Junttila, Juhani
Northern Ostrobothnia Hospital District · University of Oulu
7 papers on CoChatORCID 0000-0002-8896-1281
Most cited papers
- Verified
FinnGen provides genetic insights from a well-phenotyped isolated population
Kurki, M. I., Karjalainen, J., Palta, P., Sipilä, T. P., Kristiansson, K., Donner, K. M., Reeve, M. P., Laivuori, H., Aavikko, M., Kaunisto, M. A., et al. (2023) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 4,233
- Verified
New insights into the genetic etiology of Alzheimer’s disease and related dementias
Bellenguez, C., Küçükali, F., Jansen, I. E., Kleineidam, L., Moreno-Grau, S., Amin, N., Naj, A. C., Campos-Martin, R., Grenier-Boley, B., Andrade, V., et al. (2022) · Nature Genetics
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 2,498
- Verified
Defining the role of common variation in the genomic and biological architecture of adult human height
The Electronic Medical Records and Genomics (eMERGE) Consortium, Wood, A. R., The MIGen Consortium, The PAGE Consortium, Study, T. L. C., Esko, T., Yang, J., Vedantam, S., Pers, T. H., Gustafsson, S., et al. (2014) · Nature Genetics
Genetic Associations and EpidemiologyGenetics and Physical Performance
Cited by 1,853
- Verified
Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans
Kaasinen, E., Kuismin, O., Rajamäki, K., Ristolainen, H., Aavikko, M., Kondelin, J., Saarinen, S., Berta, D. G., Katainen, R., Hirvonen, E. A. M., et al. (2019) · Nature Communications
Acute Myeloid Leukemia ResearchEpigenetics and DNA Methylation
Cited by 92
- Verified
Association of sST2 and hs-CRP levels with new-onset atrial fibrillation in coronary artery disease
Nortamo, S., Ukkola, O., Lepojärvi, S., Kenttä, T., Kiviniemi, A., Junttila, J., Huikuri, H., & Perkiömäki, J. (2017) · International Journal of Cardiology
Atrial Fibrillation Management and OutcomesInflammatory Biomarkers in Disease Prognosis
Cited by 65
- Verified
Electrocardiographic Transmural Dispersion of Repolarization in Patients with Inherited Short QT Syndrome
Anttonen, O., Väänänen, H., Junttila, J., Huikuri, H. V., & Viitasalo, M. (2008) · Annals of Noninvasive Electrocardiology
Cardiac electrophysiology and arrhythmiasCardiovascular Effects of Exercise
Cited by 50
- Verified
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young, W. J., Lahrouchi, N., Isaacs, A., Duong, T., Foco, L., Ahmed, F., Brody, J. A., Salman, R., Noordam, R., Benjamins, J.-W., et al. (2022) · Nature Communications
Cardiac electrophysiology and arrhythmiasGenetic Associations and Epidemiology
Cited by 49
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