FOXP2

por Nudel, Ron, Newbury, Dianne F
Publicado 2013

Reading and Language Disorders: The Importance of Both Quantity and Quality

por Newbury, Dianne F., Monaco, Anthony P., Paracchini, Silvia
Publicado 2014

Recent advances in the genetics of language impairment

por Newbury, Dianne F, Fisher, Simon E, Monaco, Anthony P
Publicado 2010

Peripheral Anomalies in USH2A Cause Central Auditory Anomalies in a Mouse Model of Usher Syndrome and CAPD

por Perrino, Peter A., Newbury, Dianne F., Fitch, R. Holly
Publicado en Genes (Basel) (2021)

Genome-Wide Association Study of Motor Coordination

por Mountford, Hayley S., Hill, Amanda, Barnett, Anna L., Newbury, Dianne F.
Publicado en Front Hum Neurosci (2021)

Genome-Wide Studies of Specific Language Impairment

por Reader, Rose H., Covill, Laura E., Nudel, Ron, Newbury, Dianne F.
Publicado en Curr Behav Neurosci Rep (2014)

Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis

por Newbury, Dianne F., Simpson, Nuala H., Thompson, Paul A., Bishop, Dorothy V. M.
Publicado en Wellcome Open Res (2018)

Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis

por Newbury, Dianne F., Simpson, Nuala H., Thompson, Paul A., Bishop, Dorothy V. M.
Publicado en Wellcome Open Res (2021)

Using Polygenic Profiles to Predict Variation in Language and Psychosocial Outcomes in Early and Middle Childhood

por Newbury, Dianne F., Gibson, Jenny L., Conti-Ramsden, Gina, Pickles, Andrew, Durkin, Kevin, Toseeb, Umar
Publicado en J Speech Lang Hear Res (2019)

Generalized Structured Component Analysis in candidate gene association studies: applications and limitations

por Thompson, Paul A., Bishop, Dorothy V. M., Eising, Else, Fisher, Simon E., Newbury, Dianne F.
Publicado en Wellcome Open Res (2020)

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

por Moralli, Daniela, Nudel, Ron, Chan, May T. M., Green, Catherine M., Volpi, Emanuela V., Benítez-Burraco, Antonio, Newbury, Dianne F., García-Bellido, Paloma
Publicado en Mol Cytogenet (2015)

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

por Chen, Xiaowei Sylvia, Reader, Rose H., Hoischen, Alexander, Veltman, Joris A., Simpson, Nuala H., Francks, Clyde, Newbury, Dianne F., Fisher, Simon E.
Publicado en Sci Rep (2017)

The Genetic Population Structure of Robinson Crusoe Island, Chile

por Mountford, Hayley S., Villanueva, Pía, Fernández, María Angélica, Jara, Lilian, De Barbieri, Zulema, Carvajal-Carmona, Luis G., Cazier, Jean-Baptiste, Newbury, Dianne F.
Publicado en Front Genet (2020)

DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits

por Scerri, Tom S., Morris, Andrew P., Buckingham, Lyn-Louise, Newbury, Dianne F., Miller, Laura L., Monaco, Anthony P., Bishop, Dorothy V.M., Paracchini, Silvia
Publicado 2011

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population

por Villanueva, Pia, Newbury, Dianne F, Jara, Lilian, De Barbieri, Zulema, Mirza, Ghazala, Palomino, Hernán M, Fernández, María Angélica, Cazier, Jean-Baptiste, Monaco, Anthony P, Palomino, Hernán
Publicado 2011

Mapping of partially overlapping de novo deletions across an autism susceptibility region [AUTS5] in two unrelated individuals affected by developmental delays with communication i...

por Newbury, Dianne F, Warburton, Pamela C, Wilson, Natalie, Bacchelli, Elena, Carone, Simona, Lamb, Janine A, Maestrini, Elena, Volpi, Emanuela V, Mohammed, Shehla, Baird, Gillian, Monaco, Anthony P
Publicado 2009

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

por Newbury, Dianne F, Mari, Francesca, Sadighi Akha, Elham, MacDermot, Kay D, Canitano, Roberto, Monaco, Anthony P, Taylor, Jenny C, Renieri, Alessandra, Fisher, Simon E, Knight, Samantha J L
Publicado 2013

Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes

por Perrino, Peter A., Talbot, Lidiya, Kirkland, Rose, Hill, Amanda, Rendall, Amanda R., Mountford, Hayley S., Taylor, Jenny, Buscarello, Alexzandrea N., Lahiri, Nayana, Saggar, Anand, Fitch, R. Holly, Newbury, Dianne F.
Publicado en Commun Biol (2020)

Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment

por Pettigrew, Kerry A., Reeves, Emily, Leavett, Ruth, Hayiou-Thomas, Marianna E., Sharma, Anahita, Simpson, Nuala H., Martinelli, Angela, Thompson, Paul, Hulme, Charles, Snowling, Margaret J., Newbury, Dianne F., Paracchini, Silvia
Publicado en PLoS One (2015)

The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts

por Shore, Robert, Covill, Laura, Pettigrew, Kerry A., Brandler, William M., Diaz, Rebeca, Xu, Yiwang, Tello, Javier A., Talcott, Joel B., Newbury, Dianne F., Stein, John, Monaco, Anthony P., Paracchini, Silvia
Publicado en Hum Mol Genet (2016)