What is he best known for?
The fields of study he is best known for:
His main research concerns Genetics, Hearing loss, Allele, Gene and Mutation.
His study in Locus, Mutation, Single-nucleotide polymorphism, Nonsyndromic deafness and Candidate gene are all subfields of Genetics.
His work on Sensorineural hearing loss as part of general Hearing loss research is frequently linked to GJB6, thereby connecting diverse disciplines of science.
His Allele research is multidisciplinary, incorporating elements of Wolfram syndrome, Diabetes mellitus genetics and Genotype.
Gene is frequently linked to Inner ear in his study.
His Point mutation study in the realm of Mutation connects with subjects such as Megakaryocyte.
His most cited work include:
- GJB2 mutations and degree of hearing loss: a multicenter study. (379 citations)
- Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics? (358 citations)
- Mutations in the human |[alpha]|-tectorin gene cause autosomal dominant non-syndromic hearing impairment (294 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Genetics, Hearing loss, Gene, Audiology and Mutation.
Locus, Single-nucleotide polymorphism, Allele, Genetic linkage and Mutation are the primary areas of interest in his Genetics study.
The Locus study combines topics in areas such as Genetic marker and Gene mapping.
His Single-nucleotide polymorphism research incorporates themes from Noise-induced hearing loss and Genetic variation.
His work in the fields of Sensorineural hearing loss overlaps with other areas such as TECTA.
Gene is closely attributed to Inner ear in his study.
He most often published in these fields:
- Genetics (49.65%)
- Hearing loss (35.31%)
- Gene (22.73%)
What were the highlights of his more recent work (between 2014-2021)?
- Genetics (49.65%)
- Cancer research (8.74%)
- Hearing loss (35.31%)
In recent papers he was focusing on the following fields of study:
Guy Van Camp spends much of his time researching Genetics, Cancer research, Hearing loss, DNA methylation and Gene.
His is involved in several facets of Genetics study, as is seen by his studies on Exome sequencing, Phenotype, Mutation, Sanger sequencing and Missense mutation.
His Cancer research study also includes fields such as
- Cancer which is related to area like Germline mutation, Exon and Exome,
- Colorectal cancer which intersects with area such as Wild type and Primary tumor.
His Hearing loss study is concerned with the field of Audiology as a whole.
Guy Van Camp has researched DNA methylation in several fields, including Carcinogenesis, Methylation, Epigenetics and Immunology.
When carried out as part of a general Gene research project, his work on Genome-wide association study and Single-nucleotide polymorphism is frequently linked to work in Keratoconus, therefore connecting diverse disciplines of study.
Between 2014 and 2021, his most popular works were:
- Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma (122 citations)
- Congenital hearing loss. (120 citations)
- Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia (71 citations)
In his most recent research, the most cited papers focused on:
Genetics, Hearing loss, Mutation, Cell biology and Cancer research are his primary areas of study.
His Genetics study frequently involves adjacent topics like Bioinformatics.
His work in the fields of Hearing loss, such as OTOF, overlaps with other areas such as MYO7A.
His study in the field of Frameshift mutation also crosses realms of Amelogenesis imperfecta.
Guy Van Camp focuses mostly in the field of Cell biology, narrowing it down to topics relating to Cochlea and, in certain cases, Synaptopathy.
His studies deal with areas such as Cancer cell, Cell culture, Neuroblastoma and Apoptosis as well as Cancer research.
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