Helen Miriam Cooper

Emailhelen.cooperhelsinkifi

Research activity per year

Education/Academic qualification

Molecular Biology, PhD, University of Tampere

Award Date: 17 Dec 2009

Fields of Science

1182 Biochemistry, cell and molecular biology
1184 Genetics, developmental biology, physiology

13 Article

Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium, FinnGen Consortium, Allara, E., Bell, S., Wang, F., Palotie, A., Daly, M., Mäkelä, T. P., Kaprio, J., Perola, M., Partanen, J., Raivio, T., Ripatti, S., Carpén, O., Raivio, M., Tienari, P., Partanen, J., Färkkilä, M., Koskela, J. & Pikkarainen, S. & 87 others, Eklund, K., Mars, N., Kauppi, P., Vaura, F., Gordin, D., Sinisalo, J., Taskinen, M.-R., Tuomi, T., Hiltunen, T., Reeve, M. P., Ruotsalainen, S., Meretoja, T., Joensuu, H., Mattson, J., Salminen, E., Karihtala, P., Pitkänen, E., Turunen, J. A., Ollila, T., Karjalainen, J., Hannula-Jouppi, K., Pussinen, P., Salminen, A., Salo, T., Rice, D., Nieminen, P., Palotie, U., Laivuori, H., Kurra, V., Heikinheimo, O., Kalliala, I., Aaltonen, L., Djousse, L., Cho, K., Inouye, M., Burgess, S., Benyamin, B., Oexle, K., Swinkels, D. W., Stefansson, K., Magnusson, M., Ganna, A., Gaziano, M., Ivey, K., Danesh, J., Pereira, A., Wood, A. M., Butterworth, A. S., Di Angelantonio, E., Kivinen, K., Tukiainen, T., Ollila, H., Saarentaus, E., Åberg, F., Kurki, M., Havulinna, A., Mehtonen, J., Palta, P., Hassan, S., Della Briotta Parolo, P., Lemmelä, S., Liu, A., Lehisto, A., Llorens, V., Heyne, H., Rämö, J., Rodosthenous, R., Strausz, S., Lee, J., Kajanne, R., Aavikko, M., Cooper, H., Öller, D., Leinonen, R., Lahtela, L. E., Kaunisto, M., Kilpeläinen, E., Sipilä, T. P., Dada, O. A., Ghazal, A., Kytölä, A., Weldatsadik, R., Donner, K. M., Luo, S., Padmanabhuni, S. S., Hovatta, I. & Mäkitie, A., 2024, In: Communications Biology. 7, 1, 17 p., 1631.
Research output: Contribution to journal › Article › Scientific › peer-review

Open Access
File
Severe neonatal MEGDHEL syndrome with a homozygous truncating mutation in SERAC1
Fellman, V., Banerjee, R., Lin, K.-L., Pulli, I., Cooper, H., Tyynismaa, H. & Kallijärvi, J., 1 Jan 2022, In: Biochimica et Biophysica Acta. Molecular Basis of Disease. 1868, 1, 8 p., 166298.
Research output: Contribution to journal › Article › Scientific › peer-review

Open Access
File
Sphingosine kinase 1 overexpression induces MFN2 fragmentation and alters mitochondrial matrix Ca2+ handling in HeLa cells
Pulli, I., Löf, C., Blom, T., Asghar, M. Y., Lassila, T., Bäck, N., Lin, K.-L., Nyström, J., Kemppainen, K., Toivola, D., Dufour, E., Sanz, A., Cooper, H., Parys, J. & Törnquist, K., Sept 2019, In: Biochimica et Biophysica Acta. Molecular Cell Research. 1866, 9, p. 1475-1486 12 p.
Research output: Contribution to journal › Article › Scientific › peer-review

Open Access
File
ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia
Cooper, H., Yang, Y., Ylikallio, E., Khairullin, R., Woldegebriel, R., Lin, K.-L., Euro, L., Lin, K.-L., Wolf, A., Trokovic, R., Isohanni, P., Kaakkola, S., Auranen, M., Lönnqvist, T., Wanrooij, S. & Tyynismaa, H., 15 Apr 2017, In: Human Molecular Genetics. 26, 8, p. 1432-1443 12 p.
Research output: Contribution to journal › Article › Scientific › peer-review

Open Access
File
Mitochondrial ROS produced via reverse electron transport extend animal lifespan
Scialò, F., Sriram, A., Fernández-Ayala, D., Gubina, N., Lohmus, M., Nelson, G., Logan, A., Cooper, H., Navas, P., Antonio Enríquez, J., Murphy, M. P. & Sanz, A., 2016, In: Cell Metabolism. 23, 4, p. 734-734 1 p.
Research output: Contribution to journal › Article › Scientific › peer-review

1 Organisation and participation in conferences, workshops, courses, seminars

Lines of Descent exhibition
Kaunisto, M. (Member of organizing committee), Aavikko, M. (Member of organizing committee) & Cooper, H. M. (Member of organizing committee)
1 Mar 2024 → 27 Oct 2024
Activity: Participating in or organising an event types › Organisation and participation in conferences, workshops, courses, seminars

Helen Miriam Cooper

Personal profile

Education/Academic qualification

Fields of Science

International and National Collaboration

Dive into details

Novel loci and biomedical consequences of iron homoeostasis variation

Severe neonatal MEGDHEL syndrome with a homozygous truncating mutation in SERAC1

Sphingosine kinase 1 overexpression induces MFN2 fragmentation and alters mitochondrial matrix Ca2+ handling in HeLa cells

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

Mitochondrial ROS produced via reverse electron transport extend animal lifespan

Lines of Descent exhibition

Helen Miriam Cooper

Personal profile

Education/Academic qualification

Fields of Science

International and National Collaboration

Publications

Novel loci and biomedical consequences of iron homoeostasis variation

Severe neonatal MEGDHEL syndrome with a homozygous truncating mutation in SERAC1

Sphingosine kinase 1 overexpression induces MFN2 fragmentation and alters mitochondrial matrix Ca2+ handling in HeLa cells

ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia

Mitochondrial ROS produced via reverse electron transport extend animal lifespan

Activities

Lines of Descent exhibition