Prevalence of iron deficiency in 62,685 women of seven race/ethnicity groups: The HEIRS Study von Barton, James C, Wiener, Howard H, Acton, Ronald T, Adams, Paul C, Eckfeldt, John H, Gordeuk, Victor R, Harris, Emily L, McLaren, Christine E, Harrison, Helen, McLaren, Gordon D, Reboussin, David M

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Abdominal pain and cirrhosis at diagnosis of hemochromatosis: Analysis of 219 referred probands with HFE p.C282Y homozygosity and a literature review von Barton, James C, Barton, J Clayborn, Patel, Neha, McLaren, Gordon D

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Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations von McLaren, Christine E, McLachlan, Stela, Garner, Chad P, Vulpe, Chris D, Gordeuk, Victor R, Eckfeldt, John H, Adams, Paul C, Acton, Ronald T, Murray, Joseph A, Leiendecker-Foster, Catherine, Snively, Beverly M, Barcellos, Lisa F, Cook, James D, McLaren, Gordon D

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Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes von Barton, James C, McLaren, Christine E, Chen, Wen-pin, Ramm, Grant A, Anderson, Gregory J, Powell, Lawrie W, Subramaniam, V. Nathan, Adams, Paul C, Phatak, Pradyumna D, Gurrin, Lyle C, Phillips, John D, Parker, Charles J, Emond, Mary J, McLaren, Gordon D

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The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda von Farrell, Colin P, Overbey, Jessica R, Naik, Hetanshi, Nance, Danielle, McLaren, Gordon D, McLaren, Christine E, Zhou, Luming, Desnick, Robert J, Parker, Charles J, Phillips, John D

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Biological Variability of Transferrin Saturation and Unsaturated Iron-Binding Capacity von Adams, Paul C., MD, Reboussin, David M., PhD, Press, Richard D., MD, Barton, James C., MD, Acton, Ronald T., PhD, Moses, Godfrey C., PhD, Leiendecker-Foster, Catherine, MS, McLaren, Gordon D., MD, Dawkins, Fitzroy W., MD, Gordeuk, Victor R., MD, Lovato, Laura, MS, Eckfeldt, John H., MD, PhD

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Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study von McLaren, Gordon D, Gordeuk, Victor R

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Randomized Trial of Physician Alerts for Thromboprophylaxis after Discharge von Piazza, Gregory, MD, MS, Anderson, Frederick A., PhD, Ortel, Thomas L., MD, PhD, Cox, Michael J., MD, Rosenberg, David J., MD, Rahimian, Shahram, MD, Pendergast, William J., MD, McLaren, Gordon D., MD, Welker, James A., DO, Akus, Jan J., MD, Stevens, Scott M., MD, Elliott, C. Gregory, MD, Freeman, Andrew L., MD, Patton, William F., MD, Dabbagh, Ousama, MD, Wyman, Allison, MS, Huang, Wei, MS, Rao, Amanda F., BS, Goldhaber, Samuel Z., MD

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HFE Mutations in Caucasian Participants of the Hemochromatosis and Iron Overload Screening Study with Serum Ferritin Level <1000 μg/L von Adams, Paul C, McLaren, Christine E, Speechley, Mark, McLaren, Gordon D, Barton, James C, Eckfeldt, John H

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Relationships of Serum Ferritin, Transferrin Saturation, and HFE Mutations and Self-Reported Diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) Study von Acton, Ronald T, Barton, James C, Passmore, Leah V, Adams, Paul C, Speechley, Mark R, Dawkins, Fitzroy W, Sholinsky, Phyliss, Reboussin, David M, McLaren, Gordon D, Harris, Emily L, Bent, Thomas C, Vogt, Thomas M, Castro, Oswaldo

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Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload von McLaren, Christine E., Emond, Mary J., Subramaniam, V. Nathan, Phatak, Pradyumna D., Barton, James C., Adams, Paul C., Goh, Justin B., McDonald, Cameron J., Powell, Lawrie W., Gurrin, Lyle C., Allen, Katrina J., Nickerson, Deborah A., Louie, Tin, Ramm, Grant A., Anderson, Gregory J., McLaren, Gordon D.

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Measurement of sulfur-containing compounds involved in the metabolism and transport of cysteamine and cystamine. Regional differences in cerebral metabolism von Pinto, John T., Khomenko, Tetyana, Szabo, Sandor, McLaren, Gordon D., Denton, Travis T., Krasnikov, Boris F., Jeitner, Thomas M., Cooper, Arthur J.L.

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Iron absorption and metabolism von Anderson, Gregory J, Frazer, David M, McLaren, Gordon D

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Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels von Secondes, Eriza S., Wallace, Daniel F., Rishi, Gautam, McLaren, Gordon D., McLaren, Christine E., Chen, Wen-Pin, Ramm, Louise E., Powell, Lawrie W., Ramm, Grant A., Barton, James C., Subramaniam, V. Nathan

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Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study von Adams, Paul, Barton, James C, McLaren, Gordon D, Acton, Ronald T, Speechley, Mark, McLaren, Christine E, Reboussin, David M, Leiendecker-Foster, Catherine, Harris, Emily L, Snively, Beverly M, Vogt, Thomas, Sholinsky, Phyliss, Thomson, Elizabeth, Dawkins, Fitzroy W, Gordeuk, Victor R, Eckfeldt, John H

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Genome-wide association study identifies genetic loci associated with iron deficiency von McLaren, Christine E, Garner, Chad P, Constantine, Clare C, McLachlan, Stela, Vulpe, Chris D, Snively, Beverly M, Gordeuk, Victor R, Nickerson, Debbie A, Cook, James D, Leiendecker-Foster, Catherine, Beckman, Kenneth B, Eckfeldt, John H, Barcellos, Lisa F, Murray, Joseph A, Adams, Paul C, Acton, Ronald T, Killeen, Anthony A, McLaren, Gordon D

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A phase 1/2, dose‐escalation trial of deferasirox for the treatment of iron overload in HFE‐related hereditary hemochromatosis von Phatak, Pradyumna, Brissot, Pierre, Wurster, Mark, Adams, Paul C, Bonkovsky, Herbert L., Gross, John, Malfertheiner, Peter, McLaren, Gordon D., Niederau, Claus, Piperno, Alberto, Powell, Lawrie W., Russo, Mark W., Stoelzel, Ulrich, Stremmel, Wolfgang, Griffel, Louis, Lynch, Nicola, Zhang, Yiyun, Pietrangelo, Antonello

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Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study von McLaren, Christine E., Barton, James C., Eckfeldt, John H., McLaren, Gordon D., Acton, Ronald T., Adams, Paul C., Henkin, Leora F., Gordeuk, Victor R., Vulpe, Chris D., Harris, Emily L., Harrison, Barbara W., Reiss, Jacob A., Snively, Beverly M.

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Stimulated erythropoiesis with secondary iron loading leads to a decrease in hepcidin despite an increase in bone morphogenetic protein 6 expression von Frazer, David M., Wilkins, Sarah J., Darshan, Deepak, Badrick, Alison C., McLaren, Gordon D., Anderson, Gregory J.

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Association Between Celiac Disease and Iron Deficiency in Caucasians, but Not Non-Caucasians von Murray, Joseph A, McLachlan, Stela, Adams, Paul C, Eckfeldt, John H, Garner, Chad P, Vulpe, Chris D, Gordeuk, Victor R, Brantner, Tricia, Leiendecker–Foster, Catherine, Killeen, Anthony A, Acton, Ronald T, Barcellos, Lisa F, Nickerson, Debbie A, Beckman, Kenneth B, McLaren, Gordon D, McLaren, Christine E

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