Works matching AU Newbury, Dianne F.

Results: 35

Scaling up early language intervention in educational settings: First steps matter.

Published in:

Oxford Review of Education, 2023, v. 49, n. 1, p. 29, doi. 10.1080/03054985.2022.2088488

By:

Ramacciotti, Mirela C. C.;
Sousa, Helena;
Silveira, Heloisa G.;
Hulme, Charles;
Snowling, Margaret J.;
Newbury, Dianne F.;
Puglisi, Marina L.

Publication type:

Article

Pathways from the early language and communication environment to literacy outcomes at the end of primary school; the roles of language development and social development.

Published in:

Oxford Review of Education, 2021, v. 47, n. 2, p. 260, doi. 10.1080/03054985.2020.1824902

By:

Gibson, Jenny L.;
Newbury, Dianne F.;
Durkin, Kevin;
Pickles, Andrew;
Conti-Ramsden, Gina;
Toseeb, Umar

Publication type:

Article

The effects of prenatal smoke exposure on language development ‐ a systematic review.

Published in:

Infant & Child Development, 2022, v. 31, n. 4, p. 1, doi. 10.1002/icd.2331

By:

Peixinho, Jessica;
Toseeb, Umar;
Mountford, Hayley S.;
Bermudez, Isabel;
Newbury, Dianne F.

Publication type:

Article

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1370, doi. 10.1038/ejhg.2014.296

By:

Simpson, Nuala H;
Ceroni, Fabiola;
Reader, Rose H;
Covill, Laura E;
Knight, Julian C;
Hennessy, Elizabeth R;
Bolton, Patrick F;
Conti-Ramsden, Gina;
O'Hare, Anne;
Baird, Gillian;
Fisher, Simon E;
Newbury, Dianne F

Publication type:

Article

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1113, doi. 10.1038/ejhg.2014.275

By:

Ceroni, Fabiola;
Simpson, Nuala H;
Francks, Clyde;
Baird, Gillian;
Conti-Ramsden, Gina;
Clark, Ann;
Bolton, Patrick F;
Hennessy, Elizabeth R;
Donnelly, Peter;
Bentley, David R;
Martin, Hilary;
Parr, Jeremy;
Pagnamenta, Alistair T;
Maestrini, Elena;
Bacchelli, Elena;
Fisher, Simon E;
Newbury, Dianne F

Publication type:

Article

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 10, p. 1165, doi. 10.1038/ejhg.2014.4

By:

Ceroni, Fabiola;
Simpson, Nuala H;
Francks, Clyde;
Baird, Gillian;
Conti-Ramsden, Gina;
Clark, Ann;
Bolton, Patrick F;
Hennessy, Elizabeth R;
Donnelly, Peter;
Bentley, David R;
Martin, Hilary;
Parr, Jeremy;
Pagnamenta, Alistair T;
Maestrini, Elena;
Bacchelli, Elena;
Fisher, Simon E;
Newbury, Dianne F

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 4, p. 361, doi. 10.1038/ejhg.2012.166

By:

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

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 6, p. 687, doi. 10.1038/ejhg.2010.251

By:

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

Publication type:

Article

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.

Published in:

Nature Genetics, 2002, v. 30, n. 1, p. 86, doi. 10.1038/ng792

By:

Fisher, Simon E.;
Francks, Clyde;
Marlow, Angela J.;
MacPhie, I. Laurence;
Newbury, Dianne F.;
Cardon, Lon R.;
Ishikawa-Brush, Yumiko;
Richardson, Alex J.;
Talcott, Joel B.;
Gayán, Javier;
Olson, Richard K.;
Pennington, Bruce F.;
Smith, Shelley D.;
DeFries, John C.;
Stein, John F.;
Monaco, Anthony P.

Publication type:

Article

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

Published in:

Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0885-5

By:

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.

Publication type:

Article

Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways.

Published in:

Human Molecular Genetics, 2023, v. 32, n. 11, p. 1932, doi. 10.1093/hmg/ddad023

By:

Wilson, Kate;
Newbury, Dianne F;
Kini, Usha

Publication type:

Article

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 12, p. 1160, doi. 10.1093/hmg/ddab111

By:

Martinelli, Angela;
Rice, Mabel L;
Talcott, Joel B;
Diaz, Rebeca;
Smith, Shelley;
Raza, Muhammad Hashim;
Snowling, Margaret J;
Hulme, Charles;
Stein, John;
Hayiou-Thomas, Marianna E;
Hawi, Ziarih;
Kent, Lindsey;
Pitt, Samantha J;
Newbury, Dianne F;
Paracchini, Silvia

Publication type:

Article

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

Published in:

Genes, 2021, v. 12, n. 2, p. 151, doi. 10.3390/genes12020151

By:

Perrino, Peter A.;
Newbury, Dianne F.;
Fitch, R. Holly;
Castillo, Ignacio del;
Kremer, Hannie

Publication type:

Article

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

Published in:

Genes, 2014, v. 5, n. 2, p. 285, doi. 10.3390/genes5020285

By:

Newbury, Dianne F.;
Monaco, Anthony P.;
Paracchini, Silvia

Publication type:

Article

Associations of HLA alleles with specific language impairment.

Published in:

Journal of Neurodevelopmental Disorders, 2014, v. 6, n. 1, p. 1

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.

Publication type:

Article

A Deletion Involving CD 38 and BST 1 Results in a Fusion Transcript in a Patient With Autism and Asthma.

Published in:

Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 2, p. 254, doi. 10.1002/aur.1365

By:

Ceroni, Fabiola;
Sagar, Angela;
Simpson, Nuala H.;
Gawthrope, Alex J.T.;
Newbury, Dianne F.;
Pinto, Dalila;
Francis, Sunday M.;
Tessman, Dorothy C.;
Cook, Edwin H.;
Monaco, Anthony P.;
Maestrini, Elena;
Pagnamenta, Alistair T.;
Jacob, Suma

Publication type:

Article

Corrigendum: Genome-wide association study of motor coordination.

Published in:

Frontiers in Human Neuroscience, 2024, p. 1, doi. 10.3389/fnhum.2024.1360116

By:

Mountford, Hayley S.;
Hill, Amanda;
Barnett, Anna L.;
Newbury, Dianne F.

Publication type:

Article

Genome-Wide Association Study of Motor Coordination.

Published in:

Frontiers in Human Neuroscience, 2024, p. 1, doi. 10.3389/fnhum.2021.669902

By:

Mountford, Hayley S.;
Hill, Amanda;
Barnett, Anna L.;
Newbury, Dianne F.

Publication type:

Article

Logical and Methodological Issues Affecting Genetic Studies of Humans Reported in Top Neuroscience Journals.

Published in:

Journal of Cognitive Neuroscience, 2018, v. 30, n. 1, p. 25, doi. 10.1162/jocn_a_01192

By:

Grabitz, Clara R.;
Button, Katherine S.;
Munafò, Marcus R.;
Newbury, Dianne F.;
Pernet, Cyril R.;
Thompson, Paul A.;
Bishop, Dorothy V. M.

Publication type:

Article

The Genetic and Molecular Basis of Developmental Language Disorder: A Review.

Published in:

Children, 2022, v. 9, n. 5, p. 586, doi. 10.3390/children9050586

By:

Mountford, Hayley S.;
Braden, Ruth;
Newbury, Dianne F.;
Morgan, Angela T.

Publication type:

Article

FOXP2.

Published in:

WIREs: Cognitive Science, 2013, v. 4, n. 5, p. 547, doi. 10.1002/wcs.1247

By:

Nudel, Ron;
Newbury, Dianne F

Publication type:

Article

Candidate gene variant effects on language disorders in Robinson Crusoe Island.

Published in:

Annals of Human Biology, 2019, v. 46, n. 2, p. 109, doi. 10.1080/03014460.2019.1622776

By:

Mountford, Hayley S.;
Villanueva, Pía;
Fernández, María Angélica;
Barbieri, Zulema De;
Cazier, Jean-Baptiste;
Newbury, Dianne F.

Publication type:

Article

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Published in:

Developmental Medicine & Child Neurology, 2014, v. 56, n. 4, p. 346, doi. 10.1111/dmcn.12294

By:

Simpson, Nuala H;
Addis, Laura;
Brandler, William M;
Slonims, Vicky;
Clark, Ann;
Watson, Jocelynne;
Scerri, Thomas S;
Hennessy, Elizabeth R;
Bolton, Patrick F;
Conti‐Ramsden, Gina;
Fairfax, Benjamin P;
Knight, Julian C;
Stein, John;
Talcott, Joel B;
O'Hare, Anne;
Baird, Gillian;
Paracchini, Silvia;
Fisher, Simon E;
Newbury, Dianne F;
Consortium, SLI

Publication type:

Article

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 2, p. 256, doi. 10.1002/ajmg.c.31791

By:

Mountford, Hayley S.;
Bishop, Dorothy V. M.;
Thompson, Paul A.;
Simpson, Nuala H.;
Newbury, Dianne F.

Publication type:

Article

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

Published in:

PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0134997

By:

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

Publication type:

Article

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure.

Published in:

PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0050321

By:

Scerri, Thomas S.;
Darki, Fahimeh;
Newbury, Dianne F.;
Whitehouse, Andrew J. O.;
Peyrard-Janvid, Myriam;
Matsson, Hans;
Ang, Qi W.;
Pennell, Craig E.;
Ring, Susan;
Stein, John;
Morris, Andrew P.;
Monaco, Anthony P.;
Kere, Juha;
Talcott, Joel B.;
Klingberg, Torkel;
Paracchini, Silvia

Publication type:

Article

Genome-Wide Association Study of Motor Coordination.

Published in:

Frontiers in Human Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnhum.2021.669902

By:

Mountford, Hayley S.;
Hill, Amanda;
Barnett, Anna L.;
Newbury, Dianne F.

Publication type:

Article

The Development of Mental Health Difficulties in Young People With and Without Developmental Language Disorder: A Gene–Environment Interplay Study Using Polygenic Scores.

Published in:

Journal of Speech, Language & Hearing Research, 2023, v. 66, p. 1639, doi. 10.1044/2023_JSLHR-22-00664

By:

Toseeb, Umar;
Vincent, John;
Oginni, Olakunle A.;
Asbury, Kathryn;
Newbury, Dianne F.

Publication type:

Article

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

Published in:

Journal of Speech, Language & Hearing Research, 2019, v. 62, n. 9, p. 3381, doi. 10.1044/2019_JSLHR-L-19-0001

By:

Newbury, Dianne F.;
Gibson, Jenny L.;
Conti-Ramsden, Gina;
Pickles, Andrew;
Durkin, Kevin;
Toseeb, Umar

Publication type:

Article

Evaluation of elements in hair samples of children with developmental language disorder (DLD).

Published in:

Nutritional Neuroscience, 2023, v. 26, n. 2, p. 138, doi. 10.1080/1028415X.2021.2022068

By:

Rashaid, Ayat Bani;
Alqhazo, Mazin;
Newbury, Dianne F.;
Kanaan, Heba;
El-khateeb, Mohammad;
Abukashabeh, Ahmad;
Al-Tamimi, Feda

Publication type:

Article

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

Published in:

Scientific Reports, 2017, p. 46105, doi. 10.1038/srep46105

By:

Chen, Xiaowei Sylvia;
Reader, Rose H.;
Hoischen, Alexander;
Veltman, Joris A.;
Simpson, Nuala H.;
Francks, Clyde;
Newbury, Dianne F.;
Fisher, Simon E.

Publication type:

Article

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation.

Published in:

Scientific Reports, 2016, p. 20369, doi. 10.1038/srep20369

By:

Prekovic, Stefan;
Đurđević, Dušica Filipović;
Csifcsák, Gábor;
Šveljo, Olivera;
Stojković, Oliver;
Janković, Milica;
Koprivšek, Katarina;
Covill, Laura E;
Lučić, Milos;
Van den Broeck, Thomas;
Helsen, Christine;
Ceroni, Fabiola;
Claessens, Frank;
Newbury, Dianne F

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2016, v. 25, n. 9, p. 1771, doi. 10.1093/hmg/ddw047

By:

Shore, Robert;
Covill, Laura;
Pettigrew, Kerry A.;
Brandler, William M.;
Diaz, Rebeca;
Yiwang Xu;
Tello, Javier A.;
Talcott, Joel B.;
Newbury, Dianne F.;
Stein, John;
Monaco, Anthony P.;
Paracchini, Silvia

Publication type:

Article

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

Published in:

Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0148-1

By:

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

Publication type:

Article

Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech.

Published in:

Cellular & Molecular Life Sciences, 2024, v. 81, n. 1, p. 1, doi. 10.1007/s00018-024-05149-8

By:

Pradhan, Aditi;
Mounford, Hayley;
Peixinho, Jessica;
Rea, Edward;
Epeslidou, Emmanouela;
Scott, Julia S.;
Cull, Joanna;
Maxwell, Susan;
Webster, Richard;
Beeson, David;
Dong, Yin Yao;
Prekovic, Stefan;
Bermudez, Isabel;
Newbury, Dianne F.

Publication type:

Article