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Biorxiv : the Preprint Server for Biology|May 7, 2026
Designed Minibinders Rewire Receptor Signaling to Enable Functional Human Myogenic ReprogrammingRiya Keshri, Zachary Foreman, Phillip Barrett, et al.Nature Genetics|September 18, 2025
Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networksChing-Huang Ho, Maxwell A Dippel, Meghan S McQuade, et al.Genome Biology|January 23, 2015
Deep sequencing of multiple regions of glial tumors reveals spatial heterogeneity for mutations in clinically relevant genesAkash Kumar, Evan A Boyle, Mari Tokita, et al.Blood|December 4, 2023
Transcriptional control of leukemogenesis by the chromatin reader SGF29Karina Barbosa, Anagha Deshpande, Marlenne Perales, et al.Human Mutation|August 13, 2015
Expanding the Molecular and Clinical Phenotype of SSR4-CDGBobby G Ng, Kimiyo Raymond, Martin Kircher, et al.Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.Science Advances|October 7, 2022
Oncogenic role of a developmentally regulated NTRK2 splice variantSiobhan S Pattwell, Sonali Arora, Nicholas Nuechterlein, et al.Nature Reviews. Methods Primers|May 22, 2023
High-content CRISPR screeningChristoph Bock, Paul Datlinger, Florence Chardon, et al.American Journal of Human Genetics|April 9, 2013
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylationBobby G Ng, Kati J Buckingham, Kimiyo Raymond, et al.Genome Research|June 27, 2013
The million mutation project: a new approach to genetics in Caenorhabditis elegansOwen Thompson, Mark Edgley, Pnina Strasbourger, et al.Pageof 47