Resultados de procura - Björn Menten

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  1. 1
    Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

    Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of publ... por Björn Menten

    Publicado 2006
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  2. 2
    Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemma

    Chromosomal mosaicism in human blastocysts: the ultimate diagnostic dilemma por Mina Popovic, L Dhaenens, Annekatrien Boel, Björn Menten, Björn Heindryckx

    Publicado 2019
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  3. 3
    WisecondorX: improved copy number detection for routine shallow whole-genome sequencing

    WisecondorX: improved copy number detection for routine shallow whole-genome sequencing por Lennart Raman, Annelies Dheedene, Matthias De Smet, Jo Van Dorpe, Björn Menten

    Publicado 2018
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  4. 4
    Array comparative genomic hybridization in male infertility

    Array comparative genomic hybridization in male infertility por Katrien Stouffs, Deborah Vandermaelen, Annelien Massart, Björn Menten, Sarah Vergult, Herman Tournaye, Willy Lissens

    Publicado 2012
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  5. 5
    Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples

    Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples por Björn Menten, Katrien Swerts, Barbara Delle Chiaie, Sandra Janssens, Karen Buysse, Jan Philippé, Frank Speleman

    Publicado 2009
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  6. 6
    Identification of long non-coding RNAs involved in neuronal development and intellectual disability

    Identification of long non-coding RNAs involved in neuronal development and intellectual disability por Eva D’haene, Eva Jacobs, Pieter‐Jan Volders, Tim De Meyer, Björn Menten, Sarah Vergult

    Publicado 2016
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  7. 7
    LNCipedia: a database for annotated human lncRNA transcript sequences and structures

    LNCipedia: a database for annotated human lncRNA transcript sequences and structures por Pieter‐Jan Volders, Kenny Helsens, Xiaowei Wang, Björn Menten, Lennart Martens, Kris Gevaert, Jo Vandesompele, Pieter Mestdagh

    Publicado 2012
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  8. 8
    BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment

    BATCH-GE: Batch analysis of Next-Generation Sequencing data for genome editing assessment por Annekatrien Boel, Wouter Steyaert, Nina De Rocker, Björn Menten, Bert Callewaert, Anne De Paepe, Paul Coucke, Andy Willaert

    Publicado 2016
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  9. 9
    Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability

    Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability por Sarah Vergult, Annelies Dheedene, Alfred Meurs, Fran Faes, Bertrand Isidor, Sandra Janssens, Agnès Gautier, Cédric Le Caignec, Björn Menten

    Publicado 2014
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  10. 10
    ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation

    ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation por Tom Sante, Sarah Vergult, Pieter‐Jan Volders, Wigard P. Kloosterman, Geert Trooskens, Katleen De Preter, Annelies Dheedene, Frank Speleman, Tim De Meyer, Björn Menten

    Publicado 2014
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  11. 11
    Extensive clinical, hormonal and genetic screening in a large consecutive series of 46,XY neonates and infants with atypical sexual development

    Extensive clinical, hormonal and genetic screening in a large consecutive series of 46,XY neonates and infants with atypical sexual development por Dorien Baetens, Wilhelm Mladenov, Barbara Delle Chiaie, Björn Menten, An Desloovere, Violeta Iotova, Bert Callewaert, Erik Van Laecke, Piet Hoebeke, Elfride De Baere, Martine Cools

    Publicado 2014
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  12. 12
    Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing?

    Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing? por Mina Popovic, Annelies Dheedene, Christina Christodoulou, Jasin Taelman, L Dhaenens, Filip Van Nieuwerburgh, Dieter Deforce, E. Van den Abbeel, Petra De Sutter, Björn Menten, Björn Heindryckx

    Publicado 2018
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  13. 13
    Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain

    Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain por Hannah Verdin, Barbara D′haene, Diane Beysen, Yana Novikova, Björn Menten, Tom Sante, Pablo Lapunzina, Julián Nevado, Claudia M.B. Carvalho, James R. Lupski, Elfride De Baere

    Publicado 2013
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  14. 14
    Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

    Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts por Lieselot Deleye, Annelies Dheedene, Dieter De Coninck, Tom Sante, Christodoulos Christodoulou, Björn Heindryckx, E. Van den Abbeel, Petra De Sutter, Dieter Deforce, Björn Menten, Filip Van Nieuwerburgh

    Publicado 2015
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  15. 15
    Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method

    Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method por Lieselot Deleye, Dieter De Coninck, Christodoulos Christodoulou, Tom Sante, Annelies Dheedene, Björn Heindryckx, E. Van den Abbeel, Petra De Sutter, Björn Menten, Dieter Deforce, Filip Van Nieuwerburgh

    Publicado 2015
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  16. 16
    Low feasibility of in vitro matured oocytes originating from cumulus complexes found during ovarian tissue preparation at the moment of gender confirmation surgery and during testosterone treatment for fertility preservation in transgender men

    Low feasibility of in vitro matured oocytes originating from cumulus complexes found during ovarian tissue preparation at the moment of gender confirmation surgery and during testo... por Sylvie Lierman, Annelies Tolpe, Ilse De Croo, Stefanie De Gheselle, Justine Defreyne, Machteld Baetens, Annelies Dheedene, Roos Colman, Björn Menten, Guy T’Sjoen, Petra De Sutter, Kelly Tilleman

    Publicado 2021
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  17. 17
    Smoothing waves in array CGH tumor profiles

    Smoothing waves in array CGH tumor profiles por Mark A. van de Wiel, Rebecca P. M. Brosens, Paul H.C. Eilers, Candy Kumps, Gerrit A. Meijer, Björn Menten, Erik A. Sistermans, Frank Speleman, Marieke E. Timmerman, Bauke Ylstra

    Publicado 2009
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  18. 18
    arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs

    arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs por Caroline Van Cauwenbergh, Kristof Van Schil, Robrecht Cannoodt, Miriam Bauwens, Thalia Van Laethem, Sarah De Jaegere, Wouter Steyaert, Tom Sante, Björn Menten, Bart P. Leroy, Frauke Coppieters, Elfride De Baere

    Publicado 2016
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  19. 19
    Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma

    Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma por Lennart Raman, Malaïka Van Der Linden, Kim Van der Eecken, Karim Vermaelen, Ingel Demedts, Veerle Surmont, Ulrike Himpe, Franceska Dedeurwaerdere, Liesbeth Ferdinande, Yolande Lievens, Kathleen Claes, Björn Menten, Jo Van Dorpe

    Publicado 2020
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  20. 20
    Shallow Whole Genome Sequencing on Circulating Cell-Free DNA Allows Reliable Noninvasive Copy-Number Profiling in Neuroblastoma Patients

    Shallow Whole Genome Sequencing on Circulating Cell-Free DNA Allows Reliable Noninvasive Copy-Number Profiling in Neuroblastoma Patients por Nadine Van Roy, Malaïka Van Der Linden, Björn Menten, Annelies Dheedene, Charlotte Vandeputte, Jo Van Dorpe, Geneviève Laureys, Marleen Renard, Tom Sante, Tim Lammens, Bram De Wilde, Frank Speleman, Katleen De Preter

    Publicado 2017
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