2023 - Research.com Medicine in Finland Leader Award
2023 - Research.com Genetics in Finland Leader Award
2022 - Research.com Best Scientist Award
2022 - Research.com Genetics and Molecular Biology in Finland Leader Award
His scientific interests lie mostly in Genome-wide association study, Genetics, Genetic association, Allele and Quantitative trait locus. His Genome-wide association study study combines topics from a wide range of disciplines, such as Odds ratio, Internal medicine, Case-control study, Polymorphism and Genetic architecture. His research brings together the fields of Disease and Genetics.
His Genetic association research also works with subjects such as
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Gene, Internal medicine and Genetic association. His work in Genetics is not limited to one particular discipline; it also encompasses Disease. The study incorporates disciplines such as SNP, Polymorphism, Bioinformatics, Quantitative trait locus and Computational biology in addition to Genome-wide association study.
The various areas that Aarno Palotie examines in his Internal medicine study include Endocrinology, Oncology and Cardiology. His studies in Genetic association integrate themes in fields like Meta-analysis, Expression quantitative trait loci, Clinical psychology and Candidate gene. His Locus research integrates issues from Genetic linkage and Haplotype.
Aarno Palotie focuses on Genetics, Genome-wide association study, Internal medicine, Genetic association and Gene. His study focuses on the intersection of Genetics and fields such as Disease with connections in the field of Biobank. Aarno Palotie interconnects Case-control study, Allele, Allele frequency, Heritability and Computational biology in the investigation of issues within Genome-wide association study.
His Internal medicine study incorporates themes from Type 2 diabetes, Oncology and Hyperlipidemia. His research investigates the link between Genetic association and topics such as Clinical psychology that cross with problems in Schizophrenia and Major depressive disorder. In his study, Mendelian randomization and Single-nucleotide polymorphism is inextricably linked to Locus, which falls within the broad field of Genetic architecture.
His scientific interests lie mostly in Genome-wide association study, Genetics, Genetic association, Exome sequencing and Gene. His Genome-wide association study study integrates concerns from other disciplines, such as Schizophrenia, Quantitative trait locus, Genetic architecture, Allele and Comorbidity. The Genetics study which covers Disease that intersects with Biobank.
He combines subjects such as Meta-analysis, Pleiotropy, Immune system and Medical genetics with his study of Genetic association. His work deals with themes such as Autism, Intellectual disability and Allele frequency, which intersect with Exome sequencing. The concepts of his Gene study are interwoven with issues in Drug discovery and Kinase activity.
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.
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha.
Nature (2016)
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)
Integrating common and rare genetic variation in diverse human populations
D M Altshuler;R A Gibbs;L Peltonen.
Nature (2010)
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Nature (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)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Nature (2014)
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)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)
In vivo amplification of the androgen receptor gene and progression of human prostate cancer.
Tapio Visakorpi;Eija Hyytinen;Pasi Koivisto;Minna Tanner.
Nature Genetics (1995)
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
Thorlakur Jonsson;Jasvinder K. Atwal;Stacy Steinberg;Jon Snaedal.
Nature (2012)
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