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Ian R. Peake
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Journal Articles

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States

Veronica H. Flood, Pamela A. Christopherson, Joan Cox Gill, Kenneth D. Friedman, Sandra L. Haberichter, Daniel B. Bellissimo, Rupa A. Udani, Mahua Dasgupta, Raymond G. Hoffmann, Margaret V. Ragni, Amy D. Shapiro, Jeanne M. Lusher, Steven R. Lentz, Thomas C. Abshire, Cindy Leissinger, W. Keith Hoots, Marilyn J. Manco-Johnson, Ralph A. Gruppo, Lisa N. Boggio, Kate T. Montgomery, Anne C. Goodeve, Paula D. James, David Lillicrap, Ian R. Peake, Robert R. Montgomery
Journal: Blood
Blood (2016) 127 (20): 2481–2488.
https://doi.org/10.1182/blood-2015-10-673681
Published: 2016
Includes: Supplemental data
Journal Articles

Characterization and Expression of an In-Frame Exon 33-34 Deletion Causing Type 1 VWD

Ashley Cartwright, PhD, Pamela A Christopherson, Crystal L. Perry, Sandra L Haberichter, PhD, Daniel Hampshire, PhD, Ian R. Peake, PhD, Anne Goodeve, PhD, Robert R Montgomery, MD, Daniel B. Bellissimo, the Zimmerman Program Investigators
Journal: Blood
Blood (2014) 124 (21): 1525.
https://doi.org/10.1182/blood.V124.21.1525.1525
Published: 2014
Journal Articles

Intracellular Retention, Enhanced Clearance, and Defective FVIII Binding Are Common Features of Von Willebrand Factor D'-D3 Domain Mutations in Patients with Von Willebrand Disease Type 1 From the European Mcmdm-1VWD Study

Reinhard Schneppenheim, MD, PhD, Ulrich Budde, MD, Javier Batlle, MD, Giancarlo Castaman, MD, Jeroen C. J. Eikenboom, MD, PhD, Augusto B. Federici, MD, Jenny Goudemand, MD, PhD, Tobias Obser, Florian Oyen, Francesco Rodeghiero, MD, Sonja Schneppenheim, MD, Ian R. Peake, PhD, Anne C. Goodeve, PhD
Journal: Blood
Blood (2012) 120 (21): 99.
https://doi.org/10.1182/blood.V120.21.99.99
Published: 2012
Journal Articles

Investigation of the Role of Copy Number Variation In the Pathogenesis of Type 1 Von Willebrand Disease

Daniel J. Hampshire, PhD, Lisa D. Bloomer, MSc, Ahlam M. Al-Buhairan, PhD, Rachael E. Coyle, Raymon N. C. P. Vijzelaar, MSc, David Lillicrap, MD, Paula D. James, MD, Jeroen C. J. Eikenboom, MD, PhD, Reinhard Schneppenheim, MD, PhD, Francesco Rodeghiero, MD, Robert R. Montgomery, MD, Ian R. Peake, PhD, Anne C. Goodeve, PhD
Journal: Blood
Blood (2010) 116 (21): 2218.
https://doi.org/10.1182/blood.V116.21.2218.2218
Published: 2010
Journal Articles

Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

Brief Report
Martina E. Daly, Ban B. Dawood, William A. Lester, Ian R. Peake, Francesco Rodeghiero, Anne C. Goodeve, Michael Makris, Jonathan T. Wilde, Andrew D. Mumford, Stephen P. Watson, Stuart J. Mundell
Journal: Blood
Blood (2009) 113 (17): 4110–4113.
https://doi.org/10.1182/blood-2008-11-190850
Published: 2009
Journal Articles

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

Thomas J. Kunicki, Augusto B. Federici, Daniel R. Salomon, James A. Koziol, Steven R. Head, Tony S. Mondala, Jeffrey D. Chismar, Luciano Baronciani, Maria Teresa Canciani, Ian R. Peake
Journal: Blood
Blood (2004) 104 (8): 2359–2367.
https://doi.org/10.1182/blood-2004-01-0349
Published: 2004
Journal Articles

Analysis of intracellular storage and regulated secretion of 3 von Willebrand disease–causing variants of von Willebrand factor

Grégoire Michaux, Lindsay J. Hewlett, Sarah L. Messenger, Anne C. Goodeve, Ian R. Peake, Martina E. Daly, Daniel F. Cutler
Journal: Blood
Blood (2003) 102 (7): 2452–2458.
https://doi.org/10.1182/blood-2003-02-0599
Published: 2003
Journal Articles

FLT3 internal tandem duplication mutations are rare in agnogenic myeloid metaplasia

Faisal M. Abu-Duhier, Anne C. Goodeve, Gill A. Wilson, Rory S. Carr, Ian R. Peake, John T. Reilly
Journal: Blood
Blood (2002) 100 (1): 364.
https://doi.org/10.1182/blood-2002-02-0536
Published: 2002
Journal Articles

A novel von Willebrand disease–causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion

Simon Allen, Adel M. Abuzenadah, Joanna Hinks, Joanna L. Blagg, Turkiz Gursel, Jørgen Ingerslev, Anne C. Goodeve, Ian R. Peake, Martina E. Daly
Journal: Blood
Blood (2000) 96 (2): 560–568.
https://doi.org/10.1182/blood.V96.2.560
Published: 2000
Journal Articles

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S

Michael Makris, Michael Leach, Nick J. Beauchamp, Martina E. Daly, Peter C. Cooper, Kingsley K. Hampton, Pauline Bayliss, Ian R. Peake, George J. Miller, F. Eric Preston
Journal: Blood
Blood (2000) 95 (6): 1935–1941.
https://doi.org/10.1182/blood.V95.6.1935
Published: 2000
Journal Articles

Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

Simon Allen, Adel M. Abuzenadah, Joanna L. Blagg, Joanna Hinks, I. Mandy Nesbitt, Anne C. Goodeve, Turkiz Gursel, Jørgen Ingerslev, Ian R. Peake, Martina E. Daly
Journal: Blood
Blood (2000) 95 (6): 2000–2007.
https://doi.org/10.1182/blood.V95.6.2000
Published: 2000