Zoekresultaten - David Allsup

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  1. 1
    Chronic Lymphocytic Leukemia Care and Beyond: Navigating the Needs of Long-Term Survivors

    Chronic Lymphocytic Leukemia Care and Beyond: Navigating the Needs of Long-Term Survivors door Stefano Molica, David Allsup

    Gepubliceerd in 2025
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  2. 2
    Expression and Activity of NOX5 in the Circulating Malignant B Cells of Hairy Cell Leukemia

    Expression and Activity of NOX5 in the Circulating Malignant B Cells of Hairy Cell Leukemia door Aura S. Kamiguti, Lena Serrander, Ke Lin, R. J. C. Harris, John C. Cawley, David Allsup, Joseph R. Slupsky, Karl‐Heinz Krause, Mirko Zuzel

    Gepubliceerd in 2005
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  3. 3
    Telomere dysfunction accurately predicts clinical outcome in chronic lymphocytic leukaemia, even in patients with early stage disease

    Telomere dysfunction accurately predicts clinical outcome in chronic lymphocytic leukaemia, even in patients with early stage disease door Thet Thet Lin, Kevin Norris, Nicole H. Heppel, Guy Pratt, James M. Allan, David Allsup, James R Bailey, Lynn Cawkwell, Robert K. Hills, Julia W. Grimstead, Rhiannon E. Jones, Bethan Britt‐Compton, Chris Fegan, Duncan M. Baird, Chris Pepper

    Gepubliceerd in 2014
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  4. 4
    A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia

    A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia door Helen E. Speedy, Maria Chiara Di Bernardo, Georgina P. Sava, Martin J.S. Dyer, Amy Holroyd, Yufei Wang, Nicola J. Sunter, Larry Mansouri, Gunnar Juliusson, Karin E. Smedby, Göran Roos, Sandrine Jayne, Aneela Majid, Claire Dearden, Emma A. Hall, Tryfonia Mainou‐Fowler, Graham Jackson, Geoffrey Summerfield, Robert J. Harris, Andrew R. Pettitt, David Allsup, James R Bailey, Guy Pratt, Chris Pepper, Chris Fegan, Richard Rosenquist, Daniel Catovsky, James M. Allan, Richard S. Houlston

    Gepubliceerd in 2013
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  5. 5
    Ibrutinib and rituximab versus fludarabine, cyclophosphamide, and rituximab for patients with previously untreated chronic lymphocytic leukaemia (FLAIR): interim analysis of a multicentre, open-label, randomised, phase 3 trial

    Ibrutinib and rituximab versus fludarabine, cyclophosphamide, and rituximab for patients with previously untreated chronic lymphocytic leukaemia (FLAIR): interim analysis of a mult... door Peter Hillmen, Alexandra Pitchford, Adrian Bloor, Angus Broom, Moya Young, Ben Kennedy, Renata Walewska, Michelle Furtado, Gavin Preston, Jeffrey R Neilson, Nicholas Pemberton, Gamal Sidra, Nicholas Morley, Kate Cwynarski, Anna Schuh, Francesco Forconi, Nagah Elmusharaf, Shankara Paneesha, Christopher P. Fox, Dena Howard, Anna Hockaday, Julia Brown, David A. Cairns, Sharon Jackson, Natasha Greatorex, Nichola Webster, Jane Shingles, Surita Dalal, Piers Patten, David Allsup, Andy C. Rawstron, Talha Munir

    Gepubliceerd in 2023
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  6. 6
    Chronic Lymphocytic Leukemia Therapy Guided by Measurable Residual Disease

    Chronic Lymphocytic Leukemia Therapy Guided by Measurable Residual Disease door Talha Munir, David A. Cairns, Adrian Bloor, David Allsup, Kate Cwynarski, Andrew R. Pettitt, Shankara Paneesha, Christopher P. Fox, Toby A. Eyre, Francesco Forconi, Nagah Elmusharaf, Ben Kennedy, John G. Gribben, Nicholas Pemberton, Oonagh Sheehy, Gavin Preston, Anna Schuh, Renata Walewska, Lelia Duley, Dena Howard, Anna Hockaday, Sharon Jackson, Natasha Greatorex, Sean Girvan, Sue Bell, Julia Brown, Nichola Webster, Surita Dalal, Ruth de Tute, Andy C. Rawstron, Piers Patten, Peter Hillmen

    Gepubliceerd in 2023
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  7. 7
    Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

    Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects door Benjamin C. Johnson, Gillian Lowe, Jane Wong Fütterer, Marie Lordkipanidzé, Deborah J. MacDonald, Michael A. Simpson, Isabel Sánchez‐Guiu, Sian Drake, Danai Bem, Vincenzo Leo, Sarah J. Fletcher, Ban B. Dawood, José Rivera, David Allsup, Tina Biss, P Bolton-Maggs, Peter Collins, Nicola Curry, Charlotte Grimley, Beki James, Michael Makris, Jayashree Motwani, Sue Pavord, Katherine Talks, Jecko Thachil, J Wilde, M. Williams, Paul Harrison, Paul Gissen, Stuart J. Mundell, Andrew Mumford, Mary E. Daly, Steve P. Watson, Neil V. Morgan

    Gepubliceerd in 2016
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  8. 8
    Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

    Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk door Dalemari Crowther-Swanepoel, Peter Broderick, Maria Chiara Di Bernardo, Sara E. Dobbins, María Torres, Mahmoud Mansouri, Clara Ruíz-Ponte, Anna Enjuanes, Richard Rosenquist, Ángel Carracedo, Jesper Jurlander, Elı́as Campo, Gunnar Juliusson, Emilio Montserrat, Karin E. Smedby, Martin J.S. Dyer, Estella Matutes, Claire Dearden, Nicola J. Sunter, Emma A. Hall, Tryfonia Mainou‐Fowler, Graham Jackson, Geoffrey Summerfield, R. J. C. Harris, Andrew R. Pettitt, David Allsup, James R Bailey, Guy Pratt, Chris Pepper, Chris Fegan, Anton Parker, David Oscier, James M. Allan, Daniel Catovsky, Richard S. Houlston

    Gepubliceerd in 2010
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  9. 9
    Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology

    Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology door Molly Went, Amit Sud, Helen E. Speedy, Nicola J. Sunter, Asta Försti, Philip Law, David C. Johnson, Fabio Mirabella, Amy Holroyd, Ni Li, Giulia Orlando, Niels Weinhold, Mark van Duin, Bowang Chen, Jonathan S. Mitchell, Larry Mansouri, Gunnar Juliusson, Karin E. Smedby, Sandrine Jayne, Aneela Majid, Claire Dearden, David Allsup, James R Bailey, Guy Pratt, Chris Pepper, Chris Fegan, Richard Rosenquist, Rowan Kuiper, Owen Stephens, Uta Bertsch, Peter Broderick, Hermann Einsele, Walter M. Gregory, Jens Hillengaß, Per Hoffmann, Graham Jackson, Karl‐Heinz Jöckel, Jolanta Nickel, Markus M. Nöthen, Miguel Inácio da Silva Filho, Hauke Thomsen, Brian A. Walker, Annemiek Broyl, Faith E. Davies, Markus Hansson, Hartmut Goldschmidt, Martin J.S. Dyer, Martin Kaiser, Pieter Sonneveld, Gareth J. Morgan, Kari Hemminki, Björn Nilsson, Daniel Catovsky, James M. Allan, Richard S. Houlston

    Gepubliceerd in 2018
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  10. 10
    Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

    Genome-wide association study identifies susceptibility loci for acute myeloid leukemia door Wei‐Yu Lin, Sarah Fordham, Eric A. Hungate, Nicola J. Sunter, Claire Elstob, Yaobo Xu, Catherine Park, Anne S. Quante, Konstantin Strauch, Christian Gieger, Andrew D. Skol, Thahira Rahman, Lara E. Sucheston‐Campbell, Junke Wang, Theresa Hahn, Alyssa Clay‐Gilmour, Gail Jones, Helen Marr, Graham Jackson, Tobias Menne, Mathew Collin, Adam Ivey, Robert K. Hills, Alan K. Burnett, Nigel H. Russell, Jude Fitzgibbon, Richard A. Larson, Michelle M. Le Beau, Wendy Stock, Olaf Heidenreich, Abrar Alharbi, David Allsup, Richard S. Houlston, Jean Norden, Anne M. Dickinson, Elisabeth Douglas, Clare Lendrem, Ann K. Daly, Louise Palm, Kim Piechocki, Sally Jeffries, Martin Bornhäuser, Christoph Röllig, Heidi Altmann, Leo Ruhnke, Désirée Kunadt, Lisa Wagenführ, Heather J. Cordell, Rebecca Darlay, Mette Klarskov Andersen, Maria Chiara Fontana, Giovanni Martinelli, Giovanni Marconi, Miguel Á. Sanz, José Cervera, Inés Gómez‐Seguí, Thomas Cluzeau, Chimène Moreilhon, Sophie Raynaud, Heinz Sill, Maria Teresa Voso, Francesco Lo‐Coco, Hervé Dombret, Meyling Cheok, Claude Preudhomme, Rosemary E. Gale, David C. Linch, Julia Gaal-Wesinger, András Masszi, Daniel Nowak, Wolf‐Karsten Hofmann, Amanda Gilkes, Kimmo Porkka, Jelena D. Milosevic Feenstra, Róbert Královics, David Grimwade, Manja Meggendorfer, Torsten Haferlach, Szilvia Krizsán, Csaba Bödör, Friedrich Stölzel, Kenan Onel, James M. Allan

    Gepubliceerd in 2021
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  11. 11
    Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

    Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease door Keren Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Mégy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka, Vincent Plagnol, Christopher J. Penkett, Kathleen Stirrups, Roberta Rizzo, Genevieve Wright, Dragana Josifova, Maria Bitner‐Glindzicz, Richard H. Scott, Emma Clement, Louise Allen, Ruth Armstrong, Angela F. Brady, Jenny Carmichael, Manali Chitre, Robert Henderson, Jane A. Hurst, Robert E. MacLaren, Elaine Murphy, Joan Paterson, Elisabeth Rosser, Dorothy Thompson, Emma Wakeling, Willem H. Ouwehand, Michel Michaelides, Anthony T. Moore, Andrew R. Webster, F. Lucy Raymond, Timothy J. Aitman, Hana Alachkar, Sonia Ali, Louise Allen, David Allsup, Gautum Ambegaonkar, Julie Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Sofie Ashford, William F. Astle, Antony Attwood, Steve Austin, Chiara Bacchelli, Tamam Bakchoul, Tadbir K. Bariana, Helen Baxendale, David Bennett, Claire Bethune, Shahnaz Bibi, Maria Bitner‐Glindzicz, Marta Bleda, Harm Boggard, Paula Bolton‐Maggs, Claire Booth, John R. Bradley, Angie Brady, Matthew A. Brown, Michael J. Browning, Christine Bryson, Siobhán O. Burns, Paul Calleja, Natalie Canham, Jenny Carmichael, Keren Carss, Mark J. Caulfield, Elizabeth Chalmers, Anita Chandra, Patrick F. Chinnery, Manali Chitre, Colin Church, Emma Clement, Emma Clement, Virginia Clowes, Gerry Coghlan, Peter Collins, Nichola Cooper, Amanda Creaser-Myers, Rosa DaCosta, Louise C. Daugherty, Sophie Davies, John S. Davis, Minka De Vries, Patrick Deegan, Sri V. V. Deevi, Charu Deshpande, Lisa Devlin, Eleanor Dewhurst, Rainer Döffinger, Natalie Dormand, Elizabeth Drewe

    Gepubliceerd in 2016
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  12. 12
    Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

    Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes door James Whitworth, Philip Smith, José-Ezequiel Martín, Hannah D. West, Andrea Luchetti, Faye Rodger, Graeme M. Clark, Keren Carss, Jonathan Stephens, Kathleen Stirrups, Chris Penkett, Rutendo Mapeta, Sofie Ashford, Karyn Mégy, Hassan Shakeel, Munaza Ahmed, Julian Adlard, Julian Barwell, Carole Brewer, Ruth Casey, Ruth Armstrong, Trevor Cole, D. Gareth Evans, Florentia Fostira, Lynn Greenhalgh, Helen Hanson, Alex Henderson, Jonathan Hoffman, Louise Izatt, Ajith Kumar, Ava Kwong, Fiona Lalloo, Kai Ren Ong, Joan Paterson, Soo‐Mi Park, Rakefet Chen‐Shtoyerman, Claire Searle, Lucy Side, Anne‐Bine Skytte, Katie Snape, Emma R. Woodward, Timothy J. Aitman, Hana Alachkar, Sonia Ali, Louise Allen, David Allsup, Gautum Ambegaonkar, Julie Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Sofie Ashford, William F. Astle, Antony Attwood, Steve Austin, Chiara Bacchelli, Tamam Bakchoul, Tadbir K. Bariana, Helen Baxendale, David Bennett, Claire Bethune, Shahnaz Bibi, Maria Bitner‐Glindzicz, Marta Bleda, Harm Boggard, Paula Bolton‐Maggs, Claire Booth, John R. Bradley, Angie Brady, Matthew A. Brown, Michael J. Browning, Christine Bryson, Siobhán O. Burns, Paul Calleja, Natalie Canham, Jenny Carmichael, Keren Carss, Mark J. Caulfield, Elizabeth Chalmers, Anita Chandra, Patrick F. Chinnery, Manali Chitre, Colin Church, Emma Clement, Emma Clement, Virginia Clowes, Gerry Coghlan, Peter Collins, Victoria Cookson, Nichola Cooper, Paul A. Corris, Amanda Creaser-Myers, Rosa DaCosta, Louise C. Daugherty, Sophie Davies, John S. Davis, Minka De Vries, Patrick Deegan, Sri V. V. Deevi

    Gepubliceerd in 2018
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  13. 13
    Whole-genome sequencing of a sporadic primary immunodeficiency cohort

    Whole-genome sequencing of a sporadic primary immunodeficiency cohort door James Thaventhiran, Hana Lango Allen, Oliver S. Burren, William Rae, Daniel Greene, Emily Staples, Zinan Zhang, James H. R. Farmery, Ilenia Simeoni, Elizabeth Rivers, Jesmeen Maimaris, Christopher J. Penkett, Jonathan Stephens, Sri V. V. Deevi, Alba Sanchis‐Juan, Nicholas Gleadall, Moira Thomas, Ravishankar Sargur, Pavels Gordins, Helen Baxendale, Matthew A. Brown, Paul Tuijnenburg, Austen Worth, Steven Hanson, Rachel Linger, Matthew Buckland, Paula Rayner-Matthews, Kimberly Gilmour, Crina Samarghitean, Suranjith L. Seneviratne, David M. Sansom, Andy G. Lynch, Karyn Mégy, Eva Ellinghaus, David Ellinghaus, Silje F. Jørgensen, Tom H. Karlsen, Kathleen Stirrups, Antony J. Cutler, Dinakantha Kumararatne, Anita Chandra, David Edgar, Archana Herwadkar, Nichola Cooper, Sofia Grigoriadou, Aarnoud Huissoon, Sarah Goddard, Stephen Jolles, Catharina Schuetz, Felix Boschann, Stephen Abbs, Zoe Adhya, Julian Adlard, Maryam Afzal, Irshad Ahmed, Munaza Ahmed, Saeed Ahmed, Timothy J. Aitman, Hana Alachkar, Jayanthi Alamelu, Raza Alikhan, Carl E. Allen, Louise Allen, David Allsup, Arif Alvi, Gautam Ambegaonkar, Ariharan Anantharachagan, Philip Ancliff, Julie A. Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Rita Arya, Sofie Ashford, William J. Astle, Anthony Attwood, Steve Austin, Yeşim Aydınok, Waqar Ayub, Christian Babbs, Chiara Bacchelli, Trevor Baglin, Tamam Bakchoul, Tadbir K. Bariana, Jonathan Barratt, Julian Barwell, John Baski, Rachel W. Bates, Joana Batista, Helen Baxendale, Gareth Baynam, David Bennett, Claire Bethune, Neha Bhatnagar, Shahnaz Bibi, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Marta Bleda

    Gepubliceerd in 2020
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  14. 14
    Whole-genome sequencing of patients with rare diseases in a national health system

    Whole-genome sequencing of patients with rare diseases in a national health system door Ernest Turro, William J. Astle, Karyn Mégy, Stefan Gräf, Daniel Greene, Olga Shamardina, Hana Lango Allen, Alba Sanchis‐Juan, Mattia Frontini, Chantal Thys, Jonathan Stephens, Rutendo Mapeta, Oliver S. Burren, Kate Downes, Matthias Haimel, Salih Tuna, Sri V. V. Deevi, Timothy J. Aitman, David Bennett, Paul Calleja, Keren Carss, Mark J. Caulfield, Patrick F. Chinnery, Peter Dixon, Daniel P. Gale, Roger James, Ania Koziell, Michael Laffan, Adam P. Levine, Eamonn R. Maher, Hugh S. Markus, Joannella Morales, Nicholas W. Morrell, Andrew Mumford, Elizabeth Ormondroyd, Stuart Rankin, Augusto Rendon, Sylvia Richardson, Irene Roberts, Noémi Roy, Moin A. Saleem, Kenneth G. C. Smith, Hannah Stark, Rhea Tan, Andreas C. Themistocleous, Adrian J. Thrasher, Hugh Watkins, Andrew R. Webster, Martin R. Wilkins, Catherine Williamson, James Whitworth, Sean Humphray, David Bentley, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, David Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John R. Bradley, Eugene Bragin, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan, Matthew Buckland

    Gepubliceerd in 2020
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  15. 15
    COVID-19 severity and mortality in patients with CLL: an update of the international ERIC and Campus CLL study

    COVID-19 severity and mortality in patients with CLL: an update of the international ERIC and Campus CLL study door Thomas Chatzikonstantinou, Anargyros Kapetanakis, Lydia Scarfò, Georgios Karakatsoulis, David Allsup, Alejandro Alonso Cabrero, Martin Andres, Darko Antić, Mónica Baile, Panagiotis Baliakas, Dominique Bron, Antonella Capasso, Sofia Chatzileontiadou, Raúl Córdoba, Juan Gonzalo Correa, Carolina Cuéllar‐García, Lorenzo De Paoli, Maria Rosaria De Paolis, Giovanni Del Poeta, Christos Demosthenous, Maria Dimou, D. Donaldson, Michael Doubek, Maria Efstathopoulou, Barbara Eichhorst, Shaimaa El‐Ashwah, Alicia Enrico, Blanca Espinet, Lucia Farina, Angela Ferrari, Myriam Foglietta, Henrik Frederiksen, Moritz Fürstenau, José A. García‐Marco, Rocío García‐Serra, Massimo Gentile, Eva Gimeno, Andreas Glenthøj, María Gomes da Silva, Odit Gutwein, Yervand Hakobyan, Yair Herishanu, José‐Ángel Hernández‐Rivas, Tobias Herold, Idanna Innocenti, Gilad Itchaki, Ozren Jakšić, Ann Janssens, Olga Kalashnikova, Elżbieta Kalicińska, Linda Karlsson, Arnon P. Kater, Sabina Kersting, Jorge Labrador, Deepesh Lad, Luca Laurenti, Mark‐David Levin, Enrico Lista, Alberto López‐García, Lara Malerba, Roberto Marasca, Monia Marchetti, Juan Marquet, Mattias Mattsson, Francesca Romana Mauro, Ivana Milošević, Fatima Mirás, Marta Morawska, Marina Motta, Talha Munir, Roberta Murru, Carsten Utoft Niemann, Raquel Nunes Rodrigues, Jacopo Olivieri, Lorella Orsucci, Maria Papaioannou, Miguel Arturo Pavlovsky, Inga Piskunova, Viola Maria Popov, Francesca Maria Quaglia, Giulia Quaresmini, Kristian Qvist, Gianluigi Reda, Gian Matteo Rigolin, Rosa Ruchlemer, Gevorg Saghumyan, Amit Shrestha, Martin Šimkovič, Martin Špaček, Paolo Sportoletti, Oana Stanca, Niki Stavroyianni, Tamar Tadmor, Doreen te Raa, Sanne H. Tonino, Livio Trentin, Ellen van der Spek, Michel van Gelder, Roel van Kampen, Marzia Varettoni

    Gepubliceerd in 2021
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  16. 16
    GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

    GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements door Peter H. Dixon, Adam P. Levine, Inês Cebola, Melanie Chan, Aliya S. Amin, Anshul Aich, Monika Mozere, Hannah Maude, Alice Mitchell, Jun Zhang, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Chris Babbs, Tamam Bakchoul, Tadbir K. Bariana, Julian Barwell, David Bennett, David Bentley, Agnieszka Bierżyńska, Tina Biss, Marta Bleda, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John Bradley, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Michael J. Browning, Rachel Buchan, Matthew Buckland, Teofila Bueser, Siobhán O. Burns, Oliver S. Burren, Paul Calleja, Gerald Carr‐White, Keren Carss, Ruth Casey, Mark J. Caulfield, John C. Chambers, Jennifer Chambers, Floria Cheng, Patrick F. Chinnery, Martin Christian, Colin Church, Naomi Clements Brod, Gerry Coghlan, Elizabeth Colby, Trevor Cole, Janine Collins, Peter Collins, Camilla Colombo, Robin Condliffe, Stuart A. Cook, Terry Cook, Nichola Cooper, Paul A. Corris, Abigail Crisp-Hihn, Nicola Curry, Cesare Danesino, Matthew J. Daniels, Louise C. Daugherty, John B. Davis, Sri V. V. Deevi, Timothy Dent, Eleanor Dewhurst, Peter H. Dixon, Kate Downes, Anna M. Drazyk, Elizabeth Drewe, Tina Dutt, David Edgar, Karen L. Edwards, William Egner, Wendy N. Erber, Marie Erwood, Maria C. Estiú, Gillian Evans, D. Gareth Evans, Tamara Everington, Mélanie Eyries, Rémi Favier, Debra Fletcher, James Fox, Amy Frary, Courtney E. French, Kathleen Freson, Mattia Frontini

    Gepubliceerd in 2022
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  17. 17
    The evolving landscape of <scp>COVID</scp>‐19 and <scp>post‐COVID</scp> condition in patients with chronic lymphocytic leukemia: A study by <scp>ERIC</scp>, the <scp>European</scp> research initiative on <scp>CLL</scp>

    The evolving landscape of <scp>COVID</scp>‐19 and <scp>post‐COVID</scp> condition in patients with chronic lymphocytic leukemia: A study by <scp>ERIC</scp>, the <scp>European</scp>... door Andrea Visentin, Thomas Chatzikonstantinou, Lydia Scarfò, Anargyros Kapetanakis, Christos Demosthenous, Georgios Karakatsoulis, Eva Minga, Dimitra Chamou, David Allsup, Alejandro Alonso Cabrero, Martin Andres, Darko Antić, Mónica Baile, Panagiotis Baliakas, Sotiria Besikli‐Dimou, Dominique Bron, Sofia Chatzileontiadou, Raúl Córdoba, Juan Gonzalo Correa, Carolina Cuéllar‐García, Lorenzo De Paoli, Maria Rosaria De Paolis, Julio Delgado, Maria Dimou, David Donaldson, Mark Catherwood, Michael Doubek, Maria Efstathopoulou, Barbara Eichhorst, Salma Elashwah, Alicia Enrico, Blanca Espinet, Lucia Farina, Angela Ferrari, Myriam Foglietta, Henrik Frederiksen, Moritz Fürstenau, José A. García‐Marco, Rocío García‐Serra, Rosa Collado, Massimo Gentile, Eva Gimeno, Andreas Glenthøj, María Gomes da Silva, Yervand Hakobyan, Yair Herishanu, José‐Ángel Hernández‐Rivas, Tobias Herold, Idanna Innocenti, Gilad Itchaki, Ozren Jakšić, Ann Janssens, Olga Kalashnikova, Elżbieta Kalicińska, Arnon P. Kater, Sabina Kersting, Jorge Labrador, Deepesh Lad, Luca Laurenti, Mark‐David Levin, Enrico Lista, Alberto López‐García, Lara Malerba, Roberto Marasca, Monia Marchetti, Juan Marquet, Mattias Mattsson, Francesca Romana Mauro, Marta Morawska, Marina Motta, Talha Munir, Roberta Murru, Carsten Utoft Niemann, Raquel Nunes Rodrigues, Jacopo Olivieri, Lorella Orsucci, Maria Papaioannou, Miguel Arturo Pavlovsky, Inga Piskunova, Viola Maria Popov, Francesca Maria Quaglia, Giulia Quaresmini, Kristian Qvist, Gian Matteo Rigolin, Rosa Ruchlemer, Martin Šimkovič, Martin Špaček, Paolo Sportoletti, Oana Stanca, Tamar Tadmor, Antonella Capasso, Giovanni Del Poeta, Odit Gutwein, Linda Karlsson, Ivana Milošević, Fatima Mirás, Gianluigi Reda, Gevorg Saghumyan, Amit Shrestha, Doreen te Raa

    Gepubliceerd in 2023
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  18. 18
    Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia

    Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia door Philip Law, Sonja I. Berndt, Helen E. Speedy, Nicola J. Camp, Georgina P. Sava, C.F. Skibola, Amy Holroyd, Joseph Vijai, Nicola J. Sunter, Alexandra Nieters, Sı́lvia Beà, Alain Monnereau, David Martin‐García, Lynn R. Goldin, Guillem Clot, Lauren R. Teras, Inés Quintela, Brenda M. Birmann, Sandrine Jayne, Wendy Cozen, Aneela Majid, Karin E. Smedby, Qing Lan, Claire Dearden, Angela Brooks‐Wilson, Emma A. Hall, Mark P. Purdue, Tryfonia Mainou‐Fowler, Claire M. Vajdic, Graham Jackson, Pierluigi Cocco, Helen Marr, Yawei Zhang, Tongzhang Zheng, Graham G. Giles, Charles Lawrence, Timothy G. Call, Mark Liebow, Mads Melbye, Bengt Glimelius, Larry Mansouri, Martha Glenn, Karen Curtin, W. Ryan Diver, Brian K. Link, Lucía Conde, Paige M. Bracci, Elizabeth A. Holly, Rebecca D. Jackson, Lesley F. Tinker, Yolanda Benavente, Paolo Boffetta, Paul Brennan, Marc Maynadie, James McKay, Demetrius Albanes, Stephanie J. Weinstein, Zhaoming Wang, Neil E. Caporaso, Lindsay M. Morton, Richard K. Severson, Elio Ríboli, Paolo Vineis, Roel Vermeulen, Melissa C. Southey, Roger L. Milne, Jacqueline Clavel, Sabine Topka, John J. Spinelli, Peter Kraft, Maria Grazia Ennas, Geoffrey Summerfield, Giovanni Maria Ferri, Robert J. Harris, Lucia Miligi, Andrew R. Pettitt, Kari E. North, David Allsup, Joseph F. Fraumeni, James R Bailey, Kenneth Offit, Guy Pratt, Henrik Hjalgrim, Chris Pepper, Stephen J. Chanock, Chris Fegan, Richard Rosenquist, Sílvia de Sanjosé, Ángel Carracedo, Martin J.S. Dyer, Daniel Catovsky, Elı́as Campo, James R. Cerhan, James M. Allan, Nathanial Rothman, Richard S. Houlston, Susan L. Slager

    Gepubliceerd in 2017
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  19. 19
    Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

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    Gepubliceerd in 2018
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    Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

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    Gepubliceerd in 2017
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