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Number of items: 7.


Scott, Robert A, Scott, Laura J, Maegi, Reedik, Marullo, Letizia, Gaulton, Kyle J, Kaakinen, Marika, Pervjakova, Natalia, Pers, Tune H, Johnson, Andrew D, Eicher, John D
et al (show 165 more authors) (2017) An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. DIABETES, 66 (11). pp. 2888-2902.


Rhodes, Christopher J, Batai, Ken, Bleda, Marta, Haimel, Matthias, Southgate, Laura, Germain, Marine, Pauciulo, Michael W, Hadinnapola, Charaka, Aman, Jurjan, Girerd, Barbara
et al (show 499 more authors) (2019) Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis. LANCET RESPIRATORY MEDICINE, 7 (3). pp. 227-238.


Bolton, Jennifer L, Hayward, Caroline, Direk, Nese, Lewis, John G, Hammond, Geoffrey L, Hill, Lesley A, Anderson, Anna, Huffman, Jennifer, Wilson, James F, Campbell, Harry
et al (show 46 more authors) (2014) Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin. PLoS Genetics, 10 (7). e1004474-.


Coffee and Caffeine Genetics Consortium, , Cornelis, Marilyn C, Byrne, Enda M ORCID: 0000-0002-9491-7797, Esko, Tõnu ORCID: 0000-0003-1982-6569, Nalls, Michael A, Ganna, Andrea ORCID: 0000-0002-8147-240X, Paynter, Nina, Monda, Keri L, Amin, Najaf ORCID: 0000-0002-8944-1771, Fischer, Krista
et al (show 148 more authors) (2015) Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Molecular psychiatry, 20 (5). pp. 647-656.


Kaakinen, Marika, Magi, Reedik, Fischer, Krista, Heikkinen, Jani, Jarvelin, Marjo-Riitta, Morris, Andrew P and Prokopenko, Inga
(2017) MARV: a tool for genome-wide multi-phenotype analysis of rare variants. BMC BIOINFORMATICS, 18 (1). 110-.


Magi, Reedik, Suleimanov, Yury V, Clarke, Geraldine M, Kaakinen, Marika, Fischer, Krista, Prokopenko, Inga and Morris, Andrew P
(2017) SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes. BMC BIOINFORMATICS, 18 (1). 25-.


Kaakinen, Marika, Magi, Reedik, Fischer, Krista, Heikkinen, Jani, Jarvelin, Marjo-Riitta, Morris, Andrew P and Prokopenko, Inga
(2017) A rare-variant test for high-dimensional data. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (8). pp. 988-994.

This list was generated on Sun Mar 10 02:44:07 2024 GMT.