Brittany N. Lasseigne

Affiliations: 
University of Alabama, Birmingham, Birmingham, AL, United States 
Area:
genetics, genomics, computational biology, bioinformatics
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"Brittany Lasseigne"
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Wilk EJ, Howton TC, Fisher JL, et al. (2023) Prioritized polycystic kidney disease drug targets and repurposing candidates from pre-cystic and cystic mouse Pkd2 model gene expression reversion. Molecular Medicine (Cambridge, Mass.). 29: 67
Libby CJ, Gc S, Benavides GA, et al. (2021) A role for GLUT3 in glioblastoma cell invasion that is not recapitulated by GLUT1. Cell Adhesion & Migration. 15: 101-115
Cochran JN, Geier EG, Bonham LW, et al. (2020) Non-Coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases. American Journal of Human Genetics
Cochran JN, McKinley EC, Cochran M, et al. (2019) Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor Molecular Case Studies. 5
Gelfman S, Dugger SA, Araujo Martins Moreno C, et al. (2019) A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS. Genome Research
Cochran ME, Cochran JN, McKinley E, et al. (2019) P3-143: UTILITY OF GENOMIC SEQUENCING IN CASES OF EARLY-ONSET AND FAMILIAL DEMENTIA Alzheimer's & Dementia. 15: P986-P986
Cochran JN, Geier EG, Acosta-Uribe J, et al. (2019) P2-126: Loss-Of-Function Coding And Non-Coding Variants In Tet2 Are Associated With Neurodegenerative Diseases Alzheimers & Dementia. 15
Lasseigne BN, Brooks JD. (2018) The Role of DNA Methylation in Renal Cell Carcinoma. Molecular Diagnosis & Therapy
Ramaker RC, Bowling KM, Lasseigne BN, et al. (2017) Post-mortem molecular profiling of three psychiatric disorders. Genome Medicine. 9: 72
Ramaker RC, Lasseigne BN, Hardigan AA, et al. (2017) RNA sequencing-based cell proliferation analysis across 19 cancers identifies a subset of proliferation-informative cancers with a common survival signature. Oncotarget
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