What is he best known for?
The fields of study he is best known for:
- Gene
- Mutation
- Internal medicine
His main research concerns Genetics, Disease, Genetic heterogeneity, Allele and Internal medicine.
Locus, Gene, Chromosome, Human genetics and Mendelian inheritance are subfields of Genetics in which his conducts study.
His Disease study combines topics in areas such as Prevalence, Genetic testing, Kidney disease and Small population size.
His study in Allele is interdisciplinary in nature, drawing from both Gene mutation, Plasmodium falciparum, Malaria vaccine, Genetic association and Genotype.
His study looks at the relationship between Internal medicine and fields such as Endocrinology, as well as how they intersect with chemical problems.
His work in Candidate gene addresses subjects such as Pedigree chart, which are connected to disciplines such as Immunology.
His most cited work include:
- Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis (573 citations)
- Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. (441 citations)
- Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33 (294 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Genetics, Allele, Internal medicine, Locus and Pediatrics.
His Gene, Haplotype, Genetic linkage, Allele frequency and Genotype investigations are all subjects of Genetics research.
His primary area of study in Gene is in the field of Phenotype.
Internal medicine is frequently linked to Endocrinology in his study.
Locus connects with themes related to Penetrance in his study.
His biological study spans a wide range of topics, including Incidence and Disease.
He most often published in these fields:
- Genetics (44.67%)
- Allele (15.16%)
- Internal medicine (12.70%)
What were the highlights of his more recent work (between 2005-2015)?
- Genetics (44.67%)
- Disease (9.84%)
- Pediatrics (11.07%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in Genetics, Disease, Pediatrics, Allele and Locus.
His works in Mendelian inheritance, Genotype, Haplotype, Polymorphism and Genetic heterogeneity are all subjects of inquiry into Genetics.
His Haplotype course of study focuses on Immunology and Missense mutation.
Josué Feingold combines subjects such as European population and Retrospective cohort study with his study of Disease.
His studies deal with areas such as Endocrinology, Internal medicine and Indel as well as Allele.
The concepts of his Locus study are interwoven with issues in Linkage disequilibrium, Negative correlation, Allele frequency, Human leukocyte antigen and ABO blood group system.
Between 2005 and 2015, his most popular works were:
- Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis (573 citations)
- Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression. (169 citations)
- Long-term outcome of presymptomatic testing in Huntington disease. (88 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Mutation
- Internal medicine
The scientist’s investigation covers issues in Genetics, Disease, Pediatrics, Mendelian inheritance and Internal medicine.
Mutation, Allele, Non-coding RNA, Human genome and RNA are the primary areas of interest in his Genetics study.
His Disease research includes elements of Monogenic disease, Multivariate analysis, Psychopathology, Genetic counseling and Depression.
His Pediatrics study integrates concerns from other disciplines, such as Fetal alcohol syndrome, Pregnancy, Borderline intellectual functioning, Neuropsychology and Corpus callosum.
The Mendelian inheritance study combines topics in areas such as Mild form, Mutation, Modifier Genes, Disease expression and Human genetics.
His Internal medicine study frequently involves adjacent topics like MEFV.
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