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Jan Haavik

Showing results (151-160 of 221) with videos related to

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Epigenetics & Chromatin|October 15, 2025
Optimizing genetic ancestry adjustment in DNA methylation studies: a comparative analysis of approachesKira D Höffler, Seyma Katrinli, Matthew W Halvorsen, et al.
Molecular Psychiatry|October 28, 2024
A burden of rare copy number variants in obsessive-compulsive disorderMatthew W Halvorsen, Elles de Schipper, Julia Bäckman, et al.
BMC Psychiatry|October 31, 2023
Neurobiological mechanisms of ECT and TMS treatment in depression: study protocol of a multimodal magnetic resonance investigationLeila Marie Frid, Ute Kessler, Olga Therese Ousdal, et al.
Biological Psychiatry|December 24, 2023
Maternal Fiber Intake During Pregnancy and Development of Attention-Deficit/Hyperactivity Disorder Symptoms Across Childhood: The Norwegian Mother, Father, and Child Cohort StudyBerit Skretting Solberg, Liv Grimstvedt Kvalvik, Johanne Telnes Instanes, et al.
Journal of Clinical Medicine|June 18, 2020
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional AnalysesBàrbara Torrico, Ester Antón-Galindo, Noèlia Fernàndez-Castillo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 19, 2015
On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysisHeike Weber, Sarah Kittel-Schneider, Julia Heupel, et al.
Human Molecular Genetics|October 2, 2007
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorderSven Cichon, Ingeborg Winge, Manuel Mattheisen, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2009
Pulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigenMohammad Alimohammadi, Noémie Dubois, Filip Sköldberg, et al.
Molecular Psychiatry|September 18, 2025
A low frequency damaging SORCS2 variant identified in a family with ADHD compromises receptor stability and quenches activityMathias Kaas, Sarah Broholt Dinesen, Ole Ahlgreen, et al.
Alzheimer'S Research & Therapy|October 28, 2024
Molecular landscape of the overlap between Alzheimer's disease and somatic insulin-related diseasesI Hyun Ruisch, Joanna Widomska, Ward De Witte, et al.
Pageof 23

Showing results (151-160 of 221) with videos related to

Sort By:
Pageof 23
Epigenetics & Chromatin|October 15, 2025
Optimizing genetic ancestry adjustment in DNA methylation studies: a comparative analysis of approachesKira D Höffler, Seyma Katrinli, Matthew W Halvorsen, et al.
Molecular Psychiatry|October 28, 2024
A burden of rare copy number variants in obsessive-compulsive disorderMatthew W Halvorsen, Elles de Schipper, Julia Bäckman, et al.
BMC Psychiatry|October 31, 2023
Neurobiological mechanisms of ECT and TMS treatment in depression: study protocol of a multimodal magnetic resonance investigationLeila Marie Frid, Ute Kessler, Olga Therese Ousdal, et al.
Biological Psychiatry|December 24, 2023
Maternal Fiber Intake During Pregnancy and Development of Attention-Deficit/Hyperactivity Disorder Symptoms Across Childhood: The Norwegian Mother, Father, and Child Cohort StudyBerit Skretting Solberg, Liv Grimstvedt Kvalvik, Johanne Telnes Instanes, et al.
Journal of Clinical Medicine|June 18, 2020
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional AnalysesBàrbara Torrico, Ester Antón-Galindo, Noèlia Fernàndez-Castillo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 19, 2015
On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysisHeike Weber, Sarah Kittel-Schneider, Julia Heupel, et al.
Human Molecular Genetics|October 2, 2007
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorderSven Cichon, Ingeborg Winge, Manuel Mattheisen, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2009
Pulmonary autoimmunity as a feature of autoimmune polyendocrine syndrome type 1 and identification of KCNRG as a bronchial autoantigenMohammad Alimohammadi, Noémie Dubois, Filip Sköldberg, et al.
Molecular Psychiatry|September 18, 2025
A low frequency damaging SORCS2 variant identified in a family with ADHD compromises receptor stability and quenches activityMathias Kaas, Sarah Broholt Dinesen, Ole Ahlgreen, et al.
Alzheimer'S Research & Therapy|October 28, 2024
Molecular landscape of the overlap between Alzheimer's disease and somatic insulin-related diseasesI Hyun Ruisch, Joanna Widomska, Ward De Witte, et al.
Pageof 23