Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A
Published in BMC medicine (22.10.2009)
Published in BMC medicine (22.10.2009)
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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways
GRISWOLD, Anthony J, DEQIONG MA, WRIGHT, Harry H, ABRAMSON, Ruth K, WILLIAMS, Scott M, MENON, Ramkumar, MARTIN, Eden R, HAINES, Jonathan L, GILBERT, John R, CUCCARO, Michael L, PERICAK-VANCE, Margaret A, CUKIER, Holly N, NATIONS, Laura D, SCHMIDT, Mike A, CHUNG, Ren-Hua, JAWORSKI, James M, SALYAKINA, Daria, KONIDARI, Loanna, WHITEHEAD, Patrice L
Published in Human molecular genetics (01.08.2012)
Published in Human molecular genetics (01.08.2012)
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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk
Salyakina, Daria, Cukier, Holly N, Lee, Joycelyn M, Sacharow, Stephanie, Nations, Laura D, Ma, Deqiong, Jaworski, James M, Konidari, Ioanna, Whitehead, Patrice L, Wright, Harry H, Abramson, Ruth K, Williams, Scott M, Menon, Ramkumar, Haines, Jonathan L, Gilbert, John R, Cuccaro, Michael L, Pericak-Vance, Margaret A
Published in PloS one (07.10.2011)
Published in PloS one (07.10.2011)
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Commentary from the DSM-5 Workgroup on Neurodevelopmental Disorders
Swedo, Susan E., M.D, Baird, Gillian, M.D, Cook, Edwin H., M.D, Happé, Francesca G., Ph.D, Harris, James C., M.D, Kaufmann, Walter E., M.D, King, Bryan H., M.D, Lord, Catherine E., Ph.D, Piven, Joseph, M.D, Rogers, Sally J., Ph.D, Spence, Sarah J., M.D., Ph.D, Wetherby, Amy, Ph.D, Wright, Harry H., M.D
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.04.2012)
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.04.2012)
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The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1
Cukier, Holly N, Lee, Joycelyn M, Ma, Deqiong, Young, Juan I, Mayo, Vera, Butler, Brittany L, Ramsook, Sandhya S, Rantus, Joseph A, Abrams, Alexander J, Whitehead, Patrice L, Wright, Harry H, Abramson, Ruth K, Haines, Jonathan L, Cuccaro, Michael L, Pericak-Vance, Margaret A, Gilbert, John R
Published in Autism research (01.12.2012)
Published in Autism research (01.12.2012)
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Investigation of autism and GABA receptor subunit genes in multiple ethnic groups
COLLINS, Ann L, DEQIONG MA, PERICAK-VANCE, Margaret A, WHITEHEAD, Patrice L, MARTIN, Eden R, WRIGHT, Harry H, ABRAMSON, Ruth K, HUSSMAN, John P, HAINES, Jonathan L, CUCCARO, Michael L, GILBERT, John R
Published in Neurogenetics (01.07.2006)
Published in Neurogenetics (01.07.2006)
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Genomic screen and follow-up analysis for autistic disorder
Shao, Yujun, Wolpert, Chantelle M, Raiford, Kimberly L, Menold, Marisa M, Donnelly, Shannon L, Ravan, Sarah A, Bass, Meredyth P, McClain, Cate, von Wendt, Lennart, Vance, Jeffery M, Abramson, Ruth H, Wright, Harry H, Ashley-Koch, Allison, Gilbert, John R, DeLong, Robert G, Cuccaro, Michael L, Pericak-Vance, Margaret A
Published in American journal of medical genetics (08.01.2002)
Published in American journal of medical genetics (08.01.2002)
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A low-cost socially assistive robot and robot-assisted intervention for children with autism spectrum disorder: field trials and lessons learned
Boccanfuso, Laura, Scarborough, Sarah, Abramson, Ruth K., Hall, Alicia V., Wright, Harry H., O’Kane, Jason M.
Published in Autonomous robots (01.03.2017)
Published in Autonomous robots (01.03.2017)
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An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
Chung, Ren-Hua, Ma, Deqiong, Wang, Kai, Hedges, Dale J, Jaworski, James M, Gilbert, John R, Cuccaro, Michael L, Wright, Harry H, Abramson, Ruth K, Konidari, Ioanna, Whitehead, Patrice L, Schellenberg, Gerard D, Hakonarson, Hakon, Haines, Jonathan L, Pericak-Vance, Margaret A, Martin, Eden R
Published in Molecular autism (04.11.2011)
Published in Molecular autism (04.11.2011)
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Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes
Rabionet, Raquel, Jaworski, James M., Ashley-Koch, Allison E., Martin, Eden R., Sutcliffe, James S., Haines, Jonathan L., DeLong, G. Robert, Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L., Gilbert, John R., Pericak-Vance, Margaret A.
Published in Neuroscience letters (06.12.2004)
Published in Neuroscience letters (06.12.2004)
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A Genome‐wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1
Ma, Deqiong, Salyakina, Daria, Jaworski, James M., Konidari, Ioanna, Whitehead, Patrice L., Andersen, Ashley N., Hoffman, Joshua D., Slifer, Susan H., Hedges, Dale J., Cukier, Holly N., Griswold, Anthony J., McCauley, Jacob L., Beecham, Gary W., Wright, Harry H., Abramson, Ruth K., Martin, Eden R., Hussman, John P., Gilbert, John R., Cuccaro, Michael L., Haines, Jonathan L., Pericak‐Vance, Margaret A.
Published in Annals of human genetics (01.05.2009)
Published in Annals of human genetics (01.05.2009)
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Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster Analysis
Cuccaro, Michael L., Tuchman, Roberto F., Hamilton, Kara L., Wright, Harry H., Abramson, Ruth K., Haines, Jonathan L., Gilbert, John R., Pericak-Vance, Margaret
Published in Journal of autism and developmental disorders (01.08.2012)
Published in Journal of autism and developmental disorders (01.08.2012)
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Factor Analysis of the Aberrant Behavior Checklist in Individuals with Autism Spectrum Disorders
Brinkley, Jason, Nations, Laura, Abramson, Ruth K, Hall, Alicia, Wright, Harry H, Gabriels, Robin, Gilbert, John R, Pericak-Vance, Margaret A. O, Cuccaro, Michael L
Published in Journal of autism and developmental disorders (01.11.2007)
Published in Journal of autism and developmental disorders (01.11.2007)
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Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
Cukier, Holly N., Rabionet, Raquel, Konidari, Ioanna, Rayner-Evans, Melissa Y., Baltos, Mary L., Wright, Harry H., Abramson, Ruth K., Martin, Eden R., Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.
Published in Neurogenetics (01.07.2010)
Published in Neurogenetics (01.07.2010)
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Accelerated head growth in early development of individuals with autism
Dementieva, Yulia A., Vance, Danica D., Donnelly, Shannon L., Elston, Leigh A., Wolpert, Chantelle M., Ravan, Sarah A., DeLong, G. Robert, Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L.
Published in Pediatric neurology (01.02.2005)
Published in Pediatric neurology (01.02.2005)
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Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders
Hadjixenofontos, Athena, Schmidt, Michael A., Whitehead, Patrice L., Konidari, Ioanna, Hedges, Dale J., Wright, Harry H., Abramson, Ruth K., Menon, Ramkumar, Williams, Scott M., Cuccaro, Michael L., Haines, Jonathan L., Gilbert, John R., Pericak‐Vance, Margaret A., Martin, Eden R., McCauley, Jacob L.
Published in Annals of human genetics (01.01.2013)
Published in Annals of human genetics (01.01.2013)
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Factor analysis of restricted and repetitive behaviors in Autism using the Autism Diagnostic interview-R
CUCCARO, Michael L, YUJAN SHAO, PERICAK-VANCE, Margaret A, GRUBBER, Janet, SLIFER, Michael, WOLPERT, Chantelle M, DONNELLY, Shannon L, ABRAMSON, Ruth K, RAVAN, Sarah A, WRIGHT, Harry H, DELONG, G. Robert
Published in Child psychiatry and human development (01.09.2003)
Published in Child psychiatry and human development (01.09.2003)
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Autism in African American Families: Clinical-phenotypic findings
Cuccaro, Michael L., Brinkley, Jason, Abramson, Ruth K., Hall, Alicia, Wright, Harry H., Hussman, John P., Gilbert, John R., Pericak-Vance, Margaret A.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.12.2007)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.12.2007)
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A de novo 1.5 Mb microdeletion on chromosome 14q23.2-23.3 in a patient with autism and spherocytosis
Griswold, Anthony J, Ma, Deqiong, Sacharow, Stephanie J, Robinson, Joycelyn L, Jaworski, James M, Wright, Harry H, Abramson, Ruth K, Lybaek, Helle, Øyen, Nina, Cuccaro, Michael L, Gilbert, John R, Pericak-Vance, Margaret A
Published in Autism research (01.06.2011)
Published in Autism research (01.06.2011)
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Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21
Cukier, Holly N., Salyakina, Daria, Blankstein, Sarah F., Robinson, Joycelyn L., Sacharow, Stephanie, Ma, Deqiong, Wright, Harry H., Abramson, Ruth K., Menon, Ramkumar, Williams, Scott M., Haines, Jonathan L., Cuccaro, Michael L., Gilbert, John R., Pericak-Vance, Margaret A.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2011)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2011)
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