Wei Wei - Concepedia

Author

Wei Wei

Also Known As

Biqing Zhu, Buyske, S., Carmen Lage, Christopher Watt, Gavin Hudson, Katie Tate, Lester, T, Richard C. Trembath, Shehla N. Mohammed, W Wei

244

Publications

8.1K

Citations

H-Index

124

Concepts

All Affiliations

University of Cambridge MRC Mitochondrial Biology Unit Sichuan University Newcastle University Medical Research Council

About

Wei Wei is an author at University of Cambridge specializing in medicine, genetics, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	34	2.5K
2	Natural Sciences	14	15	930
3	Engineering	3	3	289
4	Public Health	3	3	216
5	Health Sciences	2	2	131

Wei Wei

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia Wan‐Jin Chen, Yu Lin, Zhi‐Qi Xiong, Nature Genetics Transcriptional RegulationMendelian DisorderGenetic DisorderGeneticsDegenerative Disease	2011	477
The Fetal Basis of Amyloidogenesis: Exposure to Lead and Latent Overexpression of Amyloid Precursor Protein and β-Amyloid in the Aging Brain Riyaz Basha, Wei Wei, Saleh A. Bakheet, Journal of Neuroscience	2005	344
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes Wei Wei, Katherine Schon, Greg Elgar, Nature	2022	290
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci Josephine Purps, Sabine Siegert, Sascha Willuweit, Forensic Science International Genetics BiologyGenetic AnalysisAllelic VariantHaplotype DeterminationMolecular Ecology	2014	278
Metagenomic analysis of microbial community and function involved in cd-contaminated soil Gang Feng, Tian Xie, Xin Wang, BMC Microbiology	2018	252
Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos Vasileios I. Floros, Angela Pyle, Sabine Dietmann, Nature Cell Biology BiologyDevelopmental BiologyDnaMitochondrial FunctionMedicine	2018	243
One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs Erwei Zuo, Yijun Cai, Kui Li, Cell Research EngineeringGeneticsOne-step GenerationMolecular GeneticsMonkey Embryos	2017	211
CRISPR/Cas9-mediated targeted chromosome elimination Erwei Zuo, Xiaona Huo, Xuan Yao, Genome biology	2017	187
SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons Kirill Zaslavsky, Wenbo Zhang, Fraser P. McCready, Nature Neuroscience Neurodevelopmental DisordersHuman NeuronsMolecular NeuroscienceNeurophysiologyNeuroanatomy	2019	167
A calibrated human Y-chromosomal phylogeny based on resequencing Wei Wei, Qasim Ayub, Yuan Chen, Genome Research	2012	153

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