R. Eijk

发表

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

R. Vossen, Arnoud Boot, I. Tomlinson, 2017, British Journal of Cancer.

Integrating chromosomal aberrations and gene expression profiles to dissect rectal cancer

E. Lips, J. Oosting, C. V. D. Velde, 2008 .

Variants Modify Colorectal Cancer Risk n Lynch Syndrome

P. Devilee, I. Tomlinson, S. Verhoef, 2022 .

on Archival Tissue Using SNP Arrays

H. Morreau, E. Lips, J. Oosting, 2011 .

High‐Resolution Analysis of Genomic Copy Number Changes

B. Ylstra, G. Meijer, H. Morreau, 2010 .

Genotyping and LOH Analysis on Archival Tissue using SNP Arrays

H. Morreau, E. Lips, J. Oosting, 2010 .

Central nervous system involvement in early and late syphilis: The problem of asymptomatic neurosyphilis

E. Wolters, E. Hische, J. Bos, 1988, Journal of the Neurological Sciences.

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

Peter Devilee, Ronald van Eijk, Tamara Peelen, 1997, Nature Genetics.

Monoclonal antibody directed against a surface-exposed protein antigen common in gonococcal strains

R. Eijk, O. Ijsselmuiden, C. Agterberg, 1988 .

Solid-phase enzyme immunoassay for detection ofChlamydia trachomatis

K. H. Tjiam, M. Michel, E. Stolz, 1985, European Journal of Clinical Microbiology.

CSNK1A1 expression modifies TP53 effects on survival of colon cancer patients

H. Morreau, J. Oosting, W. Corver, 2012 .

Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas

H. Morreau, H. Vasen, C. Tops, 2008, Familial Cancer.

Diagnostic and prognostic significance of CDKN2A/CDKN2B deletions in patients with transformed mycosis fungoides and primary cutaneous CD30‐positive lymphoproliferative disease

R. Willemze, W. Zoutman, C. Tensen, 2015, The British journal of dermatology.

Enzyme-linked immunofiltration assay for rapid serodiagnosis of syphilis

M. Meinardi, H. Menke, E. Stolz, 1987, European Journal of Clinical Microbiology.

Technological advances in molecular pathology : a journey into the archives

R. Eijk, 2013 .

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Dennis E Bulman, Ronald van Eijk, Peter J Oefner, 1996, Cell.

of Genomic Copy Number Changes

B. Ylstra, G. Meijer, H. Morreau, 2011 .

The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group.

M. Beckmann, T. Sellers, M. Stratton, 2000, American journal of human genetics.

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

R. R. Frants, R. Fossdal, L. Sandkuijl, 1993, Nature Genetics.

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

R. Ophoff, H. Diener, M. Ferrari, 1995, Human Genetics.

Transfusion Syphilis, Survival of Treponema pallidum in Stored Donorblood 1

V. Vuzevski, F. Kate, R. Eijk, 1985 .

A 3-Mb Region for the Familial Hemiplegic Migraine Locus on 19p13.1–p13.2: Exclusion of PRKCSH as a Candidate Gene

M. Ferrari, H. Mohrenweiser, G. Terwindt, 1996, European journal of human genetics : EJHG.

PIK3CA kinase domain mutation identifies a subgroup of stage III colon cancer patients with poor prognosis

P. Kuppen, H. Morreau, C. Velde, 2011, Cellular Oncology.

Evaluation of the direct fluorescent antibody test for diagnosis of chlamydial infections

K. H. Tjiam, M. Michel, E. Stolz, 1985, European Journal of Clinical Microbiology.

Near‐haploidization significantly associates with oncocytic adrenocortical, thyroid, and parathyroid tumors but not with mitochondrial DNA mutations

H. Morreau, J. Oosting, W. Corver, 2014, Genes, chromosomes & cancer.

Tissue Preparation and Next-generation Sequencing Workflows for Oncology Testing

Ronald van Eijk, Stijn Crobach, R. Eijk, 2014 .

University of Groningen Beneficial Effects of the mTOR Inhibitor Everolimus in Patients with Advanced Medullary Thyroid Carcinoma

H. Gelderblom, T. Links, E. Kapiteijn, 2019 .

Does it Make Sense for Blood Transfusion Services to Continue the Time-Honored Syphilis Screening with Cardiolipin Antigen?

P. Holland, J. Leikola, W. Wagstaff, 1981 .

Solid phase enzyme immunoassay for detection of non-complicated cervical infection withChlamydia trachomatis

J. Wagenvoort, E. Stolz, R. Eijk, 1988, European Journal of Clinical Microbiology and Infectious Diseases.

Monoclonal Antibodies Against IgG Subclasses

A. Vlug, H. Brouwer, G. Lange, 1989 .

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded tissue

H. Morreau, D. Ruano, R. Eijk, 2018 .

Multiplex Ligation‐Dependent Probe Amplification for the Detection of 1p and 19q Chromosomal Loss in Oligodendroglial Tumors

P. Eilers, A. Cleton-Jansen, J. Kros, 2005, Brain pathology.

Single-Nucleotide Polymorphism Loss of Heterozygosity Analysis of the Protein Tyrosine Phosphatase Receptor Type J in Familial Colorectal Cancer

H. Morreau, A. Cleton-Jansen, P. Stanssens, 2005 .

Genetic Stability of Driver Alterations in Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type and Their Relapses: A Rationale for the Use of Molecular-Based Methods for More Effective Disease Monitoring

T. van Wezel, R. Willemze, H. Veelken, 2022, Cancers.

Apparent Lack of BRAFV600E Derived HLA Class I Presented Neoantigens Hampers Neoplastic Cell Targeting by CD8+ T Cells in Langerhans Cell Histiocytosis

L. M. Voortman, C. Hawkins, D. Roelen, 2020, Frontiers in Immunology.

E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines

P. Eilers, A. Cleton-Jansen, B. van de Water, 2006, British Journal of Cancer.

Genetic heterogeneity of familial hemiplegic migraine.

R. Ophoff, M. Ferrari, L. Sandkuijl, 1994, Genomics.

659: Somatic mutation profiles in primary colorectal cancers and matching ovarian metastases: Identification of driver and passenger mutations

G. Fleuren, H. Morreau, D. Ruano, 2014 .

Increased frequency of 20q gain and copy‐neutral loss of heterozygosity in mismatch repair proficient familial colorectal carcinomas

H. Morreau, T. van Wezel, T. Caldés, 2012, International journal of cancer.