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Profil bibliographique

Irene Antony

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

14Publications signalées
88Citations signalées
5Affiliations récentes

Les institutions déclarées

Les domaines associés

Autism Spectrum Disorder ResearchGenomics and Chromatin DynamicsPluripotent Stem Cells ResearchCRISPR and Genetic EngineeringChromatin Remodeling and Cancer

Les publications récentes

Accès ouvert 2024 article OpenAlex

Review: Child Psychiatry in the Era of Genomics: The Promise of Translational Genetics Research for the Clinic

Sarah E. Fitzpatrick, Irene Antony, Erika L. Nurmi, Thomas V. Fernandez et autres

Objective: There has been remarkable progress in recent years in understanding the genetic underpinnings of child psychiatric disorders. Concurrently, genetic testing is becoming increasingly available in the clinic. However, many clinicians report a lack of familiarity with genetics and how genetic testing …

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4 citations JAACAP Open
Accès ouvert 2024 article OpenAlex

Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder risk

Taehwan Shin, Janet H. T. Song, Michael Kosicki, Connor J. Kenny et autres

Little is known about the role of non-coding regions in the etiology of autism spectrum disorder (ASD). We examined three classes of non-coding regions: human accelerated regions (HARs), which show signatures of positive selection in humans; experimentally validated neural VISTA enhancers (VEs); …

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34 citations Cell Genomics
Accès ouvert 2023 preprint OpenAlex

Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk

Taehwan Shin, Janet H. T. Song, Michael Kosicki, Connor J. Kenny et autres

Abstract Little is known about the role of noncoding regions in the etiology of autism spectrum disorder (ASD). We examined three classes of noncoding regions: Human Accelerated Regions (HARs), which show signatures of positive selection in humans; experimentally validated neural Vista Enhancers …

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6 citations medRxiv
Accès ouvert 2022 article OpenAlex

Regulation of human cortical interneuron development by the chromatin remodeling protein CHD2

Emily M. A. Lewis, Gareth Chapman, Komal Kaushik, Julianna J. Determan et autres

Mutations in the chromodomain helicase DNA binding protein 2 (CHD2) gene are associated with neurodevelopmental disorders. However, mechanisms by which CHD2 regulates human brain development remain largely uncharacterized. Here, we used a human embryonic stem cell model of cortical interneuron (hcIN) development …

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12 citations Scientific Reports

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