Ghent University Academic Bibliography

CRISPR/Cas gene editing in the human germline

Bieke Bekaert (UGent) , Annekatrien Boel (UGent) , Gwenny Cosemans (UGent) , Lisa De Witte (UGent) , Björn Menten (UGent) and Björn Heindryckx (UGent)

(2022) SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY. 131. p.93-107

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Journal Article
A1
open access

Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts

Tine De Coster (UGent) , Heleen Masset, Olga Tsuiko, Maaike Catteeuw (UGent) , Yan Zhao, Nicolas Dierckxsens, Ainhoa Larreategui Aparicio, Eftychia Dimitriadou, Sophie Debrock, Karen Peeraer, et al.

(2022) GENOME BIOLOGY. 23(1).

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Performance and diagnostic value of genome-wide noninvasive prenatal testing in multiple gestations

Margot van Riel, Nathalie Brison, Machteld Baetens (UGent) , Bettina Blaumeiser, Francois Boemer, Laura Bourlard, Saskia Bulk, Anne De Leener, Julie Desir, Koenraad Devriendt, et al.

(2021) OBSTETRICS AND GYNECOLOGY. 137(6). p.1102-1108

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Journal Article
A1
open access

Autoimmunity in segmental vitiligo

Reinhart Speeckaert (UGent) , Jo Lambert (UGent) , Vedrana Bulat, Arno Belpaire (UGent) , Marijn Speeckaert (UGent) and Nanja van Geel

(2020) FRONTIERS IN IMMUNOLOGY. 11.

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Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome

Sofie Symoens (UGent) , Wouter Steyaert (UGent) , Lynn Demuynck (UGent) , Anne De Paepe (UGent) , Karin EM Diderich, Fransiska Malfait (UGent) and Paul Coucke (UGent)

(2017) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 173(4). p.1047-1050

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Segmental vitiligo

Nanja van Geel (UGent) and Reinhart Speeckaert (UGent)

(2017) DERMATOLOGIC CLINICS. 35(2). p.145-150

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Preimplantation genetic diagnosis for chromosomal rearrangements with the use of array comparative genomic hybridization at the blastocyst stage

CHRISTODOULOS CHRISTODOULOU (UGent) , Annelies Dheedene (UGent) , Björn Heindryckx (UGent) , Filip Van Nieuwerburgh (UGent) , Dieter Deforce (UGent) , Petra De Sutter (UGent) , Björn Menten (UGent) and Etienne Van den Abbeel (UGent)

(2017) FERTILITY AND STERILITY. 107(1). p.212-219

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open access

Identification of an AR mutation-negative class of androgen insensitivity by determining endogenous AR activity

N. C. Hornig, M. Ukat, H. U. Schweikert, O. Hiort, R. Werner, S. L. S. Drop, Martine Cools (UGent) , I. A. Hughes, L. Audi, S. F. Ahmed, et al.

(2016) JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 101(11). p.4468-4477

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New insights in segmental vitiligo: case report and review of theories

Nanja van Geel (UGent) , ILSE MOLLET (UGent) , Lieve Brochez (UGent) , MARIEKE DUTRE, Sofie De Schepper (UGent) , Evelien Verhaeghe (UGent) , Jo Lambert (UGent) and Reinhart Speeckaert (UGent)

(2012) BRITISH JOURNAL OF DERMATOLOGY. 166(2). p.240-246

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Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

Julia Vogt, Tanja Mussotter, Kathrin Bengesser, Kathleen Claes (UGent) , Josef Högel, Nadia Chuzhanova, Chuanhua Fu, Jenneke van den Ende, Victor-Felix Mautner, David N Cooper, et al.

(2012) HUMAN MUTATION. 33(11). p.1599-1609

Academic Bibliography

CRISPR/Cas gene editing in the human germline

Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts

Performance and diagnostic value of genome-wide noninvasive prenatal testing in multiple gestations

Autoimmunity in segmental vitiligo

Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome

Segmental vitiligo

Preimplantation genetic diagnosis for chromosomal rearrangements with the use of array comparative genomic hybridization at the blastocyst stage

Identification of an AR mutation-negative class of androgen insensitivity by determining endogenous AR activity

New insights in segmental vitiligo: case report and review of theories

Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

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