Výsledky vyhledávání - Chris Bizon
- Zobrazuji výsledky 1 - 15 z 15
-
1
-
2
-
3
ExEmPLAR (Extracting, Exploring, and Embedding Pathways Leading to Actionable Research): a user-friendly interface for knowledge graph mining Autor Jon-Michael Beasley, Daniel Korn, Nyssa N Tucker, Erick Tavares Marcelino Alves, Eugene Muratov, Chris Bizon, Alexander Tropsha
Vydáno 2024Artigo -
4
-
5
-
6
Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: Implications for application to clinical testing Autor Jonathan S. Berg, James P. Evans, Margaret W. Leigh, Heymut Omran, Chris Bizon, Ketan K. Mane, Michael R. Knowles, Karen E. Weck, Maimoona A. Zariwala
Vydáno 2011Artigo -
7
Increasing the diagnostic yield of exome sequencing by copy number variant analysis Autor Daniel S. Marchuk, Kristy Crooks, Natasha T. Strande, Kathleen Kaiser‐Rogers, Laura V. Milko, Alicia Brandt, Alexandra Arreola, Christian R. Tilley, Chris Bizon, Neeta L. Vora, Kirk C. Wilhelmsen, James P. Evans, Jonathan S. Berg
Vydáno 2018Artigo -
8
ClinGen Allele Registry links information about genetic variants Autor Piotr Pawliczek, Ronak Y. Patel, Lillian Ashmore, Andrew R. Jackson, Chris Bizon, Tristan Nelson, Bradford C. Powell, Robert R. Freimuth, Natasha T. Strande, Neethu Shah, Sameer Paithankar, Matt W. Wright, Selina S. Dwight, Jimmy Zhen, Melissa Landrum, Peter B. McGarvey, Lawrence Babb, Sharon E. Plon, Aleksandar Milosavljevic
Vydáno 2018Artigo -
9
Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges Autor Neeta L. Vora, Bradford C. Powell, Alicia Brandt, Natasha T. Strande, Emily Hardisty, Kelly L. Gilmore, Ann Katherine M. Foreman, Kirk C. Wilhelmsen, Chris Bizon, Jason Reilly, Phil Owen, Cynthia M. Powell, Debra Skinner, Christine Rini, Anne Drapkin Lyerly, Kim Boggess, Karen E. Weck, Jonathan S. Berg, James P. Evans
Vydáno 2017Artigo -
10
ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants Autor Ronak Y. Patel, Neethu Shah, Andrew R. Jackson, Rajarshi Ghosh, Piotr Pawliczek, Sameer Paithankar, Aaron B. Baker, Kevin Riehle, Hailin Chen, Sofia Milosavljevic, Chris Bizon, Shawn Rynearson, Tristan Nelson, Gail P. Jarvik, Heidi L. Rehm, Steven M. Harrison, Danielle R. Azzariti, Bradford C. Powell, Lawrence Babb, Sharon E. Plon, Aleksandar Milosavljevic
Vydáno 2017Artigo -
11
Biolink Model: A universal schema for knowledge graphs in clinical, biomedical, and translational science Autor Deepak Unni, Sierra Moxon, Michael Bada, Matthew Brush, Richard Bruskiewich, J. Harry Caufield, Paul A. Clemons, Vlado Dančík, Michel Dumontier, Karamarie Fecho, Gustavo Glusman, Jennifer Hadlock, Nomi L. Harris, Arpita Joshi, Tim Putman, Guangrong Qin, Stephen A. Ramsey, Kent Shefchek, Harold R. Solbrig, Karthik Soman, Anne Thessen, Melissa Haendel, Chris Bizon, Chris Mungall
Vydáno 2022Revisão -
12
Progress toward a universal biomedical data translator Autor Karamarie Fecho, Anne Thessen, Sergio E. Baranzini, Chris Bizon, Jennifer Hadlock, Sui Huang, Ryan Roper, Noel Southall, Casey Ta, Paul B. Watkins, Mark D. Williams, Hao Xu, William E. Byrd, Vlado Dančík, Marc Duby, Michel Dumontier, Gustavo Glusman, Nomi L. Harris, Eugene W. Hinderer, Greg Hyde, Adam J. Johs, Andrew I. Su, Guangrong Qin, Qian Zhu
Vydáno 2022Revisão -
13
Germline Mutations in<i>HOXB13</i>and Prostate-Cancer Risk Autor Charles M. Ewing, Anna M. Ray, Ethan M. Lange, Kimberly A. Zuhlke, Christiane M. Robbins, Waibhav Tembe, Kathleen E. Wiley, Sarah D. Isaacs, Dorhyun Johng, Yunfei Wang, Chris Bizon, Guifang Yan, Marta Gielzak, Alan W. Partin, Vijayalakshmi Shanmugam, Tyler Izatt, Shripad Sinari, David W. Craig, S. Lilly Zheng, Patrick C. Walsh, James E. Montie, Jianfeng Xu, John D. Carpten, William B. Isaacs, Kathleen A. Cooney
Vydáno 2012Artigo -
14
A Simple Standard for Sharing Ontological Mappings (SSSOM) Autor Nicolas Matentzoglu, James P. Balhoff, Susan M. Bello, Chris Bizon, Matthew Brush, Tiffany J Callahan, Christopher G. Chute, William D. Duncan, Chris T. Evelo, Davera Gabriel, John Graybeal, Alasdair Gray, Benjamin M. Gyori, Melissa Haendel, Henriette Harmse, Nomi L. Harris, Ian Harrow, Harshad Hegde, Amelia Hoyt, Charles Tapley Hoyt, Dazhi Jiao, Ernesto Jiménez-Ruiz, Simon Jupp, HyeongSik Kim, Sebastian Koehler, Thomas Liener, Qinqin Long, James Malone, James Alastair McLaughlin, Julie A. McMurry, Sierra Moxon, Monica Muñoz‐Torres, David Osumi-Sutherland, James A. Overton, Bjoern Peters, Tim Putman, Núria Queralt-Rosiñach, Kent Shefchek, Harold R. Solbrig, Anne Thessen, Tania Tudorache, Nicole Vasilevsky, Alex H. Wagner, Chris Mungall
Vydáno 2022Artigo -
15
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol Autor Leslie A. Lange, Youna Hu, He Zhang, Chenyi Xue, Ellen M. Schmidt, Zheng-Zheng Tang, Chris Bizon, Ethan M. Lange, Joshua D. Smith, Emily H. Turner, Goo Jun, Hyun Min Kang, Gina M. Peloso, Paul L. Auer, Kuo-ping Li, Jason Flannick, Ji Zhang, Christian Fuchsberger, Kyle J. Gaulton, Cecilia M. Lindgren, Adam E. Locke, Alisa K. Manning, Xueling Sim, Manuel A. Rivas, Oddgeir L. Holmen, Omri Gottesman, Yingchang Lu, Douglas M. Ruderfer, Eli A. Stahl, Qing Duan, Yun Li, Peter Durda, Shuo Jiao, Aaron Isaacs, Albert Hofman, Joshua C. Bis, Adolfo Correa, Michael Griswold, Jóhanna Jakobsdóttir, Albert V. Smith, Pamela J. Schreiner, Mary F. Feitosa, Qunyuan Zhang, Jennifer E. Huffman, Jacy R. Crosby, Christina L. Wassel, Ron Do, Nora Franceschini, Lisa W. Martin, Jennifer G. Robinson, Themistocles L. Assimes, David R. Crosslin, Elisabeth A. Rosenthal, Michael Y. Tsai, Mark J. Rieder, Deborah Farlow, Aaron R. Folsom, Thomas Lumley, Ervin R. Fox, Christopher S. Carlson, Ulrike Peters, Rebecca D. Jackson, Cornelia M. van Duijn, André G. Uitterlinden, Daniel Levy, Jerome I. Rotter, Herman A. Taylor, Vilmundur Guðnason, David S. Siscovick, Myriam Fornage, Ingrid B. Borecki, Caroline Hayward, Igor Rudan, Y. Eugene Chen, Erwin P. Böttinger, Ruth J. F. Loos, Pål Sætrom, Kristian Hveem, Michael Boehnke, Leif Groop, Mark I. McCarthy, Thomas Meitinger, Christie M. Ballantyne, Stacey Gabriel, Christopher J. O’Donnell, Wendy S. Post, Kari E. North, Alexander P. Reiner, Eric Boerwinkle, Bruce M. Psaty, David Altshuler, Sekar Kathiresan, Dan-Yu Lin, Gail P. Jarvik, L. Adrienne Cupples, Charles Kooperberg, James G. Wilson, Deborah A. Nickerson, Gonçalo R. Abecasis, Stephen S. Rich
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Computer science
Gene
Genetics
Medicine
Computational biology
Data science
Bioinformatics
Mutation
Exome
Exome sequencing
Information retrieval
Artificial intelligence
Genome
Genomics
Knowledge graph
Medical genetics
Philosophy
Allele frequency
Computer security
DNA sequencing
Data mining
Database
Engineering
Epistemology
Genetic testing
Graph
Internal medicine
Linguistics
Pathology