What is he best known for?
The fields of study he is best known for:
Genetics, Molecular biology, Cystic fibrosis, Gene and Cystic fibrosis transmembrane conductance regulator are his primary areas of study.
His is involved in several facets of Genetics study, as is seen by his studies on Human genome, Segmental duplication, Locus, Chromosome 7 and Gene mapping.
His Molecular biology study integrates concerns from other disciplines, such as Positional cloning, In situ hybridization, Somatostatin receptor, Kinase and Gene isoform.
The concepts of his Cystic fibrosis study are interwoven with issues in Endocrinology, Mutation and Polymerase chain reaction.
In general Gene, his work in Coding region, Gene expression, Exon and Alternative splicing is often linked to Substitution linking many areas of study.
His Cystic fibrosis transmembrane conductance regulator research is multidisciplinary, relying on both Dephosphorylation, Mutation, Phenotype, Frameshift mutation and Chloride channel.
His most cited work include:
- Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas (1328 citations)
- Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. (985 citations)
- MADR2 maps to 18q21 and encodes a TGFβ-regulated MAD-related protein that is functionally mutated in colorectal carcinoma (798 citations)
What are the main themes of his work throughout his whole career to date?
His main research concerns Genetics, Molecular biology, Gene, Cystic fibrosis and Gene mapping.
His is involved in several facets of Genetics study, as is seen by his studies on Exon, Locus, Chromosome 7, Genetic marker and Chromosome.
His Molecular biology research includes themes of Recombinant DNA, Transfection, DNA, Complementary DNA and Fluorescence in situ hybridization.
In his research on the topic of Cystic fibrosis, Gene mutation is strongly related with Endocrinology.
His Cystic fibrosis transmembrane conductance regulator study incorporates themes from Phenotype and Chloride channel.
His studies deal with areas such as Gastroenterology and Allele as well as Internal medicine.
He most often published in these fields:
- Genetics (55.00%)
- Molecular biology (37.14%)
- Gene (32.86%)
What were the highlights of his more recent work (between 2001-2016)?
- Genetics (55.00%)
- Internal medicine (14.64%)
- Cystic fibrosis (23.93%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Genetics, Internal medicine, Cystic fibrosis, Endocrinology and Exon.
His Genetics research focuses on Gene, Locus, Segmental duplication, Human genome and Genome.
He is interested in Cystic fibrosis transmembrane conductance regulator, which is a branch of Cystic fibrosis.
Lap-Chee Tsui has included themes like Cell culture and Allele in his Endocrinology study.
His research integrates issues of RNA splicing and Intron in his study of Exon.
The study incorporates disciplines such as Molecular biology and Single-nucleotide polymorphism in addition to Complementary DNA.
Between 2001 and 2016, his most popular works were:
- Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence (219 citations)
- Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence (219 citations)
- Human Chromosome 7: DNA Sequence and Biology (180 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Genetics, Cystic fibrosis, Segmental duplication, Human genome and Internal medicine.
His Cystic fibrosis research focuses on Cystic fibrosis transmembrane conductance regulator in particular.
Lap-Chee Tsui focuses mostly in the field of Segmental duplication, narrowing it down to matters related to Chromosome 22 and, in some cases, DNA sequencing, Chromosome 7, Chromosome 21 and Chromosome 19.
His Human genome study combines topics in areas such as Chromosome regions, Chromosome, Structural variation and Copy-number variation.
His work deals with themes such as Heterozygote advantage, Endocrinology, Genotyping and Gastroenterology, which intersect with Internal medicine.
His Exon research focuses on Missense mutation and how it connects with Allele.
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