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D

Dorothy Halliday

Oxford University Hospitals NHS Foundation Trust
H指数:30
被引数:4,236

个人简介

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荣誉奖项

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Genetic findings in people with schwannomas who do not meet clinical diagnostic criteria for NF2-related schwannomatosis
JOURNAL OF MEDICAL GENETICS
IF3.7
2024-08-290
PRE
Smith, Miriam J.; Perez-Becerril, Cristina; van der Meer, Mwee; Burghel, George J.; Waller, Sarah J.; Carney, Megan; Bunstone, Sancha; Fryer, Katherine; Bowers, Naomi L.; Hartley, Claire L.; Smith, Philip T.; Rutherford, Scott A.; Freeman, Simon R.; Lloyd, Simon K. W.; Pathmanaban, Omar N.; King, Andrew Thomas; Halliday, Dorothy; Duff, Chris; Evans, D. Gareth
NF2-related schwannomatosis and other schwannomatosis: an updated genetic and epidemiological study
JOURNAL OF MEDICAL GENETICS
IF3.7
2024-06-266
PRE
Forde, Claire; Smith, Miriam J.; Burghel, George J.; Bowers, Naomi; Roberts, Nicola; Lavin, Tim; Halliday, Jane; King, Andrew Thomas; Rutherford, Scott; Pathmanaban, Omar N.; Lloyd, Simon; Freeman, Simon; Halliday, Dorothy; Parry, Allyson; Axon, Patrick; Buttimore, Juliette; Afridi, Shazia; Obholzer, Rupert; Laitt, Roger; Thomas, Owen; Stivaros, Stavros Michael; Vassallo, Grace; Evans, D. Gareth
Radiation treatment of benign tumors in NF2-related-schwannomatosis: A national study of 266 irradiated patients showing a significant increase in malignancy/malignant progression
NEURO-ONCOLOGY ADVANCES
IF4.1
2023-03-1118
OAAI
Evans, D. Gareth; Halliday, Dorothy; Obholzer, Rupert; Afridi, Shazia; Forde, Claire; Rutherford, Scott A.; Hammerbeck-Ward, Charlotte; Lloyd, Simon K.; Freeman, Simon M.; Pathmanaban, Omar N.; Thomas, Owen M.; Laitt, Roger D.; Stivaros, Stavros; Kilday, John-Paul; Vassallo, Grace; McBain, Catherine; Lavin, Timothy; Paterson, Chay; Whitfield, Gillian; McCabe, Martin G.; Axon, Patrick R.; Halliday, Jane; Mackeith, Samuel; Parry, Allyson; Harkness, Elaine F.; Buttimore, Juliette; King, Andrew T.
Evaluation of tumour surveillance protocols and outcomes in von Hippel-Lindau disease in a national health service
BRITISH JOURNAL OF CANCER
IF6.8
2022-02-197
OA
Maher, Eamonn R.; Adlard, Julian; Barwell, Julian; Brady, Angela F.; Brennan, Paul; Cook, Jackie; Crawford, Gillian S.; Dabir, Tabib; Davidson, Rosemarie; Dyer, Rebecca; Harrison, Rachel; Forde, Claire; Halliday, Dorothy; Hanson, Helen; Hay, Eleanor; Higgs, Jenny; Jones, Mari; Lalloo, Fiona; Miedzybrodzka, Zosia; Ong, Kai Ren; Pelz, Frauke; Ruddy, Deborah; Snape, Katie; Whitworth, James; Sandford, Richard N.
Sporadic vestibular schwannoma: a molecular testing summary

散发性前庭神经鞘瘤: 分子测试总结

JOURNAL OF MEDICAL GENETICS
IF3.7
2020-06-2315
PREAI
Sadler, Katherine, V; Bowers, Naomi L.; Hartley, Claire; Smith, Philip T.; Tobi, Simon; Wallace, Andrew J.; King, Andrew; Lloyd, Simon K. W.; Rutherford, Scott; Pathmanaban, Omar N.; Hammerbeck-Ward, Charlotte; Freeman, Simon; Stapleton, Emma; Taylor, Amy; Shaw, Adam; Halliday, Dorothy; Smith, Miriam Jane; Evans, D. Gareth
Incidence of mosaicism in 1055 de novo NF2 cases: much higher than previous estimates with high utility of next-generation sequencing
GENETICS IN MEDICINE
IF6.2
2020-01-0161
OAAI
Evans, D. Gareth; Hartley, Claire L.; Smith, Philip T.; King, Andrew T.; Bowers, Naomi L.; Tobi, Simon; Wallace, Andrew J.; Perry, Mary; Anup, Raji; Lloyd, Simon K. W.; Rutherford, Scott A.; Hammerbeck-Ward, Charlotte; Pathmanaban, Omar N.; Stapleton, Emma; Freeman, Simon R.; Kellett, Mark; Halliday, Dorothy; Parry, Allyson; Gair, Juliette J.; Axon, Patrick; Laitt, Roger; Thomas, Owen; Afridi, Shazia K.; Obholzer, Rupert; Duff, Chris; Stivaros, Stavros M.; Vassallo, Grace; Harkness, Elaine F.; Smith, Miriam J.; Axon, Patrick; Gair, Juliette; Tysome, James; Donnelly, Neil; Raymond, Lucy; Hensiek, Anke; Jena, Rajesh; Macfarlane, Robert; Mannion, Richard; Nicholson, James; Muthusamy, Brinda; Taylor, Amy; Price, Richard; Rands, Gabriella; Gamazo, Nicola; Vanat, Zebunnisa; Scoffings, Daniel; Jefferies, Sarah; Knight, Richard; Lamb, Tamara; Tam, Yu Chuen; Foweraker, Karen; Harris, Fiona; Sanghera, Paul; Meade, Sara; Irving, Richard; Monksfield, Peter; Sharif, Saba; Ragge, Nicola; Murrell, Melanie; Barwell, Julian; English, Martin; Doherty, Gary; Trivedi, Rikin; Patterson, Ilse; Afridi, Shazia K.; Ferner, Rosalie E.; Obholzer, Rupert; Williams, Victoria; Hammond, Chris; Lascelles, Karine; Skilbeck, Chris; Saeed, Shakeel; Shaw, Adam; Swampillai, Angela; Thomson, Suki; Thomas, Nick; Maratos, Eleni; Barazi, Sinan; Mullin, Rebecca; Henley, Susie; Trump, Sally; Everett, Vanessa; Nunn, Terry; Nduka, Charles; Evans, D. Gareth; Anup, Raji; Duff, Chris; Freeman, Simon R.; Stapleton, Emma; Jarvis, Nicola; Kamaly-Asl, Ian; King, Andrew T.; Kellett, Mark; Kilday, John-Paul; Lloyd, Simon K.; Malluci, Connor; Mawman, Deborah; McBain, Catherine; Laitt, Roger; O'Driscoll, Martin; McCabe, Martin; Perry, Mary; Rutherford, Scott A.; Henshaw, Kirsty; Stivaros, Stavros M.; Thomas, Owen; Vassallo, Grace; Hammerbeck-Ward, Charlotte L.; Pathmanaban, Omar N.; Kurian, Jincy; Hobbs, Claire; Browne, Kate; Castle, Bruce; Crabtree, Rosie; Cogswell, Lucy; Dalton, Louise; Dodridge, Caroline; Emmanouil, Beatrice; Giele, Henk; Halliday, Dorothy; Halliday, Jane; Hanemann, C. Oliver; Howard, Wendy; Kerr, Richard; Mace, Elle; MacKeith, Sam; Parry, Allyson; Pretorius, Peter; Ramsden, James; Redman, Carolyn; Sharma, Srilakshmi; Taylor, Ros; Tomkins, Helen; Wilson, Shaun; Woolrich, Rachael
Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers

Imact研究的中期结果: BRCA2突变携带者前列腺特异性抗原筛查的证据

EUROPEAN UROLOGY
IF25.2
2019-12-01163
OAAI
Page, Elizabeth C.; Bancroft, Elizabeth K.; Brook, Mark N.; Assel, Melissa; Al Battat, Mona Hassan; Thomas, Sarah; Taylor, Natalie; Chamberlain, Anthony; Pope, Jennifer; Ni Raghallaigh, Holly; Evans, D. Gareth; Rothwell, Jeanette; Maehle, Lovise; Grindedal, Eli Marie; James, Paul; Mascarenhas, Lyon; McKinley, Joanne; Side, Lucy; Thomas, Tessy; van Asperen, Christi; Vasen, Hans; Kiemeney, Lambertus A.; Ringelberg, Janneke; Jensen, Thomas Dyrso; Osther, Palle J. S.; Helfand, Brian T.; Genova, Elena; Oldenburg, Rogier A.; Cybulski, Cezary; Wokolorczyk, Dominika; Ong, Kai-Ren; Huber, Camilla; Lam, Jimmy; Taylor, Louise; Salinas, Monica; Feliubadalo, Lidia; Oosterwijk, Jan C.; van Zelst-Stams, Wendy; Cook, Jackie; Rosario, Derek J.; Domchek, Susan; Powers, Jacquelyn; Buys, Saundra; O'Toole, Karen; Ausems, Margreet G. E. M.; Schmutzler, Rita K.; Rhiem, Kerstin; Izatt, Louise; Tripathi, Vishakha; Teixeira, Manuel R.; Cardoso, Marta; Foulkes, William D.; Aprikian, Armen; van Randeraad, Heleen; Davidson, Rosemarie; Longmuir, Mark; Ruijs, Marielle W. G.; Helderman van den Enden, Apollonia T. J. M.; Adank, Muriel; Williams, Rachel; Andrews, Lesley; Murphy, Declan G.; Halliday, Dorothy; Walker, Lisa; Liljegren, Annelie; Carlsson, Stefan; Azzabi, Ashraf; Jobson, Irene; Morton, Catherine; Shackleton, Kylie; Snape, Katie; Hanson, Helen; Harris, Marion; Tischkowitz, Marc; Taylor, Amy; Kirk, Judy; Susman, Rachel; Chen-Shtoyerman, Rakefet; Spigelman, Allan; Pachter, Nicholas; Ahmed, Munaza; Ramon y Cajal, Teresa; Zgajnar, Janez; Brewer, Carole; Gadea, Neus; Brady, Angela F.; van Os, Theo; Gallagher, David; Johannsson, Oskar; Donaldson, Alan; Barwell, Julian; Nicolai, Nicola; Friedman, Eitan; Obeid, Elias; Greenhalgh, Lynn; Murthy, Vedang; Copakova, Lucia; Saya, Sibel; McGrath, John; Cooke, Peter; Ronlund, Karina; Richardson, Kate; Henderson, Alex; Teo, Soo H.; Arun, Banu; Kast, Karin; Dias, Alexander; Aaronson, Neil K.; Ardern-Jones, Audrey; Bangma, Chris H.; Castro, Elena; Dearnaley, David; Eccles, Diana M.; Tricker, Karen; Eyfjord, Jorunn; Falconer, Alison; Foster, Christopher; Gronberg, Henrik; Hamdy, Freddie C.; Stefansdottir, Vigdis; Khoo, Vincent; Lindeman, Geoffrey J.; Lubinski, Jan; Axcrona, Karol; Mikropoulos, Christos; Mitra, Anita; Moynihan, Clare; Rennert, Gadi; Suri, Mohnish; Wilson, Penny; Dudderidge, Tim; Offman, Judith; Kote-Jarai, Zsofia; Vickers, Andrew; Lilja, Hans; Eeles, Rosalind A.
Identifying the deficiencies of current diagnostic criteria for neurofibromatosis 2 using databases of 2777 individuals with molecular testing
GENETICS IN MEDICINE
IF6.2
2019-07-0147
OAAI
Evans, D. Gareth; King, Andrew T.; Bowers, Naomi L.; Tobi, Simon; Wallace, Andrew J.; Perry, Mary; Anup, Raji; Lloyd, Simon K. L.; Rutherford, Scott A.; Hammerbeck-Ward, Charlotte; Pathmanaban, Omar N.; Stapleton, Emma; Freeman, Simon R.; Kellett, Mark; Halliday, Dorothy; Parry, Allyson; Gair, Juliette J.; Axon, Patrick; Laitt, Roger; Thomas, Owen; Afridi, Shazia; Ferner, Rosalie E.; Harkness, Elaine F.; Smith, Miriam J.; Tysome, James; Donnelly, Neil; Raymond, Lucy; Hensiek, Anke; Jena, Rajesh; Macfarlane, Robert; Mannion, Richard; Nicholson, James; Muthusamy, Brinda; Taylor, Amy; Price, Richard; Rands, Gabriella; Gamazo, Nicola; Scoffings, Zebunnisa Daniel; Jefferies, Sarah; Knight, Richard; Vanat, Tamara Lamb; Tam, Yu Chuen; Foweraker, Karen; Harris, Fiona; Heney, David; Sanghera, Paul; Irving, Richard; Monksfield, Peter; Sharif, Saba; Ragge, Nicola; Smyth, Carolyn; Barwell, Julian; English, Martin; Obholzer, Rupert; Williams, Victoria; Hammond, Chris; Lascelles, Karine; Skilbeck, Chris; Saeed, Shakeel; Shaw, Adam; Swampillai, Angela; Thomson, Suki; Thomas, Nick; Maratos, Eleni; Barazi, Sinan; Mullin, Rebecca; Henley, Susie; Trump, Sally; Everett, Vanessa; Nunn, Terry; Nduka, Charles; Duff, Chris; Jarvis, Nicola; Kamaly-Asl, Ian; Kilday, John-Paul; Malluci, Connor; Mawman, Deborah; McBain, Catherine; O'Driscoll, Martin; McCabe, Martin; Perry, Mary; Rutherford, Scott; Henshaw, Kirsty; Stivaros, Stavros; Vassallo, Grace; Hammerbeck-Ward, Charlotte; Kurian, Jincy; Blesing, Claire; Browne, Kate; Crabtree, Rosie; Cogswell, Lucy; Dalton, Louise; Dodridge, Caroline; Emmanouil, Beatrice; Giele, Henk; Hanemann, C. Oliver; Howard, Wendy; Jeyaretna, Sanjeeva; Kerr, Richard; Mace, Elle; MacKeith, Sam; May, Anne; Pretorius, Peter; Ramsden, James; Redman, Carolyn; Taylor, Srilakshmi Sharma Ros; Tomkins, Helen; Wilson, Shaun; Woolrich, Rachael
Germline pathogenic variants in PALB2 and other cancer-predisposing genes in families with hereditary diffuse gastric cancer without CDH1 mutation: a whole-exome sequencing study
LANCET GASTROENTEROLOGY & HEPATOLOGY
IF38.6
2018-07-0181
OAAI
Fewings, Eleanor; Larionov, Alexey; Redman, James; Goldgraben, Mae A.; Scarth, James; Richardson, Susan; Brewer, Carole; Davidson, Rosemarie; Ellis, Ian; Evans, D. Gareth; Halliday, Dorothy; Izatt, Louise; Marks, Peter; McConnell, Vivienne; Verbist, Louis; Mayes, Rebecca; Clark, Graeme R.; Hadfield, James; Chin, Suet-Feung; Teixeira, Manuel R.; Giger, Olivier T.; Hardwick, Richard; di Pietro, Massimiliano; O'Donovan, Maria; Pharoah, Paul; Caldas, Carlos; Fitzgerald, Rebecca C.; Tischkowitz, Marc
Schwannomatosis: a genetic and epidemiological study
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
IF7.5
2018-06-1693
OAAI
Evans, D. Gareth; Bowers, Naomi L.; Tobi, Simon; Hartley, Claire; Wallace, Andrew J.; King, Andrew T.; Lloyd, Simon K. W.; Rutherford, Scott A.; Hammerbeck-Ward, Charlotte; Pathmanaban, Omar N.; Freeman, Simon R.; Ealing, John; Kellett, Mark; Laitt, Roger; Thomas, Owen; Halliday, Dorothy; Ferner, Rosalie; Taylor, Amy; Duff, Chris; Harkness, Elaine F.; Smith, Miriam J.
Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis
NEUROLOGY
IF8.5
2015-01-1384
OAAI
Smith, Miriam J.; Isidor, Bertand; Beetz, Christian; Williams, Simon G.; Bhaskar, Sanjeev S.; Richer, Wilfrid; O'Sullivan, James; Anderson, Beverly; Daly, Sarah B.; Urquhart, Jill E.; Fryer, Alan; Rustad, Cecilie F.; Mills, Samantha J.; Samii, Amir; du Plessis, Daniel; Halliday, Dorothy; Barbarot, Sebastien; Bourdeaut, Franck; Newman, William G.; Evans, D. Gareth
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset
JOURNAL OF MEDICAL GENETICS
IF3.7
2011-01-2893
OAAI
Smith, Miriam J.; Higgs, Jenny E.; Bowers, Naomi L.; Halliday, Dorothy; Paterson, Joan; Gillespie, James; Huson, Susan M.; Freeman, Simon R.; Lloyd, Simon; Rutherford, Scott A.; King, Andrew T.; Wallace, Andrew J.; Ramsden, Richard T.; Evans, D. Gareth R.
Cardiovascular manifestations in men and women carrying a FBN1 mutation
EUROPEAN HEART JOURNAL
IF35.6
2010-08-13138
OAAI
Detaint, Delphine; Faivre, Laurence; Collod-Beroud, Gwenaelle; Child, Anne H.; Loeys, Bart L.; Binquet, Christine; Gautier, Elodie; Arbustini, Eloisa; Mayer, Karin; Arslan-Kirchner, Mine; Stheneur, Chantal; Halliday, Dorothy; Beroud, Christophe; Bonithon-Kopp, Claire; Claustres, Mireille; Plauchu, Henri; Robinson, Peter N.; Kiotsekoglou, Anatoli; De Backer, Julie; Ades, Lesley; Francke, Uta; De Paepe, Anne; Boileau, Catherine; Jondeau, Guillaume

研究方向

暂未获取到该数据
D
D. Gareth Evans
H 指数:182论文数:2,473被引数:13.4万
M
Miriam J. Smith
H 指数:50论文数:173被引数:9,290
S
Scott Rutherford
H 指数:43论文数:202被引数:9,914
A
Andrew T. King
H 指数:47论文数:236被引数:6,776
A
Allyson Parry
H 指数:23论文数:57被引数:2,294
O
Omar Pathmanaban
H 指数:29论文数:140被引数:2,753
S
Simon Freeman
H 指数:29论文数:127被引数:2,404
S
Simon Lloyd
H 指数:29论文数:259被引数:2,733
S
Shazia Afridi
H 指数:21论文数:51被引数:2,596
N
Naomi L. Bowers
H 指数:26论文数:81被引数:2,503