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Brittany Lasseigne
PeerJ Editor, Author & Reviewer
1,485 Points

Contributions by role

Author 135
Reviewer 15
Editor 1,335

Contributions by subject area

Computational Biology
Genomics
Oncology
Bioinformatics
Cell Biology
Nephrology
Biochemistry
Molecular Biology
Toxicology
Histology
Cardiology
Internal Medicine
Nutrition
Neuroscience
Surgery and Surgical Specialties
Gastroenterology and Hepatology
Pharmacology
Rheumatology
Neurology
Global Health
Translational Medicine
Cognitive Disorders
Medical Genetics
Women's Health
Emergency and Critical Care
Respiratory Medicine

Brittany N Lasseigne

PeerJ Editor, Author & Reviewer

Summary

Brittany N. Lasseigne, PhD is an Assistant Professor of Cell, Developmental and Integrative Biology at The University of Alabama at Birmingham School of Medicine. She trained in Biotechnology, Science, and Engineering at Mississippi State University (B.S.) and the University of Alabama in Huntsville (Ph.D.) and completed a postdoctoral fellowship in genetics and genomics at the HudsonAlpha Institute for Biotechnology.

Her lab develops and applies genomic- and data-driven strategies (including single-cell and long-read sequencing) to discover biological signatures that might be used to improve patient care and provide insight into the cellular and molecular processes contributing to disease, especially for diseases impacting the brain and/or kidney. Their recent work includes prioritizing drug repurposing candidates for cancers and polycystic kidney disease, evaluating preclinical models and cross-species transcriptomic signatures to improve disease modeling, and applying single-cell and long-read technologies to neurological disease tissues to understand the role that context plays in disease etiology, progression, and treatment.

The Lasseigne Lab is currently focused on integrating genomics data, functional annotations, and patient information with machine learning and regulatory network approaches across diseases that impact the brain or kidney to discover novel mechanisms in disease etiology and progression, identify genome-driven therapeutic targets and opportunities for drug repositioning and repurposing, determine clinically-relevant biomarkers, and understand how cellular context contributes to these diseases. Collectively, these distinct projects all apply genetics and genomics to human diseases and build tools to accelerate future research. Their lab also develops data science software and analytical pipelines that are open-source, well-documented, and hosted by third-party code distributors, critical for facilitating reproducibility and enabling the research community to use the methods they develop.

Bioinformatics Computational Biology Data Mining & Machine Learning Genomics Nephrology Neuroscience Oncology Pharmacology

Editorial Board Member

PeerJ - the Journal of Life & Environmental Sciences

Past or current institution affiliations

University of Alabama - Birmingham

Work details

Assistant Professor

University of Alabama - Birmingham
Cell, Developmental and Integrative Biology
Brittany N. Lasseigne, PhD is an Assistant Professor of Cell, Developmental and Integrative Biology at The University of Alabama at Birmingham School of Medicine. She trained in Biotechnology, Science, and Engineering at Mississippi State University (B.S.) and the University of Alabama in Huntsville (Ph.D.) and completed a postdoctoral fellowship in genetics and genomics at the HudsonAlpha Institute for Biotechnology. Her lab develops and applies genomic- and data-driven strategies (including single-cell and long-read sequencing) to discover biological signatures that might be used to improve patient care and provide insight into the cellular and molecular processes contributing to disease, especially for diseases impacting the brain and/or kidney. Their recent work includes prioritizing drug repurposing candidates for cancers and polycystic kidney disease, evaluating preclinical models and cross-species transcriptomic signatures to improve disease modeling, and applying single-cell and long-read technologies to neurological disease tissues to understand the role that context plays in disease etiology, progression, and treatment. The Lasseigne Lab is currently focused on integrating genomics data, functional annotations, and patient information with machine learning and regulatory network approaches across diseases that impact the brain or kidney to discover novel mechanisms in disease etiology and progression, identify genome-driven therapeutic targets and opportunities for drug repositioning and repurposing, determine clinically-relevant biomarkers, and understand how cellular context contributes to these diseases. Collectively, these distinct projects all apply genetics and genomics to human diseases and build tools to accelerate future research. Their lab also develops data science software and analytical pipelines that are open-source, well-documented, and hosted by third-party code distributors, critical for facilitating reproducibility and enabling the research community to use the methods they develop.

Websites

  • Google Scholar
  • GitHub
  • Lasseigne Lab Website

PeerJ Contributions

  • Articles 1
  • Edited 10
April 25, 2023
CINmetrics: an R package for analyzing copy number aberrations as a measure of chromosomal instability
Vishal H. Oza, Jennifer L. Fisher, Roshan Darji, Brittany N. Lasseigne
https://doi.org/10.7717/peerj.15244 PubMed 37123011

Academic Editor on

August 29, 2025
Survival predictors of lung cancer patients in ICU: the importance of acute kidney injury prediction and prevention
Jue Shen, Changsong Wang, Gang Ma, Hong-Zhi Wang, Xuezhong Xing, Biao Zhu, Jianghong Zhao, Donghao Wang, Mingou Cui
https://doi.org/10.7717/peerj.19885 PubMed 40900749
August 26, 2025
A closer look at severe acute kidney injury: risk factors and outcomes in PD-1/PD-L1 antibody treatment from a retrospective study
Yuemeng Wu, Lingfan Luo, Xin Sun, Xiaolan Ye, Yan Ren, Wei Zhang, Shuangshan Bu, Yiwen Li, Bin Zhu, Lina Shao
https://doi.org/10.7717/peerj.19886 PubMed 40895060
July 21, 2025
P21 activated kinase 6: a promising tool for predicting small cell lung cancer diagnosis and treatment response
Simei Chen, Kexin Han, Yinyi Chen, Liping Wei, Xinlu Sun, Yi Luo, Lili Wen, Liming Tan
https://doi.org/10.7717/peerj.19714 PubMed 40708824
February 27, 2025
Development of a prognostic model based on the ceRNA network in Triple-Negative Breast cancer
Yimin Zhu, Jiayu Wang, Binghe Xu
https://doi.org/10.7717/peerj.19063 PubMed 40034665
December 9, 2024
The role of CD47 in immune escape of colon cancer and its correlation with heterogeneity of tumor immune microenvironment
Qiu-Si Tian, ChunMei Zhang, Zhi-Jun Bao, ZhiGang Pei
https://doi.org/10.7717/peerj.18579 PubMed 39670101
October 30, 2024
Development and internal and external validation of a nomogram model for predicting the risk of chronic kidney disease progression in IgA nephropathy patients
Ying Zhang, Zhixin Wang, Wenwu Tang, Xinzhu Yuan, Xisheng Xie
https://doi.org/10.7717/peerj.18416 PubMed 39494280
September 18, 2024
Comprehensive analysis of macrophage-associated inflammatory genes in AMI based on bulk combined with single-cell sequencing data
Xugang Kong, Guangjun Jin
https://doi.org/10.7717/peerj.17981 PubMed 39308815
August 9, 2024
The role of lncRNAs related ceRNA regulatory network in multiple hippocampal pathological processes during the development of perioperative neurocognitive disorders
Bowen Zhou, Yuxiang Zheng, Zizheng Suo, Mingzhu Zhang, Wenjie Xu, Lijuan Wang, Dazhuang Ge, Yinyin Qu, Qiang Wang, Hui Zheng, Cheng Ni
https://doi.org/10.7717/peerj.17775 PubMed 39135955
June 4, 2024
Identification of proteins related to SIS3 by iTRAQ and PRM-based comparative proteomic analysis in cisplatin-induced acute kidney injury
Jiayan Huang, Jian Ye, Yi Gao, Yu Wang, Qing Zhao, Tanqi Lou, Weiyan Lai
https://doi.org/10.7717/peerj.17485 PubMed 38854800
May 29, 2024
Investigating molecular markers linked to acute myocardial infarction and cuproptosis: bioinformatics analysis and validation in the AMI mice model
Bingyu Wang, Jianqing Zhou, Ning An
https://doi.org/10.7717/peerj.17280 PubMed 38827298