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Circulation Research|October 26, 2018
Cerebral Cavernous Malformations Develop Through Clonal Expansion of Mutant Endothelial CellsMatthew R Detter, Daniel A Snellings, Douglas A MarchukNature Reviews. Genetics|April 25, 2025
Advances in single-cell DNA sequencing enable insights into human somatic mosaicismDiane D Shao, Andrea J Kriz, Daniel A Snellings, et al.American Journal of Human Genetics|October 22, 2019
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1Daniel A Snellings, Carol J Gallione, Dewi S Clark, et al.Nature Communications|November 3, 2023
Single-nucleus DNA sequencing reveals hidden somatic loss-of-heterozygosity in Cerebral Cavernous MalformationsAndrew K Ressler, Daniel A Snellings, Romuald Girard, et al.Bioinformatics (Oxford, England)|August 25, 2023
Gonomics: uniting high performance and readability for genomics with GoEric H Au, Christiana Fauci, Yanting Luo, et al.Circulation Research|June 24, 2021
Cerebral Cavernous Malformation: From Mechanism to TherapyDaniel A Snellings, Courtney C Hong, Aileen A Ren, et al.Biorxiv : the Preprint Server for Biology|June 12, 2025
Cell-type-specific patterns and consequences of somatic mutation in development and aging brainAndrea J Kriz, Shulin Mao, Diane D Shao, et al.Cell|November 24, 2022
Adaptive sequence divergence forged new neurodevelopmental enhancers in humansRiley J Mangan, Fernando C Alsina, Federica Mosti, et al.Nature|April 28, 2021
PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanismAileen A Ren, Daniel A Snellings, Yourong S Su, et al.Pageof 1