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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Common SNP-Based Haplotype Analysis of the 4p16.3 Huntington Disease Gene Region
Lee, Jong-Min, Gillis, Tammy, Mysore, Jayalakshmi Srinidhi, Ramos, Eliana Marisa, Myers, Richard H., Hayden, Michael R., Morrison, Patrick J., Nance, Martha, Ross, Christopher A., Margolis, Russell L., Squitieri, Ferdinando, Griguoli, Annamaria, Di Donato, Stefano, Gomez-Tortosa, Estrella, Ayuso, Carmen, Suchowersky, Oksana, Trent, Ronald J., McCusker, Elizabeth, Novelletto, Andrea, Frontali, Marina, Jones, Randi, Ashizawa, Tetsuo, Frank, Samuel, Saint-Hilaire, Marie-Helene, Hersch, Steven M., Rosas, Herminia D., Lucente, Diane, Harrison, Madaline B., Zanko, Andrea, Abramson, Ruth K., Marder, Karen, Sequeiros, Jorge, MacDonald, Marcy E., Gusella, James F.
Published in American journal of human genetics (09.03.2012)
Published in American journal of human genetics (09.03.2012)
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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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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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Pharmacotherapy of Autism Spectrum Disorder: Results from the Randomized BAART Clinical Trial
DeVane, C Lindsay, Charles, Jane M, Abramson, Ruth K, Williams, John E, Carpenter, Laura A, Raven, Sarah, Gwynette, Frampton, Stuck, Craig A, Geesey, Mark E, Bradley, Catherine, Donovan, Jennifer L, Hall, Alicia G, Sherk, Shelley T, Powers, Nancy R, Spratt, Eve, Kinsman, Anne, Kruesi, Markus J, Bragg, Jr, John E
Published in Pharmacotherapy (01.06.2019)
Published in Pharmacotherapy (01.06.2019)
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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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Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2
Cukier, Holly N, Griswold, Anthony J, Hofmann, Natalia K, Gomez, Lissette, Whitehead, Patrice L, Abramson, Ruth K, Gilbert, John R, Cuccaro, Michael L, Dykxhoorn, Derek M, Pericak-Vance, Margaret A
Published in Autism research (01.04.2020)
Published in Autism research (01.04.2020)
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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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Comparison of serum carnitine levels and clinical correlates between outpatients and acutely hospitalised individuals with bipolar disorder and schizophrenia: A cross-sectional study
Cuturic, Miroslav, Abramson, Ruth K, Breen, Robert J, Edwards, Alfred C, Levy, Elliott E
Published in The world journal of biological psychiatry (01.09.2016)
Published in The world journal of biological psychiatry (01.09.2016)
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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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Journal Article
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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TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington’s disease
Lee, Ji-Hyun, Lee, Jong-Min, Ramos, Eliana Marisa, Gillis, Tammy, Mysore, Jayalakshmi S., Kishikawa, Shotaro, Hadzi, Tiffany, Hendricks, Audrey E., Hayden, Michael R., Morrison, Patrick J., Nance, Martha, Ross, Christopher A., Margolis, Russell L., Squitieri, Ferdinando, Gellera, Cinzia, Gomez-Tortosa, Estrella, Ayuso, Carmen, Suchowersky, Oksana, Trent, Ronald J., McCusker, Elizabeth, Novelletto, Andrea, Frontali, Marina, Jones, Randi, Ashizawa, Tetsuo, Frank, Samuel, Saint-Hilaire, Marie-Helene, Hersch, Steven M., Rosas, Herminia D., Lucente, Diane, Harrison, Madaline B., Zanko, Andrea, Abramson, Ruth K., Marder, Karen, Sequeiros, Jorge, Bernhard Landwehrmeyer, G., Shoulson, Ira, Myers, Richard H., MacDonald, Marcy E., Gusella, James F.
Published in Biochemical and biophysical research communications (03.08.2012)
Published in Biochemical and biophysical research communications (03.08.2012)
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