Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marjo Riita Jarvelin"'
Autor:
Elmar W. Tobi, Diana L. Juvinao-Quintero, Justiina Ronkainen, Raffael Ott, Rossella Alfano, Mickaël Canouil, Madelon L. Geurtsen, Amna Khamis, Leanne K. Küpers, Ives Y. Lim, Patrice Perron, Giancarlo Pesce, Johanna Tuhkanen, Anne P. Starling, Toby Andrew, Elisabeth Binder, Robert Caiazzo, Jerry K.Y. Chan, Romy Gaillard, Peter D. Gluckman, Elina Keikkala, Neerja Karnani, Sanna Mustaniemi, Tim S. Nawrot, François Pattou, Michelle Plusquin, Violeta Raverdy, Kok Hian Tan, Evangelia Tzala, Katri Raikkonen, Christiane Winkler, Anette-G. Ziegler, Isabella Annesi-Maesano, Luigi Bouchard, Yap Seng Chong, Dana Dabelea, Janine F. Felix, Barbara Heude, Vincent W.V. Jaddoe, Jari Lahti, Brigitte Reimann, Marja Vääräsmäki, Amélie Bonnefond, Philippe Froguel, Sandra Hummel, Eero Kajantie, Marjo-Riita Jarvelin, Regine P.M. Steegers-Theunissen, Caitlin G. Howe, Marie-France Hivert, Sylvain Sebert
Publikováno v:
Diabetes Care
Diabetes Care, 2022, 45 (3), pp.614-623. ⟨10.2337/dc21-1701⟩
Diabetes Care, 45(3), 614-623. American Diabetes Association Inc.
Diabetes Care 45, 614-623 (2022)
Diabetes Care, 2022, 45 (3), pp.614-623. ⟨10.2337/dc21-1701⟩
Diabetes Care, 45(3), 614-623. American Diabetes Association Inc.
Diabetes Care 45, 614-623 (2022)
OBJECTIVE Maternal glycemic dysregulation during pregnancy increases the risk of adverse health outcomes in her offspring; a risk thought to be linearly related to maternal hyperglycemia. It is hypothesized that changes in offspring DNA methylation (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61bc9777913c3a7ff45f03e99fa4e8e9
https://hal.umontpellier.fr/hal-03676276
https://hal.umontpellier.fr/hal-03676276
Autor:
Marjo-Riita Jarvelin, Simone Accordini, Matthias Wielscher, Cecilie Svanes, M. Holm, Vivi Schlünssen, Karl A. Franklin, Francisco Gómez Real, Deborah Jarvis, Angelo Corsico, Bénédicte Leynaert, Jorunn Kirkeleit, Judith Garcia-Aymerich, Caroline J Lodge, Trond Riise, Shyamali C. Dharmage, Julia Dratva, Anne-Elie Carsin, Christer Janson, Chantal Raherison
Publikováno v:
Epidemiology.
Autor:
Philippe Froguel, Ndeye Coumba Ndiaye, Amélie Bonnefond, Nabila Bouatia-Naji, Aurélie Dechaume, Gérard Siest, Bernard Herbeth, Mario Falchi, Leonardo Bottolo, Rosa-Maria Guéant-Rodriguez, Cécile Lecoeur, Michel R Langlois, Yann Labrune, Aimo Ruokonen, Said El Shamieh, Maria G Stathopoulou, Anita Morandi, Claudio Maffeis, David Meyre, Joris R Delanghe, Peter Jacobson, Lars Sjöström, Lena M S Carlsson, Andrew Walley, Paul Elliott, Marjo-Riita Jarvelin, George V Dedoussis, Sophie Visvikis-Siest
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e32327 (2012)
Haptoglobin is an acute phase inflammatory marker. Its main function is to bind hemoglobin released from erythrocytes to aid its elimination, and thereby haptoglobin prevents the generation of reactive oxygen species in the blood. Haptoglobin levels
Externí odkaz:
https://doaj.org/article/cec641e79e79442fb737a5472b95a662
Autor:
Dave Evans, D.I. Boomsma, Martin D. Tobin, Germaine C. Verwoert, Ollie Raitakari, Beate St Pourcain, Debbie A Lawlor, Mika Kähönen, Jorma Viikari, Laurent Briollais, John P. Newnham, Cornelia M. van Duijn, Marcella Marinelli, Leo-Pekka Lyytikäinen, Nicholas G. Martin, Fernando Rivadeneira, Laura D Howe, Craig E. Pennell, Penelope A. Lind, Matthew W. Gillman, Lyle J. Palmer, Elisabeth Thiering, André G. Uitterlinden, Marjo Riita Jarvelin, Grant W. Montgomery, Vincent W. V. Jaddoe, Albert Hofman, John Whitfield, Terho Lehtimäki, Jesus Vioque, H. Rob Taal, Lawrence J. Beilin, P. Parmar, Jouke-Jan Hottenga, Margie Wright, Joachim Heinrich, Ville Aalto, Nicholas J. Timpson
Publikováno v:
Circ. Cardiovasc. Genet. 9, 266-278 (2016)
Circulation. Cardiovascular genetics, 9(3), 266-278. American Heart Association
Circulation-cardiovascular genetics, 9(3), 266-+. Lippincott Williams & Wilkins
Early Genetics and Lifecourse Epidemiology Consortium 2016, ' International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents ', Circulation. Cardiovascular genetics, vol. 9, no. 3, pp. 266-278 . https://doi.org/10.1161/CIRCGENETICS.115.001190
Circulation. Cardiovascular genetics, 9(3), 266-278. American Heart Association
Circulation-cardiovascular genetics, 9(3), 266-+. Lippincott Williams & Wilkins
Early Genetics and Lifecourse Epidemiology Consortium 2016, ' International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents ', Circulation. Cardiovascular genetics, vol. 9, no. 3, pp. 266-278 . https://doi.org/10.1161/CIRCGENETICS.115.001190
Background— Our aim was to identify genetic variants associated with blood pressure (BP) in childhood and adolescence. Methods and Results— Genome-wide association study data from participating European ancestry cohorts of the Early Genetics and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edaa778630883258a84a0246a117edaf
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=48093
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=48093
Autor:
David J. Balding, Julian E. Asher, Marjo-Riita Jarvelin, Phillipe Froguel, Lachlan J. M. Coin, Alexandra I.F. Blakemore, Shu-Yi Su
Publikováno v:
Bioinformatics
Bioinformatics; Vol 26
Bioinformatics; Vol 26
Motivation: Copy number variations (CNVs) are increasingly recognized as an substantial source of individual genetic variation, and hence there is a growing interest in investigating the evolutionary history of CNVs as well as their impact on complex