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Microfluidic characterisation reveals broad range of SARS-CoV-2 antibody affinity in human plasma.
Schneider MM, Emmenegger M, Xu CK, Condado Morales I, Meisl G, Turelli P, Zografou C, Zimmermann MR, Frey BM, Fiedler S, Denninger V, Jacquat RP, Madrigal L, Ilsley A, Kosmoliaptsis V, Fiegler H, Trono D, Knowles TP, Aguzzi A. Schneider MM, et al. Among authors: fiegler h. Life Sci Alliance. 2021 Nov 30;5(2):e202101270. doi: 10.26508/lsa.202101270. Print 2022 Feb. Life Sci Alliance. 2021. PMID: 34848436 Free PMC article.
Antibody Affinity Governs the Inhibition of SARS-CoV-2 Spike/ACE2 Binding in Patient Serum.
Fiedler S, Piziorska MA, Denninger V, Morgunov AS, Ilsley A, Malik AY, Schneider MM, Devenish SRA, Meisl G, Kosmoliaptsis V, Aguzzi A, Fiegler H, Knowles TPJ. Fiedler S, et al. Among authors: fiegler h. ACS Infect Dis. 2021 Aug 13;7(8):2362-2369. doi: 10.1021/acsinfecdis.1c00047. Epub 2021 Apr 20. ACS Infect Dis. 2021. PMID: 33876632
Microfluidic Antibody Affinity Profiling Reveals the Role of Memory Reactivation and Cross-Reactivity in the Defense Against SARS-CoV-2.
Denninger V, Xu CK, Meisl G, Morgunov AS, Fiedler S, Ilsley A, Emmenegger M, Malik AY, Piziorska MA, Schneider MM, Devenish SRA, Kosmoliaptsis V, Aguzzi A, Fiegler H, Knowles TPJ. Denninger V, et al. Among authors: fiegler h. ACS Infect Dis. 2022 Apr 8;8(4):790-799. doi: 10.1021/acsinfecdis.1c00486. Epub 2022 Mar 30. ACS Infect Dis. 2022. PMID: 35352558
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.
Shaw-Smith C, Redon R, Rickman L, Rio M, Willatt L, Fiegler H, Firth H, Sanlaville D, Winter R, Colleaux L, Bobrow M, Carter NP. Shaw-Smith C, et al. Among authors: fiegler h. J Med Genet. 2004 Apr;41(4):241-8. doi: 10.1136/jmg.2003.017731. J Med Genet. 2004. PMID: 15060094 Free PMC article.
Tiling path resolution mapping of constitutional 1p36 deletions by array-CGH: contiguous gene deletion or "deletion with positional effect" syndrome?
Redon R, Rio M, Gregory SG, Cooper RA, Fiegler H, Sanlaville D, Banerjee R, Scott C, Carr P, Langford C, Cormier-Daire V, Munnich A, Carter NP, Colleaux L. Redon R, et al. Among authors: fiegler h. J Med Genet. 2005 Feb;42(2):166-71. doi: 10.1136/jmg.2004.023861. J Med Genet. 2005. PMID: 15689456 Free PMC article. No abstract available.
Prenatal diagnosis by array-CGH.
Rickman L, Fiegler H, Carter NP, Bobrow M. Rickman L, et al. Among authors: fiegler h. Eur J Med Genet. 2005 Jul-Sep;48(3):232-40. doi: 10.1016/j.ejmg.2005.03.003. Eur J Med Genet. 2005. PMID: 16179219 Review.
Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
Rickman L, Fiegler H, Shaw-Smith C, Nash R, Cirigliano V, Voglino G, Ng BL, Scott C, Whittaker J, Adinolfi M, Carter NP, Bobrow M. Rickman L, et al. Among authors: fiegler h. J Med Genet. 2006 Apr;43(4):353-61. doi: 10.1136/jmg.2005.037648. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199537 Free PMC article.
Genomic array technology.
Fiegler H, Carter NP. Fiegler H, et al. Methods Cell Biol. 2004;75:769-85. doi: 10.1016/s0091-679x(04)75033-5. Methods Cell Biol. 2004. PMID: 15603452 No abstract available.
61 results