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Journal Articles

Increased Allele Frequency of GNPAT p.D519G in Compound HFE p.C282Y/p.H63D Heterozygotes with Elevated Serum Ferritin Levels

Eriza S. Secondes, BSc (Honors), Daniel F. Wallace, PhD, Gautam Rishi, PhD, Gordon D. McLaren, MD, Christine E. McLaren, PhD, Wen-Pin Chen, MS, Louise Ramm, BSc, Lawrie W. Powell, MD PhD, Grant A. Ramm, PhD, James C. Barton, MD, V. Nathan Subramaniam, PhD

Blood (2019) 134 (Supplement_1): 4807.

https://doi.org/10.1182/blood-2019-128240

Published: 2019

Journal Articles

Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease

Kam Sandhu, Kaledas Flintoff, Mark D. Chatfield, Jeannette L. Dixon, Louise E. Ramm, Grant A. Ramm, Lawrie W. Powell, V. Nathan Subramaniam, Daniel F. Wallace

Blood (2018) 132 (1): 101–110.

https://doi.org/10.1182/blood-2018-02-830562

Published: 2018

Includes: Supplemental data

Journal Articles

GNPAT p.D519G is Independently Associated with Markedly Increased Iron Stores in HFE p.C282Y Homozygotes

James C. Barton, MD, Wen-Pin Chen, MS, Mary J. Emond, PhD, Pradyumna D. Phatak, MD, V. Nathan Subramaniam, PhD, Paul C. Adams, MD, Lyle C. Gurrin, PhD, Gregory J. Anderson, BSc, MSc, PhD, Grant A. Ramm, PhD, Lawrie W. Powell, MD, PhD, Katrina J. Allen, FRACP, MD PhD, John D. Phillips, PhD, Charles J. Parker, MD, Gordon D. McLaren, MD, Christine E. McLaren, PhD

Blood (2016) 128 (22): 3617.

https://doi.org/10.1182/blood.V128.22.3617.3617

Published: 2016

Journal Articles

Pocket-sized iron regulators: one size fits all?

V. Nathan Subramaniam

Blood (2016) 128 (2): 153–154.

https://doi.org/10.1182/blood-2016-05-716043

Published: 2016

Journal Articles

Exome Sequencing Identifies a GNPAT Variant Associated with Severe Iron Overload in HFE C282Y Homozygous Men with Extreme Phenotypes; Possible Role in Regulation of Hepcidin Expression

Gordon D. McLaren, MD, Mary J. Emond, PhD, V. Nathan Subramaniam, PhD, Pradyumna D. Phatak, MD, James C. Barton, MD, Paul C. Adams, MD, Justin B. Goh, PhD, Cameron J. McDonald, PhD, Lawrie W. Powell, MD PhD, Lyle C. Gurrin, PhD, Katrina J. Allen, MBBS, PhD, Deborah A. Nickerson, PhD, Tin Louie, MS, Grant A. Ramm, PhD, Gregory J. Anderson, PhD, Christine E. McLaren, PhD

Blood (2014) 124 (21): 745.

https://doi.org/10.1182/blood.V124.21.745.745

Published: 2014

Journal Articles

An Essential Role For Transferrin Receptor 2 In Erythropoiesis During Iron Restriction

Daniel F Wallace, Cameron J McDonald, Eriza S Secondes, Lesa Ostini, Gautam Rishi, John D Hooper, Gloria Velasco, Andrew J Ramsay, Carlos López-Otín, V Nathan Subramaniam

Blood (2013) 122 (21): 429.

https://doi.org/10.1182/blood.V122.21.429.429

Published: 2013

Journal Articles

Exome Sequencing Identifies Genes and Variant Alleles Associated With Severity Of Iron Overload In Hemochromatosis HFE C282Y Homozygotes

Christine E. McLaren, PhD, Mary J. Emond, PhD, Pradyumna D. Phatak, MD, Paul C. Adams, MD, V. Nathan Subramaniam, PhD, James C. Barton, MD, Lawrie W. Powell, MD, PhD, Lyle C. Gurrin, PhD, Katrina J. Allen, MBBS, PhD, Deborah A. Nickerson, PhD, Tin Louie, MS, Grant A. Ramm, PhD, Gregory J. Anderson, PhD, Gordon D. McLaren, MD

Blood (2013) 122 (21): 179.

https://doi.org/10.1182/blood.V122.21.179.179

Published: 2013

Journal Articles

Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2

Daniel F. Wallace, Cameron J. McDonald, Lesa Ostini, V. Nathan Subramaniam

Blood (2011) 117 (10): 2960–2966.

https://doi.org/10.1182/blood-2010-08-303859

Published: 2011

Journal Articles

Ironing out doxorubicin-related cardiotoxicity

V. Nathan Subramaniam

Blood (2003) 102 (7): 2317–2318.

https://doi.org/10.1182/blood-2003-07-2517

Published: 2003

Journal Articles

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

Daniel F. Wallace, Palle Pedersen, Jeannette L. Dixon, Peter Stephenson, Jeffrey W. Searle, Lawrie W. Powell, V. Nathan Subramaniam

Blood (2002) 100 (2): 692–694.

https://doi.org/10.1182/blood.V100.2.692

Published: 2002

Includes: Supplemental data

NARROW

Increased Allele Frequency of GNPAT p.D519G in Compound HFE p.C282Y/p.H63D Heterozygotes with Elevated Serum Ferritin Levels

Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease

GNPAT p.D519G is Independently Associated with Markedly Increased Iron Stores in HFE p.C282Y Homozygotes

Pocket-sized iron regulators: one size fits all?

Exome Sequencing Identifies a GNPAT Variant Associated with Severe Iron Overload in HFE C282Y Homozygous Men with Extreme Phenotypes; Possible Role in Regulation of Hepcidin Expression

An Essential Role For Transferrin Receptor 2 In Erythropoiesis During Iron Restriction

Exome Sequencing Identifies Genes and Variant Alleles Associated With Severity Of Iron Overload In Hemochromatosis HFE C282Y Homozygotes

Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2

Ironing out doxorubicin-related cardiotoxicity

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

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American Society of Hematology

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American Society of Hematology

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