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Becker, Felicitas
90
results:
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english (79)
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1
Unified Quantification of Quantum Defects in Small-Diameter..:
Sebastian, Finn L
;
Becker, Felicitas
;
Yomogida, Yohei
...
http://arxiv.org/abs/2311.08029. , 2023
Link:
http://arxiv.org/abs/231..
?
2
Genome-wide identification and phenotypic characterization ..:
Montanucci, Ludovica
;
Lewis-Smith, David
;
Collins, Ryan L
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-023-39539-6. , 2023
Link:
https://repository.vu.lt..
?
3
GWAS meta-analysis of over 29,000 people with epilepsy iden..:
Stevelink, Remi
;
Campbell, Ciarán
;
Chen, Siwei
...
https://doi.org/10.1038/s41588-023-01485-w. , 2023
Link:
https://orbilu.uni.lu/ha..
?
4
Genome-wide identification and phenotypic characterization ..:
Montanucci, Ludovica
;
Lewis-Smith, David
;
Collins, Ryan L
...
https://eprints.gla.ac.uk/305681/1/305681.pdf. , 2023
Link:
https://eprints.gla.ac.u..
?
5
GWAS meta-analysis of over 29,000 people with epilepsy iden..:
Stevelink, Remi
;
Campbell, Ciarán
;
Chen, Siwei
...
https://eprints.gla.ac.uk/307631/1/307631.pdf. , 2023
Link:
https://eprints.gla.ac.u..
?
6
Sub-genic intolerance, ClinVar, and the epilepsies: A whole..:
Canafoglia, Laura
;
Goldstein, David B
;
Lowenstein, Daniel H
...
0eacb4d1-c0d8-4723-ac08-0ba3905057a6. , 2021
Link:
https://doi.org/10.1016/..
?
7
Shared genetic basis between genetic generalized epilepsy a..:
Stevelink, Remi
;
Luykx, Jurjen J
;
Lin, Bochao D
...
info:eu-repo/semantics/altIdentifier/doi/10.1111/epi.16922. , 2021
Link:
https://repository.vu.lt..
?
8
Shared genetic basis between genetic generalized epilepsy a..:
Stevelink, Remi
;
Luykx, Jurjen J
;
Lin, Bochao D
...
qt3d00d4x4. , 2021
Link:
https://escholarship.org..
?
9
Distinct gene-set burden patterns underlie common generaliz..:
Koko, Mahmoud
;
Krause, Roland
;
Sander, Thomas
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ebiom.2021.103588. , 2021
Link:
https://repository.vu.lt..
?
10
Testing association of rare genetic variants with resistanc..:
Wolking, Stefan
;
Moreau, Claudia
;
Nies, Anne T
...
info:eu-repo/grantAgreement/EC/FP7/279062. , 2020
Link:
https://orbilu.uni.lu/ha..
?
11
Bi-allelic GAD1 variants cause a neonatal onset syndromic d..:
Chatron, Nicolas
;
Becker, Felicitas
;
Morsy, Heba
...
https://freidok.uni-freiburg.de/data/166227. , 2020
Link:
https://freidok.uni-frei..
?
12
Testing association of rare genetic variants with resistanc..:
Wolking, Stefan
;
Moureau, Claudia
;
Niels, Anne T
...
http://eprints.gla.ac.uk/210312/7/210312.pdf. , 2020
Link:
http://eprints.gla.ac.uk..
?
13
Pharmacoresponse in genetic generalized epilepsy: a genome-..:
Wolking, Stefan
;
Schulz, Herbert
;
Nies, Anne A.T
...
uri/info:doi/10.2217/pgs-2019-0179. , 2020
Link:
http://hdl.handle.net/20..
?
14
Epilepsia / Testing association of rare genetic variants wi..:
Lerche, Holger
;
Girard, Simon
;
Krenn, Martin
...
vignette : https://repositorium.meduniwien.ac.at/titlepage/urn/urn:nbn:at:at-ubmuw:3-85205/128. , 2020
Link:
https://doi.org/10.1111/..
?
15
Testing association of rare genetic variants with resistanc..:
Wolking, Stefan
;
Moreau, Claudia
;
Nies, Anne A.T
...
uri/info:doi/10.1111/epi.16467. , 2020
Link:
http://hdl.handle.net/20..
1-15