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Author Details

Dina Halai
Royal National Orthopaedic Hospital National Health Service Trust
2010
20
18
PMIDPaper TitleJournal TitlePublished Year
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
29691228The 100â¿¿000 Genomes Project: bringing whole genome sequencing to the NHS.BMJ2018
29691228The 100â¿¿000 Genomes Project: bringing whole genome sequencing to the NHS.BMJ2018
26084801A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.Cancer Discov2015
26084801A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.Cancer Discov2015
26464424Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.J Natl Cancer Inst2015
26464424Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.J Natl Cancer Inst2015
24633157Recurrent PTPRB and PLCG1 mutations in angiosarcoma.Nat Genet2014
24633157Recurrent PTPRB and PLCG1 mutations in angiosarcoma.Nat Genet2014
23175151MicroRNA profiling of peripheral nerve sheath tumours identifies miR-29c as a tumour suppressor gene involved in tumour progression.Br J Cancer2013
23863747Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2.Nat Commun2013
23770606Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.Nat Genet2013
24162739Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.Nat Genet2013
23668430Assessment of MUC4 expression in primary bone tumours.Histopathology2013
23175151MicroRNA profiling of peripheral nerve sheath tumours identifies miR-29c as a tumour suppressor gene involved in tumour progression.Br J Cancer2013
23727862Genome-wide association study identifies two susceptibility loci for osteosarcoma.Nat Genet2013
24162739Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.Nat Genet2013
23863747Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2.Nat Commun2013
23668430Assessment of MUC4 expression in primary bone tumours.Histopathology2013
23770606Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.Nat Genet2013
23727862Genome-wide association study identifies two susceptibility loci for osteosarcoma.Nat Genet2013
22074548Frequency of Mouse Double Minute 2 (MDM2) and Mouse Double Minute 4 (MDM4) amplification in parosteal and conventional osteosarcoma subtypes.Histopathology2012
22847733An integrated functional genomics approach identifies the regulatory network directed by brachyury (T) in chordoma.J Pathol2012
22699518Sensitivity of MDM2 amplification and unexpected multiple faint alphoid 12 (alpha 12 satellite sequences) signals in atypical lipomatous tumor.Mod Pathol2012
23064415A common single-nucleotide variant in T is strongly associated with chordoma.Nat Genet2012
22074548Frequency of Mouse Double Minute 2 (MDM2) and Mouse Double Minute 4 (MDM4) amplification in parosteal and conventional osteosarcoma subtypes.Histopathology2012
23064415A common single-nucleotide variant in T is strongly associated with chordoma.Nat Genet2012
22699518Sensitivity of MDM2 amplification and unexpected multiple faint alphoid 12 (alpha 12 satellite sequences) signals in atypical lipomatous tumor.Mod Pathol2012
22847733An integrated functional genomics approach identifies the regulatory network directed by brachyury (T) in chordoma.J Pathol2012
21171078Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.J Pathol2011
21171079The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target.J Pathol2011
21171078Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.J Pathol2011
21598255IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours.J Pathol2011
22057236Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.Nat Genet2011
22057236Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.Nat Genet2011
21598255IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours.J Pathol2011
21171079The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target.J Pathol2011
20407326Primary myxoid liposarcoma of the ovary in an adolescent girl: a case report.Int J Gynecol Pathol2010
20407326Primary myxoid liposarcoma of the ovary in an adolescent girl: a case report.Int J Gynecol Pathol2010
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Collaborators

Roberto Tirabosco
University College London, UCL Cancer Institute
Co-authored papers 18
Adrienne M Flanagan
University College London, UCL Cancer Institute
Co-authored papers 18
Fernanda Amary
Royal National Orthopaedic Hospital
Co-authored papers 12
Phillip A Futreal
The University of Texas MD Anderson Cancer Center
Co-authored papers 5
Peter J Campbell
Wellcome Sanger Institute
Co-authored papers 4
Patrick S Tarpey
Wellcome Trust Sanger Institute
Co-authored papers 4
Luis Sierrases??maga
Clinica Universidad de Navarra
Co-authored papers 3
Fernando Lecanda
University of Navarra, Center for Applied Medical Research
Co-authored papers 3
Michael R Stratton
Wellcome Sanger Institute
Co-authored papers 3
Jay S Wunder
University of Toronto
Co-authored papers 3
Irene L Andrulis
University of Toronto
Co-authored papers 3
David M Thomas
Garvan Institute of Medical Research
Co-authored papers 3
David C Wedge
Manchester Cancer Research Centre, University of Manchester
Co-authored papers 3
Meredith Yeager
Frederick National Laboratory for Cancer Research
Co-authored papers 3
Donald A Barkauskas
Keck School of Medicine of the University of Southern California
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Jon Teague
Wellcome Sanger Institute
Co-authored papers 3
Robert N Hoover
National Cancer Institute
Co-authored papers 3
Neil E Caporaso
National Cancer Institute, National Institutes of Health
Co-authored papers 3
Neyssa Marina
Stanford University School of Medicine
Co-authored papers 3
Zhaoming Wang
St Jude Children's Research Hospital
Co-authored papers 3
Joseph F Fraumeni
National Cancer Institute
Co-authored papers 3
Adam Butler
Wellcome Sanger Institute
Co-authored papers 3
Susanna L Cooke
Institute of Cancer Sciences, University of Glasgow
Co-authored papers 3
Julie M Gastier-Foster
Baylor College of Medicine
Co-authored papers 3
Peter Van Loo
The Francis Crick Institute
Co-authored papers 3
Margaret A Tucker
National Cancer Institute
Co-authored papers 3
Stephen J Chanock
National Cancer Institute, National Institutes of Health
Co-authored papers 3
Lisa Mirabello
National Cancer Institute
Co-authored papers 3
Massimo Serra
IRCCS Istituto Ortopedico Rizzoli
Co-authored papers 3
Claudia Maria Hattinger
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Release 1.2