Work
By organ system and year. ◆ marks genetics, ● marks multiomics; most papers use both.
- Trang KB, Sharma P, Cook L, et al. 3D chromatin-based variant-to-gene maps across 57 human cell types reveal the cellular and genetic architecture of autoimmune disease susceptibility. Genome Biol. 2025;26:414. First author Story →
- Conery M*, Pippin JA*, Wagley Y*, Trang K*, et al. GWAS-informed data integration and non-coding CRISPRi screen illuminate genetic etiology of bone mineral density. Genome Biol. 2025;26:331. Co-first Story →
- Qiu R, Trang KB, Shalaby C, et al. Multimodal analysis of in vitro hematopoiesis reveals blood cell-specific genetic impacts on complex disease traits. bioRxiv 2025. Preprint
- Trang KB, Pahl MC, Pippin JA, et al. 3D genomic features across >50 diverse cell types reveal insights into the genomic architecture of childhood obesity. eLife 2025;13:RP95411. First author
- Mace K*, Trang KB*, Zimmerman AJ, et al. Cross-trait clustering of sub-threshold sleep genetic signals identifies EGR2 as a conserved regulator of sleep. bioRxiv 2026. Co-first · preprint
- Zimmerman AJ, Biglari S, Trang KB, et al. Cell-specific variant-to-gene mapping identifies conserved neural and glial regulators of sleep. bioRxiv 2026. Preprint
- Laub S, Tulina N, Hoffman M, Faryean JB, Ramachandran S, Trang K, et al. Integrative genomics and single-cell CRISPRi screening dissect Alzheimer GWAS non-coding variants regulating TSPAN14. Am J Hum Genet. 2026;113(6):1253–1278.
- Kusic D, Salzman M, Heil J, Grant SFA, Trang KB, et al. Genetic variation in BDNF is associated with opioid use disorder severity. Hum Genet. 2026, in press.
- Trang KB, Chesi A, Toikumo S, et al. Shared and unique 3D genomic features of substance use disorders across multiple cell types. medRxiv 2024. First author · preprint
- Nirgude S, Tichy ED, Zhang Y, Trang KB, et al. Beckwith-Wiedemann syndrome multiomic analysis of hepatoblastoma uncovers unique tumour heterogeneity and cellular landscapes. BJC Rep. 2026;4(1):25.
- Littleton SH, Trang KB, Volpe CM, et al. Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3′ UTR of FAIM2. Cell Genom. 2024;4(5):100556.
- Trang K, Grant SFA. Genetics and epigenetics in the obesity phenotyping scenario. Rev Endocr Metab Disord. 2023;24(5):775–793. First author · invited review
- Caputo T, Tran VDT, Bararpour N, Winkler C, Aguileta G, Trang KB, et al. Anti-adipogenic signals at the onset of obesity-related inflammation in white adipose tissue. Cell Mol Life Sci. 2021;78(1):227–247.
- Wigger L, Casals-Casas C, Baruchet M, Trang KB, et al. System analysis of cross-talk between nuclear receptors reveals an opposite regulation of the cell cycle by LXR and FXR in human HepaRG liver cells. PLoS One 2019;14(8):e0220894.
* co-first authors. Full list on Google Scholar.