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Saillour, Virginie
28
results:
Search for persons
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Online (28)
Mediatypes
Articles (Online) (13)
Bookchapter (Online) (1)
OpenAccess-fulltext (14)
Sorted by: Relevance
Sorted by: Year
?
1
ATP2B2 de novo variants as a cause of variable neurodevelop..:
Poggio, Elena
;
Barazzuol, Lucia
;
Salmaso, Andrea
...
Genetics in Medicine. 25 (2023) 12 - p. 100971 , 2023
Link:
https://doi.org/10.1016/..
?
2
VPS4A mutation in syndromic congenital hemolytic anemia wit..:
Lunati, Ariane
;
Petit, Arnaud
;
Lapillonne, Hélène
...
American Journal of Hematology. 96 (2021) 4 - p. , 2021
Link:
https://doi.org/10.1002/..
?
3
A variant of neonatal progeroid syndrome, or Wiedemann–Raut..:
Beauregard-Lacroix, Eliane
;
Salian, Smrithi
;
Kim, Hyunyun
...
European Journal of Human Genetics. 28 (2019) 4 - p. 461-468 , 2019
Link:
https://doi.org/10.1038/..
?
4
SNooPer: a machine learning-based method for somatic varian..:
Spinella, Jean-François
;
Mehanna, Pamela
;
Vidal, Ramon
...
BMC Genomics. 17 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/..
?
5
Genomic characterization of pediatric T-cell acute lymphobl..:
Spinella, Jean-François
;
Cassart, Pauline
;
Richer, Chantal
...
Oncotarget. 7 (2016) 40 - p. 65485-65503 , 2016
Link:
https://doi.org/10.18632..
?
6
A novel somatic mutation in ACD induces telomere lengthenin..:
Spinella, Jean-François
;
Cassart, Pauline
;
Garnier, Nicolas
...
BMC Cancer. 15 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
7
Whole-exome sequencing of a rare case of familial childhood..:
Spinella, Jean-François
;
Healy, Jasmine
;
Saillour, Virginie
...
BMC Cancer. 15 (2015) 1 - p. , 2015
Link:
https://doi.org/10.1186/..
?
8
Whole-Exome Sequencing Reveals a Rapid Change in the Freque..:
Casals, Ferran
;
Hodgkinson, Alan
;
Hussin, Julie
...
PLoS Genetics. 9 (2013) 9 - p. e1003815 , 2013
Link:
https://doi.org/10.1371/..
?
9
Joint genotype inference with germline and somatic mutation:
Bareke, Eric
;
Saillour, Virginie
;
Spinella, Jean-François
...
BMC Bioinformatics. 14 (2013) S5 - p. , 2013
Link:
https://doi.org/10.1186/..
?
10
Rare allelic forms of PRDM9 associated with childhood leuke..:
Hussin, Julie
;
Sinnett, Daniel
;
Casals, Ferran
...
Genome Research. 23 (2012) 3 - p. 419-430 , 2012
Link:
https://doi.org/10.1101/..
?
11
ngALL database : a flexible framework for the management..:
, In:
Proceedings of the ACM Conference on Bioinformatics, Computational Biology and Biomedicine
,
St-Onge, Pascal
;
Hamon, Robert
;
Saillour, Virginie
... - p. 542-544 , 2012
Link:
https://dl.acm.org/doi/1..
?
12
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Imp..:
Rucheton, Benoit
;
Ewenczyk, Claire
;
Gaignard, Pauline
...
info:eu-repo/semantics/altIdentifier/doi/10.1212/nxg.0000000000000630. , 2021
Link:
https://hal.sorbonne-uni..
?
13
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Imp..:
Rucheton, Benoit
;
Ewenczyk, Claire
;
Gaignard, Pauline
...
info:eu-repo/semantics/altIdentifier/doi/10.1212/nxg.0000000000000630. , 2021
Link:
https://hal.sorbonne-uni..
?
14
Adult Cerebellar Ataxia, Axonal Neuropathy, and Sensory Imp..:
Rucheton, Benoit
;
Ewenczyk, Claire
;
Gaignard, Pauline
...
info:eu-repo/semantics/altIdentifier/doi/10.1212/nxg.0000000000000630. , 2021
Link:
https://hal.sorbonne-uni..
?
15
A variant of neonatal progeroid syndrome, or Wiedemann–Raut..:
Beauregard-Lacroix, Eliane
;
Salian, Smrithi
;
Kim, Hyunyun
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080780/. , 2019
Link:
http://www.ncbi.nlm.nih...
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