What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Genetics, Cell biology, Allele, Hearing loss and Hair cell.
His study in Locus, Mutation, Usher syndrome, PCDH15 and Gene falls within the category of Genetics.
Andrew J. Griffith has researched Locus in several fields, including Haplotype and Frameshift mutation.
His Cell biology research incorporates elements of Stereocilia and Inner ear.
His Allele research incorporates themes from Vestibular aqueduct, Missense mutation and Pendred syndrome.
His Hearing loss study combines topics in areas such as Phenotype, Endocrinology, Internal medicine and Selective advantage.
His most cited work include:
- Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23 (440 citations)
- Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29. (367 citations)
- Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. (325 citations)
What are the main themes of his work throughout his whole career to date?
Andrew J. Griffith mainly focuses on Genetics, Hearing loss, Sensorineural hearing loss, Allele and Inner ear.
His Gene, Locus, Haplotype, Mutation and Genotype investigations are all subjects of Genetics research.
Andrew J. Griffith has included themes like Phenotype, Vestibular system and Pathology in his Hearing loss study.
The various areas that Andrew J. Griffith examines in his Allele study include Genotype-phenotype distinction and Autosomal recessive trait.
His studies deal with areas such as Cochlea and Cell biology as well as Inner ear.
The Vestibular aqueduct study combines topics in areas such as Internal medicine, Endocrinology and Pendred syndrome.
He most often published in these fields:
- Genetics (43.66%)
- Hearing loss (41.55%)
- Sensorineural hearing loss (19.72%)
What were the highlights of his more recent work (between 2013-2021)?
- Hearing loss (41.55%)
- Inner ear (16.90%)
- Vestibular aqueduct (15.49%)
In recent papers he was focusing on the following fields of study:
Andrew J. Griffith spends much of his time researching Hearing loss, Inner ear, Vestibular aqueduct, Audiology and Genetics.
His research integrates issues of Mutation, Pendred syndrome and Inflammasome in his study of Hearing loss.
As a part of the same scientific study, Andrew J. Griffith usually deals with the Mutation, concentrating on Disease progression and frequently concerns with Phenotype.
His Inner ear study integrates concerns from other disciplines, such as Acoustics, Cochlea and Cell biology.
His work on Allele and Genotype as part of general Genetics research is often related to Auditory Perceptual Disorder and Autism spectrum disorder, thus linking different fields of science.
His Hair cell research is multidisciplinary, incorporating elements of Mechanotransduction and mCherry.
Between 2013 and 2021, his most popular works were:
- TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia. (105 citations)
- Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss. (103 citations)
- Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome (77 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Hearing loss, Inner ear, Vestibular aqueduct, Vestibular system and Hair cell.
Andrew J. Griffith interconnects Genetics, Genetic heterogeneity and Allele in the investigation of issues within Hearing loss.
His biological study spans a wide range of topics, including Genotype and Exon.
His work on Stereocilia as part of general Inner ear study is frequently linked to Posterior Semicircular Canal, bridging the gap between disciplines.
The study incorporates disciplines such as Cochlea and Auditory brainstem response in addition to Vestibular aqueduct.
The concepts of his Hair cell study are interwoven with issues in Mutation, Mechanotransduction, Cell biology and Transmembrane protein.
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