2023 - Research.com Psychology in Netherlands Leader Award
2022 - Research.com Best Female Scientist Award
2017 - Royal Netherlands Academy of Arts and Sciences
2015 - Member of Academia Europaea
Her scientific interests lie mostly in Genome-wide association study, Attention deficit hyperactivity disorder, Genetics, Neuroscience and Candidate gene. Her work carried out in the field of Genome-wide association study brings together such families of science as Bipolar disorder, Hippocampal formation, Neuroimaging, Heritability and Genetic architecture. The Attention deficit hyperactivity disorder study combines topics in areas such as Conduct disorder, Twin study and Autism spectrum disorder.
As a member of one scientific family, Barbara Franke mostly works in the field of Neuroscience, focusing on Voxel-based morphometry and, on occasion, Imaging genetics, Anterior cingulate cortex, Amygdala, Atrophy and Prefrontal cortex. Barbara Franke usually deals with Candidate gene and limits it to topics linked to Phenotype and Disease. Her Single-nucleotide polymorphism study integrates concerns from other disciplines, such as Quantitative trait locus and Allele.
Her primary areas of study are Attention deficit hyperactivity disorder, Genetics, Neuroscience, Clinical psychology and Psychiatry. In her work, White matter is strongly intertwined with Audiology, which is a subfield of Attention deficit hyperactivity disorder. Genetics is represented through her Single-nucleotide polymorphism, Genome-wide association study, Candidate gene, Gene and Allele research.
Her Genome-wide association study research incorporates elements of Genetic architecture, Genetic association and Heritability. Her work in Neuroscience covers topics such as Schizophrenia which are related to areas like Bipolar disorder. Her work deals with themes such as Cognition and Aggression, which intersect with Clinical psychology.
Barbara Franke mainly focuses on Attention deficit hyperactivity disorder, Clinical psychology, Neuroimaging, Autism spectrum disorder and Genetics. Her studies deal with areas such as Genome-wide association study, Audiology, Association, Impulsivity and Neurodevelopmental disorder as well as Attention deficit hyperactivity disorder. Her Genome-wide association study research is multidisciplinary, incorporating elements of Genetic association and Genetic architecture.
Her study with Neuroimaging involves better knowledge in Neuroscience. Her Autism spectrum disorder study also includes
Her main research concerns Attention deficit hyperactivity disorder, Neuroscience, Genetic association, Clinical psychology and Autism spectrum disorder. Her biological study spans a wide range of topics, including Gut flora, Genome-wide association study, Audiology, Brain Structure and Function and Neurodevelopmental disorder. Barbara Franke has researched Genome-wide association study in several fields, including Odds ratio, Heritability and Genetic architecture.
As part of one scientific family, she deals mainly with the area of Neuroscience, narrowing it down to issues related to the Schizophrenia, and often Brain morphometry. Genetic association is the subject of her research, which falls under Single-nucleotide polymorphism. Her studies in Autism spectrum disorder integrate themes in fields like Brain asymmetry and Neuroimaging.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Common variants conferring risk of schizophrenia
Hreinn Stefansson;Hreinn Stefansson;Roel A. Ophoff;Roel A. Ophoff;Roel A. Ophoff;Stacy Steinberg;Stacy Steinberg;Ole A. Andreassen.
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Ditte Demontis;Ditte Demontis;Raymond K Walters;Raymond K Walters;Joanna Martin;Joanna Martin;Joanna Martin;Manuel Mattheisen.
Nature Genetics (2019)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Genome-wide association study identifies 74 loci associated with educational attainment
Aysu Okbay;Jonathan P. Beauchamp;Mark Alan Fontana;James J. Lee.
Common genetic variants influence human subcortical brain structures.
Derrek P. Hibar;Jason L. Stein;Jason L. Stein;Miguel E. Renteria;Alejandro Arias-Vasquez.
Many sequence variants affecting diversity of adult human height
Daniel F Gudbjartsson;G Bragi Walters;Gudmar Thorleifsson;Hreinn Stefansson.
Nature Genetics (2008)
Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis
Martine Hoogman;Janita Bralten;Derrek P. Hibar;Maarten Mennes.
The Lancet Psychiatry (2017)
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.
K. Brookes;X. Xu;W. Chen;K. Zhou.
Molecular Psychiatry (2006)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: