Medical conditions in autism spectrum disorders

por Bolton, Patrick F.
Publicado 2009

Traits Contributing to the Autistic Spectrum

por Steer, Colin D., Golding, Jean, Bolton, Patrick F.
Publicado 2010

A comparison of two studies and the prevalence and sex ratio of Neurodevelopmental conditions in Tuberous Sclerosis Complex

por Runicles, Abigail K., Tye, Charlotte, Bolton, Patrick F.
Publicado 2021

Behavioral signatures related to genetic disorders in autism

por Bruining, Hilgo, Eijkemans, Marinus JC, Kas, Martien JH, Curran, Sarah R, Vorstman, Jacob AS, Bolton, Patrick F
Publicado 2014

Autism diagnosis differentiates neurophysiological responses to faces in adults with tuberous sclerosis complex

por Tye, Charlotte, Farroni, Teresa, Volein, Ágnes, Mercure, Evelyne, Tucker, Leslie, Johnson, Mark H., Bolton, Patrick F.
Publicado 2015

Resting-State Neurophysiological Activity Patterns in Young People with ASD, ADHD, and ASD + ADHD

por Shephard, Elizabeth, Tye, Charlotte, Ashwood, Karen L., Azadi, Bahar, Asherson, Philip, Bolton, Patrick F., McLoughlin, Grainne
Publicado 2017

Actigraph-Measured Movement Correlates of Attention-Deficit/Hyperactivity Disorder (ADHD) Symptoms in Young People with Tuberous Sclerosis Complex (TSC) with and without Intellectu...

por Earnest, Tom, Shephard, Elizabeth, Tye, Charlotte, McEwen, Fiona, Woodhouse, Emma, Liang, Holan, Sheerin, Fintan, Bolton, Patrick F.
Publicado 2020

Secular changes in severity of intellectual disability in tuberous sclerosis complex: A reflection of improved identification and treatment of epileptic spasms?

por Tye, Charlotte, Thomas, Laura E., Sampson, Julian R., Lewis, Julia, O'Callaghan, Finbar, Yates, John R. W., Bolton, Patrick F.
Publicado 2018

Long‐term cognitive outcomes in tuberous sclerosis complex

por Tye, Charlotte, Mcewen, Fiona S, Liang, Holan, Underwood, Lisa, Woodhouse, Emma, Barker, Edward D, Sheerin, Fintan, Yates, John R W, Bolton, Patrick F
Publicado 2019

Screening for co‐occurring conditions in adults with autism spectrum disorder using the strengths and difficulties questionnaire: A pilot study

por Findon, James, Cadman, Tim, Stewart, Catherine S., Woodhouse, Emma, Eklund, Hanna, Hayward, Hannah, De Le Harpe Golden, Daniel, Chaplin, Eddie, Glaser, Karen, Simonoff, Emily, Murphy, Declan, Bolton, Patrick F., McEwen, Fiona S.
Publicado 2016

Associations of HLA alleles with specific language impairment

por 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
Publicado 2014

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

por 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
Publicado 2015

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

por 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
Publicado 2014

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

por 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
Publicado 2015

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

por 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
Publicado 2014

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

por 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.
Publicado 2015

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

por 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.
Publicado 2015

Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated Care

por Annear, Nicholas M. P., Appleton, Richard E., Bassi, Zahabiyah, Bhatt, Rupesh, Bolton, Patrick F., Crawford, Pamela, Crowe, Alex, Tossi, Maureen, Elmslie, Frances, Finlay, Eric, Gale, Daniel P., Henderson, Alex, Jones, Elizabeth A., Johnson, Simon R., Joss, Shelagh, Kerecuk, Larissa, Lipkin, Graham, Morrison, Patrick J., O'Callaghan, Finbar J., Cadwgan, Jill, Ong, Albert C. M., Sampson, Julian R., Shepherd, Charles, Kingswood, J. Chris
Publicado 2019

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

por Newbury, Dianne F., Winchester, Laura, Addis, Laura, Paracchini, Silvia, Buckingham, Lyn-Louise, Clark, Ann, Cohen, Wendy, Cowie, Hilary, Dworzynski, Katharina, Everitt, Andrea, Goodyer, Ian M., Hennessy, Elizabeth, Kindley, A. David, Miller, Laura L., Nasir, Jamal, O'Hare, Anne, Shaw, Duncan, Simkin, Zoe, Simonoff, Emily, Slonims, Vicky, Watson, Jocelynne, Ragoussis, Jiannis, Fisher, Simon E., Seckl, Jonathon R., Helms, Peter J., Bolton, Patrick F., Pickles, Andrew, Conti-Ramsden, Gina, Baird, Gillian, Bishop, Dorothy V.M., Monaco, Anthony P.
Publicado 2009

Synaptic, transcriptional, and chromatin genes disrupted in autism

por De Rubeis, Silvia, He, Xin, Goldberg, Arthur P., Poultney, Christopher S., Samocha, Kaitlin, Cicek, A Ercument, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F., Brownfeld, Jessica M., Cai, Jinlu, Campbell, Nicholas J., Carracedo, Angel, Chahrour, Maria H., Chiocchetti, Andreas G., Coon, Hilary, Crawford, Emily L., Crooks, Lucy, Curran, Sarah R., Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A., Gallagher, Louise, Geller, Evan, Guter, Stephen J., Hill, R. Sean, Ionita-Laza, Iuliana, Gonzalez, Patricia Jimenez, Kilpinen, Helena, Klauck, Sabine M., Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R., McInnes, Alison L., Neale, Benjamin, Owen, Michael J., Ozaki, Norio, Parellada, Mara, Parr, Jeremy R., Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J., Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A., Willsey, A. Jeremy, Yu, Timothy W., Yuen, Ryan K.C., Cook, Edwin H., Freitag, Christine M., Gill, Michael, Hultman, Christina M., Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D., Sklar, Pamela, State, Matthew W., Sutcliffe, James S., Walsh, Christopher A., Scherer, Stephen W., Zwick, Michael E., Barrett, Jeffrey C., Cutler, David J., Roeder, Kathryn, Devlin, Bernie, Daly, Mark J., Buxbaum, Joseph D.
Publicado 2014