What is she best known for?
The fields of study she is best known for:
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.
Her most cited work include:
- Bayesian Selection of Continuous-Time Markov Chain Evolutionary Models (705 citations)
- Epigenetic Predictor of Age (494 citations)
- Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application (491 citations)
What are the main themes of her work throughout her whole career to date?
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.
She most often published in these fields:
- Genetics (40.32%)
- Internal medicine (20.16%)
- Gene (15.73%)
What were the highlights of her more recent work (between 2017-2021)?
- Genetics (40.32%)
- Gene (15.73%)
- Genome-wide association study (9.27%)
In recent papers she was focusing on the following fields of study:
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.
Between 2017 and 2021, her most popular works were:
- Diagnostic Utility of Transcriptome Sequencing for Rare Mendelian Diseases (34 citations)
- IRF2BPL Is Associated with Neurological Phenotypes. (33 citations)
- Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. (33 citations)
In her most recent research, the most cited papers focused on:
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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