Kraft F - Search Results

1

CNVizard-a lightweight streamlit application for an interactive analysis of copy number variants.

Krause J, Classen C, Dey D, Lausberg E, Kessler L, Eggermann T, Kurth I, Begemann M, Kraft F. Krause J, et al. Among authors: kraft f. BMC Bioinformatics. 2024 Dec 17;25(1):376. doi: 10.1186/s12859-024-06010-2. BMC Bioinformatics. 2024. PMID: 39690401 Free PMC article.

2

Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers.

Soellner L, Kraft F, Sauer S, Begemann M, Kurth I, Elbracht M, Eggermann T. Soellner L, et al. Among authors: kraft f. Eur J Hum Genet. 2019 Jan;27(1):42-48. doi: 10.1038/s41431-018-0269-1. Epub 2018 Sep 14. Eur J Hum Genet. 2019. PMID: 30218098 Free PMC article.

3

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation.

Kraft F, Wesseler K, Begemann M, Kurth I, Elbracht M, Eggermann T. Kraft F, et al. Clin Epigenetics. 2019 Feb 15;11(1):30. doi: 10.1186/s13148-019-0629-x. Clin Epigenetics. 2019. PMID: 30770769 Free PMC article.

4

Paternal 132 bp deletion affecting KCNQ1OT1 in 11p15.5 is associated with growth retardation but does not affect imprinting.

Eggermann T, Kraft F, Lausberg E, Ergezinger K, Kunstmann E. Eggermann T, et al. Among authors: kraft f. J Med Genet. 2021 Mar;58(3):173-176. doi: 10.1136/jmedgenet-2020-106868. Epub 2020 May 23. J Med Genet. 2021. PMID: 32447323

5

Long-read sequencing to understand genome biology and cell function.

Kraft F, Kurth I. Kraft F, et al. Int J Biochem Cell Biol. 2020 Sep;126:105799. doi: 10.1016/j.biocel.2020.105799. Epub 2020 Jul 3. Int J Biochem Cell Biol. 2020. PMID: 32629027 Review.

6

Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach.

Bilo L, Ochoa E, Lee S, Dey D, Kurth I, Kraft F, Rodger F, Docquier F, Toribio A, Bottolo L, Binder G, Fekete G, Elbracht M, Maher ER, Begemann M, Eggermann T. Bilo L, et al. Among authors: kraft f. Clin Epigenetics. 2023 Mar 1;15(1):35. doi: 10.1186/s13148-023-01453-5. Clin Epigenetics. 2023. PMID: 36859312 Free PMC article.

7

Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies.

Meyer R, Begemann M, Demuth S, Kraft F, Dey D, Schüler H, Busse S, Häusler M, Zerres K, Kurth I, Eggermann T, Elbracht M. Meyer R, et al. Among authors: kraft f. Clin Genet. 2020 Oct;98(4):408-412. doi: 10.1111/cge.13819. Epub 2020 Aug 19. Clin Genet. 2020. PMID: 32720325

8

Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study.

Kessler L, Krause J, Kraft F, Amin AK, Fekete G, Lengyel A, Pinti E, Kovacs A, Lischka A, Eggermann K, Kurth I, Knopp C, Elbracht M, Begemann M, Eggermann T. Kessler L, et al. Among authors: kraft f. Clin Genet. 2024 Dec 12. doi: 10.1111/cge.14649. Online ahead of print. Clin Genet. 2024. PMID: 39663844

9

HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence.

Hübner CT, Meyer R, Kenawy A, Ambrozaityte L, Matuleviciene A, Kraft F, Begemann M, Elbracht M, Eggermann T. Hübner CT, et al. Among authors: kraft f. J Clin Endocrinol Metab. 2020 Jul 1;105(7):dgaa273. doi: 10.1210/clinem/dgaa273. J Clin Endocrinol Metab. 2020. PMID: 32421827

10

Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical Management.

Wesseler K, Kraft F, Eggermann T. Wesseler K, et al. Among authors: kraft f. Int J Mol Sci. 2019 Aug 28;20(17):4219. doi: 10.3390/ijms20174219. Int J Mol Sci. 2019. PMID: 31466347 Free PMC article. Review.

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