What is she best known for?
The fields of study she is best known for:
Françoise Clerget-Darpoux mostly deals with Genetics, Allele, Genotype, Locus and Linkage.
Her Genetics study combines topics from a wide range of disciplines, such as Disease and Presenilin.
Within one scientific family, she focuses on topics pertaining to Internal medicine under Allele, and may sometimes address concerns connected to Endocrinology.
The study incorporates disciplines such as Epitope and Rheumatoid arthritis in addition to Genotype.
Her Locus research incorporates elements of Genetic marker, Genetic heterogeneity, Hla haplotypes and Genetic model.
The Linkage study combines topics in areas such as Transmission disequilibrium test, Genome and Genome Scan.
Her most cited work include:
- Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum (587 citations)
- Effects of misspecifying genetic parameters in lod score analysis. (401 citations)
- Gene for Chronic Proximal Spinal Muscular Atrophies Maps To Chromosome-5q (315 citations)
What are the main themes of her work throughout her whole career to date?
Her primary areas of study are Genetics, Allele, Locus, Genetic linkage and Disease.
Gene, Human leukocyte antigen, Genotype, Genetic marker and Linkage are the primary areas of interest in her Genetics study.
Her biological study spans a wide range of topics, including Apolipoprotein E and Risk factor.
Her Locus study incorporates themes from Genetic heterogeneity, Genetic model and Gene mapping.
Her Genetic linkage research focuses on Linkage disequilibrium and how it connects with Genetic association.
Françoise Clerget-Darpoux interconnects Mendelian inheritance and Mutation in the investigation of issues within Disease.
She most often published in these fields:
- Genetics (74.64%)
- Allele (23.92%)
- Locus (24.40%)
What were the highlights of her more recent work (between 2004-2015)?
- Genetics (74.64%)
- Gene (19.62%)
- Locus (24.40%)
In recent papers she was focusing on the following fields of study:
Her primary areas of investigation include Genetics, Gene, Locus, Genotype and Single-nucleotide polymorphism.
Her Genetics study frequently links to other fields, such as Disease.
In Gene, Françoise Clerget-Darpoux works on issues like Odds ratio, which are connected to Pathogenesis and Young adult.
Her work investigates the relationship between Locus and topics such as Genetic marker that intersect with problems in Juvenile, Sibling and Phenotype.
Her Genotype research is multidisciplinary, incorporating perspectives in Allele and Immunology.
Her Genetic linkage study combines topics from a wide range of disciplines, such as Evolutionary biology, Genetic model and Linkage.
Between 2004 and 2015, her most popular works were:
- New classification of HLA-DRB1 alleles supports the shared epitope hypothesis of rheumatoid arthritis susceptibility. (161 citations)
- Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA (160 citations)
- Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA (160 citations)
In her most recent research, the most cited papers focused on:
Her scientific interests lie mostly in Genetics, Genotype, Immunology, Allele and Disease.
Genetics is frequently linked to snRNP in her study.
Her work in Genotype covers topics such as Locus which are related to areas like OCA2, Genetic predisposition, Melanocortin 1 receptor, Eye color and Susceptibility gene.
Her Immunology research integrates issues from Cohort study, First-degree relatives, Genetic counseling, Risk Estimate and Pediatrics.
Her research integrates issues of Monogenic disease, Human genetics and Mendelian inheritance in her study of Disease.
She works mostly in the field of Gene, limiting it down to topics relating to Odds ratio and, in certain cases, Multiple sclerosis, Human leukocyte antigen and SNP, as a part of the same area of interest.
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