Kết quả tìm kiếm - Warren Cheung

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  1. 1
    High-resolution analyses of human sperm dynamic methylome reveal thousands of novel age-related epigenetic alterations

    High-resolution analyses of human sperm dynamic methylome reveal thousands of novel age-related epigenetic alterations Bằng Mingju Cao, Xiaojian Shao, Peter Chan, Warren Cheung, Tony Kwan, Tomi Pastinen, Bernard Robaire

    Được phát hành 2020
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    Artigo
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  2. 2
    Pangenome graphs improve the analysis of structural variants in rare genetic diseases

    Pangenome graphs improve the analysis of structural variants in rare genetic diseases Bằng Cristian Groza, Carl Schwendinger-Schreck, Warren Cheung, Emily Farrow, Isabelle Thiffault, Juniper A. Lake, William B. Rizzo, Gilad D. Evrony, Tom Curran, Guillaume Bourque, Tomi Pastinen

    Được phát hành 2024
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    Artigo
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  3. 3
    Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

    Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities Bằng Anita M. Quintana, Hung‐Chun Yu, Alison Brebner, Mihaela Pupavac, Elizabeth A. Geiger, Abigail Watson, Victoria L. Castro, Warren Cheung, Shu‐Huang Chen, David Watkins, Tomi Pastinen, Flemming Skovby, Bruce Appel, David S. Rosenblatt, Tamim H. Shaikh

    Được phát hành 2017
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    Artigo
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  4. 4
    Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

    Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation Bằng Stephan Busche, Xiaojian Shao, Maxime Caron, Tony Kwan, Fiona Allum, Warren Cheung, Bing Ge, Susan Westfall, Marie-Michelle Simon, Amy Barrett, Jordana T. Bell, Mark I. McCarthy, Panos Deloukas, Mathieu Blanchette, Guillaume Bourque, Timothy D. Spector, Mark Lathrop, Tomi Pastinen, Elin Grundberg

    Được phát hành 2015
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    Artigo
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  5. 5
    Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape

    Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape Bằng Kaela M. Varberg, Esteban M. Domínguez, Boryana Koseva, Joseph M. Varberg, Ross McNally, Ayelén Moreno-Irusta, Emily R. Wesley, Khursheed Iqbal, Warren Cheung, Carl Schwendinger-Schreck, Craig Smail, Hiroaki Okae, Takahiro Arima, Michael Lydic, Kristin Holoch, Courtney Marsh, Michael J. Soares, Elin Grundberg

    Được phát hành 2023
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    Artigo
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  6. 6
    Single-cell analysis of human adipose tissue identifies depot- and disease-specific cell types

    Single-cell analysis of human adipose tissue identifies depot- and disease-specific cell types Bằng Jinchu Vijay, Marie‐Frédérique Gauthier, Rebecca Biswell, Daniel Louiselle, Jeffrey Johnston, Warren Cheung, Bradley Belden, Albéna Pramatarova, Laurent Biertho, Margaret Gibson, Marie-Michelle Simon, Haig Djambazian, Alfredo Staffa, Guillaume Bourque, Anita Laitinen, Johanna Nystedt, Marie‐Claude Vohl, Jason D. Fraser, Tomi Pastinen, André Tchernof, Elin Grundberg

    Được phát hành 2019
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    Artigo
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  7. 7
    Resolving the unsolved: Comprehensive assessment of tandem repeats at scale

    Resolving the unsolved: Comprehensive assessment of tandem repeats at scale Bằng Egor Dolzhenko, Adam C. English, Harriet Dashnow, Guilherme De Sena Brandine, Tom Mokveld, William J. Rowell, Caitlin Karniski, Zev Kronenberg, Matt C. Danzi, Warren Cheung, Chengpeng Bi, Emily Farrow, Aaron M. Wenger, Verónica Martínez‐Cerdeño, Trevor Bartley, Peng Jin, David L. Nelson, Stephan Züchner, Tomi Pastinen, Aaron R. Quinlan, Fritz J. Sedlazeck, Michael A. Eberle

    Được phát hành 2023
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    Pré-impressão
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  8. 8
    Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort

    Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort Bằng Warren Cheung, Adam F. Johnson, William J. Rowell, Emily Farrow, Richard Hall, Ana S.A. Cohen, John C. Means, Tricia Zion, Daniel M. Portik, Christopher T. Saunders, Boryana Koseva, Chengpeng Bi, Tina K. Truong, Carl Schwendinger-Schreck, Byunggil Yoo, Jeffrey Johnston, Margaret Gibson, Gilad D. Evrony, William B. Rizzo, Isabelle Thiffault, Scott T. Younger, Tom Curran, Aaron M. Wenger, Elin Grundberg, Tomi Pastinen

    Được phát hành 2023
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    Artigo
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  9. 9
    Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

    Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome Bằng Warren Cheung, Xiaojian Shao, Andréanne Morin, Valérie Siroux, Tony Kwan, Bing Ge, Dylan Aïssi, Lu Chen, Louella Vasquez, Fiona Allum, Frédéric Guénard, Emmanuelle Bouzigon, Marie-Michelle Simon, Elodie Boulier, Adriana Redensek, Stephen Watt, Avik Datta, Laura Clarke, Paul Flicek, Daniel G. Mead, Dirk S. Paul, Stephan Beck, Guillaume Bourque, Mark Lathrop, André Tchernof, Marie‐Claude Vohl, Florence Démenais, Isabelle Pin, Kate Downes, Hendrick Stunnenberg, Nicole Soranzo, Tomi Pastinen, Elin Grundberg

    Được phát hành 2019
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    Errata/Corrigenda
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  10. 10
    Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

    Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome Bằng Warren Cheung, Xiaojian Shao, Andréanne Morin, Valérie Siroux, Tony Kwan, Bing Ge, Dylan Aïssi, Lu Chen, Louella Vasquez, Fiona Allum, Frédéric Guénard, Emmanuelle Bouzigon, Marie-Michelle Simon, Elodie Boulier, Adriana Redensek, Stephen Watt, Avik Datta, Laura Clarke, Paul Flicek, Daniel G. Mead, Dirk S. Paul, Stephan Beck, Guillaume Bourque, Mark Lathrop, André Tchernof, Marie‐Claude Vohl, Florence Démenais, Isabelle Pin, Kate Downes, Hendrick Stunnenberg, Nicole Soranzo, Tomi Pastinen, Elin Grundberg

    Được phát hành 2017
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    Artigo
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  11. 11
    H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

    H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis Bằng Ashot S. Harutyunyan, Brian Krug, Haifeng Chen, Simon Papillon‐Cavanagh, Michele Zeinieh, Nicolas Jay, Shriya Deshmukh, Carol Chen, Jad I. Belle, Leonie G. Mikael, Dylan M. Marchione, Rui Li, Hamid Nikbakht, Bo Hu, Gaël Cagnone, Warren Cheung, Abdulshakour Mohammadnia, Denise Béchet, Damien Faury, Melissa K. McConechy, Manav Pathania, Siddhant U. Jain, Benjamin Ellezam, Alexander G. Weil, Alexandre Montpetit, Paolo Salomoni, Tomi Pastinen, Chao Lü, Peter W. Lewis, Benjamin A. García, Claudia L. Kleinman, Nada Jabado, Jacek Majewski

    Được phát hành 2019
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    Artigo
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  12. 12
    Increased DNA methylation variability in type 1 diabetes across three immune effector cell types

    Increased DNA methylation variability in type 1 diabetes across three immune effector cell types Bằng Dirk S. Paul, Andrew E. Teschendorff, Mary Dang, Robert Lowe, Mohammed I. Hawa, Simone Ecker, Huriya Beyan, Stephanie Cunningham, Alexandra Fouts, Anita Ramelius, Frances Burden, Samantha Farrow, Sophia Rowlston, Karola Rehnström, Mattia Frontini, Kate Downes, Stephan Busche, Warren Cheung, Bing Ge, Marie-Michelle Simon, David Bujold, Tony Kwan, Guillaume Bourque, Avik Datta, Ernesto Lowy, Laura Clarke, Paul Flicek, Emanuele Libertini, Simon Heath, Marta Gut, Marta Gut, Willem H. Ouwehand, Tomi Pastinen, Nicole Soranzo, Sabine E. Hofer, Beate Karges, Thomas Meißner, Bernhard O. Boehm, Corrado Cilio, Helena Elding Larsson, Åke Lernmark, Andrea K. Steck, Vardhman K. Rakyan, Stephan Beck, Richard David Leslie

    Được phát hành 2016
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    Artigo
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  13. 13
    Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

    Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells Bằng Lu Chen, Bing Ge, Francesco Paolo Casale, Louella Vasquez, Tony Kwan, Diego Garrido-Martín, Stephen Watt, Ying Yan, Kousik Kundu, Simone Ecker, Avik Datta, David Richardson, Frances Burden, Daniel G. Mead, Alice Mann, José M. Fernández, Sophia Rowlston, Steven P. Wilder, Samantha Farrow, Xiaojian Shao, John Lambourne, Adriana Redensek, Cornelis A. Albers, Vyacheslav Amstislavskiy, Sofie Ashford, Kim Berentsen, Lorenzo Bomba, Guillaume Bourque, David Bujold, Stephan Busche, Maxime Caron, Shu‐Huang Chen, Warren Cheung, Olivier Delaneau, Emmanouil T. Dermitzakis, Heather Elding, Irina Colgiu, Frederik Otzen Bagger, Paul Flicek, Ehsan Habibi, Valentina Iotchkova, Eva M. Janssen‐Megens, Bowon Kim, Hans Lehrach, Ernesto Lowy, Amit Mandoli, Filomena Matarese, Matthew T. Maurano, John Morris, Véra Pancaldi, Farzin Pourfarzad, Karola Rehnström, Augusto Rendon, Thomas S. Risch, Nilofar Sharifi, Marie-Michelle Simon, Marc Sultan, Alfonso Valencia, Klaudia Walter, Shuang-Yin Wang, Mattia Frontini, Stylianos E. Antonarakis, Laura Clarke, Marie‐Laure Yaspo, Stephan Beck, Roderic Guigó, Daniel Rico, Joost H.A. Martens, Willem H. Ouwehand, Taco W. Kuijpers, Dirk S. Paul, Hendrik G. Stunnenberg, Oliver Stegle, Kate Downes, Tomi Pastinen, Nicole Soranzo

    Được phát hành 2016
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    Artigo
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  14. 14
    Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes

    Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes Bằng Ana S.A. Cohen, Emily Farrow, Ahmed Abdelmoity, Joseph T. Alaimo, Shivarajan Amudhavalli, John T. Anderson, Lalit Bansal, Lauren Bartik, Primo Baybayan, Bradley Belden, Courtney Berrios, Rebecca Biswell, Pawel Buczkowicz, Orion J. Buske, Shreyasee Chakraborty, Warren Cheung, Keith A. Coffman, Ashley M. Cooper, Laura Cross, Tom Curran, Thuy Tien T. Dang, Mary Elfrink, Kendra Engleman, Erin Fecske, Cynthia Fieser, Keely Fitzgerald, Emily Fleming, Randi Gadea, Jennifer Gannon, Rose Gelineau‐Morel, Margaret Gibson, Jeffrey A. Goldstein, Elin Grundberg, Kelsee Halpin, Brian S. Harvey, Bryce A. Heese, Wendy Hein, Suzanne Herd, Susan Hughes, Mohammed Ilyas, Jill D. Jacobson, Janda Jenkins, Jiang Shao, Jeffrey Johnston, Kathryn Keeler, Jonas Korlach, Jennifer Kussmann, Christine Lambert, Caitlin E. Lawson, Jean‐Baptiste Le Pichon, J. Steven Leeder, Vicki C. Little, Daniel Louiselle, Michael Lypka, Brittany McDonald, Neil Miller, Ann Modrcin, Annapoorna Nair, Shelby H. Neal, Christopher M. Oermann, Donna Pacicca, Kailash Pawar, Nyshele Posey, Nigel Price, Laura Puckett, Julio Quezada, Nikita Raje, William J. Rowell, Eric T. Rush, Venkatesh Sampath, Carol Saunders, Caitlin Schwager, Richard M. Schwend, Elizabeth Shaffer, Craig Smail, Sarah Soden, Meghan E. Strenk, Bonnie Sullivan, Brooke Sweeney, Jade Tam‐Williams, Adam M. Walter, Holly Welsh, Aaron M. Wenger, Laurel K. Willig, Yun Yan, Scott T. Younger, Dihong Zhou, Tricia Zion, Isabelle Thiffault, Tomi Pastinen

    Được phát hành 2022
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    Artigo
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  15. 15
    Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture

    Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture Bằng Hou‐Feng Zheng, Vincenzo Forgetta, Yi‐Hsiang Hsu, Karol Estrada, Alberto Roselló‐Díez, Paul Leo, Chitra Lekha Dahia, Kyung Hyun Park‐Min, Jonathan H. Tobias, Charles Kooperberg, Aaron Kleinman, Unnur Styrkársdóttir, Yongmei Liu, Charlotta Uggla, Daniel S. Evans, Carrie M. Nielson, Klaudia Walter, U. Pettersson, Shane McCarthy, Joel Eriksson, Tony Kwan, Mila Jhamai, Katerina Trajanoska, Yasin Memari, Josine L. Min, Jie Huang, Petr Danecek, Beth Wilmot, Rui Li, Wen‐Chi Chou, Lauren E. Mokry, Alireza Moayyeri, Melina Claussnitzer, Chia‐Ho Cheng, Warren Cheung, Carolina Medina‐Gómez, Bing Ge, Shu‐Huang Chen, Kwangbom Choi, Ling Oei, James A. Fraser, Robert Kraaij, Matthew Hibbs, Celia L. Gregson, Denis Paquette, Albert Hofman, Carl Wibom, Gregory J. Tranah, Mhairi Marshall, Brooke Gardiner, Katie Cremin, Paul L. Auer, Li Hsu, Susan M. Ring, Joyce Y. Tung, Gudmar Thorleifsson, Anke W. Enneman, Natasja M. van Schoor, C.P.G.M. de Groot, Nathalie van der Velde, Beatrice Melin, John P. Kemp, Claus Christiansen, Adrian Sayers, Yanhua Zhou, Sophie Caldérari, Frank J.A. van Rooij, Chris Carlson, Annette Peters, Soizik Berlivet, Josée Dostie, André G. Uitterlinden, Stephen R. Williams, Charles R. Farber, Daniel Grinberg, Andrea Z. LaCroix, Jeff Haessler, Daniel I. Chasman, Franco Giulianini, Lynda M. Rose, Paul M. Ridker, John A. Eisman, Tuan V. Nguyen, Jacqueline R. Center, Xavier Nogués, Natalia García‐Giralt, Lenore J. Launer, Vilmundur Guðnason, Dan Mellström, Liesbeth Vandenput, Najaf Amin, Cornelia M. van Duijn, Magnus K. Karlsson, Östen Ljunggren, Olle Svensson, Göran Hallmans, François Rousseau, Sylvie Giroux, J L Bussière, Pascal P. Arp

    Được phát hành 2015
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    Artigo
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  16. 16
    The Transcription Factor Encyclopedia

    The Transcription Factor Encyclopedia Bằng Dimas Yusuf, Stefanie Butland, Magdalena I. Swanson, Eugene Bolotin, Amy Ticoll, Warren Cheung, Xiao Yu Cindy Zhang, Christopher Td Dickman, Debra L. Fulton, Jonathan Lim, Jake Schnabl, Oscar HP Ramos, Mireille Vasseur-Cognet, Charles N. de Leeuw, Elizabeth M. Simpson, Gerhart U. Ryffel, Eric W.‐F. Lam, Ralf Kist, Miranda Wilson, Raquel Marco-Ferreres, Jan J. Brosens, Leonardo Beccari, Paola Bovolenta, Bérénice A. Benayoun, Lara J. Monteiro, Helma D.C. Schwenen, Lars Grøntved, Elizabeth D. Wederell, Susanne Mandrup, Reiner A. Veitia, Harini Chakravarthy, Pamela A. Hoodless, Maria Michela Mancarelli, Bruce E. Torbett, Alison H. Banham, Sekhar P. Reddy, Rebecca Cullum, Michaela Liedtke, Mario P. Tschan, Michelle Vaz, Angie Rizzino, Mariastella Zannini, Seth Frietze, Peggy Farnham, Astrid Eijkelenboom, Philip J. Brown, David Laperrière, Dominique Leprince, Tiziana de Cristofaro, Kelly L. Prince, Marrit Putker, Luis del Peso, Gieri Camenisch, Roland H. Wenger, Michał Mikula, Marieke Rozendaal, Sylvie Mader, Jerzy Ostrowski, Simon J. Rhodes, Capucine Van Rechem, Gaylor Boulay, Sam W.Z. Olechnowicz, Mary B. Breslin, Michael S. Lan, Kyster K. Nanan, Michael Wegner, Juan Hou, Rachel D. Mullen, Stephanie C. Colvin, Peter J. Noy, Carol F. Webb, Matthew E. Witek, Scott Ferrell, Juliet M. Daniel, Jason Y. Park, Scott A. Waldman, Daniel J. Peet, Michael J. Taggart, Padma-Sheela Jayaraman, Julien J. Karrich, Bianca Blom, Farhad Vesuna, Henriette O’Geen, Yunfu Sun, Richard M. Gronostajski, Mark W. Woodcroft, Margaret R. Hough, Edwin Chen, G Nicholas Europe-Finner, Magdalena Karolczak‐Bayatti, Jarrod Bailey, Oliver Hankinson, Venu Raman, David P. LeBrun, Shyam Biswal, Christopher J. Harvey, Jason P. DeBruyne, John B. Hogenesch, Robert F. Hevner, Christophe Héligon

    Được phát hành 2012
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    Artigo
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