日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Inferring fungal cis-regulatory networks from genome sequences via unsupervised and interpretable representation learning

通过无监督和可解释的表征学习从基因组序列推断真菌顺式调控网络

Moses, Alan M; Stajich, Jason E; Gasch, Audrey P; Knowles, David A

Deriving Mendelian Randomization-Based Causal Networks of Brain Imaging Phenotypes and Bipolar Disorder

基于孟德尔随机化的脑成像表型与双相情感障碍因果网络构建

O'Connell, Shane; Brown, Brielin C; Cannon, Dara M; Broin, Pilib Ó; Parker, Nadine; Alnæs, Dag; Westlye, Lars T; Banerjee, Saikat; Nabulsi, Leila; Corley, Emma; Andreassen, Ole A; Knowles, David A; Mullins, Niamh

Cas13d-mediated isoform-specific RNA knockdown with a unified computational and experimental toolbox

利用统一的计算和实验工具箱实现 Cas13d 介导的异构体特异性 RNA 敲低

Schertzer, Megan D; Stirn, Andrew; Isaev, Keren; Pereira, Laura; Park, Stella H; Das, Anjali; Réal, Aline; Jeffery, Erin D; Harbison, Claire; Wessels, Hans-Hermann; Sheynkman, Gloria M; Sanjana, Neville E; Knowles, David A

Large-scale causal discovery using interventional data sheds light on gene network structure in k562 cells

利用干预数据进行大规模因果发现,揭示了K562细胞中的基因网络结构

Brown, Brielin C; Tokolyi, Alex; Morris, John A; Lappalainen, Tuuli; Knowles, David A

Leveraging functional annotations to map rare variants associated with Alzheimer disease with gruyere

利用功能注释将与阿尔茨海默病相关的罕见变异与格鲁耶尔奶酪进行比对

Das, Anjali; Lakhani, Chirag; Terwagne, Chloé; Lin, Jui-Shan T; Naito, Tatsuhiko; Raj, Towfique; Knowles, David A

Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice

儿童交替性偏瘫与Atp1a3基因突变相关,揭示了小鼠神经系统多种改变。

Terrey, Markus; Krivoshein, Georgii; Adamson, Scott I; Arystarkhova, Elena; Anderson, Laura; Szwec, John; McKee, Shelby; Jones, Holly; Perkins, Sara; Selvam, Vijay; Piec, Pierre-Alexandre; Chhaya, Dweet; Dehn, Ari; Zuberi, Aamir; Murray, Stephen A; Morsci, Natalia S; Sweadner, Kathleen J; Knowles, David A; Tolner, Else A; van den Maagdenberg, Arn M J M; Lutz, Cathleen M

Mapping genetic effects on splicing in ten thousand post-mortem brain samples reveals novel mediators of neurological disease risk

通过对一万份死后脑组织样本进行基因剪接效应分析,揭示了神经系统疾病风险的新介质。

Réal, Aline; Bp, Kailash; Dredge, Winston H; Muller, Benjamin Z; Jang, Beomjin; Tokolyi, Alex; Won, Hong-Hee; Humphrey, Jack; Raj, Towfique; Knowles, David A

CONVEX APPROACHES TO ISOLATE THE SHARED AND DISTINCT GENETIC STRUCTURES OF SUBPHENOTYPES IN HETEROGENEOUS COMPLEX TRAITS

利用凸方法分离异质复杂性状中亚表型的共有和独特遗传结构

Banerjee, Saikat; O'Connell, Shane; Colbert, Sarah M C; Mullins, Niamh; Knowles, David A

Leveraging functional annotations to map rare variants associated with Alzheimer's disease with gruyere

利用功能注释将与阿尔茨海默病相关的罕见变异与格鲁耶尔奶酪进行比对

Das, Anjali; Lakhani, Chirag; Terwagne, Chloé; Lin, Jui-Shan T; Naito, Tatsuhiko; Raj, Towfique; Knowles, David A

Perplexity as a Metric for Isoform Diversity in the Human Transcriptome

困惑度作为人类转录组中异构体多样性的指标

Schertzer, Megan D; Park, Stella H; Su, Jiayu; Sheynkman, Gloria M; Knowles, David A