ResearcherID Thomson Reuters  

Herault, Yann
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ResearcherID: B-5500-2012
URL: http://www.researcherid.com/rid/B-5500-2012
ORCID: http://orcid.org/0000-0001-7049-6900
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This list contains papers that I have authored.

publication(s)  
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1.  Title: Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome
 Author(s): Iacono, G.; Dubos, A.; Méziane, H.; et al.
 Source: Nucleic Acids Res Published: 2018
 DOI: 10.1093/nar/gky196 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/29554304
added
08-Apr-18
2.  Title: A Fast, Easy, and Customizable Eight-Color Flow Cytometric Method for Analysis of the Cellular Content of Bronchoalveolar Lavage Fluid in the Mouse
 Author(s): Daubeuf, F.; Becker, J.; Aguilar-Pimentel, J. A.; et al.
 Source: Curr Protoc Mouse Biol Volume: 7 Issue: 2 Pages: 88-99 Published: 2017
 DOI: 10.1002/cpmo.26 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/28628216
added
27-Aug-17
3.  Title: A Fast, Easy, and Customizable Eight-Color Flow Cytometric Method for Analysis of the Cellular Content of Bronchoalveolar Lavage Fluid in the Mouse
 Author(s): Daubeuf, F.; Becker, J.; Aguilar-Pimentel, J. A.; et al.
 Source: Curr Protoc Mouse Biol Volume: 7 Issue: 2 Pages: 88-99 Published: 2017
 DOI: 10.1002/cpmo.26 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/28628216
added
03-Dec-17
4.  Title: A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
 Author(s): Bowl, M. R.; Simon, M. M.; Ingham, N. J.; et al.
 Source: Nat Commun Volume: 8 Issue: 1 Pages: 886 Published: 2017
 DOI: 10.1038/s41467-017-00595-4 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/29026089
added
17-Oct-17
5.  Title: A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
 Author(s): Bowl, M. R.; Simon, M. M.; Ingham, N. J.; et al.
 Source: Nat Commun Volume: 8 Issue: 1 Pages: 886 Published: 2017
 DOI: 10.1038/s41467-017-00595-4 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/29026089
added
03-Dec-17
6.  Title: Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies
 Author(s): Wendling, O.; Champy, M. F.; Jaubert, S.; et al.
 Source: Sci Rep Volume: 7 Issue: 1 Pages: 9618 Published: 2017
 DOI: 10.1038/s41598-017-08845-7 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/28851918
added
01-Sep-17
7.  Title: Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies
 Author(s): Wendling, O.; Champy, M. F.; Jaubert, S.; et al.
 Source: Sci Rep Volume: 7 Issue: 1 Pages: 9618 Published: 2017
 DOI: 10.1038/s41598-017-08845-7 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/28851918
added
17-Oct-17
8.  Title: Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies
 Author(s): Wendling, O.; Champy, M. F.; Jaubert, S.; et al.
 Source: Sci Rep Volume: 7 Issue: 1 Pages: 9618 Published: 2017
 DOI: 10.1038/s41598-017-08845-7 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/28851918
added
03-Dec-17
9.  Title: Corrigendum: High-throughput discovery of novel developmental phenotypes
 Author(s): Dickinson, M. E.; Flenniken, A. M.; Ji, X.; et al.
 Source: Nature Volume: 551 Issue: 7680 Pages: 398 Published: 2017
 DOI: 10.1038/nature24643 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/29144450
added
03-Dec-17
10.  Title: Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium
 Author(s): Meehan, T. F.; Conte, N.; West, D. B.; et al.
 Source: Nat Genet Volume: 49 Issue: 8 Pages: 1231-1238 Published: 2017
 DOI: 10.1038/ng.3901 /  Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/28650483
added
27-Aug-17
publication(s)  
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