Lifeng Tian
Jiangxi Maternal and Child Health Hospital(CN)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders, Pancreatic function and diabetes, Attention Deficit Hyperactivity Disorder
Most-Cited Works
- → Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing(2013)468 cited
- → Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases(2016)318 cited
- → Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism(2015)301 cited
- → ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor(2019)216 cited
- → Mutations in PDGFRB Cause Autosomal-Dominant Infantile Myofibromatosis(2013)205 cited
- → GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers(2016)178 cited
- → Rare variant associations with plasma protein levels in the UK Biobank(2023)162 cited
- → Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1(2014)117 cited
- → Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly(2018)99 cited
- → Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder(2016)73 cited