Ghent University Academic Bibliography

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Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences

Anna Summerer, Victor-Felix Mautner, Meena Upadhyaya, Kathleen Claes (UGent) , Josef Högel, David N Cooper, Ludwine Messiaen and Hildegard Kehrer-Sawatzki

(2018) HUMAN GENETICS. 137(6-7). p.511-520

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journalArticle
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open access

GC content of Early Metazoan genes and its impact on gene expression levels in mammalian cell lines

Ismail Sahin Gül (UGent) , Jens Staal (UGent) , Paco Hulpiau (UGent) , Evi De Keuckelaere (UGent) , Kai Kamm, Tom Deroo (UGent) , Ellen Sanders (UGent) , Katrien Staes (UGent) , Yasmine Driege (UGent) , Yvan Saeys (UGent) , et al.

(2018) GENOME BIOLOGY AND EVOLUTION. 10(3). p.909-917

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journalArticle
A1
open access

Identification of long non-coding RNAs involved in neuronal development and intellectual disability

Eva D'haene (UGent) , Eva Jacobs (UGent) , Pieter-Jan Volders (UGent) , Tim De Meyer (UGent) , Björn Menten (UGent) and Sarah Vergult (UGent)

(2016) SCIENTIFIC REPORTS. 6.

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journalArticle
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open access

Trisomy 21 alters DNA methylation in parent-of-origin-dependent and independent manners

Antônio Francisco Alves da Silva, Filipe Brum Machado, Érika Cristina Pavarino, Joice Matos Biselli-Périco, Bruna Lancia Zampieri, Ronaldo da Silva Francisco Junior, Pedro Thyago Mozer Rodrigues, Douglas Terra Machado, Cíntia Barros Santos-Rebouças, Maria Gomes Fernandes, et al.

(2016) PLOS ONE. 11(4).

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journalArticle
A1
open access

DNA methylation landscapes of human fetal development

Roderick C Slieker, Matthias S Roost, Liesbeth van Iperen, H Eka D Suchiman, Elmar W Tobi, Françoise Carlotti, Eelco JP de Koning, P Eline Slagboom, Bastiaan T Heijmans and Susana Marina Chuva de Sousa Lopes (UGent)

(2015) PLOS GENETICS. 11(10).

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journalArticle
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open access

Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

Hannah Verdin (UGent) , Ana Fernández-Miñán, Sara Benito-Sanz, Sandra Janssens (UGent) , Bert Callewaert (UGent) , Kathleen De Waele (UGent) , Jean De Schepper (UGent) , Inge François, Björn Menten (UGent) , Karen E Heath, et al.

(2015) SCIENTIFIC REPORTS. 5.

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We are all individuals...: bioinformatics in the personalized medicine era

Leander Van Neste and Wim Van Criekinge (UGent)

(2015) CELLULAR ONCOLOGY. 38(1). p.29-37

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journalArticle
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open access

SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data

Sandra Steyaert (UGent) , Wim Van Criekinge (UGent) , Ayla De Paepe, Simon Denil (UGent) , Klaas Mensaert (UGent) , Katrien Vandepitte, Wim Vanden Berghe (UGent) , Geert Trooskens (UGent) and Tim De Meyer (UGent)

(2014) NUCLEIC ACIDS RESEARCH. 42(20).

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Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

Sarah Vergult (UGent) , Ellen Van Binsbergen, Tom Sante (UGent) , Silke Nowak (UGent) , Olivier Vanakker (UGent) , Kathleen Claes (UGent) , Bruce Poppe (UGent) , Nathalie Van der Aa, Markus J van Roosmalen, Karen Duran, et al.

(2014) EUROPEAN JOURNAL OF HUMAN GENETICS. 22(5). p.652-659

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Quantification of integrated HIV DNA by repetitive-sampling Alu-HIV PCR on the basis of Poisson statistics

Ward De Spiegelaere (UGent) , Eva Malatinková (UGent) , Lindsay Lynch, Filip Van Nieuwerburgh (UGent) , Peter Messiaen (UGent) , Una O'Doherty and Linos Vandekerckhove (UGent)

(2014) CLINICAL CHEMISTRY. 60(6). p.886-895

Academic Bibliography

Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences

GC content of Early Metazoan genes and its impact on gene expression levels in mammalian cell lines

Identification of long non-coding RNAs involved in neuronal development and intellectual disability

Trisomy 21 alters DNA methylation in parent-of-origin-dependent and independent manners

DNA methylation landscapes of human fetal development

Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

We are all individuals...: bioinformatics in the personalized medicine era

SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data

Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

Quantification of integrated HIV DNA by repetitive-sampling Alu-HIV PCR on the basis of Poisson statistics

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