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Bacchelli, Elena
185
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Online (185)
Mediatypes
Articles (Online) (37)
OpenAccess-fulltext (148)
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1
Genomic analysis of 116 autism families strengthens known r..:
Viggiano, Marta
;
Ceroni, Fabiola
;
Visconti, Paola
...
npj Genomic Medicine. 9 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
2
Cluster Headache Genomewide Association Study and Meta‐Anal..:
Winsvold, Bendik S.
;
Harder, Aster V. E.
;
Ran, Caroline
...
Annals of Neurology. 94 (2023) 4 - p. 713-726 , 2023
Link:
https://doi.org/10.1002/..
?
3
Contribution of CACNA1H Variants in Autism Spectrum Disorde..:
Viggiano, Marta
;
D'Andrea, Tiziano
;
Cameli, Cinzia
...
Frontiers in Psychiatry. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
4
Dissecting the multifaceted contribution of the mitochondri..:
Caporali, Leonardo
;
Fiorini, Claudio
;
Palombo, Flavia
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
5
An increased burden of rare exonic variants in NRXN1 microd..:
Cameli, Cinzia
;
Viggiano, Marta
;
Rochat, Magali J.
...
Journal of Cellular and Molecular Medicine. 25 (2021) 5 - p. 2459-2470 , 2021
Link:
https://doi.org/10.1111/..
?
6
Brain Magnetic Resonance Findings in 117 Children with Auti..:
Rochat, Magali Jane
;
Distefano, Giacomo
;
Maffei, Monica
...
Brain Sciences. 10 (2020) 10 - p. 741 , 2020
Link:
https://doi.org/10.3390/..
?
7
An integrated analysis of rare CNV and exome variation in A..:
Bacchelli, Elena
;
Cameli, Cinzia
;
Viggiano, Marta
...
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
8
The role of rare compound heterozygous events in autism spe..:
Lin, Bochao Danae
;
Colas, Fabrice
;
Nijman, Isaac J.
...
Translational Psychiatry. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
9
Analysis of a Sardinian Multiplex Family with Autism Spectr..:
Bacchelli, Elena
;
Loi, Eleonora
;
Cameli, Cinzia
...
Journal of Clinical Medicine. 8 (2019) 2 - p. 212 , 2019
Link:
https://doi.org/10.3390/..
?
10
ELMOD3‐SH2D6 gene fusion as a possible co‐star actor in aut..:
Loi, Eleonora
;
Moi, Loredana
;
Blois, Sylvain
...
Journal of Cellular and Molecular Medicine. 24 (2019) 2 - p. 2064-2069 , 2019
Link:
https://doi.org/10.1111/..
?
11
Contribution of ultrarare variants in mTOR pathway genes to..:
Pippucci, Tommaso
;
Licchetta, Laura
;
Baldassari, Sara
...
Annals of Clinical and Translational Neurology. 6 (2019) 3 - p. 475-485 , 2019
Link:
https://doi.org/10.1002/..
?
12
Integrated DNA methylation analysis identifies topographica..:
Antonelli, Manila
;
Fadda, Antonio
;
Loi, Eleonora
...
Oncotarget. 9 (2018) 17 - p. 13807-13821 , 2018
Link:
https://doi.org/10.18632..
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13
Genetic variation in CHRNA7 and CHRFAM7A is associated with..:
Cameli, Cinzia
;
Bacchelli, Elena
;
De Paola, Maria
...
European Journal of Human Genetics. 26 (2018) 12 - p. 1824-1831 , 2018
Link:
https://doi.org/10.1038/..
?
14
A genome-wide analysis in cluster headache points to nepril..:
Bacchelli, Elena
;
Cainazzo, Maria Michela
;
Cameli, Cinzia
...
The Journal of Headache and Pain. 17 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
?
15
Lack of replication of previous autism spectrum disorder GW..:
Torrico, Bàrbara
;
Chiocchetti, Andreas G.
;
Bacchelli, Elena
...
Autism Research. 10 (2016) 2 - p. 202-211 , 2016
Link:
https://doi.org/10.1002/..
1-15