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Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort.
Retterer K, Scuffins J, Schmidt D, Lewis R, Pineda-Alvarez D, Stafford A, Schmidt L, Warren S, Gibellini F, Kondakova A, Blair A, Bale S, Matyakhina L, Meck J, Aradhya S, Haverfield E. Retterer K, et al. Among authors: lewis r. Genet Med. 2015 Aug;17(8):623-9. doi: 10.1038/gim.2014.160. Epub 2014 Nov 6. Genet Med. 2015. PMID: 25356966 Free article.
Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy.
Truty R, Patil N, Sankar R, Sullivan J, Millichap J, Carvill G, Entezam A, Esplin ED, Fuller A, Hogue M, Johnson B, Khouzam A, Kobayashi Y, Lewis R, Nykamp K, Riethmaier D, Westbrook J, Zeman M, Nussbaum RL, Aradhya S. Truty R, et al. Among authors: lewis r. Epilepsia Open. 2019 Jul 1;4(3):397-408. doi: 10.1002/epi4.12348. eCollection 2019 Sep. Epilepsia Open. 2019. PMID: 31440721 Free PMC article.
Gastroschisis associated changes in the placental transcriptome.
Jongen M, Reddin I, Cave S, Cashmore L, Pond J, Cleal JK, Hall NJ, Lewis RM. Jongen M, et al. Among authors: lewis rm. Placenta. 2024 Jun 4;154:38-41. doi: 10.1016/j.placenta.2024.06.001. Online ahead of print. Placenta. 2024. PMID: 38870840
Faith Community Nursing: Impacting Community-Based Care.
Burt S, Lewis R, Braithwaite Y. Burt S, et al. Among authors: lewis r. J Christ Nurs. 2024 Jul-Sep 01;41(3):160-165. doi: 10.1097/CNJ.0000000000001178. Epub 2024 Jun 10. J Christ Nurs. 2024. PMID: 38853314
6,630 results