List of works - Yichuan Liu

A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock.

scientific article

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

scientific article published on 01 July 2019

Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients

scientific article published on 08 January 2022

Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios

scientific article published on 10 September 2019

Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population

scientific article published on 06 May 2022

Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies.

scientific article published on 27 March 2018

Common variants at 5q33.1 predispose to migraine in African-American children.

scientific article

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

scientific article published on 18 September 2017

Comprehensive analysis of gene expression in human retina and supporting tissues.

scientific article published on 14 March 2014

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

scientific article

Domain Altering SNPs in the Human Proteome and Their Impact on Signaling Pathways ⬇️

scientific article published on September 23, 2010

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

scientific article published on 18 January 2016

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

scientific article published on 21 August 2017

Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data

scientific article published on 21 March 2022

Genetic correlations between COVID-19 and a variety of traits and diseases

scientific article published in 2021

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children.

scientific article

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

scientific article

Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humans

scientific article

Mapping Splicing Quantitative Trait Loci in RNA-Seq

scientific article published on 16 February 2015

Mapping Splicing Quantitative Trait Loci in RNA-Seq.

scientific article

Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa

scientific article published on 29 January 2019

Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans

scientific article published on 02 November 2020

Modular composition predicts kinase/substrate interactions.

scientific article

PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distribution

scientific article published on 20 December 2013

RNA-Seq identifies novel myocardial gene expression signatures of heart failure

scientific article

Testing Genetic Association With Rare Variants in Admixed Populations ⬇️

scientific article published on October 2, 2012

Tissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases

scientific article published on 06 February 2014

List of works by Yichuan Liu

A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock.

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients

Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios

Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population

Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies.

Common variants at 5q33.1 predispose to migraine in African-American children.

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

Comprehensive analysis of gene expression in human retina and supporting tissues.

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments.

Domain Altering SNPs in the Human Proteome and Their Impact on Signaling Pathways ⬇️

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data

Genetic correlations between COVID-19 and a variety of traits and diseases

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children.

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humans

Mapping Splicing Quantitative Trait Loci in RNA-Seq

Mapping Splicing Quantitative Trait Loci in RNA-Seq.

Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa

Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans

Modular composition predicts kinase/substrate interactions.

PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distribution

RNA-Seq identifies novel myocardial gene expression signatures of heart failure

Testing Genetic Association With Rare Variants in Admixed Populations ⬇️

Tissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases