2013 - Fellow of the Royal Society of Canada Academy of Science
Her primary areas of investigation include Genetics, Genome-wide association study, Protein tyrosine phosphatase, Cell biology and Phosphorylation. Many of her studies on Genetics apply to Disease as well. Her study in Genome-wide association study is interdisciplinary in nature, drawing from both Allele, Immunology, Primary biliary cirrhosis and Genetic association.
The various areas that Katherine A. Siminovitch examines in her Immunology study include Genotyping and Haplotype. Her Protein tyrosine phosphatase study integrates concerns from other disciplines, such as Molecular biology, Receptor tyrosine kinase and Proto-oncogene tyrosine-protein kinase Src. Her Cell biology study combines topics in areas such as Wiskott–Aldrich syndrome protein and T cell, T-cell receptor.
Her scientific interests lie mostly in Genetics, Immunology, Cell biology, Single-nucleotide polymorphism and Protein tyrosine phosphatase. Her Genetics study is mostly concerned with Locus, Genome-wide association study, Gene, Allele and Haplotype. Katherine A. Siminovitch combines subjects such as Disease and Inflammatory bowel disease with her study of Immunology.
Her work deals with themes such as Wiskott–Aldrich syndrome protein and T cell, T-cell receptor, which intersect with Cell biology. Her studies deal with areas such as Human leukocyte antigen and Bioinformatics as well as Single-nucleotide polymorphism. Her study looks at the intersection of Protein tyrosine phosphatase and topics like Proto-oncogene tyrosine-protein kinase Src with Tyrosine kinase.
Her scientific interests lie mostly in Genetics, Immunology, Single-nucleotide polymorphism, Genome-wide association study and Internal medicine. Her study in Locus, Haplotype, Allele, Allele frequency and Imputation is carried out as part of her Genetics studies. Her study on Immunology is mostly dedicated to connecting different topics, such as Gene.
The concepts of her Single-nucleotide polymorphism study are interwoven with issues in Regulation of gene expression, X chromosome and Genetic predisposition. Her biological study spans a wide range of topics, including Bioinformatics, Linkage disequilibrium, Disease, Genetic association and Candidate gene. Her studies in Internal medicine integrate themes in fields like Gastroenterology and Endocrinology.
Her primary scientific interests are in Genetics, Single-nucleotide polymorphism, Genome-wide association study, Immunology and Haplotype. Her Single-nucleotide polymorphism study is concerned with Gene in general. Her research integrates issues of Interferon and Virus in her study of Gene.
Her Genome-wide association study research is multidisciplinary, incorporating elements of Bioinformatics, Disease, Genetic association, Missing heritability problem and Candidate gene. The Immunology study combines topics in areas such as Case-control study and Genotype. Her Haplotype research incorporates themes from Human leukocyte antigen and Locus.
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.
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Yukinori Okada;Yukinori Okada;Di Wu;Di Wu;Di Wu;Gosia Trynka;Gosia Trynka;Towfique Raj;Towfique Raj.
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
Eli A Stahl;Soumya Raychaudhuri;Soumya Raychaudhuri;Elaine F Remmers;Gang Xie.
Nature Genetics (2010)
Functional variants of OCTN cation transporter genes are associated with Crohn disease.
Vanya D Peltekova;Richard F Wintle;Laurence A Rubin;Laurence A Rubin;Christopher I Amos.
Nature Genetics (2004)
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.
John D. Rioux;Mark J. Daly;Mark S. Silverberg;Kerstin Lindblad.
Nature Genetics (2001)
Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis
Soumya Raychaudhuri;Cynthia Sandor;Eli A. Stahl;Eli A. Stahl;Jan Freudenberg.
Nature Genetics (2012)
Motheaten and viable motheaten mice have mutations in the haematopoietic cell phosphatase gene
Hing Wo Tsui;Katherine A. Siminovitch;Katherine A. Siminovitch;Loretta de Souza;Florence W.L. Tsui;Florence W.L. Tsui.
Nature Genetics (1993)
Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
Gideon M. Hirschfield;Xiangdong Liu;Chun Xu;Yue Lu.
The New England Journal of Medicine (2009)
Recruitment and activation of PTP1C in negative regulation of antigen receptor signaling by Fc gamma RIIB1.
Daniele D'Ambrosio;Keli L. Hippen;Stacey A. Minskoff;Ira Mellman.
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.
John D. Rioux;Mark S. Silverberg;Mark J. Daly;A. Hillary Steinhart.
American Journal of Human Genetics (2000)
Pervasive sharing of genetic effects in autoimmune disease.
Chris Cotsapas;Benjamin F. Voight;Benjamin F. Voight;Elizabeth Rossin;Kasper Lage;Kasper Lage;Kasper Lage.
PLOS Genetics (2011)
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: