Irene Roberts

1995–2025 年に発表

93
論文数
19,253
被引用数
70
h 指数
89
i10 指数

被引用数

Irene Roberts の年別被引用数1982 年: 被引用 1 件1995 年: 被引用 8 件1996 年: 被引用 31 件1997 年: 被引用 44 件1998 年: 被引用 48 件1999 年: 被引用 54 件2000 年: 被引用 33 件2001 年: 被引用 42 件2002 年: 被引用 50 件2003 年: 被引用 89 件2004 年: 被引用 86 件2005 年: 被引用 85 件2006 年: 被引用 75 件2007 年: 被引用 108 件2008 年: 被引用 114 件2009 年: 被引用 107 件2010 年: 被引用 96 件2011 年: 被引用 110 件2012 年: 被引用 88 件2013 年: 被引用 80 件2014 年: 被引用 89 件2015 年: 被引用 86 件2016 年: 被引用 99 件2017 年: 被引用 67 件2018 年: 被引用 87 件2019 年: 被引用 324 件2020 年: 被引用 405 件2021 年: 被引用 497 件2022 年: 被引用 465 件2023 年: 被引用 439 件2024 年: 被引用 870 件2025 年: 被引用 381 件2026 年: 被引用 6 件1983〜1994 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,047 件、この内訳の 25.3%イギリス: 引用元論文 903 件、この内訳の 11.2%ドイツ: 引用元論文 527 件、この内訳の 6.5%イタリア: 引用元論文 465 件、この内訳の 5.8%中国: 引用元論文 460 件、この内訳の 5.7%フランス: 引用元論文 406 件、この内訳の 5%オランダ: 引用元論文 285 件、この内訳の 3.5%カナダ: 引用元論文 284 件、この内訳の 3.5%オーストラリア: 引用元論文 229 件、この内訳の 2.8%スペイン: 引用元論文 222 件、この内訳の 2.7%日本: 引用元論文 199 件、この内訳の 2.5%スイス: 引用元論文 160 件、この内訳の 2%
0%25.3%その他 23.5%

分野

  • Medicine61.8%
  • Biochemistry, Genetics and Molecular Biology25.4%
  • Immunology and Microbiology10.2%
  • Neuroscience0.9%
  • Computer Science0.5%
  • Nursing0.3%
  • その他0.9%

トピック

  • Acute Myeloid Leukemia Research6.4%
  • Mesenchymal stem cell research3.8%
  • Hemoglobinopathies and Related Disorders3.2%
  • Immune Cell Function and Interaction3.1%
  • Myeloproliferative Neoplasms: Diagnosis and Treatment2.6%
  • Hematopoietic Stem Cell Transplantation2.6%
  • その他78.3%

共著者

全論文

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  1. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joop H. Jansen, Rashmi Kanagal‐Shamanna, Hagop M. Kantarjian, Christian P. Kratz, Xiaoqiu Li, Megan S. Lim, Keith R. Loeb, Sanam Loghavi, Andrea N. Marcogliese, Soheil Meshinchi, Phillip Michaels, Kikkeri N. Naresh, Yasodha Natkunam, Reza Nejati, German Ott, Eric Padron, Keyur P. Patel, Nikhil Patkar, Jennifer Picarsic, Uwe Platzbecker, Irene Roberts, Anna Schuh, William A. Sewell, Reiner Siebert, Prashant Tembhare, Jeffrey Tyner, Srđan Verstovšek, Wei Wang, Brent L. Wood, Wenbin Xiao, Cecilia C.S. Yeung, Andreas Hochhaus - Leukemia 2022 被引用: 3,904

  2. Decoding human fetal liver haematopoiesis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jaume Bacardit, Andrew Fuller, Ben Millar, Barbara Innes, Susan Lindsay, Michael J. T. Stubbington, Monika S. Kowalczyk, Bo Li, Orr Ashenberg, Marcin Tabaka, Danielle Dionne, Timothy L. Tickle, Michal Slyper, Orit Rozenblatt-Rosen, Andrew Filby, Peter Carey, Alexandra-Chloé Villani, Anindita Roy, Aviv Regev, Alain Chédotal, Irene Roberts, Berthold Göttgens, Sam Behjati, Elisa Laurenti, Sarah A. Teichmann, Muzlifah Haniffa - Nature, Nat. 2019 被引用: 649

  3. Whole-genome sequencing of patients with rare diseases in a national health system

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 R. Bentley, NIHR BioResource for the 100,000 Genomes Project, 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 R. Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme C. 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 ほか 412 名 - Nature, Nat. 2020 被引用: 582

  4. Blood and immune development in human fetal bone marrow and Down syndrome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Lisgo, Petra Balogh, Kerstin B. Meyer, Elena Prigmore, Kirsty Ambridge, Mika Sarkin Jain, Mirjana Efremova, Keir Pickard, Thomas Creasey, Jaume Bacardit, Deborah J. Henderson, Jonathan Coxhead, Andrew Filby, Rafiqul Hussain, David Dixon, David McDonald, Dorin-Mirel Popescu, Monika S. Kowalczyk, Bo Li, Orr Ashenberg, Marcin Tabaka, Danielle Dionne, Timothy L. Tickle, Michal Slyper, Orit Rozenblatt–Rosen, Aviv Regev, Sam Behjati, Elisa Laurenti, Nicola K. Wilson, Anindita Roy, Berthold Göttgens, Irene Roberts, Sarah A. Teichmann, Muzlifah Haniffa - Nature 2021 被引用: 159

  5. Yolk sac cell atlas reveals multiorgan functions during human early development

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bayanne Olabi, Mohi Miah, Chloe Admane, Dorin-Mirel Popescu, Meghan Acres, David Dixon, Thomas Ness, Rowen Coulthard, Steven Lisgo, Deborah J. Henderson, Emma Dann, Chenqu Suo, Sarah Kinston, Jong-Eun Park, Krzysztof Polański, John C. Marioni, Stijn van Dongen, Kerstin B. Meyer, Marella de Bruijn, James Palis, Sam Behjati, Elisa Laurenti, Nicola K. Wilson, Roser Vento‐Tormo, Alain Chédotal, Omer Ali Bayraktar, Irene Roberts, Laura Jardine, Berthold Göttgens, Sarah A. Teichmann, Muzlifah Haniffa - Science 2023 被引用: 98

  6. Germline selection shapes human mitochondrial DNA diversity

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Catherine Williamson, NIHR BioResource–Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot, Sofie Ashford, Christopher J. Penkett, Kathleen Stirrups, Augusto Rendon, Willem H. Ouwehand, John R. Bradley, F. Lucy Raymond, Mark Caulfield, Ernest Turro, Patrick F. Chinnery, Aarnoud Huissoon, Abigail Crisp-Hihn, Adam Shaw, Adam J. Mead, Adam P. Levine, Adrian J. Thrasher, Agnieszka Bierżyńska, Ahamad Hassan, Ajith Kumar, Alba Sanchis‐Juan, Alex Richter, Allan Lawrie, Amy Frary, Andrea H. Németh, Andrea Olschewski, Andreas C. Themistocleous, Andrew C. Browning, Andrew Mumford, Andrew M. Schaefer, Andrew Marshall, Andrew O.M. Wilkie, Andrew Peacock, Andrew R. Harper, Andrew R. Webster, Andrew S.C. Rice, Angela Pyle, Ania Koziell, Anna M. Drazyk, Anne M. Kelly, Annette Wagner, Anthony Attwood, Anthony De Soyza, Anthony M. Vandersteen, Anthony T. Moore, Anton Vonk Noordegraaf, Anupama Rao, Archana Herwadkar, Arjan C. Houweling, Arjune Sen, Augusto Rendon, Austen Worth, Barbara Girerd, Bella Madan, Brian T. Wilson, Carmen Bugarin Diz, Carmen Treacy, Carole Brewer, Carolyn Campbell, Carolyn M. Millar, Catherine Roughley, Catherine Titterton, Catherine Williamson, Cecilia Compton, Cesare Danesino, Chantal Thys, Charaka Hadinnapola, Charu Deshpande ほか 305 名 - Science 2019 被引用: 251

  7. Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Katherine R. Bull, Holger Cario, Deirdre Cilliers, Valerio Conti, E. Graham Davies, Fatima Dhalla, Beatriz Diez Dacal, Dong Yin, James E. Dunford, Renzo Guerrini, Adrian L. Harris, Jane Hartley, Georg A. Holländer, M K Javaid, Maureen A. Kane, Déirdre Kelly, Dominic F. Kelly, Samantha J.L. Knight, Alexandra Y. Kreins, Erika Kvikstad, Craig B. Langman, Tracy Lester, Kate E Lines, Simon Lord, Xin Lü, Sahar Mansour, Adnan Manzur, Reza Maroofian, Brian D. Marsden, Joanne Mason, Simon J. McGowan, Davide Mei, Hana Mlčochová, Yoshiko Murakami, Andrea H. Németh, Steven Okoli, Elizabeth Ormondroyd, Lilian Bomme Ousager, Jacqueline Palace, Smita Y. Patel, Melissa M. Pentony, Christopher W. Pugh, Abolfazl Rad, Archana Ramesh, Simone G. Riva, Irene Roberts, Noémi Roy, Outi Salminen, Kyleen D. Schilling, Caroline Scott, Arjune Sen, Conrad Smith, Mark Stevenson, Rajesh V. Thakker, Stephen R.F. Twigg, Holm H. Uhlig, Richard van Wijk, Barbara Vona, Steven A. Wall, Jing Wang, Hugh Watkins, Jaroslav Žák, Anna Schuh, Usha Kini, Andrew O.M. Wilkie, Niko Popitsch, Jenny C. Taylor - Genome Medicine 2023 被引用: 72

  8. Single-Cell Analyses Reveal Megakaryocyte-Biased Hematopoiesis in Myelofibrosis and Identify Mutant Clone-Specific Targets

    著者: , , , , , , , , , , , , , , , , , , , , - Molecular Cell 2020 被引用: 177

  9. Transitions in lineage specification and gene regulatory networks in hematopoietic stem/progenitor cells over human development

    著者: , , , , , , , , , , , , , , , , - Cell Reports 2021 被引用: 88

  10. Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity

    著者: , , , , , , - Science 1995 被引用: 1,299

  11. Graft invariant natural killer T-cell dose predicts risk of acute graft-versus-host disease in allogeneic hematopoietic stem cell transplantation

    著者: , , , , , , , , , , , , , , , , - Blood 2012 被引用: 162

  12. Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stefan N. Constantinescu, Paresh Vyas, Dirk Heckl, Jan‐Henning Klusmann - Cancer Cell 2019 被引用: 145

  13. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Paula Rayner-Matthews, Olga Shamardina, Florent Soubrier, Laura Southgate, Jay Suntharalingam, Mark Toshner, Richard C. Trembath, Anton Vonk Noordegraaf, Martin R. Wilkins, Stephen J. Wort, John Wharton, Stefan Gräf, Nicholas W. Morrell, Timothy J. Aitman, David Bennett, Mark J. Caulfield, Patrick F. Chinnery, Daniel P. Gale, Ania Koziell, Taco W. Kuijpers, Michael Laffan, Eamonn R. Maher, Hugh S. Markus, Willem H. Ouwehand, David J. Perry, F. Lucy Raymond, Irene Roberts, Kenneth G. C. Smith, Adrian J. Thrasher, Hugh Watkins, Catherine Williamson, Geoffrey Woods, Sofie Ashford, John R. Bradley, Debra Fletcher, Tracey Hammerton, Roger James, Nathalie Kingston, Willem H. Ouwehand, Christopher J. Penkett, F. Lucy Raymond, Kathleen Stirrups, Marijke Veltman, Tim Young, Sofie Ashford, Matthew A. Brown, Emma Clement, John Davis, Eleanor Dewhurst, Marie Erwood, Amy Frary, Rachel Linger, Sofia Papadia, Karola Rehnström, Hannah Stark, David Allsup, Steve Austin, Tamam Bakchoul, Tadbir K. Bariana, Paula Bolton‐Maggs, Elizabeth Chalmers, Peter Collins, Wendy N. Erber, Tamara Everington, Rémi Favier, Kathleen Freson, Bruce Furie, Michael Gattens, Keith Gomez, Daniel Greene ほか 225 名 - Circulation 2017 被引用: 145

  14. Single-cell profiling of human bone marrow progenitors reveals mechanisms of failing erythropoiesis in Diamond-Blackfan anemia

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Science Translational Medicine 2021 被引用: 70

  15. The innate sensor ZBP1-IRF3 axis regulates cell proliferation in multiple myeloma

    著者: , , , , , , , , , , , , , , , - Haematologica 2021 被引用: 43

  16. Systems medicine dissection of chr1q-amp reveals a novel PBX1-FOXM1 axis for targeted therapy in multiple myeloma

    著者: , , , , , , , , , , , , , , , , , , - Blood 2022 被引用: 34

  17. Recommendations regarding splenectomy in hereditary hemolytic anemias

    著者: , , , , , , , , , , , , , , , , , , , , , - Haematologica 2017 被引用: 216

  18. GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter J. Campbell, Paresh Vyas - Blood 2013 被引用: 206

  19. Prospective, Observational Study of Outcomes in Neonates With Severe Thrombocytopenia

    著者: , , , , , , , , - PEDIATRICS 2009 被引用: 189

  20. H3K79me2/3 controls enhancer–promoter interactions and activation of the pan-cancer stem cell marker PROM1/CD133 in MLL-AF4 leukemia cells

    著者: , , , , , , , , , , , , , , , , , , , , - Leukemia 2020 被引用: 67

  21. MLL-AF4 cooperates with PAF1 and FACT to drive high-density enhancer interactions in leukemia

    著者: , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2023 被引用: 25

  22. Identification of mesenchymal stem/progenitor cells in human first-trimester fetal blood, liver, and bone marrow

    著者: , , , , , - Blood 2001 被引用: 1,353

  23. Discovery of a CD10-negative B-progenitor in human fetal life identifies unique ontogeny-related developmental programs

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Blood 2019 被引用: 94

  24. The genome-wide impact of trisomy 21 on DNA methylation and its implications for hematopoiesis

    著者: , , , , , , , , , , , , , , , , , , , , - Nature Communications 2021 被引用: 62