Laura Hecher
Publications
- 2024
Complex structural variation and nonsense variant in trans cause VPS50-related disorder
Hecher, L., Gorski-Alberts, E., Begemann, M., Herwig, J., Lausberg, E., Hillebrand, G., Volk, A. E., Kurth, I., Kraft, F. & Kutsche, K., 29.08.2024, In: J MED GENET. 61, 9, p. 833-838 6 p.Research output: SCORING: Contribution to journal › Case report › Research › peer-review
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes
Rinaldi, B., Bayat, A., Zachariassen, L. G., Sun, J-H., Ge, Y-H., Zhao, D., Bonde, K., Madsen, L. H., Awad, I. A. A., Bagiran, D., Sbeih, A., Shah, S. M., El-Sayed, S., Lyngby, S. M., Pedersen, M. G., Stenum-Berg, C., Walker, L. C., Krey, I., Delahaye-Duriez, A., Emrick, L. T., Sully, K., Murali, C. N., Burrage, L. C., Plaud Gonzalez, J. A., Parnes, M., Friedman, J., Isidor, B., Lefranc, J., Redon, S., Heron, D., Mignot, C., Keren, B., Fradin, M., Dubourg, C., Mercier, S., Besnard, T., Cogne, B., Deb, W., Rivier, C., Milani, D., Bedeschi, M. F., Di Napoli, C., Grilli, F., Marchisio, P., Koudijs, S., Veenma, D., Argilli, E., Lynch, S. A., Au, P. Y. B., Ayala Valenzuela, F. E., Brown, C., Masser-Frye, D., Jones, M., Patron Romero, L., Li, W. L., Thorpe, E., Hecher, L., Johannsen, J., Denecke, J., McNiven, V., Szuto, A., Wakeling, E., Cruz, V., Sency, V., Wang, H., Piard, J., Kortüm, F., Herget, T., Bierhals, T., Condell, A., Zeev, B. B., Kaur, S., Christodoulou, J., Piton, A., Zweier, C., Kraus, C., Micalizzi, A., Trivisano, M., Specchio, N., Lesca, G., Møller, R. S., Tümer, Z., Musgaard, M., Gerard, B., Lemke, J. R., Shi, Y. S. & Kristensen, A. S., 03.05.2024, In: BRAIN. 147, 5, p. 1837-1855 19 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Association between Tubulointerstitial Nephritis and Uveitis Syndrome and Small-Vessel CNS Vasculitis
Grinstein, L., Hecher, L., Weiss, D., Johannsen, J. & Denecke, J., 04.2024, In: NEUROPEDIATRICS. 55, 2, p. 117-123 7 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2023
INPP4A-related genetic and phenotypic spectrum and functional relevance of subcellular targeting of INPP4A isoforms
Hecher, L., Harms, F. L., Lisfeld, J., Alawi, M., Denecke, J. & Kutsche, K., 04.2023, In: NEUROGENETICS. 24, 2, p. 79-93 15 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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
- 2022
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
- 2020
The Clinical Picture of a Bilateral Perisylvian Syndrome as the Initial Symptom of Mega-Corpus-Callosum Syndrome due to a MAST1-Gene Mutation
Hecher, L., Johannsen, J., Bierhals, T., Buhk, J-H., Hempel, M. & Denecke, J., 12.2020, In: NEUROPEDIATRICS. 51, 6, p. 435-439 5 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2019
Excessive Seizure Clusters in an Otherwise Well-Controlled Epilepsy as a Possible Hallmark of Untreated Vitamin B6-Responsive Epilepsy due to a Homozygous PLPBP Missense Variant
Johannsen, J., Bierhals, T., Deindl, P., Hecher, L., Hermann, K., Hempel, M., Kloth, K. & Denecke, J., 12.2019, In: J PEDIATR GENET. 8, 4, p. 222-225 4 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
Dysregulation of a specific immune-related network of genes biologically defines a subset of schizophrenia
Trossbach, S. V., Hecher, L., Schafflick, D., Deenen, R., Popa, O., Lautwein, T., Tschirner, S., Köhrer, K., Fehsel, K., Papazova, I., Malchow, B., Hasan, A., Winterer, G., Schmitt, A., Meyer Zu Hörste, G., Falkai, P. & Korth, C., 31.05.2019, In: TRANSL PSYCHIAT. 9, 1, p. 156Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2016
Misassembly of full-length Disrupted-in-Schizophrenia 1 protein is linked to altered dopamine homeostasis and behavioral deficits
Trossbach, S. V., Bader, V., Hecher, L., Pum, M. E., Masoud, S. T., Prikulis, I., Schäble, S., de Souza Silva, M. A., Su, P., Boulat, B., Chwiesko, C., Poschmann, G., Stühler, K., Lohr, K. M., Stout, K. A., Oskamp, A., Godsave, S. F., Müller-Schiffmann, A., Bilzer, T., Steiner, H., Peters, P. J., Sauvage, M., Ramsey, A. J., Miller, G. W., Liu, F., Seeman, P., Brandon, N. J., Huston, J. P. & Korth, C., 11.2016, In: MOL PSYCHIATR. 21, 11, p. 1561-1572 12 p.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
- 2014
REVERSE-TRANSLATING BIOLOGICAL MARKERS FOR DISC1-ASSOCIATED BEHAVIORAL DISORDERS TO HUMAN PATIENTS
Hecher, L., 17.04.2014, Schizophrenia Research - Abstracts of the 4th Biennial Schizophrenia International Research Conference.Research output: SCORING: Contribution to book/anthology › Conference contribution - Poster › Research