Search Results - Gasser, Valentina C. M

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  1. 1
    Skeletal metalation of lactams through a carbonyl-to-nickel-exchange logic

    Skeletal metalation of lactams through a carbonyl-to-nickel-exchange logic by Zhong, Hongyu, Egger, Dominic T., Gasser, Valentina C. M., Finkelstein, Patrick, Keim, Loris, Seidel, Merlin Z., Trapp, Nils, Morandi, Bill

    Published in Nature communications
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  2. 2
    The advent of electrophilic hydroxylamine-derived reagents for the direct preparation of unprotected amines

    The advent of electrophilic hydroxylamine-derived reagents for the direct preparation of unprotected amines by Gasser, Valentina C. M, Makai, Szabolcs, Morandi, Bill

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  3. 3
    Synthesis of N‑Alkyl Anilines from Arenes via Iron-Promoted Aromatic C–H Amination

    Synthesis of N‑Alkyl Anilines from Arenes via Iron-Promoted Aromatic C–H Amination by Falk, Eric, Gasser, Valentina C. M, Morandi, Bill

    Published in Organic letters
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  4. 4
    A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

    A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease by Holmans, P., Moskvina, V., Jones, L., Sharma, M., Vedernikov, A., Buchel, F., Saad, M., Bras, J. M., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., Gibbs, J. R., Schulte, C., Durr, A., Guerreiro, R., Hernandez, D., Brice, A., Stefansson, H., Majamaa, K., Gasser, T., Heutink, P., Wood, N. W., Martinez, M., Singleton, A. B., Nalls, M. A., Hardy, J., Morris, H. R., Williams, N. M.

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  5. 5
    Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

    Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease by Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., Buchel, F., Sharma, M., Gibbs, J. R., Schulte, C., Moskvina, V., Durr, A., Holmans, P., Kilarski, L. L., Guerreiro, R., Hernandez, D. G., Brice, A., Ylikotila, P., Stefansson, H., Majamaa, K., Morris, H. R., Williams, N., Gasser, T., Heutink, P., Wood, N. W., Hardy, J., Martinez, M., Singleton, A. B., Nalls, M. A.

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  6. 6
    Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

    Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease by Keller, M. F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., Mittag, F., chel, F. B., Sharma, M., Gibbs, J. R., Schulte, C., Moskvina, V., Durr, A., Holmans, P., Kilarski, L. L., Guerreiro, R., Hernandez, D. G., Brice, A., Ylikotila, P., Stefansson, H., Majamaa, K., Morris, H. R., Williams, N., Gasser, T., Heutink, P., Wood, N. W., Hardy, J., Martinez, M., Singleton, A. B., Nalls, M. A.

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