Meili Fan

7PUBLICATIONS
22CO-AUTHORS
Cell and nuclear divisionDevelopmental genetics (incl. sex determination)Neurology and neuromuscular diseasesHaematological tumoursImmunogenetics (incl. genetic immunology)
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Publications (7)

|Oct 08, 2026
X;7 Translocation at p21.1 and q31.31 Disrupting DMD: A Multiomics Study of a Male Dystrophinopathy Case.

|Jul 08, 2026
Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

|Jan 12, 2026
Detection of pathogenic novel intronic splicing variants in the KIDINS220 gene causes motor developmental delay.

Lu Bai, Yu Hei, Rujin Tian

|Apr 14, 2025
Intron Variant Cause DICER1 Syndrome With Pleuropulmonary Blastoma.

Rujin Tian, Yixiao Li, Lin Zhong

|Apr 14, 2025
Combination of Synonymous and Missense Mutations in JAK3 Gene Contributes to Severe Combined Immunodeficiency in One Child.

Xingcui Wang, Rujin Tian, Haozheng Zhang

|Nov 20, 2024
Potential role of ARG1 c.57G > A variant in Argininemia.

Yixiao Li, Rujin Tian, Dong Wang

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Frequent Collaborators

2 joint publications

Dong Wang

2 joint publications

Rujin Tian

2 joint publications

Haozheng Zhang

2 joint publications

Zhongtao Gai