Lifeng Tian, Ph.D.
Affiliations: | 2007 | University of the Sciences in Philadelphia |
Area:
BiochemistryGoogle:
"Lifeng Tian"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Randy Zauhar | grad student | 2007 | University of the Sciences in Philadelphia | |
| (Computational approaches to molecular shape and electrostatics.) | ||||
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Publications
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| Wu Y, Xia Y, Li P, et al. (2020) Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndrome. Orphanet Journal of Rare Diseases. 15: 101 |
| Fuster-García C, García-García G, Jaijo T, et al. (2019) Expanding the Genetic Landscape of Usher-Like Phenotypes. Investigative Ophthalmology & Visual Science. 60: 4701-4710 |
| Liu Y, Chang X, Glessner J, et al. (2019) Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios. Frontiers in Genetics. 10: 819 |
| Qu HQ, Wang X, Tian L, et al. (2019) Application of ACMG criteria to classify variants in the human gene mutation database. Journal of Human Genetics |
| Li D, March ME, Gutierrez-Uzquiza A, et al. (2019) ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor. Nature Medicine |
| Li D, Wenger TL, Seiler C, et al. (2018) Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly. Human Molecular Genetics |
| Sanchez-Navarro I, R J da Silva L, Blanco-Kelly F, et al. (2018) Combining targeted panel-based resequencing and copy-number variation analysis for the diagnosis of inherited syndromic retinopathies and associated ciliopathies. Scientific Reports. 8: 5285 |
| Chang X, Li D, Tian L, et al. (2017) Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964). The Journal of Pediatrics |
| Zhang Y, Tian L, Sleiman P, et al. (2017) Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk loci. European Journal of Human Genetics : Ejhg |
| Li D, Streeten EA, Chan A, et al. (2017) Exome sequencing reveals mutations in AIRE as a cause of isolated hypoparathyroidism. The Journal of Clinical Endocrinology and Metabolism |