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Mutations of the BCR-ABL-kinase domain occur in a minority of patients with stable complete cytogenetic response to imatinib

Leukemia, 2007-03, Vol.21 (3), p.489-493

2007

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Characterization of BCR-ABL deletion mutants from patients with chronic myeloid leukemia

Leukemia, 2008-06, Vol.22 (6), p.1184-1190

2008

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Common mutation in methylenetetrahydrofolate reductase : Correlation with homocysteine metabolism and late-onset vascular disease

Circulation (New York, N.Y.), 1996-12, Vol.94 (12), p.3074-3078

1996

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

Clinical genetics, 2007-06, Vol.71 (6), p.518-529

2007

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End-stage liver disease without hemochromatosis associated with elevated hepatic iron index

Journal of hepatology, 1998-08, Vol.29 (2), p.257-262

1998

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Ischemic stroke in the elderly : role of the common factor V mutation causing resistance to activated protein C

Stroke (1970), 1996, Vol.27 (1), p.44-48

1996

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Detection of prevalent genetic alterations predisposing to hemochromatosis and other common human diseases

Clinical chemistry (Baltimore, Md.), 2000-10, Vol.46 (10), p.1526-1528

Press, R D

2000

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Linked Linear Amplification: A New Method for the Amplification of DNA

Clinical chemistry (Baltimore, Md.), 2001-01, Vol.47 (1), p.31-40

2001

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Multicenter evaluation of PCR methods for the detection of factor V Leiden (R506Q) genotypes

Clinical chemistry (Baltimore, Md.), 1998-06, Vol.44 (6), p.1356-1358

1998

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Hepatic iron overload: Direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis

American journal of clinical pathology, 1998-05, Vol.109 (5), p.577-584

1998

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GeneClinics Medical Genetics Knowledge Base

Molecular diagnosis, 1999-09, Vol.4 (3), p.256-256

Press, R D

1999

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Hereditary hemochromatosis: impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease

Archives of pathology & laboratory medicine (1976), 1999-11, Vol.123 (11), p.1053-1059

Press, R D

1999

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Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes

American journal of clinical pathology, 2001-03, Vol.115 (3), p.439-447

2001

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Exclusivity in testing for patented disease genes

Molecular diagnosis, 1999-03, Vol.4 (1), p.72-73

Press, R D

1999

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Analyte-specific reagents

Molecular diagnosis, 1999-03, Vol.4 (1), p.71-71

Press, R D

1999

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Effect of glycation of low-density lipoprotein on the immunological determination of apolipoprotein B

Clinical chemistry (Baltimore, Md.), 1989-11, Vol.35 (11), p.2219

1989

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Iron beware: A common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low‐risk, but not high‐risk groups

Hepatology (Baltimore, Md.), 2000-02, Vol.31 (2), p.540-542

Press, Richard D.

2000

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Hemochromatosis and Iron-Overload Screening in a Racially Diverse Population

The New England journal of medicine, 2005-04, Vol.352 (17), p.1769-1778

2005

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Crohn's disease is caused by mutations in the bacterial response protein NOD2

Molecular diagnosis, 2001-12, Vol.6 (4), p.347-348

Press, R D

2001

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New Food and Drug Administration-based oversight over genetic testing

Molecular diagnosis, 2001-12, Vol.6 (4), p.348-349

Press, R D

2001

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Biological Variability of Transferrin Saturation and Unsaturated Iron-Binding Capacity

The American journal of medicine, 2007-11, Vol.120 (11), p.999.e1-999.e7

2007

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Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

Molecular diagnosis, 2001-09, Vol.6 (3), p.212-213

Press, R D

2001

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Pharmacologic inhibition of the Bcr-Abl kinase with STI571: a novel, safe, and effective therapy for chronic myeloid leukemia

Molecular diagnosis, 2001-09, Vol.6 (3), p.211-213

Press, R D

2001

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Clinical news update

Molecular diagnosis, 2001-03, Vol.6 (1), p.69-70

Press, R D

2001

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Mutations of the BCR-ABL-kinase domain occur in a minority of patients with stable complete cytogenetic response to imatinib

Characterization of BCR-ABL deletion mutants from patients with chronic myeloid leukemia

Development and evaluation of a secondary reference panel for BCR-ABL1 quantification on the International Scale

Common mutation in methylenetetrahydrofolate reductase : Correlation with homocysteine metabolism and late-onset vascular disease

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

End-stage liver disease without hemochromatosis associated with elevated hepatic iron index

Ischemic stroke in the elderly : role of the common factor V mutation causing resistance to activated protein C

Detection of prevalent genetic alterations predisposing to hemochromatosis and other common human diseases

Linked Linear Amplification: A New Method for the Amplification of DNA

Multicenter evaluation of PCR methods for the detection of factor V Leiden (R506Q) genotypes

Hepatic iron overload: Direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis

GeneClinics Medical Genetics Knowledge Base

Hereditary hemochromatosis: impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease

Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes

Exclusivity in testing for patented disease genes

Analyte-specific reagents

Effect of glycation of low-density lipoprotein on the immunological determination of apolipoprotein B

Iron beware: A common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low‐risk, but not high‐risk groups

Hemochromatosis and Iron-Overload Screening in a Racially Diverse Population

Crohn's disease is caused by mutations in the bacterial response protein NOD2

New Food and Drug Administration-based oversight over genetic testing

Biological Variability of Transferrin Saturation and Unsaturated Iron-Binding Capacity

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening

Pharmacologic inhibition of the Bcr-Abl kinase with STI571: a novel, safe, and effective therapy for chronic myeloid leukemia

Clinical news update

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