Guan Ning Lin
Guan Ning Lin
School of Biomedical Engineering, Shanghai Jiao Tong University
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A proteome-scale map of the human interactome network
T Rolland, M Taşan, B Charloteaux, SJ Pevzner, Q Zhong, N Sahni, S Yi, ...
Cell 159 (5), 1212-1226, 2014
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation
JJ Michaelson, Y Shi, M Gujral, H Zheng, D Malhotra, X Jin, M Jian, G Liu, ...
Cell 151 (7), 1431-1442, 2012
A critical assessment of Mus musculusgene function prediction using integrated genomic evidence
L Peņa-Castillo, M Tasan, CL Myers, H Lee, T Joshi, C Zhang, Y Guan, ...
Genome biology 9 (S1), S2, 2008
Comparisons among two fertile and three male-sterile mitochondrial genomes of maize
JO Allen, CM Fauron, P Minx, L Roark, S Oddiraju, GN Lin, L Meyer, ...
Genetics 177 (2), 1173-1192, 2007
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
R Corominas*, X Yang*, GN Lin*, S Kang*, Y Shen, L Ghamsari, M Broly, ...
Nature Communications 5 (3650), 2014
Spatiotemporal 16p11. 2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases
GN Lin, R Corominas, I Lemmens, X Yang, J Tavernier, DE Hill, M Vidal, ...
Neuron 85 (4), 742-754, 2015
Frequency and complexity of de novo structural mutation in autism
WM Brandler, D Antaki, M Gujral, A Noor, G Rosanio, TR Chapman, ...
The American Journal of Human Genetics 98 (4), 667-679, 2016
MutPred2: inferring the molecular and phenotypic impact of amino acid variants
V Pejaver, J Urresti, J Lugo-Martinez, KA Pagel, GN Lin, HJ Nam, M Mort, ...
BioRxiv, 134981, 2017
SeqRate: sequence-based protein folding type classification and rates prediction
GN Lin, Z Wang, D Xu, J Cheng
BMC bioinformatics 11 (3), S1, 2010
Polytomy identification in microbial phylogenetic reconstruction
GN Lin, C Zhang, D Xu
BMC systems biology 5 (S3), S2, 2011
ComPhy: prokaryotic composite distance phylogenies inferred from whole-genome gene sets
GN Lin, Z Cai, G Lin, S Chakraborty, D Xu
BMC bioinformatics 10 (S1), S5, 2009
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants
KA Pagel, V Pejaver, GN Lin, HJ Nam, M Mort, DN Cooper, J Sebat, ...
Bioinformatics 33 (14), i389-i398, 2017
De novo mutations from whole exome sequencing in neurodevelopmental and psychiatric disorders: from discovery to application
W Wang, R Corominas, GN Lin
Frontiers in genetics 10, 258, 2019
An integrated probabilistic approach for gene function prediction using multiple sources of high-throughput data
C Zhang, T Joshi, GN Lin, D Xu
International journal of computational biology and drug design 1 (3), 254-274, 2008
GeneFAS: GeneFAS: A Tool for the Prediction of Gene function Using Multiple Sources of Data
T Joshi, C Zhang, GN Lin, Z Song, D Xu
Genomics Protocols, 369-386, 2008
A comparison framework and guideline of clustering methods for mass cytometry data
X Liu, W Song, BY Wong, T Zhang, S Yu, GN Lin, X Ding
Genome Biology 20 (1), 297, 2019
PsyMuKB: A De Novo Variant Knowledge Base Integrating Transcriptional and Translational Information to Identify Isoform-specific Mutations in Developmental Disorders
GN Lin, S Guo, X Tan, W Wang, W Qian, W Song, J Wang, S Yu, Z Wang, ...
bioRxiv, 715813, 2019
NFU-Enabled FASTA: moving bioinformatics applications onto wide area networks
EJ Baker, GN Lin, H Liu, R Kosuri
Source code for biology and medicine 2 (1), 8, 2007
LT Eremenko, GV Oreshko, MA Fadeev
Bulletin of the Academy of Sciences of the USSR, Division of chemical …, 1989
PsyMuKB: an integrative de novo variant knowledge base for developmental disorders
GN Lin, S Guo, X Tan, W Wang, W Qian, W Song, J Wang, S Yu, Z Wang, ...
Genomics, Proteomics & Bioinformatics 17 (4), 453-464, 2019
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