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Year | Number of Results |
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2019 | 1 |
2021 | 1 |
2023 | 3 |
2024 | 1 |
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Page 1
Rare variant association on unrelated individuals in case-control studies using aggregation tests: existing methods and current limitations.
Brief Bioinform. 2023 Sep 22;24(6):bbad412. doi: 10.1093/bib/bbad412.
Brief Bioinform. 2023.
PMID: 37974506
Review.
ORVAL: a novel platform for the prediction and exploration of disease-causing oligogenic variant combinations.
Renaux A, Papadimitriou S, Versbraegen N, Nachtegael C, Boutry S, Nowé A, Smits G, Lenaerts T.
Renaux A, et al. Among authors: boutry s.
Nucleic Acids Res. 2019 Jul 2;47(W1):W93-W98. doi: 10.1093/nar/gkz437.
Nucleic Acids Res. 2019.
PMID: 31147699
Free PMC article.
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CCNF (Cyclin F) as a Candidate Gene for Familial Hodgkin Lymphoma: Additional Evidence for the Importance of Mitotic Checkpoint Defects in Tumorigenesis.
Khoury E, Maalouf H, Mendola A, Boutry S, Camboni A, D'Angiolella V, Choquet S, Landman-Parker J, Besson C, Poirel HA, Limaye N.
Khoury E, et al. Among authors: boutry s.
Hemasphere. 2023 Nov 16;7(12):e985. doi: 10.1097/HS9.0000000000000985. eCollection 2023 Dec.
Hemasphere. 2023.
PMID: 38026792
Free PMC article.
No abstract available.
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Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations.
Brouillard P, Schlögel MJ, Homayun Sepehr N, Helaers R, Queisser A, Fastré E, Boutry S, Schmitz S, Clapuyt P, Hammer F, Dompmartin A, Weitz-Tuoretmaa A, Laranne J, Pasquesoone L, Vilain C, Boon LM, Vikkula M.
Brouillard P, et al. Among authors: boutry s.
Orphanet J Rare Dis. 2021 Jun 10;16(1):267. doi: 10.1186/s13023-021-01898-y.
Orphanet J Rare Dis. 2021.
PMID: 34112235
Free PMC article.
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Excalibur: A new ensemble method based on an optimal combination of aggregation tests for rare-variant association testing for sequencing data.
Boutry S, Helaers R, Lenaerts T, Vikkula M.
Boutry S, et al.
PLoS Comput Biol. 2023 Sep 14;19(9):e1011488. doi: 10.1371/journal.pcbi.1011488. eCollection 2023 Sep.
PLoS Comput Biol. 2023.
PMID: 37708232
Free PMC article.
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Somatic Loss-of-Function PIK3R1 and Activating Non-hotspot PIK3CA Mutations Associated with Capillary Malformation with Dilated Veins (CMDV).
De Bortoli M, Queisser A, Pham VC, Dompmartin A, Helaers R, Boutry S, Claus C, De Roo AK, Hammer F, Brouillard P, Abdelilah-Seyfried S, Boon LM, Vikkula M.
De Bortoli M, et al. Among authors: boutry s.
J Invest Dermatol. 2024 Feb 29:S0022-202X(24)00164-7. doi: 10.1016/j.jid.2024.01.033. Online ahead of print.
J Invest Dermatol. 2024.
PMID: 38431221
Free article.
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