FOXP2

door Nudel, Ron, Newbury, Dianne F
Gepubliceerd in 2013

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

door Newbury, Dianne F., Monaco, Anthony P., Paracchini, Silvia
Gepubliceerd in 2014

Recent advances in the genetics of language impairment

door Newbury, Dianne F, Fisher, Simon E, Monaco, Anthony P
Gepubliceerd in 2010

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

door Perrino, Peter A., Newbury, Dianne F., Fitch, R. Holly
Gepubliceerd in Genes (Basel) (2021)

Genome-Wide Association Study of Motor Coordination

door Mountford, Hayley S., Hill, Amanda, Barnett, Anna L., Newbury, Dianne F.
Gepubliceerd in Front Hum Neurosci (2021)

Genome-Wide Studies of Specific Language Impairment

door Reader, Rose H., Covill, Laura E., Nudel, Ron, Newbury, Dianne F.
Gepubliceerd in 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

door Newbury, Dianne F., Simpson, Nuala H., Thompson, Paul A., Bishop, Dorothy V. M.
Gepubliceerd in Wellcome Open Res (2018)

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

door Newbury, Dianne F., Simpson, Nuala H., Thompson, Paul A., Bishop, Dorothy V. M.
Gepubliceerd in Wellcome Open Res (2021)

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

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

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

door Thompson, Paul A., Bishop, Dorothy V. M., Eising, Else, Fisher, Simon E., Newbury, Dianne F.
Gepubliceerd in Wellcome Open Res (2020)

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

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

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

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

The Genetic Population Structure of Robinson Crusoe Island, Chile

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

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

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

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

door 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
Gepubliceerd in 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...

door 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
Gepubliceerd in 2009

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

door 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
Gepubliceerd in 2013

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

door 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.
Gepubliceerd in 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

door 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
Gepubliceerd in PLoS One (2015)

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

door 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
Gepubliceerd in Hum Mol Genet (2016)