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Publications

Clinical and genomic characterization of Klebsiella pneumoniae infections in Dhaka, Bangladesh.

Kawser Z, Sridhar S, Kar S, et al. Clinical and genomic characterization of Klebsiella pneumoniae infections in Dhaka, Bangladesh. Journal of global antimicrobial resistance. 2024. doi:10.1016/j.jgar.2024.12.016

Venous Endothelial Cell Transcriptomic Profiling Implicates METAP1 in Preeclampsia.

Pabón MA, Weisbrod RM, Castro C, et al. Venous Endothelial Cell Transcriptomic Profiling Implicates METAP1 in Preeclampsia. Circulation research. 2024. doi:10.1161/CIRCRESAHA.124.324606

Ischemic Stroke in Women: Understanding Sex-Specific Risk Factors, Treatment Considerations, and Outcomes.

Eng PC, Tan LLY, Kimball TN, Prapiadou S, Tan BYQ. Ischemic Stroke in Women: Understanding Sex-Specific Risk Factors, Treatment Considerations, and Outcomes. Journal of cardiovascular development and disease. 2024;11(12). doi:10.3390/jcdd11120382

LDB1 establishes multi-enhancer networks to regulate gene expression.

Aboreden NG, Lam JC, Goel VY, et al. LDB1 establishes multi-enhancer networks to regulate gene expression. Molecular cell. 2024. doi:10.1016/j.molcel.2024.11.037

LDB1 establishes multi-enhancer networks to regulate gene expression.

Aboreden NG, Lam JC, Goel VY, et al. LDB1 establishes multi-enhancer networks to regulate gene expression. Molecular cell. 2024. doi:10.1016/j.molcel.2024.11.037

Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.

Sabeh P, Dumas SA, Maios C, et al. Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.11.009

Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.

Sabeh P, Dumas SA, Maios C, et al. Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability. American journal of human genetics. 2024. doi:10.1016/j.ajhg.2024.11.009

MaAsLin 3: Refining and extending generalized multivariable linear models for meta-omic association discovery.

Nickols WA, Kuntz T, Shen J, et al. MaAsLin 3: Refining and extending generalized multivariable linear models for meta-omic association discovery. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.12.13.628459

Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts.

Kals M, Wilson L, Levey DF, et al. Genetic vulnerability and adverse mental health outcomes following mild traumatic brain injury: a meta-analysis of CENTER-TBI and TRACK-TBI cohorts. EClinicalMedicine. 2024;78:102956. doi:10.1016/j.eclinm.2024.102956

The Scalable Variant Call Representation: Enabling Genetic Analysis Beyond One Million Genomes.

Poterba T, Vittal C, King D, et al. The Scalable Variant Call Representation: Enabling Genetic Analysis Beyond One Million Genomes. Bioinformatics (Oxford, England). 2024. doi:10.1093/bioinformatics/btae746