Rezultati pretrage - Anne‐Katrin Emde
- Prikaz rezultata 1 – 19 od 19
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Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS od Anne‐Katrin Emde, Marcel H. Schulz, David Weese, Ruping Sun, Martin Vingron, Vera M. Kalscheuer, Stefan A. Haas, Knut Reinert
Izdano 2012Artigo -
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Genome-wide somatic variant calling using localized colored de Bruijn graphs od Giuseppe Narzisi, André Corvelo, Kanika Arora, Ewa A. Bergmann, Minita Shah, Rajeeva Musunuri, Anne‐Katrin Emde, Nicolas Robine, Vladimir Vacic, Michael C. Zody
Izdano 2018Artigo -
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Disease variants in genomes of 44 centenarians od Yun Freudenberg‐Hua, Jan Freudenberg, Vladimir Vacic, Avinash Abhyankar, Anne‐Katrin Emde, Danny Ben‐Avraham, Nir Barzilai, Dayna M. Oschwald, Erika Christen, Jeremy Koppel, Blaine Greenwald, Robert B. Darnell, Søren Germer, Gil Atzmon, Peter Davies
Izdano 2014Artigo -
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Human papillomavirus and the landscape of secondary genetic alterations in oral cancers od Maura L. Gillison, Keiko Akagi, Weihong Xiao, Bo Jiang, Robert K. L. Pickard, Jingfeng Li, Benjamin Swanson, Amit Agrawal, Mark Zucker, Birgit Stache-Crain, Anne-Katrin Emde, Heather Geiger, Nicolas Robine, Kevin R. Coombes, David E. Symer
Izdano 2018Artigo -
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Genetic mechanisms of primary chemotherapy resistance in pediatric acute myeloid leukemia od Nicole McNeer, John Philip, Heather Geiger, Rhonda E. Ries, Vincent‐Philippe Lavallée, Michael F. Walsh, Minita Shah, Kanika Arora, Anne‐Katrin Emde, Nicolas Robine, Todd A. Alonzo, E. Anders Kolb, Alan S. Gamis, Malcolm A. Smith, Daniela S. Gerhard, Jaime Guidry-Auvil, Soheil Meshinchi, Alex Kentsis
Izdano 2019Artigo -
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Diverse tumorigenic consequences of human papillomavirus integration in primary oropharyngeal cancers od David E. Symer, Keiko Akagi, Heather Geiger, Song Yang, Gaiyun Li, Anne‐Katrin Emde, Weihong Xiao, Bo Jiang, André Corvelo, Nora C. Toussaint, Jingfeng Li, Amit Agrawal, Enver Özer, Adel K. El‐Naggar, Zoe Du, Jitesh B. Shewale, Birgit Stache-Crain, Mark Zucker, Nicolas Robine, Kevin R. Coombes, Maura L. Gillison
Izdano 2021Artigo -
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Detection of a Recurrent <i>DNAJB1-PRKACA</i> Chimeric Transcript in Fibrolamellar Hepatocellular Carcinoma od Joshua N. Honeyman, Elana P. Simon, Nicolas Robine, Rachel Chiaroni-Clarke, David G. Darcy, Irene Isabel P. Lim, Caroline E. Gleason, Jennifer M. Murphy, Brad R. Rosenberg, Lydia Teegan, Constantin N. Takacs, Sergio Botero, R.L. Belote, Søren Germer, Anne‐Katrin Emde, Vladimir Vacic, Umesh Bhanot, Michael P. LaQuaglia, Sanford M. Simon
Izdano 2014Artigo -
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Comparative sequencing analysis reveals high genomic concordance between matched primary and metastatic colorectal cancer lesions od A. Rose Brannon, Efsevia Vakiani, Brooke E. Sylvester, Sasinya N. Scott, Gregory McDermott, Ronak Shah, Krishan Kania, Agnès Viale, Dayna M. Oschwald, Vladimir Vacic, Anne‐Katrin Emde, Andrea Cercek, Rona Yaeger, Nancy E. Kemeny, Leonard B. Saltz, Jinru Shia, Michael I. D’Angelica, Martin R. Weiser, David B. Solit, Michael F. Berger
Izdano 2014Artigo -
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Somatic whole genome dynamics of precancer in Barrett’s esophagus reveals features associated with disease progression od Thomas G. Paulson, Patricia C. Galipeau, Kenji Oman, Carissa A. Sanchez, Mary K. Kuhner, Lucian P. Smith, Kevin Hadi, Minita Shah, Kanika Arora, Jennifer M. G. Shelton, Molly Johnson, André Corvelo, Carlo C. Maley, Xiaotong Yao, Rashesh Sanghvi, Elisa Venturini, Anne‐Katrin Emde, Benjamin Hubert, Marcin Imieliński, Nicolas Robine, Brian J. Reid, Xiaohong Li
Izdano 2022Artigo -
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The gout epidemic in French Polynesia: a modelling study of data from the Ma’i u’u epidemiological survey od Tristan Pascart, Kaja A. Wasik, Cristian Preda, Valérie Chune, Jérémie Torterat, Nicolas Prud’homme, Maryline Nassih, Agathe Martin, Julien Le Masson, Vahinetua Rodière, Sylvain Frogier, Georges Canova, Jean-Paul Pescheux, Charles Shan Sei Fan, Charlotte Jauffret, Patrick Claeys, Sarah LeBaron von Baeyer, Stephane E. Castel, Anne‐Katrin Emde, Laura M. Yerges-Armstrong, Keolu Fox, Megan Leask, Jean‐Jacques Vitagliano, Sahara Graf, Laurène Norberciak, Jacques Raynal, Nicola Dalbeth, Tony R. Merriman, Thomas Bardin, Erwan Oehler
Izdano 2024Artigo -
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PGBD5 promotes site-specific oncogenic mutations in human tumors od Anton G. Henssen, Richard P. Koche, Jiali Zhuang, Eileen Jiang, Casie Reed, Amy Eisenberg, Eric Still, Ian C. MacArthur, Elias Rodríguez-Fos, Santiago González, Montserrat Puiggròs, Andrew N. Blackford, Christopher E. Mason, Elisa de Stanchina, Mithat Gönen, Anne-Katrin Emde, Minita Shah, Kanika Arora, Catherine Reeves, Nicholas D. Socci, Elizabeth J. Perlman, Cristina R. Antonescu, Charles W.M. Roberts, Hanno Steen, Elizabeth A. Mullen, Stephen P. Jackson, David Torrents, Zhiping Weng, Scott A. Armstrong, Alex Kentsis
Izdano 2017Artigo -
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Next-Generation Rapid Autopsies Enable Tumor Evolution Tracking and Generation of Preclinical Models od David J. Pisapia, Steven Salvatore, Chantal Pauli, Erika Hissong, Kenneth Wha Eng, Davide Prandi, Verena-Wilbeth Sailer, Brian D. Robinson, Kyung Park, Joanna Cyrta, Scott T. Tagawa, Myriam Kossaï, Jacqueline Fontugne, Robert Kim, Alexandros Sigaras, Rema Rao, Danielle Pancirer, Bishoy M. Faltas, Rohan Bareja, Ana M. Molina, David M. Nanus, Prajwal Rajappa, Mark M. Souweidane, Jeffrey P. Greenfield, Anne-Katrin Emde, Nicolas Robine, Olivier Elemento, Andrea Sboner, Francesca Demichelis, Himisha Beltran, Mark A. Rubin, Juan Miguel Mosquera
Izdano 2017Artigo -
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Whole-Exome Sequencing of Metastatic Cancer and Biomarkers of Treatment Response od Himisha Beltran, Kenneth Eng, Juan Miguel Mosquera, Alexandros Sigaras, Alessandro Romanel, Hanna Rennert, Myriam Kossaï, Chantal Pauli, Bishoy M. Faltas, Jacqueline Fontugne, Kyung Park, Jason R. Banfelder, Davide Prandi, Neel S. Madhukar, Tuo Zhang, Jessica Padilla, Noah Greco, Terra J. McNary, Erick Herrscher, David Wilkes, Theresa Y. MacDonald, Hui Xue, Vladimir Vacic, Anne-Katrin Emde, Dayna M. Oschwald, Adrian Y. Tan, Zhengming Chen, Colin C. Collins, Martin Gleave, Yuzhuo Wang, Dimple Chakravarty, Marc Schiffman, Robert Kim, Fabien Campagne, Brian D. Robinson, David M. Nanus, Scott T. Tagawa, Jenny Xiang, Agata Smogorzewska, Francesca Demichelis, David S. Rickman, Andrea Sboner, Olivier Elemento, Mark A. Rubin
Izdano 2015Artigo -
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Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs od Kevin Hadi, Xiaotong Yao, Julie M. Behr, Aditya Deshpande, Charalampos Xanthopoulakis, Huasong Tian, Sarah Kudman, Joel Rosiene, Madison Darmofal, Joseph DeRose, Rick Mortensen, Emily M. Adney, Alon Shaiber, Zoran Gajic, Michael Sigouros, Kenneth Eng, Jeremiah A. Wala, Kazimierz O. Wrzeszczyński, Kanika Arora, Minita Shah, Anne-Katrin Emde, Vanessa Felice, Mayu O. Frank, Robert B. Darnell, Mahmoud Ghandi, Franklin W. Huang, Sally M. Dewhurst, John Maciejowski, Titia de Lange, Jeremy Setton, Nadeem Riaz, Jorge S. Reis‐Filho, Simon N. Powell, David A. Knowles, Ed Reznik, Bud Mishra, Rameen Beroukhim, Michael C. Zody, Nicolas Robine, Kenji Oman, Carissa A. Sanchez, Mary K. Kuhner, Lucian P. Smith, Patricia C. Galipeau, Thomas G. Paulson, Brian J. Reid, Xiaohong Li, David Wilkes, Andrea Sboner, Juan Miguel Mosquera, Olivier Elemento, Marcin Imieliński
Izdano 2020Artigo -
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program od Daniel Taliun, Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres, Sarah A. Gagliano Taliun, André Corvelo, Stephanie M. Gogarten, Hyun Min Kang, Achilleas Pitsillides, Jonathon LeFaive, Seung‐been Lee, Xiaowen Tian, Brian L. Browning, Sayantan Das, Anne‐Katrin Emde, Wayne E. Clarke, Douglas P. Loesch, Amol C. Shetty, Thomas W. Blackwell, Albert V. Smith, Quenna Wong, Xiaoming Liu, Matthew P. Conomos, Dean Bobo, François Aguet, Christine M. Albert, Álvaro Alonso, Kristin Ardlie, Dan E. Arking, Stella Aslibekyan, Paul L. Auer, John Barnard, R. Graham Barr, Lucas Barwick, Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Daniel I. Chasman, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie Emery, Celeste Eng, Diane Fatkin, Tasha E. Fingerlin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Robert C. Kaplan, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos
Izdano 2021Artigo -
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program od Daniel Taliun, Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres, Sarah A. Gagliano Taliun, André Corvelo, Stephanie M. Gogarten, Hyun Min Kang, Achilleas Pitsillides, Jonathon LeFaive, Seung‐been Lee, Xiaowen Tian, Brian L. Browning, Sayantan Das, Anne‐Katrin Emde, Wayne E. Clarke, Douglas P. Loesch, Amol C. Shetty, Thomas W. Blackwell, Quenna Wong, François Aguet, Christine M. Albert, Álvaro Alonso, Kristin Ardlie, Stella Aslibekyan, Paul L. Auer, John Barnard, R. Graham Barr, Lewis C. Becker, Rebecca Beer, Emelia J. Benjamin, Lawrence F. Bielak, John Blangero, Michael Boehnke, Donald W. Bowden, Jennifer A. Brody, Esteban G. Burchard, Brian E. Cade, James F. Casella, Brandon Chalazan, Yii‐Der Ida Chen, Michael H. Cho, Seung Hoan Choi, Mina K. Chung, Clary B. Clish, Adolfo Correa, Joanne E. Curran, Brian Custer, Dawood Darbar, Michelle Daya, Mariza de Andrade, Dawn L. DeMeo, Susan K. Dutcher, Patrick T. Ellinor, Leslie Emery, Diane Fatkin, Lukas Forer, Myriam Fornage, Nora Franceschini, Christian Fuchsberger, Stephanie M. Fullerton, Søren Germer, Mark T. Gladwin, Daniel J. Gottlieb, Xiuqing Guo, Michael E. Hall, Jiang He, Nancy L. Heard‐Costa, Susan R. Heckbert, Marguerite R. Irvin, Jill M. Johnsen, Andrew D. Johnson, Sharon L. R. Kardia, Tanika N. Kelly, Shannon Kelly, Eimear E. Kenny, Douglas P. Kiel, Robert Klemmer, Barbara A. Konkle, Charles Kooperberg, Anna Köttgen, Leslie A. Lange, Jessica Lasky‐Su, Daniel Levy, Xihong Lin, Keng‐Han Lin, Chunyu Liu, Ruth J. F. Loos, Lori Garman, Robert E. Gerszten, Steven A. Lubitz, Kathryn L. Lunetta, Angel C. Y. Mak, Ani Manichaikul, Alisa K. Manning, Rasika A. Mathias, David D. McManus, Stephen T. McGarvey
Izdano 2019Pré-impressão
Alati za pretragu:
Povezani predmeti
Biology
Genetics
Gene
Genome
Cancer research
Computer science
DNA sequencing
Medicine
Cancer
Computational biology
Genotype
Internal medicine
Mutation
Single-nucleotide polymorphism
DNA
1000 Genomes Project
Bioinformatics
Breakpoint
DNA damage
Economics
Genome instability
Oncology
Pathology
Precision medicine
Structural variation
Benchmark (surveying)
Chromosomal translocation
Context (archaeology)
Environmental health
Exome sequencing