Canlyniadau Chwilio - Joep de Ligt

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  1. 1
    Real-Time Genomics for Tracking Severe Acute Respiratory Syndrome Coronavirus 2 Border Incursions after Virus Elimination, New Zealand

    Real-Time Genomics for Tracking Severe Acute Respiratory Syndrome Coronavirus 2 Border Incursions after Virus Elimination, New Zealand gan Jordan Douglas, Jemma L. Geoghegan, James Hadfield, Remco Bouckaert, Matthew Storey, Xiaoyun Ren, Joep de Ligt, Nigel French, David Welch

    Cyhoeddwyd 2021
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  2. 2
    Tracing the international arrivals of SARS-CoV-2 Omicron variants after Aotearoa New Zealand reopened its border

    Tracing the international arrivals of SARS-CoV-2 Omicron variants after Aotearoa New Zealand reopened its border gan Jordan Douglas, David J. Winter, Andrea McNeill, Sam Carr, Michael Bunce, Nigel French, James Hadfield, Joep de Ligt, David Welch, Jemma L. Geoghegan

    Cyhoeddwyd 2022
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  3. 3
    Genomic epidemiology of Delta SARS-CoV-2 during transition from elimination to suppression in Aotearoa New Zealand

    Genomic epidemiology of Delta SARS-CoV-2 during transition from elimination to suppression in Aotearoa New Zealand gan Lauren Jelley, Jordan Douglas, Xiaoyun Ren, David J. Winter, Andrea McNeill, Q. Sue Huang, Nigel French, David Welch, James Hadfield, Joep de Ligt, Jemma L. Geoghegan

    Cyhoeddwyd 2022
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  4. 4
    Mobster: accurate detection of mobile element insertions in next generation sequencing data

    Mobster: accurate detection of mobile element insertions in next generation sequencing data gan Djie Tjwan Thung, Joep de Ligt, Lisenka E.L.M. Vissers, Marloes Steehouwer, Mark Kroon, Petra de Vries, P. Eline Slagboom, Kai Ye, Joris A. Veltman, Jayne Y. Hehir‐Kwa

    Cyhoeddwyd 2014
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  5. 5
    Cancer cells copy migratory behavior and exchange signaling networks via extracellular vesicles

    Cancer cells copy migratory behavior and exchange signaling networks via extracellular vesicles gan Sander Christiaan Steenbeek, Thang V. Pham, Joep de Ligt, Anoek Zomer, Jaco C. Knol, Sander R. Piersma, Tim Schelfhorst, Rick Huisjes, Raymond M. Schiffelers, Edwin Cuppen, Connie R. Jiménez, Jacco van Rheenen

    Cyhoeddwyd 2018
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  6. 6
    Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer

    Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer gan Myrthe Jager, Francis Blokzijl, Ewart Kuijk, Johanna Bertl, Maria Vougioukalaki, Roel Janssen, Nicolle Besselink, Sander Boymans, Joep de Ligt, Jakob Skou Pedersen, Jan H.J. Hoeijmakers, Joris Pothof, Ruben van Boxtel, Edwin Cuppen

    Cyhoeddwyd 2019
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  7. 7
    Novel genetic causes for cerebral visual impairment

    Novel genetic causes for cerebral visual impairment gan Daniëlle G.M. Bosch, F. Nienke Boonstra, Nicole de Leeuw, Rolph Pfundt, Willy M. Nillesen, Joep de Ligt, Christian Gilissen, Shalini N. Jhangiani, James R. Lupski, Frans P.M. Cremers, Bert BA de Vries

    Cyhoeddwyd 2015
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  8. 8
    Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer

    Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer gan Jarno Drost, Ruben van Boxtel, Francis Blokzijl, Tomohiro Mizutani, Nobuo Sasaki, Valentina Sasselli, Joep de Ligt, Sam Behjati, Judith E. Grolleman, Tom van Wezel, Serena Nik‐Zainal, Roland P. Kuiper, Edwin Cuppen, Hans Clevers

    Cyhoeddwyd 2017
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  9. 9
    Genetic dissection of colorectal cancer progression by orthotopic transplantation of engineered cancer organoids

    Genetic dissection of colorectal cancer progression by orthotopic transplantation of engineered cancer organoids gan Arianna Fumagalli, Jarno Drost, Saskia J.E. Suijkerbuijk, Ruben van Boxtel, Joep de Ligt, G. Johan A. Offerhaus, Harry Begthel, Evelyne Beerling, Ee Hong Tan, Owen J. Sansom, Edwin Cuppen, Hans Clevers, Jacco van Rheenen

    Cyhoeddwyd 2017
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  10. 10
    Genomic landscape of rat strain and substrain variation

    Genomic landscape of rat strain and substrain variation gan Roel Hermsen, Joep de Ligt, Wim Spee, Francis Blokzijl, Sebastian Schäfer, Eleonora Adami, Sander Boymans, Stephen C. Flink, Ruben van Boxtel, Robin H. van der Weide, Timothy J. Aitman, Norbert Hübner, Marieke Simonis, Boris Tabakoff, Victor Guryev, Edwin Cuppen

    Cyhoeddwyd 2015
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  11. 11
    Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing

    Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing gan Joep de Ligt, Philip M. Boone, Rolph Pfundt, Lisenka E.L.M. Vissers, Todd Richmond, Joel Geoghegan, Kathleen O’Moore, Nicole de Leeuw, Christine J. Shaw, Han G. Brunner, James R. Lupski, Joris A. Veltman, Jayne Y. Hehir‐Kwa

    Cyhoeddwyd 2013
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  12. 12
    Mapping and phasing of structural variation in patient genomes using nanopore sequencing

    Mapping and phasing of structural variation in patient genomes using nanopore sequencing gan Mircea Cretu Stancu, Markus J. van Roosmalen, Ivo Renkens, Marleen M. Nieboer, Sjors Middelkamp, Joep de Ligt, Giulia Pregno, Daniela Giachino, Giorgia Mandrile, Jose Espejo Valle-Inclán, Jerome Korzelius, Ewart de Bruijn, Edwin Cuppen, Michael E. Talkowski, Tobias Marschall, Jeroen de Ridder, Wigard P. Kloosterman

    Cyhoeddwyd 2017
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  13. 13
    Genomic epidemiology reveals transmission patterns and dynamics of SARS-CoV-2 in Aotearoa New Zealand

    Genomic epidemiology reveals transmission patterns and dynamics of SARS-CoV-2 in Aotearoa New Zealand gan Jemma L. Geoghegan, Xiaoyun Ren, Matthew Storey, James Hadfield, Lauren Jelley, Sarah Jefferies, Jill Sherwood, Shevaun Paine, Q. Sue Huang, Jordan Douglas, Fábio K. Mendes, Andrew Sporle, Michael G. Baker, David R. Murdoch, Nigel French, Colin R Simpson, David Welch, Alexei J. Drummond, Edward C. Holmes, Sebastián Duchêne, Joep de Ligt

    Cyhoeddwyd 2020
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  14. 14
    Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome

    Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome gan Lisenka E.L.M. Vissers, Monica Bonetti, Jeroen Overman, Willy M. Nillesen, Suzanna G.M. Frints, Joep de Ligt, Giuseppe Zampino, Ana Justino, José Carlos Machado, Marga Schepens, Han G. Brunner, Joris A. Veltman, Hans Scheffer, Piet Gros, José Luís Costa, Marco Tartaglia, Ineke van der Burgt, Helger G. Yntema, Jeroen den Hertog

    Cyhoeddwyd 2014
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  15. 15
    Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

    Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability gan Joep de Ligt, Marjolein H. Willemsen, Bregje W.M. van Bon, Tjitske Kleefstra, Helger G. Yntema, Thessa Kroes, Anneke T. Vulto-van Silfhout, David A. Koolen, Petra de Vries, Christian Gilissen, Marisol del Rosario, Alexander Hoischen, Hans Scheffer, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman, Lisenka E.L.M. Vissers

    Cyhoeddwyd 2012
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  16. 16
    Genomic Evidence of In-Flight Transmission of SARS-CoV-2 Despite Predeparture Testing

    Genomic Evidence of In-Flight Transmission of SARS-CoV-2 Despite Predeparture Testing gan Tara Swadi, Jemma L. Geoghegan, Tom Devine, Caroline McElnay, Jillian Sherwood, Phil Shoemack, Xiaoyun Ren, Matt Storey, Sarah Jefferies, Erasmus Smit, James Hadfield, Aoife Kenny, Lauren Jelley, Andrew Sporle, Andrea McNeill, G. Edwin Reynolds, Kip Mouldey, Lindsay Lowe, Gerard J.B. Sonder, Alexei J. Drummond, Q. Sue Huang, David Welch, Edward C. Holmes, Nigel French, Colin R Simpson, Joep de Ligt

    Cyhoeddwyd 2021
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  17. 17
    Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver

    Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver gan Meritxell Huch, Helmuth Gehart, Ruben van Boxtel, Karien M. Hamer, Francis Blokzijl, Monique M.A. Verstegen, Ewa Ellis, Martien van Wenum, Sabine A. Fuchs, Joep de Ligt, Marc van de Wetering, Nobuo Sasaki, Susanne J. Boers, Hans Kemperman, Jeroen de Jonge, Jan N.M. IJzermans, Edward E. S. Nieuwenhuis, Ruurdtje Hoekstra, Stephen C. Strom, Robert Vries, Luc J. W. van der Laan, Edwin Cuppen, Hans Clevers

    Cyhoeddwyd 2014
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  18. 18
    Next‐generation genetic testing for retinitis pigmentosa

    Next‐generation genetic testing for retinitis pigmentosa gan Kornelia Neveling, Rob W.J. Collin, Christian Gilissen, Ramon A. C. van Huet, Linda Visser, Michael Kwint, Sabine Gijsen, Marijke N. Zonneveld, Nienke Wieskamp, Joep de Ligt, Anna M. Siemiatkowska, Lies H. Hoefsloot, Michael F. Buckley, Ulrich Kellner, Kari Branham, Anneke I. den Hollander, Alexander Hoischen, Carel B. Hoyng, B. Jeroen Klevering, L. Ingeborgh van den Born, Joris A. Veltman, Frans P.M. Cremers, Hans Scheffer

    Cyhoeddwyd 2012
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  19. 19
    NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability

    NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability gan Daniëlle G.M. Bosch, F. Nienke Boonstra, Claudia Gonzaga‐Jauregui, Mafei Xu, Joep de Ligt, Shalini N. Jhangiani, Wojciech Wiszniewski, Donna M. Muzny, Helger G. Yntema, Rolph Pfundt, Lisenka E.L.M. Vissers, Liesbeth Spruijt, Ellen A.W. Blokland, Chun‐An Chen, Richard A. Lewis, Sophia Y. Tsai, Richard A. Gibbs, Ming‐Jer Tsai, James R. Lupski, Huda Y. Zoghbi, Frans P.M. Cremers, Bert B.A. de Vries, Christian P. Schaaf

    Cyhoeddwyd 2014
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  20. 20
    <i>GATAD2B</i>loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in<i>Drosophila</i>

    <i>GATAD2B</i>loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in<i>Drosophi... gan Marjolein H. Willemsen, Bonnie Nijhof, Michaela Fencková, Willy M. Nillesen, Ernie M.H.F. Bongers, Anna Castells‐Nobau, Lenke Asztalos, Erika Viràgh, Bregje W.M. van Bon, Emre Tezel, Joris A. Veltman, Han G. Brunner, Bert B.A. de Vries, Joep de Ligt, Helger G. Yntema, Hans van Bokhoven, Bertrand Isidor, Cédric Le Caignec, Elsa Lorino, Zoltán Asztalos, David A. Koolen, Lisenka E.L.M. Vissers, Annette Schenck, Tjitske Kleefstra

    Cyhoeddwyd 2013
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