Clyde Francks mainly investigates Genetics, Genome-wide association study, Single-nucleotide polymorphism, Locus and Neuroscience. Much of his study explores Genetics relationship to Autism. His studies in Genome-wide association study integrate themes in fields like Anatomy & histology, Schizophrenia, Medical genetics, Hippocampal formation and Human brain.
His work on SNP, ANK3 and Tag SNP as part of general Single-nucleotide polymorphism research is often related to Poison control, thus linking different fields of science. In the field of Neuroscience, his study on Basal ganglia, Putamen and Caudate nucleus overlaps with subjects such as Striatum. He has included themes like Alzheimer's Disease Neuroimaging Initiative, Clinical psychology, Neuroimaging and Neuropsychology in his Voxel-based morphometry study.
The scientist’s investigation covers issues in Neuroscience, Genetics, Brain asymmetry, Genome-wide association study and Human brain. His Neuroscience research is multidisciplinary, incorporating perspectives in Gene expression and Genetic architecture. His research related to Single-nucleotide polymorphism, Locus, Genetic linkage, Gene and Allele might be considered part of Genetics.
His Brain asymmetry research focuses on Autism spectrum disorder and how it connects with Attention deficit hyperactivity disorder and Clinical psychology. His Genome-wide association study research is multidisciplinary, relying on both Rapid automatized naming and Reading. His Human brain study combines topics in areas such as White matter, Forebrain and Laterality.
Clyde Francks mostly deals with Brain asymmetry, Neuroscience, Human brain, Autism and Autism spectrum disorder. His research integrates issues of Neuroimaging and Genetic association in his study of Brain asymmetry. His work carried out in the field of Neuroscience brings together such families of science as Divergence and Genetic architecture.
His Human brain study which covers White matter that intersects with Genetic correlation. His Autism study also includes
His main research concerns Neuroimaging, Neuroscience, Attention deficit hyperactivity disorder, Autism spectrum disorder and Major depressive disorder. His Neuroimaging research incorporates themes from Brain asymmetry, Lateralization of brain function, Meta-analysis and Clinical psychology. His Neuroscience study typically links adjacent topics like Schizophrenia.
His biological study spans a wide range of topics, including Genome-wide association study and Genetic variation. His Genome-wide association study research integrates issues from Cerebral cortex, Cortex, Brain mapping and Genetic architecture. Clyde Francks interconnects SNP, Genetics, Heritability, Polymorphism and Dyslexia in the investigation of issues within Bipolar disorder.
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Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium
Anthony Bailey;Amaia Hervas;Nicola Matthews;Sarah Palferman.
Human Molecular Genetics (1998)
Common genetic variants influence human subcortical brain structures.
Derrek P. Hibar;Jason L. Stein;Jason L. Stein;Miguel E. Renteria;Alejandro Arias-Vasquez.
Meta-analysis and imputation refines the association of 15q25 with smoking quantity
Jason Z. Liu;Federica Tozzi;Dawn M. Waterworth;Sreekumar G. Pillai.
Nature Genetics (2010)
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
Paul M. Thompson;Jason L. Stein;Sarah E. Medland;Derrek P. Hibar.
Brain Imaging and Behavior (2014)
A genome-wide investigation of SNPs and CNVs in schizophrenia
Anna C. Need;Dongliang Ge;Michael E. Weale;Jessica Maia.
PLOS Genetics (2009)
α-5/α-3 nicotinic receptor subunit alleles increase risk for heavy smoking
W. Berrettini;W. Berrettini;X. Yuan;F. Tozzi;K. Song.
Molecular Psychiatry (2008)
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
Clyde Francks;S. Maegawa;J. Laurén;B. S. Abrahams.
Molecular Psychiatry (2007)
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
María Soler Artigas;Daan W. Loth;Louise V. Wain;Sina A. Gharib.
Nature Genetics (2011)
A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder
Simon E. Fisher;Clyde Francks;James T. McCracken;James J. McGough.
American Journal of Human Genetics (2002)
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