What is he best known for?
The fields of study he is best known for:
Mark Leppert focuses on Genetics, Gene, Genetic linkage, Mutation and Genetic marker.
His study in Locus, Gene mapping, Allele, Genetic heterogeneity and Haplotype falls under the purview of Genetics.
The concepts of his Gene study are interwoven with issues in Molecular biology, Adenomatous polyposis coli and DNA.
His Genetic linkage study combines topics from a wide range of disciplines, such as Genetic analysis, Spinal muscular atrophy, Spinal muscular atrophies, Tandem repeat and Chromosome 7.
His Mutation research includes themes of Pathology, Hyperkalemic periodic paralysis and Exon.
His biological study deals with issues like Chromosome, which deal with fields such as Restriction fragment and Complete linkage.
His most cited work include:
- Genetic alterations during colorectal-tumor development. (5645 citations)
- A haplotype map of the human genome (5144 citations)
- The International HapMap Project (5051 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Genetics, DNA sequencing, DNA, Polymorphism and Chromosome.
His Genetic linkage, Nucleic acid sequence, Genetic marker, Restriction fragment and Gene mapping study are his primary interests in Genetics.
His research on Genetic linkage also deals with topics like
- Locus which connect with Allele and Genotype,
- Haplotype which intersects with area such as Single-nucleotide polymorphism.
He combines subjects such as Restriction fragment length polymorphism and Allele frequency with his study of Gene mapping.
His DNA study integrates concerns from other disciplines, such as Chromosome 15 and Molecular cloning.
His Gene research includes elements of Molecular biology, Internal medicine and Adenomatous polyposis coli.
He most often published in these fields:
- Genetics (82.41%)
- DNA sequencing (27.27%)
- DNA (26.28%)
What were the highlights of his more recent work (between 2005-2020)?
- Genetics (82.41%)
- Single-nucleotide polymorphism (5.14%)
- Haplotype (6.92%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Genetics, Single-nucleotide polymorphism, Haplotype, Gene and Internal medicine.
His research related to Genetic association, Locus, Genetic linkage, Allele and Genome-wide association study might be considered part of Genetics.
In his research, Body mass index is intimately related to Genomics, which falls under the overarching field of Single-nucleotide polymorphism.
His Haplotype study combines topics in areas such as Genetic determinism, Case-control study, Gene mapping and Heritability.
His work on Missense mutation, Sanger sequencing and Exon as part of general Gene research is frequently linked to Congenital diaphragmatic hernia, thereby connecting diverse disciplines of science.
Mark Leppert has included themes like Pathology, Endocrinology, Oncology and Cardiology in his Internal medicine study.
Between 2005 and 2020, his most popular works were:
- A second generation human haplotype map of over 3.1 million SNPs (3819 citations)
- Genome-wide detection and characterization of positive selection in human populations (1413 citations)
- A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes (924 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Mutation
- Internal medicine
Genetics, Single-nucleotide polymorphism, Haplotype, Genome-wide association study and Genetic association are his primary areas of study.
Allele, Locus, Genetic linkage, Gene and Frameshift mutation are the subjects of his Genetics studies.
The concepts of his Gene study are interwoven with issues in DNA and Cohort.
His Single-nucleotide polymorphism research is multidisciplinary, incorporating elements of Secondary hypertension and Internal medicine.
His Haplotype research is mostly focused on the topic International HapMap Project.
His Genetic association research includes elements of Molecular biology, Retinal, Blood serum and Genetic predisposition.
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