Chennen K[au] - Search Results

Year	Number of Results
2013	1
2014	2
2016	1
2017	2
2018	1
2019	2
2020	2
2023	1
2024	1

1

[Bardet-Biedl syndrome: cilia and obesity - from genes to integrative approaches].

Chennen K, Scerbo MJ, Dollfus H, Poch O, Marion V. Chennen K, et al. Med Sci (Paris). 2014 Nov;30(11):1034-9. doi: 10.1051/medsci/20143011018. Epub 2014 Nov 10. Med Sci (Paris). 2014. PMID: 25388586 Free article. Review. French.

2

MISTIC: A prediction tool to reveal disease-relevant deleterious missense variants.

Chennen K, Weber T, Lornage X, Kress A, Böhm J, Thompson J, Laporte J, Poch O. Chennen K, et al. PLoS One. 2020 Jul 31;15(7):e0236962. doi: 10.1371/journal.pone.0236962. eCollection 2020. PLoS One. 2020. PMID: 32735577 Free PMC article.

3

CeGAL: Redefining a Widespread Fungal-Specific Transcription Factor Family Using an In Silico Error-Tracking Approach.

Mayer C, Vogt A, Uslu T, Scalzitti N, Chennen K, Poch O, Thompson JD. Mayer C, et al. Among authors: chennen k. J Fungi (Basel). 2023 Mar 29;9(4):424. doi: 10.3390/jof9040424. J Fungi (Basel). 2023. PMID: 37108879 Free PMC article.

4

Insights into Ciliary Genes and Evolution from Multi-Level Phylogenetic Profiling.

Nevers Y, Prasad MK, Poidevin L, Chennen K, Allot A, Kress A, Ripp R, Thompson JD, Dollfus H, Poch O, Lecompte O. Nevers Y, et al. Among authors: chennen k. Mol Biol Evol. 2017 Aug 1;34(8):2016-2034. doi: 10.1093/molbev/msx146. Mol Biol Evol. 2017. PMID: 28460059 Free PMC article.

5

MyGeneFriends: A Social Network Linking Genes, Genetic Diseases, and Researchers.

Allot A, Chennen K, Nevers Y, Poidevin L, Kress A, Ripp R, Thompson JD, Poch O, Lecompte O. Allot A, et al. Among authors: chennen k. J Med Internet Res. 2017 Jun 16;19(6):e212. doi: 10.2196/jmir.6676. J Med Internet Res. 2017. PMID: 28623182 Free PMC article.

6

Novel IQCE variations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish.

Estrada-Cuzcano A, Etard C, Delvallée C, Stoetzel C, Schaefer E, Scheidecker S, Geoffroy V, Schneider A, Studer F, Mattioli F, Chennen K, Sigaudy S, Plassard D, Poch O, Piton A, Strahle U, Muller J, Dollfus H. Estrada-Cuzcano A, et al. Among authors: chennen k. Hum Mutat. 2020 Jan;41(1):240-254. doi: 10.1002/humu.23924. Epub 2019 Oct 17. Hum Mutat. 2020. PMID: 31549751

7

A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi.

Stoetzel C, Bär S, De Craene JO, Scheidecker S, Etard C, Chicher J, Reck JR, Perrault I, Geoffroy V, Chennen K, Strähle U, Hammann P, Friant S, Dollfus H. Stoetzel C, et al. Among authors: chennen k. Nat Commun. 2016 Nov 24;7:13586. doi: 10.1038/ncomms13586. Nat Commun. 2016. PMID: 27882921 Free PMC article.

8

Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Laugel-Haushalter V, Morkmued S, Stoetzel C, Geoffroy V, Muller J, Boland A, Deleuze JF, Chennen K, Pitiphat W, Dollfus H, Niederreither K, Bloch-Zupan A, Pungchanchaikul P. Laugel-Haushalter V, et al. Among authors: chennen k. Front Physiol. 2018 Sep 26;9:1329. doi: 10.3389/fphys.2018.01329. eCollection 2018. Front Physiol. 2018. PMID: 30319441 Free PMC article.

9

Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.

Mary L, Chennen K, Stoetzel C, Antin M, Leuvrey A, Nourisson E, Alanio-Detton E, Antal MC, Attié-Bitach T, Bouvagnet P, Bouvier R, Buenerd A, Clémenson A, Devisme L, Gasser B, Gilbert-Dussardier B, Guimiot F, Khau Van Kien P, Leroy B, Loget P, Martinovic J, Pelluard F, Perez MJ, Petit F, Pinson L, Rooryck-Thambo C, Poch O, Dollfus H, Schaefer E, Muller J. Mary L, et al. Among authors: chennen k. Clin Genet. 2019 Mar;95(3):384-397. doi: 10.1111/cge.13500. Clin Genet. 2019. PMID: 30614526

10

Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage.

Okutman O, Gürbüz AS, Büyük U, Real E, Leconte R, Chennen K, Mayer C, Muller J, Le May N, Viville S. Okutman O, et al. Among authors: chennen k. J Assist Reprod Genet. 2024 Feb;41(2):311-322. doi: 10.1007/s10815-023-03009-1. Epub 2024 Jan 5. J Assist Reprod Genet. 2024. PMID: 38177974

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