What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Genetics, Gene, Molecular biology, IRF6 and Van der Woude syndrome.
Brian C. Schutte regularly links together related areas like Etiology in his Genetics studies.
His Gene research is multidisciplinary, incorporating elements of Chemokine and Antimicrobial peptides.
The concepts of his IRF6 study are interwoven with issues in Genetic variation and Haplotype.
His study in Van der Woude syndrome is interdisciplinary in nature, drawing from both Linkage disequilibrium, Popliteal pterygium syndrome, TFAP2A, Haploinsufficiency and Genotype.
His studies in Mutation integrate themes in fields like Transfection, Receptor, TLR4, Pathophysiology and In vivo.
His most cited work include:
- TLR4 mutations are associated with endotoxin hyporesponsiveness in humans. (1797 citations)
- Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. (644 citations)
- Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. (477 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Genetics, IRF6, Van der Woude syndrome, Gene and Molecular biology.
His is involved in several facets of Genetics study, as is seen by his studies on Locus, Missense mutation, Mutation, Candidate gene and Genotype.
His IRF6 study deals with Surgery intersecting with Dermatology.
Brian C. Schutte has researched Van der Woude syndrome in several fields, including Popliteal pterygium syndrome, Haploinsufficiency, Chromosome, Penetrance and Hypodontia.
The various areas that Brian C. Schutte examines in his Gene study include Antimicrobial and Antimicrobial peptides.
In Molecular biology, Brian C. Schutte works on issues like Enhancer, which are connected to Binding site.
He most often published in these fields:
- Genetics (35.16%)
- IRF6 (26.56%)
- Van der Woude syndrome (26.56%)
What were the highlights of his more recent work (between 2012-2021)?
- IRF6 (26.56%)
- Genetics (35.16%)
- Van der Woude syndrome (26.56%)
In recent papers he was focusing on the following fields of study:
His primary scientific interests are in IRF6, Genetics, Van der Woude syndrome, Gene and Interferon regulatory factors.
His IRF6 study combines topics from a wide range of disciplines, such as TFAP2A, Endocrinology, Exome and Cell biology.
His research links Cohort with Genetics.
Many of his studies involve connections with topics such as Popliteal pterygium syndrome and Van der Woude syndrome.
He combines subjects such as Enhancer, Embryonic stem cell, Molecular biology and Effector with his study of Interferon regulatory factors.
His Mutation research includes themes of Haploinsufficiency and Genome-wide association study.
Between 2012 and 2021, his most popular works were:
- Dominant mutations in GRHL3 cause Van der Woude syndrome and disrupt oral periderm development (126 citations)
- Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci (104 citations)
- Interferon Regulatory Factor 6 promotes differentiation of the periderm by activating expression of Grainyhead-like 3 (83 citations)
In his most recent research, the most cited papers focused on:
His primary areas of study are Genetics, IRF6, Van der Woude syndrome, Interferon regulatory factors and Popliteal pterygium syndrome.
His work is connected to Mutation, Candidate gene and Gene, as a part of Genetics.
His IRF6 research includes elements of Craniofacial, Craniofacial abnormality, Anatomy and Mandible.
His Van der Woude syndrome study frequently draws parallels with other fields, such as Popliteal pterygium.
His work carried out in the field of Interferon regulatory factors brings together such families of science as Enhancer, Embryonic stem cell, Molecular biology and Effector.
His Popliteal pterygium syndrome research incorporates themes from Syndactyly and Exome.
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