Her main research concerns Genome-wide association study, Genetics, Genetic association, Gene and Bioinformatics. Her Genome-wide association study study combines topics in areas such as Internal medicine, Kidney disease, Locus and Candidate gene. Her Genetics research includes elements of Menarche and Renal function.
Her Genetic association research is multidisciplinary, incorporating elements of Pulse pressure and Blood pressure. Her work in Gene covers topics such as Premature ovarian failure which are related to areas like Sterility, Protein family, Menopause and Mutation. Her studies in Bioinformatics integrate themes in fields like Mendelian randomization, Disease and DNA repair.
Her scientific interests lie mostly in Genetics, Genome-wide association study, Genetic association, Internal medicine and Gene. Genetics and Premature ovarian failure are commonly linked in her work. Her Genome-wide association study research is multidisciplinary, relying on both Evolutionary biology, SNP, Bioinformatics, Locus and Kidney.
Her study explores the link between Locus and topics such as Blood pressure that cross with problems in Genetic analysis. She has researched Genetic association in several fields, including Pulse pressure, Polymorphism, Quantitative trait locus, Menopause and Minor allele frequency. Cinzia Sala has included themes like Endocrinology and Immunology in her Internal medicine study.
Cinzia Sala focuses on Genome-wide association study, Genetics, Blood pressure, Evolutionary biology and Genetic association. Her research in Genome-wide association study intersects with topics in Bioinformatics, 1000 Genomes Project, Heritability, Imputation and Genetic variation. Many of her studies involve connections with topics such as Renal function and Genetics.
Her Blood pressure research also works with subjects such as
Cinzia Sala mainly investigates Genome-wide association study, Genetics, Genetic association, Blood pressure and Disease. Her Genome-wide association study study integrates concerns from other disciplines, such as Genetic variation, Bioinformatics and Heritability. She frequently studies issues relating to Renal function and Genetics.
Her biological study spans a wide range of topics, including Gene, Locus, Medical genetics and Genome-Wide Association Analysis. The Disease study combines topics in areas such as Thyroid function, Thyroid disease, Hormone, Thyroid and Genetic testing. Minor allele frequency, Allele frequency, Whole genome sequencing and Allele is closely connected to Human genome in her research, which is encompassed under the umbrella topic of Imputation.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Jennifer E. Huffman;Eva Albrecht;Alexander Teumer;Massimo Mangino.
PLOS ONE (2015)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Anna Köttgen;Anna Köttgen;Eva Albrecht;Alexander Teumer;Veronique Vitart.
Nature Genetics (2013)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Cathy E. Elks;John R B Perry;Patrick Sulem;Daniel I. Chasman.
Nature Genetics (2010)
New gene functions in megakaryopoiesis and platelet formation
Christian Gieger;Aparna Radhakrishnan;Ana Cvejic;Weihong Tang.
Nature (2011)
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Louise V. Wain;Germaine C. Verwoert;Paul F. O'Reilly;Gang Shi.
Nature Genetics (2011)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Evangelos Evangelou;Evangelos Evangelou;Helen R. Warren;Helen R. Warren;David Mosen-Ansorena;Borbala Mifsud.
Nature Genetics (2018)
Seventy-five genetic loci influencing the human red blood cell
Pim Van Der Harst;Weihua Zhang;Irene Mateo Leach;Augusto Rendon.
Nature (2012)
A Human Homologue of the Drosophila melanogaster diaphanous Gene Is Disrupted in a Patient with Premature Ovarian Failure: Evidence for Conserved Function in Oogenesis and Implications for Human Sterility
Silvia Bione;Cinzia Sala;Chiara Manzini;Giulia Arrigo.
American Journal of Human Genetics (1998)
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Lisette Stolk;John R B Perry;John R B Perry;Daniel I. Chasman;Chunyan He.
Nature Genetics (2012)
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