2013 - Fellow of the American Statistical Association (ASA)
Janet S. Sinsheimer spends much of her time researching Genetics, Gene, Locus, Internal medicine and Linkage disequilibrium. Her research related to Haplotype, Single-nucleotide polymorphism, Genetic linkage, Linkage and Genome-wide association study might be considered part of Genetics. Gene and Young adult are frequently intertwined in her study.
Her biological study spans a wide range of topics, including Hypersociability, Genetic variation, Cohort and Genetic architecture. The concepts of her Internal medicine study are interwoven with issues in Endocrinology and Oncology. In her research on the topic of Chromosomal region, Allele is strongly related with Asperger syndrome.
Janet S. Sinsheimer focuses on Genetics, Internal medicine, Gene, Allele and Genotype. Locus, Single-nucleotide polymorphism, Genome-wide association study, Haplotype and Genetic association are the core of her Genetics study. Her Locus study frequently involves adjacent topics like Linkage disequilibrium.
The various areas that Janet S. Sinsheimer examines in her Single-nucleotide polymorphism study include Odds ratio and Allele frequency. Her studies in Internal medicine integrate themes in fields like Endocrinology and Oncology. The Genotype study combines topics in areas such as Offspring, Disease and Immunology.
Her primary scientific interests are in Genetics, Gene, Genome-wide association study, Hypotonia and Internal medicine. Her studies in Genome, Mitosis, H3F3B, Zebrafish and Histone are all subfields of Genetics research. Much of her study explores Gene relationship to Computational biology.
Her Genome-wide association study research incorporates themes from Univariate and Statistics, Generalized linear model, Linear regression, Covariate. Her work deals with themes such as Phenotype, Missense mutation, Intellectual disability, Neurodevelopmental disorder and Ataxia, which intersect with Hypotonia. Her research in Internal medicine tackles topics such as Oncology which are related to areas like Parkinson's disease, Men who have sex with men, Kaposi's sarcoma and Acquired immunodeficiency syndrome.
Janet S. Sinsheimer mainly focuses on Genetics, Missense mutation, Hypotonia, Gene and Phenotype. Her work in Gene expression profiling, Transcriptome and Genome-wide association study is related to Genetics. Her work focuses on many connections between Missense mutation and other disciplines, such as Ataxia, that overlap with her field of interest in eIF2B, Leukoencephalopathy, Immunology, Kinase activity and Leukodystrophy.
Her Hypotonia study combines topics in areas such as Neurodevelopmental disorder and Intellectual disability. Janet S. Sinsheimer interconnects Neuronal ceroid lipofuscinosis, Allele and Ectopic expression in the investigation of issues within Phenotype. Her research in Allele intersects with topics in WD40 repeat, CHARGE syndrome, Locus and Protein family.
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Bayesian Selection of Continuous-Time Markov Chain Evolutionary Models
Marc A. Suchard;Robert E. Weiss;Janet S. Sinsheimer.
Molecular Biology and Evolution (2001)
Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application
Rita M. Cantor;Kenneth Lange;Janet S. Sinsheimer.
American Journal of Human Genetics (2010)
Epigenetic Predictor of Age
Sven Bocklandt;Wen Lin;Mary E. Sehl;Francisco J. Sánchez.
PLOS ONE (2011)
Comparative Analysis of Proteome and Transcriptome Variation in Mouse
Anatole Ghazalpour;Brian Bennett;Vladislav A. Petyuk;Luz Orozco.
PLOS Genetics (2011)
Normal/Independent Distributions and Their Applications in Robust Regression
Kenneth Lange;Janet S. Sinsheimer.
Journal of Computational and Graphical Statistics (1993)
Familial combined hyperlipidemia is associated with upstream transcription factor 1 ( USF1 )
Päivi Pajukanta;Heidi E Lilja;Janet S Sinsheimer;Rita M Cantor.
Nature Genetics (2004)
Chromosome 1 loci in Finnish schizophrenia families
Jesper Ekelund;Iiris Hovatta;Alex Parker;Tiina Paunio.
Human Molecular Genetics (2001)
A Genomewide Screen for Autism-Spectrum Disorders: Evidence for a Major Susceptibility Locus on Chromosome 3q25-27
Mari Auranen;Raija Vanhala;Teppo Varilo;Kristin Ayers.
American Journal of Human Genetics (2002)
In vivo sequence diversity of the protease of human immunodeficiency virus type 1: presence of protease inhibitor-resistant variants in untreated subjects.
Walter J. Lech;Greg Wang;Yan Li Yang;Ying Chee.
Journal of Virology (1996)
GENETIC INFLUENCES IN END-STAGE OSTEOARTHRITIS: SIBLING RISKS OF HIP AND KNEE REPLACEMENT FOR IDIOPATHIC OSTEOARTHRITIS
Jai Chitnavis;Janet S. Sinsheimer;Kim Clipsham;John Loughlin.
Journal of Bone and Joint Surgery-british Volume (1997)
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