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De Baere, Elfride
335
results:
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Online (335)
Mediatypes
Articles (Online) (114)
Bookchapter (Online) (2)
OpenAccess-fulltext (219)
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1
Multi-omics analysis in human retina uncovers ultraconserve..:
Lopez Soriano, Victor
;
Dueñas Rey, Alfredo
;
Mukherjee, Rajarshi
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
2
Combining a prioritization strategy and functional studies ..:
Dueñas Rey, Alfredo
;
del Pozo Valero, Marta
;
Bouckaert, Manon
...
Genome Medicine. 16 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
3
Proof-of-concept for multiple AON delivery by a single U7sn..:
Suárez-Herrera, Nuria
;
Riswick, Iris B.
;
Vázquez-Domínguez, Irene
...
Molecular Therapy. 32 (2024) 3 - p. 837-851 , 2024
Link:
https://doi.org/10.1016/..
?
4
Towards Uncovering the Role of Incomplete Penetrance in Mac..:
Hitti-Malin, Rebekkah J.
;
Panneman, Daan M.
;
Corradi, Zelia
...
Biomolecules. 14 (2024) 3 - p. 367 , 2024
Link:
https://doi.org/10.3390/..
?
5
Author Correction: Multi-omics analysis in human retina unc..:
Lopez Soriano, Victor
;
Dueñas Rey, Alfredo
;
Mukherjee, Rajarshi
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
6
Comparative 3D genome analysis between neural retina and re..:
D'haene, Eva
;
López-Soriano, Víctor
;
Martínez-García, Pedro Manuel
...
Genome Biology. 25 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
7
Mutations in SAMD7 cause autosomal-recessive macular dystro..:
Bauwens, Miriam
;
Celik, Elifnaz
;
Zur, Dinah
...
The American Journal of Human Genetics. 111 (2024) 2 - p. 393-402 , 2024
Link:
https://doi.org/10.1016/..
?
8
Evolutionary origin of Hoxc13-dependent skin appendages in ..:
Carron, Marjolein
;
Sachslehner, Attila Placido
;
Cicekdal, Munevver Burcu
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
9
Autozygome‐guided exome‐first study in a consanguineous coh..:
Del Pozo‐Valero, Marta
;
Almoallem, Basamat
;
Dueñas Rey, Alfredo
...
Clinical Genetics. 106 (2024) 2 - p. 127-139 , 2024
Link:
https://doi.org/10.1111/..
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10
Compendium of Clinical Variant Classification for 2,246 Uni..:
Cornelis, Stéphanie S.
;
Bauwens, Miriam
;
Haer-Wigman, Lonneke
...
Human Mutation. 2023 (2023) - p. 1-12 , 2023
Link:
https://doi.org/10.1155/..
?
11
HRAS‐related epidermal nevus syndromes: Expansion of the sp..:
Beyens, Aude
;
Lietaer, Charlotte
;
Claes, Kathleen
...
Clinical Genetics. 103 (2023) 6 - p. 709-713 , 2023
Link:
https://doi.org/10.1111/..
?
12
Paediatric cataract surgery with 27G vitrectomy instrumenta..:
Chan, Hwei Wuen
;
Van den Broeck, Filip
;
Cools, Axelle
...
Frontiers in Medicine. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
13
The Role of MCM9 in the Etiology of Sertoli Cell-Only Syndr..:
Potorac, Iulia
;
Laterre, Marie
;
Malaise, Olivier
...
Journal of Clinical Medicine. 12 (2023) 3 - p. 990 , 2023
Link:
https://doi.org/10.3390/..
?
14
New Noncoding Base Pair Mutation at the Identical Locus as ..:
Small, Kent W.
;
Van de Sompele, Stijn
;
Avetisjan, Jessica
...
Journal of VitreoRetinal Diseases. 7 (2023) 1 - p. 33-42 , 2023
Link:
https://doi.org/10.1177/..
?
15
Response to Beretich and Beretich:
Vockley, Jerry
;
Brunetti-Pierri, Nicola
;
Chung, Wendy K.
...
Genetics in Medicine. 25 (2023) 10 - p. 100903 , 2023
Link:
https://doi.org/10.1016/..
1-15