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Saillour, Virginie
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1

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..
 
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2

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..
 
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3

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..
 
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4

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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5

KMT2E-ASNS: a novel relapse-specific fusion gene in early T..:

Khater, Fida ; Lajoie, Mathieu ; Langlois, Sylvie...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374844/.  , 2017
Link: http://www.ncbi.nlm.nih...
 
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6

SNooPer: a machine learning-based method for somatic varian..:

Spinella, Jean-François ; Mehanna, Pamela ; Vidal, Ramon...
http://www.biomedcentral.com/1471-2164/17/912.  , 2016
Link: http://www.biomedcentral..
 
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7

Whole-exome sequencing of a rare case of familial childhood..:

Spinella, Jean-François ; Healy, Jasmine ; Saillour, Virginie...
http://www.biomedcentral.com/1471-2407/15/539.  , 2015
Link: http://www.biomedcentral..
 
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8

A novel somatic mutation in ACD induces telomere lengthenin..:

Spinella, Jean-François ; Cassart, Pauline ; Garnier, Nicolas...
http://www.biomedcentral.com/1471-2407/15/621.  , 2015
Link: http://www.biomedcentral..
 
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9

Joint genotype inference with germline and somatic mutation:

Bareke, Eric ; Saillour, Virginie ; Spinella, Jean-François...
http://www.biomedcentral.com/1471-2105/14/S5/S3.  , 2013
Link: http://www.biomedcentral..
 
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10

Rare allelic forms of PRDM9 associated with childhood leuke..:

Hussin, Julie ; Sinnett, Daniel ; Casals, Ferran...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589531.  , 2013
Link: http://www.ncbi.nlm.nih...
 
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11

Whole-exome sequencing reveals a rapid change in the freque..:

Casals, Ferran ; Hodgkinson, Alan ; Hussin, Julie...
https://constellation.uqac.ca/5142/.  , 2013
Link: https://constellation.uq..
 
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12

Whole-exome sequencing reveals a rapid change in the freque..:

Ferran Casals ; Alan Hodgkinson ; Julie Hussin...
http://europepmc.org/articles/PMC3784517?pdf=render.  , 2013
Link: https://doi.org/10.1371/..
 
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13

Custom oligonucleotide array-based CGH: a reliable diagnost..:

Vasson, Aurélie ; Leroux, Céline ; Orhant, Lucie...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746255.  , 2013
Link: http://www.ncbi.nlm.nih...
 
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14

Social and clinical vulnerability in stroke and STEMI manag..:

Jérome Berge ; Gaultier Marnat ; Emmanuel Ellie...
https://bmjopen.bmj.com/content/14/1/e073933.full.  , 2024
Link: https://doi.org/10.1136/..
 
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