Ghent University Academic Bibliography

Show Sort by

Your filters: cql: author="Vermeesch, Joris" or (type any "bookEditor journalEditor issueEditor" and editor="Vermees...

Add to list
- Conference Paper
- C3
- open access
Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation

Griet De Clercq (UGent) , Lies Vantomme (UGent) , Bert Callewaert (UGent) , Barbara Dewaele, Joris Vermeesch, Annelies Dheedene (UGent) and Björn Menten (UGent)

(2023) Genomics of Rare Disease 2023 Conference, Abstracts.
Add to list
- Conference Paper
- C3
Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation

Griet De Clercq (UGent) , Lies Vantomme (UGent) , Bert Callewaert (UGent) , Sarah Vergult (UGent) , Wouter De Coster, Mojca Strazisar, Tim De Pooter, Barbara Dewaele, Joris Vermeesch, Annelies Dheedene (UGent) , et al.

(2023) European Society for Human Genetics (ESHG) Conference 2023, Abstracts.
Add to list
- Journal Article
- A2
- open access
Pushing the boundaries : concurrent Hodgkin lymphoma and breast cancer treatment with preservation of pregnancy : a case report

Charlotte Lejeune, Daan Dierickx, Hans Wildiers, Lore Lannoo, Kristel Van Calsteren, Vincent Vandecaveye, Björn Menten (UGent) , Joris Vermeesch and Frédéric Amant

(2022) GYNECOLOGIC ONCOLOGY REPORTS. 39.
Add to list
Prenatally detected copy number variants in a national cohort : a postnatal follow-up study

Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Desir, et al.

(2020) PRENATAL DIAGNOSIS. 40(10). p.1272-1283
Add to list
The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations

Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, et al.

(2018) PRENATAL DIAGNOSIS. 38(13). p.1120-1128

Academic Bibliography

Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation

Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation

Pushing the boundaries : concurrent Hodgkin lymphoma and breast cancer treatment with preservation of pregnancy : a case report

Prenatally detected copy number variants in a national cohort : a postnatal follow-up study

The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations

Contents

Support

Contact