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 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.
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.
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.
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.
Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis
Slaheddine Marrakchi;Philippe Guigue;Blair R. Renshaw;Anne Puel.
The New England Journal of Medicine (2011)
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.
Anne Philippe;Anne Philippe;Maria Martinez;Michel Guilloud-Bataille;Christopher Gillberg.
Human Molecular Genetics (1999)
The γ e4 allele of the apolipoprotein E gene as a potential protective factor for exudative age-related macular degeneration
Eric H. Souied;Pascale Benlian;Philippe Amouyel;Josue Feingold.
American Journal of Ophthalmology (1998)
Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33
Sandrine Marquet;Laurent Abel;Dominique Hillaire;Hélia Dessein.
Nature Genetics (1996)
Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression.
Fanny Mochel;Perrine Charles;François Seguin;Julie Barritault.
PLOS ONE (2007)
Genome Screen for Asthma and Related Phenotypes in the French EGEA Study
Marie-Hélène Dizier;Céline Besse-Schmittler;Michel Guilloud-Bataille;Isabella Annesi-Maesano.
American Journal of Respiratory and Critical Care Medicine (2000)
Association Between the Tryptophan Hydroxylase Gene and Manic-depressive Illness
Frank Bellivier;Marion Leboyer;Philippe Courtet;Catherine Buresi.
Archives of General Psychiatry (1998)
Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.
Marion Leboyer;Anne Philippe;Manuel Bouvard;Michel Guilloud-Bataille.
Biological Psychiatry (1999)
Genetic heterogeneity of Alport syndrome.
Josué Feingold;Etienne Bois;Agnès Chompert;Michel Broyer.
Kidney International (1985)
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.
Beckmann Js;Richard I;Hillaire D;Broux O.
Comptes Rendus De L Academie Des Sciences Serie Iii-sciences De La Vie-life Sciences (1991)
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