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Lindenbaum, Pierre
301
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Online (301)
Mediatypes
Articles (Online) (32)
Bookchapter (Online) (1)
OpenAccess-fulltext (268)
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?
1
TAD boundary deletion causes PITX2-related cardiac electric..:
Baudic, Manon
;
Murata, Hiroshige
;
Bosada, Fernanda M.
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
2
Spontaneous Akt2 deficiency in a colony of NOD mice exhibit..:
Hervé, Julie
;
Haurogné, Karine
;
Allard, Marie
...
Scientific Reports. 14 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
3
How local reference panels improve imputation in French pop..:
Herzig, Anthony F.
;
Velo‐Suárez, Lourdes
;
Campion, Dominique
...
Scientific Reports. 14 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
4
Generation of a patient-specific induced pluripotent stem c..:
Geryk, Michelle
;
Canac, Robin
;
Forest, Virginie
...
Stem Cell Research. 77 (2024) - p. 103396 , 2024
Link:
https://doi.org/10.1016/..
?
5
Variations in the poly-histidine repeat motif of HOXA1 cont..:
Odelin, Gaëlle
;
Faucherre, Adèle
;
Marchese, Damien
...
Nature Communications. 14 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
6
APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A ..:
Vanhoye, Xavier
;
Janin, Alexandre
;
Caillaud, Amandine
...
International Journal of Molecular Sciences. 23 (2022) 8 - p. 4281 , 2022
Link:
https://doi.org/10.3390/..
?
7
Non-coding deletion induces 3D chromatin remodelling and PI..:
Baudic, Manon
;
Murata, Hiroshigue
;
Bosada, Fernanda
...
Archives of Cardiovascular Diseases Supplements. 14 (2022) 2 - p. 209 , 2022
Link:
https://doi.org/10.1016/..
?
8
Burden of rare variants in arrhythmogenic cardiomyopathy wi..:
Goudal, Adeline
;
Karakachoff, Matilde
;
Lindenbaum, Pierre
...
Human Mutation. 43 (2022) 9 - p. 1333-1342 , 2022
Link:
https://doi.org/10.1002/..
?
9
Identification of a Gain-of-FunctionLIPCVariant as a Novel ..:
Dijk, Wieneke
;
Di Filippo, Mathilde
;
Kooijman, Sander
...
Circulation. 146 (2022) 10 - p. 724-739 , 2022
Link:
https://doi.org/10.1161/..
?
10
Moment estimators of relatedness from low-depth whole-genom..:
Herzig, Anthony F.
;
Ciullo, M.
;
Deleuze, Jean-François
...
BMC Bioinformatics. 23 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
11
Fryns type mesomelic dysplasia of the upper limbs caused by..:
Le Caignec, Cédric
;
Pichon, Olivier
;
Briand, Annaig
...
European Journal of Human Genetics. 28 (2019) 3 - p. 324-332 , 2019
Link:
https://doi.org/10.1038/..
?
12
RPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with ..:
Le Caignec, Cedric
;
Ory, Benjamin
;
Lamoureux, François
...
The American Journal of Human Genetics. 105 (2019) 5 - p. 1040-1047 , 2019
Link:
https://doi.org/10.1016/..
?
13
Integrated clinical and omics approach to rare diseases: no..:
Kim, Artem
;
Savary, Clara
;
Dubourg, Christèle
...
Brain. 142 (2018) 1 - p. 35-49 , 2018
Link:
https://doi.org/10.1093/..
?
14
bioalcidae, samjs and vcffilterjs: object-oriented formatte..:
Lindenbaum, Pierre
;
Redon, Richard
;
Hancock, John
Bioinformatics. 34 (2017) 7 - p. 1224-1225 , 2017
Link:
https://doi.org/10.1093/..
?
15
Dysfunction of the Voltage‐Gated K+Channel β2 Subunit in a ..:
Portero, Vincent
;
Le Scouarnec, Solena
;
Es‐Salah‐Lamoureux, Zeineb
...
Journal of the American Heart Association. 5 (2016) 6 - p. , 2016
Link:
https://doi.org/10.1161/..
1-15