Zobrazeno 1 - 10
of 135
pro vyhledávání: '"Susan E, Folstein"'
Autor:
Geraldine Dawson, Sven Sandin, Frederico Duque, Peter Holmans, Marion Leboyer, Aarno Palotie, Fritz Poustka, Richard Delorme, Stephen Sanders, Alistair T. Pagnamenta, Lonnie Zwaigenbaum, Bridget A. Fernandez, A. Jeremy Willsey, Christine M. Freitag, Christa Lese Martin, Elena Maestrini, Elena Bacchelli, Guiomar Oliveira, Jeremy R. Parr, Guy A. Rouleau, Jonas Bybjerg-Grauholm, Joseph Piven, Latha Soorya, Lauren A. Weiss, Jonathan Green, Carsten Bøcker Pedersen, Louise Gallagher, Regina Regan, Stephan Ripke, Thomas Werge, Pat Levitt, Aravinda Chakravarti, Joana Almeida, Kathryn Roeder, Catalina Betancur, Bernie Devlin, Benjamin M. Neale, Gillian Baird, Jakob Grove, Thomas Bourgeron, David H. Ledbetter, Eftichia Duketis, Karola Rehnström, Gerard D. Schellenberg, Jillian P. Casey, Preben Bo Mortensen, Patrick Bolton, Igor Martsenkovsky, Elise Robinson, Hakon Hakonarson, Vanessa H. Bal, Stacy Steinberg, Christopher Gillberg, Kathryn Tsang, Jacob A. S. Vorstman, Verneri Anttila, Suma Jacob, Judith Conroy, J. Haines, William M. McMahon, Edwin H. Cook, Ann P. Thompson, Inês C. Conceição, Mark J. Daly, Arthur P. Goldberg, Sarah E. Medland, Milica Pejovic-Milovancevic, David M. Hougaard, Shrikant Mane, Christina M. Hultman, Susana Mouga, Hreinn Stefansson, Ellen M. Wijsman, Andreas G. Chiocchetti, Ole Mors, Phil Lee, Richard Anney, Astrid M. Vicente, Veronica J. Vieland, K. Stefansson, Stephen W. Scherer, Teimuraz Silagadze, Pall Magnusson, Donna M. Martin, Merete Nordentoft, Peter Szatmari, Patrícia B. S. Celestino-Soper, Ann S Le-Couteur, Cátia Café, Arthur L. Beaudet, Kerstin Wittemeyer, Anders D. Børglum, Joel S. Bader, Christopher S. Poultney, Hailiang Huang, Alexander Kolevzon, Margaret A. Pericak-Vance, Joachim Hallmayer, Rita M. Cantor, Eric Fombonne, Andrew Green, Dan E. Arking, M. Daniele Fallin, Matthew W. State, Christine Ladd-Acosta, Silvia Derubeis, Raphael Bernier, Regina Waltes, David G. Amaral, Manuel Mattheisen, Abraham Reichenberg, Lambertus Klei, Daniel Moreno-De-Luca, Marie Bækvad-Hansen, Maretha V. Dejonge, Susan G. McGrew, Joseph D. Buxbaum, Hilary Coon, Jennifer Reichert, Michael Gill, Herman Vanengeland, Christine Søholm Hansen, Anthony P. Monaco, Nadia Bolshakova, John I. Nurnberger, Nancy J. Minshew, Michael T. Murtha, Thomas H. Wassink, Evald Saemundsen, Simon Wallace, Sean Brennan, Sean Ennis, A. Gulhan Ercan-Sencicek, Sven Bölte, Oscar Svantesson, Susan L. Santangelo, Andrew D. Paterson, Robert L. Hendren, Timothy W. Yu, Dalila Pinto, D.E. Grice, Alison Merikangas, Stephen J. Guter, Anthony J. Bailey, Bernadette Rogé, Christopher A. Walsh, Susan E. Folstein, Wendy Roberts, Sabine M. Klauck, Marianne Giørtz Pedersen, Tiago R. Magalhaes, John R. Gilbert, Irva Hertz-Picciotto, James S. Sutcliffe, Evdokia Anagnostou, Catarina Correia, Eric M. Morrow, Daniel H. Geschwind, Jennifer K. Lowe, Agatino Battaglia, Bozenna Iliadou, Michael L. Cuccaro, Catherine Lord
Publikováno v:
Molecular Autism
Molecular Autism, BioMed Central, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Anney, R J L, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, P H, Medland, S E, Neale, B, Robinson, E, Weiss, L A, Zwaigenbaum, L, Yu, T W, Wittemeyer, K, Willsey, A J, Wijsman, E M, Werge, T, Wassink, T H, Waltes, R, Walsh, C A, Wallace, S, Vorstman, J A S, Vieland, V J, Vicente, A M, Vanengeland, H, Tsang, K, Thompson, A P, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, M W, Soorya, L, Silagadze, T, Scherer, S W, Schellenberg, G D, Sandin, S, Sanders, S J, Saemundsen, E, Rouleau, G A, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, C S, Piven, J, Pinto, D, Pericak-Vance, M A, Pejovic-Milovancevic, M, Pedersen, M G, Pedersen, C B, Paterson, A D, Parr, J R, Pagnamenta, A T, Oliveira, G, Nurnberger, J I, Nordentoft, M, Murtha, M T, Mouga, S, Mortensen, P B, Mors, O, Morrow, E M, Moreno-De-Luca, D, Monaco, A P, Minshew, N, Merikangas, A, McMahon, W M, McGrew, S G, Mattheisen, M, Martsenkovsky, I, Martin, D M, Mane, S M, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, J K, Lord, C, Levitt, P, Martin, C L, Ledbetter, D H, Leboyer, M, Lecouteur, A S, Ladd-Acosta, C, Kolevzon, A, Klauck, S M, Jacob, S, Iliadou, B, Hultman, C M, Hougaard, D M, Hertz-Picciotto, I, Hendren, R, Hansen, C S, Haines, J L, Guter, S J, Grice, D E, Green, J M, Green, A, Goldberg, A P, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, C M, Fombonne, E, Folstein, S E, Fernandez, B, Fallin, M D, Ercan-Sencicek, A G, Ennis, S, Duque, F, Duketis, E, Delorme, R, Derubeis, S, Dejonge, M V, Dawson, G, Cuccaro, M L, Correia, C T, Conroy, J, Conceição, I C, Chiocchetti, A G, Celestino-Soper, P B S, Casey, J, Cantor, R M, Café, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, P F, Bölte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, A L, Battaglia, A, Bal, V H, Baird, G, Bailey, A J, Bækvad-Hansen, M, Bader, J S, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Børglum, A D, Buxbaum, J D, Chakravarti, A, Cook, E H, Coon, H, Geschwind, D H, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, J S, Arking, D E, Devlin, B & Daly, M J 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Bolton, P F 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, pp. 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Molecular autism, vol 8, iss 1
The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Autism, vol. 8, no. 21, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, BioMed Central, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Anney, R J L, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, P H, Medland, S E, Neale, B, Robinson, E, Weiss, L A, Zwaigenbaum, L, Yu, T W, Wittemeyer, K, Willsey, A J, Wijsman, E M, Werge, T, Wassink, T H, Waltes, R, Walsh, C A, Wallace, S, Vorstman, J A S, Vieland, V J, Vicente, A M, Vanengeland, H, Tsang, K, Thompson, A P, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, M W, Soorya, L, Silagadze, T, Scherer, S W, Schellenberg, G D, Sandin, S, Sanders, S J, Saemundsen, E, Rouleau, G A, Rogé, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnström, K, Regan, R, Poustka, F, Poultney, C S, Piven, J, Pinto, D, Pericak-Vance, M A, Pejovic-Milovancevic, M, Pedersen, M G, Pedersen, C B, Paterson, A D, Parr, J R, Pagnamenta, A T, Oliveira, G, Nurnberger, J I, Nordentoft, M, Murtha, M T, Mouga, S, Mortensen, P B, Mors, O, Morrow, E M, Moreno-De-Luca, D, Monaco, A P, Minshew, N, Merikangas, A, McMahon, W M, McGrew, S G, Mattheisen, M, Martsenkovsky, I, Martin, D M, Mane, S M, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, J K, Lord, C, Levitt, P, Martin, C L, Ledbetter, D H, Leboyer, M, Lecouteur, A S, Ladd-Acosta, C, Kolevzon, A, Klauck, S M, Jacob, S, Iliadou, B, Hultman, C M, Hougaard, D M, Hertz-Picciotto, I, Hendren, R, Hansen, C S, Haines, J L, Guter, S J, Grice, D E, Green, J M, Green, A, Goldberg, A P, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, C M, Fombonne, E, Folstein, S E, Fernandez, B, Fallin, M D, Ercan-Sencicek, A G, Ennis, S, Duque, F, Duketis, E, Delorme, R, Derubeis, S, Dejonge, M V, Dawson, G, Cuccaro, M L, Correia, C T, Conroy, J, Conceição, I C, Chiocchetti, A G, Celestino-Soper, P B S, Casey, J, Cantor, R M, Café, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, P F, Bölte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, A L, Battaglia, A, Bal, V H, Baird, G, Bailey, A J, Bækvad-Hansen, M, Bader, J S, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Børglum, A D, Buxbaum, J D, Chakravarti, A, Cook, E H, Coon, H, Geschwind, D H, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, J S, Arking, D E, Devlin, B & Daly, M J 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, 2017, 8, pp.21. ⟨10.1186/s13229-017-0137-9⟩
Bolton, P F 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Molecular Autism, vol. 8, pp. 21 . https://doi.org/10.1186/s13229-017-0137-9
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Molecular autism, vol 8, iss 1
The Autism Spectrum Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia ', Autism, vol. 8, no. 21, 21 . https://doi.org/10.1186/s13229-017-0137-9
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium - Collaborators (162): Anney RJL, Ripke S, Anttila V, Grove J, Holmans P, Huang H, Klei L, Lee PH, Medland SE, Neale B, Robinson E, Weiss LA, Zwaigenbaum L, Yu TW, Witteme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1efa92826829f7f870799b08a5c31e5
https://www.hal.inserm.fr/inserm-01535717
https://www.hal.inserm.fr/inserm-01535717
Autor:
Joana Almeida, Christian R. Marshall, Hakon Hakonarson, Bárbara Oliveira, Anthony J. Griswold, Jacob A. S. Vorstman, Bhooma Thiruvahindrapuram, Suma Jacob, Judith Conroy, Alistair T. Pagnamenta, Christelle Cabrol, Jeremy R. Parr, Daniel H. Geschwind, Nancy J. Minshew, Xiao Xu, Richard Anney, Sven Bölte, Zhuozhi Wang, Emily L. Crawford, Elsa Delaby, Margaret A. Pericak-Vance, Joachim Hallmayer, Jonathan L. Haines, Dalila Pinto, Susana Mouga, Alexander Kolevzon, Elena Bacchelli, Frederico Duque, Bernie Devlin, Latha Soorya, Cátia Café, Kirsty Wing, Jennifer K. Lowe, Ana Tryfon, Stephen J. Guter, Geraldine Dawson, Tiago R. Magalhaes, Anthony J. Bailey, Michael Gill, Peter Szatmari, Steven Gallinger, Marion Pilorge, James S. Sutcliffe, Bridget A. Fernandez, Herman van Engeland, Catalina Betancur, Guiomar Oliveira, Andrew Green, Eftichia Duketis, Bernadette Rogé, Ann Le Couteur, Evdokia Anagnostou, Michelle Cotterchio, Daniele Merico, Giovanna Pellecchia, Jonathan Green, Regina Regan, Jillian P. Casey, Guiqing Cai, Gerard D. Schellenberg, Jennifer L. Howe, Elena Maestrini, Andrew D. Paterson, L. Alison McInnes, Patrick Bolton, Edwin H. Cook, Richard Delorme, Lambertus Klei, Thomas Bourgeron, Gillian Baird, Christine M. Freitag, Beth A. Dombroski, Andreas G. Chiocchetti, Sabine M. Klauck, Susan E. Folstein, Mafalda Barbosa, Anthony P. Monaco, Marion Leboyer, Nadia Bolshakova, Fritz Poustka, Richard Holt, Kerstin Wittemeyer, Wendy Roberts, Lonnie Zwaigenbaum, Louise Gallagher, Susan G. McGrew, Joseph D. Buxbaum, Graham Casey, Simon Wallace, Catherine Lord, Sean Brennan, Robert Ziman, Alison K. Merikangas, John I. Nurnberger, Christopher Gillberg, Ellen M. Wijsman, Astrid M. Vicente, Inȇs C. Conceição, Sean Ennis, Patricia Jiménez González, Hilary Coon, Raphael Bernier, John R. Gilbert, Ann P. Thompson, Susanne Thomson, Agatino Battaglia, Maretha de Jonge, Michael L. Cuccaro, Catarina Correia, Veronica J. Vieland, Stephen W. Scherer, Pauline Chaste
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 94 (5), pp.677-694. ⟨10.1016/j.ajhg.2014.03.018⟩
American Journal of Human Genetics, 2014, 94 (5), pp.677-694. ⟨10.1016/j.ajhg.2014.03.018⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 94 (5), pp.677-694. ⟨10.1016/j.ajhg.2014.03.018⟩
American Journal of Human Genetics, 2014, 94 (5), pp.677-694. ⟨10.1016/j.ajhg.2014.03.018⟩
International audience; Rare copy-number variation (CNV) is an important source of risk for autism spectrum disorders (ASDs). We analyzed 2,446 ASD-affected families and confirmed an excess of genic deletions and duplications in affected versus contr
Autor:
Marshal F. Folstein, Susan E. Folstein
Publikováno v:
Nutrition Reviews. 68:S70-S73
In the conventional view, aging of the brain is associated with atrophy vascular abnormalities and loss of volume in hippocampus and amygdala. Cognitively, aging is associated with slowing of processing and memory loss. However, many studies of aging
Publikováno v:
Autism Research. 2:22-38
Autism spectrum disorder (ASD) and specific language impairment (SLI) are developmental disorders exhibiting language deficits, but it is unclear whether they arise from similar etiologies. Language impairments have been described in family members o
Publikováno v:
Autism Research. 1:284-296
Autism and specific language impairment (SLI) are developmental disorders that, although distinct by definition, have in common some features of both language and social behavior. The goal of this study was to further explore the extent to which spec
Publikováno v:
Autism Research. 1:193-197
Research indicates that relatives of individuals with autism have higher rates of affective disorders than both the general population and families of children with other developmental disabilities. In addition, individuals with autism have high rate
Autor:
Janet E. Lainhart, Helen Tager-Flusberg, Kelli C. Dominick, Naomi Ornstein Davis, Susan E. Folstein
Publikováno v:
Research in Developmental Disabilities. 28:145-162
The frequency, course, and inter-relationships of atypical eating, sleeping, self-injurious behavior, aggression and temper tantrums in children with autism and children with a history of language impairment (HLI), was investigated using a parent int
Autor:
Brian Winklosky, Helen Tager-Flusberg, Beth Rosen-Sheidley, Sara Putnam, Susan E. Folstein, Deborah Arin, Joseph Piven, Michael Dowd, Tilla F. Ruser, Bruce Tomblin
Publikováno v:
Journal of Autism and Developmental Disorders. 37:1323-1336
While the primary language deficit in autism has been thought to be pragmatic, and in specific language impairment (SLI) structural, recent research suggests phenomenological and possibly genetic overlap between the two syndromes. To compare communic
Autor:
Susan E. Folstein
Publikováno v:
Clinical Neuroscience Research. 6:113-117
Autism, as defined by Kanner in 1943, required two features: the abnormal development of social relationships and the obsessive desire for the maintenance of sameness. This definition was applied only to children without dysmorphic features (except m
Autor:
Susan E. Folstein, Noah K. Ndosi, Veronica V. Sarwatt, Martha Collins, Ella H. Mgalla, Raymond E. Mankoski
Publikováno v:
Journal of Autism and Developmental Disorders. 36:1039-1051
Most autism has a genetic cause although post-encephalitis cases are reported. In a case-series (N = 20) from Tanzania, 14 met research criteria for autism. Three (M:F = 1:2) had normal development to age 22, 35, and 42 months, with onset of autism u