ӳ��ý

Publications

Chromosome-length genome assemblies and cytogenomic analyses of pangolins reveal remarkable chromosome counts and plasticity.

Houck ML, Koepfli KP, Hains T, et al. Chromosome-length genome assemblies and cytogenomic analyses of pangolins reveal remarkable chromosome counts and plasticity. Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 2023;31(2):13. doi:10.1007/s10577-023-09722-y

Stepwise activities of mSWI/SNF family chromatin remodeling complexes direct T cell activation and exhaustion.

Battistello E, Hixon KA, Comstock DE, et al. Stepwise activities of mSWI/SNF family chromatin remodeling complexes direct T cell activation and exhaustion. Molecular cell. 2023;83(8):1216-1236.e12. doi:10.1016/j.molcel.2023.02.026

RNAget: an API to securely retrieve RNA quantifications.

Upchurch S, Palumbo E, Adams J, et al. RNAget: an API to securely retrieve RNA quantifications. Bioinformatics (Oxford, England). 2023;39(4). doi:10.1093/bioinformatics/btad126

Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass.

Khurshid S, Lazarte J, Pirruccello JP, et al. Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass. Nature communications. 2023;14(1):1558. doi:10.1038/s41467-023-37173-w

Passive and active markers of cortical excitability in epilepsy.

Ramantani G, Westover B, Gliske S, et al. Passive and active markers of cortical excitability in epilepsy. Epilepsia. 2023. doi:10.1111/epi.17578

It is better to light a candle than to curse the darkness: single-cell transcriptomics sheds new light on pancreas biology and disease.

Cephas AT, Hwang WL, Maitra A, Parnas O, DelGiorno KE. It is better to light a candle than to curse the darkness: single-cell transcriptomics sheds new light on pancreas biology and disease. Gut. 2023;72(6):1211-1219. doi:10.1136/gutjnl-2022-329313

Characterizing the molecular impact of KMT2D variants on the epigenetic and transcriptional landscapes in kabuki syndrome.

Jung YL, Hung C, Choi J, Lee EA, Bodamer O. Characterizing the molecular impact of KMT2D variants on the epigenetic and transcriptional landscapes in kabuki syndrome. Human molecular genetics. 2023. doi:10.1093/hmg/ddad059

Comparing genomic variant identification protocols for .

Li X, Muñoz JF, Gade L, et al. Comparing genomic variant identification protocols for . Microbial genomics. 2023;9(4). doi:10.1099/mgen.0.000979

The Use of Artificial Intelligence to Predict the Development of Atrial Fibrillation.

Pipilas D, Friedman SF, Khurshid S. The Use of Artificial Intelligence to Predict the Development of Atrial Fibrillation. Current cardiology reports. 2023;25(5):381-389. doi:10.1007/s11886-023-01859-w

Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing.

Cortés-Ciriano I, Lee JJK, Xi R, et al. Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing. Nature genetics. 2023. doi:10.1038/s41588-023-01315-z