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BMC Psychiatry
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May 5, 2021
The Eating Disorders Genetics Initiative (EDGI): study protocol
Cynthia M Bulik, Laura M Thornton, Richard Parker, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
October 19, 2021
Evaluating the interrelations between the autism polygenic score and psychiatric family history in risk for autism
Diana Schendel, Thomas Munk Laursen, Clara Albiñana, et al.
Molecular Psychiatry
|
November 14, 2024
The role of co-occurring conditions and genetics in the associations of eating disorders with attention-deficit/hyperactivity disorder and autism spectrum disorder
Gitte Bundgaard Christiansen, Liselotte Vogdrup Petersen, Hannah Chatwin, et al.
Nature Genetics
|
June 2, 2022
Genetic correlates of phenotypic heterogeneity in autism
Varun Warrier, Xinhe Zhang, Patrick Reed, et al.
Genome Biology
|
March 24, 2026
Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder
Hyeji Lee, Kahee Ko, Seoyeon Kim, et al.
Biological Psychiatry Global Open Science
|
November 14, 2025
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 Patients
Slavina B Goleva, Costin Leu, Yen-Chen Anne Feng, et al.
JAMA Psychiatry
|
June 10, 2026
Changes in Genetic Contributions to ASD and ADHD by Year of Diagnosis
Sonja LaBianca, Mette Lise Lousdal, Morten Dybdahl Krebs, et al.
Nature Communications
|
August 5, 2023
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores
Clara Albiñana, Zhihong Zhu, Andrew J Schork, et al.
Nature Genetics
|
June 29, 2022
Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
Danny Antaki, James Guevara, Adam X Maihofer, et al.
Plos One
|
April 19, 2016
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
Jesper Buchhave Poulsen, Francesco Lescai, Jakob Grove, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 136) with videos related to
Sort By:
Page
of 14
BMC Psychiatry
|
May 5, 2021
The Eating Disorders Genetics Initiative (EDGI): study protocol
Cynthia M Bulik, Laura M Thornton, Richard Parker, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
October 19, 2021
Evaluating the interrelations between the autism polygenic score and psychiatric family history in risk for autism
Diana Schendel, Thomas Munk Laursen, Clara Albiñana, et al.
Molecular Psychiatry
|
November 14, 2024
The role of co-occurring conditions and genetics in the associations of eating disorders with attention-deficit/hyperactivity disorder and autism spectrum disorder
Gitte Bundgaard Christiansen, Liselotte Vogdrup Petersen, Hannah Chatwin, et al.
Nature Genetics
|
June 2, 2022
Genetic correlates of phenotypic heterogeneity in autism
Varun Warrier, Xinhe Zhang, Patrick Reed, et al.
Genome Biology
|
March 24, 2026
Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder
Hyeji Lee, Kahee Ko, Seoyeon Kim, et al.
Biological Psychiatry Global Open Science
|
November 14, 2025
Multisite, Multiancestry Genome-Wide Association Study Meta-Analysis of Functional Seizure Disorder in a Hospital Sample of 675,680 Patients
Slavina B Goleva, Costin Leu, Yen-Chen Anne Feng, et al.
JAMA Psychiatry
|
June 10, 2026
Changes in Genetic Contributions to ASD and ADHD by Year of Diagnosis
Sonja LaBianca, Mette Lise Lousdal, Morten Dybdahl Krebs, et al.
Nature Communications
|
August 5, 2023
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores
Clara Albiñana, Zhihong Zhu, Andrew J Schork, et al.
Nature Genetics
|
June 29, 2022
Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
Danny Antaki, James Guevara, Adam X Maihofer, et al.
Plos One
|
April 19, 2016
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
Jesper Buchhave Poulsen, Francesco Lescai, Jakob Grove, et al.
Page
of 14