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11
Increased Rate of Phenocopies in All Age Groups in BRCA1/BRCA2 Mutation Kindred, but Increased Prospective Breast Cancer Risk Is Confined to BRCA2 Mutation Carriers
Increased Rate of Phenocopies in All Age Groups in BRCA1/BRCA2 Mutation Kindred, but Increased Prospective Breast Cancer Risk Is Confined to BRCA2 Mutation Carriers
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Increased Rate of Phenocopies in All Age Groups in BRCA1/BRCA2 Mutation Kindred, but Increased Prospective Breast Cancer Risk Is Confined to BRCA2 Mutation Carriers

EVANS, D. Gareth R ; INGHAM, Sarah L ; BUCHAN, Lain ; WOODWARD, Emma R ; BYERS, Helen ; HOWELL, Anthony ; MAHER, Eamonn R ; NEWMAN, William G ; LALLOO, Fiona

Cancer epidemiology, biomarkers & prevention, 2013-12, Vol.22 (12), p.2269-2276 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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12
Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries
Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries
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Prospective evaluation of a breast-cancer risk model integrating classical risk factors and polygenic risk in 15 cohorts from six countries

Hurson, Amber N ; Pal Choudhury, Parichoy ; Gao, Chi ; Hüsing, Anika ; Eriksson, Mikael ; Shi, Min ; Jones, Michael E ; Evans, D Gareth R ; Milne, Roger L ; Gaudet, Mia M ; Vachon, Celine M ; Chasman, Daniel I ; Easton, Douglas F ; Schmidt, Marjanka K ; Kraft, Peter ; Garcia-Closas, Montserrat ; Chatterjee, Nilanjan

International journal of epidemiology, 2022-01, Vol.50 (6), p.1897-1911 [Periódico revisado por pares]

England: Oxford University Press

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13
Multi-Maintenance Olaparib Therapy in Relapsed, Germline BRCA1/2-Mutant High-Grade Serous Ovarian Cancer (MOLTO): A Phase II Trial
Multi-Maintenance Olaparib Therapy in Relapsed, Germline BRCA1/2-Mutant High-Grade Serous Ovarian Cancer (MOLTO): A Phase II Trial
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Multi-Maintenance Olaparib Therapy in Relapsed, Germline BRCA1/2-Mutant High-Grade Serous Ovarian Cancer (MOLTO): A Phase II Trial

Morgan, Robert D ; Clamp, Andrew R ; White, Daniel J ; Price, Marcus ; Burghel, George J ; Ryder, W David J ; Mahmood, Reem D ; Murphy, Alexander D ; Hasan, Jurjees ; Mitchell, Claire L ; Salih, Zena ; Wheeler, Chelsey ; Buckley, Emma ; Truelove, Joanna ; King, Georgia ; Ainaoui, Yasmina ; Bhaskar, Sanjeev S ; Shaw, Joseph ; Evans, D Gareth R ; Kilerci, Bedirhan ; Pearce, Simon P ; Brady, Gerard ; Dive, Caroline ; O'Connor, James P B ; Wallace, Andrew J ; Rothwell, Dominic G ; Edmondson, Richard J ; Jayson, Gordon C

Clinical cancer research, 2023-07, Vol.29 (14), p.2602-2611 [Periódico revisado por pares]

United States

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14
Predicting the likelihood of a BRCA1/2 pathogenic variant being somatic by testing only tumour DNA in non-mucinous high-grade epithelial ovarian cancer
Predicting the likelihood of a BRCA1/2 pathogenic variant being somatic by testing only tumour DNA in non-mucinous high-grade epithelial ovarian cancer
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Predicting the likelihood of a BRCA1/2 pathogenic variant being somatic by testing only tumour DNA in non-mucinous high-grade epithelial ovarian cancer

Morgan, Robert D ; Burghel, George J ; Flaum, Nicola ; Bulman, Michael ; Smith, Philip ; Clamp, Andrew R ; Hasan, Jurjees ; Mitchell, Claire ; Salih, Zena ; Woodward, Emma R ; Lalloo, Fiona ; Shaw, Joseph ; Desai, Sudha ; Crosbie, Emma J ; Edmondson, Richard J ; Schlecht, Helene ; Wallace, Andrew J ; Jayson, Gordon C ; Evans, D Gareth R

Journal of clinical pathology, 2023-10, Vol.76 (10), p.684-689 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd and Association of Clinical Pathologists

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15
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes
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TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes

Terradas, Mariona ; Mur, Pilar ; Belhadj, Sami ; Woodward, Emma R ; Burghel, George J ; Munoz-Torres, Pau M ; Quintana, Isabel ; Navarro, Matilde ; Brunet, Joan ; Lazaro, Conxi ; Pineda, Marta ; Moreno, Victor ; Capella, Gabriel ; Evans, D Gareth R ; Valle, Laura

Gut, 2021-06, Vol.70 (6), p.1139-1146 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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16
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients
Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients
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Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients

Hexter, Adam ; Jones, Adrian ; Joe, Harry ; Heap, Laura ; Smith, Miriam J ; Wallace, Andrew J ; Halliday, Dorothy ; Parry, Allyson ; Taylor, Amy ; Raymond, Lucy ; Shaw, Adam ; Afridi, Shazia ; Obholzer, Rupert ; Axon, Patrick ; King, Andrew T ; Friedman, Jan M ; Evans, D Gareth R

Journal of medical genetics, 2015-10, Vol.52 (10), p.699-705 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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17
Prevalence of germline pathogenic BRCA1/2 variants in sequential epithelial ovarian cancer cases
Prevalence of germline pathogenic BRCA1/2 variants in sequential epithelial ovarian cancer cases
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Prevalence of germline pathogenic BRCA1/2 variants in sequential epithelial ovarian cancer cases

Morgan, Robert D ; Burghel, George J ; Flaum, Nicola ; Bulman, Michael ; Clamp, Andrew R ; Hasan, Jurjees ; Mitchell, Claire L ; Schlecht, Helene ; Woodward, Emma R ; Lallo, Fiona I ; Crosbie, Emma J ; Edmondson, Richard J ; Wallace, Andrew J ; Jayson, Gordon C ; Evans, D Gareth R

Journal of medical genetics, 2019-05, Vol.56 (5), p.301-307 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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18
Assessing individual breast cancer risk within the U.K. National Health Service Breast Screening Program: a new paradigm for cancer prevention
Assessing individual breast cancer risk within the U.K. National Health Service Breast Screening Program: a new paradigm for cancer prevention
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Assessing individual breast cancer risk within the U.K. National Health Service Breast Screening Program: a new paradigm for cancer prevention

Evans, D Gareth R ; Warwick, Jane ; Astley, Susan M ; Stavrinos, Paula ; Sahin, Sarah ; Ingham, Sarah ; McBurney, Helen ; Eckersley, Barbara ; Harvie, Michelle ; Wilson, Mary ; Beetles, Ursula ; Warren, Ruth ; Hufton, Alan ; Sergeant, Jamie C ; Newman, William G ; Buchan, Iain ; Cuzick, Jack ; Howell, Anthony

Cancer prevention research (Philadelphia, Pa.), 2012-07, Vol.5 (7), p.943-951 [Periódico revisado por pares]

United States

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19
CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing
CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing
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CNVs affecting cancer predisposing genes (CPGs) detected as incidental findings in routine germline diagnostic chromosomal microarray (CMA) testing

Innes, Josie ; Reali, Lisa ; Clayton-Smith, Jill ; Hall, Georgina ; Lim, Derek HK ; Burghel, George J ; French, Kim ; Khan, Unzela ; Walker, Daniel ; Lalloo, Fiona ; Evans, D Gareth R ; McMullan, Dominic ; Maher, Eamonn R ; Woodward, Emma R

Journal of medical genetics, 2018-02, Vol.55 (2), p.89-96 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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20
Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis
Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis
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Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis

Burkitt Wright, Emma MM ; Sach, Emma ; Sharif, Saba ; Quarrell, Oliver ; Carroll, Thomas ; Whitehouse, Richard W ; Upadhyaya, Meena ; Huson, Susan M ; Evans, D Gareth R

Journal of medical genetics, 2013-09, Vol.50 (9), p.606-613 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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