Author details

Full Name

Chiara Sabatti

Affiliation

ORCID

Career Start Year

2000

Papers

101

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37346227	Filtering the rejection set while preserving false discovery rate control.		2023
36418338	GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies.	Nat Commun	2022
31301173	Selection-adjusted inference: an application to confidence intervals for cis-eQTL effect sizes.	Biostatistics	2021
36825068	Hypotheses on a tree: new error rates and testing strategies.	Biometrika	2021
31813409	Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder.	Psychological Medicine	2021
32606377	Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder.	Mol Psychiatry	2021
34580220	False discovery rate control in genome-wide association studies with population structure.	Proc Natl Acad Sci U S A	2021
34552056	Increased activation product of complement 4 protein in plasma of individuals with schizophrenia.	Transl Psychiatry	2021
34437092	Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics.	Science	2021
31412000	Multiregion Quantification of Extracellular Signal-regulated Kinase Activity in Renal Cell Carcinoma.	Eur Urol Oncol	2020
32265451	Publisher Correction: Multi-resolution localization of causal variants across the genome.	Nature Communications	2020
32107378	Multi-resolution localization of causal variants across the genome.	Nature Communications	2020
32094344	Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates.	Transl Psychiatry	2020
32743583	Progenitor identification and SARS-CoV-2 infection in long-term human distal lung organoid cultures.	bioRxiv	2020
33238290	Progenitor identification and SARS-CoV-2 infection in human distal lung organoids.	Nature	2020
32948695	Causal inference in genetic trio studies.	Proceedings of the National Academy of Sciences of the United States of America	2020
31367044	Exome sequencing of Finnish isolates enhances rare-variant association power.	Nature	2019
31687060	MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS.	Annals of Applied Statistics	2019
31686056	Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.	Nature	2019
31684996	Genetic regulation of gene expression and splicing during a 10-year period of human aging.	Genome Biol	2019
31127124	Exploratory Gene Ontology Analysis with Interactive Visualization.	Scientific Reports	2019
31217584	Genetic analyses of diverse populations improves discovery for complex traits.	Nature	2019
30799875	Gene hunting with hidden Markov model knockoffs.	Biometrika	2019
29317916	Exposure to NO, CO, and PM is linked to regional DNA methylation differences in asthma.	Clinical Epigenetics	2018
30401458	Understanding the Hidden Complexity of Latin American Population Isolates.	Am J Hum Genet	2018
30550791	Organoid Modeling of the Tumor Immune Microenvironment.	Cell	2018
29549319	Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.	Nat Neurosci	2018
27784720	Controlling the Rate of GWAS False Discoveries.	Genetics	2017
29184211	Whole genome sequencing in psychiatric disorders: the WGSPD consortium.	Nat Neurosci	2017
29083405	Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate.	Nat Genet	2017
26712028	Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder.	Proc Natl Acad Sci U S A	2016
27153635	TreeQTL: hierarchical error control for eQTL findings.	Bioinformatics	2016
27176483	Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder.	PLoS Genet	2016
26626037	Many Phenotypes Without Many False Discoveries: Error Controlling Strategies for Multitrait Association Studies.	Genet Epidemiol	2016
26680660	Genetic Variant Selection: Learning Across Traits and Sites.	Genetics	2016
25158072	Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.	Am J Psychiatry	2015
25943422	Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder.	Brain	2015
26092716	Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort.	Genetics	2015
26709357	SLOPE-ADAPTIVE VARIABLE SELECTION VIA CONVEX OPTIMIZATION.	Annals of Applied Statistics	2015
24522887	Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees.	JAMA Psychiatry	2014
24497850	Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci.	PLoS Genet	2014
23315237	Increased paternal age and the influence on burden of genomic copy number variation in the general population.	Hum Genet	2013
22889924	Genome-wide association study of Tourette's syndrome.	Mol Psychiatry	2013
22897923	Reconstructing DNA copy number by joint segmentation of multiple sequences.	BMC Bioinformatics	2012
22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	PLoS Genet	2012
22832960	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	Transl Psychiatry	2012
21859839	A molecular screening approach to identify and characterize inhibitors of glioblastoma stem cells.	Molecular Cancer Therapeutics	2011
21489405	Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.	Biological Psychiatry	2011
21505072	Phenotype mining in CNV carriers from a population cohort.	Human Molecular Genetics	2011
21572975	RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION.	Annals of Applied Statistics	2010