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List of works by Richard D Press

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

scientific article published in June 2007

A half-log increase in BCR-ABL RNA predicts a higher risk of relapse in patients with chronic myeloid leukemia with an imatinib-induced complete cytogenetic response

scientific article

A novel germline variant in CSF3R reduces N-glycosylation and exerts potent oncogenic effects in leukemia

scientific article published on 22 October 2018

ABL kinase domain pseudoexon insertion is not uncommon in BCR-ABL transcripts

scientific article published on 7 August 2008

An international study to standardize the detection and quantitation of BCR-ABL transcripts from stabilized peripheral blood preparations by quantitative RT-PCR.

scientific article published in July 2007

An intron-derived insertion/truncation mutation in the BCR-ABL kinase domain in chronic myeloid leukemia patients undergoing kinase inhibitor therapy

scientific article

An outbreak of acute hepatitis C among recipients of intravenous immunoglobulin

scientific article

Analyte-specific reagents

scientific article published on 01 March 1999

Association of JAK2 mutation status and cytogenetic abnormalities in myeloproliferative neoplasms and myelodysplastic/myeloproliferative neoplasms.

scientific article published in May 2011

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

scientific article published on 05 February 2007

BCR-ABL PCR testing in chronic myelogenous leukemia: molecular diagnosis for targeted cancer therapy and monitoring

scientific article

BCR-ABL SH3-SH2 domain mutations in chronic myeloid leukemia patients on imatinib

scientific article

BCR-ABL mRNA levels at and after the time of a complete cytogenetic response (CCR) predict the duration of CCR in imatinib mesylate-treated patients with CML.

scientific article published on 7 February 2006

BCR-ABL1 RT-qPCR for monitoring the molecular response to tyrosine kinase inhibitors in chronic myeloid leukemia

scientific article published on 27 June 2013

BCR-ABL1 compound mutations combining key kinase domain positions confer clinical resistance to ponatinib in Ph chromosome-positive leukemia

scientific article published on 14 August 2014

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

scientific article

CRISPR-Cas9-mediated saturated mutagenesis screen predicts clinical drug resistance with improved accuracy

scientific article

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

scientific article published on February 2008

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

scientific article

Clinical Utility of Next-Generation Sequencing in Acute Myeloid Leukemia

scientific article published in February 2020

Clinical implementation of next-generation sequencing

Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening

scientific article

Clinical news update

scientific article published in March 2001

Clinical news update

scientific article published on 01 December 2000

Clinical news update

scientific article published on 01 March 2000

Clinical news update

scientific article published on 01 June 2001

Clinical news update

scientific article published on 01 June 1999

Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders

scientific article

Clonal hematopoiesis as determined by the HUMARA assay is a marker for acquired mutations in epigenetic regulators in older women

scientific article published on 25 May 2016

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

scientific article

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

scientific article published on 15 April 2005

Concurrent STAT3, DNMT3A, and TET2 mutations in T-LGL leukemia with molecularly distinct clonal hematopoiesis of indeterminate potential

scientific article published on 19 October 2016

Control of the expression of c-sis mRNA in human glioblastoma cells by phorbol ester and transforming growth factor beta 1.

scientific article published in June 1989

DNMT3A co-mutation is required for FLT3-ITD as an adverse prognostic indicator in intermediate-risk cytogenetic group AML.

scientific article published on 22 November 2017

Desirable performance characteristics for BCR-ABL measurement on an international reporting scale to allow consistent interpretation of individual patient response and comparison of response rates between clinical trials.

scientific article published on 6 August 2008

Detection of BCR-ABL1 kinase domain mutations causing imatinib resistance in chronic myelogenous leukemia

scientific article published in January 2013

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

scientific article published on 01 October 2000

Determining the rise in BCR-ABL RNA that optimally predicts a kinase domain mutation in patients with chronic myeloid leukemia on imatinib

scientific article published on 22 July 2009

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

scientific article published on 25 April 2016

Discriminating a common somatic ASXL1 mutation (c.1934dup; p.G646Wfs*12) from artifact in myeloid malignancies using NGS

scientific article published on 29 June 2018

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

scientific article published on 01 November 1989

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

scientific article published on 01 August 1998

Establishment of the first World Health Organization International Genetic Reference Panel for quantitation of BCR-ABL mRNA.

scientific article published on 18 August 2010

Exclusivity in testing for patented disease genes

scientific article published on 01 March 1999

Expression and stability of c-sis mRNA in human glioblastoma cells

scientific article published in July 1988

Food and Drug Administration approval for 2 new molecular infectious disease assays

scientific article published on 01 September 1999

GeneClinics Medical Genetics Knowledge Base

scientific article published on 01 September 1999

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

scientific article published on 01 January 2007

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

scientific article published on 01 November 2009

Hemochromatosis: a "simple" genetic trait

scientific article published on 01 August 1999

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

scientific article published in May 1998

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

scientific article

Highly accurate molecular genetic testing for HFE hereditary hemochromatosis: results from 10 years of blinded proficiency surveys by the College of American Pathologists.

scientific article

Human Papillomavirus DNA detection for cervical cancer screening

scientific article published on 01 September 2000

Identification of cytomegalovirus in a liquid-based gynecologic sample using morphology, immunohistochemistry, and DNA real-time PCR detection

scientific article published on 01 June 2004

Induction of B cell lymphomas by overexpression of a Myb oncogene truncated at either terminus

scientific article published on 01 August 1995

Insights on mechanisms of clonal evolution in chronic neutrophilic leukemia on ruxolitinib therapy

scientific article published on 16 December 2019

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

scientific article published on 01 February 2000

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

scientific article published on 01 January 1996

Laboratory practice guidelines for detecting and reporting BCR-ABL drug resistance mutations in chronic myelogenous leukemia and acute lymphoblastic leukemia: a report of the Association for Molecular Pathology.

scientific article published on 18 December 2008

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

scholarly article by Press RD et al published 1 September 2001 in Molecular Diagnosis and Therapy

Linked linear amplification: a new method for the amplification of DNA.

scientific article

MYD88 mutation analysis of a rare composite chronic lymphocyte leukemia and lymphoplasmacytic lymphoma by flow cytometry cell sorting.

scientific article published on 2 August 2015

Major molecular response in CML patients treated with tyrosine kinase inhibitors: the paradigm for monitoring targeted cancer therapy

scientific article published on 21 June 2010

Major structural alterations of the c-sis gene are not observed in a series of tumors of the human central nervous system.

scientific article published in November 1989

Measurement of BCR-ABL1 transcripts on the International Scale in the United States: current status and best practices.

scientific article published on 14 July 2016

Molecular detection of a common mutation in coagulation factor V causing thrombosis via hereditary resistance to activated protein C

scientific article published on 01 September 1995

Multi-Site PCR-based CMV viral load assessment-assays demonstrate linearity and precision, but lack numeric standardization: a report of the association for molecular pathology

scientific article published on March 2009

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

scientific article published in June 1998

Multiplex high-throughput gene mutation analysis in acute myeloid leukemia.

scientific article published in June 2012

Mutant calreticulin-expressing cells induce monocyte hyperreactivity through a paracrine mechanism

scientific article published on 17 November 2015

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

scientific article published on 25 January 2007

New Food and Drug Administration-based oversight over genetic testing

Next generation sequencing in clinical diagnostics: experiences of early adopters

scientific article published on 24 November 2014

Next-generation sequencing-defined minimal residual disease before stem cell transplantation predicts acute myeloid leukemia relapse

scientific article published on 14 June 2019

Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism

scientific article published on 01 December 1999

Overexpression of C-terminally but not N-terminally truncated Myb induces fibrosarcomas: a novel nonhematopoietic target cell for the myb oncogene

scientific article published on April 1994

Pathogen analysis and genetic predisposition testing using microelectronic arrays and isothermal amplification

scientific article published on 01 March 2000

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results

scientific article published in November 1999

Predisposition to thrombosis by a factor V mutation causing hereditary resistance to activated protein C.

scientific article

Preliminary CLIAC recommendations to regulate genetic testing

scientific article published on 01 September 2000

Quantitative BCR-ABL1 RQ-PCR fusion transcript monitoring in chronic myelogenous leukemia.

scientific article published in January 2013

Quantitative real-time PCR with automated sample preparation for diagnosis and monitoring of cytomegalovirus infection in bone marrow transplant patients.

scientific article

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

scientific article

Risk of Venous Thrombosis in Carriers of a Common Mutation in the Homocysteine Regulatory Enzyme Methylenetetrahydrofolate Reductase

scientific article published on 01 March 1997

Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke.

scientific article

Significant clinical response to JAK1/2 inhibition in a patient with CSF3R-T618I-positive atypical chronic myeloid leukemia

scientific article

Subspecialty certification examination in molecular genetic pathology

scientific article published on 01 September 1999

TNFα facilitates clonal expansion of JAK2V617F positive cells in myeloproliferative neoplasms

scientific article published on 22 August 2011

Targeted Next-Generation Sequencing in Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia Aids Diagnosis in Challenging Cases and Identifies Frequent Spliceosome Mutations in Transformed Acute Myeloid Leukemia

scientific article published on 22 April 2016

The BCR-ABL35INS insertion/truncation mutant is kinase-inactive and does not contribute to tyrosine kinase inhibitor resistance in chronic myeloid leukemia

scientific article published on 8 September 2011

The Case for Laboratory Developed Procedures: Quality and Positive Impact on Patient Care.

scientific article published in January 2017

The cell cycle dependence of c-sis gene expression: artifactual conclusions in cells prepared by chemical but not physical techniques

scientific article published in July 1990

The clinical impact of coronavirus infection in patients with hematologic malignancies and hematopoietic stem cell transplant recipients.

scientific article published on 15 April 2015

The combination of NPM1, DNMT3A, and IDH1/2 mutations leads to inferior overall survival in AML

scientific article published on 21 June 2019

Thrombophilic mutations impart a high risk of pregnancy-related venous thrombosis

scientific article published on 01 June 2000

Transformation of chicken myelomonocytic cells by a retrovirus expressing the v-myb oncogene from the long terminal repeats of avian myeloblastosis virus but not Rous sarcoma virus

scientific article

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