Weimin Sun - Concepedia

Author

Weimin Sun

Quest Diagnostics (United States)ORCID

Also Known As

Sun Wei-Min, Sun, Weimin, W Sun, W-S Sun, W. P. Sun, W. SUN, W. Sun, WEI-MIN SUN, WEIMIN SUN, Wanlin Sun

138

Publications

2.7K

Citations

H-Index

110

Concepts

All Affiliations

Quest Diagnostics (United States)Second Military Medical University State Key Laboratory of Respiratory Disease Second Affiliated Hospital of Guangzhou Medical University Guangzhou Medical University

About

Weimin Sun is an author at Quest Diagnostics (United States) specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	38	1.5K
2	Public Health	10	10	373
3	Natural Sciences	8	8	307
4	Health Sciences	2	2	31
5	Engineering	1	1	54

Weimin Sun

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: Insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States Feras Hantash, Dana Goos, Beryl Crossley, Genetics in Medicine Fragile X SyndromeMedicineFragile X SpectrumGynecologyUnited States	2010	105
Identification and analysis of tumour-associated antigens in hepatocellular carcinoma Yi Shi, Hao‐Chien Wang, Yuan Yin, British Journal of Cancer	2005	102
Anti-Cancer Effect of Resveratrol is Associated with Induction of Apoptosis via a Mitochondrial Pathway Alignment Weimin Sun, Wei Wang, Jung Kim, Advances in experimental medicine and biology Mitochondrial Pathway AlignmentMitophagyMitochondrial FunctionApoptosisCell Death	2008	93
Induction and Regulation of the Carcinogen-Metabolizing Enzyme CYP1A1 by Marijuana Smoke and Δ <sup>9</sup> -Tetrahydrocannabinol Michael D. Roth, José A. Marques-Magallanes, Michael Yuan, American Journal of Respiratory Cell and Molecular Biology	2001	93
Qualitative assessment of FMR1 (CGG)n triplet repeat status in normal, intermediate, premutation, full mutation, and mosaic carriers in both sexes: Implications for fragile X syndrome carrier and newborn screening Feras Hantash, Dana G. Goos, David Tsao, Genetics in Medicine Genetic TestingMendelian DisorderGenetic DisorderMosaic CarriersGenetics	2010	83
Testing for variants in CYP2C19: population frequencies and testing experience in a clinical laboratory Charles M. Strom, Dana Goos, Beryl Crossley, Genetics in Medicine Allelic VariantGenetic TestingPopulation FrequenciesMedicineGenetics	2012	81
Radiation-driven lipid accumulation and dendritic cell dysfunction in cancer Fu Gao, Cong Liu, Jiaming Guo, Scientific Reports	2015	78
A Standardized DNA Variant Scoring System for Pathogenicity Assessments in Mendelian Disorders Izabela Karbassi, Glenn A. Maston, Angela Love, Human Mutation Genetic TestingGeneticsPolygenic RiskGenetic EpidemiologyPathology	2015	70
C3-symmetric peptide scaffolds are functional mimetics of trimeric CD40L Sylvie Fournel, Sébastien Wieckowski, Weimin Sun, Nature Chemical Biology Trimeric Cd40lNatural SciencesPeptide EngineeringPeptide LibraryMolecular Biology	2005	68
A Mutation in the Aryl Hydrocarbon Receptor (AHR) in a Cultured Mammalian Cell Line Identifies a Novel Region of AHR That Affects DNA Binding Weimin Sun, Jianzhong Zhang, Oliver Hankinson Journal of Biological Chemistry Chemical BiologyTryptophan MutationDna BindingBiochemistryNovel Region	1997	66

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