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Thomas Werge

Showing results (71-80 of 362) with videos related to

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Translational Psychiatry|August 16, 2022
Maternal pregnancy-related infections and autism spectrum disorder-the genetic perspectiveRon Nudel, Wesley K Thompson, Anders D Børglum, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2022
A comprehensive map of genetic relationships among diagnostic categories based on 48.6 million relative pairs from the Danish genealogyGeorgios Athanasiadis, Joeri J Meijsen, Dorte Helenius, et al.
JAMA Psychiatry|January 24, 2017
Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based StudyLouise K Hoeffding, Betina B Trabjerg, Line Olsen, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2023
Polygenic analyses show important differences between MDD symptoms collected using PHQ9 and CIDI-SFLianyun Huang, Sonja Tang, Jolien Rietkerk, et al.
Biological Psychiatry|December 6, 2023
Polygenic Analyses Show Important Differences Between Major Depressive Disorder Symptoms Measured Using Various InstrumentsLianyun Huang, Sonja Tang, Jolien Rietkerk, et al.
Schizophrenia Research|February 18, 2006
No significant association of the 5' end of neuregulin 1 and schizophrenia in a large Danish sampleAndrés Ingason, Karen Søeby, Sally Timm, et al.
Translational Psychiatry|December 14, 2023
Metabolic signature of the pathogenic 22q11.2 deletion identifies carriers and provides insight into systemic dysregulationJulie Courraud, Francesco Russo, Gonçalo Espregueira Themudo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 17, 2012
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersLinh Duong, Laura L Klitten, Rikke S Møller, et al.
Acta Neuropsychiatrica|March 28, 2020
Association between GLP-1 receptor gene polymorphisms with reward learning, anhedonia and depression diagnosisHale Yapici-Eser, Vivek Appadurai, Candan Yasemin Eren, et al.
Schizophrenia Research|August 27, 2019
Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophreniaChristiane Gasse, Theresa Wimberley, Yungpeng Wang, et al.
Pageof 37

Showing results (71-80 of 362) with videos related to

Sort By:
Pageof 37
Translational Psychiatry|August 16, 2022
Maternal pregnancy-related infections and autism spectrum disorder-the genetic perspectiveRon Nudel, Wesley K Thompson, Anders D Børglum, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2022
A comprehensive map of genetic relationships among diagnostic categories based on 48.6 million relative pairs from the Danish genealogyGeorgios Athanasiadis, Joeri J Meijsen, Dorte Helenius, et al.
JAMA Psychiatry|January 24, 2017
Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based StudyLouise K Hoeffding, Betina B Trabjerg, Line Olsen, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2023
Polygenic analyses show important differences between MDD symptoms collected using PHQ9 and CIDI-SFLianyun Huang, Sonja Tang, Jolien Rietkerk, et al.
Biological Psychiatry|December 6, 2023
Polygenic Analyses Show Important Differences Between Major Depressive Disorder Symptoms Measured Using Various InstrumentsLianyun Huang, Sonja Tang, Jolien Rietkerk, et al.
Schizophrenia Research|February 18, 2006
No significant association of the 5' end of neuregulin 1 and schizophrenia in a large Danish sampleAndrés Ingason, Karen Søeby, Sally Timm, et al.
Translational Psychiatry|December 14, 2023
Metabolic signature of the pathogenic 22q11.2 deletion identifies carriers and provides insight into systemic dysregulationJulie Courraud, Francesco Russo, Gonçalo Espregueira Themudo, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 17, 2012
Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersLinh Duong, Laura L Klitten, Rikke S Møller, et al.
Acta Neuropsychiatrica|March 28, 2020
Association between GLP-1 receptor gene polymorphisms with reward learning, anhedonia and depression diagnosisHale Yapici-Eser, Vivek Appadurai, Candan Yasemin Eren, et al.
Schizophrenia Research|August 27, 2019
Schizophrenia polygenic risk scores, urbanicity and treatment-resistant schizophreniaChristiane Gasse, Theresa Wimberley, Yungpeng Wang, et al.
Pageof 37