المؤلفون: Lisanne Vervoort, Joris R. Vermeesch

المصدر: Exploration of Medicine, Vol 4, Iss 2, Pp 166-175 (2023)

مصطلحات موضوعية: genomic disorders, low copy repeats, segmental duplications, Other systems of medicine, RZ201-999

وصف الملف: electronic resource

العلاقة: https://www.explorationpub.com/Journals/em/Article/1001131Test; https://doaj.org/toc/2692-3106Test

الوصول الحر: https://doaj.org/article/48aec05f6eab491582baa9901191bdd9Test

المؤلفون: Lisanne Vervoort, Joris Robert Vermeesch

المصدر: Genes, Vol 13, Iss 11, p 2101 (2022)

مصطلحات موضوعية: low copy repeats, genomic disorders, 22q11.2 deletion syndrome, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2073-4425/13/11/2101Test; https://doaj.org/toc/2073-4425Test

الوصول الحر: https://doaj.org/article/74bd8017d9864fb2948203a510b882faTest

المؤلفون: Lisanne Vervoort, Nicolas Dierckxsens, Zjef Pereboom, Oronzo Capozzi, Mariano Rocchi, Tamim H. Shaikh, Joris R. Vermeesch

المصدر: Frontiers in Genetics, Vol 12 (2021)

مصطلحات موضوعية: 22q11.2 deletion syndrome, segmental duplication, structural variation, chromosome 22 evolution, low copy repeats, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fgene.2021.706641/fullTest; https://doaj.org/toc/1664-8021Test

الوصول الحر: https://doaj.org/article/80837c5b433641c7b0be97029796b76dTest

المؤلفون: Bo Zhou, GiWon Shin, Lisanne Vervoort, Stephanie Greer, Yiling Huang, Tanmoy Roychowdhury, Reenal Pattni, Alexej Abyzov, Joris Vermeesch, Hanlee Ji, Alexander Urban

المصدر: European Neuropsychopharmacology. 63:e88-e89

مصطلحات موضوعية: Pharmacology, Psychiatry and Mental health, Neurology, Pharmacology (medical), Neurology (clinical), Biological Psychiatry

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0b7ca51430707904ed040bc3d2a9e6f2Test
https://doi.org/10.1016/j.euroneuro.2022.07.166Test

المؤلفون: Lisanne Vervoort, Tamim H. Shaikh, Beverly S. Emanuel, Elfi Vergaelen, Ming Xiao, Steven Pastor, Wolfram Demaerel, Donna M. McDonald-McGinn, Matthew S. Hestand, Ann Swillen, Yulia Mostovoy, Elizabeth A. Geiger, Pui-Yan Kwok, Joris Vermeesch, Bernice E. Morrow, Curtis R. Coughlin, Stephen K. Chow, Feyza Yilmaz

المصدر: Genome research, vol 29, iss 9

مصطلحات موضوعية: Primates, Genome instability, 22q11 Deletion Syndrome, Evolution, Bioinformatics, Chromosomes, Human, Pair 22, Non-allelic homologous recombination, Biology, Medical and Health Sciences, Genome, Chromosomes, Fluorescence, Repetitive Sequences, Cell Line, Evolution, Molecular, 03 medical and health sciences, 0302 clinical medicine, Chromosomal Instability, Chromosome instability, Genetics, Animals, Humans, 2.1 Biological and endogenous factors, Aetiology, Allele, In Situ Hybridization, Fluorescence, In Situ Hybridization, Genetics (clinical), Repetitive Sequences, Nucleic Acid, 030304 developmental biology, 0303 health sciences, Nucleic Acid, Research, Human Genome, Chromosome Mapping, Molecular, Low copy repeats, Biological Sciences, Evolutionary biology, Pair 22, Chromosome 22, 030217 neurology & neurosurgery, Human

وصف الملف: Print; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce69d30c7c07cbca901d9297cc285853Test
https://doi.org/10.1101/gr.248682.119Test

المؤلفون: Oronzo Capozzi, Joris Vermeesch, Nicolas Dierckxsens, Lisanne Vervoort, Tamim H. Shaikh, Mariano Rocchi, Zjef Pereboom

مصطلحات موضوعية: education.field_of_study, biology, Bonobo, Population, Haplotype, Low copy repeats, biology.organism_classification, Macaque, Rhesus macaque, Evolutionary biology, biology.animal, Human genome, education, Segmental duplication

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::80b003c27c9591037ec9f13a1573afd9Test
https://doi.org/10.1101/2020.11.04.367920Test

المؤلفون: Lisanne Vervoort (11136453), Nicolas Dierckxsens (11136456), Zjef Pereboom (11136459), Oronzo Capozzi (11136462), Mariano Rocchi (2047), Tamim H. Shaikh (11136465), Joris R. Vermeesch (11136468)

مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, 22q11.2 deletion syndrome, segmental duplication, structural variation, chromosome 22 evolution, low copy repeats

العلاقة: https://figshare.com/articles/dataset/Data_Sheet_1_22q11_2_Low_Copy_Repeats_Expanded_in_the_Human_Lineage_docx/14986101Test

الإتاحة: https://doi.org/10.3389/fgene.2021.706641.s001Test

المؤلفون: Lisanne Vervoort, Nicolas Dierckxsens, Zjef Pereboom, Oronzo Capozzi, Mariano Rocchi, Tamim H. Shaikh, Joris R. Vermeesch

مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, 22q11.2 deletion syndrome, segmental duplication, structural variation, chromosome 22 evolution, low copy repeats

العلاقة: https://figshare.com/articles/dataset/Data_Sheet_2_22q11_2_Low_Copy_Repeats_Expanded_in_the_Human_Lineage_xlsx/14986107Test

الإتاحة: https://doi.org/10.3389/fgene.2021.706641.s002Test
https://figshare.com/articles/dataset/Data_Sheet_2_22q11_2_Low_Copy_Repeats_Expanded_in_the_Human_Lineage_xlsx/14986107Test

المؤلفون: Hanlee P. Ji, Lisanne Vervoort, Reenal Pattni, Joris Vermeesch, Marcus Ho, Wing Hung Wong, Yiling Huang, Stephanie U. Greer, Bo Zhou, GiWon Shin, Alexander E. Urban

مصطلحات موضوعية: Gene duplication, CRISPR, Sequence assembly, Computational biology, Nanopore sequencing, Biology, Genome, Gene, Segmental duplication, Sequence (medicine)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78a117b633c780eecadec367cef39d7dTest
https://lirias.kuleuven.be/handle/20.500.12942/703505Test

المؤلفون: Matthew S. Hestand, Ann Swillen, Elfi Vergaelen, Jeroen Breckpot, Adrian Odrzywolski, Lisanne Vervoort, Anne S. Bassett, Ania Fiksinski, Bernice E. Morrow, Laura Yissel Rengifo, Donna M. McDonald-McGinn, Vandana Shashi, Jacob A. S. Vorstman, Tracy Heung, Wolfram Demaerel, Joris Vermeesch, Janneke Zinkstok, Koen Devriendt, Eva W.C. Chow

المصدر: Hum Mol Genet

مصطلحات موضوعية: Adult, Male, Chromosomes, Human, Pair 22, Chromosome Breakpoints, Biology, Chromosomes, Article, 03 medical and health sciences, 0302 clinical medicine, Segmental Duplications, Genomic, Genetics, DiGeorge Syndrome, Humans, International 22q11.2 Brain, Allele, Homologous Recombination, Molecular Biology, Genetics (clinical), Alleles, In Situ Hybridization, Fluorescence, 030304 developmental biology, Segmental duplication, Sequence (medicine), Whole genome sequencing, 0303 health sciences, Whole Genome Sequencing, Breakpoint, Chromosome, Chromosome Mapping, General Medicine, Chromosome Inversion, Female, Chromosome Deletion, Homologous recombination, 030217 neurology & neurosurgery, Behavior Consortium

وصف الملف: Print

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b9d251281485d3e8559478d6dd331cTest
https://pubmed.ncbi.nlm.nih.gov/31884517Test