Eamonn R. Maher
1990–2025 年に発表
- 別表記
- Eamonn R Maher
- 274
- 論文数
- 60,182
- 被引用数
- 134
- h 指数
- 271
- i10 指数
被引用数
引用元
国・地域
機関
分野
- Biochemistry, Genetics and Molecular Biology57.5%
- Medicine35.9%
- Neuroscience2.6%
- Immunology and Microbiology2%
- Agricultural and Biological Sciences0.3%
- Environmental Science0.3%
- その他1.4%
トピック
- Cancer, Hypoxia, and Metabolism7.4%
- Epigenetics and DNA Methylation4.6%
- Renal cell carcinoma treatment2.5%
- Genetic Syndromes and Imprinting2.4%
- Renal and related cancers2.2%
- RNA modifications and cancer2.1%
- その他78.8%
共著者
- Farida Latif45
- D. Gareth Evans26
- Neil V. Morgan25
- Emma R. Woodward20
- Ashraf Dallol15
- Fiona MacDonald15
- Frances M. Richards14
- Thomas Eggermann14
- Dewi Astuti13
- Richard C. Trembath13
- Fiona Lalloo12
- Louise Tee12
- Luke B. Hesson12
- Patrick J. Morrison12
- Paul Gissen12
- Wolf Reik12
- Andrea Riccio11
- Angelo Agathanggelou11
- Dean Gentle11
- Deborah Mackay11
- Mark R. Morris11
- Shanaz Pasha11
- Trevor Cole11
- Derek Lim10
全論文
- The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis
著者: Patrick H. Maxwell, Michael S. Wiesener, Gin-Wen Chang, Steven C. Clifford, Emma C. Vaux, Matthew E. Cockman, Charles C. Wykoff, Christopher W. Pugh, Eamonn R. Maher, Peter J. Ratcliffe - Nature 1999 被引用: 5,225
- Whole-genome sequencing of patients with rare diseases in a national health system
著者: 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 A. 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 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
- Fumarate is an epigenetic modifier that elicits epithelial-to-mesenchymal transition
著者: Marco Sciacovelli, Emanuel Gonçalves, Timothy Isaac Johnson, Vincent Zecchini, Ana S.H. Costa, Edoardo Gaude, Alizée Vercauteren Drubbel, Sebastian J. Theobald, Sandra Riekje Abbo, Maxine Tran, Vinothini Rajeeve, Simone Cardaci, Sarah Foster, Haiyang Yun, Pedro R. Cutillas, Anne Y. Warren, Vincent J. Gnanapragasam, Eyal Gottlieb, Kristian Franze, Brian J.P. Huntly, Eamonn R. Maher, Patrick H. Maxwell, Julio Sáez-Rodríguez, Christian Frezza - Nature 2016 被引用: 598
- VHL, the story of a tumour suppressor gene
著者: Lucy Gossage, Tim Eisen, Eamonn R. Maher - Nature reviews. Cancer 2014 被引用: 787
- Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
著者: Jenny Lord, Dominic McMullan, Ruth Y. Eberhardt, Gabriele Rinck, Susan Hamilton, E Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna Best, Georgina K. Carey, Rhiannon Mellis, Sarah Robart, Ian Berry, Kate Chandler, Deirdre Cilliers, Lara Cresswell, Sandra L. Edwards, Carol Gardiner, Alex Henderson, Simon Holden, Tessa Homfray, Tracy Lester, Rebecca Lewis, Ruth Newbury‐Ecob, Katrina Prescott, Oliver Quarrell, Simon Ramsden, Eileen Roberts, Dagmar Tapon, Madeleine Tooley, Pradeep Vasudevan, Astrid Weber, Diana Wellesley, Paul Westwood, Helen White, Michael Parker, Denise Williams, Lucy Jenkins, Richard H. Scott, Mark D. Kilby, Lyn S. Chitty, Matthew E. Hurles, Eamonn R. Maher, Mark S. Bateman, Ian Berry, Sunayna Best, Carolyn Campbell, Jenni Campbell, Georgina K. Carey, Kate Chandler, Lyn S. Chitty, Deirdre Cilliers, Kelly Cohen, Emma Collingwood, P. Constantinou, Lara Cresswell, Catherine Delmege, Ruth Y. Eberhardt, Sandra L. Edwards, Richard J. Ellis, Jerry Evans, Thomas R. Everett, Clare F Pinto, Natalie Forrester, Emma Fowler, Carol Gardiner, Susan Hamilton, Karen Healey, Alex Henderson, Simon Holden, Tessa Homfray, Rebecca Hudson, Matthew E. Hurles, Lucy Jenkins, Rebecca Keelagher, Mark D. Kilby, Tracey Lester, Rebecca Lewis, Jenny Lord, Eamonn R. Maher, Tamás Marton, Dominic McMullan, Sarju Mehta, Rhiannon Mellis, Ruth Newbury‐Ecob, Soo‐Mi Park, Michael Parker, Katrina Prescott, Elena Prigmore, Oliver Quarrell, E Quinlan-Jones, Simon Ramsden, Gabriele Rinck, Sarah Robart, Eileen Roberts, Jayne Rowland, Richard H. Scott, James Steer, Dagmar Tapon, Emma Taylor ほか 8 名 - The Lancet 2019 被引用: 708
- Cancer Risks Associated With GermlinePALB2Pathogenic Variants: An International Study of 524 Families
著者: Xin Yang, Goska Leslie, Alicja Doroszuk, Sandra Schneider, Jamie Allen, Brennan Decker, Alison M. Dunning, James Redman, James A. Scarth, Inga Plaskocinska, Craig Luccarini, Mitul Shah, Karen A. Pooley, Leila Dorling, Andrew Lee, Muriel A. Adank, Julian Adlard, Kristiina Aittomäki, Irene L. Andrulis, Peter Ang, Julian Barwell, Jonine L. Bernstein, Kristie Bobolis, Åke Borg, Carl Blomqvist, Kathleen Claes, Patrick Concannon, Adeline Cuggia, Julie O. Culver, Francesca Damiola, Antoine De Pauw, Orland Dı́ez, Jill S. Dolinsky, Susan M. Domchek, Christoph Engel, D. Gareth Evans, Florentia Fostira, Judy E. Garber, Lisa Golmard, Ellen L. Goode, Stephen B. Gruber, Eric Hahnen, Christopher R. Hake, Tuomas Heikkinen, Judith Hurley, Ramūnas Janavičius, Zdeněk Kleibl, Petra Kleiblová, Irene Konstantopoulou, Anders Kvist, Holly LaDuca, Ann S. G. Lee, Fabienne Lesueur, Eamonn R. Maher, Arto Mannermaa, Siranoush Manoukian, Rachel McFarland, Wendy McKinnon, Alfons Meindl, Kelly Metcalfe, Nur Aishah Mohd Taib, Jukka S. Moilanen, Katherine L. Nathanson, Susan L. Neuhausen, Pei Sze Ng, Tú Nguyen‐Dumont, Sarah M. Nielsen, Florian Obermair, Kenneth Offit, Olufunmilayo I. Olopade, Laura Ottini, Judith Penkert, Katri Pylkäs, Paolo Radice, Susan J. Ramus, Vilius Rudaitis, Lucy Side, Rachel Silva‐Smith, Valentina Silvestri, Anne‐Bine Skytte, Thomas Slavin, Jana Soukupová, Carlo Tondini, Alison H. Trainer, Gary Unzeitig, Lydia Usha, Thomas van Overeem Hansen, James Whitworth, Marie Wood, Cheng Har Yip, Sook‐Yee Yoon, Amal Yussuf, George Zogopoulos, David E. Goldgar, John L. Hopper, Georgia Chenevix‐Trench, Paul D.P. Pharoah, Sophia George, Judith Balmañà, Claude Houdayer ほか 19 名 - Journal of Clinical Oncology 2019 被引用: 418
- Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial
著者: John Burn, Harsh Sheth, Faye Elliott, Lynn Reed, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Fiona E. McRonald, Lucio Bertario, D. Gareth Evans, Anne‐Marie Gerdes, Judy W.C. Ho, Annika Lindblom, Patrick J. Morrison, Jem Rashbass, Raj Ramesar, Toni T. Seppälä, Huw Thomas, Kirsi Pylvänäinen, Gillian M. Borthwick, John C. Mathers, D. Timothy Bishop, Alex Boussioutas, Carole Brewer, Jackie Cook, Diana Eccles, Anthony Ellis, Shirley V. Hodgson, Jan Lubiński, Eamonn R. Maher, Mary Porteous, Julian R. Sampson, Rodney J. Scott, Lucy Side - The Lancet 2020 被引用: 403
- Genomic imprinting disorders: lessons on how genome, epigenome and environment interact
著者: David Monk, Deborah Mackay, Thomas Eggermann, Eamonn R. Maher, Andrea Riccio - Nature Reviews Genetics 2019 被引用: 463
- Hypoxia, Hypoxia-inducible Transcription Factors, and Renal Cancer
著者: Johannes Schödel, Steffen Grampp, Eamonn R. Maher, Holger Moch, Peter J. Ratcliffe, Paul Russo, David R. Mole - European Urology 2015 被引用: 423
- Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene
著者: Farida Latif, Kálmán Tory, James R. Gnarra, Masahiro Yao, Fuh-Mei Duh, Mary Lou Orcutt, Thomas Stackhouse, Igor Kuzmin, William S. Modi, L. Geil, Laura S. Schmidt, Fangwei Zhou, Hua Li, Ming Wei, Fan Chen, G.M. Glenn, Peter Choyke, McClellan M. Walther, Yongkai Weng, Dah-Shuhn R. Duan, Michael Dean, Damjan Glavač, Frances M. Richards, Paul A. Crossey, M.A. Ferguson‐Smith, Denis Le Paslier, llya Chumakov, Daniel Cohen, A. Craig Chinault, Eamonn R. Maher, W. Marston Linehan, Berton Zbar, Michael I. Lerman - Science 1993 被引用: 3,015
- Germline selection shapes human mitochondrial DNA diversity
著者: Wei Wei, Salih Tuna, Michael J. Keogh, Katherine R. Smith, Katherine R. Smith, Timothy J. Aitman, Phil L. Beales, David Bennett, Daniel P. Gale, Maria A. K. Bitner-Glindzicz, Graeme C. Black, Paul Brennan, Perry Elliott, Frances Flinter, R. Andrés Floto, Henry Houlden, Melita Irving, Ania Koziell, Eamonn R. Maher, Hugh S. Markus, Nicholas W. Morrell, William G. Newman, Irene Roberts, John A. Sayer, Kenneth G. C. Smith, Kenneth G. C. Smith, Jenny C. Taylor, Hugh Watkins, Andrew R. Webster, Andrew O.M. Wilkie, 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
- Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort
著者: Katie Wong, David Pitcher, Fiona Braddon, Lewis Downward, Retha Steenkamp, Nicholas M. P. Annear, Jonathan Barratt, Coralie Bingham, Constantina Chrysochou, Richard J. Coward, David Game, Siân Griffin, Matt Hall, Sally Johnson, Durga Kanigicherla, Fiona Karet Frankl, David Kavanagh, Larissa Kerecuk, Eamonn R. Maher, Shabbir H. Moochhala, Jenny Pinney, John A Sayer, Roslyn Simms, Smeeta Sinha, Shalabh Srivastava, Frederick W.K. Tam, Andrew Neil Turner, Stephen B Walsh, Aoife Waters, Patricia D. Wilson, Edwin Wong, C. Mark Taylor, Dorothea Nitsch, Moin A. Saleem, Detlef Böckenhauer, Kate Bramham, Daniel P. Gale, Sharirose Abat, Shazia Adalat, Joy O. Agbonmwandolor, Zubaidah Ahmad, Abdulfattah Alejmi, Rashid Almasarwah, Nicholas Annear, Ellie Asgari, Amanda Ayers, Jyoti Baharani, Gowrie Balasubramaniam, Felix Kpodo, Tarun Bansal, Alison Barratt, Jonathan Barratt, Megan Bates, Natalie Bayne, Janet Bendle, Sarah Benyon, Carsten Bergmann, Sunil Bhandari, Coralie Bingham, Preetham Boddana, Sally L. Bond, Fiona Braddon, Kate Bramham, Angela Branson, Stephen Brearey, Vicky Brocklebank, Sharanjit Budwal, Conor Byrne, Hugh Cairns, Brian Camilleri, Gary Campbell, A. Capell, Margaret Carmody, Marion Carson, Tracy Cathcart, Christine Catley, Karine Cesar, Melanie Chan, Houda Chea, James Chess, Chee Kay Cheung, Katy-Jane Chick, Nihil Chitalia, Martin Christian, Constantina Chrysochou, Katherine Clark, Christopher L. Clayton, Rhian Clissold, Helen Cockerill, Joshua Coelho, Elizabeth Colby, Viv Colclough, Eileen Conway, H. Terence Cook, Wendy L. Cook, Theresa Cooper, Richard J. Coward, Sarah Crosbie, Gabor Cserep, Anjali Date ほか 198 名 - The Lancet 2024 被引用: 75
- Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
著者: John Burn, Anne‐Marie Gerdes, Finlay Macrae, Jukka‐Pekka Mecklin, Gabriela Möslein, Sylviane Olschwang, Diana Eccles, D. Gareth Evans, Eamonn R. Maher, Lucio Bertario, Marie-Luise Bisgaard, Malcolm G. Dunlop, Judy Ho, Shirley V. Hodgson, Annika Lindblom, Jan Lubiński, Patrick J. Morrison, Victoria Murday, Raj Ramesar, Lucy Side, Rodney J. Scott, Huw Thomas, Hans F. A. Vasen, G Barker, Gillian Crawford, Faye Elliott, Mohammad Movahedi, Kirsi Pylvänäinen, Juul Wijnen, Riccardo Fodde, Henry T. Lynch, John C. Mathers, D. Timothy Bishop - The Lancet 2011 被引用: 951
- The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity
著者: Rune Busk Damgaard, Jennifer A. Walker, Paola Marco‐Casanova, Neil V. Morgan, Hannah Titheradge, P.R. Elliott, Duncan McHale, Eamonn R. Maher, Andrew N. J. McKenzie, David Komander - Cell 2016 被引用: 357
- Imprinting disorders
著者: Thomas Eggermann, David Monk, Guiomar Pérez de Nanclares, Masayo Kagami, Éloïse Giabicani, Andrea Riccio, Zeynep Tümer, Jennifer M. Kalish, M. Tauber, Jessica Duis, Rosanna Weksberg, Eamonn R. Maher, Matthias Begemann, Miriam Elbracht - Nature Reviews Disease Primers 2023 被引用: 79
- Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
著者: Frédéric Brioude, Jennifer M. Kalish, Alessandro Mussa, Alison Foster, Jet Bliek, Giovanni Battista Ferrero, Susanne E. Boonen, Trevor Cole, Robert J. Baker, Monica Bertoletti, Guido Cocchi, Carole Coze, Maurizio De Pellegrin, Khalid Hussain, Abdulla Ibrahim, Mark D. Kilby, Małgorzata Krajewska‐Walasek, Christian P. Kratz, E J Ladusans, Pablo Lapunzina, Yves Le Bouc, Saskia M. Maas, Fiona MacDonald, Katrin Õunap, Licia Peruzzi, Sylvie Rossignol, Silvia Russo, Caroleen Shipster, Agata Skórka, Katrina Tatton‐Brown, Jair Tenorio, Chiara Tortora, Karen Grønskov, Irène Netchine, Raoul C. M. Hennekam, Dirk Prawitt, Zeynep Tümer, Thomas Eggermann, Deborah Mackay, Andrea Riccio, Eamonn R. Maher - Nature Reviews Endocrinology 2018 被引用: 597
- PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron
著者: Neil V. Morgan, Shawn K. Westaway, Jenny E.V. Morton, Allison Gregory, Paul Gissen, Scott Sonek, Hakan Cangül, Jason Coryell, Natalie Canham, Nardo Nardocci, Giovanna Zorzi, Shanaz Pasha, Diana Rodriguez, Isabelle Desguerre, Amar Mubaidin, Enrico Bertini, Richard C. Trembath, Alessandro Simonati, Carolyn Schanen, Colin A. Johnson, Barbara Levinson, C. Geoffrey Woods, Beth Wilmot, Patricia Kramer, Jane Gitschier, Eamonn R. Maher, Susan J. Hayflick - Nature Genetics 2006 被引用: 538
- Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants
著者: David Taïeb, George B. Wanna, Maleeha Ahmad, Charlotte Lussey‐Lepoutre, Nancy D. Perrier, Svenja Nölting, Laurence Amar, Henri Timmers, Zachary G. Schwam, Anthony L. Estrera, Michael Lim, Erqi L. Pollom, Lucas K. Vitzthum, Isabelle Bourdeau, Ruth Casey, Frédéric Castinetti, Roderick Clifton‐Bligh, Eleonora P.M. Corssmit, Ronald R. de Krijger, Jaydira Del Rivero, Graeme Eisenhofer, Hans K. Ghayee, Anne‐Paule Gimenez‐Roqueplo, Ashley Grossman, Alessio Impériale, Jeroen C. Jansen, Abhishek Jha, Michiel N. Kerstens, Henricus P. M. Kunst, James K. Liu, Eamonn R. Maher, Daniele Marchioni, Leilani B Mercado-Asis, Özgür Mete, Mitsuhide Naruse, Naris Nilubol, Neeta Pandit‐Taskar, F. Sébag, Akiyo Tanabe, J Widimský, Leah Meuter, Jacques W.M. Lenders, Karel Pacák - The Lancet Diabetes & Endocrinology 2023 被引用: 87
- Hypoxia Inducible Factor-α Binding and Ubiquitylation by the von Hippel-Lindau Tumor Suppressor Protein
著者: Matthew E. Cockman, Norma Masson, David R. Mole, Panu Jaakkola, Gin-Wen Chang, Steven C. Clifford, Eamonn R. Maher, Christopher W. Pugh, Peter J. Ratcliffe, Patrick H. Maxwell - Journal of Biological Chemistry 2000 被引用: 1,047
- Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome
著者: Michael L. Nickerson, Michelle B. Warren, Jorge R. Toro, Vera Y. Matrosova, G.M. Glenn, Maria L. Turner, Paul H. Duray, Maria J. Merino, Peter L. Choyke, Christian P. Pavlovich, Nirmala Sharma, McClellan M. Walther, David J. Munroe, R Hill, Eamonn R. Maher, Cheryl R. Greenberg, Michael I. Lerman, W. Marston Linehan, Berton Zbar, Laura S. Schmidt - Cancer Cell 2002 被引用: 937
- Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment
著者: Fred H. Menko, Eamonn R. Maher, Laura S. Schmidt, Lindsay Middelton, Kristiina Aittomäki, Ian Tomlinson, Stéphane Richard, W. Marston Linehan - Familial Cancer 2014 被引用: 358
- von Hippel–Lindau disease: A clinical and scientific review
著者: Eamonn R. Maher, Hartmut P.H. Neumann, Stéphane Richard - European Journal of Human Genetics 2011 被引用: 720
- Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement
著者: David Taïeb, Svenja Nölting, Nancy D. Perrier, Martin Faßnacht, Jorge A. Carrasquillo, Ashley Grossman, Roderick Clifton‐Bligh, George B. Wanna, Zachary G. Schwam, Laurence Amar, Isabelle Bourdeau, Ruth Casey, Joakim Crona, Cheri Deal, Jaydira Del Rivero, Quan‐Yang Duh, Graeme Eisenhofer, Tito Fojo, Hans K. Ghayee, Anne‐Paule Gimenez‐Roqueplo, Anthony J. Gill, Rodney J. Hicks, Alessio Impériale, Abhishek Jha, Michiel N. Kerstens, Ronald R. de Krijger, André Lacroix, Ivica Lazúrová, Frank I. Lin, Charlotte Lussey‐Lepoutre, Eamonn R. Maher, Özgür Mete, Mitsuhide Naruse, Naris Nilubol, Mercedes Robledo, F. Sébag, Nalini S. Shah, Akiyo Tanabe, Geoffrey B. Thompson, Henri Timmers, J Widimský, William J. Young, Leah Meuter, Jacques W.M. Lenders, Karel Pacák - Nature Reviews Endocrinology 2023 被引用: 90
- Health and population effects of rare gene knockouts in adult humans with related parents
著者: Vagheesh M. Narasimhan, Karen A. Hunt, Dan Mason, Christopher L. Baker, Konrad J. Karczewski, Michael R. Barnes, Anthony Barnett, Chris Bates, Srikanth Bellary, Nicholas Bockett, Kristina Giorda, Chris Griffiths, Harry Hemingway, Zhilong Jia, M. A. Kelly, Hajrah Khawaja, Monkol Lek, Shane McCarthy, Rosie McEachan, Anne O’Donnell‐Luria, Kenneth Paigen, Constantinos A. Parisinos, Eamonn Sheridan, Laura Southgate, Louise Tee, Mark Thomas, Yali Xue, Michael Schnall-Levin, Petko M. Petkov, Chris Tyler‐Smith, Eamonn R. Maher, Richard C. Trembath, Daniel G. MacArthur, John Wright, Richard Durbin, David A. van Heel - Science 2016 被引用: 313
