List of works - Giulio Genovese

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9 ⬇️

scientific article published on July 28, 2010

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

scientific article

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

scientific article

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

scientific article

Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

scholarly article by Alicia R Martin et al published 3 May 2018 in American Journal of Human Genetics

Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer

scientific article published on 16 November 2020

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.

scientific article published on 9 April 2018

Increased burden of cardiovascular disease in carriers of APOL1 genetic variants

scientific article published on 30 December 2013

Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms.

scientific article published in April 2018

Informed conditioning on clinical covariates increases power in case-control association studies

scientific article published on 8 November 2012

Large mosaic copy number variations confer autism risk

scientific article published on 11 January 2021

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

scientific article

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Monogenic and polygenic inheritance become instruments for clonal selection

scientific article published on 24 June 2020

Mosaic mutations in blood DNA sequence are associated with solid tumor cancers

scientific article published on 6 July 2017

Non-crossover gene conversions show strong GC bias and unexpected clustering in humans

scientific article published on 25 March 2015

Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression

scientific article

Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders

scientific article published on 26 June 2017

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

scientific article published on 05 August 2010

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

scientific article published on 03 October 2016

List of works by Giulio Genovese

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9 ⬇️

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland

Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer

Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.

Increased burden of cardiovascular disease in carriers of APOL1 genetic variants

Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms.

Informed conditioning on clinical covariates increases power in case-control association studies

Large mosaic copy number variations confer autism risk

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Monogenic and polygenic inheritance become instruments for clonal selection

Mosaic mutations in blood DNA sequence are associated with solid tumor cancers

Non-crossover gene conversions show strong GC bias and unexpected clustering in humans

Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression

Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population