S. Hing

发表

Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization

F. Ross, C. Harrison, A. Moorman, 2007, Oncogene.

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

N. Sebire, E. Healy, V. Kinsler, 2013, The Journal of investigative dermatology.

Expression profile of wild‐type ETV6 in childhood acute leukaemia

K. Pritchard-Jones, V. Saha, A. Ford, 2003, British journal of haematology.

GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma

A. Flanagan, R. Tirabosco, J. Skinner, 2009, Modern Pathology.

Class III HLA Genes and Systemic Lupus Erythematosus

D. Isenberg, M. Snaith, G. Hughes, 1986 .

Prognostic classification of relapsing favorable histology Wilms tumor using cDNA microarray expression profiling and support vector machines

Simon Rogers, Colin Campbell, Javed Khan, 2004, Genes, chromosomes & cancer.

Sensitivity of MDM2 amplification and unexpected multiple faint alphoid 12 (alpha 12 satellite sequences) signals in atypical lipomatous tumor

A. Flanagan, R. Tirabosco, H. Ye, 2012, Modern Pathology.

Multiple sclerosis in north-east Scotland. An association with HLA-DQw1.

W. Mcdonald, D. Francis, S. Hing, 1987, Brain : a journal of neurology.

Primary pericardial synovial sarcoma confirmed by molecular genetic studies: a case report.

D. Hargrave, Reem Al-Saadi, S. Hing, 2007, Journal of pediatric hematology/oncology.

Haploidentical BMT with a Post-Infusion of Stem Cells Cyclophosphamide Approach Is Feasible and Leads to a High Rate of Donor Engraftment in Haemoglobinopathies Allowing Universal Application of Transplantation

S. Hing, S. Chakravorty, Richard Szydlo, 2015 .

Serologic and DNA follow-up data from HBsAg-positive patients treated with orthotopic liver transplantation.

R. Freeman, R. Jenkins, J. Zeldis, 1991, Transplantation.

8 – Molecular and Cytogenetic Analysis

L. Foroni, G. Gerrard, A. Reid, 2017 .

Clinical features of molecular pathology of solid tumours in childhood.

R. Nash, K. Pritchard-Jones, B. Messahel, 2005, The Lancet. Oncology.

Familial tumoral calcinosis and hyperostosis–hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3

A. Flanagan, T. Diss, P. O’Donnell, 2009, Skeletal Radiology.

Molecular profiling reveals frequent gain of MYCN and anaplasia‐specific loss of 4q and 14q in wilms tumor

A. Ashworth, James R. Anderson, T. Chagtai, 2011, Genes, chromosomes & cancer.

The Association of Gilbert's Syndrome with Hyperbilirubinaemia Occurring on Any of Imatinib, Dasatinib and Nilotinib in Patients with Chronic Myeloid Leukaemia (CML)

L. Foroni, S. Hing, J. Apperley, 2015 .

Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trial

Marilyn M. Li, Joshua L. Deignan, R. Butler, 2014, Journal of Clinical Pathology.

Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors.

M. Gessler, K. Pritchard-Jones, P. Grundy, 2001, The American journal of pathology.

HLA Haplotypes with C4B5; evidence for further allelic heterogeneity

S. Hing, J. Batchelor, C. Giles, 2004, Immunogenetics.

Chromosome 1q expression profiling and relapse in Wilms' tumour

Yong-jie Lu, R. Williams, K. Pritchard-Jones, 2002, The Lancet.

Genetic heterogeneity for SMARCB1, H3F3A and BRAF in a malignant childhood brain tumour: genetic–pathological correlation

T. Jacques, D. Hargrave, K. Mankad, 2015, Neuropathology and applied neurobiology.

HLA genetic determinants in familial MS. A study from the Grampian region of Scotland.

W. Mcdonald, D. Francis, S. Hing, 2008, Tissue antigens.

Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

K Fenwick, A. Ashworth, O. Dovey, 2006, The Journal of pathology.