Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Nathalie Brison"'
Autor:
Huiwen Che, Tatjana Jatsenko, Lore Lannoo, Kate Stanley, Luc Dehaspe, Leen Vancoillie, Nathalie Brison, Ilse Parijs, Kris Van Den Bogaert, Koenraad Devriendt, Sabien Severi, Ellen De Langhe, Severine Vermeire, Bram Verstockt, Kristel Van Calsteren, Joris Robert Vermeesch
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-10 (2022)
Abstract The early detection of tissue and organ damage associated with autoimmune diseases (AID) has been identified as key to improve long-term survival, but non-invasive biomarkers are lacking. Elevated cell-free DNA (cfDNA) levels have been obser
Externí odkaz:
https://doaj.org/article/3703af8193fe44ddb75b69cde0f61608
Autor:
Justyna Domaradzka, Marta Deperas, Ewa Obersztyn, Anna Kucińska-Chahwan, Nathalie Brison, Kris Van Den Bogaert, Tomasz Roszkowski, Marta Kędzior, Magdalena Bartnik-Głaska, Alicja Łuszczek, Krystyna Jakubów-Durska, Joris Robert Vermeesch, Beata Anna Nowakowska
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Background Non-invasive prenatal testing (NIPT) is a rapidly developing and widely used method in the prenatal screening. Recently, the widespread use of the NIPT caused a neglecting of the limitations of this technology. Case presentation T
Externí odkaz:
https://doaj.org/article/a67ed2280dd243d3952aab7386c1aa2c
Autor:
Liesbeth Lenaerts, PhD, Nathalie Brison, PhD, Charlotte Maggen, MD, Leen Vancoillie, PhD, Huiwen Che, MsC, Peter Vandenberghe, MD, PhD, Daan Dierickx, MD, PhD, Lucienne Michaux, MD, Phd, Barbara Dewaele, PhD, Patrick Neven, MD, PhD, Giuseppe Floris, MD, PhD, Thomas Tousseyn, MD, PhD, Lore Lannoo, MD, Tatjana Jatsenko, PhD, Isabelle Vanden Bempt, PhD, Kristel Van Calsteren, MD, PhD, Vincent Vandecaveye, MD, PhD, Luc Dehaspe, PhD, Koenraad Devriendt, MD, PhD, Eric Legius, MD, PhD, Kris Van Den Bogaert, PhD, Joris Robert Vermeesch, PhD, Frédéric Amant, MD, PhD
Publikováno v:
EClinicalMedicine, Vol 35, Iss , Pp 100856- (2021)
Background: Implausible false positive results in non-invasive prenatal testing (NIPT) have been occasionally associated with the detection of occult maternal malignancies. Hence, there is a need for approaches allowing accurate prediction of whether
Externí odkaz:
https://doaj.org/article/bef420808bcd4cd49a04531a4ded6117
Autor:
Ilse Parijs, Nathalie Brison, Leen Vancoillie, Machteld Baetens, Bettina Blaumeiser, Sébastien Boulanger, Julie Désir, Boyan Dimitrov, Nathalie Fieremans, Katrien Janssens, Sandra Janssens, Axel Marichal, Björn Menten, Colombine Meunier, Kim Van Berkel, Ann Van Den Bogaert, Koenraad Devriendt, Kris Van Den Bogaert, Joris Robert Vermeesch
Publikováno v:
European journal of human genetics
Maternally inherited 15q11-q13 duplications are generally found to cause more severe neurodevelopmental anomalies compared to paternally inherited duplications. However, this assessment is mainly inferred from the study of patient populations, causin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::503b76727ac64315911f73dbc0856eb4
https://hdl.handle.net/10067/1960390151162165141
https://hdl.handle.net/10067/1960390151162165141
Autor:
Huiwen Che, Tatjana Jatsenko, Liesbeth Lenaerts, Luc Dehaspe, Leen Vancoillie, Nathalie Brison, Ilse Parijs, Kris Van Den Bogaert, Daniela Fischerova, Ruben Heremans, Chiara Landolfo, Antonia Carla Testa, Adriaan Vanderstichele, Lore Liekens, Valentina Pomella, Agnieszka Wozniak, Christophe Dooms, Els Wauters, Sigrid Hatse, Kevin Punie, Patrick Neven, Hans Wildiers, Sabine Tejpar, Diether Lambrechts, An Coosemans, Dirk Timmerman, Peter Vandenberghe, Frédéric Amant, Joris Robert Vermeesch
Publikováno v:
Clinical chemistry, 68(9), 1164-1176. American Association for Clinical Chemistry Inc.
Background Cell-free DNA (cfDNA) analysis holds great promise for non-invasive cancer screening, diagnosis, and monitoring. We hypothesized that mining the patterns of cfDNA shallow whole-genome sequencing datasets from patients with cancer could imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40da73a4063e7fb9f0f25576145c1443
https://lirias.kuleuven.be/handle/20.500.12942/698372
https://lirias.kuleuven.be/handle/20.500.12942/698372
Autor:
Lore Lannoo, Koen Devriendt, Joris Vermeesch, Liesbeth Lenaerts, Nathalie Brison, Kristel Van Calsteren, Kris Van Den Bogaert, Huiwen Che, Frédéric Amant
Publikováno v:
Prenatal Diagnosis. 41:1264-1272
Cancer is diagnosed in one in 1000 to 1500 pregnancies. Most frequently encountered malignancies during pregnancy are breast cancer, hematological cancer, cervical cancer and malignant melanoma. Maternal cancer is associated with an increased risk of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87bea87930e87487e171fa8efd97dbd
https://doi.org/10.1002/pd.6031
https://doi.org/10.1002/pd.6031
Autor:
Leonor Palmeira, Lore Lannoo, Anne De Leener, Eva Sammels, Julie Désir, Nathalie Brison, Guillaume Smits, Vincent Bours, Annelies Dheedene, Annelies Fieuw, Kris Van Den Bogaert, Marjan De Rademaeker, Elise Vantroys, Jean-Stéphane Gatot, Laura Bourlard, Vincent Gatinois, Colombine Meunier, Koenraad Devriendt, Armelle Duquenne, François Boemer, Bettina Blaumeiser, Axel Marichal, Katrien Janssens, Joris Vermeesch, Nathalie Fieremans, Bruno Pichon, Yves Sznajer, Björn Menten, Sandra Janssens, Bernard Grisart, Machteld Baetens, Damien Lederer
Publikováno v:
Genetics in medicine
Genetics in medicine, Vol. 23, no.6, p. 1137-1142 (2021)
Genetics in medicine, Vol. 23, no.6, p. 1137-1142 (2021)
Purpose Noninvasive prenatal screening (NIPS) using cell-free DNA has transformed prenatal care. Belgium was the first country to implement and fully reimburse NIPS as a first-tier screening test offered to all pregnant women. A consortium consisting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4160c358ba3304c89c54ddec000e7f8
https://doi.org/10.1038/s41436-021-01101-4
https://doi.org/10.1038/s41436-021-01101-4
Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge
Autor:
Lore Lannoo, Khaila van Straaten, Jeroen Breckpot, Nathalie Brison, Luc De Catte, Eftychia Dimitriadou, Eric Legius, Hilde Peeters, Ilse Parijs, Olga Tsuiko, Leen Vancoillie, Joris Robert Vermeesch, Griet Van Buggenhout, Kris Van Den Bogaert, Kristel Van Calsteren, Koenraad Devriendt
Publikováno v:
European journal of human genetics : EJHG. 30(12)
Non-invasive prenatal testing has been introduced for the detection of Trisomy 13, 18, and 21. Using genome-wide screening also other "rare" autosomal trisomies (RATs) can be detected with a frequency about half the frequency of the common trisomies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96592986288e6fee27477a0e76ef8295
https://pubmed.ncbi.nlm.nih.gov/36045223
https://pubmed.ncbi.nlm.nih.gov/36045223
Autor:
Tatjana Jatsenko, Charlotte Maggen, Giuseppe Floris, Patrick Neven, Luc Dehaspe, Nathalie Brison, Anca Croitor, Darine Villela, Hanne Lefrère, Sigrid Hatse, Joris Vermeesch, Vincent Vandecaveye, Hans Wildiers, Magali Verheecke, Liesbeth Lenaerts, Maria Neofytou, Huiwen Che, Frédéric Amant
Publikováno v:
Clinical chemistry, 66(11), 1414-1423. American Association for Clinical Chemistry Inc.
Background Numerous publications have reported the incidental detection of occult malignancies upon routine noninvasive prenatal testing (NIPT). However, these studies were not designed to evaluate the NIPT performance for cancer detection. Methods W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e8c4cd78a5cd849feb8fd2c1a8650e2
https://doi.org/10.1093/clinchem/hvaa196
https://doi.org/10.1093/clinchem/hvaa196
Autor:
Nathalie Brison, Eric Legius, Kris Van Den Bogaert, Huiwen Che, Darine Villela, Masoud Zamani Esteki, Maria Neofytou, Olga Tšuiko, Thierry Voet, Joris Vermeesch, Koen Devriendt, Cindy Melotte, Eftychia Dimitriadou
Publikováno v:
Genetics in Medicine, 22(5), 962-973. Nature Publishing Group
PURPOSE: Whereas noninvasive prenatal screening for aneuploidies is widely implemented, there is an increasing need for universal approaches for noninvasive prenatal screening for monogenic diseases. Here, we present a cost-effective, generic cell-fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22b96bb06c218c967ccf95ae03790b3f
https://cris.maastrichtuniversity.nl/en/publications/f11e4336-58db-4b14-838c-30acd30fea49
https://cris.maastrichtuniversity.nl/en/publications/f11e4336-58db-4b14-838c-30acd30fea49