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Regina Waltes

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2015
The neurobiological basis of human aggression: A review on genetic and epigenetic mechanismsRegina Waltes, Andreas G Chiocchetti, Christine M Freitag
European Child & Adolescent Psychiatry|November 27, 2009
Genetics of autistic disorders: review and clinical implicationsChristine M Freitag, Wouter Staal, Sabine M Klauck, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|June 15, 2021
[Genetic risk factors and their influence on neural development in autism spectrum disorders]Christine M Freitag, Andreas G Chiocchetti, Denise Haslinger, et al.
Breast Cancer Research and Treatment|December 1, 2007
NBS1 variant I171V and breast cancer riskNatalia Bogdanova, Peter Schürmann, Regina Waltes, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 11, 2019
Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot studyRegina Waltes, Christine M Freitag, Timo Herlt, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 14, 2014
Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning rangeRegina Waltes, Johannes Gfesser, Denise Haslinger, et al.
Frontiers in Psychiatry|July 16, 2021
Anxiety Is Associated With DPPIV Alterations in Children With Selective Mutism and Social Anxiety Disorder: A Pilot StudyYulia Golub, Valeska Stonawski, Anne C Plank, et al.
American Journal of Human Genetics|May 5, 2009
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorderRegina Waltes, Reinhard Kalb, Magtouf Gatei, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 21, 2016
Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorderThorsten M Kranz, Marnie Kopp, Regina Waltes, et al.
International Journal of Cancer|October 25, 2007
Nijmegen Breakage Syndrome mutations and risk of breast cancerNatalia Bogdanova, Sergei Feshchenko, Peter Schürmann, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2015
The neurobiological basis of human aggression: A review on genetic and epigenetic mechanismsRegina Waltes, Andreas G Chiocchetti, Christine M Freitag
European Child & Adolescent Psychiatry|November 27, 2009
Genetics of autistic disorders: review and clinical implicationsChristine M Freitag, Wouter Staal, Sabine M Klauck, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie|June 15, 2021
[Genetic risk factors and their influence on neural development in autism spectrum disorders]Christine M Freitag, Andreas G Chiocchetti, Denise Haslinger, et al.
Breast Cancer Research and Treatment|December 1, 2007
NBS1 variant I171V and breast cancer riskNatalia Bogdanova, Peter Schürmann, Regina Waltes, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 11, 2019
Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot studyRegina Waltes, Christine M Freitag, Timo Herlt, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 14, 2014
Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning rangeRegina Waltes, Johannes Gfesser, Denise Haslinger, et al.
Frontiers in Psychiatry|July 16, 2021
Anxiety Is Associated With DPPIV Alterations in Children With Selective Mutism and Social Anxiety Disorder: A Pilot StudyYulia Golub, Valeska Stonawski, Anne C Plank, et al.
American Journal of Human Genetics|May 5, 2009
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorderRegina Waltes, Reinhard Kalb, Magtouf Gatei, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 21, 2016
Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorderThorsten M Kranz, Marnie Kopp, Regina Waltes, et al.
International Journal of Cancer|October 25, 2007
Nijmegen Breakage Syndrome mutations and risk of breast cancerNatalia Bogdanova, Sergei Feshchenko, Peter Schürmann, et al.
Pageof 3