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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

Association of GNPAT p.D519G with Higher Iron Phenotypes in Women with HFE p.C282Y Homozygosity

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

Blood (2017) 130 (Supplement 1): 2216.

https://doi.org/10.1182/blood.V130.Suppl_1.2216.2216

Published: 2017

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

Association of Helicobacter Pylori Infection with Iron Deficiency in Asians and Pacific Islanders but not in Caucasians, African Americans, or Hispanics

Gordon D. McLaren, MD, Joseph A. Murray, MD, Stela McLachlan, PhD, Paul C. Adams, MD, John H. Eckfeldt, MD, Chris D. Vulpe, MD, Victor R. Gordeuk, MD, Tricia Brantner, Catherine Leiendecker-Foster, M.S., CLSp(MB), Wen-Pin Chen, MS, Anthony A. Killeen, MD, Ronald T. Acton, PhD, Lisa F. Barcellos, PhD, Deborah A. Nickerson, PhD, Kenneth B. Beckman, PhD, Christine E. McLaren, PhD

Blood (2015) 126 (23): 4556.

https://doi.org/10.1182/blood.V126.23.4556.4556

Published: 2015

Journal Articles

Identification of Polymorphic Gnpat As a Risk Factor for Porphyria Cutanea Tarda

John D Phillips, PhD, Colin P Farrell, MPH, Jessica Overbey, MS, Hetanshi Naik, BS, Gordon D. McLaren, MD, Christine E McLaren, PhD, Luming Zhou, PhD, Charles J. Parker, MD

Blood (2015) 126 (23): 3353.

https://doi.org/10.1182/blood.V126.23.3353.3353

Published: 2015

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

Elevated Transferrin Saturation, Health-Related Quality Of Life and Telomere Length

Arch G. Mainous, III, PhD, Robert U. Wright, MPH, Mary M. Hulihan, MPH, Waleed O. Twal, PhD, Christine E. McLaren, PhD, Gordon D. McLaren, MD, Vanessa A. Diaz, MD, MS, W. Scott Argraves, PhD, Althea M. Grant, PhD

Blood (2013) 122 (21): 425.

https://doi.org/10.1182/blood.V122.21.425.425

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

Celiac Disease: Association with Iron Deficiency in Caucasians but Not in Non-Caucasians.

Joseph A. Murray, MD, Stela McLachlan, PhD, Paul C. Adams, MD, John H. Eckfeldt, MD, PhD, Chad P. Garner, PhD, Chris D. Vulpe, MD, PhD, Victor R. Gordeuk, MD, Tricia L. Brantner, Catherine Leiendecker-Foster, MS, CLSp(MB), Anthony A. Killeen, MD, Ronald T. Acton, PhD, Lisa F. Barcellos, PhD, Kenneth B. Beckman, PhD, Gordon D. McLaren, MD, Christine E. McLaren, PhD

Blood (2012) 120 (21): 2095.

https://doi.org/10.1182/blood.V120.21.2095.2095

Published: 2012

Journal Articles

Bivariate Mixture Models of Serum Ferritin and Transferrin Saturation Predict Stable Components Measured 12 Years Apart in a Healthy Australian Population

Christine E. McLaren, PhD, Wen-Pin Chen, MS, Nadine A. Bertalli, GradDipEp, Lidija Turkovic, MStat, Martin B. Delatycki, PhD, Graham G. Giles, PhD, Dallas R. English, PhD, John L. Hopper, PhD, Katrina J. Allen, MD, Lyle C. Gurrin, PhD

Blood (2011) 118 (21): 5281.

https://doi.org/10.1182/blood.V118.21.5281.5281

Published: 2011

Journal Articles

Associations Between Single Nucleotide Polymorphisms in Iron-Related Genes and Iron Status in Multiethnic Populations

Christine E. McLaren, PhD, Stela McLachlan, PhD, Chad P. Garner, PhD, Chris D. Vulpe, MD, PhD, Victor R. Gordeuk, MD, John H. Eckfeldt, MD, PhD, Paul C. Adams, MD, Ronald T. Acton, PhD, Joseph A. Murray, MD, Catherine Leiendecker-Foster, MS, CLSp(MB), Beverly M. Snively, PhD, Lisa F. Barcellos, PhD, James D. Cook, MD, Gordon D. McLaren, MD

Blood (2011) 118 (21): 2105.

https://doi.org/10.1182/blood.V118.21.2105.2105

Published: 2011

Journal Articles

Lack of Association between Single Nucleotide Polymorphism rs3811647 in the TF Gene and Iron Status in Patients with Iron Deficiency and Control Subjects

Gordon D. McLaren, MD, Catherine A. McCarty, PhD, MPH, Marylyn Ritchie, PhD, Stephen Turner, MS, Victor R. Gordeuk, MD, Chad P. Garner, PhD, Chris D. Vulpe, MD, PhD, Stela McLachlan, PhD, Paul C. Adams, MD, Christine E. McLaren, PhD

Blood (2010) 116 (21): 4257.

https://doi.org/10.1182/blood.V116.21.4257.4257

Published: 2010

Journal Articles

Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency.

Christine E. McLaren, Ph.D., Chad P. Garner, Ph.D., Clare C. Constantine, Ph.D., Stela Masle, Ph.D., Christopher D. Vulpe, M.D., Ph.D., Beverly M. Snively, Ph.D., James D. Cook, MD, Deborah A. Nickerson, Ph.D., Catherine Leiendecker-Foster, M.S., Kenneth B. Beckman, Ph.D., John H. Eckfeldt, M.D., Ph.D., Victor R. Gordeuk, M.D., Joseph A. Murray, M.D., Paul C. Adams, M.D., Lisa F. Barcellos, Ph.D., Anthony A. Killeen, MD, Katrina Goddard, Ph.D., David M. Reboussin, Ph.D., Gordon D. McLaren, M.D.

Blood (2009) 114 (22): 4048.

https://doi.org/10.1182/blood.V114.22.4048.4048

Published: 2009

Journal Articles

Subpopulations with Iron Deficiency, Liver Disease, or HFE Mutations Revealed by Statistical Mixture Modeling of Transferrin Saturation and Serum Ferritin Concentration in Asians, African Americans, Hispanics, and Whites.

Christine E. McLaren, PhD, Victor R. Gordeuk, M.D., Wen-Pin Chen, M.S., James C. Barton, M.D., Ronald T. Acton, Ph.D., Mark Speechley, Ph.D., Oswaldo Castro, M.D., Paul C. Adams, M.D., Beverly M. Snively, Ph.D., Emily L. Harris, Ph.D., David M. Reboussin, Ph.D., Geoffrey J. McLachlan, Ph.D., Richard Bean, Ph.D., Gordon D. McLaren, M.D.

Blood (2007) 110 (11): 2672.

https://doi.org/10.1182/blood.V110.11.2672.2672

Published: 2007

Journal Articles

Symptoms and Signs of Hemochromatosis in HFE C282Y Homozygotes Identified by Screening in Primary Care.

Gordon D. McLaren, MD, Christine E. McLaren, Ph.D., Paul C. Adams, M.D., James C. Barton, M.D., David M. Reboussin, Ph.D., Victor R. Gordeuk, M.D., Ronald T. Acton, Ph.D., Emily L. Harris, Ph.D., Mark Speechley, Ph.D., Phyliss Sholinsky, MSPH, Fitzroy W. Dawkins, M.D., Beverly M. Snively, Ph.D., Thomas Vogt, M.D., John H. Eckfeldt, M.D., Ph.D.

Blood (2006) 108 (11): 1545.

https://doi.org/10.1182/blood.V108.11.1545.1545

Published: 2006

Journal Articles

Initial Screening Transferrin Saturation Values, Serum Ferritin Concentrations, and HFE Genotypes in Native Americans and Whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

James C. Barton, MD, Ronald T. Acton, PhD, Laura Lovato, MS, Mark R. Speechley, PhD, Christine E. McLaren, PhD, Emily L. Harris, PhD, M.P.H., David M. Reboussin, PhD, Paul C. Adams, MD, Fitzroy W. Dawkins, MD, Victor R. Gordeuk, MD, Ann P. Walker, M.A.

Blood (2005) 106 (11): 3712.

https://doi.org/10.1182/blood.V106.11.3712.3712

Published: 2005

Journal Articles

Initial Screening Transferrin Saturations, Serum Ferritin Concentrations, and HFE Genotypes in Whites and Blacks in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

James C. Barton, M.D., Ronald T. Acton, Ph.D., Fitzroy W. Dawkins, M.D., Paul C. Adams, M.D., Laura Lovato, M.S., Cathy Leiendecker-Foster, M.S., Christine E. McLaren, Ph.D., David M. Reboussin, Ph.D., Mark R. Speechley, Ph.D., Victor R. Gordeuk, M.D., Gordon D. McLaren, M.D., Phyliss Sholinsky, M.S.P.H., Emily L. Harris, Ph.D., M.P.H.

Blood (2004) 104 (11): 3202.

https://doi.org/10.1182/blood.V104.11.3202.3202

Published: 2004

Journal Articles

Geographic and Racial/Ethnic Differences in HFE Mutation Frequencies and Iron Phenotypes in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Ronald T. Acton, Ph.D., Beverly M. Snively, Ph.D., James C. Barton, M.D., Paul C. Adams, M.D., John H. Eckfeldt, M.D., Ph.D., Emily L. Harris, Ph.D., Fitzroy W. Dawkins, M.D., Christine E. McLaren, Ph.D., Victor R. Gordeuk, M.D., Gordon D. McLaren, M.D., David M. Reboussin, Ph.D., Phyliss Sholinsky, M.S.P.H, Mark R. Speechley, Ph.D., Joan Holup, M.A., Cathy Leiendecker-Foster, M.S.

Blood (2004) 104 (11): 3211.

https://doi.org/10.1182/blood.V104.11.3211.3211

Published: 2004

Journal Articles

Mixture distribution analysis of phenotypic markers reflecting HFE gene mutations

Christine E. McLaren, Kuo-Tung Li, Chad P. Garner, Ernest Beutler, Victor R. Gordeuk

Blood (2003) 102 (13): 4563–4566.

https://doi.org/10.1182/blood-2003-04-1278

Published: 2003

Journal Articles

Relationship between transferrin saturation and iron stores in the African American and US Caucasian populations: analysis of data from the third National Health and Nutrition Examination Survey

Christine E. McLaren, Kuo-Tung Li, Victor R. Gordeuk, Victor Hasselblad, Gordon D. McLaren

Blood (2001) 98 (8): 2345–2351.

https://doi.org/10.1182/blood.V98.8.2345

Published: 2001

NARROW

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

Association of GNPAT p.D519G with Higher Iron Phenotypes in Women with HFE p.C282Y Homozygosity

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

Association of Helicobacter Pylori Infection with Iron Deficiency in Asians and Pacific Islanders but not in Caucasians, African Americans, or Hispanics

Identification of Polymorphic Gnpat As a Risk Factor for Porphyria Cutanea Tarda

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

Elevated Transferrin Saturation, Health-Related Quality Of Life and Telomere Length

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

Celiac Disease: Association with Iron Deficiency in Caucasians but Not in Non-Caucasians.

Bivariate Mixture Models of Serum Ferritin and Transferrin Saturation Predict Stable Components Measured 12 Years Apart in a Healthy Australian Population

Associations Between Single Nucleotide Polymorphisms in Iron-Related Genes and Iron Status in Multiethnic Populations

Lack of Association between Single Nucleotide Polymorphism rs3811647 in the TF Gene and Iron Status in Patients with Iron Deficiency and Control Subjects

Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency.

Subpopulations with Iron Deficiency, Liver Disease, or HFE Mutations Revealed by Statistical Mixture Modeling of Transferrin Saturation and Serum Ferritin Concentration in Asians, African Americans, Hispanics, and Whites.

Symptoms and Signs of Hemochromatosis in HFE C282Y Homozygotes Identified by Screening in Primary Care.

Initial Screening Transferrin Saturation Values, Serum Ferritin Concentrations, and HFE Genotypes in Native Americans and Whites in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Initial Screening Transferrin Saturations, Serum Ferritin Concentrations, and HFE Genotypes in Whites and Blacks in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Geographic and Racial/Ethnic Differences in HFE Mutation Frequencies and Iron Phenotypes in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

Mixture distribution analysis of phenotypic markers reflecting HFE gene mutations

Relationship between transferrin saturation and iron stores in the African American and US Caucasian populations: analysis of data from the third National Health and Nutrition Examination Survey

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