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Becker, Felicitas
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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/..
 
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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..
 
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8

Shared genetic basis between genetic generalized epilepsy a..:

Stevelink, Remi ; Luykx, Jurjen J ; Lin, Bochao D...
qt3d00d4x4.  , 2021
Link: https://escholarship.org..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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..
 
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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/..
 
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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..
 
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