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Dheedene, Annelies
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1

Haploinsufficiency of ZFHX3, encoding a key player in neuro..:

Pérez Baca, María del Rocío ; Jacobs, Eva Z. ; Vantomme, Lies...
The American Journal of Human Genetics.  111 (2024)  3 - p. 509-528 , 2024
Link: https://doi.org/10.1016/..
 
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2

De novo variants in SP9 cause a novel form of interneuronop..:

Tessarech, Marine ; Friocourt, Gaëlle ; Marguet, Florent...
Genetics in Medicine.  26 (2024)  5 - p. 101087 , 2024
Link: https://doi.org/10.1016/..
 
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3

Expanding the Phenotype of B3GALNT2-Related Disorders:

D'haenens, Erika ; Vergult, Sarah ; Menten, Björn...
Genes.  13 (2022)  4 - p. 694 , 2022
Link: https://doi.org/10.3390/..
 
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4

Low feasibility of in vitro matured oocytes originating fro..:

Lierman, Sylvie ; Tolpe, Annelies ; De Croo, Ilse...
Fertility and Sterility.  116 (2021)  4 - p. 1068-1076 , 2021
Link: https://doi.org/10.1016/..
 
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5

A Reassessment of Copy Number Variations in Congenital Hear..:

Meerschaut, Ilse ; Vergult, Sarah ; Dheedene, Annelies...
Genes.  12 (2021)  7 - p. 1048 , 2021
Link: https://doi.org/10.3390/..
 
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6

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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7

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/..
 
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8

Phenotypic and Molecular Heterogeneity in Mandibulofacial D..:

Shenoy, Rathika D. ; Shetty, Vikram ; Dheedene, Annelies...
The Cleft Palate-Craniofacial Journal.  59 (2021)  11 - p. 1346-1351 , 2021
Link: https://doi.org/10.1177/..
 
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9

Pathogenic variants in CDH11 impair cell adhesion and cause..:

Li, Dong ; March, Michael E. ; Fortugno, Paola...
Human Genetics.  140 (2021)  7 - p. 1061-1076 , 2021
Link: https://doi.org/10.1007/..
 
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10

Microcoria due to first duplication of 13q32.1 including th..:

Pozza, Elise ; Verdin, Hannah ; Deconinck, Hilde...
European Journal of Medical Genetics.  63 (2020)  5 - p. 103918 , 2020
Link: https://doi.org/10.1016/..
 
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11

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/..
 
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12

Expanding the molecular spectrum and the neurological pheno..:

Jacobs, Eva Z. ; Brown, Kathleen ; Byler, Melissa C....
Clinical Genetics.  99 (2020)  2 - p. 259-268 , 2020
Link: https://doi.org/10.1111/..
 
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13

PREFACE: In silico pipeline for accurate cell‐free fetal DN..:

Raman, Lennart ; Baetens, Machteld ; De Smet, Matthias...
Prenatal Diagnosis.  39 (2019)  10 - p. 925-933 , 2019
Link: https://doi.org/10.1002/..
 
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14

LINE- andAlu-containing genomic instability hotspot at 16q2..:

Szafranski, Przemyslaw ; Kośmider, Ewelina ; Liu, Qian...
Human Mutation.  39 (2018)  12 - p. 1916-1925 , 2018
Link: https://doi.org/10.1002/..
 
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15

WisecondorX: improved copy number detection for routine sha..:

Raman, Lennart ; Dheedene, Annelies ; De Smet, Matthias..
Nucleic Acids Research.  47 (2018)  4 - p. 1605-1614 , 2018
Link: https://doi.org/10.1093/..
 
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