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Matthew K Harner

Showing results (1-10 of 8) with videos related to

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Annual Review of Genomics and Human Genetics|April 25, 2025
Copy Number Variants: Deletion and Duplication SyndromesMatthew K Harner, Daniela V Bishop, Rebecca M Pollak, et al.
American Journal of Medical Genetics. Part A|August 1, 2025
Medical Multimorbidity in Patients With Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 PatientsTyler E Dietterich, Rose Mary Xavier, Maya L Lichtenstein, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
Medical Multimorbidity in Patients with Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 PatientsTyler E Dietterich, Rose Mary Xavier, Maya L Lichtenstein, et al.
Schizophrenia Bulletin Open|October 6, 2025
Obstacles, Opportunities, and Ethical Considerations for Genomic Investigations of Individuals Continuously Hospitalized with Treatment-resistant SchizophreniaRichard C Josiassen, Rose Mary Xavier, Tyler E Dietterich, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|August 1, 2025
Delineating lifetime multimorbidity associated with 16p13.11 duplication: A literature review, meta-analysis, and case studyRose Mary Xavier, Wenxin Bian, Fadhah Alshammari, et al.
Schizophrenia Research|September 18, 2020
Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndromeMatthew K Harner, Maya Lichtenstein, Martilias Farrell, et al.
Translational Psychiatry|February 19, 2020
Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literatureMartilias Farrell, Maya Lichtenstein, Matthew K Harner, et al.
Schizophrenia Bulletin|December 1, 2022
Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant PsychosisMartilias Farrell, Tyler E Dietterich, Matthew K Harner, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Annual Review of Genomics and Human Genetics|April 25, 2025
Copy Number Variants: Deletion and Duplication SyndromesMatthew K Harner, Daniela V Bishop, Rebecca M Pollak, et al.
American Journal of Medical Genetics. Part A|August 1, 2025
Medical Multimorbidity in Patients With Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 PatientsTyler E Dietterich, Rose Mary Xavier, Maya L Lichtenstein, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
Medical Multimorbidity in Patients with Treatment-Resistant Psychosis and Rare Copy Number Variants: A Retrospective Case Series of 24 PatientsTyler E Dietterich, Rose Mary Xavier, Maya L Lichtenstein, et al.
Schizophrenia Bulletin Open|October 6, 2025
Obstacles, Opportunities, and Ethical Considerations for Genomic Investigations of Individuals Continuously Hospitalized with Treatment-resistant SchizophreniaRichard C Josiassen, Rose Mary Xavier, Tyler E Dietterich, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|August 1, 2025
Delineating lifetime multimorbidity associated with 16p13.11 duplication: A literature review, meta-analysis, and case studyRose Mary Xavier, Wenxin Bian, Fadhah Alshammari, et al.
Schizophrenia Research|September 18, 2020
Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndromeMatthew K Harner, Maya Lichtenstein, Martilias Farrell, et al.
Translational Psychiatry|February 19, 2020
Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literatureMartilias Farrell, Maya Lichtenstein, Matthew K Harner, et al.
Schizophrenia Bulletin|December 1, 2022
Increased Prevalence of Rare Copy Number Variants in Treatment-Resistant PsychosisMartilias Farrell, Tyler E Dietterich, Matthew K Harner, et al.
Pageof 1