Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Diseases in Twins/genetics"'
Publikováno v:
Simony, A, Carreon, L Y, Højmark, K, Kyvik, K O & Andersen, M Ø 2016, ' Concordance Rates of Adolescent Idiopathic Scoliosis in a Danish Twin Population ', Spine, vol. 41, no. 19, pp. 1503-1507 . https://doi.org/10.1097/BRS.0000000000001681
Study design Clinical, radiological, and genetic determination of zygosity of twin pairs from the Danish Twin Registry who self-reported having adolescent idiopathic scoliosis (AIS). Objective To establish concordance rates of AIS. Summary of backgro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34ed3c01fbd2b96bba9a86d7ce92b421
https://doi.org/10.1097/brs.0000000000001681
https://doi.org/10.1097/brs.0000000000001681
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d5bb64ff8013fe21c74ee9ccbd854e4b
http://europepmc.org/articles/PMC5414070
http://europepmc.org/articles/PMC5414070
Autor:
Catharina E. M. van Beijsterveldt, Laura W. Wesseldijk, Jacqueline M. Vink, Lannie Ligthart, Christel M. Middeldorp, Meike Bartels, Dorret I. Boomsma
Publikováno v:
European child & adolescent psychiatry, 27(9), 1123-1132. D. Steinkopff-Verlag
Wesseldijk, L W, Bartels, M, Vink, J M, van Beijsterveldt, C E M, Ligthart, L, Boomsma, D I & Middeldorp, C M 2018, ' Genetic and environmental influences on conduct and antisocial personality problems in childhood, adolescence, and adulthood ', European Child and Adolescent Psychiatry, vol. 27, no. 9, pp. 1123-1132 . https://doi.org/10.1007/s00787-017-1014-y
European Child & Adolescent Psychiatry, 27, 9, pp. 1123-1132
European Child and Adolescent Psychiatry, 27(9), 1123-1132. D. Steinkopff-Verlag
European Child & Adolescent Psychiatry, 27, 1123-1132
Wesseldijk, L W, Bartels, M, Vink, J M, van Beijsterveldt, C E M, Ligthart, L, Boomsma, D I & Middeldorp, C M 2018, ' Genetic and environmental influences on conduct and antisocial personality problems in childhood, adolescence, and adulthood ', European Child and Adolescent Psychiatry, vol. 27, no. 9, pp. 1123-1132 . https://doi.org/10.1007/s00787-017-1014-y
European Child & Adolescent Psychiatry, 27, 9, pp. 1123-1132
European Child and Adolescent Psychiatry, 27(9), 1123-1132. D. Steinkopff-Verlag
European Child & Adolescent Psychiatry, 27, 1123-1132
Contains fulltext : 195163.pdf (Publisher’s version ) (Open Access) Conduct problems in children and adolescents can predict antisocial personality disorder and related problems, such as crime and conviction. We sought an explanation for such predi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c91395c49a7a8fac92df38ba07ffd30e
https://pure.amc.nl/en/publications/genetic-and-environmental-influences-on-conduct-and-antisocial-personality-problems-in-childhood-adolescence-and-adulthood(73220986-82c8-4dbd-9796-56318f0ccb75).html
https://pure.amc.nl/en/publications/genetic-and-environmental-influences-on-conduct-and-antisocial-personality-problems-in-childhood-adolescence-and-adulthood(73220986-82c8-4dbd-9796-56318f0ccb75).html
Autor:
Mashael Al-Shafai, Pankaj Kumar, Tim D. Spector, Wadha A. Al Muftah, Shaza B. Zaghlool, Jordana T. Bell, Karsten Suhre, Pei-Chien Tsai, Alessia Visconti, Mario Falchi
Publikováno v:
Clin. Epigenet. 8:13 (2016)
Al Muftah, W A, Al-Shafai, M, Zaghlool, S B, Visconti, A, Tsai, P-C, Kumar, P, Spector, T, Bell, J, Falchi, M & Suhre, K 2016, ' Epigenetic associations of type 2 diabetes and BMI in an Arab population ', Clinical Epigenetics, vol. 8, 13 . https://doi.org/10.1186/s13148-016-0177-6
Clinical Epigenetics
Al Muftah, W A, Al-Shafai, M, Zaghlool, S B, Visconti, A, Tsai, P-C, Kumar, P, Spector, T, Bell, J, Falchi, M & Suhre, K 2016, ' Epigenetic associations of type 2 diabetes and BMI in an Arab population ', Clinical Epigenetics, vol. 8, 13 . https://doi.org/10.1186/s13148-016-0177-6
Clinical Epigenetics
Background: The prevalence of type 2 diabetes (T2D) and obesity has dramatically increased within a few generations, reaching epidemic levels. In addition to genetic risk factors, epigenetic mechanisms triggered by changing environment are investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1601bd2931dad8211edd0a37953c661
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=47786
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=47786
Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::813ffb8f9fd35bc8d54038caffb5fe43
Autor:
Esben Budtz-Jørgensen, M S Olesen, Ingrid E. Christophersen, Jesper Hastrup Svendsen, Kaare Christensen, Stig Haunsø
Publikováno v:
Christophersen, I E, Budtz-Jørgensen, E, Olesen, M S, Haunsø, S, Christensen, K & Svendsen, J H 2013, ' Familial atrial fibrillation predicts increased risk of mortality : A study in Danish twins ', Circulation. Arrhythmia and electrophysiology, vol. 6, no. 1, pp. 10-15 . https://doi.org/10.1161/CIRCEP.112.971580
BACKGROUND: Atrial fibrillation (AF) is a common arrhythmia. Several studies have shown association of genetic variants with AF and that familial AF increases the risk of AF. We have previously shown a substantial heritability of AF in a twin study.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69610e3cff7b18e247697ee817aa708a
https://portal.findresearcher.sdu.dk/da/publications/0c74f52a-ef39-42fd-93a7-31e90a36b322
https://portal.findresearcher.sdu.dk/da/publications/0c74f52a-ef39-42fd-93a7-31e90a36b322
Autor:
Cécile Chevrier, Aase Sivertsen, Dorthe Grosen, Axel Skytthe, Jeffrey C. Murray, Camilla Bille, Kirsten Mølsted, Kaare Christensen
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (3), pp.162-8. ⟨10.1136/jmg.2009.069385⟩
Grosen, D, Chevrier, C, Skytthe, A, Bille, C, Mølsted, K, Sivertsen, A, Murray, J & Christensen, K 2010, ' A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark : support for the multifactorial threshold model of inheritance ', Journal of Medical Genetics, vol. 47, no. 3, pp. 162-8 . https://doi.org/10.1136/jmg.2009.069385
Journal of Medical Genetics, 2010, 47 (3), pp.162-8. ⟨10.1136/jmg.2009.069385⟩
Journal of Medical Genetics, BMJ Publishing Group, 2010, 47 (3), pp.162-8. ⟨10.1136/jmg.2009.069385⟩
Grosen, D, Chevrier, C, Skytthe, A, Bille, C, Mølsted, K, Sivertsen, A, Murray, J & Christensen, K 2010, ' A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark : support for the multifactorial threshold model of inheritance ', Journal of Medical Genetics, vol. 47, no. 3, pp. 162-8 . https://doi.org/10.1136/jmg.2009.069385
Journal of Medical Genetics, 2010, 47 (3), pp.162-8. ⟨10.1136/jmg.2009.069385⟩
Udgivelsesdato: 2010-Mar OBJECTIVES: To determine if the anatomical severity of oral clefting affects familial recurrence in a large population based sample. To provide reliable recurrence risk estimates for oral cleft for first, second, and third de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46395f7acf704669938d7c0dff7bf101
https://hal.archives-ouvertes.fr/hal-00657736
https://hal.archives-ouvertes.fr/hal-00657736
Autor:
Isabelle Laisney, Wolf-Henning Boehncke, Paul Trommler, Antje Menssen, Sigrid Vollmer, Jörg C. Prinz
Publikováno v:
European Journal of Immunology, Vol. 29, No 10 (1999) pp. 3360-3368
Psoriasis vulgaris is a common HLA-associated inflammatory skin disease. Although its etiology is still unknown, it is thought to involve T cell-mediated inflammatory mechanisms. In examining the lesional psoriatic TCR beta chain (TCRB) usage in a pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b5d54002999e0d8d9d501daabe774ab
https://pubmed.ncbi.nlm.nih.gov/10540348
https://pubmed.ncbi.nlm.nih.gov/10540348
Autor:
Thomas Pollmächer, F. Schwarzfischer, Ekkehard D. Albert, H. Schulz, Peter Geisler, Elke Kiss
Publikováno v:
Sleep. 13(4)
Narcolepsy runs in families, and recent research has revealed the human leukocyte antigen (HLA) DR2 to be a genetic marker closely associated with the disease. But, as indicated by family studies, other factors contribute to the pathogenesis of narco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1809fba78a70de022dc9bd989c18569a
https://pubmed.ncbi.nlm.nih.gov/2267476
https://pubmed.ncbi.nlm.nih.gov/2267476