Zobrazeno 1 - 10 of 45 pro vyhledávání: '"Zohreh, Talebizadeh"'
1
Akademický článek
Developing a community-led rare disease ELSI research agenda
Autor: Courtney Berrios, Macy McBeth, Andrea Bradley-Ewing, Nikolaus Schuetz, Annette Campbell, Zohreh Talebizadeh, Jeremy R. Garrett, Tamara Falicov, Francisco Martinez, Rare Voices Advisory Group, Emily A. Hurley
Publikováno v: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Background Research priorities are best defined through engagement with communities who will be impacted by the research and have lived experience of the topics to be studied. We aimed to establish a pediatric rare disease community stakehol
Externí odkaz: https://doaj.org/article/ecc2e6cebd884b14985942b261fbf8ec
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2
Akademický článek
Landscape Analysis of Neurodevelopmental Comorbidities in Newborn Screening Conditions: Challenges and Opportunities
Autor: Zohreh Talebizadeh, Valerie Hu, Monir Shababi, Amy Brower
Publikováno v: International Journal of Neonatal Screening, Vol 10, Iss 1, p 4 (2024)
Newborn screening (NBS) is a large-scale public health program in the US that screens 3.8 million newborns for up to 81 genetic conditions each year. Many of these conditions have comorbidities, including neurodevelopmental disorders (NDDs). These co
Externí odkaz: https://doaj.org/article/567055a6de72428ab348ad3c5c670307
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3
Akademický článek
The Relationship between Maternal Antibodies to Fetal Brain and Prenatal Stress Exposure in Autism Spectrum Disorder
Autor: Amy N. Costa, Bradley J. Ferguson, Emily Hawkins, Adriana Coman, Joseph Schauer, Alex Ramirez-Celis, Patrick M. Hecht, Danielle Bruce, Michael Tilley, Zohreh Talebizadeh, Judy Van de Water, David Q. Beversdorf
Publikováno v: Metabolites, Vol 13, Iss 5, p 663 (2023)
Environmental and genetic factors contribute to the etiology of autism spectrum disorder (ASD), but their interaction is less well understood. Mothers that are genetically more stress-susceptible have been found to be at increased risk of having a ch
Externí odkaz: https://doaj.org/article/14997a0a29b84046a711d934bf0d7932
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4
Akademický článek
microRNAs and Gene–Environment Interactions in Autism: Effects of Prenatal Maternal Stress and the SERT Gene on Maternal microRNA Expression
Autor: David Q. Beversdorf, Ayten Shah, Allison Jhin, Janelle Noel-MacDonnell, Patrick Hecht, Bradley J. Ferguson, Danielle Bruce, Michael Tilley, Zohreh Talebizadeh
Publikováno v: Frontiers in Psychiatry, Vol 12 (2021)
Background: Genetics and environment both are critical in autism spectrum disorder (ASD), but their interaction (G × E) is less understood. Numerous studies have shown higher incidence of stress exposures during pregnancies with children later diagn
Externí odkaz: https://doaj.org/article/3135ea189d84408a974ef22b927f3207
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6
Akademický článek
A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism.
Autor: Zohreh Talebizadeh, Dan E Arking, Valerie W Hu
Publikováno v: PLoS ONE, Vol 8, Iss 6, p e67569 (2013)
Most genome linkage scans for autism spectrum disorders (ASDs) have failed to be replicated. Recently, a new ASD phenotypic sub-classification method was developed which employed cluster analyses of severity scores from the Autism Diagnostic Intervie
Externí odkaz: https://doaj.org/article/5128c82d03a04e2fb71cf41ad397c745
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7
The AutGO Initiative: A Conceptual Framework for Developing Genetics-Outcomes Research Hypotheses
Autor: Zohreh Talebizadeh, Ayten Shah
Publikováno v: Autism Research
The increasing emphasis on translational approaches to complex neuropsychiatric and neurodevelopmental conditions research requires scientists from a broad range of disciplines to build dynamic collaborations when formulating hypotheses and framing s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cb4ecb2da2fbc395edba8136f062ae9
https://pubmed.ncbi.nlm.nih.gov/32618145
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9
The potential role of a retrotransposed gene and a long noncoding RNA in regulating an X-linked chromatin gene (KDM5C): Novel epigenetic mechanism in autism
Autor: Zohreh Talebizadeh, Ayten Shah, Luciano DiTacchio
Publikováno v: Autism research : official journal of the International Society for Autism Research. 12(7)
A growing body of evidence supports the potential role of the circadian system and chromatin remodeling genes in autism. Considering the heterogeneity and gender discrepancy in autism, and the complex nature of the epigenetic landscape, identificatio
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13d9c042a10e4fcad2c287cf558b13e9
https://pubmed.ncbi.nlm.nih.gov/31087518
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10
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37
Autor: William J. Kimberling, Patrick L. M. Huygen, James W. Askew, Katherine R. Smith, Denise M. Hoover, Kevin T. Booth, Judith B. Kenyon, Richard J.H. Smith, Shelley D. Smith, Zohreh Talebizadeh, Hela Azaiez, James D. Eudy, Melanie Bahlo, Michael S. Hildebrand
Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics
Genetics in Medicine, 21, 948-954
Genetics in Medicine, 21, 4, pp. 948-954
Purpose: The aim of this study was to determine the genetic cause of autosomal dominant non-syndromic hearing loss segregating in a multi-generational family. Methods: Clinical examination, genome-wide linkage analysis, and exome sequencing were carr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bcba4f5fd1afe3a55b277dee7d4d1a9
https://pubmed.ncbi.nlm.nih.gov/30245514
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