J. Barton

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Hemochromatosis: Mathematical models of metal metabolism in hemochromatosis

Keith F. Eckerman, Richard Wayne Leggett, R. Leggett, 2000 .

Tumor necrosis factor-alpha promoter variants and iron phenotypes in 785 hemochromatosis and iron overload screening (HEIRS) study participants.

C. McLaren, J. Barton, J. Eckfeldt, 2010, Blood cells, molecules & diseases.

HFE gene: Structure, function, mutations, and associated iron abnormalities.

J. Barton, R. Acton, C. Edwards, 2015, Gene.

A survey of 2,851 patients with hemochromatosis: symptoms and response to treatment.

R. Yip, J. Barton, P. Adams, 1999, The American journal of medicine.

Patient compliance with phlebotomy therapy for iron overload associated with hemochromatosis

D. Tucker, J. Barton, B. Hicken, 2003, American Journal of Gastroenterology.

Bilateral Subdural Hematomas in an Adult With Hereditary Factor VII Deficiency: A Complication of Sit-ups and Inversion?

J. Barton, L. Bertoli, S. O'malley, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Vibrio vulnificus infection in a hemodialysis patient receiving intravenous iron therapy.

J. Barton, R. Acton, M. T. Reymann, 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Differential staining of neutrophils and monocytes: Surface and cytoplasmic iron-binding proteins

R. Parmley, M. Lilly, J. Barton, 1988, The Histochemical Journal.

Radioimmunometric quantification of surface lactoferrin in blood mononuclear cells.

J. Barton, R. Berkow, T. W. Butler, 1994, The American journal of the medical sciences.

Immunoreactive lactoferrin in resting, activated, and neoplastic lymphocytes.

J. Barton, C. Grossi, V. Pistoia, 1990, Leukemia research.

Neutrophil lactoferrin content: Variation among mammals

R. Parmley, J. Barton, W. Blackburn, 1988, The Anatomical record.

Hemochromatosis and Iron Overload Screening (HEIRS) Study Design for an Evaluation of 100,000 Primary Care-Based Adults

E. Thomson, D. Reboussin, C. McLaren, 2003, The American journal of the medical sciences.

Iron overload and cirrhosis in referred HFE p.C282Y homozygotes with normal transferrin saturation and elevated serum ferritin.

J. Barton, P. Adams, 2020, Canadian liver journal.

Iron overload and cirrhosis in referred HFE p.C282Y homozygotes with normal transferrin saturation and elevated serum ferritin

J. Barton, P. Adams, 2020, Canadian Liver Journal.

Pagophagia in men with iron-deficiency anemia.

J. Barton, L. Bertoli, J. C. Barton, 2019, Blood cells, molecules & diseases.

Common TMPRSS6 mutations and iron, erythrocyte, and pica phenotypes in 48 women with iron deficiency or depletion.

J. Barton, Pauline L. Lee, J. C. Barton, 2012, Blood cells, molecules & diseases.

Pica associated with iron deficiency or depletion: clinical and laboratory correlates in 262 non-pregnant adult outpatients

J. Barton, L. Bertoli, J. C. Barton, 2010, BMC blood disorders.

Enhanced levels of both the membrane-bound and soluble forms of IgM Fc receptor (FcμR) in patients with chronic lymphocytic leukemia.

Randall S. Davis, S. Barnes, J. Barton, 2011, Blood.

Serum ferritin and transferrin saturation in Asians and Pacific Islanders.

D. Reboussin, T. Vogt, B. Snively, 2007, Archives of internal medicine.

Liver diseases in the hemochromatosis and iron overload screening study.

D. Reboussin, E. Harris, S. Chakrabarti, 2006, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Optimal Management Strategies for Chronic Iron Overload

J. Barton, 2012, Drugs.

A comparison between whites and blacks with severe multi-organ iron overload identified in 16,152 autopsies.

C. B. Alexander, J. Barton, R. Acton, 2009, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Drug evaluation: Deferitrin for iron overload disorders.

J. Barton, 2007, IDrugs : the investigational drugs journal.

Inheritance of two HFE mutations in African Americans: Cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency

J. Barton, R. Acton, 2001, Genetics in Medicine.

Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.

D. Reboussin, T. Vogt, B. Snively, 2008, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

Genetic screening for iron overload: No evidence of discrimination at 1 year.

C. McLaren, M. Hall, O. Castro, 2007, The Journal of family practice.

Haemochromatosis

J. Barton, P. Adams, 2007, The Lancet.

Factors affecting iron balance

J. Barton, M. Conrad, 1981, American journal of hematology.

Prevalence and characteristics of anti-HCV positivity and chronic hepatitis C virus infection in HFE p.C282Y homozygotes.

J. Barton, P. Adams, J. C. Barton, 2019, Annals of hepatology.

A rapid PCR-SSP assay for the hemochromatosis-associated Tyr250Stop mutation in the TFR2 gene.

J. Barton, R. Acton, C. Rivers, 2001, Genetic testing.

Cardiac tamponade associated with imatinib mesylate therapy of chronic myelogenous leukemia

Steven C. Jones, J. Barton, W. C. Lamberth, 2002, American journal of hematology.

Population screening for hemochromatosis: has the time finally come?

J. Barton, R. Acton, 2000, Current gastroenterology reports.

Insulin Resistance and Metabolic Syndrome: Clinical and Laboratory Associations in African Americans Without Diabetes in the Hemochromatosis and Iron Overload Screening Study.

J. Barton, R. Acton, J. C. Barton, 2018, Metabolic syndrome and related disorders.

Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study.

D. Reboussin, J. Barton, J. Eckfeldt, 2008, Thyroid : official journal of the American Thyroid Association.

HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity

J. Barton, R. Acton, J. C. Barton, 2022, Hereditas.

HFE C282Y and H63D in adults with malignancies in a community medical oncology practice

J. Barton, R. Acton, L. Bertoli, 2004, BMC Cancer.

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama

J. Barton, R. Acton, 2002, BMC Medical Genetics.

HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.

J. Barton, R. Acton, 2001, Genetic testing.

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis.

J. Barton, R. Acton, B. Rothenberg, 1997, Blood cells, molecules & diseases.

Hemochromatosis: association of severity of iron overload with genetic markers.

J. Barton, R. Acton, L. Harmon, 1996, Blood cells, molecules & diseases.

A survey of phlebotomy among persons with hemochromatosis

A. Grindon, J. Barton, P. Adams, 1999, Transfusion.

Handbook of Iron Overload Disorders: History of iron overload disorders

B. Bacon, R. Britton, J. Barton, 2010 .

Biological variability of transferrin saturation and unsaturated iron-binding capacity.

D. Reboussin, F. Dawkins, J. Barton, 2007, The American journal of medicine.

Hemochromatosis Detection in a Health Screening Program at an Alabama Forest Products Mill

T. Key, J. Barton, R. Acton, 2002, Journal of occupational and environmental medicine.

Diagnosis of hemochromatosis in family members of probands: A comparison of phenotyping and HFE genotyping

J. Barton, R. Acton, B. Rothenberg, 1999, Genetics in Medicine.

Diagnosis of hemochromatosis probands in a community hospital.

J. Barton, N. H. Barton, T. Alford, 1997, The American journal of medicine.

Iron deficiency due to excessive therapeutic phlebotomy in hemochromatosis

J. Barton, S. Bottomley, 2000, American journal of hematology.

Listeria monocytogenes Infection in Hairy Cell Leukemia: A Case Report and Literature Review

J. Barton, Hayward S Edmunds, 2018, Case reports in hematology.

Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study

D. Reboussin, C. McLaren, M. Speechley, 2007, American journal of hematology.

Relationships of serum free thyroxine and erythrocyte measures in euthyroid HFE C282Y homozygotes and control subjects: the HEIRS Study

D. Reboussin, J. Barton, J. Eckfeldt, 2010, International journal of laboratory hematology.

Factors affecting the absorption and excretion of lead in the rat

J. Barton, M. Conrad, 1978 .

Blood lead concentrations in hereditary hemochromatosis.

R. Leggett, M. Patton, J. Barton, 1994, The Journal of laboratory and clinical medicine.

Effects of iron on the absorption and retention of lead.

J. Barton, M. Conrad, S. Nuby, 1978, The Journal of laboratory and clinical medicine.

Modulation of the development of bleomycin-induced fibrosis by deferoxamine.

D. D. Briggs, W. Grizzle, J. Barton, 1988, Toxicology and applied pharmacology.

Calcium inhibition of inorganic iron absorption in rats.

R. Parmley, J. Barton, M. Conrad, 1983, Gastroenterology.

Beneficial effects of hepatitis in patients with acute myelogenous leukemia.

J. Barton, M. Conrad, 1979, Annals of internal medicine.

How I treat hemochromatosis.

J. Barton, P. Adams, 2010, Blood.

A genome‐wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study

B. Snively, S. Rich, M. Speechley, 2007, Clinical genetics.

Ultrastructural localization of lactoferrin and iron-binding protein in human neutrophils and rabbit heterophils.

M. Takagi, J. Barton, L. Boxer, 1982, The American journal of pathology.

HFE hemochromatosis and hepatic sarcoid.

J. Barton, R. Acton, B. Mcguire, 2009, The American journal of the medical sciences.

Differences in Hepatic Phenotype Between Hemochromatosis Patients With HFE C282Y Homozygosity and Other HFE Genotypes

K. Kowdley, J. Barton, S. Gordon, 2009, Journal of clinical gastroenterology.

Urticaria pigmentosa and preleukemia: evidence for reactive mast cell proliferation.

P. Emanuel, J. Barton, W. M. Sams, 1991, Journal of the American Academy of Dermatology.

A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.

J. Barton, P. Adams, 2011, Journal of hepatology.

Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study.

E. Thomson, D. Reboussin, T. Vogt, 2009, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.

D. Reboussin, C. McLaren, M. Speechley, 2007, Genetic testing.

Hemoglobin binding to A beta and HBG2 SNP association suggest a role in Alzheimer's disease.

L. Harrell, W. Hill, A. Kutlar, 2008, Neurobiology of aging.

Hemochromatosis: A brief history of hemochromatosis

J. Barton, 2000 .

Psychosocial impact of genetic testing for hemochromatosis in the HEIRS Study: a comparison of participants recruited in Canada and in the United States.

Roger T. Anderson, J. Barton, A. Walker, 2007, Genetic testing.

Management of hemochromatosis. Hemochromatosis Management Working Group.

J. Cook, P. Brissot, K. Kowdley, 1998, Annals of internal medicine.

Countries of ancestry reported by hemochromatosis probands and control subjects in central Alabama.

J. Barton, R. Acton, E. Barton, 2004, Ethnicity & disease.

Dietary iron intake and serum ferritin concentration in 213 patients homozygous for the HFEC282Y hemochromatosis mutation.

C. McLaren, M. Speechley, E. Harris, 2012, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

Serum ferritin, insulin resistance, and metabolic syndrome: clinical and laboratory associations in 769 non-hispanic whites without diabetes mellitus in the HEIRS study.

J. Barton, R. Acton, J. C. Barton, 2015, Metabolic syndrome and related disorders.

Longer survival associated with HLA‐A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA‐A and ‐B typing and haplotyping 1

J. Barton, R. Acton, J. Clayborn Barton, 2010, European journal of haematology.

Clinical guidelines: HFE hemochromatosis—screening, diagnosis and management

J. Barton, P. Adams, 2010, Nature Reviews Gastroenterology &Hepatology.

Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels.

C. McLaren, J. Barton, Wen‐Pin Chen, 2019, Blood cells, molecules & diseases.

HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high‐performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants

J. Barton, J. Eckfeldt, R. Acton, 2009, American journal of hematology.

Early age‐of‐onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A→T) in an African American male of West Indies descent

J. Barton, P. Lee, M. Kalavar, 2008, Clinical genetics.

Characteristics of participants with self‐reported hemochromatosis or iron overload at HEIRS study initial screening

D. Reboussin, C. McLaren, M. Speechley, 2008, American journal of hematology.

Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population

J. Barton, R. Acton, C. Rivers, 2004, BMC Medical Genetics.

Characteristics of HFE C282Y Homozygotes Younger than Age 30 Years

V. Felitti, J. Barton, E. Beutler, 2004, Acta Haematologica.

Hemojuvelin (HJV) mutations in persons of European, African‐American and Asian ancestry with adult onset haemochromatosis

J. Barton, E. Beutler, Pauline L. Lee, 2004, British journal of haematology.

Chelation therapy for iron overload

J. Barton, 2007, Nutrition reviews.

Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload.

J. Barton, R. Acton, E. Barton, 2001, Blood Cells, Molecules & Diseases.

Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama.

J. Barton, R. Acton, 2000, Genetic testing.

Abdominal pain and cirrhosis at diagnosis of hemochromatosis: Analysis of 219 referred probands with HFE p.C282Y homozygosity and a literature review

J. Barton, G. McLaren, J. C. Barton, 2021, PloS one.

Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes.

M. Emond, C. McLaren, L. Gurrin, 2018, Annals of hepatology.

Management of Hemochromatosis

James Barton, J. Cook, P. Brissot, 1998, Annals of Internal Medicine.

Increased risk of death from iron overload among 422 treated probands with HFE hemochromatosis and serum levels of ferritin greater than 1000 μg/L at diagnosis.

J. Barton, R. Acton, P. Adams, 2012, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Accuracy of family history of hemochromatosis or iron overload: the hemochromatosis and iron overload screening study.

B. Snively, C. McLaren, M. Speechley, 2008, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Remission of porphyria cutanea tarda after anastrozole treatment of breast cancer.

J. Barton, L. Bertoli, 2007, Clinical breast cancer.

Disparate phenotypic expression of ALAS2 R452H (nt 1407 G --> A) in two brothers, one with severe sideroblastic anemia and iron overload, hepatic cirrhosis, and hepatocellular carcinoma.

J. Barton, Pauline L. Lee, 2006, Blood cells, molecules & diseases.

Three kinships with ALAS2 P520L (c. 1559 C --> T) mutation, two in association with severe iron overload, and one with sideroblastic anemia and severe iron overload.

J. Barton, E. Beutler, R. Acton, 2006, Blood cells, molecules & diseases.

Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

B. Snively, C. McLaren, M. Speechley, 2006, Ethnicity & disease.

Phlebotomy-Mobilized Iron as a Surrogate for Liver Iron Content in Hemochromatosis Patients

J. Barton, P. Phatak, 2003, Hematology.

Common variable immunodeficiency and IgG subclass deficiency in central Alabama hemochromatosis probands homozygous for HFE C282Y.

J. Barton, R. Acton, L. Bertoli, 2003, Blood cells, molecules & diseases.

Hemochromatosis and iron therapy of Restless Legs Syndrome.

J. Barton, V. Wooten, R. Acton, 2001, Sleep medicine.

Severity of iron overload in hemochromatosis: effect of volunteer blood donation before diagnosis

J. Barton, B. Rothenberg, S. McDonnell, 2001, Transfusion.

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.

J. Barton, R. Acton, B. Rothenberg, 1999, Blood cells, molecules & diseases.

Normal transferrin saturation in hemochromatosis.

J. Barton, M. Janich, L. Bertoli, 1991, Hospital practice.

Anemia and iron kinetics in alcoholism.

J. Barton, M. Conrad, 1980, Seminars in hematology.

Serial serum ferritin measurements in untreated HFE C282Y homozygotes in the Hemochromatosis and Iron Overload Screening Study

D. Reboussin, C. McLaren, M. Speechley, 2008, International journal of laboratory hematology.

iver Diseases in the Hemochromatosis and Iron Overload creening Study

D. Reboussin, E. Harris, S. Chakrabarti, 2006 .

Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome.

J. Barton, E. Beutler, T. Gelbart, 1998, Blood.

Mild Iron Overload in an African American Man with SLC40A1 D270V

T. Gaasterland, J. Barton, Pauline L. Lee, 2012, Acta Haematologica.

SLC40A1 c.1402G→A Results in Aberrant Splicing, Ferroportin Truncation after Glycine 330, and an Autosomal Dominant Hemochromatosis Phenotype

J. Barton, Pauline L. Lee, C. West, 2007, Acta Haematologica.

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans.

C. Vulpe, V. Felitti, J. Barton, 2003, Blood cells, molecules & diseases.

Organ retention and excretion of radiolead administered intravenously in rats: A Comparison of erythrocyte‐ and plasma‐associated lead

J. Barton, M. Conrad, 2001 .

Hemochromatosis: The genetic disorder of the twenty–first century

J. Barton, L. Bertoli, 1996, Nature Network Boston.

Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary‐care population

D. Reboussin, C. McLaren, M. Speechley, 2008, American journal of hematology.

Effect of iron deficiency on bleomycin-induced lung fibrosis in the hamster.

D. D. Briggs, J. I. Kennedy, W. Grizzle, 1988, The American review of respiratory disease.

Hepatic Iron in African Americans Who Underwent Liver Biopsy

J. Barton, C. Edwards, L. Bertoli, 2014, The American journal of the medical sciences.

Diabetes in firstdegree family members: a predictor of type 2 diabetes in 159 non screening Alabama hemochromatosis probands with HFE C282Y homozygosity Running head: Diabetes, family history, and hemochromatosis

J. Barton, R. Acton, J. C. Barton, 2013 .

Association of ferroportin Q248H polymorphism with elevated levels of serum ferritin in African Americans in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.

D. Reboussin, B. Snively, C. McLaren, 2007, Blood cells, molecules & diseases.

IRON OVERLOAD IN BLOOD DONORS WITH HEMOCHROMATOSIS

J. Barton, B. Rothenberg, S. McDonnell, 2002 .

Screening for hemochromatosis in routine medical care: an evaluation of mean corpuscular volume and mean corpuscular hemoglobin.

J. Barton, B. Rothenberg, L. Bertoli, 2000, Genetic testing.

Proton Pump Inhibitors and Lower Serum Ferritin Levels in 171 HFE C282Y Homozygotes in the Hemochromatosis and Iron Overload Screening Study

C. McLaren, M. Speechley, J. Barton, 2013 .

Effects of Highly Conserved Major Histocompatibility Complex (MHC) Extended Haplotypes on Iron and Low CD8+ T Lymphocyte Phenotypes in HFE C282Y Homozygous Hemochromatosis Patients from Three Geographically Distant Areas

C. Vieira, J. Barton, B. M. da Silva, 2013, PloS one.

Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders Dupuytren's Contracture in Alabama Hfe Hemochromatosis Probands

J. Barton, Barton, J. C. Barton, 2022 .

Hemochromatosis and Severe Iron Overload Associated with Compound Heterozygosity for TFR2 R455Q and Two Novel Mutations TFR2 R396X and G792R

J. Barton, Pauline L. Lee, 2006, Acta Haematologica.

Hemochromatosis, HFE C282Y Homozygosity, and Bariatric Surgery: Report of Three Cases

J. Barton, 2004, Obesity surgery.

Attitudes about and psychosocial outcomes of HFE genotyping for hemochromatosis.

D. Tucker, D. Calhoun, J. Barton, 2004, Genetic testing.

HLA-A and -B alleles and haplotypes in 240 index patients with common variable immunodeficiency and selective IgG subclass deficiency in central Alabama

J. Barton, R. Acton, L. Bertoli, 2003, BMC Medical Genetics.

Abnormalities of flavin monooxygenase as an etiology for sideroblastic anemia

J. Barton, M. Conrad, J. Umbreit, 2000, American journal of hematology.

Acute lymphoblastic leukemia in idiopathic refractory sideroblastic anemia: Evidence for a common lymphoid and myeloid progenitor cell

J. Barton, M. Conrad, R. Parmley, 1980, American journal of hematology.

Ultrastructural silver enhancement of Prussian blue-reactive iron in hematopoietic and intestinal cells.

R. Parmley, J. Barton, D. White, 1988, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Ultrastructural cytochemistry of iron absorption.

R. Parmley, J. Barton, M. Conrad, 1978, The American journal of pathology.

GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.

M. Emond, C. McLaren, L. Gurrin, 2016, Blood cells, molecules & diseases.

Total blood lymphocyte counts in hemochromatosis probands with HFE C282Y homozygosity: relationship to severity of iron overload and HLA-A and -B alleles and haplotypes

R. Go, J. Barton, R. Acton, 2005, BMC blood disorders.

Vibrio vulnificus Bacteremia Associated with Chronic Lymphocytic Leukemia, Hypogammaglobulinemia, and Hepatic Cirrhosis: Relation to Host and Exposure Factors in 252 V. Vulnificus Infections Reported in Louisiana

J. Barton, R. Ratard, 2006, The American journal of the medical sciences.

Hemochromatosis and Vibrio vulnificus Wound Infections

J. Barton, R. Acton, 2009, Journal of clinical gastroenterology.

Iron overload and prolonged ingestion of iron supplements: Clinical features and mutation analysis of hemochromatosis‐associated genes in four cases

J. Barton, Pauline L. Lee, C. West, 2006, American journal of hematology.

Recurrent acute kidney injury associated with metastatic bronchial carcinoid.

J. Barton, L. Bertoli, J. C. Barton, 2012, The American journal of the medical sciences.

HAMP promoter mutation nc.-153C>T in 785 HEIRS Study participants

J. Barton, J. Eckfeldt, R. Acton, 2009, Haematologica.

Chromosome 6p SNP microhaplotypes and IgG3 levels in hemochromatosis probands with HFE p.C282Y homozygosity.

J. Barton, J. Guimarães, G. Porto, 2019, Blood cells, molecules & diseases.

WITHDRAWN: Chromosome 6p SNP microhaplotypes and IgG3 levels in hemochromatosis probands with HFE p.C282Y homozygosity

J. Barton, J. Guimarães, G. Porto, 2019, Blood Cells, Molecules, and Diseases.

Comparisons of CVID and IgGSD: Referring Physicians, Autoimmune Conditions, Pneumovax Reactivity, Immunoglobulin Levels, Blood Lymphocyte Subsets, and HLA-A and -B Typing in 432 Adult Index Patients

J. Barton, L. Bertoli, J. C. Barton, 2014, Journal of immunology research.

How I treat hemochromatosis.

J. Barton, P. Adams, 2010, Blood.

Heme carrier protein 1 (HCP1) genetic variants in the Hemochromatosis and Iron Overload Screening (HEIRS) Study participants.

C. McLaren, Xinjing Wang, J. Barton, 2009, Blood cells, molecules & diseases.

Iron overload in an African American woman with SS hemoglobinopathy and a promoter mutation in the X-linked erythroid-specific 5-aminolevulinate synthase (ALAS2) gene.

J. Barton, E. Beutler, Pauline L. Lee, 2004, Blood cells, molecules & diseases.

Peroxidase-containing microgranules in human neutrophils: physical, morphological, cytochemical, and secretory properties.

R. Parmley, J. Barton, W. Rice, 1987, Blood.

Cytochemistry and ultrastructural morphometry of cultured HL60 myeloid leukemia cells.

R. Parmley, J. Barton, J. M. Kinkade, 1987, Cancer research.

Ultrastructural morphology and cytochemistry of iron-deficient polymorphonuclear leukocytes.

R. Parmley, J. Barton, L. Boxer, 1986, Experimental and molecular pathology.

Ultrastructural localization of transferrin, transferrin receptor, and iron‐binding sites on human placental and duodenal microvilli

J. Barton, M. Conrad, R. Parmley, 1985, British journal of haematology.

Ultrastructural cytochemistry and radioautography of hemoglobin--iron absorption.

R. Parmley, J. Barton, M. Conrad, 1981, Experimental and molecular pathology.

Ultrastructural cytochemical identification of the siderophilic enterocyte.

R. Parmley, J. Barton, M. Conrad, 1984, Journal of Histochemistry and Cytochemistry.

Case Report: Neoplastic Meningitis with Eosinophilic Pleocytosis in Hodgkin’s Disease: A Case with Cerebellar Dysfunction and a Review of the Literature

J. Barton, C. Grossi, F. Griffin, 1988 .

Light Micnoscopic, Non-Immunologic Demonstnation of mon-Binding Proteins in Hematopoietic Cells1

R. Parmley, J. Barton, 1986 .

Serum ferritin is a biomarker for liver mortality in the Hemochromatosis and Iron Overload Screening Study.

M. Speechley, D. Alter, J. Barton, 2015, Annals of hepatology.

Implanted Central Venous Access Ports for Therapeutic Phlebotomy in Patients with HFE Hemochromatosis and other Non-thalassemia Iron Overload Disorders

J. Barton, J. C. Barton, J. Barton, 2014, The journal of vascular access.

Effects of Ethanol on the Absorption and Retention of Lead

J. Barton, M. Conrad, 1978, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

The mitochondrial nt 16189 polymorphism and hereditary hemochromatosis.

J. Barton, E. Beutler, Pauline L. Lee, 2004, Blood Cells, Molecules & Diseases.

Ferritin >1000: grand for hemochromatosis screening?

J. Barton, 2008 .

Hemochromatosis, HFE C282Y Homozygosity, and Polycystic Ovary Syndrome: Report of Two Cases and Possible Effects of Androgens and Hepcidin

J. Barton, J. C. Barton, 2011, Acta Haematologica.

Hypogonadotrophic hypogonadism due to intrasellar hemangioblastoma in von Hippel–Lindau syndrome

A. Santani, J. Barton, C. Stolle, 2009, American journal of medical genetics. Part A.

HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.

C. McLaren, M. Speechley, J. Barton, 2013, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

The aplastic anemia‐paroxysmal nocturnal hemoglobinuria syndrome

J. Barton, M. Conrad, 1979, American journal of hematology.

Polycythemia Rubra Vera and Sporadic Bilateral Renal Angiomyolipomas: A Case Report

R. Frederickson, J. Barton, Barrett P. Cary, 2022, Cureus.

Immune thrombocytopenia: effects of maternal gamma globulin infusion on maternal and fetal serum, platelet, and monocyte IgG.

J. Barton, A. Lobuglio, M. Saleh, 1987, The American journal of the medical sciences.

Sideroblastic anemia, iron overload, and ALAS2 R452S in African‐American males: Phenotype and genotype features of five unrelated patients

J. Barton, Pauline L. Lee, T. Reid, 2011, American journal of hematology.

Handbook of Iron Overload Disorders: Hemochromatosis associated with ferroportin gene ( SLC40A1 ) mutations

B. Bacon, R. Britton, J. Barton, 2010 .

Multi-Organ Iron Overload in an African-American Man with ALAS2 R452S and SLC40A1 R561G

J. Barton, M. Schwartz, N. Sussman, 2008, Acta Haematologica.

Autoimmune Conditions in 235 Hemochromatosis Probands with HFE C282Y Homozygosity and Their First-Degree Relatives

J. Barton, J. C. Barton, J. Barton, 2015, Journal of immunology research.

Mixture models of serum iron measures in population screening for hemochromatosis and iron overload.

D. Reboussin, B. Snively, C. McLaren, 2006, Translational research : the journal of laboratory and clinical medicine.

White blood cells and subtypes in HFE p.C282Y and wild-type homozygotes in the Hemochromatosis and Iron Overload Screening Study.

J. Barton, R. Acton, J. C. Barton, 2017, Blood cells, molecules & diseases.

Angioedema associated with imiquimod.

J. Barton, 2004, Journal of the American Academy of Dermatology.

Pseudochloroma: Extramedullar Hematopoietic Nodules in Chronic Myelogenous Leukemia

J. Barton, M. Poon, M. Conrad, 1979 .

Pseudochloroma: extramedullary hematopoietic nodules in chronic myelogenous leukemia.

J. Barton, M. Poon, M. Conrad, 1979, Annals of internal medicine.

Hepcidin, iron, and bacterial infection.

J. Barton, R. Acton, 2019, Vitamins and hormones.

Ancestry reported by white adults with cutaneous melanoma and control subjects in central Alabama

R. Go, J. Barton, R. Acton, 2004, BMC Cancer.

Bone metastases in malignant gastrinoma.

R. Jensen, J. Barton, B. Hirschowitz, 1986, Gastroenterology.

Ultrastructural, cytochemical, and radioautographic localization of placental iron.

R. Parmley, J. Barton, M. Conrad, 1981, The American journal of pathology.

Effect of phosphate on the absorption and retention of lead in the rat.

J. Barton, M. Conrad, 1981, The American journal of clinical nutrition.

Hemoglobin, Iron, and Bilirubin

T. Higgins, J. Barton, J. Eckfeldt, 2012 .

Isolated marrow lymphoma: An entity of possible T‐cell derivation

J. Barton, M. Conrad, L. Vogler, 1980, Cancer.

Serum Ferritin Level Predicts Advanced Hepatic Fibrosis among U.S. Patients with Phenotypic Hemochromatosis

H. El‐Serag, K. Kowdley, J. Barton, 2003, Annals of Internal Medicine.

Hemoglobin binding to Aβ and HBG2 SNP association suggest a role in Alzheimer's disease

L. Harrell, W. Hill, A. Kutlar, 2008, Neurobiology of Aging.

Current status of blastic transformation in chronic myelogenous leukemia

J. Barton, M. Conrad, 1978, American journal of hematology.

Tumor lysis syndrome in nonhematopoietic neoplasms

J. Barton, 1989, Cancer.

Genetic Testing for Disorders of Iron Homeostasis

J. Barton, Pauline L. Lee, C. Edwards, 2012 .

Acute kidney injury manifesting as renal tubular acidosis with proximal and distal renal tubular dysfunction in a dog with acute pancreatitis

J. Barton, Erin M O’Connell, Peter-John Mäntylä Noble, 2022, Journal of veterinary emergency and critical care.

Neoplastic meningitis with eosinophilic pleocytosis in Hodgkin's disease: a case with cerebellar dysfunction and a review of the literature.

J. Barton, C. Grossi, F. Griffin, 1988, The American journal of the medical sciences.

TARGET CELLS AND MOLECULAR REQUIREMENTS

J. Barton, R. Schrohenloher, W. Koopman, 1983 .

Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin.

J. Barton, E. Beutler, Pauline L. Lee, 2004, Blood.

African-centric TP53 variant increases iron accumulation and bacterial pathogenesis but improves response to malaria toxin

M. Murphy, D. George, A. Kossenkov, 2020, Nature Communications.

Hemochromatosis and iron overload: from bench to clinic.

J. Barton, 2013, The American journal of the medical sciences.

Iron overload in sideroblastic and other nonthalassemic anemias

J. Barton, S. Bottomley, C. Edwards, 2000 .

Genotypic and phenotypic heterogeneity of African Americans with primary iron overload.

J. Barton, E. Beutler, R. Acton, 2003, Blood cells, molecules & diseases.

Preleukemia in Fanconi's anemia: hematopoietic cell multinuclearity, membrane duplication, and dysgranulogenesis.

H. Findley, A. Carroll, J. Barton, 1987, Journal of submicroscopic cytology.

Hemochromatosis and iron-overload screening in a racially diverse population.

E. Thomson, D. Reboussin, B. Snively, 2005, The New England journal of medicine.

Concerns in a primary care population about genetic discrimination by insurers

E. Thomson, J. Mcewen, D. Tucker, 2005, Genetics in Medicine.

HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.

R. Go, J. Barton, R. Acton, 2005, Blood cells, molecules & diseases.

Isolated chylopericardium associated with lymphoma.

J. Barton, J. Durant, 1980, Southern medical journal.

Hereditary hemochromatosis: gene discovery and its implications for population-based screening.

F. Collins, E. Thomson, E. Clayton, 1998, JAMA.

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study

B. Snively, C. McLaren, Emily L. Harris, 2010, American journal of hematology.

Hemochromatosis : genetics, pathophysiology, diagnosis, and treatment

J. Barton, James C. Barton, Corwin Q. Edwards, 2000 .

Juvenile hemochromatosis in the southeastern United States: a report of seven cases in two kinships.

J. Barton, E. Beutler, R. Acton, 2002, Blood cells, molecules & diseases.

Estimates of European American Ancestry in African Americans Using HFE p.C282Y.

J. Barton, R. Acton, H. Wiener, 2020, Genetic testing and molecular biomarkers.

HFE mutations in African-American women with non-insulin-dependent diabetes mellitus.

J. Roseman, R. Go, J. Barton, 2001, Ethnicity & disease.

Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload

D. Nickerson, M. Emond, C. McLaren, 2015, Hepatology.

Coagulation testing of Hickman catheter blood in patients with acute leukemia.

J. Barton, M. Poon, 1986, Archives of internal medicine.

Blastic transformation of essential thrombocythemia: dual expression of myelomonoblastic/megakaryoblastic phenotypes.

R. Hoffman, J. Prchal, J. Barton, 1984, Blood.

Effects of calcium on the absorption and retention of lead.

J. Barton, M. Conrad, S. Nuby, 1978, The Journal of laboratory and clinical medicine.

Malignant hemangiopericytoma: computed tomography and magnetic resonance imaging.

R. Koehler, R. Stanley, J. Barton, 1987, The Journal of computed tomography.

Thalidomide and dexamethasone therapy of myeloma in a patient with previously untreated B‐chronic lymphocytic leukemia

J. Barton, 2003, American journal of hematology.

Assessment of total immunoreactive lactoferrin in hematopoietic cells using flow cytometry.

J. Barton, C. Grossi, T. W. Butler, 1988, Journal of immunological methods.

Thrombotic thrombocytopenic purpura in systemic sclerosis.

G. Alarcón, J. Barton, W. Blackburn, 1989, The Journal of rheumatology.

Iron, Lead, and Cobalt Absorption: Similarities and Dissimilarities 1

R. Holland, J. Barton, M. Conrad, 1981, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

ECTOPIC PELVIC KIDNEY

J. Barton, G. J. Thomas, 1936 .

Prevalence of iron deficiency in 62,685 women of seven race/ethnicity groups: The HEIRS Study

D. Reboussin, C. McLaren, E. Harris, 2020, PloS one.

HFE C282Y Homozygosity Is Associated With Lower Total and Low-Density Lipoprotein Cholesterol: The Hemochromatosis and Iron Overload Screening Study

J. Pankow, M. Speechley, J. Barton, 2009, Circulation. Cardiovascular genetics.

Diabetes in HFE Hemochromatosis

J. Barton, R. Acton, 2017, Journal of diabetes research.

Effect of Native American ancestry on iron-related phenotypes of Alabama hemochromatosis probands with HFE C282Y homozygosity

James C Barton, J. Barton, R. Acton, 2006, BMC Medical Genetics.

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in whites and blacks in the Hemochromatosis and Iron Overload Screening Study.

D. Reboussin, C. McLaren, M. Speechley, 2005, Genetic testing.

Handbook of Iron Overload Disorders

B. Bacon, R. Britton, J. Barton, 2010 .

Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study.

D. Reboussin, T. Vogt, M. Speechley, 2005, Diabetes care.

Provoked priapism in sickle cell anemia

J. Barton, J. Durant, M. Conrad, 1980, American journal of hematology.

Retention of radiolead by human erythrocytes in vitro.

J. Barton, 1989, Toxicology and applied pharmacology.

Suppression of in vitro monoclonal human rheumatoid factor synthesis by antiidiotypic antibody. Target cells and molecular requirements.

J. Barton, R. Schrohenloher, W. Koopman, 1983, The Journal of clinical investigation.

Intravenous Bevacizumab Therapy in a Patient with Hereditary Hemorrhagic Telangiectasia, ENG E137K, Alcoholic Cirrhosis, and Portal Hypertension

J. Barton, Pauline L. Lee, L. Bertoli, 2017, Case Reports in Gastroenterology.

Comparison of the unsaturated iron-binding capacity with transferrin saturation as a screening test to detect C282Y homozygotes for hemochromatosis in 101,168 participants in the hemochromatosis and iron overload screening (HEIRS) study.

D. Reboussin, C. McLaren, E. Harris, 2005, Clinical chemistry.

Neutrophil function in chronic neutrophilic leukemia: defective respiratory burst in response to phorbol esters.

J. Barton, R. Berkow, R. Joyce, 1992, Acta haematologica.

SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent.

J. Barton, R. Acton, Pauline L. Lee, 2007, Blood cells, molecules & diseases.

Stainable hepatic iron in 341 African American adults at coroner/medical examiner autopsy

J. Barton, R. Acton, R. Brissie, 2005, BMC clinical pathology.

Factors affecting the absorption and excretion of lead in the rat.

J. Barton, M. Conrad, 1978, Gastroenterology.

Ultrastructural radioautography and cytochemistry of lead absorption.

R. Parmley, J. Barton, M. Conrad, 1979, American Journal of Pathology.

Effects of vitamin D on the absorption and retention of lead.

J. Barton, J C Barton, M E Conrad, 1980, The American journal of physiology.

Bivariate Mixture Modeling of Transferrin Saturation and Serum Ferritin Concentration in Asians, African Americans, Hispanics, and Whites in the Hemochromatosis and Iron Overload Screening (heirs) Study Bivariate Mixture Modeling Was Used to Analyze Joint Population Distributions of Transferrin Satu

G. McLachlan, D. Reboussin, B. Snively, 2022 .

Potential nonresponse bias in a clinical examination after initial screening using iron phenotyping and HFE genotyping in the hemochromatosis and iron overload screening study.

D. Reboussin, M. Speechley, E. Harris, 2009, Genetic testing and molecular biomarkers.

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

D. Reboussin, C. McLaren, M. Speechley, 2004 .

HFE hemochromatosis in African Americans: prevalence estimates of iron overload and iron overload-related disease.

J. Barton, R. Acton, C. Edwards, 2022, The American journal of the medical sciences.

Drug evaluation: deferitrin (GT-56-252; NaHBED) for iron overload disorders.

J. Barton, 2007, IDrugs : the investigational drugs journal.

Handbook of Iron Overload Disorders: Pearson marrow–pancreas syndrome

B. Bacon, R. Britton, J. Barton, 2010 .

M. Emond, C. McLaren, L. Gurrin, 2015 .

Insurance, employment, and psychosocial consequences of a diagnosis of hereditary hemochromatosis in subjects without end organ damage

Christopher F. Martin, R. Sandler, B. Bacon, 2003, American Journal of Gastroenterology.

Reply:

M. Emond, C. McLaren, L. Gurrin, 2017, Hepatology.

Reply to HEP 16‐0784.R1 and HEP 16‐0898

M. Emond, C. McLaren, L. Gurrin, 2016 .

Reply to: GNPAT variant is associated with iron phenotype in healthy Taiwanese women: A population without the HFE C282Y mutation

M. Emond, C. McLaren, L. Gurrin, 2016 .

Study Site Differences in GNPAT p.D519G (rs11558492) Allele Frequencies in Men with HFE Homozygosity

M. Emond, C. McLaren, L. Gurrin, 2015 .

Probability of C282Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the hemochromatosis and iron overload screening study

C. McLaren, M. Speechley, J. Barton, 2012, Hepatology.

African Americans at risk for increased iron stores or liver disease.

E. Thomson, B. Snively, C. McLaren, 2007, The American journal of medicine.

Probability of C 282 Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the HEIRS Study

C. McLaren, M. Speechley, J. Barton, 2012 .

Survey of physician knowledge about hemochromatosis

J. Barton, R. Acton, L. Casebeer, 2002, Genetics in Medicine.

Porphyria cutanea tarda associated with HFE C282Y homozygosity, iron overload, and use of a contraceptive vaginal ring

J. Barton, C. Edwards, 2016, Journal of community hospital internal medicine perspectives.

African-centric TP53 variant increases iron accumulation and bacterial pathogenesis but improves response to malaria toxin

M. Murphy, D. George, A. Kossenkov, 2020, Nature Communications.

Handbook of Iron Overload Disorders: Complications of hemochromatosis and iron overload

B. Bacon, R. Britton, J. Barton, 2010 .

Should we treat individuals homozygous for HFE p.Cys282Tyr with ferritin 300-1000 μg/L?

J. Barton, 2017, The Lancet Haematology.

Handbook of Iron Overload Disorders: Iron overload associated with thalassemia syndromes

B. Bacon, R. Britton, J. Barton, 2010 .

Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study

B. Snively, C. McLaren, Emily L. Harris, 2010, American journal of hematology.

Haemochromatosis

J. Barton, Paul C. Adams, 2007, The Lancet.

HFE gene: Structure, function, mutations, and associated iron abnormalities.

J. Barton, R. Acton, C. Edwards, 2015, Gene.

Handbook of Iron Overload Disorders: Hereditary atransferrinemia

B. Bacon, R. Britton, J. Barton, 2010 .

Multi-Organ Iron Overload in an African-American Man with ALAS2 R452S and SLC40A1 R561G

J. Barton, M. Schwartz, N. Sussman, 2008, Acta Haematologica.

Stainable hepatic iron in 341 African American adults at coroner/medical examiner autopsy

J. Barton, R. Acton, A. K. Richardson, 2005, BMC clinical pathology.

Heritability of Iron Status Phenotype in the Hemochromatosis and Iron Overload Screening (HEIRS) Family Study

B. Snively, C. McLaren, C. Vulpe, 2008 .

Survey of physician knowledge about

J. Barton, L. Casebeer, T. Acton, 2002 .

A diagnostic approach to hyperferritinemia with a non-elevated transferrin saturation.

J. Barton, P. Adams, 2011, Journal of hepatology.

Handbook of Iron Overload Disorders: Hereditary atransferrinemia

B. Bacon, R. Britton, J. Barton, 2010 .

Purification and characterization of sideroblasts from patients with acquired and hereditary sideroblastic anaemia

J. Nieva, A. Saven, J. Prchal, 2008, British journal of haematology.