CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome
Kovanen, Leena, Donner, Kati, Kaunisto, Mari, Partonen, Timo
Published in Hypertension research (01.03.2015)
Published in Hypertension research (01.03.2015)
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CRY1 and CRY2 genetic variants in seasonality: a longitudinal and cross-sectional study
Kovanen, Leena, Donner, Kati, Kaunisto, Mari, Partonen, Timo
Published in Psychiatry research (30.08.2016)
Published in Psychiatry research (30.08.2016)
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Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design
Nuotio, Marja-Liisa, Sánez Tähtisalo, Heini, Lahtinen, Alexandra, Donner, Kati, Fyhrquist, Frej, Perola, Markus, Kontula, Kimmo K, Hiltunen, Timo P
Published in Epigenetics (02.11.2022)
Published in Epigenetics (02.11.2022)
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Complex trait susceptibilities and population diversity in a sample of 4,145 Russians
Usoltsev, Dmitrii, Kolosov, Nikita, Rotar, Oxana, Loboda, Alexander, Boyarinova, Maria, Moguchaya, Ekaterina, Kolesova, Ekaterina, Erina, Anastasia, Tolkunova, Kristina, Rezapova, Valeriia, Molotkov, Ivan, Melnik, Olesya, Freylikhman, Olga, Paskar, Nadezhda, Alieva, Asiiat, Baranova, Elena, Bazhenova, Elena, Beliaeva, Olga, Vasilyeva, Elena, Kibkalo, Sofia, Skitchenko, Rostislav, Babenko, Alina, Sergushichev, Alexey, Dushina, Alena, Lopina, Ekaterina, Basyrova, Irina, Libis, Roman, Duplyakov, Dmitrii, Cherepanova, Natalya, Donner, Kati, Laiho, Paivi, Kostareva, Anna, Konradi, Alexandra, Shlyakhto, Evgeny, Palotie, Aarno, Daly, Mark J, Artomov, Mykyta
Published in Nature communications (23.07.2024)
Published in Nature communications (23.07.2024)
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CRY2 genetic variants associate with dysthymia
Kovanen, Leena, Kaunisto, Mari, Donner, Kati, Saarikoski, Sirkku T, Partonen, Timo
Published in PloS one (08.08.2013)
Published in PloS one (08.08.2013)
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Genomic Association Analysis of Common Variants Influencing Antihypertensive Response to Hydrochlorothiazide
Turner, Stephen T, Boerwinkle, Eric, O’Connell, Jeffrey R, Bailey, Kent R, Gong, Yan, Chapman, Arlene B, McDonough, Caitrin W, Beitelshees, Amber L, Schwartz, Gary L, Gums, John G, Padmanabhan, Sandosh, Hiltunen, Timo P, Citterio, Lorena, Donner, Kati M, Hedner, Thomas, Lanzani, Chiara, Melander, Olle, Saarela, Janna, Ripatti, Samuli, Wahlstrand, Björn, Manunta, Paolo, Kontula, Kimmo, Dominiczak, Anna F, Cooper-DeHoff, Rhonda M, Johnson, Julie A
Published in Hypertension (Dallas, Tex. 1979) (01.08.2013)
Published in Hypertension (Dallas, Tex. 1979) (01.08.2013)
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Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions
Johari, Mridul, Sarparanta, Jaakko, Vihola, Anna, Jonson, Per Harald, Savarese, Marco, Jokela, Manu, Torella, Annalaura, Piluso, Giulio, Said, Edith, Vella, Norbert, Cauchi, Marija, Magot, Armelle, Magri, Francesca, Mauri, Eleonora, Kornblum, Cornelia, Reimann, Jens, Stojkovic, Tanya, Romero, Norma B., Luque, Helena, Huovinen, Sanna, Lahermo, Päivi, Donner, Kati, Comi, Giacomo Pietro, Nigro, Vincenzo, Hackman, Peter, Udd, Bjarne
Published in Acta neuropathologica (01.08.2021)
Published in Acta neuropathologica (01.08.2021)
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Genomics of asthma, allergy and chronic rhinosinusitis: novel concepts and relevance in airway mucosa
Laulajainen‐Hongisto, Anu, Lyly, Annina, Hanif, Tanzeela, Dhaygude, Kishor, Kankainen, Matti, Renkonen, Risto, Donner, Kati, Mattila, Pirkko, Jartti, Tuomas, Bousquet, Jean, Kauppi, Paula, Toppila‐Salmi, Sanna
Published in Clinical and translational allergy (28.10.2020)
Published in Clinical and translational allergy (28.10.2020)
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Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs
Hiltunen, Timo P, Donner, Kati M, Sarin, Antti-Pekka, Saarela, Janna, Ripatti, Samuli, Chapman, Arlene B, Gums, John G, Gong, Yan, Cooper-DeHoff, Rhonda M, Frau, Francesca, Glorioso, Valeria, Zaninello, Roberta, Salvi, Erika, Glorioso, Nicola, Boerwinkle, Eric, Turner, Stephen T, Johnson, Julie A, Kontula, Kimmo K
Published in Journal of the American Heart Association (01.01.2015)
Published in Journal of the American Heart Association (01.01.2015)
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PTPRD gene associated with blood pressure response to atenolol and resistant hypertension
Gong, Yan, McDonough, Caitrin W, Beitelshees, Amber L, El Rouby, Nihal, Hiltunen, Timo P, O'Connell, Jeffrey R, Padmanabhan, Sandosh, Langaee, Taimour Y, Hall, Karen, Schmidt, Siegfried O F, Curry, Jr, Robert W, Gums, John G, Donner, Kati M, Kontula, Kimmo K, Bailey, Kent R, Boerwinkle, Eric, Takahashi, Atsushi, Tanaka, Toshihiro, Kubo, Michiaki, Chapman, Arlene B, Turner, Stephen T, Pepine, Carl J, Cooper-DeHoff, Rhonda M, Johnson, Julie A
Published in Journal of hypertension (01.11.2015)
Published in Journal of hypertension (01.11.2015)
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Replicated evidence for aminoacylase 3 and nephrin gene variations to predict antihypertensive drug responses
Rimpelä, Jenni M, Kontula, Kimmo K, Fyhrquist, Frej, Donner, Kati M, Tuiskula, Annukka M, Sarin, Antti-Pekka, Mohney, Robert P, Stirdivant, Steven M, Hiltunen, Timo P
Published in Pharmacogenomics (01.04.2017)
Published in Pharmacogenomics (01.04.2017)
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Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1
Donner, Kati M, Hiltunen, Timo P, Jänne, Olli A, Sane, Timo, Kontula, Kimmo
Published in European journal of endocrinology (01.01.2013)
Published in European journal of endocrinology (01.01.2013)
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TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives
Chittani, Martina, Zaninello, Roberta, Lanzani, Chiara, Frau, Francesca, Ortu, Maria F, Salvi, Erika, Fresu, Giovanni, Citterio, Lorena, Braga, Daniele, Piras, Daniela A, Carpini, Simona Delli, Velayutham, Dinesh, Simonini, Marco, Argiolas, Giuseppe, Pozzoli, Simona, Troffa, Chiara, Glorioso, Valeria, Kontula, Kimmo K, Hiltunen, Timo P, Donner, Kati M, Turner, Stephen T, Boerwinkle, Eric, Chapman, Arlene B, Padmanabhan, Sandosh, Dominiczak, Anna F, Melander, Olle, Johnson, Julie A, Cooper-Dehoff, Rhonda M, Gong, Yan, Rivera, Natalia V, Condorelli, Gianluigi, Trimarco, Bruno, Manunta, Paolo, Cusi, Daniele, Glorioso, Nicola, Barlassina, Cristina
Published in Journal of hypertension (01.06.2015)
Published in Journal of hypertension (01.06.2015)
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Genetic Loci Associated with Allergic Sensitization in Lithuanians
Šaulienė, Ingrida, Greičiuvienė, Jūratė, Šukienė, Laura, Juškevičiūtė, Neringa, Benner, Christian, Zinkevičienė, Auksė, Ripatti, Samuli, Donner, Kati, Kainov, Denis
Published in PloS one (27.07.2015)
Published in PloS one (27.07.2015)
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Heme oxygenase-1 repeat polymorphism in septic acute kidney injury
Vilander, Laura M, Vaara, Suvi T, Donner, Kati M, Lakkisto, Päivi, Kaunisto, Mari A, Pettilä, Ville
Published in PloS one (23.05.2019)
Published in PloS one (23.05.2019)
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Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts
DONNER, Kati, SANDBACKA, Maria, LEHTOKARI, Vilma-Lotta, WALLGREN-PETTERSSON, Carina, PELIN, Katarina
Published in European journal of human genetics : EJHG (01.09.2004)
Published in European journal of human genetics : EJHG (01.09.2004)
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CYP2C9 genotype modifies activity of the renin-angiotensin-aldosterone system in hypertensive men
Donner, Kati M, Hiltunen, Timo P, Suonsyrjä, Timo, Hannila-Handelberg, Tuula, Tikkanen, Ilkka, Antikainen, Miia, Hirvonen, Ari, Kontula, Kimmo
Published in Journal of hypertension (01.10.2009)
Published in Journal of hypertension (01.10.2009)
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Mutations in the Nebulin Gene Associated with Autosomal Recessive Nemaline Myopathy
Pelin, Katarina, Hilpela, Pirta, Donner, Kati, Sewry, Caroline, Akkari, Patrick A., Wilton, Stephen D., Wattanasirichaigoon, Duangrurdee, Bang, Marie-Louise, Centner, Thomas, Hanefeld, Folker, Odent, Sylvie, Fardeau, Michel, Urtizberea, J. Andoni, Muntoni, Francesco, Dubowitz, Victor, Beggs, Alan H., Laing, Nigel G., Labeit, Siegfried, de la Chapelle, Albert, Wallgren-Pettersson, Carina
Published in Proceedings of the National Academy of Sciences - PNAS (02.03.1999)
Published in Proceedings of the National Academy of Sciences - PNAS (02.03.1999)
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