Lin, Guan Ning

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

Pejaver, V., Urresti, J., Lugo-Martinez, J., Pagel, K. A., Lin, G. N., Nam, H.-J., Mort, M., Cooper, D. N., Sebat, J., Iakoucheva, L. M., et al. (2020) · Nature Communications

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 923

Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation

Michaelson, J. J., Shi, Y., Gujral, M., Zheng, H., Malhotra, D., Jin, X., Jian, M., Liu, G., Greer, D., Bhandari, A., et al. (2012) · Cell

Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities

Cited by 544

A critical assessment of Mus musculusgene function prediction using integrated genomic evidence

Peña-Castillo, L., Tasan, M., Myers, C. L., Lee, H., Joshi, T., Zhang, C., Guan, Y., Leone, M., Pagnani, A., Kim, W. K., et al. (2008) · Genome Biology

Bioinformatics and Genomic NetworksGenomics and Phylogenetic Studies

Cited by 248

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

Lin, G. N., Corominas, R., Lemmens, I., Yang, X., Tavernier, J., Hill, D. E., Vidal, M., Sebat, J., & Iakoucheva, L. M. (2015) · Neuron

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 155

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Corominas, R., Yang, X., Lin, G. N., Kang, S., Shen, Y., Ghamsari, L., Broly, M., Rodriguez, M., Tam, S., Wanamaker, S. A., et al. (2014) · Nature Communications

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 140

Frequency and complexity of de novo structural mutation in autism

Brandler, W. M., Antaki, D., Gujral, M., Noor, A., Rosanio, G., Chapman, T. R., Barrera, D. J., Lin, G. N., Malhotra, D., Watts, A. C., et al. (2016) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 104

De novo mutations from whole exome sequencing in neurodevelopmental and psychiatric disorders: From discovery to application

Wang, W., Corominas, R., & Lin, G. N. (2019) · Frontiers in Genetics

Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders

Cited by 70

A selection pressure landscape for 870 human polygenic traits

Song, W., Shi, Y., Wang, W., Pan, W., Qian, W., Yu, S., Zhao, M., & Lin, G. N. (2021) · Nature Human Behaviour

Genetic Associations and EpidemiologyForensic and Genetic Research

Cited by 25

Haplotype Function Score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits

Song, W., Shi, Y., & Lin, G. N. (2024) · eLife

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 0

Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits

Song, W., Shi, Y., & Lin, G. N. (2024) · eLife

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 0