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Lista de obras de Martin Dugas

A European inventory of common electronic health record data elements for clinical trial feasibility

artículo científico publicado en 2014

A European inventory of data elements for patient recruitment

artículo científico publicado en 2015

A New ETV6-RUNX1 In Vivo Model Produces a Phenocopy of the Human Pb-ALL

scholarly article

A Secure Architecture to Provide a Medical Emergency Dataset for Patients in Germany and Abroad

artículo científico publicado en 2017

A Smart Device System to Identify New Phenotypical Characteristics in Movement Disorders

artículo científico publicado en 2019

A Web Service to Suggest Semantic Codes Based on the MDM-Portal

A new workflow for whole-genome sequencing of single human cells.

artículo científico publicado en 2014

A proof of concept phase I/II pilot trial of LSD1 inhibition by tranylcypromine combined with ATRA in refractory/relapsed AML patients not eligible for intensive therapy

scientific article published on 19 June 2020

AML M3 and AML M3 variant each have a distinct gene expression signature but also share patterns different from other genetically defined AML subtypes.

artículo científico publicado en 2005

AML1-ETO requires enhanced C/D box snoRNA/RNP formation to induce self-renewal and leukaemia

artículo científico publicado en 2017

AML1/ETO induces self-renewal in hematopoietic progenitor cells via the Groucho-related amino-terminal AES protein

artículo científico publicado en 2011

AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting

scientific article published on 04 February 2020

Acute myeloid leukemia with recurring chromosome abnormalities as defined by the WHO-classification: incidence of subgroups, additional genetic abnormalities, FAB subtypes and age distribution in an unselected series of 1,897 patients with acute mye

scientific article published on 01 March 2003

Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profiles

artículo científico publicado en 2002

An Approach to Virtual Karyotyping for Unbalanced Rearrangements Based on Gene Expression Data.

artículo científico publicado en 2007

An Open-Source, Standard-Compliant, and Mobile Electronic Data Capture System for Medical Research (OpenEDC): Design and Evaluation Study

artículo científico publicado en 2021

Analyses of medical data models - identifying common concepts and items in a repository of medical forms

artículo científico publicado en 2013

Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease

artículo científico publicado en 2002

Analysis of eligibility criteria from ClinicalTrials.gov

artículo científico publicado en 2014

Are physicians interested in the quality of life of their patients? usage of EHR-integrated patient reported outcomes data

artículo científico publicado en 2013

Arginine 595 is duplicated in patients with acute leukemias carrying internal tandem duplications of FLT3 and modulates its transforming potential.

artículo científico publicado en 2007

Association of contact to small children with mild course of COVID-19

artículo científico publicado en 2020

Automated Transformation of CDISC ODM to OpenClinica

artículo científico publicado en 2017

Automated UMLS-based comparison of medical forms.

artículo científico publicado en 2013

Automatic Conversion of Metadata from the Study of Health in Pomerania to ODM.

artículo científico

Azacitidine Followed By Intensive Induction/Consolidation Chemotherapy in Older Patients with Acute Myeloid Leukemia (AML): Results from the Randomized AML-AZA Trial of the Study Alliance Leukemias (SAL)

artículo científico publicado en 2014

BBCAnalyzer: a visual approach to facilitate variant calling

artículo científico publicado en 2017

BRCC3 mutations in myeloid neoplasms

artículo científico publicado en 2015

Basic4Cseq: an R/Bioconductor package for analyzing 4C-seq data

artículo científico publicado en 2014

Benchmarking of 4C-seq pipelines based on real and simulated data

artículo científico publicado en 2019

Bronchial Subepithelial Fibrosis Correlates With Airway Responsiveness to Methacholine

artículo científico publicado el 1 de julio de 1997

CD34+ gene expression profiling of individual children with very severe aplastic anemia indicates a pathogenic role of integrin receptors and the proapoptotic death ligand TRAIL.

artículo científico publicado en 2012

CDEGenerator: an online platform to learn from existing data models to build model registries

artículo científico publicado en 2018

CIS-based registration of quality of life in a single source approach

artículo científico publicado en 2011

Cancer gene prioritization by integrative analysis of mRNA expression and DNA copy number data: a comparative review

artículo científico publicado en 2012

ChIP-Chip in Primary AML Blasts Identifies Peroxiredoxin-II as An Epigenetically Silenced Tumor Suppressor.

scholarly article

Characterization of image transfer patterns in a regional trauma network

artículo científico publicado en 2014

Chronic Nodular Prurigo: A European Cross-sectional Study of Patient Perspectives on Therapeutic Goals and Satisfaction

artículo científico publicado en 2020

Clinical Trial Feasibility Study Questionnaire Analysis

artículo científico publicado en 2015

Clinical map document based on XML (cMDX): document architecture with mapping feature for reporting and analysing prostate cancer in radical prostatectomy specimens

artículo científico publicado en 2010

Clonal evolution in myelodysplastic syndromes

artículo científico publicado en 2017

Combined Analysis of Valproic Acid Induced MicroRNA and Gene Expression Changes in Acute Myeloid Leukemia.

scholarly article

Common Data Elements for Acute Coronary Syndrome: Analysis Based on the Unified Medical Language System

artículo científico publicado en 2019

Common data elements for secondary use of electronic health record data for clinical trial execution and serious adverse event reporting

artículo científico publicado en 2016

Comparative study of unsupervised dimension reduction techniques for the visualization of microarray gene expression data

artículo científico publicado en 2010

Comparison of electronic health record system functionalities to support the patient recruitment process in clinical trials

artículo científico

Compatibility Between Metadata Standards: Import Pipeline of CDISC ODM to the Samply.MDR

Compatible Data Models at Design Stage of Medical Information Systems: Leveraging Related Data Elements from the MDM Portal

scientific article published on 01 August 2019

Conducting a Multilingual Study Researching Traumatised Refugees Utilizing a Patient-Reported Outcome System

artículo científico publicado en 2018

Connecting healthcare and clinical research: Workflow optimizations through seamless integration of EHR, pseudonymization services and EDC systems

article

Converting ODM Metadata to FHIR Questionnaire Resources

artículo científico publicado en 2016

CopyDetective: Detection threshold-aware copy number variant calling in whole-exome sequencing data

scientific article published on 01 November 2020

Core Data Elements in Acute Myeloid Leukemia: A Unified Medical Language System-Based Semantic Analysis and Experts' Review

scientific article published on 12 August 2019

Cyclin A1 regulates WT1 expression in acute myeloid leukemia cells.

artículo científico publicado en 2009

DDX41 Is a Tumor Suppressor Gene Associated with Inherited and Acquired Mutations

artículo científico publicado en 2014

DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor binding

artículo científico publicado en 2012

DNA methyltransferase inhibition reverses epigenetically embedded phenotypes in lung cancer preferentially affecting polycomb target genes

artículo científico publicado en 2013

Deep Sequencing in Conjunction with Expression and Functional Analyses Reveals Activation of FGFR1 in Ewing Sarcoma

artículo científico publicado en 2015

Defective Interfering Genomes and the Full-Length Viral Genome Trigger RIG-I After Infection With Vesicular Stomatitis Virus in a Replication Dependent Manner

artículo científico publicado en 2021

Design of case report forms based on a public metadata registry: re-use of data elements to improve compatibility of data

artículo científico publicado en 2016

Detection of significantly differentially methylated regions in targeted bisulfite sequencing data

artículo científico publicado en 2013

Development and validation of an interpretable 3 day intensive care unit readmission prediction model using explainable boosting machines

artículo científico publicado en 2022

Development of best practice principles for simplifying eligibility criteria

artículo científico publicado en 2013

Distinct Expression Patterns of Human microRNAs in Myeloid Differentiation and Acute Myeloid Leukemia.

scholarly article

Does single-source create an added value? Evaluating the impact of introducing x4T into the clinical routine on workflow modifications, data quality and cost-benefit.

artículo científico publicado en 2014

Dominant-Negative Impact of PAX5/TEL on Downstream Targets of PAX5 and Essential Pre-B Cell Receptor Genes

artículo científico publicado en 2010

EMR-integrated minimal core dataset for routine health care and multiple research settings: A case study for neuroinflammatory demyelinating diseases

artículo científico publicado en 2019

EZH2 mutations and their association with PICALM-MLLT10 positive acute leukaemia

Effects of computerized decision support system implementations on patient outcomes in inpatient care: a systematic review.

artículo científico publicado en 2017

Efficiency and effectiveness evaluation of an automated multi-country patient count cohort system

artículo científico publicado en 2015

Electronic Image Documentation of Patient Reported Outcomes Using Mobile Technologies

scientific article published on 01 August 2019

Epigenetic control over the cell-intrinsic immune response antagonizes self-renewal in acute myeloid leukemia

artículo científico publicado en 2024

Epigenetic dysregulation of KCa 3.1 channels induces poor prognosis in lung cancer.

artículo científico publicado en 2015

Estimation of patient accrual rates in clinical trials based on routine data from hospital information systems

artículo científico publicado en 2009

Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data

artículo científico publicado en 2017

Evaluation of data completeness in the electronic health record for the purpose of patient recruitment into clinical trials: a retrospective analysis of element presence

artículo científico publicado en 2013

Evaluation of openEHR Repositories Regarding Standard Compliance

artículo científico publicado en 2020

Facing the challenges of chronic pruritus: a report from a multi-disciplinary medical itch centre in Germany

artículo científico publicado en 2015

Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype

artículo científico publicado en 2009

GLM-based optimization of NGS data analysis: A case study of Roche 454, Ion Torrent PGM and Illumina NextSeq sequencing data

artículo científico publicado en 2017

Gene Expression Profiling Demonstrates Similar Biological Patterns in t-AML vs. de novo AML: A Study Including 106 Patients.

artículo científico publicado en 2004

Gene Expression Profiling in AML with Normal Karyotype: A Multicenter Study Investigating Molecular Markers in 252 Cases

artículo científico publicado en 2008

Genetic alterations in human papillomavirus-associated oropharyngeal squamous cell carcinoma of patients with treatment failure

scientific article published on 28 April 2019

Genetic characterization of acquired aplastic anemia by targeted sequencing

artículo científico publicado en 2014

Genome-wide analysis of histone H3 acetylation patterns in AML identifies PRDX2 as an epigenetically silenced tumor suppressor gene

artículo científico publicado en 2011

Genomic landscape of liposarcoma.

artículo científico publicado en 2015

Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia

artículo científico publicado en 2010

Global Identification of Genomic Structural Variants In Childhood ETV6/RUNX1 (TEL/AML1) Acute Lymphoblastic Leukemias by Mate-Pair Massively Parallel Sequencing.

artículo científico publicado en 2010

Global approach to the diagnosis of leukemia using gene expression profiling

artículo científico publicado en 2005

HIS-based Kaplan-Meier plots--a single source approach for documenting and reusing routine survival information.

artículo científico publicado en 2011

HIS-based electronic documentation can significantly reduce the time from biopsy to final report for prostate tumours and supports quality management as well as clinical research

artículo científico publicado en 2009

Health-Related Quality of Life in Chronic Pruritus: An Analysis Related to Disease Etiology, Clinical Skin Conditions and Itch Intensity.

artículo científico publicado en 2015

High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray

artículo científico publicado en 2009

Histone H3 Methylation Mediates All-Trans-Retinoic Acid Responsiveness in Acute Myeloid Leukemia

scholarly article

Humanistic burden of chronic pruritus in patients with inflammatory dermatoses: Results of the European Academy of Dermatology and Venereology Network on Assessment of Severity and Burden of Pruritus (PruNet) cross-sectional trial

scientific article published on 01 September 2018

Identification Of Leukemia Suppressive Genes By Inducible Overexpression Of The DNA Methyltransferase DNMT3B During Leukemogenesis In Mice

scholarly article

Identification of Biologically Distinct and Clinically Relevant Subentities in Patients with Acute Myeloid Leukemia and Normal Karyotypes by Use of Gene Expression Profiling.

scholarly article

Identification of acute myeloid leukaemia associated microRNA expression patterns

scientific article published on 01 January 2008

Identification of the Adapter Molecule MTSS1 as a Potential Oncogene-Specific Tumor Suppressor in Acute Myeloid Leukemia

artículo científico publicado en 2015

Impact of Molecular Genetics on Outcome in Myelofibrosis Patients after Allogeneic Stem Cell Transplantation

artículo científico publicado en 2017

Impact of integrating clinical and genetic information

artículo científico publicado en 2002

Impact of trisomy 8 on expression of genes located on chromosome 8 in different AML subgroups

artículo científico publicado en 2006

Implementation of an ODM and HL7 Compliant Electronic Patient-Reported Outcome System

artículo científico publicado en 2016

Increased DNA methylation of Dnmt3b targets impairs leukemogenesis.

artículo científico publicado en 2016

Increased HDAC1 deposition at hematopoietic promoters in AML and its association with patient survival

artículo científico publicado en 2010

Infectious stimuli promote malignant B-cell acute lymphoblastic leukemia in the absence of AID

scientific article published on 05 December 2019

Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms

scientific journal article

Inhibition of the LSD1 (KDM1A) demethylase reactivates the all-trans-retinoic acid differentiation pathway in acute myeloid leukemia

artículo científico publicado en 2012

Integrated analysis of copy number alterations and gene expression: a bivariate assessment of equally directed abnormalities

artículo científico publicado en 2009

Integrating x4T-EDC into an Image-Portal to Establish an Ophthalmic Reading Center

artículo científico publicado en 2017

Integrative analyses for omics data: a Bayesian mixture model to assess the concordance of ChIP-chip and ChIP-seq measurements

artículo científico publicado en 2012

Integrative analysis of histone ChIP-seq and transcription data using Bayesian mixture models

artículo científico publicado en 2014

Integrative genomic analysis of pediatric T- cell lymphoblastic lymphoma reveals candidates of clinical significance

artículo científico publicado en 2020

InterCellar enables interactive analysis and exploration of cell-cell communication in single-cell transcriptomic data

artículo científico publicado en 2022

Interoperability Improvement of Mobile Patient Survey (MoPat) Implementing Fast Health Interoperability Resources (FHIR)

scientific article published on 01 January 2019

Interoperability in clinical research: from metadata registries to semantically annotated CDISC ODM.

artículo científico

Key Data Elements in Myeloid Leukemia

artículo científico publicado en 2016

Leukemia gene atlas--a public platform for integrative exploration of genome-wide molecular data

artículo científico publicado en 2012

Leukemia research in Germany: the Competence Network Acute and Chronic Leukemias

artículo científico

Leveraging the EHR4CR platform to support patient inclusion in academic studies: challenges and lessons learned

artículo científico publicado en 2017

Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.

artículo científico

Loss of the histone methyltransferase EZH2 induces resistance to multiple drugs in acute myeloid leukemia

artículo científico publicado en 2016

Low SMC1A protein expression predicts poor survival in acute myeloid leukemia.

artículo científico publicado en 2010

MOPAT@HOME: Electronic Patient Reported Outcomes Filled Out at Home, Evaluated at the Hospital

artículo científico publicado en 2017

MYST2 acetyltransferase expression and Histone H4 Lysine acetylation are suppressed in AML.

artículo científico publicado en 2015

Management of chronic pruritus: from the dermatological office to the specialized itch center: a review

scientific article published on 01 September 2017

Mapping turnaround times (TAT) to a generic timeline: a systematic review of TAT definitions in clinical domains.

artículo científico publicado en 2011

Medical Effect of Venous Thromboembolism Prophylaxis Systems and Common Input Categories: Preliminary Findings from a Systematic Review

artículo científico publicado en 2017

Microarrays Are a Robust Platform Suitable for Diagnostics.

scholarly article

Molecular characterization of acute leukemias by use of microarray technology

artículo científico publicado en 2003

Multicenter next-generation sequencing studies between theory and practice: harmonization of data analysis using real world myelodysplastic syndrome data

artículo científico publicado en 2020

Multidisciplinary education in medical informatics--a course for medical and informatics students.

artículo científico publicado en 2010

Mutations in the cohesin complex in acute myeloid leukemia: clinical and prognostic implications

artículo científico publicado en 2013

Myeloid leukemia with transdifferentiation plasticity developing from T-cell progenitors

artículo científico publicado en 2016

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

article

ODM Data Analysis-A tool for the automatic validation, monitoring and generation of generic descriptive statistics of patient data.

artículo científico publicado en 2018

ODMSummary: A Tool for Automatic Structured Comparison of Multiple Medical Forms Based on Semantic Annotation with the Unified Medical Language System

artículo científico publicado en 2016

ODMedit: uniform semantic annotation for data integration in medicine based on a public metadata repository.

artículo científico publicado en 2016

Operational Data Model Conversion to ResearchKit

artículo científico publicado en 2017

Patient recruitment workflow with and without a patient recruitment system

Pattern robustness of diagnostic gene expression signatures in leukemia

scientific article published on 01 March 2005

Populating the i2b2 database with heterogeneous EMR data: a semantic network approach.

artículo científico publicado en 2011

Portal of Medical Data Models: Status 2018

artículo científico publicado en 2019

Portal of medical data models: information infrastructure for medical research and healthcare

artículo científico publicado en 2016

Pragmatic MDR: a metadata repository with bottom-up standardization of medical metadata through reuse

artículo científico publicado en 2021

Profiling of histone H3 lysine 9 trimethylation levels predicts transcription factor activity and survival in acute myeloid leukemia

artículo científico publicado en 2010

Protocol feasibility workflow using an automated multi-country patient cohort system

artículo científico publicado en 2014

Qualitative and quantitative evaluation of EHR-integrated mobile patient questionnaires regarding usability and cost-efficiency.

artículo científico publicado en 2012

Quantitative comparison of microarray experiments with published leukemia related gene expression signatures

artículo científico publicado en 2009

Query engine optimization for the EHR4CR protocol feasibility scenario

artículo científico publicado en 2013

R453Plus1Toolbox: an R/Bioconductor package for analyzing Roche 454 Sequencing data

artículo científico publicado el 23 de febrero de 2011

RSVSim: an R/Bioconductor package for the simulation of structural variations

artículo científico publicado en 2013

Reconstructing clonal evolution in relapsed and non-relapsed Burkitt lymphoma

scientific article published on 14 May 2020

Recurrent Germline Variant in <i>RAD21</i> Predisposes Children to Lymphoblastic Leukemia or Lymphoma

artículo científico publicado en 2022

Repeated Digitized Assessment of Risk and Symptom Profiles During Inpatient Treatment of Affective Disorder: Observational Study

artículo científico publicado en 2020

Reviving 30 Year Old Technology: Lessons Learned from Transferring Patient Data Using Data Matrix Codes

scientific article published on 01 January 2019

Robust and Sensitive Detection of Insertions, Deletions and Point Mutations In CEBPA, a GC-Rich Content Gene, Using 454 Next-Generation Deep-Sequencing (NGS).

scholarly article

Robust and exact structural variation detection with paired-end and soft-clipped alignments: SoftSV compared with eight algorithms

artículo científico publicado en 2015

Robustness of Amplicon Deep Sequencing Underlines Its Utility in Clinical Applications

scholarly article by Vera Grossmann et al published July 2013 in The Journal of Molecular Diagnostics

Routine data from hospital information systems can support patient recruitment for clinical studies

artículo científico publicado en 2010

S100A2 induces metastasis in non-small cell lung cancer

artículo científico publicado en 2009

S2O - A software tool for integrating research data from general purpose statistic software into electronic data capture systems

artículo científico publicado en 2017

Safeguard function of PU.1 shapes the inflammatory epigenome of neutrophils

scientific article published on 25 March 2019

Semantic enrichment of medical forms - semi-automated coding of ODM-elements via web services

artículo científico

Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells

artículo científico publicado en 2009

Single source information systems to connect patient care and clinical research

scientific article published on 01 January 2009

Single-cell transcriptomics identifies potential cells of origin of MYC rhabdoid tumors

artículo científico publicado en 2022

Site-specific methylation of 18S ribosomal RNA by SNORD42A is required for Acute Myeloid Leukemia cell proliferation

scientific article published on 25 February 2020

Smarcb1 Loss Results in a Deregulation of esBAF Binding and Impacts the Expression of Neurodevelopmental Genes

artículo científico publicado en 2022

Standardising the Development of ODM Converters: The ODMToolBox

Standardized Cardiovascular Quality Assurance Forms with Multilingual Support, UMLS Coding and Medical Concept Analyses

artículo científico publicado en 2015

Standardized mappings--a framework to combine different semantic mappers into a standardized web-API.

artículo científico publicado en 2015

Standardized quality assurance forms for organ transplantations with multilingual support, open access and UMLS coding

artículo científico publicado en 2015

Steps towards single source--collecting data about quality of life within clinical information systems.

artículo científico publicado en 2010

Strategy for robust detection of insertions, deletions, and point mutations in CEBPA, a GC-rich content gene, using 454 next-generation deep-sequencing technology

artículo científico publicado en 2011

StudyPortal - A Novel Method to Visualize Study Research Networks

scientific article published on 01 January 2019

StudyPortal - Geovisualization of Study Research Networks

artículo científico publicado en 2019

Success criteria for electronic medical record implementations in low-resource settings: a systematic review

artículo científico publicado en 2015

Targeted Next-Generation Sequencing and Genome-Wide High-Resolution Copy Number DNA Arrays Allow the Identification of Five Novel RUNX1 Fusions In Hematological Malignancies.

artículo científico publicado en 2010

Temporal auto-regulation during human PU.1 locus SubTAD formation

scientific article published on 12 October 2018

The Clinical and Prognostic Influence Of Mutations In The Cohesin Complex In Acute Myeloid Leukemia

artículo científico publicado en 2013

The Gene Expression Profile in CLL Better Reflects the Igvh-Mutational Status Than the Most Common Chromosome Aberrations.

artículo científico publicado en 2004

The Interlaboratory Robustness of Next-Generation Sequencing (IRON) Study Phase II: Deep-Sequencing Analyses of Hematological Malignancies Performed by an International Network Involving 26 Laboratories

artículo científico publicado en 2012

The Pax5 Fusion Product Pax5-C20orf112 Causes Downregulation of Pre-B Cell Receptor Genes and Induces Differential Proliferation Patterns in B-Lymphoblastic Cell Lines.

scholarly article

The Portal of Medical Data Models: Where Have We Been and Where Are We Going?

artículo científico publicado en 2017

The Smart Device System for Movement Disorders: Preliminary Evaluation of Diagnostic Accuracy in a Prospective Study

artículo científico publicado en 2020

The need for harmonized structured documentation and chances of secondary use - results of a systematic analysis with automated form comparison for prostate and breast cancer

artículo científico

The single source architecture x4T to connect medical documentation and clinical research

artículo científico publicado en 2011

Towards a trial-ready mobile patient questionnaire system.

artículo científico publicado en 2014

Transcriptional Profiling Identifies Genes Differentially Regulated by the BCR/ABL Fusion Oncogene.

scholarly article

Transferring HIS data to population-based cancer registries - concept and first implementations.

artículo científico publicado en 2009

Translocation t(14;19)(q32;q13) Is a Rare Abnormality in CLL and Associated with Trisomy 12, an Unmutated IgVH Status and a Distinct Gene Expression Profile.

artículo científico publicado en 2007

Two Novel Distinct Subtypes of Myeloid Neoplasms Molecularly Associated with Histone H3K36 Methylations

artículo científico publicado en 2015

Understanding the Nature of Metadata: Systematic Review

artículo científico publicado en 2022

Using Electronic Health Records to Support Clinical Trials: A Report on Stakeholder Engagement for EHR4CR

artículo científico publicado en 2015

Using electronic health records for clinical research: the case of the EHR4CR project

artículo científico publicado en 2014

Validation of Pruritus Measures Gathered with the Electronic Patient-reported Outcome System MoPat.

artículo científico publicado en 2017

Web-Based Information Infrastructure Increases the Interrater Reliability of Medical Coders: Quasi-Experimental Study

artículo científico publicado en 2018

Web-based multi-site feasibility questionnaire tool

artículo científico publicado en 2015

What Information Does Your EHR Contain? Automatic Generation of a Clinical Metadata Warehouse (CMDW) to Support Identification and Data Access Within Distributed Clinical Research Networks

artículo científico publicado en 2017

Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype

artículo científico publicado en 2011

Workflow to improve patient recruitment for clinical trials within hospital information systems - a case-study

artículo científico publicado en 2008

[Psychooncological interventions - what do cancer patients aged 60 years or older wish for?]

artículo científico publicado en 2011

appreci8: a pipeline for precise variant calling integrating 8 tools

artículo científico publicado en 2018