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De Leener, Anne
91
results:
Search for persons
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Format
Online (91)
Mediatypes
Articles (Online) (23)
OpenAccess-fulltext (68)
Languages
english (83)
french (3)
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1
Case Report: Aggressive neural crest tumors in a child with..:
Landen, Lucie
;
De Leener, Anne
;
Le Roux, Manon
...
Frontiers in Endocrinology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
2
Congenital hydrocephalus: new Mendelian mutations and evide..:
Jacquemin, Valerie
;
Versbraegen, Nassim
;
Duerinckx, Sarah
...
Human Genomics. 17 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
3
Preclinical workup using long-read amplicon sequencing prov..:
Tsuiko, Olga
;
El Ayeb, Yasmine
;
Jatsenko, Tatjana
...
Human Reproduction. 38 (2023) 3 - p. 511-519 , 2023
Link:
https://doi.org/10.1093/..
?
4
Performance and Diagnostic Value of Genome-Wide Noninvasive..:
van Riel, Margot
;
Brison, Nathalie
;
Baetens, Machteld
...
Obstetrics & Gynecology. 137 (2021) 6 - p. 1102-1108 , 2021
Link:
https://doi.org/10.1097/..
?
5
Haplotyping-based preimplantation genetic testing reveals p..:
Tšuiko, Olga
;
Vanneste, Michiel
;
Melotte, Cindy
...
npj Genomic Medicine. 6 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
6
Comparison of the mutation spectrum and association with pr..:
Futema, Marta
;
Ramaswami, Uma
;
Tichy, Lukas
...
Atherosclerosis. 319 (2021) - p. 108-117 , 2021
Link:
https://doi.org/10.1016/..
?
7
Outcome of publicly funded nationwide first-tier noninvasiv..:
Van Den Bogaert, Kris
;
Lannoo, Lore
;
Brison, Nathalie
...
Genetics in Medicine. 23 (2021) 6 - p. 1137-1142 , 2021
Link:
https://doi.org/10.1038/..
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8
Heterogeneous colonic content: A prenatal sonographic manif..:
Dimitriou, Christos
;
Saliba, Souha
;
Peyrassol, Xavier
...
Clinical Case Reports. 8 (2020) 6 - p. 1010-1014 , 2020
Link:
https://doi.org/10.1002/..
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9
Tumor sequencing is useful to refine the analysis of germli..:
Van Marcke, Cédric
;
Helaers, Raphaël
;
De Leener, Anne
...
Breast Cancer Research. 22 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
10
Prenatally detected copy number variants in a national coho..:
Muys, Joke
;
Jacquemyn, Yves
;
Blaumeiser, Bettina
...
Prenatal Diagnosis. 40 (2020) 10 - p. 1272-1283 , 2020
Link:
https://doi.org/10.1002/..
?
11
A Belgian consensus strategy to identify familial hyperchol..:
Descamps, Olivier S.
;
Van Caenegem, Olivier
;
Hermans, Michel P.
...
Atherosclerosis. 277 (2018) - p. 369-376 , 2018
Link:
https://doi.org/10.1016/..
?
12
The Belgian MicroArray Prenatal (BEMAPRE) database: A syste..:
Muys, Joke
;
Blaumeiser, Bettina
;
Jacquemyn, Yves
...
Prenatal Diagnosis. 38 (2018) 13 - p. 1120-1128 , 2018
Link:
https://doi.org/10.1002/..
?
13
Reevaluation of ATR signaling in primary resting chronic ly..:
Beyaert, Maxime
;
Starczewska, Eliza
;
Pérez, Ana Cristina González
...
Oncotarget. 8 (2017) 34 - p. 56906-56920 , 2017
Link:
https://doi.org/10.18632..
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14
Routine use of gene panel testing in hereditary breast canc..:
van Marcke, Cedric
;
De Leener, Anne
;
Berlière, Martine
..
Critical Reviews in Oncology/Hematology. 108 (2016) - p. 33-39 , 2016
Link:
https://doi.org/10.1016/..
?
15
A Familial Heterozygous Null Mutation of MET in Autism Spec..:
Lambert, Nelle
;
Wermenbol, Vanessa
;
Pichon, Bruno
...
Autism Research. 7 (2014) 5 - p. 617-622 , 2014
Link:
https://doi.org/10.1002/..
1-15