Yizhou Yin

发表

Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype‐weighted knowledge in the CAGI SickKids5 clinical genomes challenge

Lipika R. Pal, J. Moult, Kunal Kundu, 2020, Human mutation.

Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype-weighted knowledge in the CAGI SickKids5 clinical genomes challenge

Lipika R. Pal, J. Moult, Kunal Kundu, 2019, bioRxiv.

CAGI4 SickKids clinical genomes challenge: A pipeline for identifying pathogenic variants

Lipika R. Pal, J. Moult, Kunal Kundu, 2017, Human mutation.

Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI‐5 intellectual disability challenge

Stephen J. Wilson, Lipika R. Pal, S. Brenner, 2019, Human mutation.

CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases

Aashish N. Adhikari, Lipika R. Pal, J. Gough, 2019, Human mutation.

Determination of disease phenotypes and pathogenic variants from exome sequence data in the CAGI 4 gene panel challenge

Lipika R. Pal, J. Moult, Kunal Kundu, 2017, Human mutation.

Ensemble variant interpretation methods to predict enzyme activity and assign pathogenicity in the CAGI4 NAGLU (Human N‐acetyl‐glucosaminidase) and UBE2I (Human SUMO‐ligase) challenges

Lipika R. Pal, J. Moult, Kunal Kundu, 2017, Human mutation.

Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI

Yuedong Yang, Olivier Lichtarge, Giovanni Minervini, 2017, Human mutation.

Performance of in silico tools for the evaluation of p 16 INK 4 a ( CDKN 2 A ) variants in CAGI

J. Gough, S. Brenner, E. Capriotti, 2017 .

Characterizing and comparing missense variants in monogenic disease and in cancer

J. Moult, Yizhou Yin, 2019, bioRxiv.

Assessment of methods for predicting the effects of PTEN and TPMT protein variants

Lipika R. Pal, Yaoqi Zhou, P. Radivojac, 2019, Human mutation.

Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges

Hui Ting Grace Yeo, Lipika R. Pal, Jason R. Bobe, 2017, Human mutation.

Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges

Alexander A. Morgan, Yanay Ofran, Predrag Radivojac, 2017, Human mutation.

Resolvin E1 Inhibits Corneal Allograft Rejection in High-Risk Corneal Transplantation.

Yizhou Yin, Qingqing Zhao, Min Zhao, 2018, Investigative ophthalmology & visual science.

A bacteriophage endolysin that eliminates intracellular streptococci

J. Moult, D. Gallagher, M. Lösche, 2016, eLife.

Antibody interfaces revealed through structural mining

Lipika R. Pal, J. Moult, G. Lazar, 2022, Computational and structural biotechnology journal.

Novel Antibody Interfaces Revealed Through Structural Mining

Lipika R. Pal, J. Moult, G. Lazar, 2022, bioRxiv.

Ganodermataceae: natural products and their related pharmacological functions.

Yizhou Yin, K. Tang, Juan Lin, 2007, The American journal of Chinese medicine.

Lessons from the CAGI‐4 Hopkins clinical panel challenge

Hugo Y. K. Lam, David T. Jones, Aashish N. Adhikari, 2017, Human mutation.

Assessment of predicted enzymatic activity of α‐N‐acetylglucosaminidase variants of unknown significance for CAGI 2016

Roland L. Dunbrack, Colby T. Ford, David T. Jones, 2019, Human mutation.

Prediction of methionine oxidation risk in monoclonal antibodies using a machine learning method

Kannan Sankar, Kam Hon Hoi, K. H. Hoi, 2018, mAbs.

Increasing the stability of the bacteriophage endolysin PlyC using rationale-based FoldX computational modeling.

J. Moult, Yizhou Yin, Ryan D. Heselpoth, 2015, Protein engineering, design & selection : PEDS.

CAGI4 Crohn's exome challenge: Marker SNP versus exome variant models for assigning risk of Crohn disease

Lipika R. Pal, J. Moult, Kunal Kundu, 2017, Human mutation.

Comparison of Rapid DNA Extraction Methods Applied to PCR Identification of Medicinal Mushroom Ganoderma spp.

Yizhou Yin, K. Tang, Juan Lin, 2007, Preparative Biochemistry & Biotechnology.

Resolvin D1 inhibits inflammatory response in STZ-induced diabetic retinopathy rats: Possible involvement of NLRP3 inflammasome and NF-κB signaling pathway

Yizhou Yin, Xuedong Zhang, Fei Chen, 2017, Molecular vision.

Human Mutation

Guillermo del Angel, Lipika R. Pal, P. Radivojac, 2019 .

Human Mutation

Colby T. Ford, Lipika R. Pal, Meng Wang, 2019 .

CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods

Silvio C. E. Tosatto, Julius O. B. Jacobsen, Nicholas A. Sinnott-Armstrong, 2024, Genome biology.

CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods

Nicholas A. Sinnott-Armstrong, Jonathan M. Mudge, Hui Ting Grace Yeo, 2022, Genome biology.

Human Mutation

Lipika R. Pal, J. Moult, Kunal Kundu, 2020 .