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Author Details

Daniele Cusi
Institute of Biomedical Technologies, National Research Council of Italy
1978
229
53
PMIDPaper TitleJournal TitlePublished Year
37337107Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.Nat Genet2023
37209533Dissecting the genetic heterogeneity of gastric cancer.EBioMedicine2023
37337107Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.Nat Genet2023
37480624Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer".EBioMedicine2023
37480624Corrigendum to "Dissecting the genetic heterogeneity of gastric cancer".EBioMedicine2023
37209533Dissecting the genetic heterogeneity of gastric cancer.EBioMedicine2023
35252394Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components.Front Cardiovasc Med2022
35390065Association of colorectal cancer with genetic and epigenetic variation in PEAR1-A population-based cohort study.PLoS One2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
36211488Modulation of gut microbiota: The effects of a fruits and vegetables supplement.Front Nutr2022
36057693Identification of risk loci for primary aldosteronism in genome-wide association studies.Nat Commun2022
35252394Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components.Front Cardiovasc Med2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35390065Association of colorectal cancer with genetic and epigenetic variation in PEAR1-A population-based cohort study.PLoS One2022
36211488Modulation of gut microbiota: The effects of a fruits and vegetables supplement.Front Nutr2022
36057693Identification of risk loci for primary aldosteronism in genome-wide association studies.Nat Commun2022
33589841Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.Nat Genet2021
33589841Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture.Nat Genet2021
32429735Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.Circulation2020
32429735Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.Circulation2020
31992575Klotho Gene in Human Salt-Sensitive Hypertension.Clin J Am Soc Nephrol2020
31992575Klotho Gene in Human Salt-Sensitive Hypertension.Clin J Am Soc Nephrol2020
30578417The copy number variation landscape of congenital anomalies of the kidney and urinary tract.Nat Genet2019
30578417The copy number variation landscape of congenital anomalies of the kidney and urinary tract.Nat Genet2019
30816350Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.Nat Genet2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
30816350Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.Nat Genet2019
28340119The risk of nephrolithiasis is causally related to inactive matrix Gla protein, a marker of vitamin K status: a Mendelian randomization study in a Flemish population.Nephrol Dial Transplant2018
28340119The risk of nephrolithiasis is causally related to inactive matrix Gla protein, a marker of vitamin K status: a Mendelian randomization study in a Flemish population.Nephrol Dial Transplant2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30232134Claudin-14 Gene Polymorphisms and Urine Calcium Excretion.Clin J Am Soc Nephrol2018
30232134Claudin-14 Gene Polymorphisms and Urine Calcium Excretion.Clin J Am Soc Nephrol2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
27802415Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.Hypertension2017
29020091A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia.PLoS One2017
28553957Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.Nat Genet2017
28767105Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Nat Commun2017
28449647PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population.BMC Med Genet2017
28534485Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1.Nat Commun2017
28443625Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Nat Commun2017
28613276Genetic loci associated with heart rate variability and their effects on cardiac disease risk.Nat Commun2017
28963451CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.Nat Commun2017
27802415Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.Hypertension2017
27920155<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.J Am Soc Nephrol2017
28121514Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.N Engl J Med2017
28449647PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population.BMC Med Genet2017
28121514Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.N Engl J Med2017
28443625Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Nat Commun2017
28963451CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.Nat Commun2017
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Collaborators

Erika Salvi
Co-authored papers 54
Nicola Glorioso
Co-authored papers 24
Andres Metspalu
Co-authored papers 21
Lorena Citterio
Co-authored papers 19
Alexander Teumer
University Medicine Greifswald
Co-authored papers 19
Terho Lehtim??ki
Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
Co-authored papers 19
Olli T Raitakari
Co-authored papers 18
Caroline Hayward
Co-authored papers 18
Zolt??n Kutalik
University of Lausanne
Co-authored papers 17
Annette Peters
Ludwig-Maximilians-Universitat Munchen
Co-authored papers 17
Andr?? G Uitterlinden
Erasmus University Medical Center
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Eric Boerwinkle
Baylor College of Medicine
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Martina M??ller-Nurasyid
Institute for Medical Information Processing
Co-authored papers 17
Ruth J F Loos
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Mary F Feitosa
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Mika K??h??nen
Tampere University
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Grant W Montgomery
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Nicholas G Martin
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Pim van der Harst
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Ilja M Nolte
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Albert V Smith
University of Michigan School of Public Health ann arbor
Co-authored papers 15
Vilmundur Gudnason
Co-authored papers 15
Tõnu Esko
Co-authored papers 15
Ingrid B Borecki
Co-authored papers 15
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 15
Igor Rudan
Co-authored papers 15
Reedik Mägi
Co-authored papers 15
Harold Snieder
University of Groningen, University Medical Center Groningen
Co-authored papers 15
Ozren Polasek
Co-authored papers 14
Paul M Ridker
Co-authored papers 14
Release 1.2