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Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework.
Groopman E, Mohan S, Waddell A, Wilke M, Fernandez R, Weaver M, Chen H, Liu H, Bali D, Baudet H, Clarke L, Hung C, Mao R, Pinto E Vairo F, Racacho L, Yuzyuk T, Craigen WJ, Goldstein J. Groopman E, et al. Among authors: clarke l. Mol Genet Metab. 2024 Nov;143(3):108593. doi: 10.1016/j.ymgme.2024.108593. Epub 2024 Oct 12. Mol Genet Metab. 2024. PMID: 39426251
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.
Regalado ES, Guo DC, Villamizar C, Avidan N, Gilchrist D, McGillivray B, Clarke L, Bernier F, Santos-Cortez RL, Leal SM, Bertoli-Avella AM, Shendure J, Rieder MJ, Nickerson DA; NHLBI GO Exome Sequencing Project; Milewicz DM. Regalado ES, et al. Among authors: clarke l. Circ Res. 2011 Sep 2;109(6):680-6. doi: 10.1161/CIRCRESAHA.111.248161. Epub 2011 Jul 21. Circ Res. 2011. PMID: 21778426 Free PMC article.
Lessons Learned in Virtual Launch of an Antenatal Opioid Exposure Study During the COVID-19 Pandemic.
Newman JE, Dhawan M, Clarke L, Owen S, Beiersdorfer T, Parlberg LM, Merhar S, DeMauro SB, Lorch SA, Wilson-Costello D, Ambalavanan N, Peralta-Carcelen M, Poindexter B, Davis JM, Mack N, Limperopoulos C, Bann CM. Newman JE, et al. Among authors: clarke l. Nurs Res. 2025 Jan 24. doi: 10.1097/NNR.0000000000000807. Online ahead of print. Nurs Res. 2025. PMID: 39853217
Integration of Peer Navigators Into Longitudinal Research.
Bann CM, Newman JE, Clarke L, Russell S, Dhawan M, Beiersdorfer T, DeMauro S, Wilson-Costello D, Peralta-Carcelen M, Merhar S. Bann CM, et al. Among authors: clarke l. J Obstet Gynecol Neonatal Nurs. 2025 Jan 16:S0884-2175(24)00343-5. doi: 10.1016/j.jogn.2024.11.008. Online ahead of print. J Obstet Gynecol Neonatal Nurs. 2025. PMID: 39719266 Free article.
1,476 results