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Zechuan Lin, PhD

Associate Research Scientist
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About

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Associate Research Scientist

Biography

Dr. Lin was recruited to the Adams Center from Harvard in 2024. He received his PhD at the prestigious Peking University, one of China’s highest ranked educational institutions under the tutelage of Prof. Xing Wang Deng, a fellow of the U.S. National Academy of Sciences in 2019.

Dr. Lin’s research is focused on revealing the causal relationships between genome variants, epigenetic marks, gene expression, and quantitative traits. Dr. Lin has published on complex and quantitative trait genetics during his graduate studies as first author in Lin et al. PNAS, 2020 and as co-first author in Wang*, Lin* et al., Nature Genetics, 2020.

In these high-profile publications, Dr. Lin honed the quantitative trait locus and causal inference analyses, that he is now applying at the single-cell level to Parkinson’s disease in the Parkinson Cell Atlas in 5D project.

Last Updated on November 17, 2025.

Appointments

  • Neurology

    Associate Research Scientist
    Primary

Other Departments & Organizations

Education & Training

Postdoc Research Fellow
Harvard Medical School/Brigham and Women's Hospital (2023)
PhD
Peking University, College of Life Sciences (2019)

Research

Overview

My research programs are dedicated to a central question: how to translate these complex human brain-cell-spatial gene activity map into druggable targets of human brain diseases for combating complex diseases like Parkinson's? To address this question, my group is developing novel statistical model, and also apply statistical genetics, functional genomics, and computational biology approaches to construct a brain-cell-spatial gene activity map, and then reveal novel therapeutic strategies of Parkinson’s disease by connecting brain-cell-spatial gene regulation insights with disease risk.

Research at a Glance

Publications Timeline

A big-picture view of Zechuan Lin, PhD's research output by year.
23Publications
684Citations

Publications

Featured Publications

  • Single cell eQTL mapping reveals convergent glial–neuronal risk architecture in Parkinson's disease
    Lin Z, Parker J, Nithianandam V, Mathivanan S, Wang T, Liao Z, Simmons SK, Tuncali I, Adiconis X, Haywood N, Weykopf B, Teng X, Sharma M, Yuan J, Baecher-Allan C, Dong X, Beach TG, Serrano GE, Levin JZ, Zhang S, Feany MB, Scherzer CR. Single cell eQTL mapping reveals convergent glial–neuronal risk architecture in Parkinson's disease. 2026 DOI: 10.64898/2026.04.24.720642.
    Peer-Reviewed Original Research

2026

  • Multi-locus genetic dosage shapes cognitive disease progression in Parkinson’s patients: 15-year meta-analysis of 24 cohorts
    Kang X, Lin Z, Calikusu FZ, Miller LA, Soriano S, Locascio JJ, Corvol JC, Maple-Grødem J, Fan Y, Mead K, Campbell MC, Elbaz A, Lesage S, Brice A, Hung AY, Schwarzschild MA, Hayes MT, Wills AM, Herrington TM, Liu G, Ravina B, Taba P, Kõks S, Simuni T, Forsgren L, Counsell C, Macleod AD, Beach TG, Alves G, Tysnes OB, Perlmutter JS, Heutink P, Kasten M, Mollenhauer B, Trenkwalder C, Klein C, Hepp DH, Backstrom D, Svenningsson P, Hu MT, Williams-Gray CH, Barker RA, , Scherzer CR. Multi-locus genetic dosage shapes cognitive disease progression in Parkinson’s patients: 15-year meta-analysis of 24 cohorts. Npj Parkinson's Disease 2026 DOI: 10.1038/s41531-026-01367-y.
    Peer-Reviewed Original Research
  • Experimental and computational methods for allelic imbalance analysis from single-nucleus RNA-seq data.
    Simmons SK, Adiconis X, Haywood N, Parker J, Lin Z, Liao Z, Tuncali I, Shin A, Jagadeesh K, Gosik K, Gatzen M, Smith JT, El Kodsi DN, Kuras Y, Baecher-Allan C, Serrano GE, Beach TG, Garimella K, Al'Khafaji AM, Rozenblatt-Rosen O, Regev A, Dong X, Scherzer CR, Levin JZ. Experimental and computational methods for allelic imbalance analysis from single-nucleus RNA-seq data. Genome Biol 2026 PMID: 41965748, DOI: 10.1186/s13059-026-04062-6.
    Peer-Reviewed Original Research
  • Integrating Long-Read Structural Variant Analysis with single-nucleus RNA-seq to Elucidate Gene Expression Effects in Disease.
    Kim K, Lin Z, Simmons SK, Parker J, Kearney M, Liao Z, Haywood N, Zhang J, Cline MP, Tuncali I, Sharma M, Serrano GE, Beach TG, Dong X, Popic V, Scherzer CR, Levin JZ. Integrating Long-Read Structural Variant Analysis with single-nucleus RNA-seq to Elucidate Gene Expression Effects in Disease. BioRxiv 2026 PMID: 41929179, DOI: 10.64898/2026.03.20.713192.
    Peer-Reviewed Original Research

2022

2020

Academic Achievements & Community Involvement

Honors

  • honor

    Resource-Limited Award

  • honor

    Research Grants Award

  • honor

    Multi-omics Meta-analysis (MoMa) program

Get In Touch

Contacts

Locations

  • 101 College Street

    Academic Office

    Fl 10, Ste 1029

    New Haven, CT 06510