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T

Terri McVeigh

the royal marsden nhs foundation trust

21H指数
155论文数
1.7K被引数
收录论文 45
发表时间
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Reply to Correspondence: Leveraging paired germline and somatic analysis to improve the classification of DDX41 variants回复：利用配对种系和体细胞分析改善DDX41变异的分类
errBritish Journal of Haematology
IF3.8
err2026-09-17
err0
PREAI
errTerri Patricia McVeigh; Jamshid S. Khorashad
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Somatic and germline genetic testing pathways in haematological malignancies: Best practice consensus guidelines from the 2025 national meeting organised by UK Cancer Genetics Group (UKCGG), CanGene-CanVar and the NHS England Haematological Oncology Working Group体细胞和生殖系遗传检测路径在血液系统恶性肿瘤中的应用：来自2025年由国家癌症遗传学小组（UKCGG）、CanGene-CanVar和英国国家医疗服务体系（NHS England）血液肿瘤工作组组织的全国会议的最佳实践共识指南
errBritish Journal of Haematology
IF3.8
err2026-03-03
err0
errOAAI
errB. Speight; A. Hamblin; P. Talley; O. Tsoulaki; R. Robinson; P. Dean; J. Khorashad; A. Kulasekararaj; A. L. Godfrey; A. J. Mead; T. P. McVeigh; K. Snape; Consensus Meeting Attendees
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Real-World Molecular Testing in European Early-Onset Colorectal Cancer欧洲早发性结直肠癌的真实世界分子检测
errUnited European Gastroenterology Journal
IF6.7
err2025-09-27
err0
errOAAI
errPenelope V. Edwards; Kussai Giuma Ali Eloussta; Andrew Latchford; Omar Faiz; Huw Thomas; Filomena Liccardo; Nikhil Pawa; Robert Hüneburg; Jacob Nattermann; Andrew George; Francesc Balaguer; Marc Martí; Antonino Spinelli; Caterina Foppa; Noel F. F. C. de Miranda; Irene López; Elena Hurtado; Fernando Jiménez; Marta Jiménez-Toscano; Edurne Álvaro; Gonzalo Sanz; Araceli Ballestero; José A. Rueda; Cristina Viyuela; Lorena Brandáriz; Rosario Vidal-Tocino; Damián García-Olmo; Carlos Pastor; Rogelio González-Sarmiento; Andreana N. Holowatyj; Terri McVeigh; José Perea; Kevin J. Monahan; Collaborators GEOCODE and SECOC Consortia
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UK recommendations for chimerism testing and monitoring following allogeneic haematopoietic stem cell transplantation (HSCT): Best practice consensus guidelines from the British Society for Blood and Marrow Transplant and Cellular Therapies (BSBMTCT), NHS England Genomic Laboratory Hub (GLH) Haematological Malignancies Working Group, UK Cancer Genetics Group (UKCGG) and the UK National External Quality Assessment Service for Leucocyte Immunophenotyping (UK NEQAS LI)英国关于异基因造血干细胞移植（HSCT）后嵌合体检测与监测的建议：英国血液与骨髓移植及细胞治疗学会（BSBMTCT）、英国国家医疗服务体系（NHS England）基因组实验室枢纽（GLH）血液恶性肿瘤工作组、英国癌症遗传学组（UKCGG）以及英国白细胞免疫表型外部质量评估服务（UK NEQAS LI）的最佳实践共识指南。
errBritish Journal of Haematology
IF3.8
err2025-09-09
err0
errOAAI
errAndrew Clark; Hazel Clouston; Kanchan Rao; Najeem Folarin; Josu De la Fuente; Angela Hamblin; Eduardo Olavarria; Debbie Richardson; Polly Talley; Victoria Potter; Justin Loke; Terri McVeigh; John Snowden
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Availability of benign missense variant “truthsets” for validation of functional assays: Current status and a systematic approach良性错义变异“真实集合”在功能测定验证中的可用性：现状与系统方法
errThe American Journal of Human Genetics
IF0
err2025-09-08
err0
PREAI
errCharlie F. Rowlands; Sophie Allen; Alice Garrett; Miranda Durkie; George J. Burghel; Rachel Robinson; Alison Callaway; Joanne Field; Bethan Frugtniet; Sheila Palmer-Smith; Jonathan Grant; Judith Pagan; Trudi McDevitt; Katie Snape; Helen Hanson; Terri McVeigh; Clare Turnbull
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Quantifying evidence for phenotypic specificity (PP4) for syndromic phenotypes: Large-scale integration of rare germline FH variants from diagnostic laboratory testing for HLRCC (Hereditary Leiomyomatosis and Renal Cell Cancer) and renal cancer量化综合征表型（PP4）特异性证据：大规模整合来自HLRCC（遗传性平滑肌瘤病和肾细胞癌）及肾癌诊断实验室检测的罕见生殖系FH变异
errGenetics in Medicine
IF6.2
err2025-09-04
err0
errOAAI
errSophie Allen; Charlie F. Rowlands; Samantha Butler; Miranda Durkie; Carrie Horton; Tina Pesaran; Marcy Richardson; Rachel Robinson; Alice Garrett; George J. Burghel; Alison Callaway; Joanne Field; Bethan Frugtniet; Sheila Palmer-Smith; Jonathan Grant; Judith Pagan; Trudi McDevitt; Katie Snape; Avgi Andreou; Eamonn R. Maher; Helen Hanson; Terri McVeigh; Clare Turnbull
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Li Fraumeni syndrome in the UK: clinical characteristics and outcomes of TP53 carriersLi Fraumeni综合征在英国：TP53携带者的临床特征和结局
errESMO Open
IF8.3
err2025-08-20
err0
PREAI
errE. Finn; S. Sardo Infirri; C.S. Clarke; C. Bunce; J.Y. Weng; R.W. Lee; Z. Kemp; T.P. McVeigh; R. Eeles; A. George
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UK clinical practice guidelines for the management of patients with constitutional POT1 pathogenic variants英国临床实践指南：针对携带体细胞POT1致病性变异患者的管理
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2025-05-11
err0
PREAI
errTsoulaki, Olga; Evans, D. Gareth; Sinha, Khushboo; Rajan, Neil; Bakr, Farah; Hatcher, Helen; Napolitano, Andrea; Finn, Elena; Iyengar, Sunil; Sohaib, Aslam; Sadler, Timothy J.; Forde, Claire; Woodward, Emma Roisin; McVeigh, Terri P.; Tischkowitz, Marc; Lalloo, Fiona; Hanson, Helen
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Surveillance for individuals with a strong family history of kidney cancer but no identified heritable disease: a UK consensus
errBJU INTERNATIONAL
IF4.4
err2025-03-01
err0
errOAAI
errWhitworth, James; Hanson, Helen; Youngs, Alice; Mcveigh, Terri; UK Canc Genetics Grp renalsurveillance meeting
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Breast cancer outcomes in women with ovarian cancer and a pathogenic germline BRCA mutation
errEJSO
IF2.9
err2025-03-01
err0
PREAI
errAin, Quratul; O'Connell, Rachel L.; Swarnkar, Parinita; Mcveigh, Terri; George, Angela; Tasoulis, Marios K.; Gui, Gerald P. H.; Wiggins, Jennifer; Khan, Aadil A.; Krupa, Katherine D. C.; Barry, Peter A.; Banerjee, Susana; Rusby, Jennifer E.
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Impact of NICE Guideline NG241 'Ovarian Cancer: identifying and managing familial and genetic risk' on a regional NHS family history and clinical genetics serviceNICE指南NG241 “卵巢癌: 识别和管理家族性和遗传风险” 对区域NHS家族史和临床遗传学服务的影响
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2025-02-19
err0
errOAAI
errRoe, Alexander; Forman, Andrea; Lalloo, Fiona; Mcveigh, Terri P.; Hanson, Helen; Snape, Katie
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Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10 G>T at the intron 9/exon 10 of the MAPT gene
errNEUROBIOLOGY OF AGING
IF3.5
err2025-02-01
err0
PREAI
errOlszewska, Diana A.; Fearon, Conor; Mcguigan, Christopher; Mcveigh, Terri P.; Houlden, Henry; Polke, James M.; Lawlor, Brian; Coen, Robert; Hutchinson, Michael; Hutton, Michael; Beausang, Alan; Delon, Isabelle; Brett, Francesca; Sevastou, Ioanna; Seto-Salvia, Nuria; de Silva, Rohan; Lynch, Tim
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Using cancer phenotype sex-specificity to enable unbiased penetrance estimation of SMARCA4 pathogenic variants for small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)使用癌症表型性别特异性来实现对卵巢小细胞癌，高钙血症型 (SCCOHT) 的SMARCA4致病变体的无偏外显率估计
errGENETICS IN MEDICINE
IF6.2
err2025-01-01
err0
PREAI
errWade, Isaac; Witkowski, Leora; Ahmed, Afrida; Rowlands, Charlie F.; Banerjee, Susana; Pressey, Joseph G.; Mcveigh, Terri P.; Tischkowitz, Marc D.; Foulkes, William D.; Turnbull, Clare
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The PS4-likelihood ratio calculator: flexible allocation of evidence weighting for case-control data in variant classification
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2024-09-03
err0
errOAAI
errRowlands, Charlie F.; Garrett, Alice; Allen, Sophie; Durkie, Miranda; Burghel, George J.; Robinson, Rachel; Callaway, Alison; Field, Joanne; Frugtniet, Bethan; Palmer-Smith, Sheila; Grant, Jonathan; Pagan, Judith; McDevitt, Trudi; McVeigh, Terri P.; Hanson, Helen; Whiffin, Nicola; Jones, Michael; Turnbull, Clare
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Carrier testing for partners of MUTYH variant carriers: UK Cancer Genetics Group recommendations
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2024-05-30
err0
errOAAI
errMcVeigh, Terri Patricia; Lalloo, Fiona; Monahan, Kevin J.; Latchford, Andrew; Durkie, Miranda; Mein, Rachael; Baple, Emma L.; Hanson, Helen
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Challenges in developing and implementing international best practice guidance for intermediate-risk variants in cancer susceptibility genes: APC c.3920T>A p.(Ile1307Lys) as an exemplar制定和实施癌症易感基因中等风险变异的国际最佳实践指南的挑战: APC c.3920T>A p.(Ile1307Lys) 作为范例
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2024-05-02
err2
errOAAI
errMcveigh, Terri Patricia; Lalloo, Fiona; Frayling, Ian M.; Latchford, Andrew; Snape, Katie; Durkie, Miranda; Monahan, Kevin J.; Hanson, Helen
err分享
err收藏
Extent of investigation and management of cases of 'unexplained' mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2024-03-26
err1
errOAAI
errMcVeigh, Terri Patricia; Monahan, Kevin J.; Christopher, Joseph; West, Nick; Scott, Malcolm; Murray, Jennie; Hanson, Helen
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Recommendations for laboratory workflow that better support centralised amalgamation of genomic variant data: findings from CanVIG-UK national molecular laboratory survey
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2023-12-22
err1
errOAAI
errAllen, Sophie; Loong, Lucy; Garrett, Alice; Torr, Bethany; Durkie, Miranda; Drummond, James; Callaway, Alison; Robinson, Rachel; Burghel, George J.; Hanson, Helen; Field, Joanne; McDevitt, Trudi; McVeigh, Terri P.; Bedenham, Tina; Bowles, Christopher; Bradshaw, Kirsty; Brooks, Claire; Butler, Samantha; Del Rey Jimenez, Juan Carlos; Hawkes, Lorraine; Stinton, Victoria; MacMahon, Suzanne; Owens, Martina; Palmer-Smith, Sheila; Smith, Kenneth; Tellez, James; Valganon-Petrizan, Mikel; Waskiewicz, Erik; Yau, Michael; Eccles, Diana M.; Tischkowitz, Marc; Goel, Shilpi; McRonald, Fiona; Antoniou, Antonis C.; Morris, Eva; Hardy, Steven; Turnbull, Clare
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Germline ATM Mutations Detected by Somatic DNA Sequencing in Lethal Prostate Cancer
errEUROPEAN UROLOGY
IF25.2
err2023-06-01
err4
errOAAI
errGrochot, Rafael; Carreira, Suzanne; Miranda, Susana; Figueiredo, Ines; Bertan, Claudia; Rekowski, Jan; Yuan, Wei; Ferreira, Ana; Riisnaes, Ruth; Neeb, Antje; Gurel, Bora; Fenor de la Maza, Maria de Los Dolores; Guo, Christina; Carmichael, Juliet; Westaby, Daniel; Mateo, Joaquin; Sharp, Adam; McVeigh, Terri P.; De Bono, Johann
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Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996-2020: development of a national resource of patient-level genomics laboratory records来自英国NHS区域分子基因组学实验室的种系错配修复 (MMR) 基因分析1996-2020: 患者水平基因组学实验室记录的国家资源的开发
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2022-12-26
err7
errOAAI
errLoong, Lucy; Huntley, Catherine; McRonald, Fiona; Santaniello, Francesco; Pethick, Joanna; Torr, Bethany; Allen, Sophie; Tulloch, Oliver; Goel, Shilpi; Shand, Brian; Rahman, Tameera; Luchtenborg, Margreet; Garrett, Alice; Barber, Richard; Bedenham, Tin; Bourn, David; Bradshaw, Kirsty; Brooks, Claire; Bruty, Jonathan; Burghel, George J.; Butler, Samantha; Buxton, Chris; Callaway, Alison; Callaway, Jonathan; Drummond, James; Durkie, Miranda; Field, Joanne; Jenkins, Lucy; McVeigh, Terri P.; Mountford, Roger; Nyanhete, Rodney; Petrides, Evgenia; Robinson, Rachel; Scott, Tracy; Stinton, Victoria; Tellez, James; Wallace, Andrew J.; Yarram-Smith, Laura; Sahan, Kate; Hallowell, Nina; Eccles, Diana M.; Pharoah, Paul; Tischkowitz, Marc; Antoniou, Antonis C.; Evans, D. Gareth; Lalloo, Fiona; Norbury, Gail; Morris, Eva; Burn, John; Hardy, Steven; Turnbull, Clare
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研究方向

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