I agree that this site is using cookies. You can find further informations here.
X
Plagnol, V
429  results:
Search for persons X
?
1

91 Dose tracking software implementation within a intervent..:

Plagnol, V. ; Blayac, P.M. ; Maquin, P....
Physica Medica.  68 (2019)  - p. 54 , 2019
Link: https://doi.org/10.1016/..
 
?
2

77 Volumetric modulated arc therapy breast irradiations wit..:

Bouyer, C. ; Plagnol, V. ; C.Vignolo..
Physica Medica.  68 (2019)  - p. 47 , 2019
Link: https://doi.org/10.1016/..
 
?
3

Dissecting TDP-43 gain- and loss-of-function in neurodegene..:

Sivakumar, P. ; Humphrey, J. ; Lo, K....
Neuromuscular Disorders.  28 (2018)  - p. S26 , 2018
Link: https://doi.org/10.1016/..
 
?
4

36. A DACS (Dose Archiving and Communication System) succes..:

Plagnol, V. ; Blayac, P.-M. ; Chirveches, L...
Physica Medica.  44 (2017)  - p. 43 , 2017
Link: https://doi.org/10.1016/..
 
?
5

Investigating dysfunctional RNA processing in TDP-43 mouse ..:

Sivakumar, P. ; Humphrey, J. ; Ule, A....
Neuromuscular Disorders.  27 (2017)  - p. S32 , 2017
Link: https://doi.org/10.1016/..
 
?
6

A novel missense mutation in HSF4 causes autosomal-dominant..:

Berry, V ; Pontikos, N ; Moore, A...
Eye.  32 (2017)  4 - p. 806-812 , 2017
Link: https://doi.org/10.1038/..
 
?
7

Use of high-throughput targeted exome-sequencing to screen ..:

Lopes, L.R. ; Murphy, C. ; Syrris, P....
European Journal of Medical Genetics.  58 (2015)  11 - p. 611-616 , 2015
Link: https://doi.org/10.1016/..
 
?
8

A severe collodion phenotype in the newborn period associat..:

Bland, P.J. ; Chronnell, C. ; Plagnol, V...
British Journal of Dermatology.  173 (2015)  1 - p. 285-287 , 2015
Link: https://doi.org/10.1111/..
 
?
9

High-throughput genotyping and phenotyping reveals new gene..:

Rocha Lopes, L. ; Giambartolomei, C. ; Syrris, P....
European Heart Journal.  34 (2013)  suppl 1 - p. 863-863 , 2013
Link: https://doi.org/10.1093/..
 
?
10

A missense mutation in the mouse TDP-43 gene leads to a gai..:

De Oliveira, H.M. ; Ricketts, T. ; Fisher, E....
Journal of the Neurological Sciences.  333 (2013)  - p. e438-e439 , 2013
Link: https://doi.org/10.1016/..
 
?
11

Recessive oligodontia linked to a homozygous loss-of-functi..:

AlFawaz, S. ; Fong, F. ; Plagnol, V....
Archives of Oral Biology.  58 (2013)  5 - p. 462-466 , 2013
Link: https://doi.org/10.1016/..
 
?
12

G.P.2 Mutations in the human isoprenoid synthase domain con..:

Cirak, S. ; Foley, R.A. ; Herrmann, R....
Neuromuscular Disorders.  22 (2012)  9-10 - p. 812 , 2012
Link: https://doi.org/10.1016/..
 
?
13

Exome sequencing in a family segregating for celiac disease:

Szperl, AM ; Ricaño‐Ponce, I ; Li, JK...
Clinical Genetics.  80 (2011)  2 - p. 138-147 , 2011
Link: https://doi.org/10.1111/..
 
?
14

Dissection of the genetics of Parkinson's disease identifie..:

The UK Parkinson's Disease Consortium and The Wellcome Trust Case Control Consortium 2 ; Spencer, C. C. A. ; Plagnol, V....
Human Molecular Genetics.  20 (2010)  2 - p. 345-353 , 2010
Link: https://doi.org/10.1093/..
 
?
15

Integrated Polygenic Tool Substantially Enhances Coronary A..:

Riveros-Mckay, F ; Weale, ME ; Moore, R...
https://discovery.ucl.ac.uk/id/eprint/10139552/1/hcg-14-e003304.pdf.  , 2021
Link: https://discovery.ucl.ac..
 
1-15