المؤلفون: Lindsay, Natasha, Runicles, Abigail, Johnson, Mark H., Jones, Emily J. H., Bolton, Patrick F., Charman, Tony, Tye, Charlotte

المساهمون: Tuberous Sclerosis Association

المصدر: Developmental Medicine & Child Neurology ; volume 66, issue 5, page 635-643 ; ISSN 0012-1622 1469-8749

الإتاحة: https://doi.org/10.1111/dmcn.15765Test

المؤلفون: Tye, Charlotte, McEwen, Fiona S., Liang, Holan, Woodhouse, Emma, Underwood, Lisa, Shephard, Elizabeth, Barker, Edward D., Sheerin, Fintan, Higgins, Nicholas, Steenbruggen, Juul, Bolton, Patrick F.

المساهمون: Autism Speaks, Baily Thomas Charitable Fund, Tuberous Sclerosis Association

المصدر: Epilepsia ; volume 64, issue 3 ; ISSN 0013-9580 1528-1167

الإتاحة: https://doi.org/10.1111/epi.17507Test

المؤلفون: Lindsay, Natasha, Runicles, Abigail, Johnson, Mark H., Jones, Emily J. H., Bolton, Patrick F., Charman, Tony, Tye, Charlotte

المصدر: Developmental Medicine & Child Neurology; May2024, Vol. 66 Issue 5, p635-643, 9p

مصطلحات موضوعية: TUBEROUS sclerosis, EPILEPSY, AGE groups, INFANT development, LONGITUDINAL method

المؤلفون: Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Wang, Zhuozhi, Vorstman, Jacob A. S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Marshall, Christian R., Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Griswold, Anthony J., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., De Jonge, Maretha V., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inȇs C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bolshakova, Nadia, Bacchelli, Elena, Anney, Richard, Gallinger, Steven, Cotterchio, Michelle, Casey, Graham, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, Wallace, Simon, Engeland, Herman ˜vanœ, Tryfon, Ana, Thomson, Susanne, Soorya, Latha, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, González, Patricia Jiménez, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Fernandez, Bridget A., Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bölte, Sven, Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Anagnostou, Evdokia, Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen W., http://data.europeana.eu/agent/base/147813Test, http://data.europeana.eu/agent/base/41957Test, http://data.europeana.eu/agent/base/140389Test, http://data.europeana.eu/agent/base/95030Test, Pinto, Dalila

الوصول الحر: https://www.europeana.eu/item/2048441/item_NVDTEKNVF5Y3ADIMEGS7LXXY7EUQA722?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCaTest

المؤلفون: Raznahan, Armin, Parikshak, Neelroop N, Chandran, Vijay, Blumenthal, Jonathan D, Clasen, Liv S, Alexander-Bloch, Aaron F, Zinn, Andrew R, Wangsa, Danny, Wise, Jasen, Murphy, Declan GM, Bolton, Patrick F, Ried, Thomas, Ross, Judith, Giedd, Jay N, Geschwind, Daniel H

المصدر: Proceedings of the National Academy of Sciences of the United States of America. 115(28)

مصطلحات موضوعية: Clinical Research, Biotechnology, Genetics, Rare Diseases, Human Genome, 1.1 Normal biological development and functioning, Underpinning research, Generic health relevance, Aneuploidy, Animals, Chromosomes, Human, X, Chromosomes, Human, Y, Female, Gene Dosage, Gene Expression Regulation, Genome-Wide Association Study, Humans, Kruppel-Like Transcription Factors, Male, Mice, Mice, Knockout, Models, Genetic, sex chromosomes, X-inactivation, sex differences, Turner syndrome, Klinefelter syndrome

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3nq077tbTest

المؤلفون: Magalhaes, Tiago, Conroy, Judith M., Regan, Regina, Shah, Naisha, Anney, Richard, Shields, Denis C., Abrahams, Brett S., Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Cali, Phil, Correia, Catarina, Corsello, Christina, Coutanche, Marc, Dawson, Geraldine, Jonge, Maretha de, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Foley, Suzanne, Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Holt, Richard, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Lamb, Janine A., Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lord, Catherine, Lund, Sabata C., Maestrini, Elena, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Merikangas, Alison, Miller, Judith, Minopoli, Fiorella, Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Nygren, Gudrun, Oliveira, Guiomar, Pagnamenta, Alistair T., Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Pickles, Andrew, Pinto, Dalila, Piven, Joseph, Posey, David J., Poustka, Annemarie, Poustka, Fritz, Ragoussis, Jiannis, Rogé, Bernadette, Rutter, Michael L., Sequeira, Ana F., Soorya, Latha, Sousa, Inês, Sykes, Nuala, Stoppioni, Vera, Tancredi, Raffaella, Tauber, Maïté, Thompson, Ann P., Thomson, Susanne, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Vorstman, Jacob A. S., Wallace, Simon, Wang, Kai, Wassink, Thomas H., White, Kathy, Wing, Kirsty, Wittemeyer, Kerstin, Yaspan, Brian L., Zwaigenbaum, Lonnie, Betancur, Catalina, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Geschwind, Daniel H., Haines, Jonathan L., Hallmayer, Joachim, Monaco, Anthony P., Nurnberger Jr., John I., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter, Vieland, Veronica J., Wijsman, Ellen M., Green, Andrew, Gill, Michael, Gallagher, Louise, Vicente, Astrid, Ennis, Sean, http://data.europeana.eu/agent/base/147813Test, http://data.europeana.eu/agent/base/140389Test, http://data.europeana.eu/agent/base/41957Test, http://data.europeana.eu/agent/base/95030Test, Casey, Jillian P.

الوصول الحر: https://www.europeana.eu/item/2048441/item_EU5EQYQXZS4JA265TSCF7BJ3I33FF53C?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCaTest

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

المصدر: PLoS genetics. 11(3)

مصطلحات موضوعية: SLI Consortium, Humans, Apraxias, Genetic Predisposition to Disease, Carrier Proteins, Membrane Proteins, Genetics, Population, Child, Child, Preschool, Female, Male, Genetic Association Studies, High-Throughput Nucleotide Sequencing, Exome, Preschool, Genetics, Population, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/97r7064sTest

المؤلفون: Shephard, Elizabeth, Tye, Charlotte, Ashwood, Karen L., Azadi, Bahar, Asherson, Philip, Bolton, Patrick F., McLoughlin, Grainne

المصدر: Journal of Autism and Developmental Disorders. Jan 2018 48(1):110-122.

تمت مراجعته من قبل الزملاء: Y

Page Count: 13

الواصفات: Attention Deficit Hyperactivity Disorder, Control Groups, Autism, Pervasive Developmental Disorders, Comorbidity, Neurology, Physiology, Correlation, Comparative Analysis, Profiles, Therapy, Brain Hemisphere Functions

المؤلفون: Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Wang, Zhuozhi, Vorstman, Jacob AS, Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T, Oliveira, Bárbara, Marshall, Christian R, Magalhaes, Tiago R, Lowe, Jennifer K, Howe, Jennifer L, Griswold, Anthony J, Gilbert, John, Duketis, Eftichia, Dombroski, Beth A, De Jonge, Maretha V, Cuccaro, Michael, Crawford, Emily L, Correia, Catarina T, Conroy, Judith, Conceição, Inês C, Chiocchetti, Andreas G, Casey, Jillian P, Cai, Guiqing, Cabrol, Christelle, Bolshakova, Nadia, Bacchelli, Elena, Anney, Richard, Gallinger, Steven, Cotterchio, Michelle, Casey, Graham, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, Wallace, Simon, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Soorya, Latha, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L Alison, McGrew, Susan G, Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S, Kolevzon, Alexander, González, Patricia Jiménez, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Fernandez, Bridget A, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F, Bölte, Sven, Bernier, Raphael, Baird, Gillian, Bailey, Anthony J, Anagnostou, Evdokia, Almeida, Joana, Wijsman, Ellen M, Vieland, Veronica J, Vicente, Astrid M, Schellenberg, Gerard D, Pericak-Vance, Margaret, Paterson, Andrew D, Parr, Jeremy R, Oliveira, Guiomar, Nurnberger, John I, Monaco, Anthony P, Maestrini, Elena, Klauck, Sabine M, Hakonarson, Hakon, Haines, Jonathan L, Geschwind, Daniel H, Freitag, Christine M, Folstein, Susan E, Ennis, Sean

المصدر: American Journal of Human Genetics. 94(5)

مصطلحات موضوعية: Genetics, Brain Disorders, Pediatric, Mental Health, Intellectual and Developmental Disabilities (IDD), Neurosciences, Autism, 2.1 Biological and endogenous factors, Aetiology, Child, Child Development Disorders, Pervasive, DNA Copy Number Variations, Female, Gene Regulatory Networks, Humans, Male, Metabolic Networks and Pathways, Multigene Family, Pedigree, Sequence Deletion, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2pf286f3Test

المؤلفون: Cañigueral, Roser, Palmer, Jason, Ashwood, Karen L., Azadi, Bahar, Asherson, Philip, Bolton, Patrick F., McLoughlin, Gráinne, Tye, Charlotte

المصدر: Cañigueral , R , Palmer , J , Ashwood , K L , Azadi , B , Asherson , P , Bolton , P F , McLoughlin , G & Tye , C 2021 , ' Alpha oscillatory activity during attentional control in children with Autism Spectrum Disorder (ASD), Attention-Deficit/Hyperactivity Disorder (ADHD), and ASD+ADHD ' , Journal of Child Psychology and Psychiatry and Allied Disciplines . https://doi.org/10.1111/jcpp.13514Test

مصطلحات موضوعية: ADHD, attention, Autism Spectrum Disorder, comorbidity

الإتاحة: https://doi.org/10.1111/jcpp.13514Test
https://kclpure.kcl.ac.uk/portal/en/publications/ec4cfb1f-3b9c-40bd-ba92-f2b9ddbfede8Test
http://www.scopus.com/inward/record.url?scp=85114101686&partnerID=8YFLogxKTest