about
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.Modular composition predicts kinase/substrate interactions.A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock.Mapping Splicing Quantitative Trait Loci in RNA-Seq.Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humansRNA-Seq identifies novel myocardial gene expression signatures of heart failureGenome-wide association study reveals two loci for serum magnesium concentrations in European-American children.PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distributionTissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases.Comprehensive analysis of gene expression in human retina and supporting tissues.Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies.Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).Common variants at 5q33.1 predispose to migraine in African-American children.Mapping Splicing Quantitative Trait Loci in RNA-SeqAssociation of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family TriosARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorMicroduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa
P50
Q30381277-52DA19C2-8DA4-436D-8AA6-749D44161F3DQ33616885-C23D0208-645B-4D26-ABDD-EBFEC960A16DQ34425911-09E9648C-9EF0-4AD5-BF67-4911682C6A29Q34444821-D4B8B582-322B-4097-A5FA-2BDCB7ACCB6BQ35152830-40026EFA-2410-4637-913D-7C2FB59A8E14Q36384754-0D2BAAD7-8EC9-441B-90B6-DA2DF23BAD28Q36388222-BFE833AA-C473-4FE0-B121-81FF0C93FD75Q37574150-DC6503F0-7CF5-42CF-9842-6540E0C1AC63Q37666053-CF3E7D49-445A-4CF6-8A24-F627F64D75BDQ38478741-50FADE20-D7DE-4029-9978-1839E09D53D5Q41701329-00D96125-4504-401E-99CB-2FB13462B537Q42348513-3B6A3416-8BE5-4058-825C-1CE4E5F95C62Q43082054-0FBCC100-6382-432D-A35F-4A57D3E1490AQ52339934-9BBACE2E-465C-411D-A669-5B69C0192DE8Q54481903-296F0873-7180-428E-B31C-301D2A136D37Q64913038-B189E717-3858-4693-BD07-164DAEFC0EB2Q86858193-DAB733E0-F63A-4D20-85DD-81270B8D14F2Q90266461-FFCE181B-98CC-4050-9270-C5638CCC7CF9Q91530411-C0435EE6-97F3-474F-BB49-57ED8F628F25Q92413381-DD6744FB-03C4-4598-9888-ED750468EB1E
P50
description
researcher (ORCID 0000-0003-2023-072X)
@en
name
Yichuan Liu
@en
type
label
Yichuan Liu
@en
prefLabel
Yichuan Liu
@en
P31
P496
0000-0003-2023-072X