Chiara Sabatti

Q: What Schools Are Affiliated With Chiara Sabatti

Chiara Sabatti is affiliated with the following schools: University of California, Berkeley, University of California, Los Angeles, Stanford University, University of Florence

Chiara Sabatti's AcademicInfluence.com Rankings

Chiara Sabatti

Mathematics

#4397

World Rank

#6254

Historical Rank

Statistics

#395

World Rank

#463

Historical Rank

mathematics Degrees

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Mathematics

Chiara Sabatti's Degrees

PhD Statistics University of California, Berkeley
Masters Statistics University of California, Berkeley

Why Is Chiara Sabatti Influential?

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According to Wikipedia, Chiara Sabatti is an Italian and American statistician and statistical geneticist, and a professor of biomedical data science and of statistics at Stanford University. Her research involves the analysis of high-throughput genomics data.

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Chiara Sabatti's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) (3485)
Genetic effects on gene expression across human tissues (2017) (2841)
Variance component model to account for sample structure in genome-wide association studies (2010) (2138)
Large recurrent microdeletions associated with schizophrenia (2008) (1790)
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts (2009) (909)
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population (2008) (803)
Organoid Modeling of the Tumor Immune Microenvironment (2018) (668)
Network component analysis: Reconstruction of regulatory signals in biological systems (2003) (633)
Genetic analyses of diverse populations improves discovery for complex traits (2019) (501)
Disruption of the neurexin 1 gene is associated with schizophrenia. (2009) (469)
The Human Phenome Project (2003) (398)
The DYT1 phenotype and guidelines for diagnostic testing (2000) (358)
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies (2006) (284)
Recurrent CNVs disrupt three candidate genes in schizophrenia patients. (2008) (281)
SLOPE-ADAPTIVE VARIABLE SELECTION VIA CONVEX OPTIMIZATION. (2014) (251)
Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort (2015) (241)
The impact of rare variation on gene expression across tissues (2016) (197)
Progenitor identification and SARS-CoV-2 infection in human distal lung organoids (2020) (186)
Distribution and dynamics of Lamp1-containing endocytic organelles in fibroblasts deficient in BLOC-3 (2005) (180)
False discovery rate in linkage and association genome screens for complex disorders. (2003) (179)
Inferring protein domain interactions from databases of interacting proteins (2005) (167)
The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology (2004) (166)
Co-expression pattern from DNA microarray experiments as a tool for operon prediction (2002) (153)
An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis. (2002) (152)
Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoforms (2009) (151)
Bayesian analysis of haplotypes for linkage disequilibrium mapping. (2001) (151)
Transcriptome-based determination of multiple transcription regulator activities in Escherichia coli by using network component analysis. (2004) (150)
A Quantitative Proteome Map of the Human Body (2019) (143)
The dysbindin-containing complex (BLOC-1) in brain: developmental regulation, interaction with SNARE proteins, and role in neurite outgrowth (2009) (140)
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. (2015) (123)
Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families. (2007) (119)
Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks. (2003) (118)
Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (115)
Exome sequencing of Finnish isolates enhances rare-variant association power (2019) (113)
Bayesian sparse hidden components analysis for transcription regulation networks (2005) (110)
A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales (2012) (108)
Genome-wide association study of Tourette Syndrome (2012) (102)
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. (2006) (98)
Controlling the Rate of GWAS False Discoveries (2016) (97)
Generalised Gibbs sampler and multigrid Monte Carlo for Bayesian computation (2000) (96)
Exposure to NO2, CO, and PM2.5 is linked to regional DNA methylation differences in asthma (2018) (91)
Gene hunting with hidden Markov model knockoffs (2018) (88)
The relevance of migraine in patients with Ménière's disease (2007) (87)
A Molecular Screening Approach to Identify and Characterize Inhibitors of Glioblastoma Stem Cells (2011) (85)
Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. (2014) (84)
Clinical features and associated syndromes of mal de debarquement (2008) (83)
Guidelines for association studies in Human Molecular Genetics. (2005) (81)
Homozygosity and linkage disequilibrium. (2002) (79)
Journal of the American Statistical Association: Comment (2006) (79)
Dissecting a population genome for targeted screening of disease mutations. (2001) (78)
Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder (2015) (73)
Human genetics: Variants in common diseases (2007) (70)
Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients (2011) (68)
Multi-resolution localization of causal variants across the genome (2019) (62)
Many Phenotypes Without Many False Discoveries: Error Controlling Strategies for Multitrait Association Studies (2015) (58)
Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25 (2002) (58)
Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci (2014) (55)
A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. (2006) (55)
A novel mutation in KCNA1 causes episodic ataxia without myokymia (2004) (55)
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease (2021) (54)
Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics (2020) (54)
Thresholding rules for recovering a sparse signal from microarray experiments. (2002) (50)
Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate. (2016) (48)
A generalized framework for network component analysis (2005) (45)
Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34. (2006) (44)
Gene Hunting with Knockoffs for Hidden Markov Models (2017) (43)
MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS. (2017) (42)
With Malice Towards None: Assessing Uncertainty via Equalized Coverage (2019) (42)
Increased paternal age and the influence on burden of genomic copy number variation in the general population (2013) (38)
Causal inference in genetic trio studies (2020) (38)
Understanding the Hidden Complexity of Latin American Population Isolates (2018) (38)
Volume measures for linkage disequilibrium (2006) (35)
Genetic regulation of gene expression and splicing during a 10-year period of human aging (2019) (35)
Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder. (2015) (34)
TreeQTL: hierarchical error control for eQTL findings (2015) (34)
Empirical Bayes Estimation of a Sparse Vector of Gene Expression Changes (2005) (34)
Tag SNPs chosen from HapMap perform well in several population isolates (2007) (34)
Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy (2004) (34)
Genomewide motif identification using a dictionary model (2002) (31)
Applied Statistical Genetics with R for Population-Based Association Studies (2009) (31)
Progenitor identification and SARS-CoV-2 infection in long-term human distal lung organoid cultures (2020) (29)
RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. (2009) (26)
Testing hypotheses on a tree: new error rates and controlling strategies (2017) (24)
False discovery rate control in genome-wide association studies with population structure (2021) (24)
Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates (2018) (23)
Linkage Disequilibrium and Haplotype Homozygosity in Population Samples Genotyped at a High Marker Density (2006) (23)
Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms (2009) (21)
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2018) (21)
Phenotype mining in CNV carriers from a population cohort. (2011) (20)
Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder (2006) (20)
IEEE/ACM TRANSACTIONS ON (2004) (20)
Vocabulon: a dictionary model approach for reconstruction and localization of transcription factor binding sites (2005) (19)
Reconstructing DNA copy number by joint segmentation of multiple sequences (2012) (19)
Sparse Regulatory Networks. (2010) (15)
Bayesian Gaussian Mixture Models for High-Density Genotyping Arrays (2008) (13)
Avoiding false discoveries in association studies. (2007) (12)
Distant regulatory effects of genetic variation in multiple human tissues (2016) (11)
Rejoinder: ‘Gene hunting with hidden Markov model knockoffs’ (2019) (11)
Exploratory Gene Ontology Analysis with Interactive Visualization (2018) (11)
Selection-adjusted inference: an application to confidence intervals for cis-eQTL effect sizes. (2018) (11)
Searching for consistent associations with a multi-environment knockoff filter (2021) (10)
Integrative Spatial Single-cell Analysis with Graph-based Feature Learning (2020) (10)
Filtering the Rejection Set While Preserving False Discovery Rate Control (2018) (10)
Simulated Sintering: Markov Chain Monte Carlo With Spaces of Varying Dimensions (2007) (10)
Hypotheses on a tree: new error rates and testing strategies. (2020) (9)
DISTINCT AND SHARED CONTRIBUTIONS OF DIAGNOSIS AND SYMPTOM DOMAINS TO COGNITIVE PERFORMANCE IN SEVERE MENTAL ILLNESS (2019) (9)
A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees (2009) (9)
Controlling the false discovery rate in GWAS with population structure (2020) (8)
A dictionary model for haplotyping, genotype calling, and association testing (2007) (8)
Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate (2016) (8)
Increased activation product of complement 4 protein in plasma of individuals with schizophrenia (2021) (8)
FDR control in GWAS with population structure (2020) (6)
Transfer Learning in Genome-Wide Association Studies with Knockoffs (2021) (6)
Detecting multiple replicating signals using adaptive filtering procedures (2016) (6)
Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder (2016) (6)
Measuring Dependency With Volume Tests (2002) (6)
Advances in Statistical Bioinformatics: Multivariate Linear Models for GWAS (2013) (5)
Nanoscale proteomic profiling to define diagnostic signatures and biomarkers of therapeutic activity in patients with RCC. (2013) (5)
Multiregion Quantification of Extracellular Signal-regulated Kinase Activity in Renal Cell Carcinoma. (2020) (5)
Genetic dysregulation of gene expression and splicing during a ten-year period of human aging (2019) (4)
Inferring genomic loss and location of tumor suppressor genes from high density genotypes (2005) (4)
Use of nano-immuno assay to generate rapid, quantitative nanoscale proteomic profiling of the hypoxia pathway in renal cell carcinoma clinical specimens. (2012) (4)
Controlling FDR while highlighting selected discoveries (2018) (4)
CME Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11 q 23-25 (2002) (4)
Detecting Replicating Signals using Adaptive Filtering Procedures with the Application in High-throughput Experiments (2016) (4)
Reconstructing Ancestral Haplotypes with a Dictionary Model (2005) (4)
Comments on Michael Jordan’s Essay “The AI Revolution Hasn’t Happened Yet" (2019) (4)
Progenitor identification and SARS-CoV-2 infection in human distal lung organoids (2020) (3)
Summary statistics knockoff inference empowers identification of putative causal variants in genome-wide association studies (2021) (3)
Exome sequencing of Finnish isolates enhances rare-variant association power (2019) (3)
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (3)
Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder (2019) (3)
Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder (2020) (3)
Statistical Issues in Microarray Analysis (2002) (3)
Reconstructing Hidden Regulatory Layers by Network Component Analysis : Theory and Application (2004) (2)
Controlling FDR while highlighting distinct discoveries (2018) (2)
False Discovery Rate and Multiple Comparison Procedures (2005) (2)
Publisher Correction: Multi-resolution localization of causal variants across the genome (2020) (2)
Geospatial analysis reveals distinct hotspots of severe mental illness (2022) (2)
An introduction to statistical issues in High throughput screens (2008) (2)
Response to the Letter "Gametic and Zygotic Associations" by Rong-Cai Yang (2003) (2)
Genetic Variant Selection: Learning Across Traits and Sites (2015) (2)
Genome-Wide Association Study with SLOPE (2016) (1)
Genetic regulation of gene expression and splicing during a 10-year period of human aging (2019) (1)
Mendel 13.2 Documentation (2013) (1)
Reconstructing DNA copy number by joint segmentation of multiple sequences (2012) (1)
False Discovery Rate and Correction for Multiple Comparisons in Linkage Disequilibrium Genome Screens (2002) (1)
Results of a SNP genome screen in a large Costa Rican Pedigree segregating for severe bipolar disorder (2008) (1)
Exome sequencing identifies high-impact trait-associated alleles enriched in Finns (2018) (1)
Genome-wide association (GWA) analysis in 4000 members of a Finnish birth cohort identifies common variants associated with fasting insulin levels and related metabolic traits (2008) (1)
Abstract 2283: Nano-scale proteomic profiles of response to targeted therapy in patients with RCC. (2013) (1)
Volume Measures for Linkage Disequilibrium - eScholarship (2006) (1)
Adaptive Filtering Procedures for Replicability Analysis of High-throughput Experiments (2016) (1)
Increased paternal age and the influence on burden of genomic copy number variation in the general population (2013) (0)
A genome-wide meta-analysis of association studies of Cloninger ' s Temperament Scales Service (0)
Facile single cell profiling and clonotype analysis of NSCLC immune microenvironments. (2018) (0)
Comment (2005) (0)
Characterizing the human mitochondrial proteome using a genome-wide functional linkage network (2015) (0)
Resource Organoid Modeling of the Tumor Immune Microenvironment Graphical Abstract Highlights (2018) (0)
Abstract 1280: Nano-scale phospho-proteomic analysis to define diagnostic signatures and biomarkers of therapeutic activity in cancer (2012) (0)
LEVERAGING ELECTRONIC HOSPITAL RECORDS FOR PSYCHIATRIC PHENOTYPING (2019) (0)
Machine Learning Approaches to Understanding Gene Regulation in Mouse Embryonic Stem Cells (2010) (0)
Adaptive Filtering Multiple Testing Procedures for Partial Conjunction Hypotheses (2016) (0)
Sorted L1 Penalized Estimation [R package SLOPE version 0.3.2] (2020) (0)
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power (2019) (0)
Mendel 14.2 Documentation (2014) (0)
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2018) (0)
Exploratory Gene Ontology Analysis with Interactive Visualization (2019) (0)
A Vocabulon Study of E.Coli Regulatory Sites with Feedback to Expression Array Analysis (2003) (0)
GENETICS OF SEVERE MENTAL ILLNESS: THE “PAISA PROJECT” (2019) (0)
Whole genome sequencing in psychiatric disorders: the WGSPD consortium (2017) (0)
Discussion of Gene Hunting with Hidden Markov Model Knockoffs (2018) (0)
Faculty Opinions recommendation of Association testing of the mitochondrial genome using pedigree data. (2013) (0)
Multi-resolution localization of causal variants across the genome (2020) (0)
Genetic analyses of diverse populations improves discovery for complex traits (2019) (0)
Exposure to NO2, CO, and PM2.5 is linked to regional DNA methylation differences in asthma (2018) (0)
Dictionary model for the analysis of E. Coli promoter regions (2003) (0)
Supplementary Material (nature09270-s1) (2012) (0)
1. The analysis of gene expression data: Methods and software. Giovanni Parmigiani, Elizabeth S. Garrett, Rafael A. Irizarry and Scott L. Zeger (eds), Springer, New York, 2003. No. of pages: 455. Price: EUR 89.95; £63.00; US $89.95. ISBN: 0‐387‐95577‐1 (2004) (0)
S26NLP STRATEGIES FOR ANALYZING FREE-TEXT PSYCHIATRIC ELECTRONIC HOSPITAL RECORDS (2019) (0)
Title Markov models for inferring Copy Number Variations from genotype data on Illumina platforms Permalink (2008) (0)
Title False Discovery Rate and Correction for Multiple Comparisons in Linkage Disequilibrium Genome (2002) (0)
The Statistics of Gene Mapping (2007) (0)
INTRA‐TUMOR HETEROGENEITY IN RENAL CELL CARCINOMA: IMPLICATIONS FOR PROTEOMIC ANALYSIS OF RENAL MASS BIOPSIES: MP39‐10 (2017) (0)
GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies (2022) (0)
Near-peer mentoring in data science: Two experiences at Stanford University (2022) (0)
COMMENTARY Guidelines for association studies in Human (2005) (0)
Mendel 12 Documentation (2012) (0)
A Bayesian approach to expression network component analysis (2004) (0)
603 NANO-SCALE PROTEOMIC PROFILING TO DEFINE DIAGNOSTIC SIGNATURES AND BIOMARKERS OF THERAPEUTIC ACTIVITY IN RCC (2013) (0)
GENETICS OF SEVERE MENTAL ILLNESS IN A COLOMBIAN POPULATION ISOLATE (2019) (0)
“Genomewide Motif Recognition with a Dictionary Model” (2002) (0)
False Discovery Rate and Correction for Multiple Comparisons in Association Genome Screens for Complex Disorders (2002) (0)
Contents Vol. 62, 2006 (2006) (0)
Faculty Opinions recommendation of Screening for partial conjunction hypotheses. (2013) (0)
Title Markov models for inferring Copy Number Variations from genotype data Permalink (2008) (0)
Data Science in a Time of Crisis: Lessons from the Pandemic (2022) (0)
Discussion of the Paper “Prediction, Estimation, and Attribution” by B. Efron (2020) (0)
Publisher Correction: Multi-resolution localization of causal variants across the genome (2020) (0)
GENETICS OF SEVERE MENTAL ILLNESS IN SOUTH AMERICA (2022) (0)
Interplay in the Computational Analysis of Genomic Regulatory Sequences and Microarray Expression Data (2004) (0)
THE RELATIONSHIP BETWEEN GENOME-WIDE SIGNIFICANT GWAS LOCI AND PSYCHIATRIC PHENOTYPES IN A COLOMBIAN POPULATION ISOLATE (2019) (0)
Abstract 5672: Facile generation of single-cell transcriptome and immune repertoire freshly isolated from clinical tumor specimens (2018) (0)
Abstract 987: Organoid-based characterization of patient tumors and microenvironments at single cell resolution (2018) (0)
CONTROLLING FALSE DISCOVERIES IN MAPPING MULTIPLE PHENOTYPES (2015) (0)
Acknowledgement to the Reviewers (2000) (0)
Characterization of expression quantitative trait loci in extensively phenotyped pedigrees ascertained for bipolar disorder (2015) (0)
Comment (2006) (0)
Subject Index Vol. 62, 2006 (2006) (0)

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What Schools Are Affiliated With Chiara Sabatti?

Chiara Sabatti is affiliated with the following schools:

Chiara Sabatti's Academic­Influence.com Rankings