Mario Falchi mainly focuses on Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Allele. His work deals with themes such as Genetic variation, Immunology, Disease and Chromosome 7, which intersect with Genome-wide association study. His work in Genetics is not limited to one particular discipline; it also encompasses Replication.
The various areas that Mario Falchi examines in his Internal medicine study include Quantitative trait locus and Endocrinology. His study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Childhood obesity and Medical genetics. His Allele research includes elements of Skin cancer, Nevus, Melanoma, Cutaneous melanoma and CDKN2A.
His main research concerns Genetics, Genome-wide association study, Internal medicine, Immunology and Cancer research. His study in Single-nucleotide polymorphism, Genetic association, Genetic linkage, Quantitative trait locus and Melanoma is done as part of Genetics. His studies in Genome-wide association study integrate themes in fields like Medical genetics, Disease, Allele, Locus and Genetic variation.
Mario Falchi has included themes like Endocrinology and Type 2 diabetes in his Internal medicine study. In the field of Endocrinology, his study on Body fat percentage and Insulin resistance overlaps with subjects such as Lean body mass. His research integrates issues of Cancer cell and Cancer in his study of Cancer research.
Mario Falchi mainly investigates Genome-wide association study, Cancer research, Cell biology, Internal medicine and Genetics. Genome-wide association study is the subject of his research, which falls under Single-nucleotide polymorphism. Mario Falchi interconnects Cancer cell, Cancer, Tumor marker, Microvesicles and Gene mutation in the investigation of issues within Cancer research.
His work on Intracellular as part of general Cell biology study is frequently connected to Oligodendrocyte differentiation, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His Internal medicine research includes themes of Endocrinology and Heritability. His Genetics course of study focuses on Metabolome and DNA methylation and CpG site.
Genetics, Genome-wide association study, Melanoma, Internal medicine and Cancer research are his primary areas of study. His biological study spans a wide range of topics, including Metabolome, Disease risk and Sunburn. His Genome-wide association study research integrates issues from Phenotype, Eye color, Sun exposure and Genetic variation.
His Melanoma study integrates concerns from other disciplines, such as Single-nucleotide polymorphism, Genetic predisposition and Medical genetics. In general Internal medicine study, his work on Odds ratio, Confidence interval and PDX1 often relates to the realm of Severe acute respiratory syndrome coronavirus 2 and Anosmia, thereby connecting several areas of interest. His Cancer research study combines topics from a wide range of disciplines, such as Microvesicles, Cancer, Innate immune system and Signal transduction.
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Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
Daniel G Healy;Mario Falchi;Sean S O'Sullivan;Vincenzo Bonifati.
Lancet Neurology (2008)
Real-time tracking of self-reported symptoms to predict potential COVID-19.
Cristina Menni;Ana M. Valdes;Ana M. Valdes;Maxim B. Freidin;Carole H. Sudre.
Nature Medicine (2020)
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Yurii S Aulchenko;Samuli Ripatti;Ida Lindqvist;Dorret Boomsma.
Nature Genetics (2009)
Bone mineral density, osteoporosis, and osteoporotic fractures : a genome-wide association study
J.B. Richards;F. Rivadeneira;M. Inouye;T.M. Pastinen.
The Lancet (2008)
Repeatability of published microarray gene expression analyses.
John P A Ioannidis;David B Allison;Catherine A Ball;Issa Coulibaly.
Nature Genetics (2009)
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Nicole Soranzo;Nicole Soranzo;Tim D Spector;Massimo Mangino;Brigitte Kühnel.
Nature Genetics (2009)
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
R. G. Walters;S. Jacquemont;A. Valsesia;A. Valsesia;A. Valsesia;A. J. de Smith.
Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia
Chris Wallace;Stephen J. Newhouse;Peter Braund;Feng Zhang.
American Journal of Human Genetics (2008)
New gene functions in megakaryopoiesis and platelet formation
Christian Gieger;Aparna Radhakrishnan;Ana Cvejic;Weihong Tang.
HIV protease inhibitors are potent anti-angiogenic molecules and promote regression of Kaposi sarcoma.
Cecilia Sgadari;Giovanni Barillari;Elena Toschi;Davide Carlei.
Nature Medicine (2002)
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