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Rousseau, Justine
47
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1
Mono-allelic KCNB2 variants lead to a neurodevelopmental sy..:
Bhat, Shreyas
;
Rousseau, Justine
;
Michaud, Coralie
...
The American Journal of Human Genetics. 111 (2024) 4 - p. 761-777 , 2024
Link:
https://doi.org/10.1016/..
?
2
Enhancement of inhaled micronized powder flow properties fo..:
Gresse, Eva
;
Rousseau, Justine
;
Akdim, Myriam
...
Powder Technology. 437 (2024) - p. 119576 , 2024
Link:
https://doi.org/10.1016/..
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3
Disease-relevant mutations in Kv2.2 have drastic effects on..:
Bhat, Shreyas
;
Özaydın, Deniz
;
Rousseau, Justine
..
Biophysical Journal. 123 (2024) 3 - p. 525a-526a , 2024
Link:
https://doi.org/10.1016/..
?
4
Resistance to CLnA-induced ferroptosis is acquired in Caco-..:
Cuvelier, Géraldine
;
Vermonden, Perrine
;
Rousseau, Justine
...
Frontiers in Cell Death. 2 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
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5
Null and missense mutations of ERI1 cause a recessive pheno..:
Guo, Long
;
Salian, Smrithi
;
Xue, Jing-yi
...
The American Journal of Human Genetics. 110 (2023) 7 - p. 1068-1085 , 2023
Link:
https://doi.org/10.1016/..
?
6
The ATP6V1B2 DDOD/DOORS-Associated p.Arg506* Variant Causes..:
Rousseau, Justine
;
Tene Tadoum, Samuel Boris
;
Lavertu Jolin, Marisol
...
Genes. 14 (2023) 8 - p. 1538 , 2023
Link:
https://doi.org/10.3390/..
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7
Recurrent chromosomal translocations in sarcomas create a m..:
Sudarshan, Deepthi
;
Avvakumov, Nikita
;
Lalonde, Marie-Eve
...
Genes & Development. 36 (2022) 11-12 - p. 664-683 , 2022
Link:
https://doi.org/10.1101/..
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8
Hypomorphic GINS3 variants alter DNA replication and cause ..:
McQuaid, Mary E.
;
Ahmed, Kashif
;
Tran, Stephanie
...
JCI Insight. 7 (2022) 10 - p. , 2022
Link:
https://doi.org/10.1172/..
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9
Disruption of exon-bridging interactions between the minor ..:
Olthof, Anouk M
;
White, Alisa K
;
Mieruszynski, Stephen
...
Nucleic Acids Research. 49 (2021) 6 - p. 3524-3545 , 2021
Link:
https://doi.org/10.1093/..
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10
A homozygous variant in the Lamin B receptor gene LBR resul..:
Collins, Meagan
;
Miranda, Valancy
;
Rousseau, Justine
..
Bone. 141 (2020) - p. 115601 , 2020
Link:
https://doi.org/10.1016/..
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11
Mutations in ANAPC1, Encoding a Scaffold Subunit of the Ana..:
Ajeawung, Norbert F.
;
Nguyen, Thi Tuyet Mai
;
Lu, Linchao
...
The American Journal of Human Genetics. 105 (2019) 3 - p. 625-630 , 2019
Link:
https://doi.org/10.1016/..
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12
Author Correction: CHD3 helicase domain mutations cause a n..:
Blok, Lot Snijders
;
Rousseau, Justine
;
Twist, Joanna
...
Nature Communications. 10 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
13
Author Correction: CHD3 helicase domain mutations cause a n..:
Snijders Blok, Lot
;
Rousseau, Justine
;
Twist, Joanna
...
Nature Communications. 10 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
14
Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartat..:
van Karnebeek, Clara D.M.
;
Ramos, Rúben J.
;
Wen, Xiao-Yan
...
The American Journal of Human Genetics. 105 (2019) 3 - p. 534-548 , 2019
Link:
https://doi.org/10.1016/..
?
15
CHD3 helicase domain mutations cause a neurodevelopmental s..:
Snijders Blok, Lot
;
Rousseau, Justine
;
Twist, Joanna
...
Nature Communications. 9 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
1-15