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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2005 1
2006 6
2007 3
2008 4
2009 2
2010 8
2011 11
2012 9
2013 4
2014 9
2015 11
2016 5
2017 5
2018 6
2019 7
2020 9
2021 7
2022 4
2023 5
2024 2

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101 results

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Page 1
From ecological functions to ecosystem services: linking coastal lagoons biodiversity with human well-being.
Rodrigues-Filho JL, Macêdo RL, Sarmento H, Pimenta VRA, Alonso C, Teixeira CR, Pagliosa PR, Netto SA, Santos NCL, Daura-Jorge FG, Rocha O, Horta P, Branco JO, Sartor R, Muller J, Cionek VM. Rodrigues-Filho JL, et al. Among authors: muller j. Hydrobiologia. 2023;850(12-13):2611-2653. doi: 10.1007/s10750-023-05171-0. Epub 2023 Mar 10. Hydrobiologia. 2023. PMID: 37323646 Free PMC article. Review.
WGS Revealed Novel BBS5 Pathogenic Variants, Missed by WES, Causing Ciliary Structure and Function Defects.
Karam A, Delvallée C, Estrada-Cuzcano A, Geoffroy V, Lamouche JB, Leuvrey AS, Nourisson E, Tarabeux J, Stoetzel C, Scheidecker S, Porter LF, Génin E, Redon R, Sandron F, Boland A, Deleuze JF, Le May N, Dollfus H, Muller J. Karam A, et al. Among authors: muller j. Int J Mol Sci. 2023 May 13;24(10):8729. doi: 10.3390/ijms24108729. Int J Mol Sci. 2023. PMID: 37240074 Free PMC article.
The AnnotSV webserver in 2023: updated visualization and ranking.
Geoffroy V, Lamouche JB, Guignard T, Nicaise S, Kress A, Scheidecker S, Le Béchec A, Muller J. Geoffroy V, et al. Among authors: muller j. Nucleic Acids Res. 2023 Jul 5;51(W1):W39-W45. doi: 10.1093/nar/gkad426. Nucleic Acids Res. 2023. PMID: 37216590 Free PMC article.
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
El Chehadeh S, Han KA, Kim D, Jang G, Bakhtiari S, Lim D, Kim HY, Kim J, Kim H, Wynn J, Chung WK, Vitiello G, Cutcutache I, Page M, Gecz J, Harper K, Han AR, Kim HM, Wessels M, Bayat A, Jaén AF, Selicorni A, Maitz S, de Brouwer APM, Silfhout AV, Armstrong M, Symonds J, Küry S, Isidor B, Cogné B, Nizon M, Feger C, Muller J, Torti E, Grange DK, Willems M, Kruer MC, Ko J, Piton A, Um JW. El Chehadeh S, et al. Among authors: muller j. Nat Commun. 2022 Jul 15;13(1):4112. doi: 10.1038/s41467-022-31566-z. Nat Commun. 2022. PMID: 35840571 Free PMC article.
The Economic, Medical and Psychosocial Consequences of Whole Genome Sequencing for the Genetic Diagnosis of Patients With Intellectual Disability: The DEFIDIAG Study Protocol.
Lejeune C, Robert-Viard C, Meunier-Beillard N, Borel MA, Gourvès L, Staraci S, Soilly AL, Guillemin F, Seror V, Achit H, Bouctot M, Asensio ML, Briffaut AS, Delmas C, Bruel AL, Benoit A, Simon A, Gerard B, Hadj Abdallah H, Lyonnet S, Faivre L, Thauvin-Robinet C, Odent S, Heron D, Sanlaville D, Frebourg T, Muller J, Duffourd Y, Boland A, Deleuze JF, Espérou H, Binquet C, Dollfus H. Lejeune C, et al. Among authors: muller j. Front Genet. 2022 Apr 4;13:852472. doi: 10.3389/fgene.2022.852472. eCollection 2022. Front Genet. 2022. PMID: 35444683 Free PMC article.
101 results