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- 2024
- A proteogenomic atlas of the human neural retina (2024) FRONTIERS IN GENETICS. 15.
- Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci (2024) NATURE COMMUNICATIONS. 15(1).
- Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease (2024) GENOME MEDICINE. 16(1).
- Structural variants disrupt a critical regulatory region downstream of FOXG1 (2024) Belgian Society for Human Genetics (BeSHG) Annual Symposium 2024 : Single Cells : to care or not to care, Abstracts.
- Contribution of combined stressors on density and gene expression dynamics of the copepod Temora longicornis in the North Sea (2024) MOLECULAR ECOLOGY. p.1-23
- An in-depth investigation of the microbiota and its virulence factors associated with severe udder cleft dermatitis lesions (2024) JOURNAL OF DAIRY SCIENCE. 107(5). p.3219-3234
- Myb overexpression synergizes with the loss of Pten and is a dependency factor and therapeutic target in T-cell lymphoblastic leukemia (2024) HEMASPHERE. 8(3).
- Genome-wide methylome stability and parental effects in the worldwide distributed Lombardy poplar (2024) BMC BIOLOGY. 22(1).
- Baselining physiological parameters in three muscles across three equine breeds : what can we learn from the horse? (2024) FRONTIERS IN PHYSIOLOGY. 15.
- Expression profile and gap-junctional transfer of microRNAs in the bovine cumulus-oocyte complex (2024) FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY. 12.
- Proteomics data in vitiligo : a scoping review (2024) FRONTIERS IN IMMUNOLOGY. 15.
- MicroRNA-146b negatively affects bovine embryo development and quality (2024) REPRODUCTION. 167(2).
- A dual role for PSIP1/LEDGF in T cell acute lymphoblastic leukemia (2024) SCIENCE ADVANCES. 10(44).
- How temperature modulates the expression of pathogenesis-related molecules of the cross-kingdom pathogen Lasiodiplodia hormozganensis (2024) SCIENCE OF THE TOTAL ENVIRONMENT. 927.
- High-throughput single-cell screening of viable hybridomas and patient-derived antibody-secreting cells using punchable microwells (2024) ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY. 52(1). p.426-436
- The role of Helicobacter suis, Fusobacterium gastrosuis, and the pars oesophageal microbiota in gastric ulceration in slaughter pigs receiving meal or pelleted feed (2024) VETERINARY RESEARCH. 55(1).
- A genomic urine assay for surveillance of patients with bladder cancer treated with radiotherapy (2024) EUROPEAN UROLOGY OPEN SCIENCE. 62. p.131-139
- Quantitative transcriptomic and epigenomic data analysis : a primer (2024) BIOINFORMATICS ADVANCES. 4(1).
- Hyperdimensional computing : a fast, robust, and interpretable paradigm for biological data (2024) PLOS COMPUTATIONAL BIOLOGY. 20(9).
- Loss-of-imprinting of HM13 leads to poor prognosis in clear cell renal cell carcinoma (2024) BIOMOLECULES. 14(8).
- Multimodal deregulation of imprinted gene HM13 : a pan-cancer study (2024) Long-Read Sequencing Workshop 2024, Abstracts.
- Applications of nanopore sequencing for forensic analysis (2024) Next generation sequencing (NGS) technology in DNA analysis. p.85-98
- Osteopontin characterizes bile duct-associated macrophages and correlates with liver fibrosis severity in primary sclerosing cholangitis (2024) HEPATOLOGY. 79(2). p.269-288
- Myeloid A20 is critical for alternative macrophage polarization and type-2 immune-mediated helminth resistance (2024) FRONTIERS IN IMMUNOLOGY. 15.
- Mycothione reductase as a potential target in the fight against Mycobacterium abscessus infections (2024) MSPHERE. 9(1).
- From follicle to blastocyst : microRNA-34c from follicular fluid-derived extracellular vesicles modulates blastocyst quality (2024) JOURNAL OF ANIMAL SCIENCE AND BIOTECHNOLOGY. 15(1).
- Exploring mode-of-action for acute toxicity of primary aromatic amines with D. magna using differential gene expression analysis (2024) SETAC Europe, 34th Annual Meeting, Abstracts. p.115-116
- HES6 knockdown in human hematopoietic precursor cells reduces their in vivo engraftment potential and their capacity to differentiate into erythroid cells, B cells, T cells and plasmacytoid dendritic cells (2024) HAEMATOLOGICA. 109(11). p.3578-3592
- Impact of nutrient excess on physiology and metabolism of Sulfolobus acidocaldarius (2024) FRONTIERS IN MICROBIOLOGY. 15.
- Implicit bias in diagnosing mosaicism amongst preimplantation genetic testing providers : results from a multicenter study of 36 395 blastocysts (2024) HUMAN REPRODUCTION. 39(1). p.258-274
- Pronuclear transfer rescues poor embryo development of in vitro-grown secondary mouse follicles (2024) HUMAN REPRODUCTION OPEN. 2024(1).
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder (2024)
- Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability (2024) AMERICAN JOURNAL OF HUMAN GENETICS. 111(3). p.509-528
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder (2024) 18th Troina Meeting on Genetics of Neurodevelopmental Disorders, Abstracts.
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder (2024) Belgian Society for Human Genetics (BeSHG) Annual Symposium 2024 : Single Cells : to care or not to care, Abstracts.
- Aligning genotyping and copy number data in single trophectoderm biopsies for aneuploidy prediction : uncovering incomplete concordance (2024) HUMAN REPRODUCTION OPEN. 2024(4).
- Neoantigen-targeted dendritic cell vaccination in lung cancer patients induces long-lived T cells exhibiting the full differentiation spectrum (2024) CELL REPORTS MEDICINE. 5(5).
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder (2024) MEDRXIV.
- Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing (2024) STEM CELL RESEARCH. 81.
- Effect of biphasic CAPA-IVM on ovarian tissue oocytes of transgender men (2024) HUMAN REPRODUCTION. In Human Reproduction 39(Supplement 1). p.i360-i361
- Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform (2024) CLINICAL GENETICS. p.1-13
- Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction (2024) AMERICAN JOURNAL OF HUMAN GENETICS. 111(2). p.393-402
- Towards uncovering the role of incomplete penetrance in maculopathies through sequencing of 105 disease-associated genes (2024) BIOMOLECULES. 14(3).
- Evolutionary origin of Hoxc13-dependent skin appendages in amphibians (2024) NATURE COMMUNICATIONS. 15(1).
- Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci (2024) GENOME BIOLOGY. 25(1).
- ERN-EYE virtual clinic for rare eye diseases as a successful effort towards solving complex and rare ophthalmic conditions in Europe (2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.379-380
- In memory of Ludwine Messiaen, Ph.D. (1956-2024) (2024) CLINICAL GENETICS.
- The clinical use of exome sequencing to diagnose PCD patients (2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.385-385
- The retina-specific 3D genome and the impact of structural variation in inherited retinal disease (2024)
- Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development (2024) Nature Communications. 15(1).
- CRISPR/Cas9 mediated disruption of an evolutionary conserved putative enhancer in the mab21l2 locus induces developmental eye anomalies in Xenopus tropicalis (2024) EUROPEAN JOURNAL OF HUMAN GENETICS. 32. p.247-247
- Epigenetics in personalized toxicity (2024) Personalized epigenetics : a volume in translational epigenetics. p.229-248
- The promise of omics approaches for pediatric drug development (2024) Essentials of translational pediatric drug development : from past needs to future oportunities. p.257-280
- Acoustic ejection mass spectrometry empowers ultra-fast protein biomarker quantification (2024) NATURE COMMUNICATIONS. 15(1).
- Effects of hypothermia and hypoxia on cytochrome P450‐mediated drug metabolism in neonatal Göttingen minipigs (2024) Basic & Clinical Pharmacology & Toxicology.
- Mass Spectrometry-based Profiling of Single-cell Histone Post-translational Modifications to Dissect Chromatin Heterogeneity (2024)
- ClassiCOL : LC-MS/MS analysis for ancient species classification via collagen peptide ambiguation (2024) BIORXIV.
- 2023
- Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis (2023) FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY. 11.
- A systematic approach to characterize the contribution of 5'UTR variation to inherited retinal disease (2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
- Unraveling the genetic basis of early-onset inherited retinal disease in a Saudi Arabian cohort reveals a novel RIMS2-related family (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.114-114
- An integrated approach using multi-omics data to dissect cis-regulatory role of ultraconserved non-coding elements (UCNEs) in human retina (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.5-5
- Identification and characterization of a novel retinaspecific lncRNA upstream ABCA4 with a potential role in ABCA4-associated inherited retinal disease (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.78-79
- Dual molecular effects of constitutional SF3B2 variants cause a novel dominant spliceosomopathy displaying retinitis pigmentosa or developmental skeletal anomalies (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.71-71
- Single domain antibodies to study orphan receptors and tackle their mutant counterpart with dominant-negative effect (2023) Nuclear Receptor Research Network, 15th Meeting, Abstracts.
- HIV-PULSE : a long-read sequencing assay for high-throughput near full-length HIV-1 proviral genome characterization (2023) BioRXiv.
- HIV-PULSE : a long-read sequencing assay for high-throughput near full-length HIV-1 proviral genome characterization (2023) NUCLEIC ACIDS RESEARCH. 51(20). p.e102-e102
- Single-cell profiling identifies a novel human polyclonal unconventional T cell lineage (2023) JOURNAL OF EXPERIMENTAL MEDICINE. 220(6).
- Structural variants disrupt a critical regulatory region downstream of FOXG1 (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.28-28
- BeSolveRD : the Belgian genome resource to resolve rare diseases (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.573-574
- Structural variants disrupt a critical regulatory region downstream of FOXG1 (2023) 17th Troina Meeting on Genetics of Neurodevelopmental Disorders Abstract Book. p.9-9
- Structural variants disrupt a critical regulatory region downstream of FOXG1 (2023) 15th Meeting of the Belgian Society for Neuroscience, Abstracts.
- Structural variants disrupt a critical regulatory region downstream of FOXG1 (2023) EMBO Workshop 'Gene regulatory mechanisms in neural fate decisions', Abstracts.
- Severe udder cleft dermatitis lesion transcriptomics points to an impaired skin barrier, defective wound repair and a dysregulated inflammatory response as key elements in the pathogenesis (2023) PLOS ONE. 18(7).
- Comparative transcriptomics of porcine liver-resident CD8αdim, liver CD8αhigh and circulating blood CD8αhigh NK cells reveals an intermediate phenotype of liver CD8αhigh NK cells (2023) FRONTIERS IN IMMUNOLOGY. 14.
- Cathepsin-L secreted by high-quality bovine embryos exerts an embryotrophic effect in vitro (2023) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 24(7).
- Targeted haplotyping in pharmacogenomics using Oxford Nanopore Technologies' adaptive sampling (2023) FRONTIERS IN PHARMACOLOGY. 14.
- Dynamic of training and acute exercised-induced shifts in muscular glucose transporter (GLUT) 4, 8 and 12 expression in locomotion versus posture muscles in healthy horses. (2023) Proceedings of the European College of Equine Internal Medicine (ECEIM) congress.
- Baselining physiological parameters in posture versus locomotion muscles across breeds towards tailored dietary and training management (2023) Proceedings of the European College of Equine Internal Medicine (ECEIM) congress.
- Effect of aleurone on glucose & insuline dynamics and gut microbiome of trained horses (2023) Nutrition Society Winter Conference, Abstracts.
- Dynamics of training and acute exercise-induced shifts in muscular glucose transporter (GLUT) 4, 8, and 12 expression in locomotion versus posture muscles in healthy horses (2023) FRONTIERS IN PHYSIOLOGY. 14.
- Molecular analysis of broad-spectrum induced resistance in rice by the green leaf volatile Z-3-hexenyl acetate (2023) JOURNAL OF EXPERIMENTAL BOTANY. 74(21). p.6804-6819
- RIPK1 kinase-dependent inflammation and cell death contribute to the pathogenesis of COPD (2023) EUROPEAN RESPIRATORY JOURNAL. 61(4).
- How do engineered Yarrowia lipolytica strains secrete free fatty acids : hints from comparative transcriptomics (2023) FEMS YEAST RESEARCH. 23.
- Differential protease content of mast cells and the processing of IL-33 in Alternaria alternata induced allergic airway inflammation in mice (2023) FRONTIERS IN IMMUNOLOGY. 14.
- Multimodal deregulation of imprinted gene HM13 leads to pan-cancer upregulation of putative oncogene MCTS2 (2023) The RNA processing in cancer conference : from bench to bedside.
- Cost-effectiveness of an urinary biomarker panel in combination with MRI for prostate cancer diagnosis (2023) WORLD JOURNAL OF UROLOGY. 41(6). p.1527-1532
- Challenges in neoantigen-directed therapeutics (2023) CANCER CELL. 41(1). p.15-40
- Variational autoencoders to predict DNA-methylation age and provide biological insights in age-related health and disease (2023)
- A urine-based genomic assay improves risk stratification for patients with high-risk hematuria stratified according to the American Urological Association guidelines (2023) EUROPEAN UROLOGY ONCOLOGY. 6(2). p.183-189
- Systematic comparison of experimental and human obstructive cholestasis reveals conservation of canonical pathway activation and biomarkers relevant for cholestatic liver disease (2023) GENES & DISEASES. 10(1). p.18-21
- Elucidating the combined toxicity of aflatoxin B1 and fumonisin B1 on HepG2 cells based on respirometry and transcriptome analyses (2023) BIORXIV.
- Identification of a novel idiopathic epilepsy risk locus and a variant in the CCDC85A gene in the Dutch partridge dog (2023) ANIMALS. 13(5).
- Transcriptomics reveal molecular differences in equine oocytes vitrified before and after in vitro maturation (2023) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 24(8).
- Effects of biologics treatment in type 2-high chronic rhinosinusitis with nasal polyp patients (2023) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. In Journal of Allergy and Clinical Immunology 151(2, Supplement 1). p.AB187-AB187
- A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract (2023) HUMAN GENETICS. 142(3). p.457-476
- Guar gum as galactomannan source induces dysbiosis and reduces performance in broiler chickens and dietary β-mannanase restores the gut homeostasis (2023) POULTRY SCIENCE. 102(8).
- Post-feeding transcriptomics reveals essential genes expressed in the midgut of the desert locust (2023) FRONTIERS IN PHYSIOLOGY. 14.
- New insights into the combined toxicity of aflatoxin B1 and fumonisin B1 in HepG2 cells using Seahorse respirometry analysis and RNA transcriptome sequencing (2023) ENVIRONMENT INTERNATIONAL. 175.
- Identification and profiling of a novel Bombyx mori latent virus variant acutely infecting Helicoverpa armigera and Trichoplusia ni (2023) VIRUSES-BASEL. 15(5).
- Transcriptional and translational dynamics underlying heat shock response in the thermophilic crenarchaeon Sulfolobus acidocaldarius (2023) MBIO. 14(5).
- Myeloid OTULIN deficiency couples RIPK3-dependent cell death to Nlrp3 inflammasome activation and IL-1β secretion (2023) SCIENCE IMMUNOLOGY. 8(89).
- A spatial human thymus cell atlas mapped to a continuous tissue axis (2023) BIORXIV.
- Intrathymic dendritic cell-biased precursors promote human T cell lineage specification through IRF8-driven transmembrane TNF (2023) NATURE IMMUNOLOGY. 24(3). p.474-486
- Effect on colorectal cancer bioenergetics by chronic exposure to red meat metabolites (2023) Tumor heterogeneity, plasticity and therapy, 2nd edition, Abstracts.
- Chronic exposure to dietary compounds shifts bioenergetics in colorectal cancer (2023) Ghent Gut Inflammation Group, 4th Meeting, Abstracts.
- The multi-omics single-cell landscape of sinus mucosa in uncontrolled severe chronic rhinosinusitis with nasal polyps (2023) CLINICAL IMMUNOLOGY. 256.
- Characterization of ovarian tissue oocytes from transgender men reveals poor calcium release and embryo development, which might be overcome by spindle transfer (2023) HUMAN REPRODUCTION. 38(6). p.1135-1150
- Effect of biphasic CAPA-IVM on ovarian tissue oocytes of transgender men (2023) HUMAN REPRODUCTION. In Human Reproduction 38(Supplement 1). p.i396-i397
- Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing (2023) STEM CELL RESEARCH. 67.
- Inherited pathogenic variants in neurodevelopmental disorders : a potential pitfall in triobased analysis of clinical exomes (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.460-460
- Valuable insights after one year whole exome sequencing in a fetal/prenatal setting (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.356-356
- Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos (2023) MOLECULAR THERAPY. 31(8). p.2326-2341
- Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability (2023) Research Day 2023, Abstracts.
- Long-read sequencing enables full characterization of previously unresolved structural variation (2023) Nanopore Day Paris 2023, Abstracts.
- Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability (2023) Belgian Society for Human Genetics (BeSHG) Annual Meeting 2023 : To DNA and beyond, Abstracts.
- Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation (2023) Genomics of Rare Disease 2023 Conference, Abstracts.
- Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation (2023) European Society for Human Genetics (ESHG) Conference 2023, Abstracts.
- Nuclear transfer overcomes poor embryo development of in vitro grown mouse oocytes (2023) HUMAN REPRODUCTION. 38(Supplement 1). p.i383-i384
- Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability (2023) Revolutionizing Next-Generation Sequencing, 5th Tools & Technologies Conference, Abstracts.
- MIDRIXNEO-LUNG : safety and immunogenicity of a neoantigen-presenting autologous dendritic cell therapy in resected NSCLC patients (2023) JOURNAL OF THORACIC ONCOLOGY. In Journal of Thoracic Oncology 18(11, Supplement). p.S526-S526
- CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis (2023) JOURNAL OF CLINICAL INVESTIGATION. 133(8).
- HRAS-related epidermal nevus syndromes : expansion of the spectrum with first branchial arch defects (2023) CLINICAL GENETICS. 103(6). p.709-713
- New noncoding base pair mutation at the identical locus as the original NCMD/MCDR1 in a Mexican family, suggesting a mutational hotspot (2023) JOURNAL OF VITREORETINAL DISEASES. 7(1). p.33-42
- The role of MCM9 in the etiology of Sertoli cell-only syndrome and premature ovarian insufficiency (2023) JOURNAL OF CLINICAL MEDICINE. 12(3).
- Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci (2023)
- Results of Belgian patients with RPE65-related inherited retinal dystrophy 6 months after treatment with voretigene neparvovec (2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
- Deciphering the genetic architecture of inherited retinal diseases in the Iranian population by integrated exome sequencing (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.367-367
- Benefits of whole exome sequencing to advance the genetic diagnosis in patients with differences (disorders) of sex development (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.382-383
- Targeted sequencing using single-molecule Molecular Inversion Probes reveals severe bi-allelic ABCA4 alleles in probands diagnosed with Leber congenital amaurosis (2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
- Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases (2023) HUMAN GENETICS AND GENOMICS ADVANCES. 4(1).
- Multi-omics profiling, in vitro and in vivo approaches to interpret non-coding variation in inherited retinal diseases (2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
- Compendium of clinical variant classification for 2,246 unique ABCA4 variants to clarify variant pathogenicity in Stargardt disease using a modified ACMG/AMP framework (2023) HUMAN MUTATION. 2023.
- Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development : a cross-sectional study (2023) EUROPEAN JOURNAL OF ENDOCRINOLOGY. 190(1). p.34-43
- Mapping the 3D genome of the human retina and its role in retinal disease (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.57-57
- Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium (2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
- Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci (2023) EMBO Workshop 'Enhanceropathies : Understanding enhancer function to understand human disease', Abstracts.
- The evolving role of medical geneticists in the era of gene therapy : an urgency to prepare (2023) GENETICS IN MEDICINE. 25(4).
- Paediatric cataract surgery with 27G vitrectomy instrumentation : the Ghent University Hospital experience (2023) FRONTIERS IN MEDICINE. 10.
- An in vitro enzymatic assay to elucidate the VUS problem in RPE65, a target for retinal gene therapy (2023) Research Day 2023, Abstracts.
- An in vitro enzymatic assay to elucidate the VUS problem in RPE65, a target for retinal gene therapy (2023) Belgian Society for Human Genetics (BeSHG) Annual Meeting 2023 : To DNA and beyond, Abstracts.
- Comparative 3D genome analysis between neural retina and RPE reveals diferential cis-regulatory interactions at retinal disease loci (2023) ASHG 2023 Annual Meeting, Abstracts.
- Whole genome sequencing sheds light on the dark matter of the genome in patients with inherited retinal diseases (2023) Belgian Society for Human Genetics (BeSHG) Annual Meeting 2023 : To DNA and beyond, Abstracts.
- RXFP2 : validating its role in autosomal recessive bilateral cryptorchidism and a novel association with male infertility (2023) HORMONE RESEARCH IN PAEDIATRICS. In Hormone Research in Paediatrics 96(Supplement 4). p.397-398
- Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases (2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
- Interaction map of cis-regulatory elements controlling ABCA4 in human retina (2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.323-324
- Juggling offsets unlocks RNA-seq tools for fast scalable differential usage, aberrant splicing and expression analyses (2023)
- Etiology, histology and long-term outcome of bilateral testicular regression : a large Belgian series (2023) HUMAN REPRODUCTION OPEN. 2023(4).
- Micro‐topographies induce epigenetic reprogramming and quiescence in human mesenchymal stem cells (2023) ADVANCED SCIENCE. 10(1).
- 2022
- Haplotyping pharmacogenes using TLA combined with Illumina or Nanopore sequencing (2022) SCIENTIFIC REPORTS. 12(1).
- Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophyand hearing loss (2022) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 30(Supplement 1). p.45-45
- Analyzing data independent acquisition mass spectrometry with noiseless ion-networks (2022) BioRXiv.
- Hatching is modulated by microRNA-378a-3p derived from extracellular vesicles secreted by blastocysts (2022) PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 119(12).
- Transcriptional dynamics of gametogenesis in the green seaweed Ulva mutabilis identifies an RWP-RK transcription factor linked to reproduction (2022) BMC PLANT BIOLOGY. 22(1).
- Cas9 targeted nanopore sequencing with enhanced variant calling improves CYP2D6-CYP2D7 hybrid allele genotyping (2022) PLOS GENETICS. 18(9).
- DNA methylation alterations in fractionally irradiated rats and breast cancer patients receiving radiotherapy (2022) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 23(24).
- Continuous activation of the IL-17F driven inflammatory pathway in acute and chronic digital dermatitis lesions in dairy cattle (2022) SCIENTIFIC REPORTS. 12(1).
- Enrichment of circulating trophoblasts from maternal blood using filtration-based Metacell (R) technology (2022) PLOS ONE. 17(7).
- Profiling the aerobic window of horses in response to training by means of a modified lactate minimum speed test : flatten the curve (2022) FRONTIERS IN PHYSIOLOGY. 13.
- Nanopore sequencing of a forensic combined STR and SNP multiplex (2022) FORENSIC SCIENCE INTERNATIONAL-GENETICS. 56.
- QueSTR probes : Quencher-labeled RNase H2-dependent probes for short tandem repeat genotyping (2022) SENSORS AND ACTUATORS B-CHEMICAL. 361.
- Microbial diversity and antimicrobial susceptibility in endotracheal tube biofilms recovered from mechanically ventilated COVID-19 patients (2022) BIOFILM. 4.
- Metabolism and health effects of rare sugars in a CACO-2/HepG2 coculture model (2022) NUTRIENTS. 14(3).
- DC vaccines loaded with glioma cells killed by photodynamic therapy induce Th17 anti-tumor immunity and provide a four-gene signature for glioma prognosis (2022) CELL DEATH & DISEASE. 13(12).
- Joubert syndrome (2022) Clinical ophthalmic genetics and genomics. p.274-276
- Exploring PhaLP, an open source portal for Phage Lytic Proteins, to engineer modular enzybiotics against vancomycin-resistant Enterococcus faecalis (2022) 1st Belgian Society for Viruses of Microbes (BSVoM) Symposium, Abstracts.
- Machine learning-guided engineering of modular enzybiotics to target vancomycin-resistant Enterococcus faecalis infections of the urinary tract (2022) National Symposium for Applied Biological Sciences, 26th, Abstracts.
- Exploring PhaLP, an open source portal for Phage Lytic Proteins, to engineer modular enzybiotics against vancomycin-resistant Enterococcus faecalis (2022) Viruses of Microbes 2022, Abstracts.
- A genomic urine assay to detect urinary tract recurrences in patients with bladder cancer treated with radiotherapy (2022) JOURNAL OF UROLOGY. 207(suppl. 5). p.E84-E84
- A urine-based molecular assay refines the risk stratification of the recent American Urological Association guideline on hematuria (2022) JOURNAL OF UROLOGY. 207(suppl. 5). p.E928-E929
- Technical considerations in PCR-based assay design for diagnostic DNA methylation cancer biomarkers (2022) CLINICAL EPIGENETICS. 14(1).
- Copy number gain and loss-of-imprinting lead to HM13 intron retention across multiple cancer types (2022) Epigenetics and Epigenomics in Health and Disease, Abstracts.
- A tapt1 knockout zebrafish line with aberrant lens development and impaired vision models human pediatric cataract (2022) International Zebrafish Conference (IZFS) 2022, Abstracts.
- Multigenerational DNA methylation responses to copper exposure in daphnia : potential targets for epigenetic biomarkers? (2022) CHEMOSPHERE. 308(part 1).
- Phasing of the entire CYP2D6 locus with CRISPR-Cas9 enriched Nanopore sequencing (2022) EUROPEAN JOURNAL OF HUMAN GENETICS. 30(SUPPL 1). p.509-510
- PIWI proteins play an antiviral role in Lepidopteran cell lines (2022) VIRUSES-BASEL. 14(7).
- TXNIP promotes human NK cell development but is dispensable for NK cell functionality (2022) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 23(19).
- Signatures of polygenic adaptation align with genome-wide methylation patterns in wild strawberry plants (2022) NEW PHYTOLOGIST. 235(4). p.1501-1514
- The transcription factor RUNX2 drives the generation of human NK cells and promotes tissue residency (2022) ELIFE. 11.
- IRF2 is required for development and functional maturation of human NK cells (2022) FRONTIERS IN IMMUNOLOGY. 13.
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