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Brief Report: Under-Representation of African Americans in Autism Genetic Research: A Rationale for Inclusion of Subjects Representing Diverse Family Structures
Hilton, Claudia L., Fitzgerald, Robert T., Jackson, Kelley M., Maxim, Rolanda A., Bosworth, Christopher C., Shattuck, Paul T., Geschwind, Daniel H., Constantino, John N.
Published in Journal of autism and developmental disorders (01.05.2010)
Published in Journal of autism and developmental disorders (01.05.2010)
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A Meta-Analysis of Single Case Research Studies on Aided Augmentative and Alternative Communication Systems with Individuals with Autism Spectrum Disorders
Ganz, Jennifer B., Earles-Vollrath, Theresa L., Heath, Amy K., Parker, Richard I., Rispoli, Mandy J., Duran, Jaime B.
Published in Journal of autism and developmental disorders (01.01.2012)
Published in Journal of autism and developmental disorders (01.01.2012)
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A Study on the Linkage Model Between Institutions Related to Lifelong Education for People with Developmental Disabilities Based on the K-PACE Center of Daegu University: A Perspective on the Whole Life Cycle for People with Developmental Disabilities
Kim, Young-Jun, Kim, Wha-Soo, Rhee, Kun-Yong
Published in The International journal of advanced culture technology (2022)
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Published in The International journal of advanced culture technology (2022)
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Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features
Zaki, Maha S., Accogli, Andrea, Mirzaa, Ghayda, Rahman, Fatima, Mohammed, Hiba, Porras-Hurtado, Gloria Liliana, Efthymiou, Stephanie, Maqbool, Shazia, Shukla, Anju, Vincent, John B., Hussain, Abrar, Mir, Asif, Beetz, Christian, Leubauer, Anika, Houlden, Henry, Gleeson, Joseph G., Maroofian, Reza
Published in European journal of human genetics : EJHG (01.08.2021)
Published in European journal of human genetics : EJHG (01.08.2021)
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The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay
Kirov, George, Rees, Elliott, Walters, James T.R., Escott-Price, Valentina, Georgieva, Lyudmila, Richards, Alexander L., Chambert, Kimberly D., Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J.
Published in Biological psychiatry (1969) (01.03.2014)
Published in Biological psychiatry (1969) (01.03.2014)
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Whole Exome Sequencing and Panel-Based Analysis in 176 Spanish Children with Neurodevelopmental Disorders: Focus on Autism Spectrum Disorder and/or Intellectual Disability/Global Developmental Delay
Sánchez Suárez, Ariadna, Martínez Menéndez, Beatriz, Escolar Escamilla, Eduardo, Martínez Sarries, Francisco J., Esparza Garrido, Miren Iranzu, Gil-Fournier, Belén, Ramiro León, Soraya, Rubio Gribble, Bárbara, Quesada Espinosa, Juan F., Alcaraz Romero, Andrés J.
Published in Genes (11.10.2024)
Published in Genes (11.10.2024)
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Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling
Johnson, Brett V., Alexander, Suzy, Vega, Michelle Sanchez, Domingo, Deepti, Oh, Tracey, Lines, Matthew, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Billette de Villemeur, Thierry, Koolen, David A., Sa, Joaquim, Santiago-Fernández, Olaya, Fernández-Jaén, Alberto, Goldstein, Amy, Madan-Khetarpal, Suneeta, Sullivan, Jennifer A., Bacino, Carlos A., Baker, Eva, Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Butte, Manish J., Davids, Mariska, Davidson, Jean M., Dayal, Jyoti G., Dhar, Shweta U., Douine, Emilie D., Draper, David D., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Forghani, Irman, Friedman, Noah D., Gahl, William A., Godfrey, Rena A., Hanchard, Neil A., Jiang, Yong-hui, Karaviti, Lefkothea, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lanpher, Brendan C., LeBlanc, Kimberly, Lee, Brendan H., Liu, Xue Zhong, Marwaha, Shruti, McCauley, Jacob, Morimoto, Marie, Nath, Avi, Nelson, Stan F., Newman, John H., Oglesbee, Devin, Orengo, James P., Pak, Stephen, Parker, Neil H., Phillips, John A., Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Sampson, Jacinda B., Schedl, Timothy, Shakachite, Lisa, Sharma, Prashant, Signer, Rebecca, Silverman, Edwin K., Sinsheimer, Janet S., Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wang, Lee-kai, Wangler, Michael F., Worthey, Elizabeth A., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli, Gahl, William, Sullivan, Jennifer A., Barnett, Sarah S., Perry, M. Scott, Schuette, Jane L., Smith, Laurie D., Rosenfeld, Jill A., Bhoj, Elizabeth, Kaplan, Paige, Oegema, Renske, Armstrong, Martin, Lin, Angela E., Hollander, Nicolette den, Hoffer, Mariëtte J.V., Mosher, Theresa Mihalic, Tezcan, Kamer, Penzes, Peter, Piper, Michael
Published in Biological psychiatry (1969) (15.01.2020)
Published in Biological psychiatry (1969) (15.01.2020)
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The Use of Structural Priming and Focused Recasts to Facilitate the Production of Subject- and Object-Focused Relative Clauses by School-Age Children With and Without Developmental Language Disorder
Wada, Rebekah, Gillam, Sandra Laing, Gillam, Ronald B.
Published in American journal of speech-language pathology (01.11.2020)
Published in American journal of speech-language pathology (01.11.2020)
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Harmonization of resting-state functional MRI data across multiple imaging sites via the separation of site differences into sampling bias and measurement bias
Yamashita, Ayumu, Yahata, Noriaki, Itahashi, Takashi, Lisi, Giuseppe, Yamada, Takashi, Ichikawa, Naho, Takamura, Masahiro, Yoshihara, Yujiro, Kunimatsu, Akira, Okada, Naohiro, Yamagata, Hirotaka, Matsuo, Koji, Hashimoto, Ryuichiro, Okada, Go, Sakai, Yuki, Morimoto, Jun, Narumoto, Jin, Shimada, Yasuhiro, Kasai, Kiyoto, Kato, Nobumasa, Takahashi, Hidehiko, Okamoto, Yasumasa, Tanaka, Saori C., Kawato, Mitsuo, Yamashita, Okito, Imamizu, Hiroshi
Published in PLoS biology (18.04.2019)
Published in PLoS biology (18.04.2019)
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Cross-cultural adaptation to the Brazilian Portuguese language of the Waisman Activities of Daily Living (W-ADL) for adolescents and adults with developmental disabilities
Teixeira, Renata Machado, Pereira, Eveline Torres, Maenner, Matthew J., Albuquerque, Maicon Rodrigues
Published in Sport sciences for health (01.08.2018)
Published in Sport sciences for health (01.08.2018)
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Outcomes of Two Trials of Oxygen-Saturation Targets in Preterm Infants
Tarnow-Mordi, William, Stenson, Ben, Kirby, Adrienne, Juszczak, Edmund, Donoghoe, Mark, Deshpande, Sanjeev, Morley, Colin, King, Andrew, Doyle, Lex W, Fleck, Brian W, Davis, Peter G, Halliday, Henry L, Hague, Wendy, Cairns, Pamela, Darlow, Brian A, Fielder, Alistair R, Gebski, Val, Marlow, Neil, Simmer, Karen, Tin, Win, Ghadge, Alpana, Williams, Cathy, Keech, Anthony, Wardle, Stephen P, Kecskes, Zsuzsoka, Kluckow, Martin, Gole, Glen, Evans, Nicholas, Malcolm, Girvan, Luig, Melissa, Wright, Ian, Stack, Jacqueline, Tan, Kenneth, Pritchard, Margo, Gray, Peter H, Morris, Scott, Headley, Bevan, Dargaville, Peter, Simes, R John, Brocklehurst, Peter
Published in The New England journal of medicine (25.02.2016)
Published in The New England journal of medicine (25.02.2016)
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Phenotypic manifestations of copy number variation in chromosome 16p13.11
Nagamani, Sandesh C Sreenath, Erez, Ayelet, Bader, Patricia, Lalani, Seema R, Scott, Daryl A, Scaglia, Fernando, Plon, Sharon E, Tsai, Chun-Hui, Reimschisel, Tyler, Roeder, Elizabeth, Malphrus, Amy D, Eng, Patricia A, Hixson, Patricia M, Kang, Sung-Hae L, Stankiewicz, Pawel, Patel, Ankita, Cheung, Sau Wai
Published in European journal of human genetics : EJHG (01.03.2011)
Published in European journal of human genetics : EJHG (01.03.2011)
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Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development
Ivanova, Ekaterina L., Mau-Them, Frédéric Tran, Riazuddin, Saima, Kahrizi, Kimia, Laugel, Vincent, Schaefer, Elise, de Saint Martin, Anne, Runge, Karen, Iqbal, Zafar, Spitz, Marie-Aude, Laura, Mary, Drouot, Nathalie, Gérard, Bénédicte, Deleuze, Jean-François, de Brouwer, Arjan P.M., Razzaq, Attia, Dollfus, Hélène, Assir, Muhammad Zaman, Nitchké, Patrick, Hinckelmann, Maria-Victoria, Ropers, Hilger, Riazuddin, Sheikh, Najmabadi, Hossein, van Bokhoven, Hans, Chelly, Jamel
Published in American journal of human genetics (07.09.2017)
Published in American journal of human genetics (07.09.2017)
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How much loss to follow-up is acceptable in long-term randomised trials and prospective studies?
Fewtrell, Mary S, Kennedy, Kathy, Singhal, Atul, Martin, Richard M, Ness, Andy, Hadders-Algra, Mijna, Koletzko, Berthold, Lucas, Alan
Published in Archives of disease in childhood (01.06.2008)
Published in Archives of disease in childhood (01.06.2008)
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Modeling premature brain injury and recovery
Scafidi, Joey, Fagel, Devon M., Ment, Laura R., Vaccarino, Flora M.
Published in International journal of developmental neuroscience (01.12.2009)
Published in International journal of developmental neuroscience (01.12.2009)
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Additive effect of congenital heart disease and early developmental disorders on attention-deficit/hyperactivity disorder and autism spectrum disorder: a nationwide population-based longitudinal study
Tsao, Pei-Chen, Lee, Yu-Sheng, Jeng, Mei-Jy, Hsu, Ju-Wei, Huang, Kai-Lin, Tsai, Shih-Jen, Chen, Mu-Hong, Soong, Wen-Jue, Kou, Yu Ru
Published in European child & adolescent psychiatry (01.11.2017)
Published in European child & adolescent psychiatry (01.11.2017)
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