Psychedelics as Medicines: An Emerging New Paradigm von Nichols, DE, Johnson, MW, Nichols, CD

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Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset von NICHOLS, W. C, PANKRATZ, N, MAREK, D. K, PAUCIULO, M. W, ELSAESSER, V. E, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F, FOROUD, T

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Operational degradation of organic light-emitting diodes: Mechanism and identification of chemical products von Kondakov, D. Y., Lenhart, W. C., Nichols, W. F.

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Alpha galactosidase A activity in Parkinson's disease von Alcalay, R.N., Wolf, P., Levy, O.A., Kang, U.J., Waters, C., Fahn, S., Ford, B., Kuo, S.H., Vanegas, N., Shah, H., Liong, C., Narayan, S., Pauciulo, M.W., Nichols, W.C., Gan-Or, Z., Rouleau, G.A., Chung, W.K., Oliva, P., Keutzer, J., Marder, K., Zhang, X.K.

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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease von HAUGARVOLL, K, RADEMAKERS, R, GUIDI, M, RIBOLDAZZI, G, BROWN, L, WALTER, U, BENECKE, R, BERG, D, GASSER, T, THEUNS, J, PALS, P, CRAS, P, KACHERGUS, J. M, DE DEYN, P. Paul, ENGELBORGHS, S, PICKUT, B, UITTI, R. J, FOROUD, T, NICHOLS, W. C, HAGENAH, J, KLEIN, C, SAMII, A, ZABETIAN, C. P, NUYTEMANS, K, BONIFATI, V, VAN BROECKHOVEN, C, FARRER, M. J, WSZOLEK, Z. K, ROSS, O. A, GIBSON, J. M, TAN, E.-K, GAIG, C, TOLOSA, E, GOLDWURM, S

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Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations von PANKRATZ, N, KISSELL, D. K, PAUCIULO, M. W, HALTER, C. A, RUDOLPH, A, PFEIFFER, R. F, MARDER, K. S, FOROUD, T, NICHOLS, W. C

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Informing the Human Plasma Protein Binding of Environmental Chemicals by Machine Learning in the Pharmaceutical Space: Applicability Domain and Limits of Predictability von Ingle, Brandall L, Veber, Brandon C, Nichols, John W, Tornero-Velez, Rogelio

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Variation in GIGYF2 is not associated with Parkinson disease von NICHOLS, W. C, KISSELL, D. K, FOROUD, T, PANKRATZ, N, PAUCIULO, M. W, ELSAESSER, V. E, CLARK, K. A, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F

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A mutation in myotilin causes spheroid body myopathy von FOROUD, T, PANKRATZ, N, FARLOW, M, NICHOLS, W. C, BATCHMAN, A. P, PAUCIULO, M. W, VIDAL, R, MIRAVALLE, L, GOEBEL, H. H, CUSHMAN, L. J, AZZARELLI, B, HORAK, H

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LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8 von NICHOLS, W. C, ELSAESSER, V. E, PANKRATZ, N, PAUCIULO, M. W, MAREK, D. K, HALTER, C. A, RUDOLPH, A, SHULTS, C. W, FOROUD, T

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Heterozygosity for a mutation in the Parkin gene leads to later onset Parkinson disease von FOROUD, T, UNIACKE, S. K, LIU, L, PANKRATZ, N, RUDOLPH, A, HALTER, C, SHULTS, C, MARDER, K, CONNEALLY, P. M, NICHOLS, W. C

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Unprecedented summer hypoxia in southern Cape Cod Bay: an ecological response to regional climate change? von Scully, Malcolm E, Geyer, W. Rockwell, Borkman, David, Pugh, Tracy L, Costa, Amy, Nichols, Owen C

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Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine models von Markusic, David M, Nichols, Timothy C, Merricks, Elizabeth P, Palaschak, Brett, Zolotukhin, Irene, Marsic, Damien, Zolotukhin, Sergei, Srivastava, Arun, Herzog, Roland W

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Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci von PANKRATZ, N, UNIACKE, S. K, HALTER, C. A, RUDOLPH, A, SHULTS, C. W, CONNEALLY, P. M, FOROUD, T, NICHOLS, W. C

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Risk Assessment Matrices for Workplace Hazards: Design for Usability von Jensen, Roger C, Bird, Royce L, Nichols, Blake W

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Proteome and phosphoproteome signatures of recurrence for HPV+ head and neck squamous cell carcinoma von Kaneko, Tomonori, Zeng, Peter Y. F., Liu, Xuguang, Abdo, Rober, Barrett, John W., Zhang, Qi, Nichols, Anthony C., Li, Shawn Shun-Cheng

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Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension von Koehler, R, Grünig, E, Pauciulo, M W, Hoeper, M M, Olschewski, H, Wilkens, H, Halank, M, Winkler, J, Ewert, R, Bremer, H, Kreuscher, S, Janssen, B, Nichols, W C

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Mycobacterium avium Complex Infection, Rifabutin, and Uveitis—Is There a Connection? von Nichols, Charles W.

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Moderation of hemophilia A phenotype by the factor V R506Q mutation von NICHOLS, W. C, AMANO, K, CACHERIS, P. M, FIGUEIREDO, M. S, MICHAELIDES, K, SCHWAAB, R, HOYER, L, KAUFMAN, R. J, GINSBURG, D

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Molecular Analysis of the ERGIC-53 Gene in 35 Families With Combined Factor V-Factor VIII Deficiency von Neerman-Arbez, M., Johnson, K.M., Morris, M.A., McVey, J.H., Peyvandi, F., Nichols, W.C., Ginsburg, D., Rossier, C., Antonarakis, S.E., Tuddenham, E.G.D.

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