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Thomas Werge

Showing results (81-90 of 362) with videos related to

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Schizophrenia Research|August 11, 2006
Analysis of coding-polymorphisms in NOTCH-related genes reveals NUMBL poly-glutamine repeat to be associated with schizophrenia in Brazilian and Danish subjectsSheila Passos Gregorio, Wagner F Gattaz, Hildeberto Tavares, et al.
European Journal of Epidemiology|July 8, 2026
Neonatal vitamin D levels and autoimmune disorders: a Danish population-based cohort studyHenriette Thisted Horsdal, Berit Heitmann, Sanne Grundvad Boelt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 19, 2012
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic populationPeter Saetre, Jakob Grove, Anders D Børglum, et al.
BMC Cancer|August 6, 2010
No influence of the polymorphisms CYP2C19 and CYP2D6 on the efficacy of cyclophosphamide, thalidomide, and bortezomib in patients with Multiple MyelomaAnnette J Vangsted, Karen Søeby, Tobias W Klausen, et al.
Plos Genetics|December 30, 2015
An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association StudiesWesley K Thompson, Yunpeng Wang, Andrew J Schork, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|February 8, 2011
Dystrobrevin-binding protein 1 gene (DTNBP1) variants associated with cerebrospinal fluid homovanillic acid and 5-hydroxyindoleacetic acid concentrations in healthy volunteersDimitrios Andreou, Peter Saetre, Anna K Kähler, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Deep learning-based polygenic scores enhance generalizability of psychiatric disorders predictionLeonardo Cobuccio, Arnor I Sigurdsson, Kajsa-Lotta Georgii Hellberg, et al.
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
Disruptive mutations in the serotonin transporter associate serotonin dysfunction with treatment-resistant affective disorderJonatan Fullerton Støier, Trine Nygaard Jørgensen, Thomas Sparsø, et al.
European Journal of Medical Genetics|November 14, 2015
Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a familyLinh T T Duong, Louise K Hoeffding, Kirsten B Petersen, et al.
Science Advances|June 29, 2022
Deep learning-based integration of genetics with registry data for stratification of schizophrenia and depressionRosa Lundbye Allesøe, Ron Nudel, Wesley K Thompson, et al.
Pageof 37

Showing results (81-90 of 362) with videos related to

Sort By:
Pageof 37
Schizophrenia Research|August 11, 2006
Analysis of coding-polymorphisms in NOTCH-related genes reveals NUMBL poly-glutamine repeat to be associated with schizophrenia in Brazilian and Danish subjectsSheila Passos Gregorio, Wagner F Gattaz, Hildeberto Tavares, et al.
European Journal of Epidemiology|July 8, 2026
Neonatal vitamin D levels and autoimmune disorders: a Danish population-based cohort studyHenriette Thisted Horsdal, Berit Heitmann, Sanne Grundvad Boelt, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 19, 2012
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic populationPeter Saetre, Jakob Grove, Anders D Børglum, et al.
BMC Cancer|August 6, 2010
No influence of the polymorphisms CYP2C19 and CYP2D6 on the efficacy of cyclophosphamide, thalidomide, and bortezomib in patients with Multiple MyelomaAnnette J Vangsted, Karen Søeby, Tobias W Klausen, et al.
Plos Genetics|December 30, 2015
An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association StudiesWesley K Thompson, Yunpeng Wang, Andrew J Schork, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|February 8, 2011
Dystrobrevin-binding protein 1 gene (DTNBP1) variants associated with cerebrospinal fluid homovanillic acid and 5-hydroxyindoleacetic acid concentrations in healthy volunteersDimitrios Andreou, Peter Saetre, Anna K Kähler, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2025
Deep learning-based polygenic scores enhance generalizability of psychiatric disorders predictionLeonardo Cobuccio, Arnor I Sigurdsson, Kajsa-Lotta Georgii Hellberg, et al.
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
Disruptive mutations in the serotonin transporter associate serotonin dysfunction with treatment-resistant affective disorderJonatan Fullerton Støier, Trine Nygaard Jørgensen, Thomas Sparsø, et al.
European Journal of Medical Genetics|November 14, 2015
Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a familyLinh T T Duong, Louise K Hoeffding, Kirsten B Petersen, et al.
Science Advances|June 29, 2022
Deep learning-based integration of genetics with registry data for stratification of schizophrenia and depressionRosa Lundbye Allesøe, Ron Nudel, Wesley K Thompson, et al.
Pageof 37