What is he best known for?
The fields of study he is best known for:
- Gene
- Mutation
- Internal medicine
Lee-Jun C. Wong mainly focuses on Genetics, Mitochondrial DNA, Mitochondrial disease, Mutation and Point mutation.
His work in Gene, Human mitochondrial genetics, Homoplasmy, Allele and Prenatal diagnosis are all subfields of Genetics research.
His Mitochondrial DNA research incorporates elements of Molecular biology, Mitochondrion and Polymerase chain reaction.
His Mitochondrial disease research incorporates themes from Genome, Nuclear gene, Massive parallel sequencing, Mitochondrial respiratory chain and Hypotonia.
The various areas that Lee-Jun C. Wong examines in his Mutation study include Pathology and Somatic cell.
As a part of the same scientific family, Lee-Jun C. Wong mostly works in the field of Point mutation, focusing on Lactic acidosis and, on occasion, Virology and Encephalopathy.
His most cited work include:
- The in-depth evaluation of suspected mitochondrial disease. (269 citations)
- Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses (256 citations)
- Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer. (224 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of study are Genetics, Mitochondrial DNA, Mutation, Mitochondrial disease and Molecular biology.
His work is connected to Gene, Point mutation, Missense mutation, DNA sequencing and Massive parallel sequencing, as a part of Genetics.
His Missense mutation research integrates issues from Compound heterozygosity and Myopathy.
His work deals with themes such as Genome, Mitochondrion and Pathology, which intersect with Mitochondrial DNA.
The study incorporates disciplines such as Internal medicine, Cystic fibrosis, Cystic fibrosis transmembrane conductance regulator and Endocrinology in addition to Mutation.
Lee-Jun C. Wong has researched Mitochondrial disease in several fields, including Lactic acidosis, Homoplasmy and Nuclear gene.
He most often published in these fields:
- Genetics (55.21%)
- Mitochondrial DNA (35.49%)
- Mutation (21.97%)
What were the highlights of his more recent work (between 2016-2020)?
- Genetics (55.21%)
- Mitochondrial DNA (35.49%)
- Heteroplasmy (14.93%)
In recent papers he was focusing on the following fields of study:
Lee-Jun C. Wong focuses on Genetics, Mitochondrial DNA, Heteroplasmy, Gene and Computational biology.
His research in Phenotype, Missense mutation, Exome sequencing, Mendelian inheritance and Amplicon are components of Genetics.
The concepts of his Mitochondrial DNA study are interwoven with issues in Lactic acidosis, Evolutionary biology, Myopathy, Paternal Inheritance and Mitochondrion.
Lee-Jun C. Wong has included themes like Mutation, Molecular biology, SUCLA2 and Pyruvate dehydrogenase complex in his Lactic acidosis study.
His study in Heteroplasmy is interdisciplinary in nature, drawing from both Offspring, Proband, Mitochondrial disease, Respiratory chain and Massive parallel sequencing.
His biological study spans a wide range of topics, including Comparative genomic hybridization, Mitochondrial trna, DNA sequencing and Human genome.
Between 2016 and 2020, his most popular works were:
- Biparental Inheritance of Mitochondrial DNA in Humans. (159 citations)
- Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders. (133 citations)
- Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA (69 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Mutation
- Internal medicine
Genetics, Mitochondrial DNA, Phenotype, Genotype and Gene are his primary areas of study.
Genetics is a component of his Heteroplasmy, Exome sequencing, Genetic heterogeneity, Amplicon and Missense mutation studies.
His Mitochondrial DNA research includes elements of Offspring, Cerebral atrophy, Myopathy, Paternal Inheritance and Mitochondrion.
His Mitochondrion research includes themes of FBXL4, Mitochondrial Encephalomyopathies, Human mitochondrial genetics, Microcephaly and Hypotonia.
His Genotype study incorporates themes from Collagen VI, Epidemiology, Congenital muscular dystrophy, Disease and Nonsense mutation.
His research integrates issues of Prenatal diagnosis, Fetus and Family history in his study of Gene.
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.
