Mihael H. Polymeropoulos spends much of his time researching Genetics, Gene, Gene mapping, Genetic marker and Human genome. His study brings together the fields of Parkinson's disease and Genetics. His Gene study combines topics from a wide range of disciplines, such as Molecular biology and Bioinformatics.
His work carried out in the field of Gene mapping brings together such families of science as Restriction fragment length polymorphism, Polymerase chain reaction and Allele frequency. His study in Genetic marker is interdisciplinary in nature, drawing from both Family aggregation and Degenerative disease. His studies in Human genome integrate themes in fields like Complementary DNA, Chromosome 4, Microsatellite Repeat and Atrophy.
Genetics, Gene, Gene mapping, Genetic marker and Internal medicine are his primary areas of study. The Genetics study which covers Molecular biology that intersects with Complementary DNA. Mihael H. Polymeropoulos has included themes like Parkinson's disease and Bioinformatics in his Gene study.
His Gene mapping research includes elements of Repeated sequence, Restriction fragment length polymorphism and Allele frequency. His Restriction fragment length polymorphism research incorporates themes from DNA, Molecular probe and Trinucleotide repeat expansion. His Internal medicine study integrates concerns from other disciplines, such as Endocrinology and Oncology.
Mihael H. Polymeropoulos focuses on Internal medicine, Sleep in non-human animals, Circadian rhythm, Gastroparesis and Nausea. The study incorporates disciplines such as Endocrinology and Placebo-controlled study in addition to Internal medicine. His research in Sleep in non-human animals intersects with topics in Anesthesia, Phase advance and Smith–Magenis syndrome.
His work is dedicated to discovering how Smith–Magenis syndrome, Psychiatry are connected with QT interval and Metabolite and other disciplines. His Circadian rhythm research is multidisciplinary, incorporating elements of Burden of disease and Period. In general Gastroparesis, his work in Idiopathic gastroparesis is often linked to Gastroenterology, Complete responder, Computational biology and Whole genome sequencing linking many areas of study.
Mihael H. Polymeropoulos mainly investigates Internal medicine, Gastroparesis, Atopic dermatitis, Nausea and Vomiting. His Internal medicine research focuses on Adverse effect in particular. His Adverse effect research incorporates elements of Seasickness, Motion sickness, Clinical endpoint, Clinical trial and Incidence.
His Atopic dermatitis research is multidisciplinary, incorporating perspectives in Loss function, Randomized controlled trial and Computational biology. The concepts of his Randomized controlled trial study are interwoven with issues in Dermatology and Eczema Area and Severity Index. As a part of the same scientific study, he usually deals with the Vomiting, concentrating on Placebo-controlled study and frequently concerns with Antagonist.
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Mutation in the α-synuclein gene identified in families with Parkinson's disease
Mihael H. Polymeropoulos;Christian Lavedan;Elisabeth Leroy;Susan E. Ide.
Complementary DNA sequencing : expressed sequence tags and human genome project
Mark D. Adams;Jenny M. Kelley;Jeannine D. Gocayne;Mark Dubnick.
The ubiquitin pathway in Parkinson's disease
Elisabeth Leroy;Rebecca Boyer;Georg Auburger;Barbara Leube.
The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression.
Greg Lennon;Charles Auffray;Mihael Polymeropoulos;Marcelo Bento Soares.
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
Robert Freedman;Hilary Coon;Marina Myles-Worsley;Avi Orr-Urtreger.
Proceedings of the National Academy of Sciences of the United States of America (1997)
A gene map of the human genome
G. D. Schuler;M. S. Boguski;E. A. Stewart;L. D. Stein.
Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23
Mihael H. Polymeropoulos;Joseph J. Higgins;Lawrence I. Golbe;William G. Johnson.
A Physical Map of 30,000 Human Genes
P. Deloukas;G. D. Schuler;G. Gyapay;E. M. Beasley.
Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH)
Mihael H. Polymeropoulos;Hong Xiao;Denise S. Rath;Carl R. Merril.
Nucleic Acids Research (1991)
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis
Victor L. Ruiz-Perez;Susan E. Ide;Susan E. Ide;Tim M. Strom;Bettina Lorenz.
Nature Genetics (2000)
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