Search Results - Fabian Grubert

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  1. 1
    A single-molecule long-read survey of the human transcriptome

    A single-molecule long-read survey of the human transcriptome by Donald Sharon, Hagen Tilgner, Fabian Grubert, M Snyder

    Published 2013
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  2. 2
    Defining a personal, allele-specific, and single-molecule long-read transcriptome

    Defining a personal, allele-specific, and single-molecule long-read transcriptome by Hagen Tilgner, Fabian Grubert, Donald Sharon, M Snyder

    Published 2014
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  3. 3
    A procedure for highly specific, sensitive, and unbiased whole-genome amplification

    A procedure for highly specific, sensitive, and unbiased whole-genome amplification by Xinghua Pan, Alexander E. Urban, Dean Palejev, Vincent Schulz, Fabian Grubert, Yiping Hu, M Snyder, Sherman M. Weissman

    Published 2008
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  4. 4
    Genome-wide map of regulatory interactions in the human genome

    Genome-wide map of regulatory interactions in the human genome by Nastaran Heidari, Douglas H. Phanstiel, Chao He, Fabian Grubert, Fereshteh Jahanbani, Maya Kasowski, Michael Q. Zhang, M Snyder

    Published 2014
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  5. 5
    Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome

    Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome by Jan O. Korbel, Alexander E. Urban, Fabian Grubert, Jiang Du, Thomas Royce, Peter Starr, Guoneng Zhong, Beverly S. Emanuel, Sherman M. Weissman, M Snyder, Mark Gerstein

    Published 2007
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  6. 6
    Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

    Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history by Philip M. Kim, Hugo Y. K. Lam, Alexander E. Urban, Jan O. Korbel, Jason P. Affourtit, Fabian Grubert, Xueying Chen, Sherman M. Weissman, M Snyder, Mark Gerstein

    Published 2008
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  7. 7
    Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans

    Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans by Can Cenik, Elif Sarinay Cenik, Gun Woo Byeon, Fabian Grubert, Sophie I. Candille, Damek V. Spacek, Bilal Alsallakh, Hagen Tilgner, Carlos L. Araya, Hua Tang, Emiliano P. Ricci, M Snyder

    Published 2015
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  8. 8
    Transcriptome Sequencing from Diverse Human Populations Reveals Differentiated Regulatory Architecture

    Transcriptome Sequencing from Diverse Human Populations Reveals Differentiated Regulatory Architecture by Alicia R. Martin, Helio A. Costa, Tuuli Lappalainen, Brenna M. Henn, Jeffrey M. Kidd, Muh-Ching Yee, Fabian Grubert, Howard M. Cann, M Snyder, Stephen B. Montgomery, Carlos D. Bustamante

    Published 2014
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  9. 9
    Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension

    Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension by Armando Reyes‐Palomares, Mingxia Gu, Fabian Grubert, Ivan Berest, Silin Sa, Maya Kasowski, Christian Arnold, Shuai Mao, Rohith Srivas, Yifei Miao, Dan Li, M Snyder, Marlene Rabinovitch, Judith B. Zaugg

    Published 2020
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  10. 10
    Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

    Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy by Juliane Winkelmann, Ling Lin, Barbara Schormair, Birgitte Rahbek Kornum, Juliette Faraco, Giuseppe Plazzi, Atle Melberg, F. Cornelio, Alexander E. Urban, Fabio Pizza, Francesca Poli, Fabian Grubert, Thomas Wieland, Elisabeth Graf, Joachim Hallmayer, Tim M. Strom, Emmanuel Mignot

    Published 2012
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  11. 11
    Induced Pluripotent Stem Cell Model of Pulmonary Arterial Hypertension Reveals Novel Gene Expression and Patient Specificity

    Induced Pluripotent Stem Cell Model of Pulmonary Arterial Hypertension Reveals Novel Gene Expression and Patient Specificity by Silin Sa, Mingxia Gu, James Chappell, Ning‐Yi Shao, Mohamed Ameen, Kathryn Elliott, Dan Li, Fabian Grubert, Caiyun G. Li, Shalina Taylor, Aiqin Cao, Yu Ma, Ryan Fong, Long Nguyen, Joseph C. Wu, M Snyder, Marlene Rabinovitch

    Published 2016
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  12. 12
    Variation in Transcription Factor Binding Among Humans

    Variation in Transcription Factor Binding Among Humans by Maya Kasowski, Fabian Grubert, Christopher Heffelfinger, Manoj Hariharan, Akwasi Asabere, Sebastian M. Waszak, Lukas Habegger, Joel Rozowsky, Minyi Shi, Alexander E. Urban, Mi-Young Hong, Konrad J. Karczewski, Wolfgang Huber, Sherman M. Weissman, Mark Gerstein, Jan O. Korbel, M Snyder

    Published 2010
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  13. 13
    Landscape of cohesin-mediated chromatin loops in the human genome

    Landscape of cohesin-mediated chromatin loops in the human genome by Fabian Grubert, Rohith Srivas, Damek V. Spacek, Maya Kasowski, Mariana Ruiz-Velasco, Nasa Sinnott-Armstrong, Peyton Greenside, Anil Narasimha, Qing Liu, Benjamin S. Geller, Akshay Sanghi, Michael Kulik, Silin Sa, Marlene Rabinovitch, Anshul Kundaje, Stephen Dalton, Judith B. Zaugg, M Snyder

    Published 2020
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  14. 14
    Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions

    Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions by Fabian Grubert, Judith B. Zaugg, Maya Kasowski, Oana Ursu, Damek V. Spacek, Alicia R. Martin, Peyton Greenside, Rohith Srivas, Doug Phanstiel, Aleksandra Pękowska, Nastaran Heidari, Ghia Euskirchen, Wolfgang Huber, Jonathan K. Pritchard, Carlos D. Bustamante, Lars M. Steinmetz, Anshul Kundaje, M Snyder

    Published 2015
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  15. 15
    Extensive Variation in Chromatin States Across Humans

    Extensive Variation in Chromatin States Across Humans by Maya Kasowski, Sofia Kyriazopoulou-Panagiotopoulou, Fabian Grubert, Judith B. Zaugg, Anshul Kundaje, Yuling Liu, Alan P. Boyle, Qiangfeng Cliff Zhang, Fouad Zakharia, Damek V. Spacek, Jingjing Li, Dan Xie, Anthony O. Olarerin-George, Lars M. Steinmetz, John B. Hogenesch, Manolis Kellis, Serafim Batzoglou, M Snyder

    Published 2013
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  16. 16
    Patient-Specific iPSC-Derived Endothelial Cells Uncover Pathways that Protect against Pulmonary Hypertension in BMPR2 Mutation Carriers

    Patient-Specific iPSC-Derived Endothelial Cells Uncover Pathways that Protect against Pulmonary Hypertension in BMPR2 Mutation Carriers by Mingxia Gu, Ning‐Yi Shao, Silin Sa, Dan Li, Vittavat Termglinchan, Mohamed Ameen, Ioannis Karakikes, Gustavo Sosa, Fabian Grubert, Jaecheol Lee, Aiqin Cao, Shalina Taylor, Yu Ma, Zhixin Zhao, James Chappell, Rizwan Hamid, Eric D. Austin, Joseph Gold, Joseph C. Wu, M Snyder, Marlene Rabinovitch

    Published 2016
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  17. 17
    A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans

    A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans by Chip Stewart, Deniz Kural, Michael P. Strömberg, Jerilyn A. Walker, Miriam K. Konkel, Adrian M. Stütz, Alexander E. Urban, Fabian Grubert, Hugo Y. K. Lam, Wan-Ping Lee, Michele Busby, Amit Indap, Erik Garrison, Chad D. Huff, Jinchuan Xing, M Snyder, Lynn B. Jorde, Mark A. Batzer, Jan O. Korbel, Gábor Marth

    Published 2011
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  18. 18
    Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome

    Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome by Jan O. Korbel, Alexander E. Urban, Jason P. Affourtit, Brian C. Godwin, Fabian Grubert, Jan Fredrik Simons, Philip M. Kim, Dean Palejev, Nicholas Carriero, Lei Du, Bruce E. Taillon, Zhoutao Chen, Andrea Tanzer, Abbey Saunders, Jianxiang Chi, Fengtang Yang, Nigel P. Carter, Matthew E. Hurles, Sherman M. Weissman, Timothy T. Harkins, Mark Gerstein, Michael D. Miller, M Snyder

    Published 2007
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  19. 19
    The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

    The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies by Jan O. Korbel, Tal Tirosh‐Wagner, Alexander E. Urban, Xiao–Ning Chen, Maya Kasowski, Li Dai, Fabian Grubert, Chandra Erdman, Michael Gao, K. LANGE, Eric M. Sobel, Gillian M. Barlow, Arthur S. Aylsworth, Nancy J. Carpenter, Robin D. Clark, Monika Cohen, Eric Doran, Tzipora C. Falik‐Zaccai, Susan O. Lewin, Ira T. Lott, Barbara McGillivray, John B. Moeschler, Mark J. Pettenati, Siegfried M. Pueschel, Kathleen W. Rao, Lisa G. Shaffer, Mordechai Shohat, Alexander J. Van Riper, Dorothy Warburton, Sherman M. Weissman, Mark Gerstein, M Snyder, Julie R. Korenberg

    Published 2009
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  20. 20
    Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

    Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes by Rui Chen, George I. Mias, Jennifer Li‐Pook‐Than, Lihua Jiang, Hugo Y. K. Lam, Rong Chen, Elana Miriami, Konrad J. Karczewski, Manoj Hariharan, Frederick E. Dewey, Yong Cheng, Michael J. Clark, Hogune Im, Lukas Habegger, Suganthi Balasubramanian, Maeve O’Huallachain, Joel T. Dudley, Sara Hillenmeyer, Rajini Haraksingh, Donald Sharon, Ghia Euskirchen, Phil Lacroute, Keith Bettinger, Alan P. Boyle, Maya Kasowski, Fabian Grubert, Scott Seki, Marco Garcia, Michelle Whirl‐Carrillo, Mercedes Gallardo, Marı́a A. Blasco, Peter L. Greenberg, Phyllis J. Snyder, Teri E. Klein, Russ B. Altman, Atul J. Butte, Euan A. Ashley, Mark Gerstein, Kari C. Nadeau, Hua Tang, M Snyder

    Published 2012
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