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 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
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.
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.
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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Genetic alterations during colorectal-tumor development.
Bert Vogelstein;Eric R. Fearon;Stanley R. Hamilton;Scott E. Kern.
The New England Journal of Medicine (1988)
The International HapMap Project
John W. Belmont;Paul Hardenbol;Thomas D. Willis;Fuli Yu.
A haplotype map of the human genome
John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol.
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds.
Identification and characterization of the familial adenomatous polyposis coli gene
Joanna Groden;Andrew Thliveris;Andrew Thliveris;Wade Samowitz;Mary Carlson.
Variable number of tandem repeat (VNTR) markers for human gene mapping
Yusuke Nakamura;Mark Leppert;Peter O'Connell;Roger Wolff.
Genome-wide detection and characterization of positive selection in human populations
Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller.
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
Rando Allikmets;Nanda Singh;Hui Sun;Noah F. Shroyer.
Nature Genetics (1997)
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
N. A. Singh;Carole Charlier;D. Stauffer;B. R. DuPont.
Nature Genetics (1998)
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
Ewart Ak;Morris Ca;Atkinson D;Jin W.
Nature Genetics (1993)
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