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• A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies

  Turro, E., Greene, D., Wijgaerts, A., Thys, C., Lentaigne, C., Bariana, T. K., Westbury, S. K., Kelly, A. M., Selleslag, D., Stephens, J. C., Papadia, S., Simeoni, I., Penkett, C. J., Ashford, S., Attwood, A., Austin, S., Bakchoul, T., Collins, P., Deevi, S. V. V., Favier, R. & 23 others, Kostadima, M., Lambert, M. P., Mathias, M., Millar, C. M., Peerlinck, K., Perry, D. J., Schulman, S., Whitehorn, D., Wittevrongel, C., De Maeyer, M., Rendon, A., Gomez, K., Erber, W. N., Mumford, A. D., Nurden, P., Stirrups, K., Bradley, J. R., Raymond, F. L., Laffan, M. A., Van Geet, C., Richardson, S., Freson, K. & Ouwehand, H., 2016, In : Science Translational Medicine. 8, 328, p. 1-15 15 p., 328ra30.

  Research output: Contribution to journal › Article

  • Gain of Function Mutation
  • Primary Myelofibrosis
  • Thrombocytopenia
  • Protein-Tyrosine Kinases
  • Hemorrhage
  51 Citations (Scopus)

• A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss

  Stritt, S., Nurden, P., Turro, E., Greene, D., Jansen, S. B., Westbury, S. K., Petersen, R., Astle, W. J., Marlin, S., Bariana, T. K., Kostadima, M., Lentaigne, C., Maiwald, S., Papadia, S., Kelly, A. M., Stephens, J. C., Penkett, C. J., Ashford, S., Tuna, S., Austin, S. & 26 others, Bakchoul, T., Collins, P., Favier, R., Lambert, M. P., Mathias, M., Millar, C. M., Mapeta, R., Perry, D. J., Schulman, S., Simeoni, I., Thys, C., Gomez, K., Erber, W. N., Stirrups, K., Rendon, A., Bradley, J. R., van Geet, C., Raymond, F. L., Laffan, M. A., Nurden, A. T., Nieswandt, B., Richardson, S., Freson, K., Ouwehand, W. H., Mumford, A. D. & BRIDGE-BPD Consortium, 9 Jun 2016, In : Blood. 127, 23, p. 2903-2914 12 p.

  Research output: Contribution to journal › Article
  72 Citations (Scopus)

• A mutation in PTPN11 may drive leukemic transformation in a case of essential thrombocythemia

  Guo, B., Liang, J., Allcock, R., Mirzai, B., Augustson, B., Howman, R., Fuller, K. & Erber, W., 7 Jun 2017, In : LEUKEMIA & LYMPHOMA. 59, 1, p. 245-248

  Research output: Contribution to journal › Letter

• An active, collaborative approach to learning skills in flow cytometry

  Fuller, K., Linden, M., Lee-Pullen, T., Fragall, C., Erber, W. & Roehrig, K., 1 Jun 2016, In : Advances in Physiology Education. 40, 2, p. 176-185 10 p.

  Research output: Contribution to journal › Article

  • Flow Cytometry
  • Learning
  • Students
  • Teaching
  • Data Analysis
  8 Citations (Scopus)

• A novel translocation t(10;17)(p13;q11.2) harboring two cryptic deletions identified by array-CGH and characterized by SUZ12 overexpression in a patient with chronic thrombocytosis

  Batanian, J. R., Malherbe, J. A. J. & Erber, W. N., 1 Nov 2020, In : Genes Chromosomes and Cancer. 59, 11, p. 661-666 6 p.

  Research output: Contribution to journal › Review article

  • Thrombocytosis
  • Essential Thrombocythemia
  • Myeloproliferative Disorders
  • Genes
  • Hyperplasia

• Applications of imaging flow cytometry in the diagnostic assessment of acute leukaemia

  Grimwade, L. F., Fuller, K. A. & Erber, W. N., 1 Jan 2017, In : Methods. 112, p. 39-45 7 p.

  Research output: Contribution to journal › Article

  • Flow cytometry
  • Leukemia
  • Flow Cytometry
  • Imaging techniques
  • Fluorescence
  21 Citations (Scopus)

• A retrospective audit of bacterial culture results of donated human milk in Perth, Western Australia

  Almutawif, Y., Hartmann, B., Lloyd, M., Erber, W. & Geddes, D., 1 Feb 2017, In : Early Human Development. 105, p. 1-6 6 p.

  Research output: Contribution to journal › Article

  • Western Australia
  • Milk Banks
  • Human Milk
  • Bacteria
  • Staphylococcus aureus
  14 Citations (Scopus)

• Automated enumeration of lymphoid and plasma cells in bone marrow to establish normal reference ranges

  Liang, J., Malherbe, J. A. J., Fuller, K. A., Mirzai, B., George, C., Carter, T. L., Cole, C. H., Guo, B. B., Meehan, K. & Erber, W. N., 1 Oct 2018, In : Journal of Clinical Pathology. 71, 10, p. 916-925 10 p.

  Research output: Contribution to journal › Article

  • Plasma Cells
  • Reference Values
  • Bone Marrow
  • Lymphocytes
  • Biopsy
  2 Citations (Scopus)

• Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

  Arno, G., Carss, K. J., Hull, S., Zihni, C., Robson, A. G., Fiorentino, A., Hardcastle, A. J., Holder, G. E., Cheetham, M. E., Plagnol, V., Moore, A. T., Raymond, F. L., Matter, K., Balda, M. S., Webster, A. R., UK Inherited Retinal Dis, NIHR Bioresource - Rare Dis & Erber, W., 2 Feb 2017, In : American Journal of Human Genetics. 100, 2, p. 334-342 9 p.

  Research output: Contribution to journal › Article

  Open Access
  11 Citations (Scopus)

• Blood and Bone Marrow Pathology

  Porwit, A., Mccullough, J. & Erber, W., 2011, Second ed. United Kingdon: Elsevier.

  Research output: Book/Report › Edited book/Anthology

  22 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 journal › Article
  6 Citations (Scopus)

• Circumscribed sebaceous neoplasms: a morphological, immunohistochemical and molecular analysis

  Harvey, N., Tabone, T., Erber, W. & Wood, B., 2016, In : Pathology. 48, 5, p. 454-462

  Research output: Contribution to journal › Article

  • Carcinoma
  • Adenoma
  • Mutation
  • Neoplasms
  • p53 Genes
  12 Citations (Scopus)

• Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

  NIHR-BioResource Rare Diseases Consortium, 5 Jul 2018, In : American Journal of Human Genetics. 103, 1, p. 3-18 16 p.

  Research output: Contribution to journal › Article

  Open Access

  • Neoplasm Genes
  • Phenotype
  • Neoplasms
  • Whole Genome Sequencing
  • Genetic Services
  15 Citations (Scopus)

• Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

  NIHR-BioResource Rare Diseases Consortium, 5 Jan 2017, In : American Journal of Human Genetics. 100, 1, p. 75-90 16 p.

  Research output: Contribution to journal › Article

  Open Access

  • Retinal Diseases
  • Whole Genome Sequencing
  • Molecular Pathology
  • Whole Exome Sequencing
  • Choroideremia
  148 Citations (Scopus)

• Definition of ringed sideroblasts

  Lee, S., Erber, W., Porwit, A., Tomonaga, M. & Peterson, L. C., 2011, In : International Journal of Laboratory Hematology. 32, p. e185

  Research output: Contribution to journal › Letter

  Open Access

• De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

  NIHR BioResource & Care4Rare Canada Consortium, 5 Jul 2018, In : American Journal of Human Genetics. 103, 1, p. 144-153 10 p.

  Research output: Contribution to journal › Article

  Open Access

  • Wiskott-Aldrich Syndrome Protein Family
  • Intellectual Disability
  • Actins
  • Seizures
  • Mutation
  4 Citations (Scopus)

• DETECTION OF CHROMOSOMAL ABERRATIONS ASSOCIATED WITH PROGNOSIS OF UVEAL MELANOMA USING CIRCULATING TUMOUR CELLS

  Isaacs, T., Beasley, A., Allcok, R., Khattak, A., Vermeulen, T., Freeman, J., Chen, F., Bentel, J., Calapre, L., Pereira, M., Yau, K., Mirzai, B., Erber, W., Ziman, M. & Gray, E., Oct 2017, In : Clinical & Experimental Ophthalmology. 45, p. 61-61 1 p.

  Research output: Contribution to journal › Abstract/Meeting Abstract

• Detection of cytoplasmic nucleophosmin expression by imaging flow cytometry

  Grimwade, L., Gudgin, E., Bloxham, D., Bottley, G., Vassiliou, G., Huntly, B., Scott, M. A. & Erber, W., 2012, In : Cytometry Part A. 81 A, p. 896-900

  Research output: Contribution to journal › Article

  Open Access
  11 Citations (Scopus)

• Detection of therapeutic targets in carcinomas of unknown primary

  Clynick, B., Dessauvagie, B., Strerrett, G., Harvey, N., Subramaniam, S., Herron, J., Allcock, R., Guo, B., Saunder, C., Erber, W. & Meehan, K., Sep 2017, In : Annals of Oncology. 28, 1 p.

  Research output: Contribution to journal › Abstract/Meeting Abstract

• Development of a Robust Immuno-S-FISH Protocol Using Imaging Flow Cytometry

  Fuller, K. A., Bennett, S. C., Hui, H. Y., Chakera, A. & Erber, W. N., 2016, In : Cytometry Part A. 89, 8, p. 720-730 11 p.

  Research output: Contribution to journal › Article

  • Fluorescence In Situ Hybridization
  • Flow Cytometry
  • Cell Count
  • Fluorescent Dyes
  • Suspensions
  9 Citations (Scopus)

• Diagnostic techniques in the assessment of haematological malignancies

  Erber, W., 2020, Oxford Textbook of Medicine. Warrell, DA., Cox, TM. & Firth, JD. (eds.). 6 ed. Oxford University Press

  Research output: Chapter in Book/Conference paper › Chapter

  • diagnostic techniques
  • blood
  • bone marrow
  • therapeutics
  • relapse

• Diagnostik beim zufallsbefund eosinophilie

  Sims, H. & Erber, W. N., 18 Jan 2012, In : Praxis. 101, 2, p. 123-125 3 p.

  Research output: Contribution to journal › Comment/debate

• Disruption of IKAROS activity in primitive chronic-phase CML cells mimics myeloid disease progression

  Beer, P. A., Knapp, D. J. H. F., Miller, P. H., Kannan, N., Sloma, I., Heel, K., Babovic, S., Bulaeva, E., Rabu, G., Terry, J., Druker, B. J., Loriaux, M. M., Loeb, K. R., Radich, J. P., Erber, W. & Eaves, C. J., 2015, In : Blood. 125, 3, p. 504-515

  Research output: Contribution to journal › Article

  Open Access

  • Leukemia, Myeloid, Chronic Phase
  • Emitter coupled logic circuits
  • Myeloid Cells
  • Blast Crisis
  • Disease Progression
  16 Citations (Scopus)

• Dysregulation of the intrinsic apoptotic pathway mediates megakaryocytic hyperplasia in myeloproliferative neoplasms

  Malherbe, J., Fuller, K., Mirzai, B., Kavanagh, S., So, C. C., Ip, H. W., Guo, B., Forsyth, C., Howman, R. & Erber, W., 2016, In : Journal of Clinical Pathology. 69, 11, p. 1017-1024

  Research output: Contribution to journal › Article

  Open Access

  • Megakaryocytes
  • Hyperplasia
  • Caspase 9
  • Survivin
  • Primary Myelofibrosis
  5 Citations (Scopus)

• Effects of the JAK2 mutation on the hematopoietic stem and progenitor compartment in human myeloproliferative neoplasms

  Anand, S., Stedham, F., Beer, P., Gudwin, E., Ortmann, C. A., Bench, A., Erber, W., Green, A. R. & Huntly, B. J. P., 2011, In : Blood. 118, 1, p. 177-181

  Research output: Contribution to journal › Article

  Open Access
  46 Citations (Scopus)

• EGFL7 is expressed in bone microenvironment and promotes angiogenesis via ERK, STAT3, and integrin signaling cascades

  Chim, S., Kuek, V., Chow, S. T., Lim, B., Tickner, J., Zhao, J., Chung, R., Su, Y., Zhang, G., Erber, W., Xian, C. J., Rosen, V. M. & Xu, J., Jan 2015, In : Journal of Cellular Physiology. 230, 1, p. 82-94

  Research output: Contribution to journal › Article

  Open Access

  File

  • STAT3 Transcription Factor
  • Epidermal Growth Factor
  • Bone
  • Integrins
  • Endothelial cells
  25 Citations (Scopus)

  516 Downloads (Pure)

• Essential thrombocythemia: seeing the wood for the trees

  Beer, P. A., Erber, W., Campbell, P. J. & Green, A. R., 2011, In : Blood. 118, 4, p. 1180-1181

  Research output: Contribution to journal › Letter

• Genetic characterisation of molecular targets in carcinoma of unknown primary

  Clynick, B., Dessauvagie, B., Sterrett, G., Harvey, N. T., Allcock, R. J. N., Saunders, C., Erber, W. & Meehan, K., 4 Jul 2018, In : Journal of Translational Medicine. 16, 1, 185.

  Research output: Contribution to journal › Article

  Open Access

  • Genes
  • Molecular Biology
  • Carcinoma
  • Tumors
  • Epithelial Cells
  10 Citations (Scopus)

• Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

  Lentaigne, C., Greene, D., Sivapalaratnam, S., Favier, R., Seyres, D., Thys, C., Grassi, L., Mangles, S., Sibson, K., Stubbs, M., Burden, F., Bordet, J. C., Armari-Alla, C., Erber, W., Farrow, S., Gleadall, N., Gomez, K., Megy, K., Papadia, S., Penkett, C. J. & 11 others, Sims, M. C., Stefanucci, L., Stephens, J. C., Read, R. J., Stirrups, K. E., Ouwehand, W. H., Laffan, M. A., BioResource, N., Frontini, M., Freson, K. & Turro, E., 5 Dec 2019, In : Blood. 134, 23, p. 2070-2081 12 p.

  Research output: Contribution to journal › Article

  • Platelets
  • Germ-Line Mutation
  • Thrombocytopenia
  • Genes
  • Transcription Factors
  8 Citations (Scopus)

• Germline selection shapes human mitochondrial DNA diversity

  NIHR Bioresource - Rare Dis & 100000 Genomes Project-Rare Dis, 24 May 2019, In : Science. 364, 6442, p. 749-+ 59 p.

  Research output: Contribution to journal › Article

  Open Access
  42 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 journal › Review article

  Open Access
  5 Citations (Scopus)

• Hepcidin predicts response to IV iron therapy in patients admitted to the intensive care unit: a nested cohort study

  IRONMAN Study Investigators, Australian New Zealand Intensive C & Farmer, S., 10 Sep 2018, In : Journal of Intensive Care. 6, 7 p., 60.

  Research output: Contribution to journal › Article

  Open Access
  6 Citations (Scopus)

• HER2 mRNA transcript quantitation in breast cancer

  Meehan, K., Clynick, B., Mirzai, B., Maslen, P., Harvey, J. & Erber, W. N., 11 Nov 2016, In : Clinical and Translational Oncology. p. 606-615 10 p.

  Research output: Contribution to journal › Article

  • human ERBB2 protein
  • Breast Neoplasms
  • Messenger RNA
  • Polymerase Chain Reaction
  • Formaldehyde
  4 Citations (Scopus)

• How I treat essential thrombocythemia

  Beer, P. A., Erber, W., Campbell, P. J. & Green, A. R., 2011, In : Blood. 117, 5, p. 1472-1482

  Research output: Contribution to journal › Review article
  74 Citations (Scopus)

• Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

  Westbury, S. K., Turro, E., Greene, D., Lentaigne, C., Kelly, A. M., Bariana, T. K., Simeoni, I., Pillois, X., Attwood, A., Austin, S., Jansen, S. B. G., Bakchoul, T., Crisp-Hihn, A., Erber, W., Favier, R., Foad, N., Gattens, M., Jolley, J. D., Liesner, R., Meacham, S. & 20 others, Millar, C. M., Nurden, A. T., Peerlinck, K., Perry, D. J., Poudel, P., Schulman, S., Schulze, H., Stephens, J. C., Furie, B., Robinson, P. N., Van Geet, C., Rendon, A., Gomez, K., Laffan, M. A., Lambert, M. P., Nurden, P., Ouwehand, W. H., Richardson, S., Mumford, A. D. & Freson, K., 2015, In : Genome Medicine. 7, 1, p. 1-15

  Research output: Contribution to journal › Article

  Open Access

  • Cluster Analysis
  • Blood Platelets
  • Hemorrhage
  • Phenotype
  • Genetic Heterogeneity
  79 Citations (Scopus)

• ICSH recommendations for indentification, dignostic value and quantification of schistocytes

  Zini, G., D"onofrio, G., Briggs, C., Erber, W., Lee, S. H., Mcfadden, S., Yutaka, N., Jou, J. M., Vives-Corrons, J. L. & Lesesve, J. F., 2011, In : International Journal of Laboratory Hematology. 2011, p. 10pp

  Research output: Contribution to journal › Article

  Open Access
  99 Citations (Scopus)

• Imaging flow cytometry in the assessment of leukocyte-platelet aggregates

  Hui, H., Fuller, K. A., Erber, W. N. & Linden, M. D., 1 Jan 2017, In : Methods. 112, p. 46-54 9 p.

  Research output: Contribution to journal › Article

  • Flow cytometry
  • Platelets
  • Leukocytes
  • Blood Platelets
  • Flow Cytometry
  9 Citations (Scopus)

• Imaging flow cytometry to assess chromosomal abnormalities in chronic lymphocytic leukaemia

  Hui, H., Fuller, K. A., Chuah, H., Liang, J., Sidiqi, H., Radeski, D. & Erber, W. N., 1 Feb 2018, In : Methods. 134-135, p. 32-40 9 p.

  Research output: Contribution to journal › Article

  • Flow cytometry
  • Fluorescence
  • B-Cell Chronic Lymphocytic Leukemia
  • Chromosome Aberrations
  • Fluorescence In Situ Hybridization
  6 Citations (Scopus)

• Improved classification of leukemic B-cell lymphoproliferative disorders using a transcriptional and genetic classifier

  Navarro, A., Clot, G., Martínez-Trillos, A., Pinyol, M., Jares, P., González-Farré, B., Martínez, D., Trim, N., Fernández, V., Villamor, N., Colomer, D., Costa, D., Salaverria, I., Martín-Garcia, D., Erber, W., López, C., Jayne, S., Siebert, R., Dyer, M. J. S., Wiestner, A. & 7 others, Wilson, W. H., Aymerich, M., López-Guillermo, A., Sánchez, À., Campo, E., Matutes, E. & Beà, S., 31 Aug 2017, In : Haematologica. 102, 9, p. 360-363 4 p.

  Research output: Contribution to journal › Letter

  Open Access
  8 Citations (Scopus)

• Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses

  NIHR BioResource Collaborative Group, 1 Jun 2019, In : Haematologica. 104, 6, p. e260-e264

  Research output: Contribution to journal › Letter

  Open Access
  6 Citations (Scopus)

• Intravenous iron or placebo for anaemia in intensive care: the IRONMAN multicentre randomized blinded trial: A randomized trial of IV iron in critical illness

  Litton, E., Baker, S., Erber, W. N., Farmer, S., Ferrier, J., French, C., Gummer, J., Hawkins, D., Higgins, A., Hofmann, A., De Keulenaer, B., Mcmorrow, J., Olynyk, J. K., Richards, T., Towler, S., Trengove, R. & Webb, S., Nov 2016, In : Intensive Care Medicine. 42, 11, p. 1715-1722

  Research output: Contribution to journal › Article

  • Critical Illness
  • Critical Care
  • Anemia
  • Iron
  • Placebos
  47 Citations (Scopus)

• Investigation and classification of anemia

  Erber, W., 2011, Blood and Bond Marrow Pathology. Porwit, A., McCullough, J. & Erber, W. N. (eds.). Second ed. United Kingdom: Elsevier, p. 105-114

  Research output: Chapter in Book/Conference paper › Chapter

  2 Citations (Scopus)

• Investigation of an incidental finding of eosinophilia

  Sims, H. & Erber, W., 2011, In : BMJ (CLINICAL RESEARCH ED.). 342, p. 1147-1149

  Research output: Contribution to journal › Article

  Open Access
  11 Citations (Scopus)

• Measurement of monocyte-platelet aggregates by imaging flow cytometry

  Hui, H., Fuller, K., Erber, W. & Linden, M., 2015, In : Cytometry Part A. 87, 3, p. 273-278

  Research output: Contribution to journal › Article

  • Monocytes
  • Blood Platelets
  • Flow Cytometry
  • P-Selectin
  • Platelet Activation
  16 Citations (Scopus)

• Megakaryocytes in myeloproliferative neoplasms have unique somatic mutations

  Guo, B. B., Allcock, R. J., Mirzai, B., Malherbe, J. A., Choudry, F. A., Frontini, M., Chuah, H., Liang, J., Kavanagh, S. E., Howman, R., Ouwehand, W. H., Fuller, K. A. & Erber, W., Jul 2017, In : The American Journal of Pathology. 187, 7, p. 1512–1522

  Research output: Contribution to journal › Article

  • Megakaryocytes
  • Mutation
  • Primary Myelofibrosis
  • Bone Marrow
  • Neoplasms
  3 Citations (Scopus)

• Megakaryocytic hyperplasia in myeloproliferative neoplasms is driven by disordered proliferative, apoptotic and epigenetic mechanisms

  Malherbe, J., Fuller, K., Arshad, A., Nangalia, J., Romeo, G., Hall, S., Meehan, K., Guo, B., Howman, R. & Erber, W., 2016, In : Journal of Clinical Pathology. 69, 2, p. 155-163

  Research output: Contribution to journal › Article

  Open Access

  • Megakaryocytes
  • Epigenomics
  • Hyperplasia
  • Mutation
  • Neoplasms
  14 Citations (Scopus)

• Molecular subsets of mantle cell lymphoma defined by the IGHV mutational status and SOX11 expression have distinct biologic and clinical features

  Navarro, A., Clot, G., Royo, C., Jares, P., Hadzidimitriou, A., Agathangelidis, A., Bikos, V., Darzentas, N., Papadaki, T., Salaverria, I., Pinyol, M., Puig, X., Palomero, J., Vegliante, M. C., Amador, V., Martinez-Trillos, A., Stefancikova, L., Wiestner, A., Wilson, W., Pott, C. & 13 others, Calasanz, M. J., Trim, N., Erber, W., Sander, B., Ott, G., Rosenwald, A., Colomer, D., Giné, E., Siebert, R., Lopez-Guillermo, A., Stamatopoulos, K., Beà, S. & Campo, E., 2012, In : Cancer Research. 72, 20, p. 5307-16

  Research output: Contribution to journal › Article

  Open Access
  157 Citations (Scopus)

• Mutational Analysis of BRAF Inhibitor-Associated Squamoproliferative Lesions

  Clynick, B., Tabone, T., Fuller, K., Erber, W., Meehan, K., Millward, M., Wood, B. & Harvey, N., 2015, In : JOURNAL OF MOLECULAR DIAGNOSTICS. 17, 6, p. 644-651

  Research output: Contribution to journal › Article
  6 Citations (Scopus)

• Non-nodal type of mantle cell lymphoma is a specific biological and clinical subgroup of the disease

  Royo, C., Navarro, A., Clot, G., Salaverria, I., Giné, E., Jares, P., Colomer, D., Wiestner, A., Wilson, W. H., Vegliante, M. C., Fernandez, V., Hartmann, E. M., Trim, N., Erber, W., Swerdlow, S. H., Klapper, W., Dyer, M. J. S., Vargas-Pabón, M., Ott, G., Rosenwald, A. & 4 others, Siebert, R., López-Guillermo, A., Campo, E. & Beà, S., 2012, In : Leukemia. 26, p. 1895-98

  Research output: Contribution to journal › Article
  93 Citations (Scopus)

• Normal blood cells

  Wickramasinghe, S. N. & Erber, W., 2011, Blood and Bone Marrow Pathology. Porwit, A., McCullough, J. & Erber, W. N. (eds.). Second ed. United Kingdom: Churchill Livingstone, p. 708

  Research output: Chapter in Book/Conference paper › Chapter

  3 Citations (Scopus)