C. Sabatti

发表

Large recurrent microdeletions associated with schizophrenia

Thomas W. Mühleisen, Bjarni V. Halldórsson, P. Matthews, 2008, Nature.

Sparse Regulatory Networks.

Ji Zhu, Chiara Sabatti, Nengfeng Zhou, 2010, The annals of applied statistics.

SLOPE-ADAPTIVE VARIABLE SELECTION VIA CONVEX OPTIMIZATION.

Weijie J. Su, E. Candès, C. Sabatti, 2014, The annals of applied statistics.

Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoforms

C. Sabatti, B. Matthews, Daisuke Hattori, 2009, Nature.

K. Roeder, C. Sabatti, R. Carroll, 2006 .

Clinical features and associated syndromes of mal de debarquement

C. Sabatti, G. Ishiyama, R. Baloh, 2008, Journal of Neurology.

Comments on Michael Jordan’s Essay “The AI Revolution Hasn’t Happened Yet"

John C. Duchi, E. Candès, C. Sabatti, 2019, Issue 1.

RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION.

K. Lange, C. Sabatti, R. Ophoff, 2009, The annals of applied statistics.

Thresholding rules for recovering a sparse signal from microarray experiments.

D. Geschwind, C. Sabatti, S. Karsten, 2002, Mathematical biosciences.

Transcriptome-based determination of multiple transcription regulator activities in Escherichia coli by using network component analysis.

Katy C. Kao, C. Sabatti, J. Liao, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Bayesian analysis of haplotypes for linkage disequilibrium mapping.

C. Sabatti, J. Liu, N. Risch, 2001, Genome research.

Generalised Gibbs sampler and multigrid Monte Carlo for Bayesian computation

Jun S. Liu, C. Sabatti, 2000 .

MULTILAYER KNOCKOFF FILTER: CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS.

Chiara Sabatti, Eugene Katsevich, C. Sabatti, 2017, The annals of applied statistics.

Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci

Tanya M. Teslovich, P. Elliott, M. Jarvelin, 2014, PLoS genetics.

Controlling the Rate of GWAS False Discoveries

Christine B. Peterson, E. Candès, C. Sabatti, 2016, Genetics.

Genetic Variant Selection: Learning Across Traits and Sites

C. Sabatti, Laurel Stell, 2015, Genetics.

Genome-Wide Association Study with SLOPE

C. Sabatti, M. Bogdan, Damian Brzyski, 2016 .

Gene Hunting with Knockoffs for Hidden Markov Models

E. Candès, C. Sabatti, M. Sesia, 2017 .

Many Phenotypes Without Many False Discoveries: Error Controlling Strategies for Multitrait Association Studies

Christine B. Peterson, C. Sabatti, Y. Benjamini, 2015, Genetic epidemiology.

Testing hypotheses on a tree: new error rates and controlling strategies

Yoav Benjamini, Christine B. Peterson, Chiara Sabatti, 2017, 1705.07529.

Variance component model to account for sample structure in genome-wide association studies

H. Kang, C. Sabatti, N. Freimer, 2010, Nature Genetics.

Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees.

C. Sabatti, N. Freimer, R. Cantor, 2014, JAMA psychiatry.

Inferring protein domain interactions from databases of interacting proteins

Christopher J. Lee, C. Sabatti, D. Eisenberg, 2005, Genome Biology.

Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics

Scott A. Longwell, C. Sabatti, D. Herschlag, 2020, Science.

A Quantitative Proteome Map of the Human Body

Christopher D. Brown, Katherine H. Huang, Christopher M. Lee, 2019, Cell.

Understanding the Hidden Complexity of Latin American Population Isolates.

C. Sabatti, N. Freimer, G. Bedoya, 2018, American journal of human genetics.

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

C. Sabatti, N. Freimer, R. Ophoff, 2018, bioRxiv.

The Human Phenome Project

C. Sabatti, N. Freimer, 2003, Nature Genetics.

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

C. Hoggart, L. Coin, M. McCarthy, 2008, Nature Genetics.

Simulated Sintering: Markov Chain Monte Carlo With Spaces of Varying Dimensions

Jun S. Liu, Chiara Sabatti, Jun S. Liu, 2007 .

Genetic analyses of diverse populations improves discovery for complex traits

Stephanie A. Bien, Janina M. Jeff, Sarah C. Nelson, 2019, Nature.

Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort

C. Sabatti, N. Risch, P. Kwok, 2015, Genetics.

Exome sequencing of Finnish isolates enhances rare-variant association power

Ira M. Hall, Thomas J. Nicholas, Thomas J Nicholas, 2019, Nature.

The GTEx Consortium atlas of genetic regulatory effects across human tissues

Christopher D. Brown, Katherine H. Huang, Jared L. Nedzel, 2019, Science.

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

Bronwen L. Aken, R. Wilson, C. Sabatti, 2016, Nature Genetics.

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

Christine B. Peterson, Bronwen L. Aken, R. Wilson, 2016, Nature Genetics.

Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms

C. Sabatti, R. Ophoff, H. Blauw, 2009, Human Heredity.

Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder.

Chiara Sabatti, Paul M Thompson, Nelson B Freimer, 2015, Brain : a journal of neurology.

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

Chiara Sabatti, Andrew Collins, Proton Rahman, 2006, Nature Genetics.

Integrative Spatial Single-cell Analysis with Graph-based Feature Learning

C. Sabatti, Junjie Zhu, 2020 .

Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

Thomas J. Nicholas, Thomas J Nicholas, M. Pirinen, 2018 .

An evaluation of tyramide signal amplification and archived fixed and frozen tissue in microarray gene expression analysis.

D. Geschwind, C. Sabatti, S. Karsten, 2002, Nucleic acids research.

Machine Learning Approaches to Understanding Gene Regulation in Mouse Embryonic Stem Cells

Mike J. Mason, C. Sabatti, K. Plath, 2010 .

Rejoinder: ‘Gene hunting with hidden Markov model knockoffs’

Emmanuel J. Candes, Chiara Sabatti, Matteo Sesia, 2019, Biometrika.

Discussion of Gene Hunting with Hidden Markov Model Knockoffs

E. Candès, C. Sabatti, 2018 .

Genome-wide association study of Tourette Syndrome

S. E. Stewart, A. Singleton, C. Sabatti, 2012, Molecular Psychiatry.

The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology

Chiara Sabatti, Nelson Freimer, C. Sabatti, 2004, Nature Genetics.

Empirical Bayes Estimation of a Sparse Vector of Gene Expression Changes

Chiara Sabatti, Stephen Erickson, C. Sabatti, 2005, Statistical applications in genetics and molecular biology.

Mendel 14.2 Documentation

K. Lange, C. Sabatti, R. Cantor, 2014 .

Mendel 13.2 Documentation

K. Lange, C. Sabatti, R. Cantor, 2013 .

Mendel 12 Documentation

K. Lange, C. Sabatti, R. Cantor, 2012 .

Organoid Modeling of the Tumor Immune Microenvironment

Chiara Sabatti, Grace X. Y. Zheng, Joseph C. Liao, 2018, Cell.

Controlling the Rate of GWAS False Discoveries

E. Candès, C. Sabatti, M. Bogdan, 2016, Genetics.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Stephan J Sanders, M. Daly, G. Abecasis, 2017, bioRxiv.

Controlling FDR while highlighting selected discoveries

C. Sabatti, M. Bogomolov, E. Katsevich, 2018 .

Vocabulon: a dictionary model approach for reconstruction and localization of transcription factor binding sites

Kenneth Lange, Chiara Sabatti, Lars Rohlin, 2005, Bioinform..

Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder

C. Sabatti, N. Freimer, R. Cantor, 2020, Molecular Psychiatry.

Reconstructing Hidden Regulatory Layers by Network Component Analysis : Theory and Application

C. Sabatti, J. Liao, V. Roychowdhury, 2004 .

Response to the Letter "Gametic and Zygotic Associations" by Rong-Cai Yang

C. Sabatti, N. Risch, 2003 .

Adaptive Filtering Multiple Testing Procedures for Partial Conjunction Hypotheses

A. Owen, C. Sabatti, Jingshu Wang, 2016 .

Guidelines for association studies in Human Molecular Genetics.

C. Sabatti, N. Freimer, 2005, Human molecular genetics.

Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder

C. Sabatti, N. Freimer, R. Cantor, 2016, PLoS genetics.

CONTROLLING FALSE DISCOVERIES IN MAPPING MULTIPLE PHENOTYPES

Christine B. Peterson, C. Sabatti, Y. Benjamini, 2015 .

Inferring genomic loss and location of tumor suppressor genes from high density genotypes

C. Sabatti, S. Nelson, Yohan Lee, 2005 .

INTRA‐TUMOR HETEROGENEITY IN RENAL CELL CARCINOMA: IMPLICATIONS FOR PROTEOMIC ANALYSIS OF RENAL MASS BIOPSIES: MP39‐10

C. Sabatti, J. Brooks, J. Leppert, 2017 .

IEEE/ACM TRANSACTIONS ON

Luca Benini, Tao Jiang, Stefano Lonardi, 2004 .

Data Science in a Time of Crisis: Lessons from the Pandemic

C. Sabatti, John M. Chambers, 2022, Statistical Science.

Searching for consistent associations with a multi-environment knockoff filter

Yaniv Romano, Emmanuel Candes, Chiara Sabatti, 2021, 2106.04118.

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Christian Gieger, Thomas Meitinger, Mario Falchi, 2009, Nature Genetics.

Statistical Issues in Microarray Analysis

Chiara Sabatti, C. Sabatti, 2002 .

Distant regulatory effects of genetic variation in multiple human tissues

Eleazar Eskin, Manolis Kellis, Buhm Han, 2016, bioRxiv.

Genetic regulation of gene expression and splicing during a 10-year period of human aging

David A. Knowles, Chiara Sabatti, Stephen B. Montgomery, 2019, Genome Biology.

Genetic dysregulation of gene expression and splicing during a ten-year period of human aging

David A. Knowles, Nathan S. Abell, Michael J. Gloudemans, 2019, bioRxiv.

Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate.

Christine B. Peterson, Bronwen L. Aken, R. Wilson, 2016 .

C. Sabatti, 2005 .

A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales

M. Jarvelin, N. Wray, T. Lehtimäki, 2012, Translational Psychiatry.

Near-peer mentoring in data science: Two experiences at Stanford University

C. Sabatti, Qianlan Zhao, 2022, 2211.08637.

GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies

Michaël E. Belloy, E. Candès, C. Sabatti, 2022, Nature Communications.

Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids

Tanya M. Teslovich, Y. J. Kim, M. Rieder, 2010, Nature.

Applied Statistical Genetics with R for Population-Based Association Studies

Christophe Lalanne, Chiara Sabatti, C. Sabatti, 2009 .

Selection-adjusted inference: an application to confidence intervals for cis-eQTL effect sizes.

Chiara Sabatti, Junjie Zhu, Snigdha Panigrahi, 2018, Biostatistics.

Genetic effects on gene expression across human tissues

Nicola J. Rinaldi, Ian C. McDowell, Christopher D. Brown, 2017, Nature.

A Molecular Screening Approach to Identify and Characterize Inhibitors of Glioblastoma Stem Cells

C. Sabatti, R. Damoiseaux, I. Nakano, 2011, Molecular Cancer Therapeutics.

The dysbindin-containing complex (BLOC-1) in brain: developmental regulation, interaction with SNARE proteins, and role in neurite outgrowth

C. Sabatti, J. de Vellis, L. Chan, 2009, Molecular Psychiatry.

The impact of rare variation on gene expression across tissues

Gao Wang, Mary Goldman, Brian Craft, 2016, Nature.

Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34.

C. Sabatti, N. Freimer, M. Parra, 2006, Human molecular genetics.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Elvira Bramon, Chiara Sabatti, Kari Stefansson, 2009, Human molecular genetics.

Increased paternal age and the influence on burden of genomic copy number variation in the general population

A. Uitterlinden, J. Buizer-Voskamp, L. Kiemeney, 2013, Human Genetics.

Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients

H. Stefánsson, J. Buizer-Voskamp, C. Sabatti, 2011, Biological Psychiatry.

Recurrent CNVs disrupt three candidate genes in schizophrenia patients.

J. Buizer-Voskamp, C. Sabatti, R. Ophoff, 2008, American journal of human genetics.

Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease

Christopher D. Brown, Katherine H. Huang, Christopher M. Lee, 2021, Cell.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Stephan J Sanders, M. Daly, G. Abecasis, 2017, bioRxiv.

Summary statistics knockoff inference empowers identification of putative causal variants in genome-wide association studies

Michaël E. Belloy, E. Candès, C. Sabatti, 2021, bioRxiv.

Detecting multiple replicating signals using adaptive filtering procedures

Lin Gui, Weijie J. Su, Jingshu Wang, 2016, The Annals of Statistics.

Dissecting a population genome for targeted screening of disease mutations.

C. Sabatti, L. Peltonen, M. Perola, 2001, Human molecular genetics.

Resource Organoid Modeling of the Tumor Immune Microenvironment Graphical Abstract Highlights

Grace X. Y. Zheng, Mark M. Davis, C. Sabatti, 2018 .

False discovery rate control in genome-wide association studies with population structure

J. Marchini, E. Candès, C. Sabatti, 2021, Proceedings of the National Academy of Sciences.

FDR control in GWAS with population structure

J. Marchini, E. Candès, C. Sabatti, 2021 .

Controlling the false discovery rate in GWAS with population structure

Chiara Sabatti, Jonathan Marchini, Matteo Sesia, 2020, bioRxiv.

Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families.

S. E. Stewart, C. Sabatti, W. McMahon, 2007, American journal of human genetics.

Avoiding false discoveries in association studies.

C. Sabatti, 2007, Methods in molecular biology.

COMMENTARY Guidelines for association studies in Human

C. Sabatti, N. Freimer, 2005 .

False discovery rate in linkage and association genome screens for complex disorders.

Chiara Sabatti, Nelson Freimer, C. Sabatti, 2003, Genetics.

Multi-resolution localization of causal variants across the genome

Emmanuel J. Candès, Chiara Sabatti, Eugene Katsevich, 2019, Nature Communications.

Gene hunting with hidden Markov model knockoffs

M Sesia, C Sabatti, E J Candès, 2017, Biometrika.

A generalized framework for network component analysis

Vwani P. Roychowdhury, Chiara Sabatti, James C. Liao, 2005, IEEE/ACM Transactions on Computational Biology and Bioinformatics.

Network component analysis: Reconstruction of regulatory signals in biological systems

Chiara Sabatti, James C Liao, Riccardo Boscolo, 2003, Proceedings of the National Academy of Sciences of the United States of America.

A Quantitative Proteome Map of the Human Body

Christopher D. Brown, Katherine H. Huang, Christopher M. Lee, 2019, Cell.

Causal inference in genetic trio studies

Chiara Sabatti, Matteo Sesia, Stephen Bates, 2020, Proceedings of the National Academy of Sciences.

Increased activation product of complement 4 protein in plasma of individuals with schizophrenia

C. Sabatti, A. Urban, D. Levinson, 2021, Translational Psychiatry.

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

Chiara Sabatti, Nelson B Freimer, C. Sabatti, 2006, Human molecular genetics.

Phenotype mining in CNV carriers from a population cohort.

M. Jarvelin, O. Pietiläinen, T. Paunio, 2011, Human molecular genetics.

Detecting Replicating Signals using Adaptive Filtering Procedures with the Application in High-throughput Experiments

Jingshu Wang, Weijie Su, Chiara Sabatti, 2016, 1610.03330.

Understanding the Hidden Complexity of Latin American Population Isolates

C. Sabatti, N. Freimer, G. Bedoya, 2018, bioRxiv.

Exposure to NO2, CO, and PM2.5 is linked to regional DNA methylation differences in asthma

C. Sabatti, D. Dinakarpandian, K. Nadeau, 2018, Clinical Epigenetics.

TreeQTL: hierarchical error control for eQTL findings

Christine B. Peterson, Christine B. Peterson, M. Bogomolov, 2015, bioRxiv.

Filtering the Rejection Set While Preserving False Discovery Rate Control

Marina Bogomolov, Eugene Katsevich, Chiara Sabatti, 2018, Journal of the American Statistical Association.

False Discovery Rate and Correction for Multiple Comparisons in Linkage Disequilibrium Genome Screens

C. Sabatti, N. Freimer, 2002 .

Title False Discovery Rate and Correction for Multiple Comparisons in Linkage Disequilibrium Genome

C. Sabatti, S. Service, 2002 .

False Discovery Rate and Correction for Multiple Comparisons in Association Genome Screens for Complex Disorders

C. Sabatti, N. Freimer, S. Service, 2002 .

Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks.

D. Geschwind, C. Sabatti, L. Kudo, 2003, Developmental biology.

Hypotheses on a tree: new error rates and testing strategies.

Christine B. Peterson, C. Sabatti, Y. Benjamini, 2020, Biometrika.

Progenitor identification and SARS-CoV-2 infection in human distal lung organoids

Grace X. Y. Zheng, Lisa E. Wagar, Mark M. Davis, 2020, Nature.

Progenitor identification and SARS-CoV-2 infection in long-term human distal lung organoid cultures

Grace X. Y. Zheng, Mark M. Davis, Ryan A. Flynn, 2020, bioRxiv.

Distribution and dynamics of Lamp1-containing endocytic organelles in fibroblasts deficient in BLOC-3

Chiara Sabatti, Juan M Falcón-Pérez, C. Sabatti, 2005, Journal of Cell Science.

Transfer Learning in Genome-Wide Association Studies with Knockoffs

Chiara Sabatti, Matteo Sesia, Shuangning Li, 2021, Sankhya B.

Genetic analyses of diverse populations improves discovery for complex traits

Stephanie A. Bien, Janina M. Jeff, Sarah C. Nelson, 2019, Nature.

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

S. E. Stewart, C. Sabatti, N. Freimer, 2015, The American journal of psychiatry.

Linkage Disequilibrium and Haplotype Homozygosity in Population Samples Genotyped at a High Marker Density

C. Sabatti, N. Freimer, Yuguo Chen, 2006, Human Heredity.

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

C. Sabatti, S. Nelson, R. Baloh, 2006, Human molecular genetics.

Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy

C. Sabatti, S. Nelson, R. Baloh, 2004, Neurology.

Geospatial analysis reveals distinct hotspots of severe mental illness

C. Sabatti, R. Gur, T. Teshiba, 2022, medRxiv.

The relevance of migraine in patients with Ménière's disease

C. Sabatti, G. Ishiyama, R. Baloh, 2007, Acta oto-laryngologica.

Reconstructing DNA copy number by joint segmentation of multiple sequences

Kenneth Lange, Chiara Sabatti, Zhongyang Zhang, 2012, BMC Bioinformatics.

Characterization of expression quantitative trait loci in extensively phenotyped pedigrees ascertained for bipolar disorder

C. Sabatti, N. Freimer, Y. Benjamini, 2015, bioRxiv.

Exploratory Gene Ontology Analysis with Interactive Visualization

Qian Zhao, Chiara Sabatti, Eugene Katsevich, 2018, Scientific Reports.

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

Nicola J. Rinaldi, Ian C. McDowell, Christopher D. Brown, 2018, Nature Communications.

Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25

C. Sabatti, R. Baloh, T. Bosley, 2002, Neurology.

CME Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11 q 23-25

C. Sabatti, S. Nelson, R. Baloh, 2002 .

Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder

Chiara Sabatti, Nelson Freimer, Joseph DeYoung, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees

C. Sabatti, M. Parra, G. Bedoya, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

DISTINCT AND SHARED CONTRIBUTIONS OF DIAGNOSIS AND SYMPTOM DOMAINS TO COGNITIVE PERFORMANCE IN SEVERE MENTAL ILLNESS

C. Sabatti, N. Freimer, R. Gur, 2019, European Neuropsychopharmacology.

Homozygosity and linkage disequilibrium.

Chiara Sabatti, C. Sabatti, N. Risch, 2002, Genetics.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium

Hailiang Huang, Chiara Sabatti, Kevin Eggan, 2017, bioRxiv.

Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder

C. Sabatti, N. Freimer, R. Ophoff, 2019, Psychological Medicine.

Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder

C. Sabatti, N. Freimer, R. Cantor, 2015, Proceedings of the National Academy of Sciences.

Bayesian sparse hidden components analysis for transcription regulation networks

Chiara Sabatti, Gareth M. James, Gareth M. James, 2005, Bioinform..

Human genetics: Variants in common diseases

Chiara Sabatti, Nelson B. Freimer, C. Sabatti, 2007, Nature.

Reconstructing Ancestral Haplotypes with a Dictionary Model

Kenneth Lange, Chiara Sabatti, Kristin L. Ayers, 2005, J. Comput. Biol..

Progenitor identification and SARS-CoV-2 infection in human distal lung organoids

Grace X. Y. Zheng, Ryan A. Flynn, T. Mikkelsen, 2020, Nature.

The DYT1 phenotype and guidelines for diagnostic testing

C. Sabatti, N. Risch, M. Brin, 2000, Neurology.

Volume measures for linkage disequilibrium

Chiara Sabatti, Chia-Ho Lin, Yuguo Chen, 2006, BMC Genetics.

Measuring Dependency With Volume Tests

Chiara Sabatti, C. Sabatti, 2002 .

A novel mutation in KCNA1 causes episodic ataxia without myokymia

C. Sabatti, S. Nelson, J. Jen, 2004, Human mutation.

A genome-wide meta-analysis of association studies of Cloninger ' s Temperament Scales Service

T. Lehtimäki, C. Sabatti, J. Viikari, 2022 .

Co-expression pattern from DNA microarray experiments as a tool for operon prediction

Chiara Sabatti, Lars Rohlin, James C. Liao, 2002, Nucleic Acids Res..

With Malice Towards None: Assessing Uncertainty via Equalized Coverage pdf

Emmanuel J. Candès, Yaniv Romano, Chiara Sabatti, 2019, ArXiv.

Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

Karen L. Mohlke, Luigi Ferrucci, Florian Kronenberg, 2012, PLoS genetics.

Genetic regulation of gene expression and splicing during a 10-year period of human aging

David A. Knowles, Nathan S. Abell, Michael J. Gloudemans, 2019, Genome Biology.

Genetic effects on gene expression across human tissues

Ian C. McDowell, Christopher D. Brown, Eun Yong Kang, 2018 .

Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics

Mary Goldman, Brian Craft, Jingchun Zhu, 2016, Nature Communications.

Catch me if you can: Signal localization with knockoff e-values

C. Sabatti, Paula Gablenz, 2023, 2306.09976.

Exploring the Phenotypic Consequences of Tissue Specific Gene Exploring the Phenotypic Consequences of Tissue Specific Gene Expression Variation Inferred from GWAS Summary Statistics Expression Variation Inferred from GWAS Summary Statistics

Ian C. McDowell, Christopher D. Brown, Eun Yong Kang, 2021 .

Tag SNPs chosen from HapMap perform well in several population isolates

C. Sabatti, N. Freimer, S. Service, 2007, Genetic epidemiology.

Journal of the American Statistical Association: Comment

K. Roeder, C. Sabatti, R. Carroll, 2006 .

Exposure to NO2, CO, and PM2.5 is linked to regional DNA methylation differences in asthma

C. Sabatti, D. Dinakarpandian, K. Nadeau, 2018, Clinical Epigenetics.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Pall I. Olason, H. Stefánsson, D. Rujescu, 2009, Human molecular genetics.

Increased paternal age and the influence on burden of genomic copy number variation in the general population

J. Buizer-Voskamp, L. Kiemeney, C. Sabatti, 2013, Human Genetics.

A dictionary model for haplotyping, genotype calling, and association testing

Kenneth Lange, Chiara Sabatti, K. Lange, 2007, Genetic epidemiology.

A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales

M. Jarvelin, N. Wray, T. Lehtimäki, 2012, Translational Psychiatry.

Bayesian Gaussian Mixture Models for High-Density Genotyping Arrays

Kenneth Lange, Chiara Sabatti, K. Lange, 2008, Journal of the American Statistical Association.

Title Markov models for inferring Copy Number Variations from genotype data on Illumina platforms Permalink

C. Sabatti, J. Veldink, Hui Wang, 2008 .

Title Markov models for inferring Copy Number Variations from genotype data Permalink

C. Sabatti, J. Veldink, Hui Wang, 2008 .