Follow
Matthew T. Weirauch
Matthew T. Weirauch
Other namesMatt Weirauch, Matthew Weirauch
Verified email at cchmc.org
Title
Cited by
Year
Macrophage memories of early-life injury drive neonatal nociceptive priming
AJ Dourson, AO Fadaka, AM Warshak, A Paranjpe, B Weinhaus, ...
Cell Reports 43 (5), 2024
2024
Filaggrin loss-of-function variants are associated with atopic dermatitis phenotypes in a diverse, early-life prospective cohort
SJ Virolainen, L Satish, JM Biagini, H Chaib, WC Chang, PJ Dexheimer, ...
JCI insight 9 (9), 2024
12024
Human cytomegalovirus infection coopts chromatin organization to diminish TEAD1 transcription factor activity
K Sayeed, S Parameswaran, MJ Beucler, LE Edsall, A VonHandorf, ...
bioRxiv, 2024.04. 12.588762, 2024
2024
Shared and distinct interactions of type 1 and type 2 Epstein-Barr Nuclear Antigen 2 with the human genome
KCMF Viel, S Parameswaran, OA Donmez, CR Forney, MR Hass, C Yin, ...
BMC genomics 25 (1), 273, 2024
2024
Non-coding autoimmune risk variant defines role for ICOS in T peripheral helper cell development
T Kim, M Martínez-Bonet, Q Wang, N Hackert, JA Sparks, Y Baglaenko, ...
Nature Communications 15 (1), 2150, 2024
12024
Broad de-regulated U2AF1 splicing is prognostic and augments leukemic transformation via protein arginine methyltransferase activation
M Venkatasubramanian, L Schwartz, N Ramachandra, J Bennett, ...
bioRxiv, 2024
2024
Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis
MS Shook, X Lu, X Chen, S Parameswaran, L Edsall, MP Trimarchi, ...
The American Journal of Human Genetics 111 (2), 280-294, 2024
12024
The transcription factor ZEB2 drives the formation of age-associated B cells
D Dai, S Gu, X Han, H Ding, Y Jiang, X Zhang, C Yao, S Hong, J Zhang, ...
Science 383 (6681), 413-421, 2024
272024
Splicing neoantigen discovery with SNAF reveals shared targets for cancer immunotherapy
G Li, S Mahajan, S Ma, ED Jeffery, X Zhang, A Bhattacharjee, ...
Science Translational Medicine 16 (730), eade2886, 2024
62024
Inter-cellular mRNA Transfer Alters Human Pluripotent Stem Cell State
Y Yoneyama, RR Zhang, M Kimura, Y Cai, M Adam, S Parameswaran, ...
bioRxiv, 2024.06. 27.600209, 2024
2024
Accessible chromatin maps of inflammatory bowel disease intestine nominate cell-type mediators of genetic disease risk
JA Wayman, Z Yang, E Angerman, E Bonkowski, I Jurickova, X Chen, ...
bioRxiv, 2024.02. 09.579678, 2024
2024
TET1 regulates responses to house dust mite by altering chromatin accessibility, DNA methylation, and gene expression in airway epithelial cells
AP Brown, S Parameswaran, L Cai, S Elston, C Pham, A Barski, ...
Research Square, 2023
2023
Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation
D Torre, YS Fstkchyan, JSY Ho, Y Cheon, RS Patel, EJ Degrace, ...
Molecular cell 83 (23), 4255-4271. e9, 2023
62023
Identification of a regulatory pathway governing TRAF1 via an arthritis-associated non-coding variant
Q Wang, M Martínez-Bonet, T Kim, JA Sparks, K Ishigaki, X Chen, ...
Cell genomics 3 (11), 2023
32023
Effector memory T cells induce innate inflammation by triggering DNA damage and a non-canonical STING pathway in dendritic cells
HE Meibers, KA Warrick, A VonHandorf, CN Vallez, K Kawarizadeh, ...
Cell reports 42 (10), 2023
32023
VExD: a curated resource for human gene expression alterations following viral infection
PJ Dexheimer, M Pujato, KM Roskin, MT Weirauch
G3: Genes, Genomes, Genetics 13 (10), jkad176, 2023
2023
After the Infection: A Survey of Pathogens and Non-communicable Human Disease
M Lape, D Schnell, S Parameswaran, K Ernst, N Salomonis, LJ Martin, ...
medRxiv, 2023
2023
Lineage tracing of newly accrued nuclei in skeletal myofibers uncovers distinct transcripts and interplay between nuclear populations
C Sun, CO Swoboda, MJ Petrany, S Parameswaran, A VonHandorf, ...
bioRxiv, 2023
22023
High-throughput identification of functional regulatory SNPs in systemic lupus erythematosus
Q Wang, T Kim, M Martínez-Bonet, VRC Aguiar, S Sim, J Cui, JA Sparks, ...
bioRxiv, 2023.08. 16.553538, 2023
2023
A functional mechanism for a non-coding variant near AGTR2 associated with risk for preterm birth
L Wang, RM Rossi, X Chen, J Chen, J Runyon, M Chawla, D Miller, ...
BMC medicine 21 (1), 258, 2023
12023
The system can't perform the operation now. Try again later.
Articles 1–20