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2. De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette’s Disorder and Autism

Author

Cappi, Carolina, Oliphant, Melody E, Péter, Zsanett, Zai, Gwyneth, Conceição do Rosário, Maria, Sullivan, Catherine AW, Gupta, Abha R, Hoffman, Ellen J, Virdee, Manmeet, Olfson, Emily, Abdallah, Sarah B, Willsey, A Jeremy, Shavitt, Roseli G, Miguel, Euripedes C, Kennedy, James L, Richter, Margaret A, and Fernandez, Thomas V

Subjects
Biological Sciences, Genetics, Mental Health, Pediatric, Brain Disorders, Human Genome, Neurosciences, Clinical Research, Biotechnology, Prevention, Intellectual and Developmental Disabilities (IDD), Serious Mental Illness, Autism, 2.1 Biological and endogenous factors, Aetiology, Mental health, Autism Spectrum Disorder, Autistic Disorder, Calcium-Binding Proteins, Child, DNA, DNA-Binding Proteins, Humans, Mutation, Obsessive-Compulsive Disorder, Tourette Syndrome, Transcription Factors, CHD8, Obsessive-compulsive disorder, SCUBE1, Tourette, Whole-exome sequencing, Medical and Health Sciences, Psychology and Cognitive Sciences, Psychiatry, Biological sciences, Biomedical and clinical sciences, Psychology
Abstract

BackgroundObsessive-compulsive disorder (OCD) is a debilitating neuropsychiatric disorder with a genetic risk component, yet identification of high-confidence risk genes has been challenging. In recent years, risk gene discovery in other complex psychiatric disorders has been achieved by studying rare de novo (DN) coding variants.MethodsWe performed whole-exome sequencing in 222 OCD parent-child trios (184 trios after quality control), comparing DN variant frequencies with 777 previously sequenced unaffected trios. We estimated the contribution of DN mutations to OCD risk and the number of genes involved. Finally, we looked for gene enrichment in other datasets and canonical pathways.ResultsDN likely gene disrupting and predicted damaging missense variants are enriched in OCD probands (rate ratio, 1.52; p = .0005) and contribute to risk. We identified 2 high-confidence risk genes, each containing 2 DN damaging variants in unrelated probands: CHD8 and SCUBE1. We estimate that 34% of DN damaging variants in OCD contribute to risk and that DN damaging variants in approximately 335 genes contribute to risk in 22% of OCD cases. Furthermore, genes harboring DN damaging variants in OCD are enriched for those reported in neurodevelopmental disorders, particularly Tourette's disorder and autism spectrum disorder. An exploratory network analysis reveals significant functional connectivity and enrichment in canonical pathways, biological processes, and disease networks.ConclusionsOur findings show a pathway toward systematic gene discovery in OCD via identification of DN damaging variants. Sequencing larger cohorts of OCD parent-child trios will reveal more OCD risk genes and will provide needed insights into underlying disease biology.

Published
2020

3. High-throughput functional analysis of autism genes in zebrafish identifies convergence in dopaminergic and neuroimmune pathways

Author

Weinschutz Mendes, Hellen, Neelakantan, Uma, Liu, Yunqing, Fitzpatrick, Sarah E., Chen, Tianying, Wu, Weimiao, Pruitt, April, Jin, David S., Jamadagni, Priyanka, Carlson, Marina, Lacadie, Cheryl M., Enriquez, Kristen D., Li, Ningshan, Zhao, Dejian, Ijaz, Sundas, Sakai, Catalina, Szi, Christina, Rooney, Brendan, Ghosh, Marcus, Nwabudike, Ijeoma, Gorodezky, Andrea, Chowdhury, Sumedha, Zaheer, Meeraal, McLaughlin, Sarah, Fernandez, Joseph M., Wu, Jia, Eilbott, Jeffrey A., Vander Wyk, Brent, Rihel, Jason, Papademetris, Xenophon, Wang, Zuoheng, and Hoffman, Ellen J.

Published
2023
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9. Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2

Author

Hoffman, Ellen J, Turner, Katherine J, Fernandez, Joseph M, Cifuentes, Daniel, Ghosh, Marcus, Ijaz, Sundas, Jain, Roshan A, Kubo, Fumi, Bill, Brent R, Baier, Herwig, Granato, Michael, Barresi, Michael JF, Wilson, Stephen W, Rihel, Jason, State, Matthew W, and Giraldez, Antonio J

Subjects
Pharmacology and Pharmaceutical Sciences, Biomedical and Clinical Sciences, Behavioral and Social Science, Prevention, Genetics, Neurosciences, Mental Health, Intellectual and Developmental Disabilities (IDD), Pediatric, Basic Behavioral and Social Science, Brain Disorders, Autism, 2.1 Biological and endogenous factors, Aetiology, Animals, Animals, Genetically Modified, Autistic Disorder, Disease Models, Animal, Estrogens, Gene Expression Regulation, Genistein, Green Fluorescent Proteins, Humans, Larva, Luminescent Proteins, Membrane Proteins, Motor Activity, Mutation, Nerve Tissue Proteins, Phenotype, Phytoestrogens, Psychotropic Drugs, Seizures, Sleep-Wake Transition Disorders, Vesicular Glutamate Transport Protein 2, Zebrafish, Psychology, Cognitive Sciences, Neurology & Neurosurgery, Biological psychology
Abstract

Autism spectrum disorders (ASDs) are a group of devastating neurodevelopmental syndromes that affect up to 1 in 68 children. Despite advances in the identification of ASD risk genes, the mechanisms underlying ASDs remain unknown. Homozygous loss-of-function mutations in Contactin Associated Protein-like 2 (CNTNAP2) are strongly linked to ASDs. Here we investigate the function of Cntnap2 and undertake pharmacological screens to identify phenotypic suppressors. We find that zebrafish cntnap2 mutants display GABAergic deficits, particularly in the forebrain, and sensitivity to drug-induced seizures. High-throughput behavioral profiling identifies nighttime hyperactivity in cntnap2 mutants, while pharmacological testing reveals dysregulation of GABAergic and glutamatergic systems. Finally, we find that estrogen receptor agonists elicit a behavioral fingerprint anti-correlative to that of cntnap2 mutants and show that the phytoestrogen biochanin A specifically reverses the mutant behavioral phenotype. These results identify estrogenic compounds as phenotypic suppressors and illuminate novel pharmacological pathways with relevance to autism.

Published
2016

10. Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene

Author

Fernandez, Thomas V., primary, Williams, Zsanett P., additional, Kline, Tina, additional, Rajendran, Shreenath, additional, Augustine, Farhan, additional, Wright, Nicole, additional, Sullivan, Catherine A. W., additional, Olfson, Emily, additional, Abdallah, Sarah B., additional, Liu, Wenzhong, additional, Hoffman, Ellen J., additional, Gupta, Abha R., additional, and Singer, Harvey S., additional

Published
2023
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13. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

Author

Jin, Sheng Chih, Dong, Weilai, Kundishora, Adam J., Panchagnula, Shreyas, Moreno-De-Luca, Andres, Furey, Charuta G., Allocco, August A., Walker, Rebecca L., Nelson-Williams, Carol, Smith, Hannah, Dunbar, Ashley, Conine, Sierra, Lu, Qiongshi, Zeng, Xue, Sierant, Michael C., Knight, James R., Sullivan, William, Duy, Phan Q., DeSpenza, Tyrone, Reeves, Benjamin C., Karimy, Jason K., Marlier, Arnaud, Castaldi, Christopher, Tikhonova, Irina R., Li, Boyang, Peña, Helena Perez, Broach, James R., Kabachelor, Edith M., Ssenyonga, Peter, Hehnly, Christine, Ge, Li, Keren, Boris, Timberlake, Andrew T., Goto, June, Mangano, Francesco T., Johnston, James M., Butler, William E., Warf, Benjamin C., Smith, Edward R., Schiff, Steven J., Limbrick, Jr, David D., Heuer, Gregory, Jackson, Eric M., Iskandar, Bermans J., Mane, Shrikant, Haider, Shozeb, Guclu, Bulent, Bayri, Yasar, Sahin, Yener, Duncan, Charles C., Apuzzo, Michael L. J., DiLuna, Michael L., Hoffman, Ellen J., Sestan, Nenad, Ment, Laura R., Alper, Seth L., Bilguvar, Kaya, Geschwind, Daniel H., Günel, Murat, Lifton, Richard P., and Kahle, Kristopher T.

Published
2020
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17. Contributors

Author

Ansari, Rida, primary, Appelbaum, Lior, additional, Bartel, W. Philip, additional, Bonan, Carla Denise, additional, Brennan, Caroline H., additional, Burton, Edward A., additional, Carvan III, Michael J., additional, Clark, Karl J., additional, Da Silva, Rosane Souza, additional, Demin, Konstantin A., additional, De Santis, Flavia, additional, Di Donato, Vincenzo, additional, Dreosti, Elena, additional, Ekker, Marc, additional, Facciol, Amanda, additional, Flik, Gert, additional, Gerlai, Robert T., additional, Gorissen, Marnix, additional, Grieco, Fabrizio, additional, Guo, Su, additional, Heeren, Amanda A., additional, Higgs, Dennis M., additional, Hoffman, Ellen J., additional, Howe, Kerstin, additional, Hua, Khang, additional, Jenett, Arnim, additional, Kalueff, Allan V., additional, Kalyviotis, Konstantinos, additional, Kenney, Justin W., additional, Lakstygal, Anton M., additional, Lee, Han B., additional, Marquez-Legorreta, Emmanuel, additional, Miller, Noam, additional, Modhurima, Rodsy, additional, Neuhauss, Stephan C.F., additional, Noldus, Lucas P.J.J., additional, Norton, William HJ., additional, Pantazis, Periklis, additional, Parichy, David M., additional, Piber, Marielle, additional, Postlethwait, John H., additional, Pritchett, David, additional, Qin, Hanyu, additional, Rihel, Jason, additional, Schlegel, Domino K., additional, Scott, Ethan K., additional, Stankiewicz, Alexander, additional, Stednitz, S.J., additional, Tegelenbosch, Ruud A.J., additional, Terriente, Javier, additional, Tran, Steven, additional, Tsang, Benjamin, additional, Tsuda, Sachiko, additional, van den Bos, Ruud, additional, Van Laar, Victor S., additional, Vianna, Monica Ryff Moreira Roca, additional, Washbourne, P., additional, Winberg, Svante, additional, Xu, Jiale, additional, Zada, David, additional, and Zhdanova, Irina V., additional

Published
2021
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19. Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

Author

Willsey, A Jeremy, Sanders, Stephan J, Li, Mingfeng, Dong, Shan, Tebbenkamp, Andrew T, Muhle, Rebecca A, Reilly, Steven K, Lin, Leon, Fertuzinhos, Sofia, Miller, Jeremy A, Murtha, Michael T, Bichsel, Candace, Niu, Wei, Cotney, Justin, Ercan-Sencicek, A Gulhan, Gockley, Jake, Gupta, Abha R, Han, Wenqi, He, Xin, Hoffman, Ellen J, Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M, Lein, Ed S, Wei, Liping, Noonan, James P, Roeder, Kathryn, Devlin, Bernie, Sestan, Nenad, and State, Matthew W

Subjects
Biological Sciences, Bioinformatics and Computational Biology, Genetics, Neurosciences, Mental Health, Intellectual and Developmental Disabilities (IDD), Pediatric, Brain Disorders, Clinical Research, Autism, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Neurological, Mental health, Animals, Brain, Child Development Disorders, Pervasive, Exome, Female, Fetus, Gene Expression Profiling, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Mice, Mutation, Neurons, Prefrontal Cortex, Sequence Analysis, DNA, Medical and Health Sciences, Developmental Biology, Biological sciences, Biomedical and clinical sciences
Abstract

Autism spectrum disorder (ASD) is a complex developmental syndrome of unknown etiology. Recent studies employing exome- and genome-wide sequencing have identified nine high-confidence ASD (hcASD) genes. Working from the hypothesis that ASD-associated mutations in these biologically pleiotropic genes will disrupt intersecting developmental processes to contribute to a common phenotype, we have attempted to identify time periods, brain regions, and cell types in which these genes converge. We have constructed coexpression networks based on the hcASD "seed" genes, leveraging a rich expression data set encompassing multiple human brain regions across human development and into adulthood. By assessing enrichment of an independent set of probable ASD (pASD) genes, derived from the same sequencing studies, we demonstrate a key point of convergence in midfetal layer 5/6 cortical projection neurons. This approach informs when, where, and in what cell types mutations in these specific genes may be productively studied to clarify ASD pathophysiology.

Published
2013

22. Brain Registration and Evaluation for Zebrafish

Author

Jin, David S., Neelakantan, Uma, Lacadie, Cheryl M., Tianying Chen, Rooney, Brendan, Liu, Yunqing, Wu, Weimiao, Wang, Zuoheng, Papademetris, Xenophon, and Hoffman, Ellen J.

Abstract

This repository contains three zipped folders: 1. bin.zip: The scripts and files to be placed into the bin directory. 2. pre-processing.zip: Initial preprocessing scripts for generating maximum intensity projections and their summary documents. 3. test.zip: Twodatasets containing confocal microscope z-stack image files (.lif) of larvalbrains ofzebrafishmutants of two autism risk genes (Weinschutz Mendes et al. 2023).

Published
2023
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27. Progress in Cytogenetics: Implications for Child Psychopathology

Author

Hoffman, Ellen J. and State, Matthew W.

Abstract

Objective: This review considers the impact of chromosomal studies on the understanding of childhood neuropsychiatric syndromes, highlighting key discoveries, advances in technology, and new challenges faced by clinicians trying to interpret recent findings. Method: We review the literature on the genetics of child psychiatric disorders, including autism, childhood-onset schizophrenia, attention-deficit/hyperactivity disorder, and Tourette syndrome, with a focus on studies of chromosomal structure. Results: Over several decades, cytogenetic investigations have led to key findings relevant to child psychiatry. During this time, technology has transitioned from light microscopy to molecular cytogenetics to microarray-based detection of structural variation, resulting in a dramatic increase in the resolution of such approaches. Each of these methods has contributed to the understanding of the genetic bases of developmental neuropsychiatric disorders. Moreover, the implementation of microarray technology has prompted a reconceptualization of the nature of human genetic variation, demonstrating that both the sequence of DNA as well as the fine structure of chromosomes vary in affected and unaffected individuals. Conclusions: The study of chromosomal variation at high resolution continues to be a promising area of research that is yielding critical data regarding the genetic underpinnings of childhood psychiatric disorders. Preliminary data indicate that apparently identical submicroscopic variations in chromosomal structure may predispose to a very broad range of phenotypes. These findings suggest that disruption of the same basic neurodevelopmental mechanisms, such as synapse function, may result in outcomes that span a broad sweep of DSM-IV psychiatric diagnoses. (Contains 3 figures.)

Published
2010
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29. PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets

Author

DeSpenza, Tyrone, primary, Carlson, Marina, additional, Panchagnula, Shreyas, additional, Robert, Stephanie, additional, Duy, Phan Q., additional, Mermin-Bunnell, Nell, additional, Reeves, Benjamin C., additional, Kundishora, Adam, additional, Elsamadicy, Aladine A., additional, Smith, Hannah, additional, Ocken, Jack, additional, Alper, Seth L., additional, Jin, Sheng Chih, additional, Hoffman, Ellen J., additional, and Kahle, Kristopher T., additional

Published
2021
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40. A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes

Author

Kroll, François, primary, Powell, Gareth T, additional, Ghosh, Marcus, additional, Gestri, Gaia, additional, Antinucci, Paride, additional, Hearn, Timothy J, additional, Tunbak, Hande, additional, Lim, Sumi, additional, Dennis, Harvey W, additional, Fernandez, Joseph M, additional, Whitmore, David, additional, Dreosti, Elena, additional, Wilson, Stephen W, additional, Hoffman, Ellen J, additional, and Rihel, Jason, additional

Published
2021
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41. Kroll et al., 2020. A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes

Author

Kroll, François, Powell, Gareth T, Ghosh, Marcus, Gestri, Gaia, Antinucci, Paride, Hearn, Timothy J, Tunbak, Hande, Lim, Sumi, Dennis, Harvey W, Fernandez, Joseph M, Whitmore, David, Dreosti, Elena, Wilson, Stephen W, Hoffman, Ellen J, and Rihel, Jason

Abstract

Data and code for Kroll, F. et al.2020. A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes. https://doi.org/10.1101/2020.06.04.133462 You can also navigate through the files at:https://github.com/francoiskroll/f0knockout (Some heavierfiles are only included inthe Zenodo repository) If you use some of the data or code, please cite! ___ Contact: Twitter: @francois_kroll Email: francois@kroll.be

Published
2020
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42. Norm-Referenced Tests

Author

Anagnostou, Evdokia, primary, Mankad, Deepali, additional, Diehl, Joshua, additional, Lord, Catherine, additional, Butler, Sarah, additional, McDuffie, Andrea, additional, Shull, Lisa, additional, Ashbaugh, Kristen, additional, Koegel, Robert L., additional, Volkmar, Fred R., additional, Naples, Adam, additional, Doggett, Rebecca, additional, Hooper, Stephen R., additional, Casanova, Manuel, additional, Hoffman, Ellen J., additional, McFadden, Kate, additional, Anderson, George M., additional, Gupta, Abha R., additional, DiLullo, Nicholas M., additional, Minshew, Nancy J., additional, Burner, Karen, additional, Bernier, Raphael, additional, Pelphrey, Kevin A., additional, Perszyk, Danielle, additional, Willsey, A. Jeremy, additional, Krasno, Anna M., additional, Campbell, Daniel, additional, Spear-Swerling, Louise, additional, Kuschner, Emily S., additional, Corbett, Eugenia, additional, Noonan, Jacqueline A., additional, Takeuchi, Yoshihiro, additional, Tassé, Marc J., additional, Grover, Matthew, additional, Lyons, Megan, additional, Tyson, Katherine, additional, Fein, Deborah, additional, Berger, Michael, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Dunn, Debra, additional, and Pilato, Madison, additional

Published
2013
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43. Maintenance of Treatment Effects

Author

Hutchins, Tiffany, primary, Vivanti, Giacomo, additional, Mateljevic, Natasa, additional, Jou, Roger J., additional, Shic, Frederick, additional, Cornew, Lauren, additional, Roberts, Timothy P. L., additional, Oakes, Leona, additional, Gray, Sarah A. O., additional, Ray-Subramanian, Corey, additional, Stubbe, Dorothy, additional, Mueller, Vannesa T., additional, Singh, Anjileen, additional, Zierhut, Cynthia, additional, Rogers, Sally J., additional, Sulkes, Stephen, additional, Wilczynski, Susan, additional, Rue, Hanna C., additional, Gabig, Cheryl Smith, additional, Offit, Paul A., additional, Scott, Haleigh, additional, Havercamp, Susan M., additional, Voos, Avery, additional, Westphal, Alexander, additional, Roesser, Jessica L., additional, Avini, Mitrah E., additional, Scahill, Lawrence David, additional, Lickenbrock, Diane M., additional, Boucher, Jill, additional, Gaigg, Sebastian, additional, Bowler, Dermot, additional, Solages, Martine, additional, Grindstaff, Jemma, additional, Shea, Victoria, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Farmer, Miranda, additional, Pilato, Madison, additional, Macy, Kelly, additional, Moyle, Maura, additional, Plowgian, Claire, additional, Marti, Itxaso, additional, Geno, Danielle, additional, McDuffie, Andrea, additional, Schoen, Sarah, additional, Miller, Lucy, additional, Solomon, Marjorie, additional, Hyman, Susan, additional, Dinstein, Ilan, additional, Behrman, Marlene, additional, Parvez, Rizwan, additional, Aaronson, Benjamin, additional, Bernier, Raphael, additional, Kent, Lindsey, additional, Lestrud, Michelle, additional, Volkmar, Fred R., additional, Dereu, Mieke, additional, Brucker, Pamela, additional, Hoffman, Ellen J., additional, Johnson, Kristin, additional, Edelson, Lisa, additional, El-Fishawy, Paul, additional, Hillegers, Manon H. J., additional, Aalst, Karen, additional, Esposito, Gianluca, additional, Mouridsen, Svend Erik, additional, Koegel, Lynn, additional, Koegel, Robert L., additional, Park, Mi Na, additional, Lee, Su Mei, additional, Zampella, Casey, additional, Bennetto, Loisa, additional, Brown, Ted, additional, Lewis, Moira, additional, Reilly, Beau, additional, Lee, Evon Batey, additional, Melchior, Sarah, additional, Marcus, Lee, additional, Murdoch, John D., additional, Gaag, Jan Van der Rutger, additional, Sanders, Stephan, additional, Kim, Jinah, additional, Gulsrud, Amanda C., additional, and Capece, Lindsey, additional

Published
2013
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44. Motivation

Author

Hutchins, Tiffany, primary, Vivanti, Giacomo, additional, Mateljevic, Natasa, additional, Jou, Roger J., additional, Shic, Frederick, additional, Cornew, Lauren, additional, Roberts, Timothy P. L., additional, Oakes, Leona, additional, Gray, Sarah A. O., additional, Ray-Subramanian, Corey, additional, Stubbe, Dorothy, additional, Mueller, Vannesa T., additional, Singh, Anjileen, additional, Zierhut, Cynthia, additional, Rogers, Sally J., additional, Sulkes, Stephen, additional, Wilczynski, Susan, additional, Rue, Hanna C., additional, Gabig, Cheryl Smith, additional, Offit, Paul A., additional, Scott, Haleigh, additional, Havercamp, Susan M., additional, Voos, Avery, additional, Westphal, Alexander, additional, Roesser, Jessica L., additional, Avini, Mitrah E., additional, Scahill, Lawrence David, additional, Lickenbrock, Diane M., additional, Boucher, Jill, additional, Gaigg, Sebastian, additional, Bowler, Dermot, additional, Solages, Martine, additional, Grindstaff, Jemma, additional, Shea, Victoria, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Farmer, Miranda, additional, Pilato, Madison, additional, Macy, Kelly, additional, Moyle, Maura, additional, Plowgian, Claire, additional, Marti, Itxaso, additional, Geno, Danielle, additional, McDuffie, Andrea, additional, Schoen, Sarah, additional, Miller, Lucy, additional, Solomon, Marjorie, additional, Hyman, Susan, additional, Dinstein, Ilan, additional, Behrman, Marlene, additional, Parvez, Rizwan, additional, Aaronson, Benjamin, additional, Bernier, Raphael, additional, Kent, Lindsey, additional, Lestrud, Michelle, additional, Volkmar, Fred R., additional, Dereu, Mieke, additional, Brucker, Pamela, additional, Hoffman, Ellen J., additional, Johnson, Kristin, additional, Edelson, Lisa, additional, El-Fishawy, Paul, additional, Hillegers, Manon H. J., additional, Aalst, Karen, additional, Esposito, Gianluca, additional, Mouridsen, Svend Erik, additional, Koegel, Lynn, additional, Koegel, Robert L., additional, Park, Mi Na, additional, Lee, Su Mei, additional, Zampella, Casey, additional, Bennetto, Loisa, additional, Brown, Ted, additional, Lewis, Moira, additional, Reilly, Beau, additional, Lee, Evon Batey, additional, Melchior, Sarah, additional, Marcus, Lee, additional, Murdoch, John D., additional, Gaag, Jan Van der Rutger, additional, Sanders, Stephan, additional, Kim, Jinah, additional, Gulsrud, Amanda C., additional, and Capece, Lindsey, additional

Published
2013
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45. Navane (Thiothixene)

Author

Anagnostou, Evdokia, primary, Mankad, Deepali, additional, Diehl, Joshua, additional, Lord, Catherine, additional, Butler, Sarah, additional, McDuffie, Andrea, additional, Shull, Lisa, additional, Ashbaugh, Kristen, additional, Koegel, Robert L., additional, Volkmar, Fred R., additional, Naples, Adam, additional, Doggett, Rebecca, additional, Hooper, Stephen R., additional, Casanova, Manuel, additional, Hoffman, Ellen J., additional, McFadden, Kate, additional, Anderson, George M., additional, Gupta, Abha R., additional, DiLullo, Nicholas M., additional, Minshew, Nancy J., additional, Burner, Karen, additional, Bernier, Raphael, additional, Pelphrey, Kevin A., additional, Perszyk, Danielle, additional, Willsey, A. Jeremy, additional, Krasno, Anna M., additional, Campbell, Daniel, additional, Spear-Swerling, Louise, additional, Kuschner, Emily S., additional, Corbett, Eugenia, additional, Noonan, Jacqueline A., additional, Takeuchi, Yoshihiro, additional, Tassé, Marc J., additional, Grover, Matthew, additional, Lyons, Megan, additional, Tyson, Katherine, additional, Fein, Deborah, additional, Berger, Michael, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Dunn, Debra, additional, and Pilato, Madison, additional

Published
2013
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46. Monotonic Voice

Author

Hutchins, Tiffany, primary, Vivanti, Giacomo, additional, Mateljevic, Natasa, additional, Jou, Roger J., additional, Shic, Frederick, additional, Cornew, Lauren, additional, Roberts, Timothy P. L., additional, Oakes, Leona, additional, Gray, Sarah A. O., additional, Ray-Subramanian, Corey, additional, Stubbe, Dorothy, additional, Mueller, Vannesa T., additional, Singh, Anjileen, additional, Zierhut, Cynthia, additional, Rogers, Sally J., additional, Sulkes, Stephen, additional, Wilczynski, Susan, additional, Rue, Hanna C., additional, Gabig, Cheryl Smith, additional, Offit, Paul A., additional, Scott, Haleigh, additional, Havercamp, Susan M., additional, Voos, Avery, additional, Westphal, Alexander, additional, Roesser, Jessica L., additional, Avini, Mitrah E., additional, Scahill, Lawrence David, additional, Lickenbrock, Diane M., additional, Boucher, Jill, additional, Gaigg, Sebastian, additional, Bowler, Dermot, additional, Solages, Martine, additional, Grindstaff, Jemma, additional, Shea, Victoria, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Farmer, Miranda, additional, Pilato, Madison, additional, Macy, Kelly, additional, Moyle, Maura, additional, Plowgian, Claire, additional, Marti, Itxaso, additional, Geno, Danielle, additional, McDuffie, Andrea, additional, Schoen, Sarah, additional, Miller, Lucy, additional, Solomon, Marjorie, additional, Hyman, Susan, additional, Dinstein, Ilan, additional, Behrman, Marlene, additional, Parvez, Rizwan, additional, Aaronson, Benjamin, additional, Bernier, Raphael, additional, Kent, Lindsey, additional, Lestrud, Michelle, additional, Volkmar, Fred R., additional, Dereu, Mieke, additional, Brucker, Pamela, additional, Hoffman, Ellen J., additional, Johnson, Kristin, additional, Edelson, Lisa, additional, El-Fishawy, Paul, additional, Hillegers, Manon H. J., additional, Aalst, Karen, additional, Esposito, Gianluca, additional, Mouridsen, Svend Erik, additional, Koegel, Lynn, additional, Koegel, Robert L., additional, Park, Mi Na, additional, Lee, Su Mei, additional, Zampella, Casey, additional, Bennetto, Loisa, additional, Brown, Ted, additional, Lewis, Moira, additional, Reilly, Beau, additional, Lee, Evon Batey, additional, Melchior, Sarah, additional, Marcus, Lee, additional, Murdoch, John D., additional, Gaag, Jan Van der Rutger, additional, Sanders, Stephan, additional, Kim, Jinah, additional, Gulsrud, Amanda C., additional, and Capece, Lindsey, additional

Published
2013
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47. Memory Development

Author

Hutchins, Tiffany, primary, Vivanti, Giacomo, additional, Mateljevic, Natasa, additional, Jou, Roger J., additional, Shic, Frederick, additional, Cornew, Lauren, additional, Roberts, Timothy P. L., additional, Oakes, Leona, additional, Gray, Sarah A. O., additional, Ray-Subramanian, Corey, additional, Stubbe, Dorothy, additional, Mueller, Vannesa T., additional, Singh, Anjileen, additional, Zierhut, Cynthia, additional, Rogers, Sally J., additional, Sulkes, Stephen, additional, Wilczynski, Susan, additional, Rue, Hanna C., additional, Gabig, Cheryl Smith, additional, Offit, Paul A., additional, Scott, Haleigh, additional, Havercamp, Susan M., additional, Voos, Avery, additional, Westphal, Alexander, additional, Roesser, Jessica L., additional, Avini, Mitrah E., additional, Scahill, Lawrence David, additional, Lickenbrock, Diane M., additional, Boucher, Jill, additional, Gaigg, Sebastian, additional, Bowler, Dermot, additional, Solages, Martine, additional, Grindstaff, Jemma, additional, Shea, Victoria, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Farmer, Miranda, additional, Pilato, Madison, additional, Macy, Kelly, additional, Moyle, Maura, additional, Plowgian, Claire, additional, Marti, Itxaso, additional, Geno, Danielle, additional, McDuffie, Andrea, additional, Schoen, Sarah, additional, Miller, Lucy, additional, Solomon, Marjorie, additional, Hyman, Susan, additional, Dinstein, Ilan, additional, Behrman, Marlene, additional, Parvez, Rizwan, additional, Aaronson, Benjamin, additional, Bernier, Raphael, additional, Kent, Lindsey, additional, Lestrud, Michelle, additional, Volkmar, Fred R., additional, Dereu, Mieke, additional, Brucker, Pamela, additional, Hoffman, Ellen J., additional, Johnson, Kristin, additional, Edelson, Lisa, additional, El-Fishawy, Paul, additional, Hillegers, Manon H. J., additional, Aalst, Karen, additional, Esposito, Gianluca, additional, Mouridsen, Svend Erik, additional, Koegel, Lynn, additional, Koegel, Robert L., additional, Park, Mi Na, additional, Lee, Su Mei, additional, Zampella, Casey, additional, Bennetto, Loisa, additional, Brown, Ted, additional, Lewis, Moira, additional, Reilly, Beau, additional, Lee, Evon Batey, additional, Melchior, Sarah, additional, Marcus, Lee, additional, Murdoch, John D., additional, Gaag, Jan Van der Rutger, additional, Sanders, Stephan, additional, Kim, Jinah, additional, Gulsrud, Amanda C., additional, and Capece, Lindsey, additional

Published
2013
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48. NEPSY-II

Author

Anagnostou, Evdokia, primary, Mankad, Deepali, additional, Diehl, Joshua, additional, Lord, Catherine, additional, Butler, Sarah, additional, McDuffie, Andrea, additional, Shull, Lisa, additional, Ashbaugh, Kristen, additional, Koegel, Robert L., additional, Volkmar, Fred R., additional, Naples, Adam, additional, Doggett, Rebecca, additional, Hooper, Stephen R., additional, Casanova, Manuel, additional, Hoffman, Ellen J., additional, McFadden, Kate, additional, Anderson, George M., additional, Gupta, Abha R., additional, DiLullo, Nicholas M., additional, Minshew, Nancy J., additional, Burner, Karen, additional, Bernier, Raphael, additional, Pelphrey, Kevin A., additional, Perszyk, Danielle, additional, Willsey, A. Jeremy, additional, Krasno, Anna M., additional, Campbell, Daniel, additional, Spear-Swerling, Louise, additional, Kuschner, Emily S., additional, Corbett, Eugenia, additional, Noonan, Jacqueline A., additional, Takeuchi, Yoshihiro, additional, Tassé, Marc J., additional, Grover, Matthew, additional, Lyons, Megan, additional, Tyson, Katherine, additional, Fein, Deborah, additional, Berger, Michael, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Dunn, Debra, additional, and Pilato, Madison, additional

Published
2013
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49. Nonsymbolic Communication

Author

Anagnostou, Evdokia, primary, Mankad, Deepali, additional, Diehl, Joshua, additional, Lord, Catherine, additional, Butler, Sarah, additional, McDuffie, Andrea, additional, Shull, Lisa, additional, Ashbaugh, Kristen, additional, Koegel, Robert L., additional, Volkmar, Fred R., additional, Naples, Adam, additional, Doggett, Rebecca, additional, Hooper, Stephen R., additional, Casanova, Manuel, additional, Hoffman, Ellen J., additional, McFadden, Kate, additional, Anderson, George M., additional, Gupta, Abha R., additional, DiLullo, Nicholas M., additional, Minshew, Nancy J., additional, Burner, Karen, additional, Bernier, Raphael, additional, Pelphrey, Kevin A., additional, Perszyk, Danielle, additional, Willsey, A. Jeremy, additional, Krasno, Anna M., additional, Campbell, Daniel, additional, Spear-Swerling, Louise, additional, Kuschner, Emily S., additional, Corbett, Eugenia, additional, Noonan, Jacqueline A., additional, Takeuchi, Yoshihiro, additional, Tassé, Marc J., additional, Grover, Matthew, additional, Lyons, Megan, additional, Tyson, Katherine, additional, Fein, Deborah, additional, Berger, Michael, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Dunn, Debra, additional, and Pilato, Madison, additional

Published
2013
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50. Noncontingent Reinforcement (NCI)

Author

Anagnostou, Evdokia, primary, Mankad, Deepali, additional, Diehl, Joshua, additional, Lord, Catherine, additional, Butler, Sarah, additional, McDuffie, Andrea, additional, Shull, Lisa, additional, Ashbaugh, Kristen, additional, Koegel, Robert L., additional, Volkmar, Fred R., additional, Naples, Adam, additional, Doggett, Rebecca, additional, Hooper, Stephen R., additional, Casanova, Manuel, additional, Hoffman, Ellen J., additional, McFadden, Kate, additional, Anderson, George M., additional, Gupta, Abha R., additional, DiLullo, Nicholas M., additional, Minshew, Nancy J., additional, Burner, Karen, additional, Bernier, Raphael, additional, Pelphrey, Kevin A., additional, Perszyk, Danielle, additional, Willsey, A. Jeremy, additional, Krasno, Anna M., additional, Campbell, Daniel, additional, Spear-Swerling, Louise, additional, Kuschner, Emily S., additional, Corbett, Eugenia, additional, Noonan, Jacqueline A., additional, Takeuchi, Yoshihiro, additional, Tassé, Marc J., additional, Grover, Matthew, additional, Lyons, Megan, additional, Tyson, Katherine, additional, Fein, Deborah, additional, Berger, Michael, additional, Early, Maureen, additional, Wink, Logan, additional, Erickson, Craig, additional, McDougle, Christopher J., additional, Dunn, Debra, additional, and Pilato, Madison, additional

Published
2013
Full Text
View/download PDF

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