Her main research concerns Genetics, Genome-wide association study, Autism, Copy-number variation and Genetic linkage. Genetics is frequently linked to Autism spectrum disorder in her study. Her Genome-wide association study research is multidisciplinary, incorporating elements of Schizophrenia, Neuroimaging, Genetic association, Clinical psychology and Genetic variation.
Her research in Schizophrenia tackles topics such as Bipolar disorder which are related to areas like Major depressive disorder and Genetic heterogeneity. The study incorporates disciplines such as Gene duplication, Psychosis and Genetic architecture in addition to Copy-number variation. Rita M. Cantor has included themes like Genetic determinism and Polymorphic Microsatellite Marker in her Genetic linkage study.
Rita M. Cantor spends much of her time researching Genetics, Genome-wide association study, Genetic linkage, Allele and Locus. Her research investigates the connection with Genetics and areas like Autism which intersect with concerns in Genetic heterogeneity. Her research in Genome-wide association study focuses on subjects like Case-control study, which are connected to Odds ratio.
Her study in Genetic linkage is interdisciplinary in nature, drawing from both Quantitative trait locus, Chromosome, Linkage and Genetic marker. Her Allele research includes elements of Immunology and Candidate gene. Her Genetic association study incorporates themes from Bipolar disorder and Schizophrenia.
Her scientific interests lie mostly in Genetics, Genome-wide association study, Bipolar disorder, Genetic association and Quantitative trait locus. She frequently studies issues relating to Disease and Genetics. Her studies deal with areas such as Genetic linkage, Autism spectrum disorder, Locus, Heritability and Genetic variation as well as Genome-wide association study.
The various areas that she examines in her Bipolar disorder study include Whole blood, Schizophrenia, Transcriptome, Clinical psychology and Brain size. Rita M. Cantor has researched Genetic association in several fields, including Genetic architecture, Genetic heterogeneity, Psychiatry and Genomics. The Quantitative trait locus study combines topics in areas such as Expression quantitative trait loci, Linkage disequilibrium and Gene expression profiling.
Her primary scientific interests are in Genome-wide association study, Genetics, Bipolar disorder, Genetic association and Locus. Her studies in Genome-wide association study integrate themes in fields like Odds ratio, Quantitative trait locus, Developmental psychology, Genetic linkage and Genetic variation. The concepts of her Quantitative trait locus study are interwoven with issues in Linkage disequilibrium and Bioinformatics.
Her Genetics research includes themes of Autism and Autism spectrum disorder. Her Bipolar disorder study combines topics from a wide range of disciplines, such as Schizophrenia, Disease and Comorbidity. Rita M. Cantor focuses mostly in the field of Genetic association, narrowing it down to matters related to Genomics and, in some cases, Meta-analysis, Genotyping, Dysbiosis, Histone methylation and Psychiatric genetics.
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.
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters.
Human polymorphism at microRNAs and microRNA target sites.
Liuqing Yang;Chunru Lin;Chunyu Jin;Joy C. Yang.
Frontiers in Genetics (2013)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
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)
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.
Genome-wide association study identifies five new schizophrenia loci
Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
Irina Voineagu;Xinchen Wang;Patrick G Johnston;Jennifer K Lowe.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J. Sanders;A. Gulhan Ercan-Sencicek;Vanessa Hus;Rui Luo.
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang;Haitao Zhang;Deqiong Ma;Maja Bucan.
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: