Ghent University Academic Bibliography

Mark

journalArticle
A1
open access

Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes : a comparative evaluation of upstream whole-genome amplification methods

Lieselot Deleye (UGent) , Yannick Gansemans (UGent) , Dieter De Coninck (UGent) , Filip Van Nieuwerburgh (UGent) and Dieter Deforce (UGent)

(2018) PLOS ONE. 13(4).

Mark

Chromosomal mosaicism in human blastocysts : the ultimate challenge of preimplantation genetic testing?

Mina Popovic (UGent) , Annelies Dheedene (UGent) , CHRISTODOULOS CHRISTODOULOU (UGent) , Jasin Taelman (UGent) , Lien Dhaenens (UGent) , Filip Van Nieuwerburgh (UGent) , Dieter Deforce (UGent) , Etienne Van den Abbeel (UGent) , Petra De Sutter (UGent) , Björn Menten (UGent) , et al.

(2018) HUMAN REPRODUCTION. 33(7). p.1342-1354

Mark

journalArticle
A1
open access

Performance of four modern whole genome amplification methods for copy number variant detection in single cells

Lieselot Deleye (UGent) , Laurentijn Tilleman (UGent) , Ann-Sophie Vander Plaetsen (UGent) , Senne Cornelis (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2017) SCIENTIFIC REPORTS. 7.

Mark

journalArticle
A1
open access

CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana

Nico De Storme (UGent) , Burcu Nur Keçeli (UGent) , Linda Zamariola (UGent) , Geert Angenon (UGent) and Danny Geelen (UGent)

(2016) BMC PLANT BIOLOGY. 16.

Mark

journalArticle
A1
open access

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

Lieselot Deleye (UGent) , Dieter De Coninck (UGent) , CHRISTODOULOS CHRISTODOULOU (UGent) , Tom Sante (UGent) , Annelies Dheedene (UGent) , Björn Heindryckx (UGent) , Etienne Van den Abbeel (UGent) , Petra De Sutter (UGent) , Björn Menten (UGent) , Dieter Deforce (UGent) , et al.

(2015) SCIENTIFIC REPORTS. 5.

Mark

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

Lieselot Deleye (UGent) , Annelies Dheedene (UGent) , Dieter De Coninck (UGent) , Tom Sante (UGent) , CHRISTODOULOS CHRISTODOULOU (UGent) , Björn Heindryckx (UGent) , Etienne Van den Abbeel (UGent) , Petra De Sutter (UGent) , Dieter Deforce (UGent) , Björn Menten (UGent) , et al.

(2015) FERTILITY AND STERILITY. 104(5). p.1276-1285

Mark

journalArticle
A1
open access

Deregulation of the replisome factor MCMBP prompts oncogenesis in colorectal carcinomas through chromosomal instability

Mauricio Alberto Quimbaya Gomez (UGent) , Eric Raspé (UGent) , Geertrui Denecker (UGent) , Bram De Craene (UGent) , Ria Roelandt (UGent) , Wim Declercq (UGent) , Xavier Sagaert, Lieven De Veylder (UGent) and Geert Berx (UGent)

(2014) NEOPLASIA. 16(9). p.694-709

Mark

Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type I-associated glomus tumors

Douglas R Stewart, Alexander Pemov, Eline Baert, Hilde Brems, Raf Sciot, Kathleen Claes (UGent) , Evgenia Pak, Amalia Dutra, Chyi-Chia Richard Lee and Eric Legius

(2012) GENES CHROMOSOMES & CANCER. 51(5). p.429-437

Mark

The base number of 'loxoscaphoid' Asplenium species and its implication for cytoevolution in Aspleniaceae

Elke Bellefroid (UGent) , Siti Khadijah Rambe, Olivier Leroux (UGent) and Ronnie Viane (UGent)

(2010) ANNALS OF BOTANY. 106(1). p.157-171

Mark

Risk of spontaneous abortion in singleton and twin pregnancies after IVF/ICSI

Philippe Tummers (UGent) , Petra De Sutter (UGent) and Marc Dhont (UGent)

(2003) HUMAN REPRODUCTION. 18(8). p.1720-1723

Academic Bibliography

Massively parallel sequencing of micro-manipulated cells targeting a comprehensive panel of disease-causing genes : a comparative evaluation of upstream whole-genome amplification methods

Chromosomal mosaicism in human blastocysts : the ultimate challenge of preimplantation genetic testing?

Performance of four modern whole genome amplification methods for copy number variant detection in single cells

CENH3-GFP: a visual marker for gametophytic and somatic ploidy determination in Arabidopsis thaliana

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

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

Deregulation of the replisome factor MCMBP prompts oncogenesis in colorectal carcinomas through chromosomal instability

Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type I-associated glomus tumors

The base number of 'loxoscaphoid' Asplenium species and its implication for cytoevolution in Aspleniaceae

Risk of spontaneous abortion in singleton and twin pregnancies after IVF/ICSI

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