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

Year Number of Results
2008 6
2009 3
2010 4
2011 4
2013 3
2014 5
2015 1
2016 2
2017 5
2018 2
2019 4
2020 4
2022 3
2023 4
2024 0

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44 results

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Page 1
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons.
Asadollahi R, Delvendahl I, Muff R, Tan G, Rodríguez DG, Turan S, Russo M, Oneda B, Joset P, Boonsawat P, Masood R, Mocera M, Ivanovski I, Baumer A, Bachmann-Gagescu R, Schlapbach R, Rehrauer H, Steindl K, Begemann A, Reis A, Winkler J, Winner B, Müller M, Rauch A. Asadollahi R, et al. Among authors: oneda b. Hum Mol Genet. 2023 Jun 19;32(13):2192-2204. doi: 10.1093/hmg/ddad048. Hum Mol Genet. 2023. PMID: 37010102 Free PMC article.
Microarrays in prenatal diagnosis.
Oneda B, Rauch A. Oneda B, et al. Best Pract Res Clin Obstet Gynaecol. 2017 Jul;42:53-63. doi: 10.1016/j.bpobgyn.2017.01.003. Epub 2017 Jan 23. Best Pract Res Clin Obstet Gynaecol. 2017. PMID: 28215395 Review.
Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders.
Oneda B, Asadollahi R, Azzarello-Burri S, Niedrist D, Baldinger R, Masood R, Schinzel A, Latal B, Jenni OG, Rauch A. Oneda B, et al. Mol Syndromol. 2017 Aug;8(5):266-271. doi: 10.1159/000477189. Epub 2017 Jun 13. Mol Syndromol. 2017. PMID: 28878611 Free PMC article.
Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay.
Rieger M, Moutton S, Verheyen S, Steindl K, Popp B, Leheup B, Bonnet C, Oneda B, Rauch A, Reis A, Krumbiegel M, Hüffmeier U. Rieger M, et al. Among authors: oneda b. Eur J Med Genet. 2023 Jan;66(1):104669. doi: 10.1016/j.ejmg.2022.104669. Epub 2022 Nov 12. Eur J Med Genet. 2023. PMID: 36379434
Assessing clinical utility of preconception expanded carrier screening regarding residual risk for neurodevelopmental disorders.
Boonsawat P, Horn AHC, Steindl K, Baumer A, Joset P, Kraemer D, Bahr A, Ivanovski I, Cabello EM, Papik M, Zweier M, Oneda B, Sirleto P, Burkhardt T, Sticht H, Rauch A. Boonsawat P, et al. Among authors: oneda b. NPJ Genom Med. 2022 Jul 29;7(1):45. doi: 10.1038/s41525-022-00316-x. NPJ Genom Med. 2022. PMID: 35906228 Free PMC article.
Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, Datar C, Verma IC, Puri RD, Zollino M, Bachmann-Gagescu R, Niedrist D, Papik M, Figueiro-Silva J, Masood R, Zweier M, Kraemer D, Lincoln S, Rodan L; Undiagnosed Diseases Network (UDN); Passemard S, Drunat S, Verloes A, Horn AHC, Sticht H, Steinfeld R, Plecko B, Latal B, Jenni O, Asadollahi R, Rauch A. Boonsawat P, et al. Among authors: oneda b. Genet Med. 2019 Sep;21(9):2043-2058. doi: 10.1038/s41436-019-0464-7. Epub 2019 Mar 7. Genet Med. 2019. PMID: 30842647 Free PMC article.
44 results