| human | Q5 |
| P496 | ORCID iD | 0000-0002-0400-9542 |
| P2038 | ResearchGate profile ID | Edwin_Cuppen |
| P184 | doctoral advisor | Bé Wieringa | Q54297130 |
| P108 | employer | University Medical Center Utrecht | Q2456800 |
| Hubrecht Institute | Q2512544 | ||
| P735 | given name | Edwin | Q240931 |
| Edwin | Q240931 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q90598019 | 5-Fluorouracil treatment induces characteristic T>G mutations in human cancer |
| Q89555837 | A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns |
| Q31087541 | A functional screen identifies specific microRNAs capable of inhibiting human melanoma cell viability |
| Q33321064 | A genome-wide SNP panel for mapping and association studies in the rat. |
| Q30425836 | A hypomorphic mutation in Lpin1 induces progressively improving neuropathy and lipodystrophy in the rat |
| Q28592623 | A novel mutant allele of Ncx1: a single amino acid substitution leads to cardiac dysfunction |
| Q37094235 | A systematic genome-wide analysis of zebrafish protein-coding gene function |
| Q30481194 | Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries |
| Q38007323 | Application of exome sequencing in the search for genetic causes of rare disorders of copper metabolism |
| Q36493253 | Approaches to microRNA discovery |
| Q92023072 | Biallelic variants in POLR3GL cause endosteal hyperostosis and oligodontia |
| Q24800430 | CASCAD: a database of annotated candidate single nucleotide polymorphisms associated with expressed sequences |
| Q24812255 | CONREAL web server: identification and visualization of conserved transcription factor binding sites |
| Q89121167 | Cancer cells copy migratory behavior and exchange signaling networks via extracellular vesicles |
| Q30419099 | Cell autonomous lipin 1 function is essential for development and maintenance of white and brown adipose tissue |
| Q39222413 | Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring |
| Q21184064 | Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer |
| Q92916364 | Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer |
| Q27853105 | Detailed imaging and genetic analysis reveal a secondary BRAF(L505H) resistance mutation and extensive intrapatient heterogeneity in metastatic BRAF mutant melanoma patients treated with vemurafenib |
| Q28506643 | Diabetes risk gene and Wnt effector Tcf7l2/TCF4 controls hepatic response to perinatal and adult metabolic demand |
| Q112703012 | Different responses to DNA damage determine ageing differences between organs |
| Q24337521 | Dominant-negative ALK2 allele associates with congenital heart defects |
| Q28592916 | E2F7 represses a network of oscillating cell cycle genes to control S-phase progression |
| Q43219651 | ENU mutagenesis to generate genetically modified rat models |
| Q64290587 | Early divergence of mutational processes in human fetal tissues |
| Q24814007 | Efficient single nucleotide polymorphism discovery in laboratory rat strains using wild rat-derived SNP candidates |
| Q31024384 | Efficient target-selected mutagenesis in zebrafish |
| Q40064881 | Epigenomic annotation of gene regulatory alterations during evolution of the primate brain. |
| Q38099306 | Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology |
| Q51901493 | Exploring conservation of transcription factor binding sites with CONREAL. |
| Q34066126 | Functional microRNA screening using a comprehensive lentiviral human microRNA expression library |
| Q28303521 | Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients |
| Q30862430 | GENOTRACE: cDNA-based local GENOme assembly from TRACE archives |
| Q63804582 | Generation of Genetically Modified Rodents Using Random ENU Mutagenesis |
| Q33712981 | Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers |
| Q34871454 | Haplotype block structure is conserved across mammals |
| Q34021045 | High-throughput target-selected gene inactivation in zebrafish |
| Q46045138 | Highly Efficient ENU Mutagenesis in Zebrafish. |
| Q39750772 | Hyperactivation of the G12-mediated signaling pathway in Caenorhabditis elegans induces a developmental growth arrest via protein kinase C. |
| Q28117422 | Identification and molecular characterization of BP75, a novel bromodomain-containing protein |
| Q43104046 | Identification of Srp9 as a febrile seizure susceptibility gene |
| Q31014484 | Identification of factors required for meristem function in Arabidopsis using a novel next generation sequencing fast forward genetics approach |
| Q30494611 | Identification of genetic modifiers of behavioral phenotypes in serotonin transporter knockout rats |
| Q30421160 | Incomplete segregation of MYH11 variants with thoracic aortic aneurysms and dissections and patent ductus arteriosus |
| Q50325174 | KOUNCIL: Kidney-Oriented Understanding of Correcting Ciliopathies. |
| Q28254408 | Long-term culture of genome-stable bipotent stem cells from adult human liver |
| Q64244995 | Long-term expanding human airway organoids for disease modeling |
| Q24652239 | Mammalian mirtron genes |
| Q44794525 | Mapping and phasing of structural variation in patient genomes using nanopore sequencing |
| Q37711814 | Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. |
| Q47351515 | Measuring mutation accumulation in single human adult stem cells by whole-genome sequencing of organoid cultures |
| Q40665907 | Mechanisms of Therapy Resistance in Patient-Derived Xenograft Models of BRCA1-Deficient Breast Cancer |
| Q28580846 | Melanocortin receptor 4 deficiency affects body weight regulation, grooming behavior, and substrate preference in the rat |
| Q40010591 | Methods for small RNA preparation for digital gene expression profiling by next-generation sequencing |
| Q37609839 | Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells |
| Q92306014 | Molecular tumour boards and molecular diagnostics for patients with cancer in the Netherlands: experiences, challenges, and aspirations |
| Q37451936 | Next-generation sequencing approaches in genetic rodent model systems to study functional effects of human genetic variation |
| Q28610872 | Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects |
| Q42478363 | No link of serotonin 2C receptor editing to serotonin transporter genotype |
| Q27678049 | Nucleosomal DNA binding drives the recognition of H3K36-methylated nucleosomes by the PSIP1-PWWP domain |
| Q34456438 | Organoid models of human and mouse ductal pancreatic cancer |
| Q101226336 | Pan-cancer landscape of homologous recombination deficiency |
| Q91824416 | Pancreatic cancer organoids recapitulate disease and allow personalized drug screening |
| Q28302536 | Phylogenetic shadowing and computational identification of human microRNA genes |
| Q28592590 | Planar cell polarity defects and defective Vangl2 trafficking in mutants for the COPII gene Sec24b |
| Q64054064 | Portrait of a cancer: mutational signature analyses for cancer diagnostics |
| Q112746644 | Precancerous liver diseases do not cause increased mutagenesis in liver stem cells |
| Q41547803 | Predicting clinical benefit from everolimus in patients with advanced solid tumors, the CPCT-03 study |
| Q38406426 | Primary colorectal cancers and their subsequent hepatic metastases are genetically different: implications for selection of patients for targeted treatment |
| Q53473853 | Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT. |
| Q91695649 | Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants |
| Q39772700 | Proteins interacting with Caenorhabditis elegans Galpha subunits |
| Q98204998 | Publisher Correction: The mutational impact of culturing human pluripotent and adult stem cells |
| Q30480845 | RAP-1 and the RAL-1/exocyst pathway coordinate hypodermal cell organization in Caenorhabditis elegans |
| Q43227093 | Rats go genomic. |
| Q112292167 | Reconstructing single-cell karyotype alterations in colorectal cancer identifies punctuated and gradual diversification patterns |
| Q34012712 | Reduced rates of gene loss, gene silencing, and gene mutation in Dnmt1-deficient embryonic stem cells. |
| Q52423597 | Sequential cancer mutations in cultured human intestinal stem cells. |
| Q46011131 | Serotonin transporter deficiency increases abdominal fat in female, but not male rats. |
| Q24628976 | Small RNA expression and strain specificity in the rat |
| Q96135754 | Sperm DNA damage causes genomic instability in early embryonic development |
| Q39141920 | Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease |
| Q28387704 | Systematic biases in DNA copy number originate from isolation procedures |
| Q44714383 | Target-selected mutagenesis of the rat. |
| Q35937517 | Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material |
| Q46744970 | The Atp1a1 gene from inbred Dahl salt sensitive rats does not contain the A1079T missense transversion |
| Q31120231 | The Genomic Scrapheap Challenge; Extracting Relevant Data from Unmapped Whole Genome Sequencing Reads, Including Strain Specific Genomic Segments, in Rats |
| Q48179359 | The PLETHORA Gene Regulatory Network Guides Growth and Cell Differentiation in Arabidopsis Roots |
| Q92147951 | The molecular genetic make-up of male breast cancer |
| Q95300102 | The mutational impact of culturing human pluripotent and adult stem cells |
| Q34430352 | The neuronal nitric oxide synthase PDZ motif binds to -G(D,E)XV* carboxyterminal sequences. |
| Q63866011 | The serotonin transporter knock-out rat: a review |
| Q28567372 | The serotonin transporter plays an important role in male sexual behavior: a study in serotonin transporter knockout rats |
| Q48161214 | Toward effective software solutions for big biology |
| Q35681731 | Translational regulation shapes the molecular landscape of complex disease phenotypes. |
| Q92129277 | Tubuloids derived from human adult kidney and urine for personalized disease modeling |
| Q114123787 | Unscrambling cancer genomes via integrated analysis of structural variation and copy number |
| Q47799650 | Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer. |
| Q38797398 | Wnt-induced transcriptional activation is exclusively mediated by TCF/LEF. |
| Q37174307 | Zebrafish as a cancer model |
| Q47074039 | Zebrafish with mutations in mismatch repair genes develop neurofibromas and other tumors |
| Q27320810 | miR-127 protects proximal tubule cells against ischemia/reperfusion: identification of kinesin family member 3B as miR-127 target |
| Q54297130 | Bé Wieringa | doctoral student | P185 |
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