Fei Yi - Concepedia

Author

Fei Yi

Salk Institute for Biological Studies ORCID

Also Known As

Chen, Rujin, F Yi, F. Yi, FEI YI, Fangzhao Yi, Fei Yi, Fei. Yi (7956590), Fuhua Yi, Yi Fei, Yi, Fangjun

104

Publications

5.5K

Citations

H-Index

118

Concepts

All Affiliations

Salk Institute for Biological Studies China Medical University Chinese Academy of Sciences Institute of Biophysics Center of Regenerative Medicine in Barcelona

About

Fei Yi is an author at Salk Institute for Biological Studies specializing in medicine, cell biology, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	24	2.2K
2	Natural Sciences	5	5	178
3	Health Sciences	3	3	260
4	Social Sciences	3	3	136
5	Engineering	1	1	116

Fei Yi

Publications

4.6K

Citations

H-Index

Page 1

	Year	Citations
A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging Weiqi Zhang, Jingyi Li, Keiichiro Suzuki, Science	2015	534
Progressive degeneration of human neural stem cells caused by pathogenic LRRK2 Guang‐Hui Liu, Jing Qu, Keiichiro Suzuki, Nature NeuroregenerationDevelopmental BiologyProgressive DegenerationMedicineAdult Stem Cell	2012	337
Autism-associated SHANK3 haploinsufficiency causes <i>I</i> <sub>h</sub> channelopathy in human neurons Fei Yi, Tamás Dankó, Salomé Calado Botelho, Science	2016	326
Repression of Nanog Gene Transcription by Tcf3 Limits Embryonic Stem Cell Self-Renewal Laura Pereira, Fei Yi, Bradley J. Merrill Molecular and Cellular Biology	2006	304
Opposing effects of Tcf3 and Tcf1 control Wnt stimulation of embryonic stem cell self-renewal Fei Yi, Laura Pereira, Jackson A. Hoffman, Nature Cell Biology Induced Pluripotent Stem CellDevelopmental BiologyMedicineAdult Stem CellStem Cell Research	2011	301
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 ChangHui Pak, Tamás Dankó, Yingsha Zhang, Cell stem cell Neurodegenerative DiseasesSynaptic PlasticityNeurological DisorderSynaptic TransmissionPsychiatric Genetics	2015	225
Targeted Gene Correction of Laminopathy-Associated LMNA Mutations in Patient-Specific iPSCs Guang‐Hui Liu, Keiichiro Suzuki, Jing Qu, Cell stem cell Genetic DisorderGeneticsGene CorrectionPathologyMolecular Genetics	2011	217
PTEN deficiency reprogrammes human neural stem cells towards a glioblastoma stem cell-like phenotype Shunlei Duan, Guohong Yuan, Xiaomeng Liu, Nature Communications	2015	166
Tcf3 Functions as a Steady-State Limiter of Transcriptional Programs of Mouse Embryonic Stem Cell Self-Renewal Fei Yi, Laura Pereira, Bradley J. Merrill Stem Cells	2008	161
<scp>ATM</scp> ‐ <scp>CHK</scp> 2‐Beclin 1 axis promotes autophagy to maintain <scp>ROS</scp> homeostasis under oxidative stress Qiqiang Guo, Shanshan Wang, Shanshan Zhang, The EMBO Journal Redox SignalingCell AutophagySignal TransductionMolecular PathwayPhysiology	2020	139

Page 1