Research ExplorerScientific StaffMathias Woidy Publications

Mathias Woidy

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ORCID: 0000-0003-2393-3738
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Publications

  1. SCORING: Journal article › Research › Peer-reviewed

  2. Accumulation of α-synuclein mediates podocyte injury in Fabry nephropathy

    Braun, F., Abed, A., Sellung, D., Rogg, M., Woidy, M., Eikrem, O., Wanner, N., Gambardella, J., Laufer, S. D., Haas, F., Wong, M. N., Dumoulin, B., Rischke, P., Mühlig, A. K., Sachs, W., von Cossel, K., Schulz, K., Muschol, N., Gersting, S. W., Muntau, A. C., Kretz, O., Hahn, O., Rinschen, M. M., Mauer, M., Bork, T., Grahammer, F., Liang, W., Eierhoff, T., Römer, W., Hansen, A., Meyer-Schwesinger, C., Iaccarino, G., Tøndel, C., Marti, H-P., Najafian, B., Puelles, V. G., Schell, C. & Huber, T. B., 01.06.2023, In: J CLIN INVEST. 133, 11, e157782.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  3. Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

    Schneeberger, P. E., Kortüm, F., Korenke, G. C., Alawi, M., Santer, R., Woidy, M., Buhas, D., Fox, S., Juusola, J., Alfadhel, M., Webb, B. D., Coci, E. G., Abou Jamra, R., Siekmeyer, M., Biskup, S., Heller, C., Maier, E. M., Javaher-Haghighi, P., Bedeschi, M. F., Ajmone, P. F., Iascone, M., Peeters, H., Ballon, K., Jaeken, J., Rodríguez Alonso, A., Palomares-Bralo, M., Santos-Simarro, F., Meuwissen, M. E. C., Beysen, D., Kooy, R. F., Houlden, H., Murphy, D., Doosti, M., Karimiani, E. G., Mojarrad, M., Maroofian, R., Noskova, L., Kmoch, S., Honzik, T., Cope, H., Sanchez-Valle, A., Undiagnosed Diseases Network, Gelb, B. D., Kurth, I., Hempel, M. & Kutsche, K., 01.08.2020, In: BRAIN. 143, 8, p. 2437-2453 17 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  4. Dominant KPNA3 Mutations Cause Infantile Onset Hereditary Spastic Paraplegia

    Schob, C., Hempel, M., Brozkova, D. S., Jiang, H., Kim, S. Y., Batzir, N. A., Orenstein, N., Bierhals, T., Johannsen, J., Meszarosova, A. U., Chae, J-H., Seeman, P., Woidy, M., Fang, F., Kubisch, C., Kindler, S. & Denecke, J., 11.2021, In: ANN NEUROL. 90, 5, p. 738-750 13 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  5. Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency

    Lotz-Havla, A. S., Woidy, M., Guder, P., Schmiesing, J., Erdmann, R., Waterham, H. R., Muntau, A. C. & Gersting, S. W., 2021, In: FRONT GENET. 12, 726174.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  6. iBRET Screen of the ABCD1 Peroxisomal Network and Mutation-Induced Network Perturbations

    Lotz-Havla, A. S., Woidy, M., Guder, P., Friedel, C. C., Klingbeil, J. M., Bulau, A-M., Schultze, A., Dahmen, I., Noll-Puchta, H., Kemp, S., Erdmann, R., Zimmer, R., Muntau, A. C. & Gersting, S. W., 03.09.2021, In: J PROTEOME RES. 20, 9, p. 4366-4380 15 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  7. Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26

    Guder, P., Lotz-Havla, A. S., Woidy, M., Reiß, D. D., Danecka, M. K., Schatz, U. A., Becker, M., Ensenauer, R., Pagel, P., Büttner, L., Muntau, A. C. & Gersting, S. W., 03.2019, In: BBA-MOL CELL RES. 1866, 3, p. 518-531 14 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  8. Long-Term Antibody Response to SARS-CoV-2 in Children

    Dunay, G. A., Barroso, M., Woidy, M., Danecka, M. K., Engels, G., Hermann, K., Neumann, F. S., Paul, K., Beime, J., Escherich, G., Fehse, K., Grinstein, L., Haniel, F., Haupt, L. J., Hecher, L., Kehl, T., Kemen, C., Kemper, M. J., Kobbe, R., Kohl, A., Klokow, T., Nörz, D., Olfe, J., Schlenker, F., Schmiesing, J., Schrum, J., Sibbertsen, F., Stock, P., Tiede, S., Vettorazzi, E., Zazara, D. E., Zapf, A., Lütgehetmann, M., Oh, J., Mir, T. S., Muntau, A. C., Gersting, S. W. & C19.CHILD Study Group, 01.2023, In: J CLIN IMMUNOL. 43, 1, p. 46-56 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  9. Mapping the functional landscape of frequent phenylalanine hydroxylase (PAH) genotypes promotes personalised medicine in phenylketonuria

    Danecka, M. K., Woidy, M., Zschocke, J., Feillet, F., Muntau, A. C. & Gersting, S. W., 03.2015, In: J MED GENET. 52, 3, p. 175-185 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  10. Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism

    Eichinger, A., Danecka, M. K., Möglich, T., Borsch, J., Woidy, M., Büttner, L., Muntau, A. C. & Gersting, S. W., 15.05.2018, In: HUM MOL GENET. 27, 10, p. 1732-1742 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  11. Specific CD4+ T Cell Responses to Ancestral SARS-CoV-2 in Children Increase With Age and Show Cross-Reactivity to Beta Variant

    Paul, K., Sibbertsen, F., Weiskopf, D., Lütgehetmann, M., Barroso, M., Danecka, M. K., Glau, L., Hecher, L., Hermann, K., Kohl, A., Oh, J., Wiesch, J. S. Z., Sette, A., Tolosa, E., Vettorazzi, E., Woidy, M., Zapf, A., Zazara, D. E., Mir, T. S., Muntau, A. C., Gersting, S. W. & Dunay, G. A., 15.07.2022, In: FRONT IMMUNOL. 13, p. 867577 867577.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  12. SCORING: Review article › Research

  13. Inborn errors of metabolism and the human interactome: a systems medicine approach

    Woidy, M., Muntau, A. C. & Gersting, S. W., 05.2018, In: J INHERIT METAB DIS. 41, 3, p. 285-296 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Review article › Research

  14. Conference abstract in journal › Research › Peer-reviewed

  15. A personalized medicine approach for phenylketonuria patients

    Gundorova, P., Danecka, M. K., Woidy, M. & Gersting, S. W., 16.08.2022, In: J INHERIT METAB DIS. 45, S1, p. 473 SSIEM22-2133.

    Research output: SCORING: Contribution to journal › Conference abstract in journal › Research › peer-review

  16. Functional studies drive treatment of phenylketonuria to become personalized

    Gundorova, P., Danecka, M. K., Woidy, M., Kasten, V., Muntau, A. C. & Gersting, S. W., 04.01.2024, In: EUR J HUM GENET. 32, Suppl 1, p. 698 P19.044.D.

    Research output: SCORING: Contribution to journal › Conference abstract in journal › Research › peer-review

  17. Chapter › Research › Peer-reviewed

  18. Disorders of Carbohydrate Absorption, Transmembrane Transport and Metabolism

    Derks, T., Lubout, C., Woidy, M. & Santer, R., 01.2022, Physician’s Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases. Blau, N., Vici, C. D., Ferreira, C. R., Vianey-Saban, C. & van Karnebeek, C. D. M. (eds.). 2 ed. Springer Nature Switzerland, p. 649-700 52 p.

    Research output: SCORING: Contribution to book/anthology › Chapter › Research › peer-review