Jill Finlayson

Dr

  • The University of Western Australia (M504), 35 Stirling Highway,

    6009 Perth

    Australia

  • 108 Citations
  • 5 h-Index
20102016
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Research Output 2010 2016

  • 108 Citations
  • 5 h-Index
  • 19 Article
  • 3 Review article
  • 1 Letter
Article
5 Citations (Scopus)

Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: Laboratory diagnosis and clinical importance

Chow, A., Ghassemifar, R. & Finlayson, J., 2013, In : Pathology. 45, 6, p. 591-594

Research output: Contribution to journalArticle

4 Citations (Scopus)

A molecular tool to assess the pathological relevance of alpha-globin DNA variants

Qadah, T., Finlayson, J., Newbound, C., Pell, N., Jennens, M., Holmes, P., Grey, D., Beilby, J. & Ghassemifar, R., 2012, In : Pathology. 44, 4, p. 337-341

Research output: Contribution to journalArticle

4 Citations (Scopus)

BRAF mutation detection in hairy cell leukaemia from archival haematolymphoid specimens

Thomas, C., Amanuel, B., Finlayson, J., Grieu-Iacopetta, F., Spagnolo, D. & Erber, W., 2015, In : Pathology. 47, 4, p. 349-354

Research output: Contribution to journalArticle

3 Citations (Scopus)

Differential expression of the Bcl-2 and Bax isoforms in CD19 positive B-lymphocytes isolated from patients diagnosed with chronic lymphocytic leukaemia

Ghassemifar, R., Forster, L., Finlayson, J., Calogero, T., Augustson, B., Joske, D. & Cull, G., 2012, In : Pathology. 44, 7, p. 632-7

Research output: Contribution to journalArticle

6 Citations (Scopus)

Differential gene expression analysis in early and late erythroid progenitor cells in β-thalassaemia

Forster, L., Mccooke, J., Bellgard, M., Joske, D., Finlayson, J. & Ghassemifar, R., 2015, In : British Journal of Haematology. 170, 2, p. 257-267

Research output: Contribution to journalArticle

Erythroid Precursor Cells
Thalassemia
Gene Expression
Globins
Genes
1 Citation (Scopus)
Amino Acid Substitution
Transcription
Substitution reactions
Amino Acids
Computer Simulation
2 Citations (Scopus)

Hb East Timor [β(EF4)Asn ― His,AAC>CAC (HBB c.241A>C)], A Variant Hemoglobin associated with Normal Hematology

Finlayson, J., Ghassemifar, R., Holmes, P., Grey, D., Figliomeni, L., Newbound, C., Pell, N., Kersten, M., Jennens, M., Macaulay, C., Greenwood, L. & Beilby, J., 2010, In : Hemoglobin. 34, 6, p. 561-564

Research output: Contribution to journalArticle

2 Citations (Scopus)

Identification and characterization of two novel and differentially expressed isoforms of human α2-and α1-globin genes

Ghassemifar, R., Forster, L., Qadah, T. & Finlayson, J., 2012, In : Hemoglobin. 36, 5, p. 421-32

Research output: Contribution to journalArticle

4 Citations (Scopus)

Incidence of c-Cbl mutations in human acute myeloid leukaemias in an Australian patient cohort

Ghassemifar, R., Thien, C., Finlayson, J., Joske, D., Cull, G. M., Augustson, B. & Langdon, W., 2011, In : Pathology. 43, 3, p. 261-265

Research output: Contribution to journalArticle

8 Citations (Scopus)

In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A)(α2)]

Qadah, T. H. W., Finlayson, J. & Ghassemifar, R., 2012, In : Hemoglobin. 36, 1, p. 38-46

Research output: Contribution to journalArticle

1 Citation (Scopus)
RNA Splice Sites
Nonsense Codon
Point Mutation
Exons
Genes
1 Citation (Scopus)
Globins
Point Mutation
Mutation
Genes
Transfection
3 Citations (Scopus)

Molecular and cellular characterization of a new α-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon

Qadah, T., Finlayson, J., Newbound, C., Pell, N., Pascoe, M., Greenwood, L., Holmes, P., Grey, D., Beilby, A. & Ghassemifar, R., 2012, In : Hemoglobin. 36, 3, p. 244-52

Research output: Contribution to journalArticle

1 Citation (Scopus)

Molecular characterization of Hb hamilton hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain

Qadah, T., Finlayson, J., North, E. & Ghassemifar, R., 2015, In : Hemoglobin. 39, 2, p. 88-94

Research output: Contribution to journalArticle

Globins
Nonsense Codon
Thalassemia
Mutation
Exons
3 Citations (Scopus)

RNF187 is Downregulated Following NF-?B Inhibition in Late Erythroblasts

Forster, L., Finlayson, J. & Ghassemifar, R., 2016, In : Biochemical Genetics. 54, 5, p. 714-721

Research output: Contribution to journalArticle

erythroblasts
Erythroblasts
Down-Regulation
Genes
Gene expression
26 Citations (Scopus)

Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification

Phylipsen, M., Prior, J. F., Lim, E., Lingam, N., Vogelaar, I. P., Giordano, P. C., Finlayson, J. & Harteveld, C. L., 2010, In : Blood Cells, Molecules, and Diseases. 44, p. 146-151

Research output: Contribution to journalArticle

2 Citations (Scopus)

The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT

Forster, L., Ardakani, R. M., Qadah, T., Finlayson, J. & Ghassemifar, R., 2015, In : Hemoglobin. 39, 5, p. 334-339

Research output: Contribution to journalArticle

Thalassemia
Globins
Genes
Mutation
Nucleotides
12 Citations (Scopus)

Two New α1 Globin Gene Point Mutations: Hb Nedlands (HBA1:c.86C>T) [α28(B9)Ala―Val] and Hb Queens Park (HBA1:c.98T>A) [α32(B13)Met―Lys]

Phylipsen, M., Prior, J. F., Lim, E., Lingam, N., Finlayson, J., Arkesteijn, S. G. J., Harteveld, C. L. & Giordano, P. C., 2010, In : Hemoglobin. 34, 2, p. 123-126

Research output: Contribution to journalArticle

α-Thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA

Finlayson, J., Ghassemifar, R., Holmes, P., Grey, D., Newbound, C., Pell, N., Jennens, M., Greenwood, L. & Beilby, J., 2012, In : Hemoglobin. 36, 5, p. 511-515

Research output: Contribution to journalArticle

Letter
3 Citations (Scopus)

Cell cycle, proliferation and apoptosis in erythroblasts cultured from patients with β-thalassaemia major

Forster, L., Cornwall, S., Finlayson, J. & Ghassemifar, R., 1 Nov 2016, In : British Journal of Haematology. 175, 3, p. 539-542 4 p.

Research output: Contribution to journalLetter

Review article
2 Citations (Scopus)

Hb Lynwood [α107(G14) (–T) (α2) HBA2:c.323delT)] in Conjunction with the α3.7 Deletion Produces a Moderately Severe α-Thalassemia Phenotype

Finlayson, J., Ghassemifar, R., Holmes, P., Grey, D., Newbound, C., Pell, N., Jennens, M., Macaulay, C., Greenwood, L. & Beilby, J., 2011, In : Hemoglobin. 35, 2, p. 142-146

Research output: Contribution to journalReview article

4 Citations (Scopus)

Hematologic Features of Hepatosplenic T-Cell Lymphoma

Erber, W. & Finlayson, J., 1 Feb 2012, In : American Journal of Clinical Pathology. 137, p. 334-335

Research output: Contribution to journalReview article

Open Access
11 Citations (Scopus)

Transfusion-related acute lung injury in a neutropenic patient

Finlayson, J., Grey, D., Kavanagh, L. & Witt, C., 2011, In : Internal Medicine Journal. 41, 8, p. 638-641

Research output: Contribution to journalReview article