Mayo Clinic


Klinik

Standort der Organisation:
Rochester, MN, Vereinigte Staaten von Amerika (USA)


Publikationen in Kooperation mit FAU-Wissenschaftlerinnen und Wissenschaftlern


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Okumura, N., Hayashi, R., Nakano, M., Tashiro, K., Yoshii, K., Aleff, R.,... Koizumi, N. (2019). Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal Dystrophy. Cornea, 38(7), 799-805. https://dx.doi.org/10.1097/ICO.0000000000001952
Konrad, E., Nardini, N., Caliebe, A., Nagel, I., Young, D., Horvath, G.,... Zweier, C. (2019). CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum. Genetics in Medicine. https://dx.doi.org/10.1038/s41436-019-0585-z
Okumura, N., Hayashi, R., Nakano, M., Yoshii, K., Tashiro, K., Sato, T.,... Koizumi, N. (2019). Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal Dystrophy. Investigative Ophthalmology & Visual Science, 60(2), 779-786. https://dx.doi.org/10.1167/iovs.18-25760
Buckley, M.A., Woods, N.T., Tyrer, J.P., Mendoza-Fandino, G., Lawrenson, K., Hazelett, D.J.,... Freedman, M.L. (2019). Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility Locus. Cancer Research, 79(3). https://dx.doi.org/10.1158/0008-5472.CAN-17-3864
Wartenberg, K.E., Hwang, D.Y., Häusler, K.G., Muehlschlegel, S., Sakowitz, O.W., Madžar, D.,... Varelas, P.N. (2019). Gap Analysis Regarding Prognostication in Neurocritical Care: A Joint Statement from the German Neurocritical Care Society and the Neurocritical Care Society. Neurocritical Care. https://dx.doi.org/10.1007/s12028-019-00769-6
Yang, Y., Wu, L., Shu, X., Lu, Y., Shu, X.-O., Cai, Q.,... Long, J. (2019). Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk. Cancer Research, 79(3). https://dx.doi.org/10.1158/0008-5472.CAN-18-2726
Ruddy, K.J., Schaid, D.J., Partridge, A.H., Larson, N.B., Batzler, A., Häberle, L.,... Fasching, P. (2019). Genetic predictors of chemotherapy-related amenorrhea in women with breast cancer. Fertility and Sterility. https://dx.doi.org/10.1016/j.fertnstert.2019.05.018
Wang, R., Canavese, F., Intravooth, T., Singer, W., & Hilz, M.-J. (2019). German Validation of the Composite Autonomic Symptom Score 31. In NEUROLOGY. Philadelphia, PA, US: PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS.
Martinez, A.P., Fritchie, K.J., Weiss, S.W., Agaimy, A., Haller, F., Huang, H.-Y.,... Folpe, A.L. (2019). Histiocyte-rich rhabdomyoblastic tumor: rhabdomyosarcoma, rhabdomyoma, or rhabdomyoblastic tumor of uncertain malignant potential? A histologically distinctive rhabdomyoblastic tumor in search of a place in the classification of skeletal muscle neoplasms. Modern Pathology, 32(3), 446-457. https://dx.doi.org/10.1038/s41379-018-0145-0
Wang, E.W., Zanation, A.M., Gardner, P.A., Schwartz, T.H., Eloy, J.A., Adappa, N.D.,... Van Koevering, K. (2019). ICAR: endoscopic skull-base surgery. International Forum of Allergy and Rhinology, 9, S145-S365. https://dx.doi.org/10.1002/alr.22326
Vachon, C.M., Scott, C.G., Tamimi, R.M., Thompson, D.J., Fasching, P., Stone, J.,... Garcia-Closas, M. (2019). Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk. Breast Cancer Research, 21. https://dx.doi.org/10.1186/s13058-019-1138-8
Williams, S.B., Hudgins, H.K., Ray-Zack, M.D., Chamie, K., Smaldone, M.C., Boorjian, S.A.,... Gore, J.L. (2019). Systematic Review of Factors Associated with the Utilization of Radical Cystectomy for Bladder Cancer. European Urology Oncology, 2(2), 119-125. https://dx.doi.org/10.1016/j.euo.2018.07.006
Michal, M., Agaimy, A., Folpe, A.L., Zambo, I., Kebrle, R., Horch, R.E.,... Michal, M. (2019). Tenosynovitis With Psammomatous Calcifications A Distinctive Trauma-Associated Subtype of Idiopathic Calcifying Tenosynovitis With a Predilection for the Distal extremities of Middle-Aged Women-A Report of 23 Cases. American Journal of Surgical Pathology, 43(2), 261-267. https://dx.doi.org/10.1097/PAS.0000000000001182
Reinhardt, A., Stichel, D., Schrimpf, D., Sahm, F., Korshunov, A., Reuss, D.E.,... Capper, D. (2018). Anaplastic astrocytoma with piloid features, a novel molecular class of IDH wildtype glioma with recurrent MAPK pathway, CDKN2A/B and ATRX alterations. Acta Neuropathologica, 136(2), 273-291. https://dx.doi.org/10.1007/s00401-018-1837-8
Komori, Y., Okumura, N., Hayashi, R., Nakano, M., Tashiro, K., Yoshii, K.,... Koizumi, N. (2018). Association of rs613872 and trinucleotide repeat expansion in the TCF4 gene in Fuchs endothelial corneal dystrophy in Germany.
Lewczuk, P., Riederer, P., O'Bryant, S.E., Verbeek, M.M., Dubois, B., Visser, P.J.,... Kornhuber, J. (2018). Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry. World Journal of Biological Psychiatry, 19(4), 244-328. https://dx.doi.org/10.1080/15622975.2017.1375556
Blok, L.S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H.,... Campeau, P.M. (2018). CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 9(1). https://dx.doi.org/10.1038/s41467-018-06014-6
Keller, K.E., Bhattacharya, S.K., Borras, T., Brunner, T.M., Chansangpetch, S., Clark, A.F.,... Stamer, W.D. (2018). Consensus recommendations for trabecular meshwork cell isolation, characterization and culture. Experimental Eye Research, 171, 164-173. https://dx.doi.org/10.1016/j.exer.2018.03.001
Chen, H., Douglas, J., Gordon, W., Thompson, D., Couch, F., Fasching, P.,... Lindstroem, S. (2018). Evidence for a shared genetic basis between breast cancer and mammographic density phenotypes. In CANCER RESEARCH. Chicago, IL, US: PHILADELPHIA: AMER ASSOC CANCER RESEARCH.
Sievers, P., Stichel, D., Schrimpf, D., Sahm, F., Koelsche, C., Reuss, D.E.,... Von Deimling, A. (2018). FGFR1:TACC1 fusion is a frequent event in molecularly defined extraventricular neurocytoma. Acta Neuropathologica, 136(2), 293-302. https://dx.doi.org/10.1007/s00401-018-1882-3

Zuletzt aktualisiert 2016-29-04 um 08:06