Publications by authors named "Dina Halai"

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1
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.

N Engl J Med· November 2021

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The 100 000 Genomes Project: bringing whole genome sequencing to the NHS.
Clare Turnbull, Richard H Scott, Ellen Thomas, Louise Jones, Nirupa Murugaesu, Dina Halai

BMJ· April 2018

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Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.
Joshua N Sampson, William A Wheeler, Meredith Yeager, Orestis Panagiotou, Zhaoming Wang, Dina Halai

J Natl Cancer Inst· December 2015

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A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.
Lisa Mirabello, Roelof Koster, Branden S Moriarity, Logan G Spector, Paul S Meltzer, Dina Halai

Cancer Discov· September 2015

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Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
Sam Behjati, Patrick S Tarpey, Helen Sheldon, Inigo Martincorena, Peter Van Loo, Dina Halai

Nat Genet· April 2014

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Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2.
Paul Guilhamon, Malihe Eskandarpour, Dina Halai, Gareth A Wilson, Andrew Feber

Nat Commun· January 2014

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Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.
Sam Behjati, Patrick S Tarpey, Nadège Presneau, Susanne Scheipl, Nischalan Pillay, Dina Halai

Nat Genet· December 2013

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Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.
Patrick S Tarpey, Sam Behjati, Susanna L Cooke, Peter Van Loo, David C Wedge, Dina Halai

Nat Genet· August 2013

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Assessment of MUC4 expression in primary bone tumours.
Roberto Tirabosco, Fitim Berisha, Hongtao Ye, Dina Halai, M Fernanda Amary

Histopathology· July 2013

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Genome-wide association study identifies two susceptibility loci for osteosarcoma.
Sharon A Savage, Lisa Mirabello, Zhaoming Wang, Julie M Gastier-Foster, Richard Gorlick, Dina Halai

Nat Genet· July 2013

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An integrated functional genomics approach identifies the regulatory network directed by brachyury (T) in chordoma.
Andrew C Nelson, Nischalan Pillay, Stephen Henderson, Nadège Presneau, Roberto Tirabosco, Dina Halai

J Pathol· November 2012

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A common single-nucleotide variant in T is strongly associated with chordoma.
Nischalan Pillay, Vincent Plagnol, Patrick S Tarpey, Samira B Lobo, Nadège Presneau, Dina Halai

Nat Genet· November 2012

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Sensitivity of MDM2 amplification and unexpected multiple faint alphoid 12 (alpha 12 satellite sequences) signals in atypical lipomatous tumor.
Takeshi Kashima, Dina Halai, Hongtao Ye, Sandra Nalini Hing, David Delaney

Mod Pathol· October 2012

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Frequency of Mouse Double Minute 2 (MDM2) and Mouse Double Minute 4 (MDM4) amplification in parosteal and conventional osteosarcoma subtypes.
Laure A E Duhamel, Hongtao Ye, Dina Halai, Bernadine D Idowu, Nadège Presneau

Histopathology· January 2012

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Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2.
M Fernanda Amary, Stephen Damato, Dina Halai, Malihe Eskandarpour, Fitim Berisha

Nat Genet· November 2011

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IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours.
M Fernanda Amary, Krisztian Bacsi, Francesca Maggiani, Stephen Damato, Dina Halai

J Pathol· July 2011

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Role of the transcription factor T (brachyury) in the pathogenesis of sporadic chordoma: a genetic and functional-based study.
Nadège Presneau, Asem Shalaby, Hongtao Ye, Nischalan Pillay, Dina Halai

J Pathol· February 2011

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The role of epidermal growth factor receptor in chordoma pathogenesis: a potential therapeutic target.
Asem Shalaby, Nadège Presneau, Hongtao Ye, Dina Halai, Fitim Berisha

J Pathol· February 2011

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Primary myxoid liposarcoma of the ovary in an adolescent girl: a case report.
Roberto Tirabosco, Rupali Arora, Hongtao Ye, Carol Brunell, Dina Halai

Int J Gynecol Pathol· May 2010

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