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The Prostate, ISSN 1097-0045, 2019, Volume 79, Issue 10, pp. 1099 - 1105
...), the concept and tools for assessing the validity of reported GRS values from tests (narrow‐sense validity) are underdeveloped. Methods We propose two benchmarks for assessing the narrow... 
prostate cancer (PCa) | genetic risk score (GRS) | clinical validity | Genetic Predisposition to Disease | Prostatic Neoplasms - genetics | Risk Assessment | Gene Frequency | Humans | Middle Aged | Risk Factors | Alleles | Benchmarking | Male | Polymorphism, Single Nucleotide | Prostatic Neoplasms - diagnosis | Genetic research | Prostate cancer | Risk factors | Benchmarks | Validity | Single-nucleotide polymorphism | Calibration | Risk assessment
Journal Article
Journal of clinical oncology, ISSN 1527-7755, 2018, Volume 36, Issue 4, pp. 414 - 424
textabstractPurpose: Guidelines are limited for genetic testing for prostate cancer (PCA). The goal of this conference was to develop an expert... 
CONSORTIUM | SURVIVAL | ONCOLOGY | MEN | GERMLINE MUTATIONS | HOXB13 G84E MUTATION | CARRIERS | MISMATCH REPAIR DEFICIENCY | BREAST | BRCA2 MUTATION | ACCURACY | Special
Journal Article
by Sotoodehnia, Nona and Isaacs, Aaron and de Bakker, Paul I W and Dörr, Marcus and Newton-Cheh, Christopher and Nolte, Ilja M and van der Harst, Pim and Müller, Martina and Eijgelsheim, Mark and Alonso, Alvaro and Hicks, Andrew A and Padmanabhan, Sandosh and Hayward, Caroline and Smith, Albert Vernon and Polasek, Ozren and Giovannone, Steven and Fu, Jingyuan and Magnani, Jared W and Marciante, Kristin D and Pfeufer, Arne and Gharib, Sina A and Teumer, Alexander and Li, Man and Bis, Joshua C and Rivadeneira, Fernando and Aspelund, Thor and Köttgen, Anna and Johnson, Toby and Rice, Kenneth and Sie, Mark P S and Wang, Ying A and Klopp, Norman and Fuchsberger, Christian and Wild, Sarah H and Leach, Irene Mateo and Estrada, Karol and Völker, Uwe and Wright, Alan F and Asselbergs, Folkert W and Qu, Jiaxiang and Chakravarti, Aravinda and Sinner, Moritz F and Kors, Jan A and Petersmann, Astrid and Harris, Tamara B and Soliman, Elsayed Z and Munroe, Patricia B and Psaty, Bruce M and Oostra, Ben A and Cupples, L Adrienne and Perz, Siegfried and de Boer, Rudolf A and Uitterlinden, André G and Völzke, Henry and Spector, Timothy D and Liu, Fang-Yu and Boerwinkle, Eric and Dominiczak, Anna F and Rotter, Jerome I and van Herpen, Gé and Levy, Daniel and Wichmann, H-Erich and van Gilst, Wiek H and Witteman, Jacqueline C M and Kroemer, Heyo K and Kao, W H Linda and Heckbert, Susan R and Meitinger, Thomas and Hofman, Albert and Campbell, Harry and Folsom, Aaron R and van Veldhuisen, Dirk J and Schwienbacher, Christine and O'Donnell, Christopher J and Volpato, Claudia Beu and Caulfield, Mark J and Connell, John M and Launer, Lenore and Lu, Xiaowen and Franke, Lude and Fehrmann, Rudolf S N and te Meerman, Gerard and Groen, Harry J M and Weersma, Rinse K and van den Berg, Leonard H and Wijmenga, Cisca and Ophoff, Roel A and Navis, Gerjan and Rudan, Igor and Snieder, Harold and Wilson, James F and Pramstaller, Peter P and Siscovick, David S and Wang, Thomas J and Gudnason, Vilmundur and van Duijn, Cornelia M and Felix, Stephan B and Fishman, Glenn I and Jamshidi, Yalda and Ch Stricker, Bruno H and ...
Nature genetics, ISSN 1546-1718, 2010, Volume 42, Issue 12, pp. 1068 - 1076
Journal Article
by Jankowski, Janusz A Z and de Caestecker, John and Love, Sharon B and Reilly, Gavin and Watson, Peter and Sanders, Scott and Ang, Yeng and Morris, Danielle and Bhandari, Pradeep and Brooks, Claire and Attwood, Stephen and Harrison, Rebecca and Barr, Hugh and Moayyedi, Paul and Ragunath, Krish and Rameh, Bashir and Fullarton, Grant and Tucker, Art and Penman, Ian and Rodgers, Colin and Neale, James and Edwards, Cathryn and Wise, Adelyn and Jones, Stephen and Church, Nicholas and Vaidya, Kishor and Balata, Sherzad and Todd, John and Gibbons, Michael and Johnston, David and Anderson, Mark and Davies, Gareth and Dickey, William and Murdock, Andrew and Turner, Graham and Goddard, Andrew and Gore, Stephen and Haigh, Chris and Harding, Timothy and Jackson, Lucina and Murray, Iain and Worthingon, Joy and Lee, Thomas and Lim, Peik Loon and McLoughlin, James and Macdonald, Christopher and Mairs, Philip and Monk, David and Preston, Sean and Pugh, Stirling and Smart, Howard and Soliman, Ashraf and Isaacs, Peter and Aldulaimi, David and Trudgill, Nigel and Teare, Julian and Benhamida, Abduljalil and Bell, Andrew and Boulton-Jones, Robert and Daneshmend, Tawfique and Suzuki, Hisaharu and Cullen, Sue and Fitzgerald, Rebecca and Ransford, Rupert and Rahman, Mohammad Mesbahur and Tebala, Giovanni Domenico and Hallissey, Michael and Kelly, Carrie and Hickish, Tamas and Taha, Ali and Rademaker, Johan and Whitehead, Mark and Kelly, Sean and Phull, Perminder and Sharma, Naveen and Perry, Ian and Sankara-Raman, Vankatraman and Ali, Haythem and Khan, Iqbal and Curtis, Howard and Wadley, Martin and Stone, Adam and Sukumaran, Sumesh and Higham, Andrew and Lewis, Stephen and Haycock, Adam and Usselmann, Bernhard and Johnston, Simon Douglas and Tham, Tony and Campbell, Stewart and Douds, Andrew and Dunn, Jason and Sargeant, Ian and Narain, Mark and Maynard, Nick and Chilton, Andrew and Green, Susi and Loft, Duncan and Decadt, Bart and Mendall, Michael and ... and AspECT Trial Team
The Lancet (British edition), ISSN 0140-6736, 2018, Volume 392, Issue 10145, pp. 400 - 408
Journal Article
2013, The SAGE Key Concepts Series, ISBN 144621057X
...A mark scheme is a set of criteria used when assessing a piece of work in a test or assessment. It is usual to write the mark scheme at the same time... 
Book Chapter
Lancet Infectious Diseases, The, ISSN 1473-3099, 2011, Volume 11, Issue 12, pp. 907 - 915
Journal Article
Nature genetics, ISSN 1546-1718, 2012, Volume 44, Issue 12, pp. 1336 - 1340
Journal Article