An investigation of NFXL1, a gene implicated in a study of specific language impairment

by Nudel, Ron
Published 2016

FOXP2

by Nudel, Ron, Newbury, Dianne F
Published 2013

Genome-Wide Studies of Specific Language Impairment

by Reader, Rose H., Covill, Laura E., Nudel, Ron, Newbury, Dianne F.
Published 2014

Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2

by Moralli, Daniela, Nudel, Ron, Chan, May T. M., Green, Catherine M., Volpi, Emanuela V., Benítez-Burraco, Antonio, Newbury, Dianne F., García-Bellido, Paloma
Published 2015

Associations of HLA alleles with specific language impairment

by Nudel, Ron, Simpson, Nuala H, Baird, Gillian, O’Hare, Anne, Conti-Ramsden, Gina, Bolton, Patrick F, Hennessy, Elizabeth R, Monaco, Anthony P, Knight, Julian C, Winney, Bruce, Fisher, Simon E, Newbury, Dianne F
Published 2014

Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes

by Pettigrew, Kerry A., Frinton, Emily, Nudel, Ron, Chan, May T. M., Thompson, Paul, Hayiou-Thomas, Marianna E., Talcott, Joel B., Stein, John, Monaco, Anthony P., Hulme, Charles, Snowling, Margaret J., Newbury, Dianne F., Paracchini, Silvia
Published 2016

Correction: Exome Sequencing in an Admixed Isolated Population IndicatesNFXL1 Variants Confer a Risk for Specific Language Impairment

by Villanueva, Pía, Nudel, Ron, Hoischen, Alexander, Fernández, María Angélica, Simpson, Nuala H., Gilissen, Christian, Reader, Rose H., Jara, Lillian, Magdalena Echeverry, María, Francks, Clyde, Baird, Gillian, Conti-Ramsden, Gina, O’Hare, Anne, Bolton, Patrick F., Hennessy, Elizabeth R., Palomino, Hernán, Carvajal-Carmona, Luis, Veltman, Joris A., Cazier, Jean-Baptiste, Barbieri, Zulema De, Fisher, Simon E., Newbury, Dianne F.
Published 2015

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

by Villanueva, Pía, Nudel, Ron, Hoischen, Alexander, Fernández, María Angélica, Simpson, Nuala H., Gilissen, Christian, Reader, Rose H., Jara, Lillian, Echeverry, Maria Magdalena, Francks, Clyde, Baird, Gillian, Conti-Ramsden, Gina, O’Hare, Anne, Bolton, Patrick F., Hennessy, Elizabeth R., Palomino, Hernán, Carvajal-Carmona, Luis, Veltman, Joris A., Cazier, Jean-Baptiste, De Barbieri, Zulema, Fisher, Simon E., Newbury, Dianne F.
Published 2015

VarElect: the phenotype-based variation prioritizer of the GeneCards Suite

by Stelzer, Gil, Plaschkes, Inbar, Oz-Levi, Danit, Alkelai, Anna, Olender, Tsviya, Zimmerman, Shahar, Twik, Michal, Belinky, Frida, Fishilevich, Simon, Nudel, Ron, Guan-Golan, Yaron, Warshawsky, David, Dahary, Dvir, Kohn, Asher, Mazor, Yaron, Kaplan, Sergey, Iny Stein, Tsippi, Baris, Hagit N., Rappaport, Noa, Safran, Marilyn, Lancet, Doron
Published 2016