World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
67
Citations
37512
World Ranking
8024
National Ranking
3635

Overview

Chiara Sabatti is affiliated with Stanford University in the United States, focusing on research in biochemistry, genetics, and molecular biology. Their scholarly work spans 62 publications in these main fields, with notable subfield contributions in genetics, molecular biology, statistics and probability, biomedical engineering, and pulmonary and respiratory medicine.

The scientist's research covers a broad range of topics, including genetic associations and epidemiology, gene expression and cancer classification, genetic and phenotypic traits in livestock, genetic mapping and diversity in plants and animals, statistical methods in clinical trials, advanced causal inference techniques, and single-cell and spatial transcriptomics.

Chiara Sabatti has authored multiple papers published in several prominent venues. Notable recent papers include:

  • Determinants of telomere length across human tissues, 2020, Science
  • Progenitor identification and SARS-CoV-2 infection in human distal lung organoids, 2020, Nature
  • Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics, 2021, Science
  • Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease, 2021, Cell
  • False discovery rate control in genome-wide association studies with population structure, 2021, Proceedings of the National Academy of Sciences

The frequent coauthors collaborating with Chiara Sabatti include Emmanuel J. Candès, Matteo Sesia, Zihuai He, Stephen Bates, and Benjamin B. Chu. The scientist's work has appeared regularly in venues such as bioRxiv (Cold Spring Harbor Laboratory), arXiv (Cornell University), Nature Communications, Science, and the Proceedings of the National Academy of Sciences.

This profile reflects a research career centered on the intersection of genetics, molecular biology, and statistical methodology applied to complex biological and medical questions, with a record of collaboration and publication in high-impact journals and preprint platforms.

Best Publications

  • The GTEx Consortium atlas of genetic regulatory effects across human tissues

    F Aguet;AN Barbeira;R Bonazzola;A Brown

  • Biological, clinical and population relevance of 95 loci for blood lipids

    Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson

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

    Hyun Min Kang;Jae Hoon Sul;Noah A. Zaitlen

  • Large recurrent microdeletions associated with schizophrenia

    Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen

  • Organoid Modeling of the Tumor Immune Microenvironment.

    James T. Neal;Xingnan Li;Junjie Zhu;Valeria Giangarra

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

    Alvaro N. Barbeira;Scott P. Dickinson;Rodrigo Bonazzola;Jiamao Zheng

  • Genetic analyses of diverse populations improves discovery for complex traits

    Genevieve L. Wojcik;Mariaelisa Graff;Katherine K. Nishimura;Ran Tao

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

    Yurii S Aulchenko;Samuli Ripatti;Ida Lindqvist;Dorret Boomsma

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

    Chiara Sabatti;Anna-Liisa Hartikainen;Anneli Pouta

  • Network component analysis: Reconstruction of regulatory signals in biological systems

    James C. Liao;Riccardo Boscolo;Young-Lyeol Yang;Linh My Tran

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

    Z Dastani;Hivert M-F.;Hivert M-F.;N Timpson;Perry Jrb.;Perry Jrb.

  • Disruption of the neurexin 1 gene is associated with schizophrenia

    Dan Rujescu;Andres Ingason;Andres Ingason;Sven Cichon;Olli P.H. Pietiläinen

  • The Human Phenome Project

    Nelson Freimer;Chiara Sabatti

  • The DYT1 phenotype and guidelines for diagnostic testing

    Susan B Bressman;C Sabatti;Deborah Raymond;D de Leon

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

    Ameen A. Salahudeen;Ameen A. Salahudeen;Shannon S. Choi;Arjun Rustagi;Junjie Zhu

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

    Yambazi Banda;Mark N. Kvale;Thomas J. Hoffmann;Stephanie E. Hesselson

  • Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

    Terry Vrijenhoek;Jacobine E. Buizer-Voskamp;Inge van der Stelt;Eric Strengman

  • SLOPE { Adaptive Variable Selection via Convex Optimization

    Małgorzata Bogdan;Ewout van den Berg;Chiara Sabatti;Weijie Su

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

    Joseph DeYoung;Maria Karayiorgou;J Louw Roos

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

    Chiara Sabatti;Nelson Freimer

Frequent Co-Authors

Nelson B. Freimer
Nelson B. Freimer University of California, Los Angeles
Victor I. Reus
Victor I. Reus University of California, San Francisco
Roel A. Ophoff
Roel A. Ophoff University of California, Los Angeles
Carrie E. Bearden
Carrie E. Bearden University of California, Los Angeles
Emmanuel J. Candès
Emmanuel J. Candès Stanford University
Javier I. Escobar
Javier I. Escobar Rutgers, The State University of New Jersey
Andrés Ruiz-Linares
Andrés Ruiz-Linares Fudan University
Rita M. Cantor
Rita M. Cantor University of California, Los Angeles
Samuli Ripatti
Samuli Ripatti University of Helsinki
Aarno Palotie
Aarno Palotie University of Helsinki

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