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  • Wendy Erber
2012

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 journalArticle

Open Access
10 Citations (Scopus)
2016
6 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 journalArticle

Open Access
5 Citations (Scopus)
2013

Developments in the immunophenotypic analysis of haematological malignancies

Heel, K., Tabone, T., Roehrig, K., Maslen, P., Meehan, K., Grimwade, L. F. & Erber, W., 2013, In : Blood Reviews. 27, 4, p. 193-207

Research output: Contribution to journalArticle

5 Citations (Scopus)
2017

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 journalArticle

21 Citations (Scopus)
2015

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 journalArticle

6 Citations (Scopus)
2012

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
5 Citations (Scopus)

Red Blood Cell Disorders

Erber, W., 2012, Clinical Pharmacology. Bennett, B. & Sharma (eds.). 11 ed. United States: Churchill Livingstone, p. 509-521

Research output: Chapter in Book/Conference paperChapter

2 Citations (Scopus)
2017

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 journalLetter

Open Access
7 Citations (Scopus)
2016

TGF-α and IL-6 plasma levels selectively identify CML patients who fail to achieve an early molecular response or progress in the first year of therapy

Nievergall, E., Reynolds, J., Kok, C. H. H., Watkins, D. B. B., Biondo, M., Busfield, S. J. J., Vairo, G., Fuller, K. A., Erber, W. N., Sadras, T., Grose, R., Yeung, D. T. T., Lopez, A. F. F., Hiwase, D. K. K., Hughes, T. P. P. & White, D. L. L., 2016, In : Leukemia. 30, 6, p. 1263-1272 10 p.

Research output: Contribution to journalArticle

22 Citations (Scopus)
2017

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 journalLetter

2018

Red blood cell disorders

Sidiqi, H. & Erber, W., May 2018, Clinical Pharmacology. Bennett, PN., Brown, MJ. & Sharma, P. (eds.). 12 ed. China: Churchill Linvingstone, p. 528-542

Research output: Chapter in Book/Conference paperChapter

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 journalArticle

5 Citations (Scopus)
2019

“Immuno-flowFISH” for the Assessment of Cytogenetic Abnormalities in Chronic Lymphocytic Leukemia

Hui, H. Y. L., Clarke, K. M., Fuller, K. A., Stanley, J., Chuah, H. H., Ng, T. F., Cheah, C., McQuillan, A. & Erber, W. N., 1 May 2019, In : Cytometry Part A. 95, 5, p. 521-533 13 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)
2017

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 journalArticle

3 Citations (Scopus)
2014

Guidelines on the use of multicolour flow cytometry in the diagnosis of haematological neoplasms

Johansson, U., Bloxham, D. M., Couzens, S., Jesson, J., Morilla, R. M., Erber, W. & Macey, M. G., 2014, In : British Journal of Haematology. 165, 4, p. 455-488

Research output: Contribution to journalArticle

Open Access
57 Citations (Scopus)
2017

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 journalArticle

Open Access
133 Citations (Scopus)
2020

Whole-genome sequencing of patients with rare diseases in a national health system

NIHR BioResource for the 100,000 Genomes Project, 2 Jul 2020, In : Nature. 583, 7814, p. 96-102 7 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)
2018

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 journalArticle

Open Access
3 Citations (Scopus)
2019

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 journalLetter

Open Access
5 Citations (Scopus)
2012

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 journalArticle

90 Citations (Scopus)
2017

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 journalArticle

9 Citations (Scopus)
2016

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 journalArticle

9 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 journalArticle

Open Access
12 Citations (Scopus)
2014

Gray platelet syndrome: Proinflammatory megakaryocytes and α-granule loss cause myelofibrosis and confer metastasis resistance in mice

Guerrero, J. A., Bennett, C., Van Der Weyden, L., Mckinney, H., Chin, M., Nurden, P., Mcintyre, Z., Cambridge, E. L., Estabel, J., Wardle-Jones, H., Speak, A. O., Erber, W., Rendon, A., Ouwehand, W. H. & Ghevaert, C. J. G., 2014, In : Blood. 124, 24, p. 3624-3635

Research output: Contribution to journalArticle

Open Access
53 Citations (Scopus)
2015

Somatic mutations in glioblastoma are associated with methylguanine-DNA methyltransferase methylation

Mcdonald, K. L., Tabone, T., Nowak, A. & Erber, W., 2015, In : Oncology Letters. 9, 5, p. 2063-2067

Research output: Contribution to journalArticle

Open Access
6 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 journalArticle

16 Citations (Scopus)

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 journalArticle

Open Access
14 Citations (Scopus)
2016

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 journalArticle

48 Citations (Scopus)
2014

Chronic neutrophilic leukemia with plasma cell dyscrasia: friends or relatives?

Erber, W. & Reilly, J. T., 2014, In : LEUKEMIA & LYMPHOMA. 55, 2, p. 240-242

Research output: Contribution to journalLetter

3 Citations (Scopus)
2016

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 journalArticle

68 Citations (Scopus)
2020

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 paperChapter

2015

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 journalArticle

Open Access
File
25 Citations (Scopus)
480 Downloads (Pure)
2013

Angiogenic factors in bone local environment

Chim, S., Tickner, J., Chow, S. T., Kuek, V., Guo, B., Zhang, G., Rosen, V., Erber, W. & Xu, J., 2013, In : Cytokine and Growth Factor Reviews. 24, 3, p. 297-310

Research output: Contribution to journalReview article

131 Citations (Scopus)
2018

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 journalArticle

Open Access
11 Citations (Scopus)
2017

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 journalArticle

13 Citations (Scopus)
2018
Open Access
9 Citations (Scopus)
2017

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 journalAbstract/Meeting Abstract

2019
2016

NPNT is expressed by osteoblasts and mediates angiogenesis via the activation of extracellular signal-regulated kinase

Kuek, V., Yang, Z., Chim, S., Zhu, S., Xu, H., Chow, S. T., Tickner, J., Rosen, V., Erber, W., Li, X., An, Q., Qian, Y. & Xu, J., 26 Oct 2016, In : Scientific Reports. 6, p. 1-13 13 p., 36210.

Research output: Contribution to journalArticle

Open Access
File
7 Citations (Scopus)
368 Downloads (Pure)
2019

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 journalArticle

Open Access
34 Citations (Scopus)
2018

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 journalArticle

Open Access
4 Citations (Scopus)

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Farmery, J. H. R., Smith, M. L., Huissoon, A., Furnell, A., Mead, A., Levine, A. P., Manzur, A., Thrasher, A., Greenhalgh, A., Parker, A., Sanchis-Juan, A., Richter, A., Gardham, A., Lawrie, A., Sohal, A., Creaser-Myers, A., Frary, A., Greinacher, A., Themistocleous, A., Peacock, A. J. & 329 others, Marshall, A., Mumford, A., Rice, A., Webster, A., Brady, A., Koziell, A., Manson, A., Chandra, A., Hensiek, A., Veld, A. H. I. T., Maw, A., Kelly, A. M., Moore, A., Vonk Noordegraaf, A., Attwood, A., Herwadkar, A., Ghofrani, A., Houweling, A. C., Girerd, B., Furie, B., Treacy, C. M., Millar, C. M., Sewell, C., Roughley, C., Titterton, C., Williamson, C., Hadinnapola, C., Deshpande, C., Toh, C. H., Bacchelli, C., Patch, C., Geet, C. V., Babbs, C., Bryson, C., Penkett, C. J., Rhodes, C. J., Watt, C., Bethune, C., Booth, C., Lentaigne, C., McJannet, C., Church, C., French, C., Samarghitean, C., Halmagyi, C., Gale, D., Greene, D., Hart, D., Allsup, D., Bennett, D., Edgar, D., Kiely, D. G., Gosal, D., Perry, D. J., Keeling, D., Montani, D., Shipley, D., Whitehorn, D., Fletcher, D., Krishnakumar, D., Grozeva, D., Kumararatne, D., Thompson, D., Josifova, D., Maher, E., Wong, E. K. S., Murphy, E., Dewhurst, E., Louka, E., Rosser, E., Chalmers, E., Colby, E., Drewe, E., McDermott, E., Thomas, E., Staples, E., Clement, E., Matthews, E., Wakeling, E., Oksenhendler, E., Turro, E., Reid, E., Wassmer, E., Raymond, F. L., Hu, F., Kennedy, F., Soubrier, F., Flinter, F., Kovacs, G., Polwarth, G., Ambegaonkar, G., Arno, G., Hudson, G., Woods, G., Coghlan, G., Hayman, G., Arumugakani, G., Schotte, G., Cook, H. T., Alachkar, H., Lango Allen, H., Lango-Allen, H., Stark, H., Stauss, H., Schulze, H., Boggard, H. J., Baxendale, H., Dolling, H., Firth, H., Gall, H., Watson, H., Longhurst, H., Markus, H. S., Watkins, H., Simeoni, I., Emmerson, I., Roberts, I., Quinti, I., Wanjiku, I., Gibbs, J. S. R., Thaventhiran, J., Whitworth, J., Hurst, J., Collins, J., Suntharalingam, J., Payne, J., Thachil, J., Martin, J. M., Carmichael, J., Maimaris, J., Paterson, J., Pepke-Zaba, J., Heemskerk, J. W. M., Gebhart, J., Davis, J., Pasi, J., Bradley, J. R., Wharton, J., Stephens, J., Rankin, J., Anderson, J., Vogt, J., Von Ziegenweldt, J., Rehnstrom, K., Megy, K., Talks, K., Peerlinck, K., Yates, K., Freson, K., Stirrups, K., Gomez, K., Smith, K. G. C., Rue-Albrecht, K., Gilmour, K., Masati, L., Scelsi, L., Southgate, L., Ranganathan, L., Ginsberg, L., Devlin, L., Willcocks, L., Ormondroyd, L., Lorenzo, L., Harper, L., Allen, L., Daugherty, L., Chitre, M., Kurian, M., Humbert, M., Tischkowitz, M., Bitner-Glindzicz, M., Erwood, M., Scully, M., Veltman, M., Caulfield, M., Layton, M., McCarthy, M., Ponsford, M., Toshner, M., Bleda, M., Wilkins, M., Mathias, M., Reilly, M., Afzal, M., Brown, M., Rondina, M., Stubbs, M., Haimel, M., Lees, M., Laffan, M. A., Browning, M., Gattens, M., Richards, M., Michaelides, M., Lambert, M. P., Makris, M., De Vries, M., Mahdi-Rogers, M., Saleem, M., Thomas, M., Holder, M., Eyries, M., Clements-Brod, N., Canham, N., Dormand, N., Zuydam, N. V., Kingston, N., Ghali, N., Cooper, N., Morrell, N. W., Yeatman, N., Roy, N., Shamardina, O., Alavijeh, O. S., Gresele, P., Nurden, P., Chinnery, P., Deegan, P., Yong, P., Man, P. Y. W., Corris, P. A., Calleja, P., Gissen, P., Bolton-Maggs, P., Rayner-Matthews, P., Ghataorhe, P. K., Gordins, P., Stein, P., Collins, P., Dixon, P., Kelleher, P., Ancliff, P., Yu, P., Tait, R. C., Linger, R., Doffinger, R., Machado, R., Kazmi, R., Sargur, R., Favier, R., Tan, R., Liesner, R., Antrobus, R., Sandford, R., Scott, R., Trembath, R., Horvath, R., Hadden, R., Mackenzieross, R. V., Henderson, R., MacLaren, R., James, R., Ghurye, R., Dacosta, R., Hague, R., Mapeta, R., Armstrong, R., Noorani, S., Murng, S., Santra, S., Tuna, S., Johnson, S., Chong, S., Lear, S., Walker, S., Goddard, S., Mangles, S., Westbury, S., Mehta, S., Hackett, S., Nejentsev, S., Moledina, S., Bibi, S., Meehan, S., Othman, S., Revel-Vilk, S., Holden, S., McGowan, S., Staines, S., Savic, S., Burns, S., Grigoriadou, S., Papadia, S., Ashford, S., Schulman, S., Ali, S., Park, S. M., Davies, S., Stock, S., Ali, S., Deevi, S. V. V., Gräf, S., Ghio, S., Wort, S. J., Jolles, S., Austin, S., Welch, S., Meacham, S., Rankin, S., Walker, S., Seneviratne, S., Holder, S., Sivapalaratnam, S., Richardson, S., Kuijpers, T. W., Kuijpers, T. W., Bariana, T. K., Bakchoul, T., Everington, T., Renton, T., Young, T., Aitman, T., Warner, T. Q., Vale, T., Hammerton, T., Pollock, V., Matser, V., Cookson, V., Clowes, V., Qasim, W., Wei, W., Erber, W. N., Ouwehand, W. H., Astle, W., Egner, W., Turek, W., Henskens, Y., Tan, Y. & Lynch, A. G., 1 Dec 2018, In : Scientific Reports. 8, 1, 1300.

Research output: Contribution to journalArticle

Open Access
9 Citations (Scopus)
2020

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

Primary Immunodeficiency Consortium for the NIHR Bioresource, 2 Jul 2020, In : Nature. 583, 7814, p. 90-95 6 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)
2014

Transcriptional diversity during lineage commitment of human blood progenitors

Chen, L., Kostadima, M., Martens, J., Canu, G., Garcia, S., Turro, E., Downes, K., Macaulay, I., Bielczyk-Maczynska, E., Coe, S., Farrow, S., Poudel, P., Burden, F., Jansen, S. B. G., Astle, W., Attwood, A., Bariana, T., De Bono, B., Breschi, A., Chambers, J. C. & 46 others, Choudry, F. A., Clarke, L., Coupland, P., Van Der Ent, M., Erber, W., Jansen, J. H., Favier, R., Fenech, M. E., Foad, N., Freson, K., Van Geet, C., Gomez, K., Guigo, R., Hampshire, D., Kelly, A. M., Kerstens, H. H. D., Kooner, J. S., Laffan, M., Lentaigne, C., Labalette, C., Martin, T., Meacham, S., Mumford, A., Nurnberg, S., Palumbo, E., Van Der Reijden, B. A., Richardson, D., Sammut, S. J., Slodkowicz, G., Tamuri, A. U., Vasquez, L., Voss, K., Watt, S., Westbury, S., Flicek, P., Loos, R., Goldman, N., Bertone, P., Read, RJ., Richardson, S., Cvejic, A., Soranzo, N., Ouwehand, W. H., Stunnenberg, H. G., Frontini, M. & Rendon, A., 26 Sep 2014, In : Science. 345, 6204, p. 1-10 1251033.

Research output: Contribution to journalArticle

Open Access
143 Citations (Scopus)
2012

Diagnostik beim zufallsbefund eosinophilie

Translated title of the contribution: Diagnostics in the incidental finding of eosinophiliaSims, H. & Erber, W. N., 18 Jan 2012, In : Praxis. 101, 2, p. 123-125 3 p.

Research output: Contribution to journalComment/debate

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 journalArticle

Open Access
152 Citations (Scopus)
2016

TGFα expression in myeloid malignancies

Kavanagh, S., Mirzai, B., Fuller, K. & Erber, W., 2016, In : Journal of Clinical Pathology. 69, 6, p. 543-546

Research output: Contribution to journalArticle

Open Access
1 Citation (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 journalArticle

4 Citations (Scopus)
2015

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 journalArticle

Open Access
75 Citations (Scopus)