Søgeresultater - Harrison Brand

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  1. 1
    ESTABLISHMENT OF A CRISPR/CAS9-BASED GENOME EDITING PLATFORM FOR THE GENERATION OF AN OFF-THE-SHELF ALLOGENEIC CAR-T CELL MODEL

    ESTABLISHMENT OF A CRISPR/CAS9-BASED GENOME EDITING PLATFORM FOR THE GENERATION OF AN OFF-THE-SHELF ALLOGENEIC CAR-T CELL MODEL af SCG Lima, Harrison Brand, LC Batista, DMC Fantacini, MGB Coelho, FA Castro, Dimas Tadeu Covas, LEB Souza

    Udgivet 2021
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  2. 2
    Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing

    Low Incidence of Off-Target Mutations in Individual CRISPR-Cas9 and TALEN Targeted Human Stem Cell Clones Detected by Whole-Genome Sequencing af Adrian Veres, Bridget S. Gosis, Qiurong Ding, Ryan L. Collins, Ashok Ragavendran, Harrison Brand, Serkan Erdin, Chad A. Cowan, Michael E. Talkowski, Kiran Musunuru

    Udgivet 2014
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  3. 3
    De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

    De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families af Jonathan R. Belyeu, Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier, Meenal Gupta, Thomas J. Nicholas, Joseph Brown, Lisa Baird, Bernie Devlin, Stephan Sanders, Lynn B. Jorde, Michael E. Talkowski, Aaron R. Quinlan

    Udgivet 2021
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  4. 4
    Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation

    Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation af Harrison Brand, Ryan L. Collins, Carrie Hanscom, Jill A. Rosenfeld, Vamsee Pillalamarri, Matthew R. Stone, Fontina Kelley, Tamara Mason, Lauren Margolin, Stacey Eggert, Elyse Mitchell, Jennelle C. Hodge, James F. Gusella, Stephan Sanders, Michael E. Talkowski

    Udgivet 2015
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  5. 5
    GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data

    GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data af Mehrtash Babadi, Jack Fu, Samuel K. Lee, Andrey N. Smirnov, Laura D. Gauthier, Mark Walker, David Benjamin, Xuefang Zhao, Konrad J. Karczewski, Isaac Wong, Ryan L. Collins, Alba Sanchis‐Juan, Harrison Brand, Eric Banks, Michael E. Talkowski

    Udgivet 2023
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  6. 6
    <i>CHD8</i> regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors

    <i>CHD8</i> regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors af Aarathi Sugathan, Marta Biagioli, Christelle Golzio, Serkan Erdin, Ian Blumenthal, Poornima Manavalan, Ashok Ragavendran, Harrison Brand, Diane Lucente, Judith H. Miles, Steven D. Sheridan, Alexei Stortchevoi, Manolis Kellis, Stephen J. Haggarty, Nicholas Katsanis, James F. Gusella, Michael E. Talkowski

    Udgivet 2014
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  7. 7
    High-Resolution and Noninvasive Fetal Exome Screening

    High-Resolution and Noninvasive Fetal Exome Screening af Harrison Brand, Christopher W. Whelan, Michael H. Duyzend, John Lemanski, Monica Salani, Stephanie P. Hao, Isaac Wong, Elise Valkanas, Caroline Cusick, Casie A. Genetti, Lori Dobson, Courtney Studwell, Kathleen Gianforcaro, Louise Wilkins‐Haug, Stephanie Guseh, Benjamin Currall, Kathryn J. Gray, Michael E. Talkowski

    Udgivet 2023
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  8. 8
    Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9

    Efficient Ablation of Genes in Human Hematopoietic Stem and Effector Cells using CRISPR/Cas9 af Pankaj Kumar Mandal, Leonardo M. R. Ferreira, Ryan L. Collins, Torsten Meißner, Christian L. Boutwell, Max Friesen, Vladimir Vrbanac, Brian S. Garrison, Alexei Stortchevoi, David Bryder, Kiran Musunuru, Harrison Brand, Andrew M. Tager, Todd M. Allen, Michael E. Talkowski, Derrick J. Rossi, Chad A. Cowan

    Udgivet 2014
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  9. 9
    High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

    High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios af Marta Byrska-Bishop, Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison Regier, André Corvelo, Wayne E. Clarke, Rajeeva Musunuri, Kshithija Nagulapalli, Susan Fairley, Alexi Runnels, Lara Winterkorn, Ernesto Lowy, Paul Flicek, Søren Germer, Harrison Brand, Ira M. Hall, Michael E. Talkowski, Giuseppe Narzisi, Michael C. Zody

    Udgivet 2021
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  10. 10
    Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate

    Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate af Zena Wolf, Harrison Brand, John R. Shaffer, Elizabeth J. Leslie, Boaz Arzi, Cali E. Willet, Timothy C. Cox, Toby McHenry, Nicole Narayan, Eleanor Feingold, Wang Xioajing, Sliskovic Saundra, Nili Karmi, Noa Safra, Carla Sanchez, Frederic W.‐B. Deleyiannis, Jeffrey C. Murray, Claire M. Wade, Mary L. Marazita, Danika L. Bannasch

    Udgivet 2015
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  11. 11
    Rare germline structural variants increase risk for pediatric solid tumors

    Rare germline structural variants increase risk for pediatric solid tumors af Riaz Gillani, Ryan L. Collins, Jett Crowdis, Amanda Garza, Jill K. Jones, Mark Walker, Alba Sanchis-Juan, Christopher W. Whelan, Emma Pierce‐Hoffman, Michael E. Talkowski, Harrison Brand, Kevin M. Haigis, Jaclyn LoPiccolo, Saud H. AlDubayan, Alexander Gusev, Brian D. Crompton, Katherine A. Janeway, Eliezer M. Van Allen

    Udgivet 2025
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  12. 12
    Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders

    Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders af Harrison Brand, Vamsee Pillalamarri, Ryan L. Collins, Stacey Eggert, Colm Ó'Dúshláine, Ellen B. Braaten, Matthew R. Stone, Kimberly Chambert, Nathan D. Doty, Carrie Hanscom, Jill A. Rosenfeld, Hillary L. Ditmars, Jessica E. Blais, Ryan E. Mills, Charles Lee, James F. Gusella, Steven A. McCarroll, Jordan W. Smoller, Michael E. Talkowski, Alysa E. Doyle

    Udgivet 2014
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  13. 13
    Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies

    Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies af Xuefang Zhao, Ryan L. Collins, Wan‐Ping Lee, Alexandra M. Weber, Yukyung Jun, Qihui Zhu, Ben Weisburd, Yongqing Huang, Peter A. Audano, Harold Wang, Mark Walker, Chelsea Lowther, Jack Fu, Mark Gerstein, Scott E. Devine, Tobias Marschall, Jan O. Korbel, Evan E. Eichler, Mark Chaisson, Charles Lee, Ryan E. Mills, Harrison Brand, Michael E. Talkowski

    Udgivet 2021
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  14. 14
    A harmonized public resource of deeply sequenced diverse human genomes

    A harmonized public resource of deeply sequenced diverse human genomes af Zan Koenig, Mary T. Yohannes, Lethukuthula L. Nkambule, Xuefang Zhao, Julia K. Goodrich, Heesu Ally Kim, Michael W. Wilson, Grace Tiao, Stephanie P. Hao, Nareh Sahakian, Katherine R. Chao, Mark Walker, Yunfei Lyu, Heidi L. Rehm, Benjamin M. Neale, Michael E. Talkowski, Mark J. Daly, Harrison Brand, Konrad J. Karczewski, Elizabeth G. Atkinson, Alicia R. Martin

    Udgivet 2023
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  15. 15
    A harmonized public resource of deeply sequenced diverse human genomes

    A harmonized public resource of deeply sequenced diverse human genomes af Zan Koenig, Mary T. Yohannes, Lethukuthula L. Nkambule, Xuefang Zhao, Julia K. Goodrich, Heesu Ally Kim, Michael W. Wilson, Grace Tiao, Stephanie P. Hao, Nareh Sahakian, Katherine R. Chao, Mark A. Walker, Yunfei Lyu, Heidi L. Rehm, Benjamin M. Neale, Michael E. Talkowski, Mark J. Daly, Harrison Brand, Konrad J. Karczewski, Elizabeth G. Atkinson, Alicia R. Martin

    Udgivet 2024
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  16. 16
    Loss of δ-catenin function in severe autism

    Loss of δ-catenin function in severe autism af Tychele N. Turner, Kamal Sharma, Edwin C. Oh, Yangfan P. Liu, Ryan L. Collins, Maria X. Sosa, Dallas R. Auer, Harrison Brand, Stephan Sanders, Daniel Moreno‐De‐Luca, Vasyl Pihur, Teri M. Plona, Kristen Pike, Daniel Soppet, Michael W. Smith, Sau Wai Cheung, Christa Lese Martin, Matthew W. State, Michael E. Talkowski, Edwin H. Cook, Richard L. Huganir, Nicholas Katsanis, Aravinda Chakravarti

    Udgivet 2015
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  17. 17
    Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis

    Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis af Zehra Ordulu, Tammy Kammin, Harrison Brand, Vamsee Pillalamarri, Claire Redin, Ryan L. Collins, Ian Blumenthal, Carrie Hanscom, Shahrin Pereira, India Bradley, Barbara F. Crandall, Pamela Gerrol, Mark A. Hayden, Naveed Hussain, Bibi Kanengisser‐Pines, Sibel Kantarci, Brynn Levy, Michael J. Macera, Fabiola Quintero‐Rivera, Erica Spiegel, Blair Stevens, Janet E. Ulm, Dorothy Warburton, Louise Wilkins‐Haug, Naomi Yachelevich, James F. Gusella, Michael E. Talkowski, Cynthia C. Morton

    Udgivet 2016
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  18. 18
    Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

    Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting af Kimberly K. Diaz Perez, Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho, Bridget Carter, Toby McHenry, Madison R. Bishop, Luz Consuelo Valencia‐Ramirez, Claudia Restrepo, Jacqueline T. Hecht, Lina M. Moreno Uribe, George L. Wehby, Seth M. Weinberg, Terri H. Beaty, Jeffrey C. Murray, Eleanor Feingold, Mary L. Marazita, David J. Cutler, Michael P. Epstein, Harrison Brand, Elizabeth J. Leslie

    Udgivet 2023
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  19. 19
    Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

    Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome af Ryan L. Collins, Harrison Brand, Claire Redin, Carrie Hanscom, Caroline Antolik, Matthew R. Stone, Joseph Glessner, Tamara Mason, Giulia Pregno, Naghmeh Dorrani, Giorgia Mandrile, Daniela Giachino, Danielle Perrin, Cole Walsh, Michelle Cipicchio, Maura Costello, Alexei Stortchevoi, Joon‐Yong An, Benjamin Currall, Catarina M. Seabra, Ashok Ragavendran, Lauren Margolin, Julián A. Martínez-Agosto, Diane Lucente, Brynn Levy, Stephan Sanders, Ronald J. Wapner, Fabiola Quintero‐Rivera, Wigard P. Kloosterman, Michael E. Talkowski

    Udgivet 2017
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  20. 20
    Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

    Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios af Madison R. Bishop, Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay, Jacqueline B. Hetmanski, Margaret A. Taub, Lina Moreno‐Uribe, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton, George L. Wehby, Jacqueline T. Hecht, Frederic W.‐B. Deleyiannis, Seth M. Weinberg, Yah Huei Wu‐Chou, Philip K. Chen, Harrison Brand, Michael P. Epstein, Ingo Ruczinski, Jeffrey C. Murray, Terri H. Beaty, Eleanor Feingold, Robert J. Lipinski, David J. Cutler, Mary L. Marazita, Elizabeth J. Leslie

    Udgivet 2020
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