R. Acton

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

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.

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.

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

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

Association of a 9.2-kilobase Pvu II class I major histocompatibility complex restriction fragment length polymorphism with ankylosing spondylitis.

J. Reveille, B. Barger, R. Acton, 1987, Arthritis and rheumatism.

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.

frican Americans at Risk for Increased Iron Stores r Liver Disease

B. Snively, M. Speechley, E. Harris, 2007 .

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.

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

B. Snively, C. McLaren, J. Murray, 2011, PloS one.

HLA antigens and gold toxicity in American blacks with rheumatoid arthritis

G. Alarcón, B. Barger, R. Acton, 2004, Rheumatology International.

The complement component C4 in black Americans with Type 1 (insulin-dependent) diabetes mellitus

J. Roseman, B. Budowle, R. Go, 1984, Diabetologia.

Properdin factor B in black Type 1 (insulin-dependent) diabetic patients

J. Roseman, B. Budowle, R. Go, 1982, Diabetologia.

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.

Genetic association of 11 beta-hydroxysteroid dehydrogenase type 2 (HSD11B2) flanking microsatellites with essential hypertension in blacks.

D. Warnock, D. Callen, R. Acton, 1996, Hypertension.

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

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

Gestational diabetes mellitus among African-American women.

J. Roseman, R. Go, B. Barger, 1991, Diabetes/metabolism reviews.

Genetic predisposition to acute lymphocytic leukemia in American blacks. A pediatric oncology group study

J. Roseman, B. Budowle, R. Go, 1985, Cancer.

DR antigens in systemic sclerosis: lack of clinical correlations.

B. Barger, R. Acton, C. Wasner, 2008, Tissue antigens.

DR antigens and gold toxicity in white rheumatoid arthritis patients.

G. Alarcón, B. Barger, R. Acton, 1984, Arthritis and rheumatism.

Short communications The complement component C4 in black Americans with Type I (insulin-dependent) diabetes mellitus

B. Budowle, B. Barger, R. Acton, 1984 .

Population genetic analyses of insulin dependent diabetes mellitus using HLA allele frequencies

J. Roseman, R. Go, B. Barger, 1983, Clinical genetics.

Short Communications Properdin Factor B in Black Type 1 (Insulin-Dependent) Diabetic Patients

J. Roseman, B. Budowle, B. Barger, 1982 .

Associations of properdin factor B with melanoma.

J. Roseman, C. Balch, B. Budowle, 1982, Cancer genetics and cytogenetics.

Properdin factor B and acute lymphocytic leukemia (ALL)

B. Budowle, R. Go, B. Barger, 1982, Cancer.

HLA associations with insulin-dependent diabetes mellitus in a sample of the American Black population.

J. Roseman, B. Barger, R. Acton, 2008, Tissue antigens.

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.

DNA analysis of HLA-DR and DQ genes in American blacks with systemic lupus erythematosus.

J. Reveille, R. Schrohenloher, B. Barger, 1989, Arthritis and rheumatism.

Genes within and flanking the major histocompatibility region are risk factors for diabetes, insulin resistance, hypertension, and microalbuminuria in African-American women.

J. Roseman, H. Taylor, R. Go, 1997, Transplantation proceedings.

Futility of Predicting Onset of Type I Diabetes Mellitus

B. Barger, R. Acton, R. Clements, 1987, Diabetes Care.

HLA-A, -B, and -DR Associations in Type I Diabetes Mellitus with Onset After Age Forty

J. Roseman, R. Go, B. Barger, 1982, Diabetes.

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.

Glucokinase gene in gestational diabetes mellitus: population association study and molecular scanning

M. Permutt, J. Roseman, R. Go, 2004, Diabetologia.

The relationship between maternal serum zinc levels during pregnancy and birthweight.

J. Roseman, G. Cutter, R. Go, 1991, Early human development.

A positive association between maternal serum zinc concentration and birth weight.

J. Roseman, G. Cutter, R. Go, 1990, The American journal of clinical nutrition.

LARGE-SCALE PRODUCTION OF MURINE LYMPHOBLASTOID CELL: LINES EXPRESSING DIFFERENTIATION ALLOANTIGENS

K. Wise, R. Acton, P. Barstad, 1977 .

Pediatric Oncology 1

R. Acton, G. Humphrey, G. Grindey, 1981, Cancer Treatment and Research.

Title Association Between Celiac Disease and Iron Deficiency in Caucasians , but not Non-Caucasians Permalink

D. Nickerson, K. Beckman, C. McLaren, 2013 .

Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians.

D. Nickerson, K. Beckman, C. McLaren, 2013, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

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

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

HFE hemochromatosis and hepatic sarcoid.

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

Results communication and patient education after screening for possible hemochromatosis and iron overload: experience from the HEIRS Study of a large ethnically and linguistically diverse group

E. Thomson, K. Lohman, D. Tucker, 2007, Genetics in Medicine.

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.

A novel DRB1 allele in DR2-positive American blacks.

T. Hodge, R. Acton, J. Demopulos, 1991, Human immunology.

RFLP Standardization Report for DQ Alpha/HindIII

P. A. Biro, J. Tiercy, R. Acton, 1989 .

Evidence for the “Genetic Admixture Hypothesis” That the Increased Incidence of IDDM Among African Americans Compared to Africans is Due in Large Part to Susceptibility Gene(s) Which Entered Through Admixture with the European American Gene Pool

J. Roseman, R. Go, R. Acton, 1994 .

Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y

R. Acton, J. C. Barton, James C Barton, 2022, PloS one.

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.

A primer for predicting risk of disease in HFE-linked hemochromatosis.

A. Walker, R. Acton, P. Adams, 2001, Genetic testing.

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.

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.

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.

Restriction fragment polymorphisms of the HLA‐DR, HLA‐DQ, and insulin gene regions in IDDM: The GAW5 data

M. Skolnick, M. Permutt, R. Spielman, 1989, Genetic epidemiology.

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.

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.

Screening for hemochromatosis and iron overload: satisfaction with results notification and understanding of mailed results in unaffected participants of the HEIRS study.

K. Lohman, M. Hall, A. Walker, 2008, Genetic testing.

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.

Predictors of belief that genetic test information about hemochromatosis should be shared with family members.

J. A. Crabb, Roger T. Anderson, E. Thomson, 2006, Genetic testing.

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.

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.

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.

Comparative immunological studies with the oyster,Crassostrea virginica

R. Acton, K. Wolf, E. Edward Evans, 1967, In Vitro.

Molecular genetic testing for adult‐onset disorders: The evolving laboratory, physician, patient interface

R. Acton, 1997, Journal of clinical laboratory analysis.

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.

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.

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.

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.

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.

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.

Hemochromatosis and Vibrio vulnificus Wound Infections

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

Restriction fragment length polymorphism analysis of HLA-DR, DQ, DP and C4 alleles in Caucasians with systemic lupus erythematosus.

J. Reveille, R. Schrohenloher, B. Barger, 1991, The Journal of rheumatology.

PHENOTYPES OF THE FOURTH COMPLEMENT COMPONENT (C4) IN BLACK AMERICANS FROM THE SOUTHEASTERN UNITED STATES

J. Roseman, B. Budowle, B. Barger, 1983, Journal of immunogenetics.

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

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

Familial polyarteritis nodosa: a serologic and immunogenetic analysis.

J. Reveille, B. Barger, R. Acton, 1989, The Journal of rheumatology.

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.

X-linked codominant genes control all types of non-major histocompatibility complex-restricted cytotoxicity.

D. Zarcone, C. Grossi, R. Acton, 1991, Human immunology.

New vistas. In the etiology, genetics, pathogenesis and natural history of juvenile-onset diabetes.

J. Roseman, R. Acton, 1978, Journal of the Medical Association of the State of Alabama.

Evidence for Genetic Admixture as a Determinant in the Occurrence of Insulin-dependent Diabetes Mellitus in U.S. Blacks

J. Roseman, B. Budowle, R. Go, 1982, Diabetes.

Re: Methotrexate in the treatment of arthritis and connective tissue disease.

B. Barger, R. Acton, W. Koopman, 1988, Cleveland Clinic journal of medicine.

DR2 positivity and response to methotrexate in rheumatoid arthritis.

G. Alarcón, B. Barger, R. Acton, 1986, Arthritis and rheumatism.

Characterization of a teleost immunoglobulin: the immune macroglobulin from the channel catfish, Ictalurus punctatus.

H. K. Dupree, R. Acton, J. Bennett, 1973, Comparative biochemistry and physiology. B, Comparative biochemistry.

Phylogeny of immunoglobulins. Characterization of a 14S immunoglobulin from the gar, Lepisosteus osseus.

H. K. Dupree, R. Acton, J. Bennett, 1971, Biochemistry.

Toxicity of methotrexate in rheumatoid arthritis.

J. J. Johnson, G. Alarcón, B. Barger, 1987, The Journal of rheumatology.

Associations of MHC genes with levels of caries-inducing organisms and caries severity in African-American women.

J. Roseman, R. Go, P. Caufield, 1999, Human immunology.

Comparative Immunology

R. Stroud, R. Acton, B. Painter, 1969, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Immunogenetic predictors of gestational diabetes in american blacks

J. Roseman, L. Perkins, R. Goldenberg, 1990 .

Abnormalities of 21-hydroxylase gene ratio and adrenal steroidogenesis in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to acute adrenal stimulation.

R. Azziz, R. Acton, H. Zacur, 1991, The Journal of clinical endocrinology and metabolism.

Pseudogene/functional gene ratio in late-onset 21-hydroxylase-deficient adrenal hyperplasia.

R. Azziz, R. Acton, H. Zacur, 1990, American journal of obstetrics and gynecology.

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.

Contemporary Topics in Immunobiology

R. L. Carter, M. Hanna, V. Nussenzweig, 1974, Springer US.

Adrenal and Endocrine Tumors in Children

T. Pysher, R. Acton, G. Humphrey, 1983, Cancer Treatment and Research.

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.

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.

Pancreatic Tumors in Children

R. Acton, G. Humphrey, G. Grindey, 1982, Cancer Treatment and Research.

Induced Bactericidal Response in the California Spiny Lobster Panulirus interruptus 1

R. Acton, E. E. Evans, P. Weinheimer, 1969, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Secondary and Tertiary Responses of the Induced Bactericidin from the West Indian Spiny Lobster, Panulirus argus

R. Acton, B. Painter, E. E. Evans, 1969, Journal of bacteriology.

Specificity of the Induced Bactericidin of the West Indian Spiny Lobster, Panulirus argus

R. Acton, E. E. Evans, P. Weinheimer, 1969, Journal of bacteriology.

Isolation and partial characterization of the human homologue of Thy-1

C. Balch, R. Acton, E. Ades, 1980, The Journal of experimental medicine.

Hemagglutinins: Primitive Receptor Molecules Operative in Invertebrate Defense Mechanisms *

R. Acton, P. Weinheimer, 1974 .

Physical and chemical characterization of an oyster hemagglutinin.

R. Schrohenloher, R. Acton, J. Bennett, 1969, The Journal of biological chemistry.

A bactericidal system in the lobster Homarus americanus.

R. Acton, E. E. Evans, P. Weinheimer, 1969, Journal of invertebrate pathology.

Lack of a bactericidal response in the earthworm Lumbricus terrestris after immunization with bacterial antigens.

E. Cooper, R. Acton, E. E. Evans, 1969, Journal of invertebrate pathology.

Induced Bactericidal Response in a Sipunculid Worm

R. Acton, J. Cushing, E. E. Evans, 1969, Nature.

An Induced Bactericidin in the Spiny Lobster, Panulirus argus ∗

R. Acton, E. E. Evans, P. Weinheimer, 1968, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Bacteriophage Clearance in the Oyster (Crassostrea virginica)

R. Acton, E. E. Evans, 1968, Journal of bacteriology.

Attempt to induce a bactericidal response in the oyster

R. Acton, E. E. Evans, P. Weinheimer, 1969, Journal of bacteriology.

Interaction of murine T-cell surface antigens with Mycoplasma hyorhinis.

K. Wise, R. Acton, P. B. Asa, 1979, Advances in Experimental Medicine and Biology.

Origin of the minor glycoproteins of murine leukemia viruses

K. Wise, R. Compans, R. Acton, 1978, Journal of virology.

Production of Milligram Quantities of H-2K and Thy-1 Alloantigens by Large-Scale Mammalian Cell Culture

R. Acton, J. Lynn, R. M. Cox, 1977, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Growth properties and alloantigenic expression of murine lymphoblastoid cell lines

R. Acton, R. Zwerner, Robert K. ZWERNERt, 1975, The Journal of experimental medicine.

The carbohydrate composition of immunoglobulins G.

R. Acton, J. Bennett, W. Niedermeier, 1971, Biochimica et biophysica acta.

Propagation and scaling-up of suspension cultures.

R. Acton, P. Barstad, R. Zwerner, 1979, Methods in enzymology.

Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease.

J. Roseman, R. Go, L. Perkins, 1994, The American journal of clinical nutrition.

Productive murine leukemia virus (MuLV) infection of EL4 T-lymphoblastoid cells: selective elevation of H-2 surface expression and possible association of Thy-1 antigen with viruses.

K. Wise, R. Acton, S. L. Henley, 1984, Advances in experimental medicine and biology.

ALTERED EXPRESSION OF T-LYMPHOID CELL SURFACE ANTIGENS ASSOCIATED WITH VIRAL INFECTION

K. Wise, R. Acton, S. L. Henley, 1979 .

Purification and characterization of mouse brain Thy-1.2 differentiation alloantigen

R. Acton, M. Tomana, L. D. Mcclain, 1978, Brain Research.

Design of a large‐scale mammalian cell, suspension culture facility

R. Acton, J. Lynn, 1975 .

Description and operation of a large-scale, mammalian cell, suspension culture facility

R. Acton, J. Lynn, 1977 .

VKORC1 polymorphisms, haplotypes and haplotype groups on warfarin dose among African-Americans and European-Americans.

Nianjun Liu, T Mark Beasley, Donna K Arnett, 2008, Pharmacogenomics.

SSCP analysis and sequencing of the human prion protein gene (PRNP) detects two different 24 bp deletions in an atypical Alzheimer's disease family.

L. Harrell, R. Go, R. Perry, 1995, American journal of medical genetics.

Species distribution of J chain.

J. Mestecky, R. Acton, P. Weinheimer, 1971, Journal of immunology.

Immunoglobulin and Complement Systems of Amphibian Serum

R. Acton, E. E. Evans, D. Legler, 1969 .

The Potential Use of HLA to Predict Risk of Malignant Diseases and Outcome of Therapy

B. Barger, R. Acton, 1981 .

Variations among sublines of inbred AKR mice.

R. Acton, E. Boyse, E. Blankenhorn, 1973, Nature: New biology.

The developmental appearance on Thy-1 in mouse reaggregating brain cell cultures.

R. Acton, N. Seeds, R. Zwerner, 1977, Developmental biology.

A technique for the detection of variable electrophoretic patterns of hair proteins

B. Budowle, R. Acton, 1981 .

Immunogenetics of Melanoma

J. Roseman, C. Balch, S. Soong, 1982 .

Evolution of the Immune Response

R. Acton, J. Bennett, E. E. Evans, 1970 .

T2 Bacteriophage Clearance in the Lemon Shark∗

W. J. Russell, A. Lucas, R. Acton, 1968, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Purification and characterization of two classes of immunoglobulins from the marine toad, Bufo marinus.

R. Acton, J. Bennett, W. Niedermeier, 1972, Biochemistry.

Selective Subnormal IgG1 in 54 Adult Index Patients with Frequent or Severe Bacterial Respiratory Tract Infections

R. Acton, L. Bertoli, J. C. Barton, 2016, Journal of immunology research.

Selective subnormal IgG3 in 121 adult index patients with frequent or severe bacterial respiratory tract infections.

R. Acton, L. Bertoli, J. C. Barton, 2016, Cellular immunology.

Assessing Genetic Risk of Cancer

L. Nabell, R. Acton, 2004 .

Genetic predictors of coronary heart disease risk factors in premenopausal African-American women.

H. Taylor, M. Weaver, O. Strickland, 2005, Ethnicity & disease.

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

D. Nickerson, K. Beckman, B. Snively, 2009, PloS one.

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

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

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

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

Kidney function influences warfarin responsiveness and hemorrhagic complications.

N. Limdi, T. Beasley, G. Mcgwin, 2009, Journal of the American Society of Nephrology : JASN.

HLA-Bw35 and gold toxicity in rheumatoid arthritis.

G. Alarcón, B. Barger, R. Acton, 1985, Arthritis and rheumatism.

HLA in ankylosing spondylitis: is HLA-B27 the only MHC gene involved in disease pathogenesis?

J. Reveille, R. Go, B. Barger, 1994, Seminars in arthritis and rheumatism.

HLA restriction fragment length polymorphisms associated with insulin-dependent diabetes mellitus and the seronegative spondyloarthropathies

J. Reveille, T. Hodge, B. Barger, 1985, Bioscience reports.

PROPERDIN FACTOR B POLYMORPHISM IN BLACK AMERICANS

B. Budowle, B. Barger, R. Acton, 1981, Journal of immunogenetics.

Seronegative rheumatoid arthritis and B7-CREG: disparate results.

G. Alarcón, B. Barger, R. Acton, 1983, Arthritis and rheumatism.

RFLP Standardization Report for DR Beta/HindIII

R. Fauchet, M. Hammond, J. Tiercy, 1989 .

Analyses of HLA linkage in white families with multiple cases of seropositive rheumatoid arthritis.

G. Alarcón, R. Go, B. Barger, 1987, Arthritis and rheumatism.

The carbohydrate composition of immunoglobulins from diverse species of vertebrates.

R. Acton, L. Clem, J. Bennett, 1972, Journal of immunology.

Tetrameric immune macroglobulins in three orders of bony fishes.

R. Acton, E. Shelton, J. Bennett, 1971, Proceedings of the National Academy of Sciences of the United States of America.

Restriction fragment length polymorphism analysis in ankylosing spondylitis.

J. Reveille, B. Barger, R. Acton, 1988, The American journal of medicine.

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.

Genetic analysis of IDDM: The GAW5 multiplex family dataset

H. Kolb, R. Fimmers, M. Baur, 1989, Genetic epidemiology.

Familial studies in human brucellosis.

G. Alarcón, R. Go, E. Gotuzzo, 2008, Tissue antigens.

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

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

Patient acceptability of genotypic testing for hemochromatosis in primary care

E. Thomson, D. Tucker, B. Snively, 2005, Genetics in Medicine.

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

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

Investigation of association of 13 polymorphisms in eight genes in southeastern African American Alzheimer disease patients as compared to age-matched controls.

L. Harrell, R. Go, R. Perry, 2001, American journal of medical genetics.

A simple methodology for the routine production and partial purification of human lymphoblastoid interferon.

R. Acton, P. Neame, 1984, Advances in experimental medicine and biology.

Eukaryotic Cell Cultures: Basics and Applications

D. Lynn, R. Acton, J. Lynn, 1984, Advances in Experimental Medicine and Biology.

The role of TNF and its receptors in Alzheimer’s disease

R. Go, R. Perry, R. Acton, 2001, Neurobiology of Aging.

Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: the NIMH Alzheimer Disease Genetics Initiative.

M. Albert, M. McInnis, D. Blacker, 2000, American journal of medical genetics.

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.

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.

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.

Hemochromatosis in a Lithuanian with HFE C282Y homozygosity and C282Y allele frequencies in the Baltic Sea region

R. Acton, C. Rivers, James C. Barton, 2001, European journal of haematology.

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.

Factors associated with IgG levels in adults with IgG subclass deficiency

R. Acton, L. Bertoli, J. C. Barton, 2021, BMC immunology.

Influence of CYP2C9 and VKORC1 on warfarin dose, anticoagulation attainment and maintenance among European-Americans and African-Americans.

N. Limdi, T. Beasley, G. Mcgwin, 2008, Pharmacogenomics.

Biological Sciences: N-Terminal Sequences of Immunoglobulin Heavy and Light Chains from Three Species of Lower Vertebrates

R. Acton, J. Bennett, E. E. Evans, 1970, Nature.

Molecular analysis of HLA-D region genes in seropositive rheumatoid arthritis.

G. Alarcón, B. Barger, R. Acton, 1989, Tissue antigens.

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.

Undiagnosed diabetes and impaired fasting glucose in HFE C282Y homozygotes and HFE wild-type controls in the HEIRS Study

D. Reboussin, C. McLaren, O. Castro, 2016, BMJ Open Diabetes Research and Care.

Risk Factors for Insulin Resistance, Metabolic Syndrome, and Diabetes in 248 HFE C282Y Homozygotes Identified by Population Screening in the HEIRS Study.

R. Acton, P. Adams, J. C. Barton, 2016, Metabolic syndrome and related disorders.

Isolation and physico-chemical characterization of the "IgM-like" immunologlobulin from the stingray Dasyatis americana.

R. Acton, E. Shelton, J. Bennett, 1971, Journal of immunology.

Isolation and characterization of the immune macroglobulin from the paddlefish, Polyodon spathula.

H. K. Dupree, R. Schrohenloher, R. Acton, 1971, The Journal of biological chemistry.

Phylogeny of immunoglobulins--purification and physico-chemical characterization of the immune macroglobulin from the turtle, Pseudemus seripta.

R. Acton, E. Shelton, J. Bennett, 1972, Immunochemistry.

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.

An evaluation of suspension culture systems for the growth of murine lymphoblastoid lines expressing TL and Thy‐1 alloantigens

D. Lynn, R. Acton, R. Zwerner, 1975 .

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.

HLA-A and -B Type and Haplotype Frequencies in IgG Subclass Deficiency Subgroups

R. Acton, L. Bertoli, J. C. Barton, 2020, Archivum Immunologiae et Therapiae Experimentalis.

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 .

Molecular genetic studies of rheumatoid arthritis.

G. Alarcón, B. Barger, R. Acton, 1988, The American journal of medicine.

Prevalence and risk factors of microalbuminuria in a cohort of African-American women with gestational diabetes.

J. Roseman, R. Go, R. Acton, 2001, Diabetes care.

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 .

Reactions of sipunculid coelomic fluid with erythrocytes.

R. Acton, J. Cushing, E. E. Evans, 1970, Life sciences.

Increase of HLA-DR 4 in Melanoma Patients from Alabama 1

J. Roseman, C. Balch, S. Soong, 2006 .

Enhanced in vitro IgM rheumatoid factor synthesis in seropositive rheumatoid arthritis families

G. Alarcón, R. Go, R. Schrohenloher, 2004, Rheumatology International.

The Effect of Genetic Risk Information and Health Risk Assessment on Compliance with Preventive Behaviors

J. Roseman, R. Go, R. Bamberg, 1990 .

Platelet counts in HFE p.C282Y/p.C282Y and wt/wt post-screening clinical evaluation participants.

R. Acton, James C. Barton, J. Barton, 2023, Platelets.

Non-alcoholic fatty liver disease in hemochromatosis probands with iron overload and HFE p.C282Y/p.C282Y

R. Acton, James C. Barton, J. Barton, 2023, BMC Gastroenterology.

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.

Diabetes in First-Degree Family Members: A Predictor of Type 2 Diabetes in 159 Nonscreening Alabama Hemochromatosis Probands With HFE C282Y Homozygosity

R. Acton, J. C. Barton, James C. Barton, 2013, Diabetes Care.

Risk Factors for Gestational Diabetes in Black Population

J. Roseman, R. Go, L. Perkins, 1990, Diabetes Care.

Impact of hemochromatosis screening in patients with indeterminate results: The hemochromatosis and iron overload screening study

E. Thomson, D. Tucker, M. Hall, 2006, Genetics in Medicine.

Seronegative rheumatoid arthritis. A distinct immunogenetic disease?

G. Alarcón, B. Barger, R. Acton, 1982, Arthritis and rheumatism.

Comparison of HLA phenotypes among African Americans from Alabama, Maryland, and North Carolina.

R. Go, R. Acton, W. Bias, 1993, Transplantation proceedings.

DR antigen distribution in Blacks with rheumatoid arthritis.

G. Alarcón, B. Barger, R. Acton, 1983, The Journal of rheumatology.

Increased Prevalence of Mitral Valve Prolapse in IDDM

R. Acton, David S. H. Bel, 1996, Diabetes Care.

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

B. Snively, C. McLaren, J. Murray, 2011, PloS one.

Immunological capabilities of the oyster Crassostrea virginica.

R. Acton, J. Bennett, E. E. Evans, 1969, Comparative biochemistry and physiology.

Association of factor B with ischemic heart disease (IHD).

J. Roseman, G. Cutter, R. Go, 1984, Progress in clinical and biological research.

A method for dialysis of microsamples.

B. Budowle, B. Barger, R. Acton, 1981, Analytical biochemistry.

RFLP Standardization Report for BF/HindIII

R. Acton, S. V. Tonder, S. Cutbush, 1989 .

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

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

Survey of physician knowledge about hemochromatosis

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

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.

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

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

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

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

Characterization of adult patients with IgG subclass deficiency and subnormal IgG2

R. Acton, L. Bertoli, J. C. Barton, 2020, PloS one.

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 .

Association of HLA-linked factor B with gestational diabetes mellitus in black women.

B. Budowle, R. Go, B. Barger, 1988, American journal of obstetrics and gynecology.

Scleroderma: DR antigens, autoantibodies and clinical manifestations.

B. Barger, R. Acton, P. Lanyon, 1987, Clinical and experimental rheumatology.

Complement-dependent systems and the phylogeny of immunity

R. Acton, B. Painter, D. Legler, 1967, In Vitro.

Comparison of HLA Antigens and DNA Polymorphisms in Parentage Testing

R. Go, R. Acton, L. Harman, 1990 .