Publications

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Hübel, C., Gaspar, H. A., Coleman, J. R. I., Hanscombe, K. B., Purves, K., Prokopenko, I., Graff, M., Ngwa, J. S., Workalemahu, T., O’Reilly, P. F., Bulik, C. M., Breen, G., ADHD Working Group of the Psychiatric Genomics Consortium, Meta-Analyses of Glucose- and Insulin-related traits Consortium (MAGIC), Autism Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Eating Disorders Working Group of the Psychiatric Genomics Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, OCD & Tourette Syndrome Working Group of the Psychiatric Genomics Consortium ... International Headache Genetics Consortium (2019). Genetic correlations of psychiatric traits with body composition and glycemic traits are sex- and age-dependent. Nature Communications, 10(1), Article 5765. https://doi.org/10.1038/s41467-019-13544-0
Hübel, C., Gaspar, H. A., Coleman, J. R. I., Finucane, H., Purves, K. L., Hanscombe, K. B., Prokopenko, I., Graff, M., Ngwa, J. S., Workalemahu, T., O'Reilly, P. F., Bulik, C. M., Breen, G., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Tourette Syndrome/Obsessive-Compulsive Disorder Working Group of the Psychiatric Genomics Consortium, MAGIC Investigators & Eating Disorders Working Group of the Psychiatric Genomics Consortium (2019). Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 180(6), 428-438. https://doi.org/10.1002/ajmg.b.32709
Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Wang, W., Pardiñas, A. F., Rajagopal, V. M., Als, T. D., T Nguyen, H., Girdhar, K., Boocock, J., Roussos, P., Fromer, M., Kramer, R., Domenici, E., Gamazon, E. R., Purcell, S., Demontis, D., Børglum, A. D. ... iPSYCH-GEMS Schizophrenia Working Group (2019). Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics, 51(4), 659-674. https://doi.org/10.1038/s41588-019-0364-4
Huebner, A. K., Maier, H., Maul, A., Nietzsche, S., Herrmann, T., Praetorius, J. & Hübner, C. A. (2019). Early Hearing Loss upon Disruption of Slc4a10 in C57BL/6 Mice. Journal of the Association for Research in Otolaryngology, 20(3), 233-245. https://doi.org/10.1007/s10162-019-00719-1
Iena, F. M., Vegger, J. B., Thomsen, J. S., Brüel, A. & Lebeck, J. (2019). The Effect of High-Fat Diet on Adipose Tissue Glycerol Metabolism Is Influenced by Sex and GLP-1 Agonist Treatment. Poster session presented at American Diabetes Association 79th Scientific Sessions, San Francisco, California, United States.
Janssens, V., Gaide Chevronnay, H. P., Marie, S., Vincent, M.-F., Van Der Smissen, P., Nevo, N., Vainio, S., Nielsen, R., Christensen, E. I., Jouret, F., Antignac, C., Pierreux, C. E. & Courtoy, P. J. (2019). Protection of Cystinotic Mice by Kidney-Specific Megalin Ablation Supports an Endocytosis-Based Mechanism for Nephropathic Cystinosis Progression. Journal of the American Society of Nephrology : JASN, 30(11), 2177-2190. https://doi.org/10.1681/ASN.2019040371
Jensen, T. B., Bartels, D., Sædder, E. A., Poulsen, B. K., Andersen, S. E., Christensen, M. M. H., Nielsen, L. & Christensen, H. R. (2019). Implementation of TNF-biosimilars (Infliximab and Eternacept) in Danish departments of rheumatology. Annals of the Rheumatic Diseases, 78(Suppl. 2), 237-237. Article OP0310. https://doi.org/10.1136/annrheumdis-2019-eular.1383
Kaiser, K., Gyllborg, D., Procházka, J., Salašová, A., Kompaníková, P., Molina, F. L., Laguna-Goya, R., Radaszkiewicz, T., Harnoš, J., Procházková, M., Potěšil, D., Barker, R. A., Casado, Á. G., Zdráhal, Z., Sedláček, R., Arenas, E., Villaescusa, J. C. & Bryja, V. (2019). WNT5A is transported via lipoprotein particles in the cerebrospinal fluid to regulate hindbrain morphogenesis. Nature Communications, 10(1), Article 1498. https://doi.org/10.1038/s41467-019-09298-4
Kaleviste, E., Saare, M., Leahy, T. R., Bondet, V., Duffy, D., Mogensen, T. H., Jørgensen, S. E., Nurm, H., Ip, W., Davies, E. G., Sauer, S., Syvänen, A. C., Milani, L., Peterson, P. & Kisand, K. (2019). Interferon signature in patients with STAT1 gain-of-function mutation is epigenetically determined. European Journal of Immunology, 49(5), 790-800. https://doi.org/10.1002/eji.201847955