Exploring causal associations between interleukins, their receptors, and acute respiratory distress syndrome: a bidirectional-Mendelian Randomization study

in Genetics of Common and Rare Diseases

• Jia-wei Ma
• Ji-chun Tang
• Hong-zhi Fang

Case report: A case of holocarboxylase synthetase deficiency with respiratory tract as the initial symptom

in Genetics of Common and Rare Diseases

• Haiying Zou
• Li Yang
• Renlong Zhang
• Yao Qin

Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from Mali

in Genetics of Common and Rare Diseases

• Salia Bamba
• Lala Sidibé
• Seybou H. Diallo
• Lassana Cissé
• Kékouta Dembélé
• Abdoulaye Yalcouyé
• Weizhen Ji
• Mohamed Emile Dembélé
• Salimata Diarra
• Alassane dit Baneye Maiga

Retraction: CircSETD3 (Hsa_circ_0000567) suppresses Hepatoblastoma pathogenesis via targeting the mir-423-3p/Bcl-2-interacting mediator of cell death axis

in Genetics of Common and Rare Diseases

Genetic screening of α-thalassemia fusion gene using routine flow-through hybridization

in Genetics of Common and Rare Diseases

• Yingbei Huang
• Aiping Ju
• Lihong Zheng
• Biqiu Xu
• Liang Liang
• Youqiong Li