Bioinformatics-based analysis of the relationship between STC1 expression and immune infiltration in gastric cancer

in Cancer Genetics and Oncogenomics

• Weijun Ma
• Xiaoli Ma
• Yaoqi Li

Roles of organic anion transporting polypeptides in hepatocellular carcinoma

in Cancer Genetics and Oncogenomics

• Hubert Chen

Mitochondrial genome complexity in Erodium stephanianum (Geraniaceae): nanopore sequencing reveals chloroplast gene transfer and DNA rearrangements

in Genomics of Plants and the Phytoecosystem

• Xinchen Xu
• Qingfei Meng
• Na Li
• Zichuan Zou
• Haonan Yang
• Ang Li
• Fusheng Ge
• Jian Meng
• Zixue Ding

Robust consensus nuclear and cell segmentation

in Computational Genomics

• Melis O. Irfan
• Eduardo A. González-Solares
• Tristan Whitmarsh
• Alireza Molaeinezhad
• Mohammad Al Sa’d
• Claire M. Mulvey
• Marta Páez Ribes
• Atefeh Fatemi
• Dario Bressan
• Nicholas A. Walton

Correction: Reduced T-cell stemness underlies Th17 expansion and graft dysfunction in kidney transplant recipients

in Stem Cell Research

• Chang Liu
• Hao Jiang
• Andu Zhu
• Chen Xu
• Zhenfan Wang
• Guocai Mao
• Minjun Jiang
• Jianchun Chen
• Zheng Ma
• Jiaqian Qi

Expanded newborn screening for inborn errors of metabolism and genetic variants in Xinjiang, China

in Genetics of Common and Rare Diseases

• Huiwen Zhang
• Haoyue Tian
• Wencheng Dai
• Luhan Zhang
• Gang Guo
• Guifeng Ding

Dopamine D2 receptor gene Taq 1A polymorphism: genetic architecture in Indian population and comparison to global populations

in Evolutionary, Population, and Conservation Genetics

• Amrita Chaudhary
• Pradeep Kumar
• Bechan Sharma
• Vandana Rai

Identification and characterization of signature genes related to fetoplacental vascular endothelial cell programming in gestational diabetes mellitus using bioinformatics analysis

in Computational Genomics

• Chunhong Liu
• Caicheng Wei
• Yulan Lu
• Fu Chai
• Chunfang Wang
• Yonglong Zeng
• Huatuo Huang

Two novel cases with PIGQ-CDG: expansion of the genotype–phenotype spectrum and evaluation of GestaltMatcher as a diagnostic tool

in Genetics of Common and Rare Diseases

• Katarína Kušíková
• Tzung-Chien Hsieh
• Mateja Pfeifer
• Christine Fauth
• Yoshiko Murakami
• Franco Laccone
• Daniela Karall
• Walter Bonfig
• Helen Stewart
• Denisa Weis

Circ-malat1 promotes gastric cell growth via miR-154-5p/CCND2

in RNA

• Lina Li
• Liuqing Yang
• Yuzhen Wang
• Kejun Nan

Advancing artificial intelligence ethics in health and genomics: lessons from a public survey in South Korea

in ELSI in Science and Genetics

• Jungim Lee
• Wonhoo Yoo
• Hannah Kim

Aerobic exercise-induced lactate production: a novel opportunity for remodeling the tumor microenvironment

in Epigenomics and Epigenetics

• Xin Zhou
• Jinliang Jiang
• Jingjing Liu
• Qinglu Wang
• Ying Luo
• Liping Wu

Identification of a PATL2 missense variant (c.877G>T) disrupting canonical splicing and contributing to female infertility

in Statistical Genetics and Methodology

• Hongyan Li
• Yue Lin
• Weixu Ma
• Ting Yu
• Lingfeng Dong
• Yankun Chen
• Shuming Fan
• Guoqun Luo
• Jingwen Zhang
• Ge Song

The effect of different teaching models on improving nursing humanistic care competencies: a network meta-analysis

in ELSI in Science and Genetics

• Xiao Meixia
• Xiong Qin
• Jiang Rong
• Li Lingxia
• Fu Wenhao

Case Report: The nonsense variation of the cardiac transcription factor NKX2-5 has been identified in a Chinese family with nonsyndromic congenital heart disease

in Genetics of Common and Rare Diseases

• Haixia Zhang
• Jing Chen
• He Wang
• Qinqin Xiang
• Shanling Liu

Genome-wide identification of GATA family genes in sweet potato (Ipomoea batatas L.) and their expression patterns under abiotic stress

in Genomics of Plants and the Phytoecosystem

• Chong Wang
• Mengjiao Lan
• Manqiu Xiao
• Ying Peng
• Hao Pan
• Jiaqi Deng
• Wensheng Wu

Correction: A non-invasive method for screening mitochondrial diabetes

in Genetics of Common and Rare Diseases

• Hangyu Fang
• Xiaoe Li
• Shuping Wang
• Mei Zhang
• Victor Wei Zhang
• Chao Xu

Comprehensive bioinformatics analysis of malignant transformation and potential therapeutic possibility of lung adenocarcinoma after lipopolysaccharide induction

in Cancer Genetics and Oncogenomics

• Wanjie Xu
• Jing Zhang
• Xinyu Zhang
• Xue Wang
• Yiluo Xie
• Shengping Min
• Xiaojing Wang
• Chaoqun Lian

Identification of variants in SWI/SNF complex genes associated with neurodevelopmental disorders

in Genetics of Common and Rare Diseases

• Chen Liang
• Haihong Shi
• Yanjuan Chen
• Xia Wang
• Jieyuan Jin
• Liqun Su
• Lijun Tang
• Huihong Li
• Fei Ling
• Haoxian Li

Retraction: EZH2-mediated microRNA-375 upregulation promotes progression of breast cancer via the inhibition of FOXO1 and the p53 signaling pathway

in Cancer Genetics

Development and validation of mPCR-CEFA for detecting multiple deletion and non-deletion thalassemia genotypes

in Genetics of Common and Rare Diseases

• Jingping Xu
• Baoyan Ren
• Qixun Fang
• Kangfeng Lin
• Xingan Xing
• Jingting Lin

Correction: Clinical impact of pharmacogenomics in pediatric care: insights extracted from clinical exome sequencing

in Pharmacogenetics and Pharmacogenomics

• Simran Maggo
• Yachen Pan
• Dejerianne Ostrow
• Jenny Q. Nguyen
• Jaclyn A. Biegel
• Matthew A. Deardorff
• Xiaowu Gai

Identification of a novel microdeletion at 9q21.13 in a family with epilepsy, intellectual disability, and speech disorders and literature review

in Genetics of Common and Rare Diseases

• Liqing Jiang
• Jiaqi Li
• Aizhong Han
• Fei Hou
• Xiaotong Wei
• Yanjun Tian

A novel vasculogenic mimicry-related nomogram predicts prognosis in hepatocellular carcinoma

in Cancer Genetics and Oncogenomics

• Yun Zhong
• Fadian Ding
• Han Zhang
• Denghan Zhang
• Xiang Zhang
• Shangeng Weng