Significant sparse polygenic risk scores across 813 traits in UK Biobank von Tanigawa, Yosuke, Qian, Junyang, Venkataraman, Guhan, Justesen, Johanne Marie, Li, Ruilin, Tibshirani, Robert, Hastie, Trevor, Rivas, Manuel A

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A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank von Qian, Junyang, Tanigawa, Yosuke, Du, Wenfei, Aguirre, Matthew, Chang, Chris, Tibshirani, Robert, Rivas, Manuel A, Hastie, Trevor

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A cross-population atlas of genetic associations for 220 human phenotypes von Sakaue, Saori, Kanai, Masahiro, Tanigawa, Yosuke, Karjalainen, Juha, Kurki, Mitja, Koshiba, Seizo, Narita, Akira, Konuma, Takahiro, Yamamoto, Kenichi, Akiyama, Masato, Ishigaki, Kazuyoshi, Suzuki, Akari, Suzuki, Ken, Obara, Wataru, Yamaji, Ken, Takahashi, Kazuhisa, Asai, Satoshi, Takahashi, Yasuo, Suzuki, Takao, Shinozaki, Nobuaki, Yamaguchi, Hiroki, Minami, Shiro, Murayama, Shigeo, Yoshimori, Kozo, Nagayama, Satoshi, Obata, Daisuke, Higashiyama, Masahiko, Masumoto, Akihide, Koretsune, Yukihiro, Ito, Kaoru, Terao, Chikashi, Yamauchi, Toshimasa, Komuro, Issei, Kadowaki, Takashi, Tamiya, Gen, Yamamoto, Masayuki, Nakamura, Yusuke, Kubo, Michiaki, Murakami, Yoshinori, Yamamoto, Kazuhiko, Kamatani, Yoichiro, Palotie, Aarno, Rivas, Manuel A., Daly, Mark J., Matsuda, Koichi, Okada, Yukinori

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Genetics of 35 blood and urine biomarkers in the UK Biobank von Sinnott-Armstrong, Nasa, Tanigawa, Yosuke, Amar, David, Mars, Nina, Benner, Christian, Aguirre, Matthew, Venkataraman, Guhan Ram, Wainberg, Michael, Ollila, Hanna M., Kiiskinen, Tuomo, Havulinna, Aki S., Pirruccello, James P., Qian, Junyang, Shcherbina, Anna, Rodriguez, Fatima, Assimes, Themistocles L., Agarwala, Vineeta, Tibshirani, Robert, Hastie, Trevor, Ripatti, Samuli, Pritchard, Jonathan K., Daly, Mark J., Rivas, Manuel A.

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Testing for an unusual distribution of rare variants von Neale, Benjamin M, Rivas, Manuel A, Voight, Benjamin F, Altshuler, David, Devlin, Bernie, Orho-Melander, Marju, Kathiresan, Sekar, Purcell, Shaun M, Roeder, Kathryn, Daly, Mark J

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The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease von Moutsianas, Loukas, Agarwala, Vineeta, Fuchsberger, Christian, Flannick, Jason, Rivas, Manuel A, Gaulton, Kyle J, Albers, Patrick K, McVean, Gil, Boehnke, Michael, Altshuler, David, McCarthy, Mark I

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Phenome-wide Burden of Copy-Number Variation in the UK Biobank von Aguirre, Matthew, Rivas, Manuel A., Priest, James

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Association of accelerometer-derived sleep measures with lifetime psychiatric diagnoses: A cross-sectional study of 89,205 participants from the UK Biobank von Wainberg, Michael, Jones, Samuel E, Beaupre, Lindsay Melhuish, Hill, Sean L, Felsky, Daniel, Rivas, Manuel A, Lim, Andrew S P, Ollila, Hanna M, Tripathy, Shreejoy J

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Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases von DeBoever, Christopher, Tanigawa, Yosuke, Aguirre, Matthew, McInnes, Greg, Lavertu, Adam, Rivas, Manuel A.

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Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide von Ruderfer, Douglas M., Walsh, Colin G., Aguirre, Matthew W., Tanigawa, Yosuke, Ribeiro, Jessica D., Franklin, Joseph C., Rivas, Manuel A.

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Opportunities and challenges for transcriptome-wide association studies von Wainberg, Michael, Sinnott-Armstrong, Nasa, Mancuso, Nicholas, Barbeira, Alvaro N., Knowles, David A., Golan, David, Ermel, Raili, Ruusalepp, Arno, Quertermous, Thomas, Hao, Ke, Björkegren, Johan L. M., Im, Hae Kyung, Pasaniuc, Bogdan, Rivas, Manuel A., Kundaje, Anshul

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Time trajectories in the transcriptomic response to exercise - a meta-analysis von Amar, David, Lindholm, Malene E., Norrbom, Jessica, Wheeler, Matthew T., Rivas, Manuel A., Ashley, Euan A.

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Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics von McInnes, Gregory, Tanigawa, Yosuke, DeBoever, Chris, Lavertu, Adam, Olivieri, Julia Eve, Aguirre, Matthew, Rivas, Manuel A

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A framework for variation discovery and genotyping using next-generation DNA sequencing data von DePristo, Mark A, Banks, Eric, Poplin, Ryan, Garimella, Kiran V, Maguire, Jared R, Hartl, Christopher, Philippakis, Anthony A, del Angel, Guillermo, Rivas, Manuel A, Hanna, Matt, McKenna, Aaron, Fennell, Tim J, Kernytsky, Andrew M, Sivachenko, Andrey Y, Cibulskis, Kristian, Gabriel, Stacey B, Altshuler, David, Daly, Mark J

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Mortality and survival in systemic sclerosis: Systematic review and meta-analysis von Rubio-Rivas, Manuel, MD, Royo, Cristina, MD, Simeón, Carmen Pilar, MD, PhD, Corbella, Xavier, MD, PhD, Fonollosa, Vicent, MD, PhD

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Homogeneity in the association of body mass index with type 2 diabetes across the UK Biobank: A Mendelian randomization study von Wainberg, Michael, Mahajan, Anubha, Kundaje, Anshul, McCarthy, Mark I, Ingelsson, Erik, Sinnott-Armstrong, Nasa, Rivas, Manuel A

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Rare and common variant discovery in complex disease: the IBD case study von Venkataraman, Guhan R, Rivas, Manuel A

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GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background von Sinnott-Armstrong, Nasa, Naqvi, Sahin, Rivas, Manuel, Pritchard, Jonathan K

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Covariant Formulation of the Brain’s Emerging Ohm’s Law von Rivas, Manuel, Reina, Manuel

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Impact of Spatial and Spectral Granularity on the Performance of SDM Networks Based on Spatial Superchannel Switching von Shariati, Behnam, Rivas-Moscoso, Jose Manuel, Marom, Dan M., Ben-Ezra, Shalva, Klonidis, Dimitrios, Velasco, Luis, Tomkos, Ioannis

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