Literature DB >> 26114769

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.

Pía Villanueva, Ron Nudel, Alexander Hoischen, María Angélica Fernández, Nuala H Simpson, Christian Gilissen, Rose H Reader, Lillian Jara, María Magdalena Echeverry, Clyde Francks, Gillian Baird, Gina Conti-Ramsden, Anne O'Hare, Patrick F Bolton, Elizabeth R Hennessy, Hernán Palomino, Luis Carvajal-Carmona, Joris A Veltman, Jean-Baptiste Cazier, Zulema De Barbieri, Simon E Fisher, Dianne F Newbury.   

Abstract

Entities:  

Year:  2015        PMID: 26114769      PMCID: PMC4483266          DOI: 10.1371/journal.pgen.1005336

Source DB:  PubMed          Journal:  PLoS Genet        ISSN: 1553-7390            Impact factor:   5.917


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The name of the ninth author is incorrect. Maria Magdalena Echeverry should read María Magdalena Echeverry. The affiliation for Pía Villanueva is incorrect. The affiliation should read Department of Speech, Language and Hearing Sciences, Faculty of Medicine, University of Chile, Santiago, Chile. The affiliation for Anne O’Hare is incorrect. The affiliation should read Child Life & Health, School of Clinical Sciences, University of Edinburgh, Edinburgh, United Kingdom. There is an error in the first paragraph of page 4. The sentence: "The contribution of identified risk variants is subsequently validated by performing targeted sequencing of candidate genes in a UK-based cohort of individuals affected by SLI," should read: "The contribution of identified risk variants is subsequently validated by performing targeted sequencing of a candidate gene in a UK-based cohort of individuals affected by SLI." There are errors in the Author Contributions. The correct contributions are: Conceived and designed the experiments: PV RN AH MAF CG LJ CF GB GCR AOH PFB ERH SLIC HP LCC JAV JBC ZDB SEF DFN Performed the Chilean fieldwork: PV MAF LJ ZDB Performed the genetic experiments: RN AH NHS CG RHR LCC JAV JBC SEF DFN Analyzed the phenotypic data: PV MAF LJ HP ZDB DFN Analyzed the genetic data: RN AH NHS CG RHR LCC JBC SEF DFN Contributed reagents/materials/analysis tools: PV AH MAF CG LJ MME GB GCR AOH PFB ERH SLIC LCC JAV ZDB SEF DFN Wrote the manuscript: PV RN JBC SEF DFN
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1.  Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.

Authors:  Pía Villanueva; Ron Nudel; Alexander Hoischen; María Angélica Fernández; Nuala H Simpson; Christian Gilissen; Rose H Reader; Lillian Jara; María Magdalena Echeverry; Maria Magdalena Echeverry; Clyde Francks; Gillian Baird; Gina Conti-Ramsden; Anne O'Hare; Patrick F Bolton; Elizabeth R Hennessy; Hernán Palomino; Luis Carvajal-Carmona; Joris A Veltman; Jean-Baptiste Cazier; Zulema De Barbieri; Simon E Fisher; Dianne F Newbury
Journal:  PLoS Genet       Date:  2015-03-17       Impact factor: 5.917

  1 in total
  2 in total

1.  Sex chromosome aneuploidies and copy-number variants: a further explanation for neurodevelopmental prognosis variability?

Authors:  Jessica Le Gall; Mathilde Nizon; Olivier Pichon; Joris Andrieux; Séverine Audebert-Bellanger; Sabine Baron; Claire Beneteau; Frédéric Bilan; Odile Boute; Tiffany Busa; Valérie Cormier-Daire; Claude Ferec; Mélanie Fradin; Brigitte Gilbert-Dussardier; Sylvie Jaillard; Aia Jønch; Dominique Martin-Coignard; Sandra Mercier; Sébastien Moutton; Caroline Rooryck; Elise Schaefer; Marie Vincent; Damien Sanlaville; Cédric Le Caignec; Sébastien Jacquemont; Albert David; Bertrand Isidor
Journal:  Eur J Hum Genet       Date:  2017-06-14       Impact factor: 4.246

2.  A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).

Authors:  Erin M Andres; Huma Hafeez; Adnan Yousaf; Sheikh Riazuddin; Mabel L Rice; Muhammad Asim Raza Basra; Muhammad Hashim Raza
Journal:  Eur J Hum Genet       Date:  2019-04-11       Impact factor: 4.246

  2 in total

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