Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

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Florian Kraft

Dr.
RWTH Aachen University
Institut für Humangenetik
Pauwelsstraße 30, 52074 Aachen, Germany
Aachen 52074
+49 241 8037569
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. 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. Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach. Clin Epigenetics. 2023 03 01; 15(1):35. PMID: 36859312; PMCID: PMC9979536.
      Citations: 1     Fields:    Translation:Cells
    2. Gaebler AJ, Fakour N, St?hr F, Zweerings J, Taebi A, Suslova M, Dukart J, Hipp JF, Adhikari BM, Kochunov P, Muthukumaraswamy SD, Forsyth A, Eggermann T, Kraft F, Kurth I, Paulzen M, Gr?nder G, Schneider F, Mathiak K. Functional connectivity signatures of NMDAR dysfunction in schizophrenia-integrating findings from imaging genetics and pharmaco-fMRI. Transl Psychiatry. 2023 02 16; 13(1):59. PMID: 36797233; PMCID: PMC9935542.
      Citations: 3     Fields:    Translation:Humans
    3. Kleinle S, Scholz V, Benet-Pag?s A, Wohlfrom T, Gehling S, Scharf F, Rost S, Prott EC, Grinzinger S, Hotter A, Haug V, Niemeier S, Wiethoff-Ubrig L, Hagenacker T, Goldhahn K, von Moers A, Walter MC, Reilich P, Eggermann K, Kraft F, Kurth I, Erdmann H, Holinski-Feder E, Neuhann T, Abicht A, Prott EC, Grinzinger S, Hotter A, Haug V, Niemeier S, Wiethoff-Ubrig L, Goldhahn K, von Moers A, Walter MC, Reilich P, Eggermann K, Kraft F, Kurth I. Closing the Gap - Detection of 5q-Spinal Muscular Atrophy by Short-Read Next-Generation Sequencing and Unexpected Results in a Diagnostic Patient Cohort. J Neuromuscul Dis. 2023; 10(5):835-846. PMID: 37424474.
      Citations: 1     Fields:    Translation:Humans
    4. Kraft F, Gangfuss A, Mohassel P, Schara-Schmidt U, Roos A, K?lbel H, Hentschel A, Czech A, Nguyen C, Stenzel W, Preu?e C. New Insights into the Neuromyogenic Spectrum of a Gain of Function Mutation in SPTLC1. Genes (Basel). 2022 05 17; 13(5). PMID: 35627278; PMCID: PMC9140917.
      Citations: 1     Fields:    Translation:Humans
    5. Haag N, Tan EC, Begemann M, Buschmann L, Kraft F, Holschbach P, Lai AHM, Brett M, Mochida GH, DiTroia S, Pais L, Neil JE, Al-Saffar M, Bastaki L, Walsh CA, Kurth I, Knopp C. Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. Eur J Hum Genet. 2021 11; 29(11):1663-1668. PMID: 34413497; PMCID: PMC8560748.
      Citations: 5     Fields:    Translation:Humans
    6. Lausberg E, Dewulf JP, Wiame E, Salvarinova R, van Karnebeek CD, Klemm P, Ohl K, Mull M, Braunschweig T, Weis J, Sommer CJ, Stollbrink-Peschgens C, Choukair D, Oommen PT, Borkhardt A, Wagner N, Meyer R, Eggermann T, Begemann M, Van Schaftingen E, Tenbrock K, van den Heuvel L, Elbracht M, Kurth I, Kraft F, Gie?elmann S, Holz A, Demuth S, Haase C, Debray FG, Libioulle C, Surowy H, Wieczorek D, H?usler M. C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. J Clin Invest. 2021 06 15; 131(12). PMID: 33945503; PMCID: PMC8203463.
      Citations: 5     Fields:    Translation:HumansAnimalsCells
    7. Meyer R, Begemann M, Demuth S, Kraft F, Dey D, Busse S, Zerres K, Kurth I, Eggermann T, Elbracht M, Sch?ler H, H?usler M. Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. Clin Genet. 2020 10; 98(4):408-412. PMID: 32720325.
      Citations: 8     Fields:    Translation:Humans
    8. Eggermann T, Kraft F, Kloth K, Hempel M, Klopocki E, H?ning I, Kunstmann E. Heterogeneous phenotypes in families with duplications of the paternal allele within the imprinting center 1 (H19/IGF2:TSS-DMR) in 11p15.5. Clin Genet. 2020 10; 98(4):418-419. PMID: 33294970.
      Citations: 2     Fields:    Translation:HumansCells
    9. Hedberg-Oldfors C, Meyer R, Nolte K, Abdul Rahim Y, Lindberg C, Karason K, Thuestad IJ, Visuttijai K, Geijer M, Begemann M, Kraft F, Lausberg E, Hitpass L, Luna EJ, Koschmieder S, Gramlich M, Gess B, Elbracht M, Weis J, Kurth I, Oldfors A, Knopp C, G?tzl R, Lochm?ller H. Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles. Brain. 2020 08 01; 143(8):2406-2420. PMID: 32779703; PMCID: PMC7447519.
      Citations: 11     Fields:    Translation:HumansCells
    10. Kraft F, Kurth I. Long-read sequencing to understand genome biology and cell function. Int J Biochem Cell Biol. 2020 09; 126:105799. PMID: 32629027.
      Citations: 13     Fields:    Translation:HumansAnimalsCells
    11. Meyer R, Kenawy A, Ambrozaityte L, Matuleviciene A, Kraft F, Begemann M, Elbracht M, Eggermann T, H?bner CT. HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence. J Clin Endocrinol Metab. 2020 07 01; 105(7). PMID: 32421827.
      Citations: 5     Fields:    Translation:Humans
    12. Eggermann T, Kraft F, Lausberg E, Ergezinger K, Kunstmann E. Paternal 132 bp deletion affecting KCNQ1OT1 in 11p15.5 is associated with growth retardation but does not affect imprinting. J Med Genet. 2021 03; 58(3):173-176. PMID: 32447323.
      Citations: 5     Fields:    Translation:HumansCells
    13. Kotolloshi R, Mirzakhani K, Ahlburg J, Kraft F, Pungsrinont T, Baniahmad A. Thyroid hormone induces cellular senescence in prostate cancer cells through induction of DEC1. J Steroid Biochem Mol Biol. 2020 07; 201:105689. PMID: 32360904.
      Citations: 5     Fields:    Translation:HumansCells
    14. Kraft F, van Rootselaar AF, Giesselmann S, Tschernoster N, Altmueller J, Delpu Y, Avarello MDM, Vijfhuizen LS, Kroes T, Reif PS, Rosenow F, Kurth I, Rafehi H, FAME consortium, Klein KM, Labauge P, Bennett MF, Bahlo M, Gecz J, Corbett MA, Tijssen MAJ, van den Maagdenberg AMJM, Florian RT, Leit?o E, Kaya S, Klebe S, Magnin E, Buratti J, K?hnel T, Schr?der C, Lamiral A, Keren B, Nava C, Bouteiller D, Forlani S, Jornea L, Kubica R, Ye T, Plassard D, Jost B, Meyer V, Deleuze JF, Rudolf G, Hirsch E, Ganos C, Vidailhet M, Thivard L, Mathieu A, Bourgeron T, Steenpass L, Horsthemke B, LeGuern E, Depienne C. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3. Nat Commun. 2019 10 29; 10(1):4919. PMID: 31664039; PMCID: PMC6820781.
      Citations: 61     Fields:    Translation:HumansCells
    15. Begemann M, Waszak SM, Robinson GW, Sharma T, Knopp C, Kraft F, Moser O, Mynarek M, Guerrini-Rousseau L, Brugieres L, Pietsch T, Bowers DC, Chintagumpala M, Sahm F, Korbel JO, Rutkowski S, Eggermann T, Gajjar A, Northcott P, Elbracht M, Pfister SM, Kontny U, Kurth I, J?ger N, Varlet P. Germline GPR161 Mutations Predispose to Pediatric Medulloblastoma. J Clin Oncol. 2020 01 01; 38(1):43-50. PMID: 31609649; PMCID: PMC6943973.
      Citations: 31     Fields:    Translation:HumansCells
    16. Wesseler K, Kraft F, Eggermann T. Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders: Characterization of Basic Mechanisms to Improve Clinical Management. Int J Mol Sci. 2019 Aug 28; 20(17). PMID: 31466347; PMCID: PMC6747273.
      Citations: 3     Fields:    Translation:HumansCells
    17. Kraft F, Wesseler K, Begemann M, Kurth I, Elbracht M, Eggermann T. Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation. Clin Epigenetics. 2019 02 15; 11(1):30. PMID: 30770769; PMCID: PMC6377752.
      Citations: 8     Fields:    Translation:HumansCells
    18. Kraft F, Haag N, Korenke GC, Knopp C, Mull M, Bergmann M, Weis J, Elbracht M, Begemann M, Kurth I, Karsai G, H?nisch B, Othman A, Suriyanarayanan S, Steiner R, Schr?der JM, Hornemann T. DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humans. J Clin Invest. 2019 03 01; 129(3):1229-1239. PMID: 30620338; PMCID: PMC6391115.
      Citations: 28     Fields:    Translation:HumansCells
    19. Roell D, Hessenkemper W, Kraft F, Hauschild M, Bartsch S, Abraham TE, Houtsmuller AB, Matusch R, van Royen ME, Baniahmad A, R?sler TW. Halogen-substituted anthranilic acid derivatives provide a novel chemical platform for androgen receptor antagonists. J Steroid Biochem Mol Biol. 2019 04; 188:59-70. PMID: 30615932.
      Citations: 7     Fields:    Translation:HumansAnimalsCells
    20. Elbracht M, Kraft F, Begemann M, Holschbach P, Mull M, Kurth I, Hehr U, Kabat IM, M?ller B, H?usler M. Familial NEDD4L variant in periventricular nodular heterotopia and in a fetus with hypokinesia and flexion contractures. Mol Genet Genomic Med. 2018 11; 6(6):1255-1260. PMID: 30393983; PMCID: PMC6305664.
      Citations: 4     Fields:    Translation:Humans
    21. Soellner L, Kraft F, Sauer S, Begemann M, Kurth I, Elbracht M, Eggermann T. Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers. Eur J Hum Genet. 2019 01; 27(1):42-48. PMID: 30218098; PMCID: PMC6303262.
      Citations: 7     Fields:    Translation:HumansCells
    22. Drube S, Grimlowski R, Kraft F, Andreas N, Dudeck J, Weber F, Drube J, Reich D, Dudeck A, Kamradt T, Deppermann C, Fr?bel J, Stegner D, R?diger M, G?pfert C, Nieswandt B. The Neurobeachin-like 2 Protein Regulates Mast Cell Homeostasis. J Immunol. 2017 10 15; 199(8):2948-2957. PMID: 28887433.
      Citations: 10     Fields:    Translation:AnimalsCells
    23. Drube S, Kraft F, Dudeck J, Weber F, Meininger I, Beyer M, Irmler I, Stumm R, Yakovleva T, Gaestel M, Dudeck A, Kamradt T, M?ller AL, G?pfert C, H?fner N, Sch?tz D. MK2/3 Are Pivotal for IL-33-Induced and Mast Cell-Dependent Leukocyte Recruitment and the Resulting Skin Inflammation. J Immunol. 2016 11 01; 197(9):3662-3668. PMID: 27694493.
      Citations: 28     Fields:    Translation:AnimalsCells
    24. Foertsch F, Szambowska A, Weise A, Zielinski A, Schlott B, Kraft F, Mrasek K, Borgmann K, Pospiech H, Grosse F, Melle C. S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci. Cell Cycle. 2016 Oct 17; 15(20):2766-79. PMID: 27590262; PMCID: PMC5053559.
      Citations: 3     Fields:    Translation:HumansCells
    25. Esmaeili M, Jennek S, Ludwig S, Klitzsch A, Kraft F, Melle C, Baniahmad A. The tumor suppressor ING1b is a novel corepressor for the androgen receptor and induces cellular senescence in prostate cancer cells. J Mol Cell Biol. 2016 06; 8(3):207-20. PMID: 26993046.
      Citations: 19     Fields:    Translation:HumansAnimalsCells
    26. Kraft F, Schmidt C, Van Aken H, Zarbock A. Inflammatory response and extracorporeal circulation. Best Pract Res Clin Anaesthesiol. 2015 Jun; 29(2):113-23. PMID: 26060024.
      Citations: 25     Fields:    Translation:HumansAnimals
    27. Thiele M, Rabe S, Hessenkemper W, Roell D, Bartsch S, Kraft F, Abraham TE, Houtsmuller AB, van Royen ME, Giannis A, Baniahmad A. Novel Nor-Homo- and Spiro-Oxetan- Steroids Target the Human Androgen Receptor and Act as Antiandrogens. Curr Med Chem. 2015; 22(9):1156-1167. PMID: 24934352.
      Citations: 2     Fields:    
    28. Eckey M, Kraft F, Kob R, Escher N, Asim M, Fischer H, Fritsche MK, Melle C, Baniahmad A. The corepressor activity of Alien is controlled by CREB-binding protein/p300. FEBS J. 2013 Apr; 280(8):1861-8. PMID: 23441852.
      Citations:    Fields:    Translation:HumansCells
    29. Lorenz V, Hessenkemper W, Kyrylenko S, Kraft F, Baniahmad A, R?diger J. Sodium butyrate induces cellular senescence in neuroblastoma and prostate cancer cells. Horm Mol Biol Clin Investig. 2011 Oct 01; 7(1):265-72. PMID: 25961265.
      Citations: 12     Fields:    

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