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Veronika Vaclavik
60
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Search for persons
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Online (60)
Mediatypes
Articles (Online) (23)
Bookchapter (Online) (3)
OpenAccess-fulltext (34)
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?
1
Detection of elusive DNA copy-number variations in heredita..:
Quinodoz, Mathieu
;
Kaminska, Karolina
;
Cancellieri, Francesca
...
The American Journal of Human Genetics. 111 (2024) 4 - p. 701-713 , 2024
Link:
https://doi.org/10.1016/..
?
2
Macular dystrophy in Kabuki syndrome due to de novo KMT2D v..:
Vaclavik, Veronika
;
Navarro, Aurelie
;
Jacot-Guillarmod, Alain
...
Graefe's Archive for Clinical and Experimental Ophthalmology. 262 (2024) 6 - p. 1737-1744 , 2024
Link:
https://doi.org/10.1007/..
?
3
GNB1-Related Rod-Cone Dystrophy: A Case Report:
Conti, Giovanni Marco
;
Cancellieri, Francesca
;
Quinodoz, Mathieu
...
Case Reports in Ophthalmology. 15 (2024) 1 - p. 230-237 , 2024
Link:
https://doi.org/10.1159/..
?
4
Genetics of retinitis pigmentosa and other hereditary retin..:
Conti, Giovanni Marco
;
Vaclavik, Veronika
;
Rivolta, Carlo
...
Ophthalmic Research. , 2023
Link:
https://doi.org/10.1159/..
?
5
Coats-like Vasculopathy in Inherited Retinal Disease:
Daich Varela, Malena
;
Conti, Giovanni Marco
;
Malka, Samantha
...
Ophthalmology. 130 (2023) 12 - p. 1327-1335 , 2023
Link:
https://doi.org/10.1016/..
?
6
Acute bilateral blindness due to diffuse outer retinopathy ..:
Gurtler, Nicolas
;
Bughin, Alice
;
Vaclavik, Veronika
..
BMC Ophthalmology. 23 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
7
Multi-omics approach dissects cis-regulatory mechanisms und..:
Van de Sompele, Stijn
;
Small, Kent W.
;
Cicekdal, Munevver Burcu
...
The American Journal of Human Genetics. 109 (2022) 11 - p. 2029-2048 , 2022
Link:
https://doi.org/10.1016/..
?
8
Contributors:
, In:
Clinical Ophthalmic Genetics and Genomics
,
Aleman, Tomas S.
;
Amati-Bonneau, Patrizia
;
Arveiler, Benoît
... - p. xi-xiv , 2022
Link:
https://doi.org/10.1016/..
?
9
Contribution of Whole-Genome Sequencing and Transcript Anal..:
Poncet, Anaïs F.
;
Grunewald, Olivier
;
Vaclavik, Veronika
...
International Journal of Molecular Sciences. 23 (2022) 8 - p. 4294 , 2022
Link:
https://doi.org/10.3390/..
?
10
NewCOL6A6Variant Causes Autosomal Dominant Retinitis Pigmen..:
Vaclavik, Veronika
;
Tiab, Leila
;
Sun, Young Joo
...
Investigative Opthalmology & Visual Science. 63 (2022) 3 - p. 23 , 2022
Link:
https://doi.org/10.1167/..
?
11
Stargardt Macular Dystrophy:
, In:
Hereditary Chorioretinal Disorders; Retina Atlas
,
Vaclavik, Veronika
- p. 85-94 , 2020
Link:
https://doi.org/10.1007/..
?
12
Malattia Leventinese:
, In:
Hereditary Chorioretinal Disorders; Retina Atlas
,
Vaclavik, Veronika
- p. 107-117 , 2020
Link:
https://doi.org/10.1007/..
?
13
Correction: Habibi I. et al. "Clinical and Genetic Findings..:
Habibi, Imen
;
Falfoul, Yosra
;
Todorova, Margarita G.
...
Genes. 11 (2020) 5 - p. 503 , 2020
Link:
https://doi.org/10.3390/..
?
14
Clinical and Genetic Findings of Autosomal Recessive Bestro..:
Habibi, Imen
;
Falfoul, Yosra
;
Todorova, Margarita G.
...
Genes. 10 (2019) 12 - p. 953 , 2019
Link:
https://doi.org/10.3390/..
?
15
Statins in ophthalmology:
Ooi, Kenneth G.-J.
;
Khoo, Pauline
;
Vaclavik, Veronika
.
Survey of Ophthalmology. 64 (2019) 3 - p. 401-432 , 2019
Link:
https://doi.org/10.1016/..
1-15