Nelson B. Freimer mostly deals with Genetics, Genome-wide association study, Genetic association, Schizophrenia and Bipolar disorder. His Genetics study frequently draws connections between adjacent fields such as Body mass index. Genome-wide association study is a primary field of his research addressed under Single-nucleotide polymorphism.
The Genetic association study combines topics in areas such as Meta-analysis and Hemodynamics. His Schizophrenia study combines topics in areas such as Alzheimer's Disease Neuroimaging Initiative, Psychosis, Neuroscience and Bioinformatics. His work carried out in the field of Bipolar disorder brings together such families of science as Cardiology, Thalamus, Major depressive disorder, Genetic heterogeneity and Computational biology.
His main research concerns Genetics, Genome-wide association study, Bipolar disorder, Genetic association and Psychiatry. His studies in Locus, Linkage disequilibrium, Genetic linkage, Single-nucleotide polymorphism and Allele are all subfields of Genetics research. The various areas that Nelson B. Freimer examines in his Single-nucleotide polymorphism study include Internal medicine and Genotyping.
His Genome-wide association study research includes themes of Quantitative trait locus, Genetic architecture, Tourette syndrome and Copy-number variation. His research in Bipolar disorder intersects with topics in Schizophrenia and Clinical psychology. His work carried out in the field of Schizophrenia brings together such families of science as Major depressive disorder and Psychosis.
Nelson B. Freimer mainly focuses on Genetics, Genome-wide association study, Gene, Bipolar disorder and Hyperlipidemia. His study in Phenotype, Exome sequencing, Genetic association, Quantitative trait locus and Allele are all subfields of Genetics. His work in Genetic association addresses subjects such as Structural variation, which are connected to disciplines such as Genotype.
The various areas that Nelson B. Freimer examines in his Genome-wide association study study include Genome and Copy-number variation. His studies deal with areas such as Neuroscience, Cell adhesion molecule and Tourette syndrome as well as Gene. His Bipolar disorder research incorporates elements of Pedigree chart, Druggability, Expression quantitative trait loci, Prefrontal cortex and Neurocognitive.
Nelson B. Freimer mainly investigates Genetics, Genome-wide association study, Gene, Bipolar disorder and Copy-number variation. As part of his studies on Genetics, Nelson B. Freimer often connects relevant areas like Disease. His Genome-wide association study study incorporates themes from Genotyping and Genome, Deep sequencing, Genomics.
In general Gene, his work in Expression quantitative trait loci, Druggability and Gene expression is often linked to Furin linking many areas of study. His work deals with themes such as Major depressive disorder, Genetic heterogeneity and Psychosis, which intersect with Bipolar disorder. His studies in Copy-number variation integrate themes in fields like Microarray, SNP genotyping and Pedigree chart.
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Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters.
Nature (2014)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Genome-wide association study identifies five new schizophrenia loci
Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)
Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Nature (2010)
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)
Variance component model to account for sample structure in genome-wide association studies
Hyun Min Kang;Jae Hoon Sul;Noah A. Zaitlen.
Nature Genetics (2010)
Mutational processes of simple-sequence repeat loci in human populations.
A Di Rienzo;A C Peterson;J C Garza;A M Valdes.
Proceedings of the National Academy of Sciences of the United States of America (1994)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Nature (2008)
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