., Li, Yun, Zhang, Guosheng, Duan, Qing, Karczewski, Konrad J., Guo, Yiran, Tragante, Vinicius, North, Kari E., Cushman, Mary, Asselbergs, Folkert W., Wilson, James G., Lange, Leslie A., Drenos, Fotios, Reiner, Alex P., Barnes, Michael R., Keating, Brendan J.
Published in Journal of lipid research (01.09.2015)
Published in Journal of lipid research (01.09.2015)
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Two variants of the C-reactive protein gene are associated with risk of pre-eclampsia in an American Indian population
Best, Lyle G, Saxena, Richa, Anderson, Cindy M, Barnes, Michael R, Hakonarson, Hakon, Falcon, Gilbert, Martin, Candelaria, Castillo, Berta Almoguera, Karumanchi, Ananth, Keplin, Kylie, Pearson, Nichole, Lamb, Felicia, Bercier, Shellee, Keating, Brendan J
Published in PloS one (05.08.2013)
Published in PloS one (05.08.2013)
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Genetic analysis of impaired trimethylamine metabolism using whole exome sequencing
Guo, Yiran, Hwang, Liang-Dar, Li, Jiankang, Eades, Jason, Yu, Chung Wen, Mansfield, Corrine, Burdick-Will, Alexis, Chang, Xiao, Chen, Yulan, Duke, Fujiko F, Zhang, Jianguo, Fakharzadeh, Steven, Fennessey, Paul, Keating, Brendan J, Jiang, Hui, Hakonarson, Hakon, Reed, Danielle R, Preti, George
Published in BMC medical genetics (15.02.2017)
Published in BMC medical genetics (15.02.2017)
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