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Fiona Lalloo

1991–2025 年に発表

117
論文数
18,769
被引用数
67
h 指数
107
i10 指数

被引用数

Fiona Lalloo の年別被引用数1987 年: 被引用 1 件1988 年: 被引用 1 件1993 年: 被引用 2 件1994 年: 被引用 2 件1995 年: 被引用 2 件1996 年: 被引用 3 件1997 年: 被引用 16 件1998 年: 被引用 8 件1999 年: 被引用 5 件2000 年: 被引用 8 件2001 年: 被引用 6 件2002 年: 被引用 8 件2003 年: 被引用 12 件2004 年: 被引用 34 件2005 年: 被引用 60 件2006 年: 被引用 77 件2007 年: 被引用 94 件2008 年: 被引用 93 件2009 年: 被引用 103 件2010 年: 被引用 160 件2011 年: 被引用 131 件2012 年: 被引用 146 件2013 年: 被引用 166 件2014 年: 被引用 181 件2015 年: 被引用 146 件2016 年: 被引用 163 件2017 年: 被引用 164 件2018 年: 被引用 137 件2019 年: 被引用 549 件2020 年: 被引用 651 件2021 年: 被引用 526 件2022 年: 被引用 454 件2023 年: 被引用 354 件2024 年: 被引用 495 件2025 年: 被引用 176 件2026 年: 被引用 1 件1989〜1992 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 1,732 件、この内訳の 20.7%イギリス: 引用元論文 885 件、この内訳の 10.6%カナダ: 引用元論文 428 件、この内訳の 5.1%オーストラリア: 引用元論文 404 件、この内訳の 4.8%イタリア: 引用元論文 392 件、この内訳の 4.7%ドイツ: 引用元論文 386 件、この内訳の 4.6%オランダ: 引用元論文 385 件、この内訳の 4.6%フランス: 引用元論文 332 件、この内訳の 4%スペイン: 引用元論文 304 件、この内訳の 3.7%中国: 引用元論文 262 件、この内訳の 3.1%スウェーデン: 引用元論文 186 件、この内訳の 2.2%デンマーク: 引用元論文 166 件、この内訳の 2%
0%20.7%その他 29.9%

機関

分野

  • Medicine48.8%
  • Biochemistry, Genetics and Molecular Biology47.8%
  • Computer Science0.5%
  • Immunology and Microbiology0.5%
  • Neuroscience0.4%
  • Pharmacology, Toxicology and Pharmaceutics0.4%
  • その他1.6%

トピック

  • BRCA gene mutations in cancer13%
  • Genetic factors in colorectal cancer8.2%
  • Cancer Genomics and Diagnostics4.7%
  • DNA Repair Mechanisms3.6%
  • Ovarian cancer diagnosis and treatment3.3%
  • Breast Cancer Treatment Studies3.2%
  • その他64%

共著者

全論文

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  1. Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies

    著者: Antonis C. Antoniou, Paul D.P. Pharoah, Steven A. Narod, Harvey A. Risch, J.E. Eyfjörd, John L. Hopper, Niklas Loman, Håkan Olsson, Oskar T. Johannsson, Åke Borg, Barbara Pasini, Paolo Radice, Siranoush Manoukian, Diana Eccles, Nelson L.S. Tang, Edith Oláh, Hoda Anton‐Culver, Ellen Warner, Jan Lubiński, Jacek Gronwald, Bohdan Górski, Hrafn Tulinius, Steinunn Thorlacius, Hannaleena Eerola, Heli Nevanlinna, Kirsi Syrjäkoski, Olli Kallioniemi, Deborah J. Thompson, Chris Evans, Julian Peto, Fiona Lalloo, D. Gareth Evans, Douglas F. Easton - The American Journal of Human Genetics 2003 被引用: 3,685

  2. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    著者: Mev Dominguez–Valentin, Julian R. Sampson, Toni T. Seppälä, Sanne W. ten Broeke, John‐Paul Plazzer, Sigve Nakken, Christoph Engel, Stefan Aretz, Mark A. Jenkins, Lone Sunde, Inge Bernstein, Gabriel Capellá, Francesc Balaguer, Huw Thomas, D. Gareth Evans, John Burn, Marc S. Greenblatt, Eivind Hovig, Wouter H. de Vos tot Nederveen Cappel, Rolf H. Sijmons, Lucio Bertario, Maria Grazia Tibiletti, Giulia Martina Cavestro, Annika Lindblom, Adriana Della Valle, Francisco López‐Köstner, Nathan Gluck, Lior H. Katz, Karl Heinimann, Carlos Vaccaro, Reinhard Büttner, Heike Görgens, Elke Holinski‐Feder, Monika Morak, Stefanie Holzapfel, Robert Hüneburg, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Hans K. Schackert, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane M. Lindor, Steven Gallinger, Loı̈c Le Marchand, Polly A. Newcomb, Jane C. Figueiredo, Stephen N. Thibodeau, Karin Wadt, Christina Therkildsen, Henrik Okkels, Zohreh Ketabi, Leticia Moreira, Ariadna Sánchez, Miquel Serra‐Burriel, Marta Pineda, Matilde Navarro, Ignacio Blanco, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Oliver G. Denton, Ian M. Frayling, Einar Andreas Rødland, Hans F. A. Vasen, Miriam Mints, Florencia Neffa, Patricia Esperón, Karin Álvarez, Revital Kariv, Guy Rosner, Tamara Alejandra Piñero, María Laura González, Pablo Kalfayan, Douglas Tjandra, Ingrid Winship, Finlay Macrae, Gabriela Möslein, Jukka‐Pekka Mecklin, Maartje Nielsen, Pål Møller - Genetics in Medicine 2019 被引用: 649

  3. Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG)

    著者: Kevin Monahan, Nicola Bradshaw, Sunil Dolwani, Bianca DeSouza, Malcolm G. Dunlop, James E. East, Mohammad Ilyas, Asha Kaur, Fiona Lalloo, Andrew Latchford, Matthew D. Rutter, Ian Tomlinson, Huw Thomas, James Hill - Gut 2019 被引用: 473

  4. Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

    著者: Pål Møller, Toni T. Seppälä, Inge Bernstein, Elke Holinski‐Feder, Paulo Sala, D. Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf H. Sijmons, Jacqueline Jeffries, Hans F. A. Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Mark A. Jenkins, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Laura Renkonen‐Sinisalo, Mev Dominguez–Valentin, Ian M. Frayling, John‐Paul Plazzer, Kirsi Pylvänäinen, Maurizio Genuardi, Jukka‐Pekka Mecklin, Gabriela Moeslein, Julian R. Sampson, Gabriel Capellá - Gut 2017 被引用: 573

  5. Birth incidence and prevalence of tumor‐prone syndromes: Estimates from a UK family genetic register service

    著者: D. Gareth Evans, Elizabeth Howard, Clare Giblin, Tara Clancy, Harrison C. Spencer, Susan Huson, Fiona Lalloo - American Journal of Medical Genetics Part A 2010 被引用: 997

  6. Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

    著者: Pål Møller, Toni T. Seppälä, Inge Bernstein, Elke Holinski‐Feder, Paola Sala, D. Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf H. Sijmons, Jacqueline Jeffries, Hans F. A. Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Laura Renkonen‐Sinisalo, Ian M. Frayling, John‐Paul Plazzer, Kirsi Pylvänäinen, Julian R. Sampson, Gabriel Capellá, Jukka‐Pekka Mecklin, Gabriela Möslein - Gut 2015 被引用: 545

  7. The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome

    著者: Emma J. Crosbie, Emma J. Crosbie, Neil Ryan, Mark J. Arends, Tjalling Bosse, John Burn, Joanna M. Cornes, Robin Crawford, Diana Eccles, Ian M. Frayling, Sadaf Ghaem-Maghami, Heather Hampel, Noah D. Kauff, Henry C. Kitchener, Sarah J. Kitson, Ranjit Manchanda, Raymond F.T. McMahon, Kevin Monahan, Usha Menon, Pål Møller, Gabriela Möslein, Adam N. Rosenthal, Peter Sasieni, Mourad W. Seif, Naveena Singh, Pauline Skarrott, Tristan Snowsill, R. Steele, Marc Tischkowitz, Angel Alonso Sanchez, Mark J. Arends, James M. Bolton, Tjalling Bosse, John Burn, Emma J. Crosbie, Emma J. Crosbie, David N. Church, Joanna M. Cornes, Robin Crawford, K. J. Donnelly, Diana Eccles, Richard J. Edmondson, D. Gareth Evans, Ian M. Frayling, Sadaf Ghaem-Maghami, Paula Gollop, Selina Goodman, Heather Hampel, Shirley Hodgson, Noah D. Kauff, Henry C. Kitchener, Sarah J. Kitson, Fiona Lalloo, Anne Lowry, Ranjit Manchanda, Raymond F.T. McMahon, Rhona J. McVey, Usha Menon, Tracie Miles, Gabriela Möslein, Pål Møller, Kevin Monahan, Adam N. Rosenthal, Neil Ryan, Peter Sasieni, Mourad W. Seif, Pauline Skarrott, Naveena Singh, Tristan Snowsill, R. Steele, Astrid Stormoken, Helen F. Stringfellow, Marc Tischkowitz, Andrew J. Wallace, Luciya Whyte, Nafisa Wilkinson, Godfrey Wilson, Jo Wilson, Nick Wood, D. Gareth Evans - Genetics in Medicine 2019 被引用: 235

  8. Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

    著者: Mev Dominguez–Valentin, Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein, Mark A. Jenkins, Christoph Engel, Stefan Aretz, Maartje Nielsen, Gabriel Capellá, Francesc Balaguer, D. Gareth Evans, John Burn, Elke Holinski‐Feder, Lucio Bertario, Bernardo Bonanni, Annika Lindblom, Zohar Levi, Finlay Macrae, Ingrid Winship, John‐Paul Plazzer, Rolf H. Sijmons, Luigi Laghi, Adriana Della Valle, Karl Heinimann, Tadeusz Dębniak, Robert Fruscio, Francisco Lopez-Koestner, Karin Alvarez-Valenzuela, Lior H. Katz, Ido Laish, E Vainer, Carlos Vaccaro, Dirce Maria Carraro, Kevin Monahan, Elizabeth Half, Áine Stakelum, D. C. Winter, Rory Kennelly, Nathan Gluck, Harsh Sheth, Naim Abu‐Freha, Marc S. Greenblatt, Bernard Rossi, Mábel Bohórquez, Giulia Martina Cavestro, Leonardo S. Lino‐Silva, Karoline Horisberger, Maria Grazia Tibiletti, Ivana do Nascimento, Huw Thomas, Norma Rossi, Leandro Apolinário da Silva, Attila Zaránd, Juan Ruiz‐Bañobre, Vincent Heuveline, Jukka‐Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, Anna Lepistö, Païvi Peltomäki, Christina Therkildsen, Mia Gebauer Madsen, Stefan Kobbelgaard Burgdorf, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane M. Lindor, Steven Gallinger, Loı̈c Le Marchand, Polly A. Newcomb, Jane C. Figueiredo, Daniel D. Buchanan, Stephen N. Thibodeau, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Evelin Schröck, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Claudia Perne, Robert Hüneburg, Silke Redler, Reinhard Büttner, Jürgen Weitz, Marta Pineda, Núria Dueñas, Joan Brunet Vidal, Leticia Moreira, Ariadna Sánchez, Eivind Hovig, Sigve Nakken, Kate Green, Fiona Lalloo, James Hill, Emma J. Crosbie, Miriam Mints, Yael Goldberg ほか 16 名 - EClinicalMedicine 2023 被引用: 110

  9. Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells

    著者: Philip S. Robinson, Laura E. Thomas, Federico Abascal, Hyunchul Jung, Luke M. R. Harvey, Hannah D. West, Sigurgeir Ólafsson, Bernard C. H. Lee, Tim Coorens, Henry Lee-Six, Laura Butlin, Nicola Lander, Rebekah Truscott, Mathijs A. Sanders, Stefanie V. Lensing, Simon J. A. Buczacki, Rogier ten Hoopen, Nicholas Coleman, Roxanne Brunton-Sim, Simon Rushbrook, Kourosh Saeb‐Parsy, Fiona Lalloo, Peter J. Campbell, Iñigo Martincorena, Julian R. Sampson, Michael R. Stratton - Nature Communications 2022 被引用: 61

  10. Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD

    著者: Katrina Andrews, David B. Ascher, Douglas E. V. Pires, Daniel R. Barnes, Lindsey Vialard, Ruth Casey, Nicola Bradshaw, Julian Adlard, Simon Aylwin, Paul Brennan, Carole Brewer, Trevor Cole, Jackie Cook, Rosemarie Davidson, Alan Donaldson, Alan Fryer, Lynn Greenhalgh, Shirley V. Hodgson, Richard Irving, Fiona Lalloo, Michelle McConachie, Vivienne McConnell, Patrick J. Morrison, Victoria Murday, Soo‐Mi Park, Helen Simpson, Katie Snape, Susan E. Stewart, Susan Tomkins, Yvonne Wallis, Louise Izatt, David Goudie, Robert S. Lindsay, Colin Perry, Emma R. Woodward, Antonis C. Antoniou, Eamonn R. Maher - Journal of Medical Genetics 2018 被引用: 251

  11. UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variants in cancer predisposition genes: RAD51C, RAD51D, BRIP1 and PALB2

    著者: Helen Hanson, Anjana Kulkarni, Lucy Loong, Grace Kavanaugh, Bethany Torr, Sophie Allen, Munaza Ahmed, Antonis C. Antoniou, Ruth Cleaver, Tabib Dabir, D. Gareth Evans, Ellen Golightly, Rosalyn Jewell, Kelly Kohut, Ranjit Manchanda, Alex Murray, Jennie Murray, Kai‐Ren Ong, Adam N. Rosenthal, Emma R. Woodward, Diana Eccles, Clare Turnbull, Marc Tischkowitz, On behalf of Consensus meeting attendees, Fiona Lalloo - Journal of Medical Genetics 2022 被引用: 44

  12. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

    著者: Hans F. A. Vasen, Ignacio Blanco, Katja Aktan–Collan, Jessica P. Gopie, Ángel Alonso, Stefan Aretz, Inge Bernstein, Lucio Bertario, John Burn, Gabriel Capellá, Chrystelle Colas, Christoph Engel, Ian M. Frayling, Maurizio Genuardi, Karl Heinimann, Frederik J. Hes, Shirley V. Hodgson, John A. Karagiannis, Fiona Lalloo, Annika Lindblom, Jukka‐Pekka Mecklin, Pål Møller, T Myrhøj, Fokko M. Nagengast, Yann Parc, Maurizio Ponz de Leòn, Laura Renkonen‐Sinisalo, Julian R. Sampson, Astrid Stormorken, Rolf H. Sijmons, Sabine Tejpar, Huw Thomas, Nils Rahner, Juul Wijnen, Heikki Järvinen, Gabriela Möslein - Gut 2013 被引用: 744

  13. Germline mutations in RAD51D confer susceptibility to ovarian cancer

    著者: Chey Loveday, Clare Turnbull, Emma Ramsay, Deborah Hughes, Elise Ruark, Jessica Frankum, Georgina R. Bowden, Bolot Kalmyrzaev, Margaret Warren-Perry, Katie Snape, Julian Adlard, Julian Barwell, Jonathan Berg, Angela F. Brady, Carole Brewer, Glen Brice, Cyril Chapman, Jackie Cook, Rosemarie Davidson, Alan Donaldson, Fiona Douglas, Lynn Greenhalgh, Alex Henderson, Louise Izatt, Ajith Kumar, Fiona Lalloo, Zosia Miedzybrodzka, Patrick J. Morrison, Joan Paterson, Mary Porteous, Mark T. Rogers, Susan Shanley, Lisa Walker, Diana Eccles, D. Gareth Evans, Anthony Renwick, Sheila Seal, Christopher J. Lord, Alan Ashworth, Jorge S. Reis‐Filho, Antonis C. Antoniou, Nazneen Rahman - Nature Genetics 2011 被引用: 537

  14. The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

    著者: Antonis C. Antoniou, Alex Cunningham, Julian Peto, D. Gareth Evans, Fiona Lalloo, Steven A. Narod, Harvey A. Risch, Jórunn E. Eyfjörd, John L. Hopper, Melissa C. Southey, Håkan Olsson, Oskar T. Johannsson, Åke Borg, B Passini, Paolo Radice, Siranoush Manoukian, Diana Eccles, Nelson L.S. Tang, Edith Oláh, Hoda Anton‐Culver, Ellen Warner, Jan Lubiński, Jacek Gronwald, Bohdan Górski, Laufey Tryggvadóttír, Kirsi Syrjäkoski, O-P Kallioniemi, Hannaleena Eerola, Heli Nevanlinna, Paul D.P. Pharoah, Douglas F. Easton - British Journal of Cancer 2008 被引用: 535

  15. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

    著者: Manuel A. R. Ferreira, Eric R. Gamazon, Fares Al‐Ejeh, Kristiina Aittomäki, Irene L. Andrulis, Hoda Anton‐Culver, Aðalgeir Arason, Volker Arndt, Kristan J. Aronson, Banu Arun, Ella Asseryanis, Jacopo Azzollini, Judith Balmañà, Daniel R. Barnes, Daniel Barrowdale, Matthias W. Beckmann, Sabine Behrens, Javier Benı́tez, Marina Bermisheva, Katarzyna Białkowska, Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Manjeet K. Bolla, Åke Borg, Hiltrud Brauch, Hermann Brenner, Annegien Broeks, Barbara Burwinkel, Trinidad Caldés, Maria A. Caligo, Daniele Campa, Ian Campbell, Federico Canzian, Jonathan Carter, Brian D. Carter, Jose E. Castelao, Jenny Chang‐Claude, Stephen J. Chanock, Hans Christiansen, Wendy K. Chung, Kathleen Claes, Christine L. Clarke, EMBRACE Collaborators, Julian Adlard, Munaza Ahmed, Julian Barwell, Angela Brady, Carole Brewer, Jackie Cook, Rosemarie Davidson, Alan C. Donaldson, Jacqueline Eason, Ros Eeles, D. Gareth Evans, Helen Gregory, Helen Hanson, Alex Henderson, Shirley Hodgson, Louise Izatt, Michael J. Kennedy, Fiona Lalloo, Clare Miller, Patrick J. Morrison, Kai‐Ren Ong, Jo Perkins, Mary Porteous, Mark T. Rogers, Lucy Side, Katie Snape, Lisa Walker, Patricia A. Harrington, GC-HBOC Study Collaborators, Norbert Arnold, Bernd Auber, Nadja Bogdanova-Markov, Julika Borde, Almuth Caliebe, Nina Ditsch, Bernd Dworniczak, Stefanie Engert, Ulrike Faust, Andrea Gehrig, Eric Hahnen, Jan Hauke, Julia Hentschel, Natalie Herold, Ellen Honisch, Walter Just, Karin Kast, Mirjam Larsen, Johannes Lemke, Huu Phuc Nguyen, Dieter Niederacher, Claus‐Eric Ott, Konrad Platzer, Esther Pohl‐Rescigno, Juliane Ramser, Kerstin Rhiem, Doris Steinemann ほか 218 名 - Nature Communications 2019 被引用: 138

  16. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

    著者: Aung Ko Win, James G. Dowty, Jeanette C. Reece, Grant Lee, Allyson Templeton, John‐Paul Plazzer, Daniel D. Buchanan, Kiwamu Akagi, Seçil Ak Aksoy, Ángel Alonso, Karin Álvarez, David J. Amor, Ravindran Ankathil, Stefan Aretz, Julie Arnold, Melyssa Aronson, Rachel Austin, A Bäckman, Sanne W. ten Broeke, Verónica Barca-Tierno, Julian Barwell, Inge Bernstein, Pascaline Berthet, Beate Betz, Yves‐Jean Bignon, Talya Boisjoli, Valérie Bonadona, Laurent Briollais, Joan Brunet, Karolin Bucksch, Bruno Buecher, Reinhard Buettner, John Burn, Trinidad Caldés, Gabriel Capellá, Olivier Caron, Graham Casey, Min Hoe Chew, Yun‐Hee Choi, James M. Church, Mark Clendenning, Chrystelle Colas, Elisa J. Cops, Isabelle Coupier, Marcia Cruz‐Correa, Albert de la Chapelle, Niels de Wind, Tadeusz Dębniak, Adriana Della Valle, Capuccine Delnatte, Marion Dhooge, Mev Dominguez–Valentin, Youenn Drouet, Floor A.M. Duijkers, Christoph Engel, Patricia Esperón, D. Gareth Evans, Aı́da Falcón de Vargas, Jane C. Figueiredo, William D. Foulkes, Emmanuelle Fourme, Thierry Frébourg, Steven Gallinger, Pilar Garré, Maurizio Genuardi, Anne‐Marie Gerdes, Lauren M. Gima, Sophie Giraud, Annabel Goodwin, Heike Görgens, Kate Green, José G. Guillem, Carmen Guillén‐Ponce, Roselyne Guimbaud, Rodrigo Santa Cruz Guindalini, Elizabeth Half, Michael J. Hall, Heather Hampel, Thomas van Overeem Hansen, Karl Heinimann, Frederik J. Hes, James Hill, Judy Ho, Elke Holinski‐Feder, Nicoline Hoogerbrugge, Robert Hüneburg, Vanessa Huntley, Paul A. James, Uffe Birk Jensen, Thomas John, Wan Khairunnisa Wan Juhari, Matthew F. Kalady, Fay Kastrinos, Matthias Kloor, Maija R.J. Kohonen‐Corish, Lotte Krogh, Sonia S. Kupfer, Uri Ladabaum, Kristina Lagerstedt‐Robinson, Fiona Lalloo ほか 112 名 - The Lancet Oncology 2021 被引用: 118

  17. Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

    著者: Fiona Lalloo, A. Kulkarni, Cindy Chau, Maartje Nielsen, Michael Sheaff, Jeremy Steele, Remco van Doorn, Karin Wadt, Monica Hamill, Beth Torr, Marc Tischkowitz, Delphi respondents, Munaza Ahmed, Svetlana Bajalica‐Lagercrantz, Ana Blatnik, Joan Brunet, Ruth Cleaver, Chrystelle Colas, Tabib Dabir, D. Gareth Evans, Shirin Feshtali, Paola Ghiorzo, Lise Graversen, Klaus Griewank, Hildur Helgadóttir, Rosalyn Jewell, Kelly Kohut, Henrik Lorentzen, Daniela Massi, Guy S. Missotten, Alex Murray, Jennie Murray, Ernest Nadal, Kai Ren Ong, Josep M. Piulats, Susana Puig, Neil Rajan, Simone Ribero, Galateau Salle, Àlex Teulé, Emma Tham, Barbara van Paassen, Robin De Putter, Robert M. Verdijk, Anja Wagner, Emma R. Woodward, Helen Hanson - European Journal of Human Genetics 2023 被引用: 53

  18. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

    著者: Elizabeth Bancroft, Elizabeth Page, Mark N. Brook, Sarah Thomas, Natalie Taylor, Jennifer Pope, Jana McHugh, Ann-Britt Jones, Questa Karlsson, Susan Merson, Kai Ren Ong, Jonathan Hoffman, Camilla Huber, Lovise Mæhle, Eli Marie Grindedal, Astrid Stormorken, D. Gareth Evans, Jeanette Rothwell, Fiona Lalloo, Angela F. Brady, Marion Bartlett, Katie Snape, Helen Hanson, Paul A. James, Joanne McKinley, Lyon Mascarenhas, Sapna Syngal, Chinedu Ukaegbu, Lucy Side, Tessy Thomas, Julian Barwell, Manuel R. Teixeira, Louise Izatt, Mohnish Suri, Finlay Macrae, Nicola Poplawski, Rakefet Chen‐Shtoyerman, Munaza Ahmed, Hannah Musgrave, Nicola Nicolai, Lynn Greenhalgh, Carole Brewer, Nicholas Pachter, Allan D. Spigelman, Ashraf Azzabi, Brian T. Helfand, Dorothy Halliday, Saundra S. Buys, Teresa Ramón y Cajal, Alan Donaldson, Kathleen A. Cooney, Marion Harris, John McGrath, Rosemarie Davidson, Amy Taylor, Peter Cooke, Kathryn Myhill, Matthew Hogben, Neil K. Aaronson, Audrey Ardern‐Jones, Chris H. Bangma, Elena Castro, David P. Dearnaley, Alexander Dias, Tim Dudderidge, Diana M Eccles, Kate Green, Jórunn E. Eyfjörd, Alison Falconer, Christopher S. Foster, Henrik Grönberg, Freddie C. Hamdy, Oskar T. Johannsson, Vincent Khoo, Hans Lilja, Geoffrey J. Lindeman, Jan Lubiński, Karol Axcrona, Christos Mikropoulos, Anita Mitra, Clare Moynihan, Holly Ní Raghallaigh, Gad Rennert, Rebecca Collier, Lisa K. Adams, Julian Adlard, Rosa Alfonso, Saira Ali, Angela Andrew, Luís Araújo, Nazya Azam, Darran Ball, Queenstone Barker, Alon Basevitch, Barbara Benton, Cheryl Berlin, Nicola Bermingham, Leah H. Biller, Angela Bloss, Matilda Bradford ほか 218 名 - The Lancet Oncology 2021 被引用: 93

  19. Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected Individuals

    著者: Claire Forde, Derek Lim, Yousef Alwan, George J. Burghel, Laura Butland, Ruth Cleaver, Abhijit Dixit, D. Gareth Evans, Helen Hanson, Fiona Lalloo, Pedro Oliveira, Lindsey Vialard, Yvonne Wallis, Eamonn R. Maher, Emma R. Woodward - European Urology Oncology 2019 被引用: 92

  20. Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary network

    著者: Alice Garrett, Alison Callaway, Miranda Durkie, Cankut Çubuk, Mary Alikian, George J. Burghel, Rachel Robinson, Louise Izatt, Sabrina Talukdar, Lucy Side, Treena Cranston, Sheila Palmer-Smith, Diana Baralle, Ian Berry, James Drummond, Andrew J. Wallace, Gail Norbury, Diana Eccles, Sian Ellard, Fiona Lalloo, D. Gareth Evans, Emma R. Woodward, Marc Tischkowitz, Helen Hanson, Clare Turnbull - Journal of Medical Genetics 2020 被引用: 54

  21. Uptake of bilateral-risk-reducing-mastectomy: Prospective analysis of 7195 women at high-risk of breast cancer

    著者: D. Gareth Evans, Ashu Gandhi, Julie Wisely, Tara Clancy, Emma R. Woodward, James Harvey, Lyndsey Highton, John Murphy, Lester Barr, Sacha J. Howell, Fiona Lalloo, Elaine F. Harkness, Anthony Howell - The Breast 2021 被引用: 31

  22. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

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