Teemu Kuulasmaa
Teemu Kuulasmaa
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The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
RJ Strawbridge, J Dupuis, I Prokopenko, A Barker, E Ahlqvist, D Rybin, ...
Diabetes 60 (10), 2624-2634, 2011
Changes in insulin sensitivity and insulin release in relation to glycemia and glucose tolerance in 6,414 Finnish men
A Stančáková, M Javorský, T Kuulasmaa, SM Haffner, J Kuusisto, ...
Diabetes 58 (5), 1212-1221, 2009
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Y Lu, FR Day, S Gustafsson, ML Buchkovich, J Na, V Bataille, ...
Nature communications 7 (1), 10495, 2016
New insights into the genetic etiology of Alzheimer’s disease and related dementias
C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ...
Nature genetics 54 (4), 412-436, 2022
Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men
A Stančáková, T Kuulasmaa, J Paananen, AU Jackson, LL Bonnycastle, ...
Diabetes 58 (9), 2129-2136, 2009
Variants of transcription factor 7-like 2 (TCF7L2) gene predict conversion to type 2 diabetes in the Finnish Diabetes Prevention Study and are associated with …
J Wang, J Kuusisto, M Vänttinen, T Kuulasmaa, J Lindström, J Tuomilehto, ...
Diabetologia 50, 1192-1200, 2007
Insulin sensitivity, insulin release and glucagon-like peptide-1 levels in persons with impaired fasting glucose and/or impaired glucose tolerance in the EUGENE2 study
M Laakso, J Zilinskaite, T Hansen, TW Boesgaard, M Vänttinen, ...
Diabetologia 51, 502-511, 2008
The Metabolic Syndrome in Men study: a resource for studies of metabolic and cardiovascular diseases
M Laakso, J Kuusisto, A Stančáková, T Kuulasmaa, P Pajukanta, AJ Lusis, ...
Journal of lipid research 58 (3), 481-493, 2017
Enhanced polyamine catabolism alters homeostatic control of white adipose tissue mass, energy expenditure, and glucose metabolism
E Pirinen, T Kuulasmaa, M Pietilä, S Heikkinen, M Tusa, P Itkonen, ...
Molecular and cellular biology 27 (13), 4953-4967, 2007
The trans-ancestral genomic architecture of glycemic traits
J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ...
Nature genetics 53 (6), 840-860, 2021
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass
MC Zillikens, S Demissie, YH Hsu, LM Yerges-Armstrong, WC Chou, ...
Nature communications 8 (1), 1-13, 2017
Association of risk variants for type 2 diabetes and hyperglycemia with gestational diabetes
H Huopio, H Cederberg, J Vangipurapu, H Hakkarainen, M Pääkkönen, ...
European journal of endocrinology 169 (3), 291-297, 2013
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I De Rojas, S Moreno-Grau, N Tesi, B Grenier-Boley, V Andrade, ...
Nature communications 12 (1), 3417, 2021
Single nucleotide polymorphisms in the peroxisome proliferator–activated receptor δ gene are associated with skeletal muscle glucose uptake
M Vänttinen, P Nuutila, T Kuulasmaa, J Pihlajamäki, K Hällsten, ...
Diabetes 54 (12), 3587-3591, 2005
Single Nucleotide Polymorphisms of the Peroxisome Proliferator–Activated Receptor-α Gene (PPARA) Influence the Conversion From Impaired Glucose Tolerance …
L Andrulionyte, T Kuulasmaa, JL Chiasson, M Laakso, ...
Diabetes 56 (4), 1181-1186, 2007
Detection of novel gene variants associated with congenital hypothyroidism in a Finnish patient cohort
C Löf, K Patyra, T Kuulasmaa, J Vangipurapu, H Undeutsch, H Jaeschke, ...
Thyroid 26 (9), 1215-1224, 2016
Microbiota-related metabolites and the risk of type 2 diabetes
J Vangipurapu, L Fernandes Silva, T Kuulasmaa, U Smith, M Laakso
Diabetes care 43 (6), 1319-1325, 2020
New insights on the genetic etiology of Alzheimer’s and related dementia
C Bellenguez, F Küçükali, I Jansen, V Andrade, S Moreno-Grau, N Amin, ...
MedRxiv, 2020.10. 01.20200659, 2020
Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics
H Koutnikova, M Laakso, L Lu, R Combe, J Paananen, T Kuulasmaa, ...
PLoS genetics 5 (8), e1000591, 2009
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