Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Twins, Monozygotic/genetics"'
Autor:
Martin Dalgaard Villumsen, Jacob v. B. Hjelmborg, Kaare Christensen, Merete Osler, Martin Balslev Jørgensen, Marie Kim Wium-Andersen
Publikováno v:
Osler, M, Villumsen, M D, Jørgensen, M B, Hjelmborg, J V B, Christensen, K & Wium-Andersen, M K 2022, ' Familial risk and heritability of ischemic heart disease and stroke in Danish twins ', Scandinavian Journal of Public Health, vol. 50, no. 2, pp. 199-204 . https://doi.org/10.1177/1403494820953322
Aim: Our aim was to explore whether familial factors influence the risk of ischemic heart disease, stroke, and their co-occurrence. Methods: In total, 23,498 monozygotic and 39,540 same-sex dizygotic twins from the Danish Twin Registry were followed
Autor:
Jesper Lund, Martin Jakob Larsen, Qihua Tan, Weilong Li, Jan Baumbach, Lene Christiansen, Shuxia Li, Jonas Mengel-From, Kaare Christensen, Afsaneh Mohammadnejad, Tanja Maria Michel, Jacob v. B. Hjelmborg
Publikováno v:
Mohammadnejad, A, Baumbach, J, Li, W, Lund, J, Larsen, M J, Li, S, Mengel-From, J, Sheldrick-Michel, T M, Christiansen, L, Christensen, K, Hjelmborg, J & Tan, Q 2021, ' Differential lncRNA expression profiling of cognitive function in middle and old aged monozygotic twins using generalized association analysis ', Journal of Psychiatric Research, vol. 140, pp. 197-204 . https://doi.org/10.1016/j.jpsychires.2021.05.074
Cognitive impairment is the most prominent symptom in neurodegenerative disorders affecting quality of life and mortality. However, despite years of research, the molecular mechanism underlying the regulation of cognitive function and its impairment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f6011b00a9d3115cc4a9d69d46e459d
https://portal.findresearcher.sdu.dk/da/publications/e9299092-164c-418a-a1dd-61aad0e0e8a7
https://portal.findresearcher.sdu.dk/da/publications/e9299092-164c-418a-a1dd-61aad0e0e8a7
Autor:
Kan, C, Pedersen, N L, Christensen, K, Bornstein, S R, Licinio, J, MacCabe, J H, Ismail, K, Rijsdijk, F
Publikováno v:
Molecular Psychiatry
Kan, C, Pedersen, N L, Christensen, K, Bornstein, S R, Licinio, J, MacCabe, J H, Ismail, K & Rijsdijk, F 2016, ' Genetic overlap between type 2 diabetes and depression in Swedish and Danish twin registries ', Molecular Psychiatry, vol. 21, no. 7, pp. 903-909 . https://doi.org/10.1038/mp.2016.28
Kan, C, Pedersen, N L, Christensen, K, Bornstein, S R, Licinio, J, MacCabe, J H, Ismail, K & Rijsdijk, F 2016, ' Genetic overlap between type 2 diabetes and depression in Swedish and Danish twin registries ', Molecular Psychiatry, vol. 21, no. 7, pp. 903-909 . https://doi.org/10.1038/mp.2016.28
A bidirectional association between type 2 diabetes (T2DM) and depression has been consistently reported. Depression is associated with worse biomedical outcomes and increased mortality. The mechanisms underlying the association of T2DM with depressi
Autor:
Matthaei, Johannes, Tzvetkov, Mladen V, Strube, Jakob, Sehrt, Daniel, Sachse-Seeboth, Cordula, Hjelmborg, Jacob v. B., Möller, Sören, Halekoh, Ulrich, Hofmann, Ute, Schwab, Matthias, Kerb, Reinhold, Brockmöller, Jürgen
Publikováno v:
Matthaei, J, Tzvetkov, M V, Strube, J, Sehrt, D, Sachse-Seeboth, C, Hjelmborg, J V B, Möller, S, Halekoh, U, Hofmann, U, Schwab, M, Kerb, R & Brockmöller, J 2016, ' Heritability of caffeine metabolism : Environmental effects masking genetic effects on CYP1A2 activity but not on NAT2 ', Clinical Pharmacology & Therapeutics, vol. 100, no. 6, pp. 606-616 . https://doi.org/10.1002/cpt.444
Heritability of caffeine pharmacokinetics and cytochrome P450 1A2 (CYP1A2) activity is controversial. Here, we analyzed the pharmacokinetics of caffeine, an in vivo probe drug for CYP1A2 and arylamine N-acetyltransferase 2 (NAT2) activity, in monozyg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::1ff4e5cd2dd5d73af006082d3f0cada4
https://portal.findresearcher.sdu.dk/da/publications/505827fa-2eef-4b06-a5cf-bf68b63fa2b3
https://portal.findresearcher.sdu.dk/da/publications/505827fa-2eef-4b06-a5cf-bf68b63fa2b3
Publikováno v:
Magaard Koldby, K, Nygaard, M, Christensen, K & Christiansen, L 2016, ' Somatically acquired structural genetic differences : a longitudinal study of elderly Danish twins ', European Journal of Human Genetics, vol. 24, no. 10, pp. 1506–1510 . https://doi.org/10.1038/ejhg.2016.34
Structural genetic variants like copy number variants (CNVs) comprise a large part of human genetic variation and may be inherited as well as somatically acquired. Recent studies have reported the presence of somatically acquired structural variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::164e16b1dea29b31b255268f50a66d30
https://europepmc.org/articles/PMC5027681/
https://europepmc.org/articles/PMC5027681/
Publikováno v:
Skousgaard, S G, Skytthe, A, Möller, S, Overgaard, S & Brandt, L 2016, ' Sex differences in risk and heritability estimates on primary knee osteoarthritis leading to total knee arthroplasty : a nationwide population based follow up study in Danish twins ', Arthritis Research & Therapy
, vol. 18, 46 . https://doi.org/10.1186/s13075-016-0939-8
Arthritis Research & Therapy
, vol. 18, 46 . https://doi.org/10.1186/s13075-016-0939-8
Arthritis Research & Therapy
Background: Symptomatic knee osteoarthritis is a highly age and sex associated complex disease. Little is known about the causes behind this age and sex associated increase, or if genetic and environmental factors impacts differently by gender. Our s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65b7db53d12fafac1df58fe7d0253c0a
https://findresearcher.sdu.dk:8443/ws/files/123311794/Sex_differences_in_risk_and_heritability_estimates_on_primary_knee_osteoarthritis.pdf
https://findresearcher.sdu.dk:8443/ws/files/123311794/Sex_differences_in_risk_and_heritability_estimates_on_primary_knee_osteoarthritis.pdf
Autor:
Jacob v. B. Hjelmborg, Jaakko Kaprio, Hans-Olov Adami, Kamila Czene, Sören Möller, Niels V. Holm, Ulrich Halekoh, Eero Pukkala, Axel Skytthe, Kaare Christensen, Klaus K. Holst, Lorelei A. Mucci, Thomas H. Scheike, Jennifer R. Harris
Publikováno v:
Möller, S, Mucci, L A, Harris, J R, Scheike, T, Holst, K, Halekoh, U, Adami, H-O, Czene, K, Christensen, K, Holm, N V, Pukkala, E, Skytthe, A, Kaprio, J & Hjelmborg, J B 2016, ' The Heritability of Breast Cancer among women in the Nordic Twin Study of Cancer ', Cancer Epidemiology, Biomarkers & Prevention, vol. 25, no. 1, pp. 145-150 . https://doi.org/10.1158/1055-9965.EPI-15-0913
Background: Family history is an established risk factor for breast cancer. Although some important genetic factors have been identified, the extent to which familial risk can be attributed to genetic factors versus common environment remains unclear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a246ea0da00b207eeb5367bf3a33ca2a
https://findresearcher.sdu.dk:8443/ws/files/135183543/The_Heritability_of_Breast_Cancer_among_women_in_the_Nordic_Twin_Study_of_Cancer.pdf
https://findresearcher.sdu.dk:8443/ws/files/135183543/The_Heritability_of_Breast_Cancer_among_women_in_the_Nordic_Twin_Study_of_Cancer.pdf
Autor:
Philip McGuire, Kazunori Matsumoto, Ulrich Ettinger, Charmaine Borg, Sheena Owens, Timothea Toulopoulou, Neeltje E.M. van Haren, Claire Orrells, Mei-Hua Hall, Anne Schmechtig, Veena Kumari, Robin M. Murray, Marco Picchioni
Publikováno v:
Schizophrenia Bulletin, 38(1), 192-203. Oxford University Press
Frontostriatal networks mediating important cognitive and motor functions have been shown to be abnormal structurally and functionally in schizophrenia. However, the influence of genetic risk for schizophrenia on structural abnormalities in these are
Autor:
Daniel Sehrt, Matthias Schwab, Mladen V. Tzvetkov, Cordula Sachse-Seeboth, Ute Hofmann, Sören Möller, Ulrich Halekoh, Jacob v. B. Hjelmborg, Jürgen Brockmöller, Johannes Matthaei, Reinhold Kerb
Publikováno v:
Matthaei, J, Brockmöller, J, Tzvetkov, M, Sehrt, D, Sachse-Seeboth, C, Hjelmborg, J V B, Möller, S, Halekoh, U, Hofmann, U, Schwab, M & Kerb, R 2015, ' Heritability of metoprolol and torsemide pharmacokinetics ', Clinical Pharmacology and Therapeutics, vol. 98, no. 6, pp. 611-621 . https://doi.org/10.1002/cpt.258
Genetic variation in the pharmacokinetics of metoprolol and torsemide due to polymorphisms in CYP2D6, CYP2C9, and OATP1B1 has been extensively studied. However, it is still unknown how much of the variation in pharmacokinetics of these two clinically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab3eee0207e12981e67f226bbf1b3c87
https://portal.findresearcher.sdu.dk/da/publications/09c139b8-a310-4344-b293-642eaed23ec0
https://portal.findresearcher.sdu.dk/da/publications/09c139b8-a310-4344-b293-642eaed23ec0
Autor:
Lorelei A. Mucci, Thomas H. Scheike, Kaare Christensen, Klaus K. Holst, Jacob v. B. Hjelmborg, Kamila Czene, Axel Skytthe, Julia Kutschke, Jaakko Kaprio, Eero Pukkala, Hans-Olov Adami, Jennifer R. Harris, Tellervo Korhonen
Publikováno v:
Hjelmborg, J V B, Korhonen, T, Holst, K, Skytthe, A, Pukkala, E, Kutschke, J, Harris, J, Mucci, L, Christensen, K, Czene, K, Adami, H-O, Scheike, T H & Kaprio, J 2017, ' Lung cancer, genetic predisposition and smoking: the Nordic Twin Study of Cancer ', Thorax, vol. 72, no. 11, pp. 1021-1027 . https://doi.org/10.1136/thoraxjnl-2015-207921
Background We aimed to disentangle genetic and environmental causes in lung cancer while considering smoking status. Methods Four Nordic twin cohorts (43 512 monozygotic (MZ) and 71 895 same sex dizygotic (DZ) twin individuals) had smoking data befor