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Personal profile

Keywords

  • 3111 Biomedicine
  • 318 Medical biotechnology
  • histocompatibility
  • 1184 Genetics, developmental biology, physiology
  • immunognetics
  • 1182 Biochemistry, cell and molecular biology

International and National Collaboration Publications and projects within past five years.

Publications 1977 2019

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events A GENIUS-CHD Study of Individual Participant Data

CARDIo-GRAMPlusC4D Consortium, Patel, R. S., Schmidt, A. F., Kuukasjarvi, P., Nikus, K., Vlachopoulou, E., Lokki, M-L. & Sinisalo, J., Apr 2019, In : Circulation-Genomic and precision medicine. 12, 4, 12 p., 002471.

Research output: Contribution to journalArticleScientificpeer-review

Subsequent Event Risk in Individuals With Established Coronary Heart Disease Design and Rationale of the GENIUS-CHD Consortium

Patel, R. S., Tragante, V., Schmidt, A. F., McCubrey, R. O., Holmes, M., Howe, L. J., Direk, K., Akerblom, A., Leander, K., Virani, S. S., Kaminski, K. A., Muehlschlegel, J. D., Allayee, H., Almgren, P., Alver, M., Baranova, E., Behloui, H., Boeckx, B., Braund, P. S., Breitling, L. P. & 161 othersDelgado, G., Duarte, N. E., Dube, M-P., Dufresne, L., Eriksson, N., Foco, L., Scholz, M., Gijsberts, C. M., Glinge, C., Gong, Y., Hartiala, J., Heydarpour, M., Hubacek, J. A., Kleber, M., Kofink, D., Kotti, S., Kuukasjarvi, P., Lee, V-V., Leiherer, A., Lenzini, P. A., Levin, D., Lyytikainen, L-P., Martinelli, N., Mons, U., Nelson, C. P., Nikus, K., Pilbrow, A. P., Ploski, R., Sun, Y., Tanck, M. W. T., Tang, W. H. W., Trompet, S., van der Laan, S. W., Van Setten, J., Vilmundarson, R. O., Anselmi, C. V., Vlachopoulou, E., Al Ali, L., Boerwinkle, E., Briguori, C., Carlquist, J. F., Carruthers, K. F., Casu, G., Deanfield, J., Deloukas, P., Dudbridge, F., Engstrom, T., Fitzpatrick, N., Fox, K., Gigante, B., James, S., Lokki, M-L., Lotufo, P. A., Marziliano, N., Mordi, I. R., Muhlestein, J. B., Newton-Cheh, C., Pitha, J., Saely, C. H., Samman-Tahhan, A., Sandesara, P. B., Teren, A., Timmis, A., Van de Werf, F., Wauters, E., Wilde, A. A. M., Ford, I., Stott, D. J., Algra, A., Andreassi, M. G., Ardissino, D., Arsenault, B. J., Ballantyne, C. M., Bergmeijer, T. O., Bezzina, C. R., Body, S. C., Boersma, E. H., Bogaty, P., Bots, M. L., Brenner, H., Brugts, J. J., Burkhardt, R., Carpeggiani, C., Condorelli, G., Cooper-DeHoff, R. M., Cresci, S., Danchin, N., de Faire, U., Doughty, R. N., Drexel, H., Engert, J. C., Fox, K. A. A., Girelli, D., Grobbee, D. E., Hagstrom, E., Hazen, S. L., Held, C., Hemingway, H., Hoefer, I. E., Hovingh, G. K., Jabbari, R., Johnson, J. A., Jukema, J. W., Kaczor, M. P., Kahonen, M., Kettner, J., Kiliszek, M., Klungel, O. H., Lagerqvist, B., Lambrechts, D., Laurikka, J. O., Lehtimaki, T., Lindholm, D., Mahmoodi, B. K., Maitland-van der Zee, A. H., McPherson, R., Melander, O., Metspalu, A., Niemcunowicz-Janica, A., Olivieri, O., Opolski, G., Palmer, C. N., Pasterkamp, G., Pepine, C. J., Pereira, A. C., Pilote, L., Quyyumi, A. A., Richards, A. M., Sanak, M., Siegbahn, A., Simon, T., Sinisalo, J., Smith, J. G., Spertus, J. A., Stender, S., Stewart, A. F. R., Szczeklik, W., Szpakowicz, A., Tardif, J-C., ten Berg, J. M., Tfelt-Hansen, J., Thanassoulis, G., Thiery, J., Torp-Pedersen, C., van der Graaf, Y., Visseren, F. L. J., Waltenberger, J., Weeke, P. E., Van der Harst, P., Lang, C. C., Sattar, N., Cameron, V. A., Anderson, J. L., Brophy, J. M., Pare, G., Horne, B. D., Marz, W., Wallentin, L., Samani, N. J., Hingorani, A. D. & Asselbergs, F. W., Apr 2019, In : Circulation-Genomic and precision medicine. 12, 4, 16 p., 002470.

Research output: Contribution to journalArticleScientificpeer-review

The complexity and diversity of major histocompatibility complex challenge disease association studies

Lokki, M-L. & Paakkanen, R., Jan 2019, In : HLA. 93, 1, p. 3-15 13 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

Atrial Fibrillation Genetics Conso, Int Stroke Genetics Consortium, Pulit, S. L., Lyytikäinen, L-P., Seppälä, I., Malik, R., Sinisalo, J., Vlachopoulou, E., Lokki, M-L., Tatlisumak, T. & Happola, O., Dec 2018, In : Neurology Genetics. 4, 6, 8 p., 293.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Clinical features of patients with homozygous complement C4A or C4B deficiency

Liesmaa, I., Paakkanen, R., Järvinen, A., Valtonen, V. & Lokki, M-L., 21 Jun 2018, In : PLoS One. 13, 6, 13 p., 0199305.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Projects 2011 2016

Activities 1983 2017

31st European Immunogenetics and Histocompatibility Conference

Marja-Liisa Lokki (Attendee), Elisa Lahtela (Poster Presentation), Marja Satu Johanna Marchesani (Speaker: Presenter), Johanna Marjut Tolva (Speaker: Presenter)
30 May 20172 Jun 2017

Activity: Participating in or organising an event typesOrganisation and participation in conferences, workshops, courses, seminars

29th European immunogenetics and histocompatibility conference

Marja-Liisa Lokki (Attendee), Efthymia Vlachopoulou (Speaker: Presenter)
26 Apr 201529 Apr 2015

Activity: Participating in or organising an event typesOrganisation and participation in conferences, workshops, courses, seminars

Supervision of Licentiate thesis (MD)

Marja-Liisa Lokki (Supervisor)
2015

Activity: Examination typesSupervision of other thesis (Master's, Licentiate)

Circulation. Cardiovascular genetics (Journal)

Marja-Liisa Lokki (Reviewer)
2015 → …

Activity: Publication peer-review and editorial work typesPeer review of manuscripts

Steven Mack

Marja-Liisa Lokki (Host)
14 Sep 201517 Sep 2015

Activity: Hosting a visitor typesAcademic visit at UH