T. Rosseel

发表

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11

A. Vral, W. Foulkes, L. Forétova, 2018, Human mutation.

False-positive results in metagenomic virus discovery: a strong case for follow-up diagnosis.

K. De Clercq, B. Pardon, O. Ozhelvaci, 2014, Transboundary and emerging diseases.

Evaluation of convenient pretreatment protocols for RNA virus metagenomics in serum and tissue samples.

O. Ozhelvaci, G. Freimanis, T. Rosseel, 2015, Journal of virological methods.

Next-Generation Sequencing in Veterinary Medicine: How Can the Massive Amount of Information Arising from High-Throughput Technologies Improve Diagnosis, Control, and Management of Infectious Diseases?

R. Orton, I. Monne, A. Fusaro, 2014, Methods in molecular biology.

Genome sequencing by random priming methods for viral identification

T. Rosseel, Toon Rosseel, 2015 .

Multi-omics profiling, in vitro and in vivo enhancer assays dissect the cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy

C. Rivolta, J. Tena, J. Gómez-Skarmeta, 2022, bioRxiv.

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy

C. Rivolta, J. Tena, J. Gómez-Skarmeta, 2022, American journal of human genetics.

Identification and complete genome sequencing of paramyxoviruses in mallard ducks (Anas platyrhynchos) using random access amplification and next generation sequencing technologies

B. Lambrecht, T. P. van den Berg, F. Vandenbussche, 2011, Virology Journal.

What's in a strain? Viral metagenomics identifies genetic variation and contaminating circoviruses in laboratory isolates of pigeon paramyxovirus type 1.

M. Steensels, B. Lambrecht, T. P. van den Berg, 2013, Virus research.

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development

R. Veitia, L. Looijenga, H. Stoop, 2016, Genetics in Medicine.

Dealing with Pseudogenes in in the Next Generation Era

K. De Leeneer, T. Rosseel, Kathleen B. M. Claes, 2021, Methods in Molecular Biology.

Loss of adipocyte phospholipase gene PLAAT3 causes lipodystrophy and insulin resistance due to inactivated arachidonic acid-mediated PPARγ signaling

C. Depienne, B. Poppe, D. Hemelsoet, 2021, bioRxiv.

ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants

F. Cremers, K. Carss, G. Arno, 2019, Genetics in Medicine.

Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

J. van den Ende, M. McKibbin, C. Inglehearn, 2018, Genetics in Medicine.

Accurate detection and quantification of epigenetic and genetic second hits in BRCA1 and BRCA2-associated hereditary breast and ovarian cancer reveals multiple co-acting second hits.

A. Vral, M. V. Van Bockstal, D. Deforce, 2018, Cancer letters.

Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss

B. Menten, G. Arno, M. De Bruyne, 2021, Frontiers in Cell and Developmental Biology.

DNase SISPA-Next Generation Sequencing Confirms Schmallenberg Virus in Belgian Field Samples and Identifies Genetic Variation in Europe

Matthias Scheuch, Dirk Höper, N. De Regge, 2012, PloS one.

The Origin of Biased Sequence Depth in Sequence-Independent Nucleic Acid Amplification and Optimization for Efficient Massive Parallel Sequencing

M. Beer, B. Hoffmann, T. P. van den Berg, 2013, PloS one.

Complete Genome Sequence of Bovine Polyomavirus Type 1 from Aborted Cattle, Isolated in Belgium in 2014

F. Vandenbussche, L. Delooz, E. Mathijs, 2016, Genome Announcements.

Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients

M. Blok, S. Tejpar, K. Claes, 2021, Cancers.

Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss, and reduced male fertility

C. Bachert, C. Rivolta, P. Farinelli, 2020, Human mutation.

Full-Genome Sequencing of Four Bluetongue Virus Serotype 11 Viruses.

B. Hoffmann, K. De Clercq, S. Zientara, 2015, Transboundary and emerging diseases.

A novel duplication involving PRDM13 in a Turkish family supports its role in North Carolina macular dystrophy (NCMD/MCDR1)

M. Pericak-Vance, J. Vance, Stijn Van de Sompele, 2021, Molecular vision.

Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

J. van den Ende, M. McKibbin, C. Inglehearn, 2018, Genetics in Medicine.

Extensive Genetic Variability Linked to IS26 Insertions in the fljB Promoter Region of Atypical Monophasic Variants of Salmonella enterica Serovar Typhimurium

V. Jasson, P. Wattiau, K. Dierick, 2015, Applied and Environmental Microbiology.

Phenocopy of a heterozygous carrier of X-linked retinitis pigmentosa due to mosaicism for a RHO variant

M. De Bruyne, J. de Zaeytijd, C. van Cauwenbergh, 2021, Scientific Reports.

Next-generation sequencing shows West Nile virus quasispecies diversification after a single passage in a carrion crow (Corvus corone) in vivo infection model.

B. Lambrecht, R. Orton, S. Lecollinet, 2015, The Journal of general virology.

ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

James M. Hodge, E. Burnside, Y. Kamatani, 2023, Clinical cancer research : an official journal of the American Association for Cancer Research.

ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants

F. Cremers, K. Carss, G. Arno, 2019, Genetics in Medicine.

Phylogeographic analysis of avian influenza viruses isolated from Charadriiformes in Belgium confirms intercontinental reassortment in gulls

B. Lambrecht, D. Vangeluwe, T. P. van den Berg, 2012, Archives of Virology.

Dealing with Pseudogenes in Molecular Diagnostics in the Next Generation Sequencing Era.

K. Claes, K. De Leeneer, T. Rosseel, 2021, Methods in molecular biology.

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling

P. Verloo, D. Hemelsoet, M. Taquet, 2023, Nature Genetics.