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Yizhou Yin
Yizhou Yin
Visterra Inc.
Verified email at ibbr.umd.edu
Title
Cited by
Cited by
Year
Ganodermataceae: Natural Products and Their Related Pharmacological Functions
X Zhou, J Lin, Y Yin, J Zhao, X Sun, K Tang
The American journal of Chinese medicine 35 (04), 559-574, 2007
2712007
A bacteriophage endolysin that eliminates intracellular streptococci
Y Shen, M Barros, T Vennemann, DT Gallagher, Y Yin, SB Linden, ...
Elife 5, e13152, 2016
742016
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
R Daneshjou, Y Wang, Y Bromberg, S Bovo, PL Martelli, G Babbi, ...
Human mutation 38 (9), 1182-1192, 2017
472017
Comparison of Rapid DNA Extraction Methods Applied to PCR Identification of Medicinal Mushroom Ganoderma spp.
X Zhou, Q Li, J Zhao, K Tang, J Lin, Y Yin
Preparative Biochemistry and Biotechnology 37 (4), 369-380, 2007
432007
Prediction of methionine oxidation risk in monoclonal antibodies using a machine learning method
K Sankar, KH Hoi, Y Yin, P Ramachandran, N Andersen, A Hilderbrand, ...
mAbs 10 (8), 1281-1290, 2018
412018
Identification of medicinal Ganoderma species based on PCR with specific primers and PCR-RFLP
Z Xuanwei, L Qizhang, Y Yizhou, C Yiyuan, L Juan
Planta medica 74 (02), 197-200, 2008
352008
Increasing the stability of the bacteriophage endolysin PlyC using rationale-based FoldX computational modeling
RD Heselpoth, Y Yin, J Moult, DC Nelson
Protein Engineering, Design and Selection 28 (4), 85-92, 2015
342015
Assessment of methods for predicting the effects of PTEN and TPMT protein variants
V Pejaver, G Babbi, R Casadio, L Folkman, P Katsonis, K Kundu, ...
Human mutation 40 (9), 1495-1506, 2019
182019
CAGI4 Crohn's exome challenge: Marker SNP versus exome variant models for assigning risk of Crohn disease
LR Pal, K Kundu, Y Yin, J Moult
Human mutation 38 (9), 1225-1234, 2017
182017
Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges
B Cai, B Li, N Kiga, J Thusberg, T Bergquist, YC Chen, N Niknafs, ...
Human mutation 38 (9), 1266-1276, 2017
182017
Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI‐5 intellectual disability challenge
M Carraro, AM Monzon, L Chiricosta, F Reggiani, MC Aspromonte, ...
Human mutation 40 (9), 1330-1345, 2019
172019
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI
M Carraro, G Minervini, M Giollo, Y Bromberg, E Capriotti, R Casadio, ...
Human mutation 38 (9), 1042-1050, 2017
162017
Ensemble variant interpretation methods to predict enzyme activity and assign pathogenicity in the CAGI4 NAGLU (Human N‐acetyl‐glucosaminidase) and UBE2I (Human SUMO‐ligase …
Y Yin, K Kundu, LR Pal, J Moult
Human mutation 38 (9), 1109-1122, 2017
162017
Assessment of predicted enzymatic activity of α‐N‐acetylglucosaminidase variants of unknown significance for CAGI 2016
WT Clark, L Kasak, C Bakolitsa, Z Hu, G Andreoletti, G Babbi, Y Bromberg, ...
Human mutation 40 (9), 1519-1529, 2019
142019
CAGI4 SickKids clinical genomes challenge: A pipeline for identifying pathogenic variants
LR Pal, K Kundu, Y Yin, J Moult
Human mutation 38 (9), 1169-1181, 2017
122017
CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases
L Kasak, JM Hunter, R Udani, C Bakolitsa, Z Hu, AN Adhikari, G Babbi, ...
Human mutation 40 (9), 1373-1391, 2019
112019
Participation in research program: a novel course in undergraduate education of life science
X Zhou, J Lin, Y Yin, X Sun, K Tang
Biochemistry and Molecular Biology Education 35 (5), 322-327, 2007
112007
Lessons from the CAGI‐4 Hopkins clinical panel challenge
JM Chandonia, A Adhikari, M Carraro, A Chhibber, GR Cutting, Y Fu, ...
Human mutation 38 (9), 1155-1168, 2017
92017
The development of biotechnology education in China
X Zhou, J Lin, L Zhang, Z Chen, Y Yin, B Guo, X Sun, K Tang
Biochemistry and Molecular Biology Education 34 (2), 141-147, 2006
92006
Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype‐weighted knowledge in the CAGI SickKids5 clinical genomes challenge
LR Pal, K Kundu, Y Yin, J Moult
Human mutation 41 (2), 347-362, 2020
72020
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