Miller M - Search Results

1

The National Academies' Roundtable on Genomics and Precision Health: Where we have been and where we are heading.

Ginsburg G, Penny M, Feero WG, Miller M, Addie S, Beachy SH. Ginsburg G, et al. Among authors: miller m. Am J Hum Genet. 2021 Oct 7;108(10):1817-1822. doi: 10.1016/j.ajhg.2021.08.015. Am J Hum Genet. 2021. PMID: 34626581 Free PMC article. Review.

2

Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Greenwood CM, Fujiwara TM, Boothroyd LJ, Miller MA, Frappier D, Fanning EA, Schurr E, Morgan K. Greenwood CM, et al. Among authors: miller ma. Am J Hum Genet. 2000 Aug;67(2):405-16. doi: 10.1086/303012. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10882571 Free PMC article.

3

cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 protein.

Bressler SL, Gray MD, Sopher BL, Hu Q, Hearn MG, Pham DG, Dinulos MB, Fukuchi K, Sisodia SS, Miller MA, Disteche CM, Martin GM. Bressler SL, et al. Among authors: miller ma. Hum Mol Genet. 1996 Oct;5(10):1589-98. doi: 10.1093/hmg/5.10.1589. Hum Mol Genet. 1996. PMID: 8894693

4

De novo mutations producing unstable hemoglobins or hemoglobins M : I. Establishment of a Depository and use of data to test for an association of de novo mutation with advanced parental age.

Stamatoyannopoulos G, Nute PE, Miller M. Stamatoyannopoulos G, et al. Among authors: miller m. Hum Genet. 1981 Oct;58(4):396-404. doi: 10.1007/BF00282822. Hum Genet. 1981. PMID: 28035506

5

Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy.

Kohn H, Manowitz P, Miller M, Kling A. Kohn H, et al. Among authors: miller m. Hum Genet. 1988 May;79(1):8-12. doi: 10.1007/BF00291701. Hum Genet. 1988. PMID: 3366464

6

De novo mutations producing unstable hemoglobins or hemoglobins M. I. Establishment of a depository and use of data to test for an association of de novo mutation with advanced parental age.

Stamatoyannopoulos G, Nute PE, Miller M. Stamatoyannopoulos G, et al. Among authors: miller m. Hum Genet. 1981;58(4):396-404. Hum Genet. 1981. PMID: 7327561 No abstract available.

7

Expert consensus on the benefits of neuraminidase in conventional influenza vaccines: a Delphi study.

Youhanna J, Puig-Barberà J, Miller MS, Molrine D, Hadi M, Bapat S, Iheanacho I, Dodman S, Fikre T, Swinburn P; ADD-NA (Adding Neuraminidase) Delphi panel. Youhanna J, et al. Among authors: miller ms. BMC Infect Dis. 2025 Jan 11;25(1):53. doi: 10.1186/s12879-024-10277-4. BMC Infect Dis. 2025. PMID: 39794704

8

TDP43 autoregulation gives rise to dominant negative isoforms that are tightly controlled by transcriptional and post-translational mechanisms.

Dykstra MM, Weskamp K, Gómez NB, Waksmacki J, Tank E, Glineburg MR, Snyder A, Pinarbasi E, Bekier M, Li X, Miller MR, Bai J, Shahzad S, Nedumaran N, Wieland C, Stewart C, Willey S, Grotewold N, McBride J, Moran JJ, Suryakumar AV, Lucas M, Tessier PM, Ward M, Todd PK, Barmada SJ. Dykstra MM, et al. Among authors: miller mr. Cell Rep. 2025 Jan 8;44(1):115113. doi: 10.1016/j.celrep.2024.115113. Online ahead of print. Cell Rep. 2025. PMID: 39792557

9

Long-term performance and stability of implanted neural interfaces in individuals with lower limb loss.

Petros E, Miller M, Dunning JL, Pinault G, Tyler DJ, Triolo RJ, Charkhkar H. Petros E, et al. Among authors: miller m. J Neural Eng. 2025 Jan 9. doi: 10.1088/1741-2552/ada829. Online ahead of print. J Neural Eng. 2025. PMID: 39787696

10

The prevalence of obesity in children with CHD: what has changed over the past decade in Southwestern Ontario?

Frewen N, Sharma A, Subasri M, Miller MR, Mansukhani G, Filler G, Norozi K. Frewen N, et al. Among authors: miller mr. Cardiol Young. 2025 Jan 9:1-6. doi: 10.1017/S1047951124036497. Online ahead of print. Cardiol Young. 2025. PMID: 39780469

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