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المؤلفون: Laurene, Ben Aim, Eamonn R, Maher, Alberto, Cascon, Anne, Barlier, Sophie, Giraud, Tonino, Ercolino, Pascal, Pigny, Roderick J, Clifton-Bligh, Delphine, Mirebeau-Prunier, Amira, Mohamed, Judith, Favier, Anne-Paule, Gimenez-Roqueplo, Francesca, Schiavi, Rodrigo A, Toledo, Patricia L, Dahia, Mercedes, Robledo, Jean Pierre, Bayley, Nelly, Burnichon
المصدر: Journal of medical genetics. 59(8)
مصطلحات موضوعية: Paraganglioma, Succinate Dehydrogenase, Adrenal Gland Neoplasms, Humans, Genetic Testing, Pheochromocytoma, Germ-Line Mutation
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المؤلفون: Emilia M. Swietlik, Daniel Greene, Na Zhu, Karyn Megy, Marcella Cogliano, Smitha Rajaram, Divya Pandya, Tobias Tilly, Katie A. Lutz, Carrie C.L. Welch, Michael W. Pauciulo, Laura Southgate, Jennifer M. Martin, Carmen M. Treacy, Christopher J. Penkett, Jonathan C. Stephens, Harm J. Bogaard, Colin Church, Gerry Coghlan, Anna W. Coleman, Robin Condliffe, Christina A. Eichstaedt, Mélanie Eyries, Henning Gall, Stefano Ghio, Barbara Girerd, Ekkehard Grünig, Simon Holden, Luke Howard, Marc Humbert, David G. Kiely, Gabor Kovacs, Jim Lordan, Rajiv D. Machado, Robert V. MacKenzie Ross, Colm McCabe, Shahin Moledina, David Montani, Horst Olschewski, Joanna Pepke-Zaba, Laura Price, Christopher J. Rhodes, Werner Seeger, Florent Soubrier, Jay Suntharalingam, Mark R. Toshner, Anton Vonk Noordegraaf, John Wharton, James M. Wild, Stephen John Wort, Allan Lawrie, Martin R. Wilkins, Richard C. Trembath, Yufeng Shen, Wendy K. Chung, Andrew J. Swift, William C. Nichols, Nicholas W. Morrell, Stefan Gräf, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David J. Allsup, 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 Bariana, Julian Barwell, Joana Batista, Helen E. Baxendale, Phil L. Beales, David L. Bennett, Agnieszka Bierzynska, Tina Biss, Maria A.K. Bitner-Glindzicz, Graeme C. Black, Marta Bleda, Iulia Blesneac, Detlef Bockenhauer, Sara Boyce, John R. Bradley, Gerome Breen, Paul Brennan, Carole Brewer, Matthew Brown, Andrew C. Browning, Michael J. Browning, Rachel J. Buchan, Matthew S. Buckland, Teofila Bueser, Carmen Bugarin Diz, John Burn, Siobhan O. Burns, Oliver S. Burren, Nigel Burrows, Carolyn Campbell, Gerald Carr-White, Keren Carss, Ruth Casey, Mark J. Caulfield, Jenny Chambers, John Chambers, Melanie M.Y. Chan, Floria Cheng, Patrick F. Chinnery, Manali Chitre, Martin T. Christian, Jill Clayton-Smith, Maureen Cleary, Naomi Clements Brod, Elizabeth Colby, Trevor R.P. Cole, Janine Collins, Peter W. Collins, Cecilia J. Compton, H. Terence Cook, Stuart Cook, Nichola Cooper, Paul A. Corris, Nicola S. Curry, Matthew J. Daniels, Mehul Dattani, Louise C. Daugherty, John Davis, Anthony De Soyza, Sri V.V. Deevi, Timothy Dent, Charu Deshpande, Eleanor F. Dewhurst, Peter H. Dixon, Sofia Douzgou, Kate Downes, Anna M. Drazyk, Elizabeth Drewe, Daniel Duarte, Tina Dutt, J. David M. Edgar, Karen Edwards, William Egner, Melanie N. Ekani, Perry Elliott, Wendy N. Erber, Marie Erwood, Maria C. Estiu, Dafydd Gareth Evans, Gillian Evans, Tamara Everington, Hiva Fassihi, Remi Favier, Debra Fletcher, Frances A. Flinter, R. Andres Floto, Tom Fowler, James Fox, Amy J. Frary, Courtney E. French, Kathleen Freson, Mattia Frontini, Abigail Furnell, Daniel P. Gale, Vijeya Ganesan, Michael Gattens, Hossein-Ardeschir Ghofrani, J. Simon R. Gibbs, Kate Gibson, Kimberly C. Gilmour, Nicholas S. Gleadall, Sarah Goddard, Keith Gomez, Pavels Gordins, David Gosal, Jodie Graham, Luigi Grassi, Lynn Greenhalgh, Andreas Greinacher, Paolo Gresele, Philip Griffiths, Sofia Grigoriadou, Detelina Grozeva, Mark Gurnell, Scott Hackett, Charaka Hadinnapola, Rosie Hague, William M. Hague, Matthias Haimel, Matthew Hall, Helen L. Hanson, Eshika Haque, Kirsty Harkness, Andrew R. Harper, Claire L. Harris, Daniel Hart, Ahamad Hassan, Grant Hayman, Alex Henderson, Archana Herwadkar, Jonathan Hoffman, Rita Horvath, Henry Houlden, Arjan C. Houweling, Fengyuan Hu, Gavin Hudson, Aarnoud P. Huissoon, Matthew Hurles, Melita Irving, Louise Izatt, Roger James, Sally A. Johnson, Stephen Jolles, Jennifer Jolley, Dragana Josifova, Neringa Jurkute, Mary A. Kasanicki, Hanadi Kazkaz, Rashid Kazmi, Peter Kelleher, Anne M Kelly, Wilf Kelsall, Carly Kempster, Nathalie Kingston, Nils Koelling, Myrto Kostadima, Ania Koziell, Roman Kreuzhuber, Taco W. Kuijpers, Ajith Kumar, Dinakantha Kumararatne, Manju A. Kurian, Michael A. Laffan, Fiona Lalloo, Michele Lambert, Hana Lango Allen, D. Mark Layton, Claire Lentaigne, Tracy Lester, Adam P. Levine, Rachel Linger, Hilary Longhurst, Lorena E. Lorenzo, Eleni Louka, Paul A. Lyons, Bella Madan, Eamonn R. Maher, Jesmeen Maimaris, Samantha Malka, Sarah Mangles, Rutendo Mapeta, Kevin J. Marchbank, Stephen Marks, Hugh S. Markus, Hanns-Ulrich Marschall, Andrew Marshall, Mary Mathias, Emma Matthews, Heather Maxwell, Paul McAlinden, Mark I. McCarthy, Harriet McKinney, Stuart Meacham, Adam J. Mead, Sarju G. Mehta, Michel Michaelides, Carolyn Millar, Shehla N. Mohammed, Anthony T. Moore, Monika Mozere, Keith W. Muir, Andrew D. Mumford, Andrea H. Nemeth, William G. Newman, Michael Newnham, Sadia Noorani, Paquita Nurden, Jennifer O’Sullivan, Samya Obaji, Chris Odhams, Steven Okoli, Andrea Olschewski, Kai Ren Ong, S. Helen Oram, Elizabeth Ormondroyd, Willem H. Ouwehand, Claire Palles, Sofia Papadia, Soo-Mi Park, David Parry, Smita Patel, Joan Paterson, Andrew Peacock, Simon H. Pearce, Kathelijne Peerlinck, Romina Petersen, Clarissa Pilkington, Kenneth E.S. Poole, Bethan Psaila, Angela Pyle, Richard Quinton, Shamima Rahman, Anupama Rao, F. Lucy Raymond, Paula J. Rayner-Matthews, Augusto Rendon, Tara Renton, Andrew S.C. Rice, Alex Richter, Leema Robert, Irene Roberts, Sarah J. Rose, Robert Ross-Russell, Catherine Roughley, Noemi B.A. Roy, Deborah M. Ruddy, Omid Sadeghi-Alavijeh, Moin A. Saleem, Nilesh Samani, Crina Samarghitean, Alba Sanchis-Juan, Ravishankar B. Sargur, Robert N. Sarkany, Simon Satchell, Sinisa Savic, Genevieve Sayer, John A. Sayer, Laura Scelsi, Andrew M. Schaefer, Sol Schulman, Richard Scott, Marie Scully, Claire Searle, Arjune Sen, W.A. Carrock Sewell, Denis Seyres, Neil Shah, Olga Shamardina, Susan E. Shapiro, Adam C. Shaw, Keith Sibson, Lucy Side, Ilenia Simeoni, Michael A. Simpson, Matthew C. Sims, Suthesh Sivapalaratnam, Damian Smedley, Katherine R. Smith, Kenneth G.C. Smith, Katie Snape, Nicole Soranzo, Olivera Spasic-Boskovic, Simon Staines, Emily Staples, Hannah Stark, Kathleen E. Stirrups, Alex Stuckey, Petros Syrris, R. Campbell Tait, Kate Talks, Rhea Y.Y. Tan, Jenny C. Taylor, John M. Taylor, James E. Thaventhiran, Andreas C. Themistocleous, David Thomas, Ellen Thomas, Moira J. Thomas, Patrick Thomas, Kate Thomson, Adrian J. Thrasher, Chantal Thys, Marc Tischkowitz, Catherine Titterton, Cheng-Hock Toh, Ian P. Tomlinson, Matthew Traylor, Paul Treadaway, Salih Tuna, Ernest Turro, Philip Twiss, Tom Vale, Chris Van Geet, Natalie van Zuydam, Anthony M Vandersteen, Marta Vazquez-Lopez, Julie von Ziegenweidt, Annette Wagner, Quinten Waisfisz, Neil Walker, Suellen M. Walker, James S. Ware, Hugh Watkins, Christopher Watt, Andrew R. Webster, Lucy Wedderburn, Wei Wei, Steven B. Welch, Julie Wessels, Sarah K. Westbury, John-Paul Westwood, Deborah Whitehorn, James Whitworth, Andrew O.M. Wilkie, Catherine Williamson, Brian T. Wilson, Edwin K.S. Wong, Nicholas Wood, Yvette Wood, Christopher Geoffrey Woods, Emma R. Woodward, Austen Worth, Michael Wright, Katherine Yates, Patrick F.K. Yong, Timothy Young, Ping Yu, Patrick Yu-Wai-Man, Eliska Zlamalova, Russel Hirsch, R. James White, Marc Simon, David Badesch, Erika Rosenzweig, Charles Burger, Murali Chakinala, Thenappan Thenappan, Greg Elliott, Robert Simms, Harrison Farber, Robert Frantz, Jean Elwing, Nicholas Hill, Dunbar Ivy, James Klinger, Steven Nathan, Ronald Oudiz, Ivan Robbins, Robert Schilz, Terry Fortin, Jeffrey Wilt, Delphine Yung, Eric Austin, Ferhaan Ahmad, Nitin Bhatt, Tim Lahm, Adaani Frost, Zeenat Safdar, Zia Rehman, Robert Walter, Fernando Torres, Sahil Bakshi, Stephen Archer, Rahul Argula, Christopher Barnett, Raymond Benza, Ankit Desai, Veeranna Maddipati
المساهمون: University of Cambridge [UK] (CAM), Columbia University [New York], University of Sheffield [Sheffield], University of Cincinnati (UC), St George's, University of London, Vrije Universiteit Amsterdam [Amsterdam] (VU), Golden Jubilee National Hospital, Glasgow, Royal Free Hospital [London, UK], Heidelberg University Hospital [Heidelberg], Service de Génétique Cytogénétique et Embryologie [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Institute of cardiometabolism and nutrition (ICAN), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), Technische Hochschule Mittelhessen - University of Applied Sciences [Giessen] (THM), Fondazione IRCCS Policlinico San Matteo, Hypertension pulmonaire : physiopathologie et innovation thérapeutique (HPPIT), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Saclay, Universität Heidelberg [Heidelberg], Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Imperial College London, Royal Hallamshire Hospital, University of Graz, Freeman Hospital, Royal United Hospitals Bath (RUH), Great Ormond Street Hospital for Children [London] (GOSH), Royal Papworth Hospital, Cambridge Biomedical Campus, Cambridge, United Kingdom., King‘s College London, Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Karl-Franzens-Universität [Graz, Autriche], Pulmonary medicine, ACS - Pulmonary hypertension & thrombosis, Swietlik, Emilia [0000-0002-4095-8489], Megy, Karyn [0000-0002-2826-3879], Tilly, Tobias [0000-0002-6762-5342], Stephens, Jonathan [0000-0003-2020-9330], Toshner, Mark [0000-0002-3969-6143], Morrell, Nicholas [0000-0001-5700-9792], Graf, Stefan [0000-0002-1315-8873], Apollo - University of Cambridge Repository, Unité de Recherche sur les Maladies Cardiovasculaires, du Métabolisme et de la Nutrition = Research Unit on Cardiovascular and Metabolic Diseases (ICAN), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Institut de Cardiométabolisme et Nutrition = Institute of Cardiometabolism and Nutrition [CHU Pitié Salpêtrière] (IHU ICAN), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Karl-Franzens-Universität Graz, HAL-SU, Gestionnaire, British Heart Foundation, The Academy of Medical Sciences
المصدر: Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine, American Heart Association, 2020, ⟨10.1161/CIRCGEN.120.003155⟩
Circulation. Genomic and Precision Medicine
Circulation. Genomic and precision medicine, 14(1):e003155. Lippincott Williams and Wilkins Ltd.
morrell 2021, ' Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension ', Circulation. Genomic and precision medicine, vol. 14, no. 1, e003155 . https://doi.org/10.1161/CIRCGEN.120.003155
Circulation: Genomic and Precision Medicine, 2020, ⟨10.1161/CIRCGEN.120.003155⟩مصطلحات موضوعية: 0301 basic medicine, Candidate gene, Cardiac & Cardiovascular Systems, genetic association studies, 030204 cardiovascular system & hematology, Biology, Bayesian inference, 03 medical and health sciences, 0302 clinical medicine, Missing heritability problem, pulmonary hypertension, medicine, Family history, Gene, Genetics & Heredity, Genetics, family history, Science & Technology, [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, Kinase insert domain receptor, computed tomography, General Medicine, Original Articles, medicine.disease, Pulmonary hypertension, Phenotype, 3. Good health, 030104 developmental biology, Cardiovascular System & Cardiology, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, Life Sciences & Biomedicine, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, vascular endothelial growth factor receptor
وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::524b66714d301fd180ea8d1d09ee8e86
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المؤلفون: Diana Walsh, Graeme R. Clark, Ezequiel Martin, Neil V. Morgan, Louise Tee, Hannah Titheradge, Evan Reid, Mary O'Driscoll, Eamonn R. Maher, Bryndis Yngvadottir
المساهمون: Martin, Ezequiel [0000-0002-0051-8868], Reid, Evan [0000-0003-1623-7304], Maher, Eamonn R [0000-0002-6226-6918], Apollo - University of Cambridge Repository
المصدر: Brain Communications
مصطلحات موضوعية: 0301 basic medicine, Genetics, cerebral palsy, business.industry, General Engineering, autosomal recessive, medicine.disease, inherited, Cerebral palsy, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Spastic cerebral palsy, Genetic linkage, Paralysis, Spastic, Missense mutation, Medicine, Original Article, medicine.symptom, business, 030217 neurology & neurosurgery, Loss function, Exome sequencing
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::963925c09b25fd4fb0d71debf31d4f84
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المؤلفون: Lynn Rochester, John T. O'Brien, Joanna Knee, Alistair S. Hall, Paul Dark, Miles D. Witham, Laurie Oliva, Kim Down, Eleanor Anderson, Gary Nestor, James Wason, Camille Carroll, Rebecca Maier, Eamonn R. Maher, Gail Mountain
المساهمون: Witham, Miles D [0000-0002-1967-0990], Carroll, Camille B [0000-0001-7472-953X], Apollo - University of Cambridge Repository
المصدر: Witham, M D, Anderson, E, Carroll, C, Dark, P, Down, K, Hall, A S, Knee, J, Maher, E H, Maier, R H, Mountain, G A, Nestor, G, O'Brien, J T, Oliva, L, Watson, J & Rochester, L 2020, ' Ensuring that COVID-19 Research is Inclusive-guidance from the NIHR INCLUDE project ', BMJ Open . https://doi.org/10.1136/bmjopen-2020-043634
BMJ Open, Vol 10, Iss 11 (2020)
Witham, MD, Dark, PM, Down, K, Knee, J, Maher, ER, Maier, RH, Mountain, GA, Nestor, G, Oliva, L, Wason, J & Group, NIHR CRN INCLUDE S 2020, ' Ensuring that COVID-19 research is inclusive: guidance from the NIHR INCLUDE project. ', BMJ Open . https://doi.org/10.1136/bmjopen-2020-043634
BMJ Openمصطلحات موضوعية: medicine.medical_specialty, Biomedical Research, Coronavirus disease 2019 (COVID-19), statistics & research methods, Psychological intervention, Ethnic group, Humans, Medicine, Minority Groups, Community engagement, SARS-CoV-2, business.industry, Public health, Clinical study design, public health, COVID-19, General Medicine, Public relations, Intervention (law), Identification (information), business, Research methods
وصف الملف: text/xml; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e31b58ff21e22486465ad72e5a06990
https://research.manchester.ac.uk/en/publications/f0b7b393-08f9-4f4d-8250-9f2fcb0121c0 -
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المؤلفون: Ruth T Casey, Hartmut P. H. Neumann, Eamonn R. Maher
المساهمون: Maher, Eamonn [0000-0002-6226-6918], Apollo - University of Cambridge Repository
المصدر: Hum Mol Genet
مصطلحات موضوعية: 0301 basic medicine, Evidence-based practice, Invited Review Article, Adrenal Gland Neoplasms, Pheochromocytoma, Biology, Bioinformatics, Paraganglioma, 03 medical and health sciences, 0302 clinical medicine, Genotype, Genetics, medicine, Humans, Genetic Testing, Precision Medicine, Molecular Biology, Genetics (clinical), Germ-Line Mutation, Genetic heterogeneity, General Medicine, Precision medicine, medicine.disease, Clinical Practice, Succinate Dehydrogenase, 030104 developmental biology, 030220 oncology & carcinogenesis, Signal Transduction
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d7ea84a78c8bba740b3a03e9ba8e6cc
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المؤلفون: Steven C Clifford, Matthew E Cockman, Alan C Smallwood, David R Mole, Emma R Woodward, Patrick H Maxwell, Peter J Ratcliffe, Eamonn R Maher
المصدر: Human Molecular Genetics. 30:844-845
مصطلحات موضوعية: Genetics, General Medicine, Molecular Biology, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7c8c2b0345bf54d32d24aac00b83af2f
https://doi.org/10.1093/hmg/ddab037 -
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المؤلفون: Venkata R. Bulusu, Philip Smith, James Whitworth, Basetti Madhu, Graeme R. Clark, Thomas Roberts, Alison Marker, Kieren Allinson, Ruth T Casey, Soo-Mi Park, Mel Maranian, Olivier Giger, Eguzkine Ochoa, Jose Ezequiel Martin, Colin Watts, Rogier ten Hoopen, Joanne Anstee, Fay Rodger, Eamonn R. Maher, Luis Miguel Pino Campos, Benjamin G. Challis
المساهمون: Madhu, Basetti [0000-0001-5844-856X], Campos, Luis [0000-0002-4317-0013], Maher, Eamonn R [0000-0002-6226-6918], Apollo - University of Cambridge Repository, Maher, Eamonn R. [0000-0002-6226-6918]
المصدر: Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reportsمصطلحات موضوعية: 0301 basic medicine, Epigenomics, Male, SDHA, Adrenal Gland Neoplasms, medicine.disease_cause, Germline, Epigenesis, Genetic, 0302 clinical medicine, Renal cell carcinoma, Paraganglioma, Genes, Regulator, Promoter Regions, Genetic, 45/90, Mutation, Multidisciplinary, Molecular medicine, GiST, article, High-Throughput Nucleotide Sequencing, Middle Aged, Succinate Dehydrogenase, Oncology, Medicine, Female, Adult, Adolescent, Gastrointestinal Stromal Tumors, Science, 45/22, 45/23, Pheochromocytoma, 692/4028, 03 medical and health sciences, medicine, Humans, Loss function, Germ-Line Mutation, Aged, 45/91, business.industry, Membrane Proteins, DNA Methylation, medicine.disease, 692/4017, 030104 developmental biology, Mutation testing, Cancer research, business, Transcriptome, 030217 neurology & neurosurgery
وصف الملف: application/pdf; text/xml
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5941746c1b6527ac8d94245524e35a9c
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المؤلفون: Zerin, Hyder, Adele, Fairclough, Mike, Groom, Joan, Getty, Elizabeth, Alexander, Elke M, van Veen, Guy, Makin, Chitra, Sethuraman, Vivian, Tang, D Gareth, Evans, Eamonn R, Maher, Emma R, Woodward
المصدر: Journal of medical genetics. 58(9)
مصطلحات موضوعية: Comparative Genomic Hybridization, DNA Copy Number Variations, Biopsy, Infant, Immunohistochemistry, Magnetic Resonance Imaging, Kidney Neoplasms, Repressor Proteins, Phenotype, Cytogenetic Analysis, Humans, Female, Genetic Predisposition to Disease, Genetic Association Studies, Germ-Line Mutation, In Situ Hybridization, Fluorescence, Sequence Deletion
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المؤلفون: Finlay A. Macrae, Toni T. Seppälä, Gillian M. Borthwick, Anne-Marie Gerdes, D. Gareth Evans, Fiona E McRonald, Lynn Reed, Huw Thomas, Julian R. Sampson, Jackie Cook, Shirley Hodgson, Mary Porteous, Jukka-Pekka Mecklin, Lucy Side, Anthony Ellis, John Burn, Carole Brewer, Lucio Bertario, Kirsi Pylvänäinen, D. Timothy Bishop, Diana Eccles, Alex Boussioutas, Faye Elliott, Rodney J. Scott, Jem Rashbass, Patrick J. Morrison, Harsh Sheth, Gabriela Möslein, Raj Ramesar, John C. Mathers, Jan Lubinski, Annika Lindblom, Judy W. C. Ho, Eamonn R. Maher
المساهمون: HUS Abdominal Center, Clinicum, II kirurgian klinikka, Helsinki University Hospital Area
المصدر: Burn, J, Sheth, H, Elliott, F, Reed, L, Macrae, F, Mecklin, J P, Möslein, G, McRonald, F E, Bertario, L, Evans, D G, Gerdes, A M, Ho, J W C, Lindblom, A, Morrison, P J, Rashbass, J, Ramesar, R, Seppälä, T, Thomas, H J W, Pylvänäinen, K, Borthwick, G M, Mathers, J C, Bishop, D T, Boussioutas, A, Brewer, C, Cook, J, Eccles, D, Ellis, A, Hodgson, S V, Lubinski, J, Maher, E R, Porteous, M EM, Sampson, J, Scott, R J, Side, L & CAPP2 Investigators 2020, ' 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 ', The Lancet, vol. 395, no. 10240, pp. 1855-1863 . https://doi.org/10.1016/S0140-6736(20)30366-4
Evans, D G & et al. 2020, ' 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 ', Lancet, vol. 395, no. 10240, pp. 1855-1863 . https://doi.org/10.1016/S0140-6736(20)30366-4مصطلحات موضوعية: RESISTANT STARCH, Placebo-controlled study, 030204 cardiovascular system & hematology, 0302 clinical medicine, Life Tables, 030212 general & internal medicine, 11 Medical and Health Sciences, media_common, RISK, Aspirin, education.field_of_study, Anti-Inflammatory Agents, Non-Steroidal, LOW-DOSE ASPIRIN, General Medicine, Lynch syndrome, 3. Good health, Intention to Treat Analysis, Anti-Inflammatory Agents, Non-Steroidal/adverse effects, medicine.drug, CHEMOPREVENTION, medicine.medical_specialty, Heterozygote, 3122 Cancers, Population, NEOPLASIA, Aspirin/adverse effects, Placebo, CAPP2 Investigators, Medication Adherence, 03 medical and health sciences, Double-Blind Method, Internal medicine, General & Internal Medicine, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, BENEFITS, medicine, media_common.cataloged_instance, Humans, European union, education, Proportional Hazards Models, Intention-to-treat analysis, Cancer prevention, business.industry, MORTALITY, 3126 Surgery, anesthesiology, intensive care, radiology, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, business, Follow-Up Studies
وصف الملف: application/pdf; text
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b883398de7c0cc7e549ca68d176f77a1
https://curis.ku.dk/portal/da/publications/cancer-prevention-with-aspirin-in-hereditary-colorectal-cancer-lynch-syndrome-10year-followup-and-registrybased-20year-data-in-the-capp2-study(731041a4-aa9f-42c7-b9db-83326e8b4a6d).html -
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المؤلفون: Xin, Yang, Goska, Leslie, Alicja, Doroszuk, Sandra, Schneider, Jamie, Allen, Brennan, Decker, Alison M, Dunning, James, Redman, James, Scarth, Inga, Plaskocinska, Craig, Luccarini, Mitul, Shah, Karen, 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 B M, Claes, Patrick, Concannon, Adeline, Cuggia, Julie O, Culver, Francesca, Damiola, Antoine, de Pauw, Orland, Diez, Jill S, Dolinsky, Susan M, Domchek, Christoph, Engel, D Gareth, Evans, Florentia, Fostira, Judy, Garber, Lisa, Golmard, Ellen L, Goode, Stephen B, Gruber, Eric, Hahnen, Christopher, Hake, Tuomas, Heikkinen, Judith E, Hurley, Ramunas, Janavicius, Zdenek, Kleibl, Petra, Kleiblova, 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, Moilanen, Katherine L, Nathanson, Susan, Neuhausen, Pei Sze, Ng, Tu, 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, Soukupova, 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, Goldgar, John L, Hopper, Georgia, Chenevix-Trench, Paul, Pharoah, Sophia H L, George, Judith, Balmaña, Claude, Houdayer, Paul, James, Zaki, El-Haffaf, Hans, Ehrencrona, Marketa, Janatova, Paolo, Peterlongo, Heli, Nevanlinna, Rita, Schmutzler, Soo-Hwang, Teo, Mark, Robson, Tuya, Pal, Fergus, Couch, Jeffrey N, Weitzel, Aaron, Elliott, Melissa, Southey, Robert, Winqvist, Douglas F, Easton, William D, Foulkes, Antonis C, Antoniou, Marc, Tischkowitz
المصدر: J Clin Oncol
مصطلحات موضوعية: Adult, Aged, 80 and over, Male, Ovarian Neoplasms, Risk, Internationality, Age Factors, Middle Aged, Breast Neoplasms, Male, Pancreatic Neoplasms, Neoplasms, RAPID COMMUNICATIONS, Humans, Female, Genetic Predisposition to Disease, Fanconi Anemia Complementation Group N Protein, Germ-Line Mutation, Aged
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::cf42d4788d5d2d210088fc88878c6fa8
https://pubmed.ncbi.nlm.nih.gov/31841383