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American Journal of Human Genetics|April 2, 2021
Opportunities and challenges for the computational interpretation of rare variation in clinically important genesGregory McInnes, Andrew G Sharo, Megan L Koleske, et al.Molecular & Cellular Proteomics : MCP|April 22, 2016
Quantitative Tagless Copurification: A Method to Validate and Identify Protein-Protein InteractionsMaxim Shatsky, Ming Dong, Haichuan Liu, et al.Proceedings of the National Academy of Sciences of the United States of America|October 7, 2009
Survey of large protein complexes in D. vulgaris reveals great structural diversityBong-Gyoon Han, Ming Dong, Haichuan Liu, et al.Biorxiv : the Preprint Server for Biology|May 7, 2026
Advances in Protein Function Prediction from the Fifth CAFA ChallengeM Clara De Paolis Kaluza, Rashika Ramola, Parnal Joshi, et al.Frontiers in Immunology|August 15, 2022
Investigation of the causal etiology in a patient with T-B+NK+ immunodeficiencyRobert Sertori, Jian-Xin Lin, Esteban Martinez, et al.RNA (New York, N.Y.)|February 18, 2006
The RNA Ontology Consortium: an open invitation to the RNA communityNeocles B Leontis, Russ B Altman, Helen M Berman, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 15, 2022
Newborn screening for neurodevelopmental diseases: Are we there yet?Wendy K Chung, Jonathan S Berg, Jeffrey R Botkin, et al.Journal of Proteome Research|October 27, 2012
High-throughput isolation and characterization of untagged membrane protein complexes: outer membrane complexes of Desulfovibrio vulgarisPeter J Walian, Simon Allen, Maxim Shatsky, et al.Human Mutation|May 30, 2019
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challengesGregory McInnes, Roxana Daneshjou, Panagiostis Katsonis, et al.NPJ Genomic Medicine|September 24, 2021
Application of full-genome analysis to diagnose rare monogenic disordersJoseph T Shieh, Monica Penon-Portmann, Karen H Y Wong, et al.Pageof 19