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Authors: Mulin Jun Li
Journal Article
CAUSALdb2: an updated database for causal variants of complex traits Open Access
Nucleic Acids Research, Volume 53, Issue D1, 6 January 2025, Pages D1295–D1301, https://doi.org/10.1093/nar/gkae1096
Published: 18 November 2024
Journal Article
webTWAS 2.0: update platform for identifying complex disease susceptibility genes through transcriptome-wide association study Open Access
Nucleic Acids Research, Volume 53, Issue D1, 6 January 2025, Pages D1261–D1269, https://doi.org/10.1093/nar/gkae1022
Published: 11 November 2024
Journal Article
SingleQ: a comprehensive database of single-cell expression quantitative trait loci (sc-eQTLs) cross human tissues Open Access
in
Database
Database, Volume 2024, 2024, baae010, https://doi.org/10.1093/database/baae010
Published: 09 March 2024
Journal Article
ADAR1 links R-loop homeostasis to ATR activation in replication stress response Open Access
Nucleic Acids Research, Volume 51, Issue 21, 27 November 2023, Pages 11668–11687, https://doi.org/10.1093/nar/gkad839
Published: 13 October 2023
Journal Article
QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes Open Access
Nucleic Acids Research, Volume 51, Issue D1, 6 January 2023, Pages D1122–D1128, https://doi.org/10.1093/nar/gkac1020
Published: 04 November 2022
Journal Article
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Open Access
Nucleic Acids Research, Volume 50, Issue 6, 8 April 2022, Page e34, https://doi.org/10.1093/nar/gkab1234
Published: 20 December 2021
Journal Article
webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study Open Access
Nucleic Acids Research, Volume 50, Issue D1, 7 January 2022, Pages D1123–D1130, https://doi.org/10.1093/nar/gkab957
Published: 20 October 2021
Journal Article
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases Open Access
Nucleic Acids Research, Volume 50, Issue D1, 7 January 2022, Pages D1408–D1416, https://doi.org/10.1093/nar/gkab853
Published: 27 September 2021
Journal Article
vSampler: fast and annotation-based matched variant sampling tool Free
Bioinformatics, Volume 37, Issue 13, July 2021, Pages 1915–1917, https://doi.org/10.1093/bioinformatics/btaa883
Published: 16 October 2020
Journal Article
HRP2–DPF3a–BAF complex coordinates histone modification and chromatin remodeling to regulate myogenic gene transcription Open Access
Nucleic Acids Research, Volume 48, Issue 12, 09 July 2020, Pages 6563–6582, https://doi.org/10.1093/nar/gkaa441
Published: 27 May 2020
Journal Article
Methods and resources to access mutation-dependent effects on cancer drug treatment Free
Briefings in Bioinformatics, Volume 21, Issue 6, November 2020, Pages 1886–1903, https://doi.org/10.1093/bib/bbz109
Published: 21 November 2019
Journal Article
CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies Open Access
Nucleic Acids Research, Volume 48, Issue D1, 08 January 2020, Pages D807–D816, https://doi.org/10.1093/nar/gkz1026
Published: 06 November 2019
Journal Article
QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes Open Access
Nucleic Acids Research, Volume 48, Issue D1, 08 January 2020, Pages D983–D991, https://doi.org/10.1093/nar/gkz888
Published: 10 October 2019
Journal Article
regBase: whole genome base-wise aggregation and functional prediction for human non-coding regulatory variants Open Access
Nucleic Acids Research, Volume 47, Issue 21, 02 December 2019, Page e134, https://doi.org/10.1093/nar/gkz774
Published: 12 September 2019
Journal Article
WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation counts Open Access
Nucleic Acids Research, Volume 47, Issue 16, 19 September 2019, Page e96, https://doi.org/10.1093/nar/gkz566
Published: 09 July 2019
Journal Article
EDITOR'S CHOICE
Neurobiological substrates underlying the effect of genomic risk for depression on the conversion of amnestic mild cognitive impairment Free
in
Brain
Brain, Volume 141, Issue 12, December 2018, Pages 3457–3471, https://doi.org/10.1093/brain/awy277
Published: 14 November 2018
Journal Article
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits Open Access
Nucleic Acids Research, Volume 46, Issue W1, 2 July 2018, Pages W114–W120, https://doi.org/10.1093/nar/gky407
Published: 16 May 2018
Journal Article
A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissues Free
Bioinformatics, Volume 34, Issue 18, September 2018, Pages 3145–3150, https://doi.org/10.1093/bioinformatics/bty318
Published: 26 April 2018
Journal Article
Integrated transcriptomic and regulatory network analyses identify microRNA-200c as a novel repressor of human pluripotent stem cell-derived cardiomyocyte differentiation and maturation Get access
Cardiovascular Research, Volume 114, Issue 6, 01 May 2018, Pages 894–906, https://doi.org/10.1093/cvr/cvy019
Published: 24 January 2018
Journal Article
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers Open Access
Nucleic Acids Research, Volume 45, Issue W1, 3 July 2017, Pages W215–W221, https://doi.org/10.1093/nar/gkx400
Published: 08 May 2017
