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Louise K Hoeffding

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Nordic Journal of Psychiatry|June 28, 2016
Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studiesLouise K Hoeffding, Anders Rosengren, Johan H Thygesen, et al.
Schizophrenia Bulletin|January 8, 2016
Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register StudyAnders Vangkilde, Line Olsen, Louise K Hoeffding, 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.
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.
Trials|August 11, 2017
A manual-based vocational rehabilitation program for patients with an acquired brain injury: study protocol of a pragmatic randomized controlled trial (RCT)Louise K Hoeffding, Maria Haahr Nielsen, Morten A Rasmussen, et al.
Nordic Journal of Psychiatry|November 13, 2015
Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disordersLouise K Hoeffding, Linh T T Duong, Andrés Ingason, et al.
BMC Neurology|October 17, 2018
Comorbidity of migraine with ADHD in adultsThomas Folkmann Hansen, Louise K Hoeffding, Lisette Kogelman, et al.
Translational Psychiatry|October 10, 2018
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorderTimothy Hughes, Ida E Sønderby, Tatiana Polushina, et al.
The Lancet. Psychiatry|June 11, 2018
Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort studyLine Olsen, Thomas Sparsø, Shantel M Weinsheimer, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Nordic Journal of Psychiatry|June 28, 2016
Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studiesLouise K Hoeffding, Anders Rosengren, Johan H Thygesen, et al.
Schizophrenia Bulletin|January 8, 2016
Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register StudyAnders Vangkilde, Line Olsen, Louise K Hoeffding, 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.
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.
Trials|August 11, 2017
A manual-based vocational rehabilitation program for patients with an acquired brain injury: study protocol of a pragmatic randomized controlled trial (RCT)Louise K Hoeffding, Maria Haahr Nielsen, Morten A Rasmussen, et al.
Nordic Journal of Psychiatry|November 13, 2015
Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disordersLouise K Hoeffding, Linh T T Duong, Andrés Ingason, et al.
BMC Neurology|October 17, 2018
Comorbidity of migraine with ADHD in adultsThomas Folkmann Hansen, Louise K Hoeffding, Lisette Kogelman, et al.
Translational Psychiatry|October 10, 2018
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorderTimothy Hughes, Ida E Sønderby, Tatiana Polushina, et al.
The Lancet. Psychiatry|June 11, 2018
Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort studyLine Olsen, Thomas Sparsø, Shantel M Weinsheimer, et al.
Pageof 1