Resultados da busca - Venner, Eric

Evolutionary Trace Annotation of Protein Function in the Structural Proteome por Erdin, Serkan, Ward, R. Matthew, Venner, Eric, Lichtarge, Olivier

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Function prediction from networks of local evolutionary similarity in protein structure por Erdin, Serkan, Venner, Eric, Lisewski, Andreas Martin, Lichtarge, Olivier

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ETAscape: analyzing protein networks to predict enzymatic function and substrates in Cytoscape por Bachman, Benjamin J., Venner, Eric, Lua, Rhonald C., Erdin, Serkan, Lichtarge, Olivier

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Accurate Protein Structure Annotation through Competitive Diffusion of Enzymatic Functions over a Network of Local Evolutionary Similarities por Venner, Eric, Lisewski, Andreas Martin, Erdin, Serkan, Ward, R. Matthew, Amin, Shivas R., Lichtarge, Olivier

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The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System por Feofanova, Elena Valeryevna, Zhang, Guo-Qiang, Lhatoo, Samden, Metcalf, Ginger A, Boerwinkle, Eric, Venner, Eric

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Evolutionary Trace Annotation Server: automated enzyme function prediction in protein structures using 3D templates por Matthew Ward, R., Venner, Eric, Daines, Bryce, Murray, Stephen, Erdin, Serkan, Kristensen, David M., Lichtarge, Olivier

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ARBoR: an identity and security solution for clinical reporting por Venner, Eric, Murugan, Mullai, Hale, Walker, Jones, Jordan M, Lu, Shan, Yi, Victoria, Gibbs, Richard A

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Accounting for epistatic interactions improves the functional analysis of protein structures por Wilkins, Angela D., Venner, Eric, Marciano, David C., Erdin, Serkan, Atri, Benu, Lua, Rhonald C., Lichtarge, Olivier

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Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia por Liu, Jidong, Ding, Guolian, Zou, Kexin, Jiang, Ziru, Zhang, Junyu, Lu, Yunhua, Pignata, Antonella, Venner, Eric, Liu, Pengfei, Liu, Zhandong, Wangler, Michael F., Sun, Zheng

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Artificial Intelligence and Cardiovascular Genetics por Krittanawong, Chayakrit, Johnson, Kipp W., Choi, Edward, Kaplin, Scott, Venner, Eric, Murugan, Mullai, Wang, Zhen, Glicksberg, Benjamin S., Amos, Christopher I., Schatz, Michael C., Tang, W. H. Wilson

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Harmonizing variant classification for return of results in the All of Us Research Program por Harrison, Steven M., Austin‐Tse, Christina A., Kim, Serra, Lebo, Matthew, Leon, Annette, Murdock, David, Radhakrishnan, Aparna, Shirts, Brian H., Steeves, Marcie, Venner, Eric, Gibbs, Richard A., Jarvik, Gail P., Rehm, Heidi L.

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Exome variant discrepancies due to reference-genome differences por Li, He, Dawood, Moez, Khayat, Michael M., Farek, Jesse R., Jhangiani, Shalini N., Khan, Ziad M., Mitani, Tadahiro, Coban-Akdemir, Zeynep, Lupski, James R., Venner, Eric, Posey, Jennifer E., Sabo, Aniko, Gibbs, Richard A.

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Neptune: An environment for the delivery of genomic medicine por Venner, Eric, Yi, Victoria, Murdock, David, Kalla, Sara E., Wu, Tsung-Jung, Sabo, Aniko, Li, Shoudong, Meng, Qingchang, Tian, Xia, Murugan, Mullai, Cohen, Michelle, Kovar, Christie, Wei, Wei-Qi, Chung, Wendy K., Weng, Chunhua, Wiesner, Georgia L., Jarvik, Gail P., Muzny, Donna, Gibbs, Richard A.

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Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients with Left Ventricular Non-Compaction por Miszalski-Jamka, Karol, Jefferies, John L., Mazur, Wojciech, Głowacki, Jan, Hu, Jianhong, Lazar, Monika, Gibbs, Richard A., Liczko, Jacek, Kłyś, Jan, Venner, Eric, Muzny, Donna M., Rycaj, Jarosław, Białkowski, Jacek, Kluczewska, Ewa, Kalarus, Zbigniew, Jhangiani, Shalini, Al-Khalidi, Hussein, Kukulski, Tomasz, Lupski, James R., Craigen, William J., Bainbridge, Matthew N.

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Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program por Venner, Eric, Muzny, Donna, Smith, Joshua D., Walker, Kimberly, Neben, Cynthia L., Lockwood, Christina M., Empey, Phillip E., Metcalf, Ginger A., Kachulis, Chris, Mian, Sana, Musick, Anjene, Rehm, Heidi L., Harrison, Steven, Gabriel, Stacey, Gibbs, Richard A., Nickerson, Deborah, Zhou, Alicia Y., Doheny, Kimberly, Ozenberger, Bradley, Topper, Scott E., Lennon, Niall J.

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Best practices for the interpretation and reporting of clinical whole genome sequencing por Austin-Tse, Christina A., Jobanputra, Vaidehi, Perry, Denise L., Bick, David, Taft, Ryan J., Venner, Eric, Gibbs, Richard A., Young, Ted, Barnett, Sarah, Belmont, John W., Boczek, Nicole, Chowdhury, Shimul, Ellsworth, Katarzyna A., Guha, Saurav, Kulkarni, Shashikant, Marcou, Cherisse, Meng, Linyan, Murdock, David R., Rehman, Atteeq U., Spiteri, Elizabeth, Thomas-Wilson, Amanda, Kearney, Hutton M., Rehm, Heidi L.

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Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example por Aronson, Samuel, Babb, Lawrence, Ames, Darren, Gibbs, Richard A, Venner, Eric, Connelly, John J, Marsolo, Keith, Weng, Chunhua, Williams, Marc S, Hartzler, Andrea L, Liang, Wayne H, Ralston, James D, Devine, Emily Beth, Murphy, Shawn, Chute, Christopher G, Caraballo, Pedro J, Kullo, Iftikhar J, Freimuth, Robert R, Rasmussen, Luke V, Wehbe, Firas H, Peterson, Josh F, Robinson, Jamie R, Wiley, Ken, Overby Taylor, Casey

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The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results por Kullo, Iftikhar J., Olson, Janet, Fan, Xiao, Jose, Merin, Safarova, Maya, Breitkopf, Carmen Radecki, Winkler, Erin, Kochan, David C., Snipes, Sara, Pacyna, Joel E., Carney, Meaghan, Chute, Christopher G., Gupta, Jyoti, Jose, Sheethal, Venner, Eric, Murugan, Mullai, Jiang, Yunyun, Zordok, Magdi, Farwati, Medhat, Philogene, Maraisha, Smith, Erica, Shaibi, Gabriel Q., Caraballo, Pedro, Freimuth, Robert, Lindor, Noralane M., Sharp, Richard, Thibodeau, Stephen N.

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Genomic considerations for FHIR®; eMERGE implementation lessons por Murugan, Mullai, Babb, Lawrence J., Taylor, Casey Overby, Rasmussen, Luke V., Freimuth, Robert R., Venner, Eric, Yan, Fei, Yi, Victoria, Granite, Stephen J., Zouk, Hana, Aronson, Samuel J., Power, Kevin, Fedotov, Alex, Crosslin, David R., Fasel, David, Jarvik, Gail P., Hakonarson, Hakon, Bangash, Hana, Kullo, Iftikhar J., Connolly, John J., Nestor, Jordan G., Caraballo, Pedro J., Wei, WeiQi, Wiley, Ken, Rehm, Heidi L., Gibbs, Richard A.

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Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel por Chiang, Theodore, Liu, Xiuping, Wu, Tsung-Jung, Hu, Jianhong, Sedlazeck, Fritz J., White, Simon, Schaid, Daniel, Andrade, Mariza de, Jarvik, Gail P., Crosslin, David, Stanaway, Ian, Carrell, David S., Connolly, John J., Hakonarson, Hakon, Groopman, Emily E., Gharavi, Ali G., Fedotov, Alexander, Bi, Weimin, Leduc, Magalie S., Murdock, David R., Jiang, Yunyun, Meng, Linyan, Eng, Christine M., Wen, Shu, Yang, Yaping, Muzny, Donna M., Boerwinkle, Eric, Salerno, William, Venner, Eric, Gibbs, Richard A.

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