Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Harry H Wright"'
Autor:
Daria Salyakina, Holly N Cukier, Joycelyn M Lee, Stephanie Sacharow, Laura D Nations, Deqiong Ma, James M Jaworski, Ioanna Konidari, Patrice L Whitehead, Harry H Wright, Ruth K Abramson, Scott M Williams, Ramkumar Menon, Jonathan L Haines, John R Gilbert, Michael L Cuccaro, Margaret A Pericak-Vance
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26049 (2011)
Copy number variations (CNVs) are a major cause of genetic disruption in the human genome with far more nucleotides being altered by duplications and deletions than by single nucleotide polymorphisms (SNPs). In the multifaceted etiology of autism spe
Externí odkaz:
https://doaj.org/article/a763b4dff8ec48fdad221a499acb13ca
Publikováno v:
Pharmacoepidemiology ISBN: 9780203743669
Pharmacoepidemiology
Pharmacoepidemiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e836a869c4f200e906469ddea712313
https://doi.org/10.1201/9780203743669-29
https://doi.org/10.1201/9780203743669-29
Autor:
Ruth K. Abramson, Alicia Hall, Laura Boccanfuso, Jason M. O'Kane, Harry H. Wright, Sarah Scarborough
Publikováno v:
Autonomous Robots. 41:637-655
Recent research has employed socially assistive robots as catalysts for social interaction and improved communication in young children with autism spectrum disorder (ASD). Studies describe observed therapeutic outcomes such as increased speech, soci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f3ebd69e6af84e3e21674954b1a0737
https://doi.org/10.1007/s10514-016-9554-4
https://doi.org/10.1007/s10514-016-9554-4
Autor:
Michael A. Schmidt, Patrice L. Whitehead, Dale J. Hedges, Jonathan L. Haines, Scott M. Williams, Harry H. Wright, Michael L. Cuccaro, Ruth K. Abramson, Athena Hadjixenofontos, Ramkumar Menon, John R. Gilbert, Ioanna Konidari, Eden R. Martin, Jacob L. McCauley, Margaret A. Pericak-Vance
Publikováno v:
Annals of Human Genetics. 77:9-21
Despite the increasing speculation that oxidative stress and abnormal energy metabolism may play a role in Autism Spectrum Disorders (ASD), and the observation that patients with mitochondrial defects have symptoms consistent with ASD, there are no c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44232254d4aa0c1dfd43d8dfa37ec992
https://doi.org/10.1111/j.1469-1809.2012.00736.x
https://doi.org/10.1111/j.1469-1809.2012.00736.x
Autor:
Patrice L. Whitehead, Harry H. Wright, Margaret A. Pericak-Vance, Vera Mayo, Michael L. Cuccaro, Juan I. Young, John R. Gilbert, Brittany L. Butler, Joycelyn M. Lee, Sandhya S. Ramsook, Alexander J. Abrams, Jonathan L. Haines, Ruth K. Abramson, Deqiong Ma, Joseph A. Rantus, Holly N. Cukier
Publikováno v:
Autism Research. 5:385-397
The methyl-CpG-binding domain (MBD) gene family was first linked to autism over a decade ago when Rett syndrome, which falls under the umbrella of autism spectrum disorders (ASDs), was revealed to be predominantly caused by MECP2 mutations. Since tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be285acf764647b7e08239d5486c1610
https://doi.org/10.1002/aur.1251
https://doi.org/10.1002/aur.1251
Autor:
Ren-Hua Chung, Harry H. Wright, Laura D. Nations, Michael L. Cuccaro, Anthony J. Griswold, Ramkumar Menon, Patrice L. Whitehead, Ruth K. Abramson, Daria Salyakina, James M. Jaworski, Michael A. Schmidt, Holly N. Cukier, Ioanna Konidari, Eden R. Martin, Jonathan L. Haines, Margaret A. Pericak-Vance, Deqiong Ma, Scott M. Williams, John R. Gilbert
Publikováno v:
Human Molecular Genetics. 21:3513-3523
Autism spectrum disorders (ASDs) are highly heritable, yet relatively few associated genetic loci have been replicated. Copy number variations (CNVs) have been implicated in autism; however, the majority of loci contribute to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a1a9e5eb5b14a69590aa2d72f982080
https://doi.org/10.1093/hmg/dds164
https://doi.org/10.1093/hmg/dds164
Autor:
Roberto Tuchman, Kara Hamilton, John R. Gilbert, Michael L. Cuccaro, Ruth K. Abramson, Harry H. Wright, Jonathan L. Haines, Margaret A. Pericak-Vance
Publikováno v:
Journal of Autism and Developmental Disorders. 42:1630-1641
Epilepsy co-occurs frequently in autism spectrum disorders (ASD). Understanding this co-occurrence requires a better understanding of the ASD-epilepsy phenotype (or phenotypes). To address this, we conducted latent class cluster analysis (LCCA) on an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae56cca28564fb8cc9425dd10417b47
https://doi.org/10.1007/s10803-011-1402-y
https://doi.org/10.1007/s10803-011-1402-y
Autor:
Ioanna Konidari, Stephanie Sacharow, Harry H. Wright, R. Henson, Ruth K. Abramson, James M. Jaworski, Joycelyn L. Robinson, Margaret A. Pericak-Vance, J. R. Gilbert, Daria Salyakina, Patrice L. Whitehead, David Cuadra Martínez, Deqiong Ma, Michael L. Cuccaro
Publikováno v:
Autism Research. 3:303-310
Asperger disorder (ASP) is one of the autism spectrum disorders (ASD) and is differentiated from autism largely on the absence of clinically significant cognitive and language delays. Analysis of a homogenous subset of families with ASP may help to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92108b3ff317e7a51354e188497a2ede
https://doi.org/10.1002/aur.158
https://doi.org/10.1002/aur.158
Autor:
Ruth K. Abramson, Raquel Rabionet, Mary L. Baltos, Holly N. Cukier, Ioanna Konidari, Eden R. Martin, Melissa Y. Rayner-Evans, Margaret A. Pericak-Vance, Michael L. Cuccaro, Harry H. Wright, John R. Gilbert
Publikováno v:
neurogenetics. 11:291-303
Misregulation of the methyl-CpG-binding protein 2 (MECP2) gene has been found to cause a myriad of neurological disorders including autism, mental retardation, seizures, learning disabilities, and Rett syndrome. We hypothesized that mutations in othe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a07108027fc49005bc835b8f421290e
https://doi.org/10.1007/s10048-009-0228-7
https://doi.org/10.1007/s10048-009-0228-7
Autor:
Ruth K. Abramson, Michael L. Cuccaro, Holly N. Cukier, Eden R. Martin, James M. Jaworski, Margaret A. Pericak-Vance, Ioanna Konidari, Harry H. Wright, Raquel Rabionet, J. R. Gilbert, Deqiong Ma
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :477-483
Autism is a heritable neurodevelopmental disorder with substantial genetic heterogeneity. Studies point to possible links between autism and two serotonin related genes: SLC6A4 and ITGB3 with a sex-specific genetic effect and interaction between the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c75fc050e64edca107f1deb9791a21c
https://doi.org/10.1002/ajmg.b.31003
https://doi.org/10.1002/ajmg.b.31003