Causal Relationships Between Serum Metabolites and Coronary Heart Disease Risk: A Mendelian Randomization Study

in Statistical Genetics and Methodology

• Xiao-Yan Meng
• Yong-Qing Zhu
• Ying-Jie Zhang
• Wei Sun
• Shu-Ang Li

CLMT: Graph Contrastive Learning Model for Microbe-Drug Associations Prediction with Transformer

in Computational Genomics

• Liqi Xiao
• Junlong Wu
• Liu Fan
• Lei Wang
• Xianyou Zhu

A rare variation of ERCC8 gene cause Cockayne Syndrome in a Chinese family

in Genetics of Aging

• Fengjuan Ding
• HOU FEI
• Bowen Zhao
• Hua Jin

Editorial: Integrative genetics and multi-omics of complex human disorders

in Computational Genomics

• Hongsheng Gui
• Christopher J. Lessard
• Jinhui Liu
• Miaoxin Li
• Indra Adrianto

LINC00461 SNPs rs933647 and rs201864123 modify the risk of adenoid hypertrophy susceptibility for children in South China

in Genetics of Common and Rare Diseases

Exploration of cfDNA landscape in NIPT and clinical utilities of cfDNA based gene expression inference in prenatal diagnostics

in Human and Medical Genomics

• Ruo Jia
• Jianjiang Zhu
• Feng Zhang
• Yangbo Sun
• Bin Zhang
• Yang Du
• Hong Qi

Comprehensive analysis of non-coding RNA-mediated endothelial cell-specific regulatory circuits in coronary artery disease risk

in Computational Genomics

• Boshui Huang
• Zhijie Lai
• Xiaoyu Wang
• Qinhao Zhang
• Tingting Hu
• Fulong Yu
• Shuxian Zhou
• Yan Zhang
• Juan Meng

Arteriovenous Cerebral High Flow Shunts: genetic analysis of patients from a pediatric tertiary care center

in Genetics of Common and Rare Diseases

• Ferruccio Romano
• Patrizia De Marco
• Giulia Amico
• Marisa Mallamaci
• Marco Pavanello
• Gianluca Piatelli
• Marcello Scala
• Federico Zara
• Francesca Faravelli
• Mariasavina Severino

Case Report: area of focus Clinical Presentation and KMT2D Gene Mutation at the c.15535C>T Site in a Case of Kabuki Syndrome

in Genetics of Common and Rare Diseases

• Wen Li
• Mengjie Lin
• Jinwei Dao
• Li Shi
• Wei Yi
• Jia Lei
• Yaxian Song
• Jiaolou Dong
• Meiwei Zhao
• Xu Yushan

Chromosome 1 Variants Associated with Decreased HIV Set-point Viral Load Correlate with PRKAB2 Expression Changes

in Human and Medical Genomics

• Riley H Tough
• Paul J Mclaren

De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis

in Computational Genomics

• Hong-Jun Yan
• Wenhui Liu
• Min-Xing Xu
• Peng-Yu Wang
• Yu-Jie Gu
• Hua Li
• Sheng Luo

Detection of a novel large fragment deletion in the alpha-globin gene cluster using CNVplex technology

in Genetics of Common and Rare Diseases

• Jianfei Xu
• Liang Hu
• Lijuan Wen
• Xianzhen Cao
• Hongyan Xu
• Qi Luo
• Yuhong Long
• Jiting Yu
• Lifang Sun
• Fengxiang Wei

Retrospective Analysis of Inflammatory Biomarkers and Prognosis in Non-Small Cell Lung Cancer Without Adenocarcinoma In Situ

in Cancer Genetics and Oncogenomics

• Qing Zhao
• Songping Cui
• Bin Hu
• Shuo Chen

Cancer Classification in High Dimensional Microarray Gene Expressions by Feature Selection using Eagle Prey Optimization

in Computational Genomics

• Swetha Dhamercherla
• Damodar Reddy Edla
• Suresh Dara

Transcriptomic signature can distinguish chronic neutrophilic leukemia from ambiguous neutrophilic leukemias

in Cancer Genetics and Oncogenomics

• Chao Guo
• Zhen-Ling Li

Novel Homozygous ACVRL1 Missense Variant in a Family with Hereditary Hemorrhagic Telangiectasia and Pulmonary Arterial Hypertension: Findings Suggesting a Hypomorphic Allele

in Genetics of Common and Rare Diseases

• Akash Mathavan
• Akshay Mathavan
• Urszula Krekora
• Adityanarayan Rao
• Marc S Zumberg
• Jeb Justice
• Pinar Bayrak-Toydemir
• Jamie McDonald
• Ali Ataya