Хайлтын үр дүнгүүд - Raheleh Rahbari
- 20-н 1 - 20 үр дүнгүүдийг харуулж байна
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Understanding the Genomic Structure of Copy-Number Variation of the Low-Affinity Fcγ Receptor Region Allows Confirmation of the Association of<i>FCGR3B</i>Deletion with Rheumatoid... -н Raheleh Rahbari, Luciana W. Zuccherato, German Tischler, Belinda Chihota, Hasret Ozturk, Sara Saleem, Eduardo Tarazona‐Santos, Lee R. Machado, Edward J. Hollox
Хэвлэсэн 2016Artigo -
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Detection of structural mosaicism from targeted and whole-genome sequencing data -н Daniel A. King, Alejandro Sifrim, Tomas Fitzgerald, Raheleh Rahbari, Emma Hobson, Tessa Homfray, Sahar Mansour, Sarju Mehta, Mohammed Shehla, Susan Tomkins, Pradeep Vasudevan, Matthew E. Hurles
Хэвлэсэн 2017Artigo -
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Timing, rates and spectra of human germline mutation -н Raheleh Rahbari, Arthur Wüster, Sarah Lindsay, Robert J. Hardwick, Ludmil B. Alexandrov, Saeed Al Turki, Anna F. Dominiczak, Andrew D. Morris, David J. Porteous, Blair H. Smith, Michael R. Stratton, Matthew E. Hurles
Хэвлэсэн 2015Artigo -
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Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes -н Vagheesh M. Narasimhan, Raheleh Rahbari, Aylwyn Scally, Arthur Wüster, Dan Mason, Yali Xue, John Wright, Richard C. Trembath, Eamonn R. Maher, David A. van Heel, Adam Auton, Matthew E. Hurles, Chris Tyler‐Smith, Richard Durbin
Хэвлэсэн 2017Artigo -
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Insights into non-crossover recombination from long-read sperm sequencing -н Regev Schweiger, Sang-Jin Lee, Chenxi Zhou, Tsun-Po Yang, Katie Smith, Stacy Li, Rashesh Sanghvi, Matthew D. C. Neville, Emily Mitchell, Ayrun Nessa, Sam Wadge, Kerrin S. Small, Peter J. Campbell, Peter H. Sudmant, Raheleh Rahbari, Richard Durbin
Хэвлэсэн 2024Pré-impressão -
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Inherent mosaicism and extensive mutation of human placentas -н Tim H. H. Coorens, Thomas R. W. Oliver, Rashesh Sanghvi, Ulla Sovio, Emma Cook, Roser Vento‐Tormo, Muzlifah Haniffa, Matthew D. Young, Raheleh Rahbari, Neil J. Sebire, Peter J. Campbell, D. Stephen Charnock‐Jones, Gordon C. S. Smith, Sam Behjati
Хэвлэсэн 2021Artigo -
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Genetic and chemotherapeutic influences on germline hypermutation -н Joanna Kaplanis, Benjamin Ide, Rashesh Sanghvi, Matthew D. C. Neville, Petr Danecek, Tim H. H. Coorens, Elena Prigmore, Patrick Short, Giuseppe Gallone, Jeremy F. McRae, Loukas Moutsianas, Chris A. Odhams, Jenny Carmichael, Angela Barnicoat, Helen V. Firth, Patrick O’Brien, Raheleh Rahbari, Matthew E. Hurles
Хэвлэсэн 2022Artigo -
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Increased somatic mutation burdens in normal human cells due to defective DNA polymerases -н Philip S. Robinson, Tim H. H. Coorens, Claire Palles, Emily Mitchell, Federico Abascal, Sigurgeir Ólafsson, Bernard C. H. Lee, Andrew Lawson, Henry Lee-Six, Luiza Moore, Mathijs A. Sanders, James Hewinson, Lynn Martin, Claudia M.A. Pinna, Sara Galavotti, Raheleh Rahbari, Peter J. Campbell, Iñigo Martincorena, Ian Tomlinson, Michael R. Stratton
Хэвлэсэн 2021Artigo -
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Extensive phylogenies of human development inferred from somatic mutations -н Tim H. H. Coorens, Luiza Moore, Philip S. Robinson, Rashesh Sanghvi, Joseph Christopher, James Hewinson, Moritz J. Przybilla, Andrew Lawson, Michael Spencer Chapman, Alex Cagan, Thomas R. W. Oliver, Matthew D. C. Neville, Yvette Hooks, Ayesha Noorani, Thomas J. Mitchell, Rebecca C. Fitzgerald, Peter J. Campbell, Iñigo Martincorena, Raheleh Rahbari, Michael R. Stratton
Хэвлэсэн 2021Artigo -
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Common clonal origin of conventional T cells and induced regulatory T cells in breast cancer patients -н Maria Xydia, Raheleh Rahbari, Eliana Ruggiero, Iain C. Macaulay, Maxime Tarabichi, Robert Lohmayer, Stefan Wilkening, Tillmann Michels, Daniel V. Brown, Sebastiaan Vanuytven, Svetlana Mastitskaya, Sean Laidlaw, Niels Grabe, Maria Pritsch, Raffaele Fronza, Klaus Hexel, Steffen Schmitt, Michael Müller‐Steinhardt, Niels Halama, Christoph Domschke, Manfred Schmidt, Christof von Kalle, Florian Schütz, Thierry Voet, Philipp Beckhove
Хэвлэсэн 2021Artigo -
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The mutational landscape of normal human endometrial epithelium -н Luiza Moore, Daniel Leongamornlert, Tim H. H. Coorens, Mathijs A. Sanders, Peter Ellis, Stefan C. Dentro, Kevin J. Dawson, Timothy Butler, Raheleh Rahbari, Thomas J. Mitchell, Francesco Maura, Jyoti Nangalia, Patrick Tarpey, Simon Brunner, Henry Lee-Six, Yvette Hooks, Sarah Moody, Krishnaa T. Mahbubani, Mercedes Jimenez‐Liñan, Jan J. Brosens, Christine A. Iacobuzio‐Donahue, Iñigo Martincorena, Kourosh Saeb‐Parsy, Peter J. Campbell, Michael R. Stratton
Хэвлэсэн 2020Artigo -
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Convergent somatic mutations in metabolism genes in chronic liver disease -н Stanley Ng, Foad J. Rouhani, Simon Brunner, Natalia Brzozowska, Sarah J. Aitken, Ming Yang, Federico Abascal, Luiza Moore, Efterpi Nikitopoulou, Lia Chappell, Daniel Leongamornlert, Aleksandra Ivovic, Philip S. Robinson, Timothy Butler, Mathijs A. Sanders, Nicholas Williams, Tim H. H. Coorens, Jon W. Teague, Keiran Raine, Adam P. Butler, Yvette Hooks, Beverley Wilson, Natalie Birtchnell, Huw Naylor, Susan Davies, Michael R. Stratton, Iñigo Martincorena, Raheleh Rahbari, Christian Frezza, Matthew Hoare, Peter J. Campbell
Хэвлэсэн 2021Artigo -
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The mutational landscape of human somatic and germline cells -н Luiza Moore, Alex Cagan, Tim H. H. Coorens, Matthew D. C. Neville, Rashesh Sanghvi, Mathijs A. Sanders, Thomas R. W. Oliver, Daniel Leongamornlert, Peter Ellis, Ayesha Noorani, Thomas J. Mitchell, Timothy Butler, Yvette Hooks, Anne Y. Warren, Mette Jorgensen, Kevin J. Dawson, Andrew Menzies, Laura P. O’Neill, Calli Latimer, Mabel Teng, Ruben van Boxtel, Christine A. Iacobuzio‐Donahue, Iñigo Martincorena, Rakesh Heer, Peter J. Campbell, Rebecca C. Fitzgerald, Michael R. Stratton, Raheleh Rahbari
Хэвлэсэн 2021Artigo -
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Somatic mutation landscapes at single-molecule resolution -н Federico Abascal, Luke M. R. Harvey, Emily Mitchell, Andrew Lawson, Stefanie V. Lensing, Peter Ellis, Andrew J. C. Russell, Raul E. Alcantara, Adrian Baez‐Ortega, Yichen Wang, Eugene Jing Kwa, Henry Lee-Six, Alex Cagan, Tim H. H. Coorens, Michael Spencer Chapman, Sigurgeir Ólafsson, Steven Leonard, David Jones, Heather E. Machado, Megan Davies, Nina Friesgaard Øbro, Krishnaa T. Mahubani, Kieren Allinson, Moritz Gerstung, Kourosh Saeb‐Parsy, David G. Kent, Elisa Laurenti, Michael R. Stratton, Raheleh Rahbari, Peter J. Campbell, Robert J. Osborne, Iñigo Martincorena
Хэвлэсэн 2021Artigo -
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The long-term effects of chemotherapy on normal blood cells -н Emily Mitchell, My H. Pham, Anna Clay, Rashesh Sanghvi, Nicholas Williams, Sandra Pietsch, Joanne I. Hsu, Hyunchul Jung, Aditi Vedi, Sarah Moody, Jingwei Wang, Daniel Leongamornlert, Michael Spencer Chapman, Ellie Dunstone, Anna Santarsieri, Alex Cagan, Heather E. Machado, E. Joanna Baxter, George Follows, Daniel J. Hodson, Ultan McDermott, Gary J. Doherty, Iñigo Martincorena, Laura Humphreys, Krishnaa T. Mahbubani, Kourosh Saeb‐Parsy, Koichi Takahashi, Margaret A. Goodell, David G. Kent, Elisa Laurenti, Peter J. Campbell, Raheleh Rahbari, Jyoti Nangalia, Michael R. Stratton
Хэвлэсэн 2025Artigo -
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Somatic mutations reveal asymmetric cellular dynamics in the early human embryo -н Young Seok Ju, Iñigo Martincorena, Moritz Gerstung, Mia Petljak, Ludmil B. Alexandrov, Raheleh Rahbari, David C. Wedge, Helen Davies, Manasa Ramakrishna, Anthony Fullam, Sancha Martin, Christopher Alder, Nikita Patel, Stephen J. Gamble, Sarah O’Meara, Dilip D. Giri, Torril Sauer, Sarah E. Pinder, Colin A. Purdie, Åke Borg, Henk G. Stunnenberg, Marc J. van de Vijver, Benita Kiat Tee Tan, Carlos Caldas, Andrew Tutt, Naoto T. Ueno, Laura van ‘t Veer, John W.M. Martens, Christos Sotiriou, Stian Knappskog, Paul N. Span, Sunil R. Lakhani, Jórunn E. Eyfjörd, Anne‐Lise Børresen‐Dale, Andrea L. Richardson, Alastair M. Thompson, Alain Viari, Matthew E. Hurles, Serena Nik‐Zainal, Peter J. Campbell, Michael R. Stratton
Хэвлэсэн 2017Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Gene
Genetics
Mutation
Somatic cell
Germline
Germline mutation
Genome
Computational biology
Mutation rate
Cancer research
Demography
Population
Sociology
Cancer
Cell
DNA
DNA damage
Embryogenesis
Evolutionary biology
Exome sequencing
Immunology
Medicine
Copy-number variation
DNA sequencing
Embryo
Embryonic stem cell
Endocrinology
Exome
Germline mosaicism