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NAR Genomics and Bioinformatics|March 5, 2026
Mapping the inter- and intra-genic codon-usage landscape in Homo sapiensMaahil Arshad, Matthew Uchmanowicz, Vanshika Rana, et al.
Genomics|December 28, 1999
Molecular characterization of zyme/protease M/neurosin (PRSS9), a hormonally regulated kallikrein-like serine proteaseG M Yousef, L Y Luo, S W Scherer, et al.
Chemical Communications (Cambridge, England)|September 25, 2002
Agostic deformations based on electron delocalization in the alkyllithium-complex [(2-(Me3Si)2CLiC5H4N)2W Scherer, P Sirsch, M Grosche, et al.
Human Molecular Genetics|January 1, 1995
Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agentsJ Thacker, C E Tambini, P J Simpson, et al.
Seminars in Pediatric Neurology|May 18, 2011
The Cerebral Palsy Demonstration Project: a multidimensional research approach to cerebral palsyMichael Shevell, Steven P Miller, Stephen W Scherer, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 19, 2026
Large Models for Small Tables: Adapting Tabular Foundation Models to EHR DataRui Zhu, Xiaopu Zhou, Ivy Liang, et al.
Molecular and Cellular Biology|May 29, 2000
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instabilityA Hellman, A Rahat, S W Scherer, et al.
Genomics|May 16, 2001
Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNAK Hannula, M Lipsanen-Nyman, S W Scherer, et al.
Human Mutation|October 23, 2012
Mechanisms of formation of structural variation in a fully sequenced human genomeAndy Wing Chun Pang, Ohsuke Migita, Jeffrey R Macdonald, et al.
Cell|December 28, 2020
Phase Separation as a Missing Mechanism for Interpretation of Disease MutationsBrian Tsang, Iva Pritišanac, Stephen W Scherer, et al.
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