Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Harkonmäki, Karoliina
Silventoinen, Karri
Levälahti, Esko
Pitkäniemi, Janne
Huunan-Seppälä, Antti
Klaukka, Timo
Koskenvuo, Markku
Kaprio, Jaakko
and
Bishop, Steve
2008.
The Genetic Liability to Disability Retirement: A 30-Year Follow-Up Study of 24,000 Finnish Twins.
PLoS ONE,
Vol. 3,
Issue. 10,
p.
e3402.
Martin, Sean A
Haren, Matthew T
Taylor, Anne W
Middleton, Sue M
and
Wittert, Gary A
2008.
Chronic disease prevalence and associations in a cohort of Australian men: The Florey Adelaide Male Ageing Study (FAMAS).
BMC Public Health,
Vol. 8,
Issue. 1,
Kendler, Kenneth S.
Fiske, Amy
Gardner, Charles O.
and
Gatz, Margaret
2009.
Delineation of Two Genetic Pathways to Major Depression.
Biological Psychiatry,
Vol. 65,
Issue. 9,
p.
808.
Obel, Niels
Christensen, Kaare
Petersen, Inge
Sørensen, Thorkild I. A.
and
Skytthe, Axel
2010.
Genetic and Environmental Influences on Risk of Death due to Infections Assessed in Danish Twins, 1943–2001.
American Journal of Epidemiology,
Vol. 171,
Issue. 9,
p.
1007.
Svedberg, Pia
Ropponen, Annina
Alexanderson, Kristina
Lichtenstein, Paul
and
Narusyte, Jurgita
2012.
Genetic Susceptibility to Sickness Absence is Similar Among Women and Men: Findings From a Swedish Twin Cohort.
Twin Research and Human Genetics,
Vol. 15,
Issue. 5,
p.
642.
Bell, Jordana T
and
Spector, Tim D
2012.
DNA methylation studies using twins: what are they telling us?.
Genome Biology,
Vol. 13,
Issue. 10,
p.
172.
Vaccarino, Loredana
Vitale, Silvana
Caruso, Marco
Palmeri, Marisa
Scola, Letizia
Bova, Manuela
Caruso, Calogero
Massenti, Maria Fatima
Vitale, Francesco
Novo, Salvatore
Lio, Domenico
and
Forte, Giusi Irma
2013.
Myocardial infarction marker levels are influenced by prothrombin and tumor necrosis factor-α gene polymorphisms in young patients.
Cytokine,
Vol. 61,
Issue. 1,
p.
218.
Castillo-Fernandez, Juan E
Spector, Tim D
and
Bell, Jordana T
2014.
Epigenetics of discordant monozygotic twins: implications for disease.
Genome Medicine,
Vol. 6,
Issue. 7,
Salo, Perttu P.
Vaara, Satu
Kettunen, Johannes
Pirinen, Matti
Sarin, Antti-Pekka
Huikuri, Heikki
Karhunen, Pekka J.
Eskola, Markku
Nikus, Kjell
Lokki, Marja-Liisa
Ripatti, Samuli
Havulinna, Aki S.
Salomaa, Veikko
Palotie, Aarno
Nieminen, Markku S.
Sinisalo, Juha
Perola, Markus
and
Dubé, Marie-Pierre
2015.
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population.
PLOS ONE,
Vol. 10,
Issue. 10,
p.
e0140576.
Silventoinen, Karri
Hjelmborg, Jacob
Möller, Sören
Ripatti, Samuli
Skythe, Axel
Tikkanen, Emmi
Pedersen, Nancy L
Magnusson, Patrik KE
Christensen, Kaare
and
Kaprio, Jaakko
2017.
Family aggregation of cardiovascular disease mortality: a register-based prospective study of pooled Nordic twin cohorts.
International Journal of Epidemiology,
Vol. 46,
Issue. 4,
p.
1223.
Yang, Liping
Yang, Yushuang
Si, Daoyuan
Shi, Kaiyao
Liu, Dongna
Meng, Heyu
and
Meng, Fanbo
2017.
High expression of long chain acyl‑coenzyme A synthetase�1 in peripheral blood may be a molecular marker for assessing the risk of acute myocardial infarction.
Experimental and Therapeutic Medicine,
Dahlqwist, Elisabeth
Magnusson, Patrik K. E.
Pawitan, Yudi
and
Sjölander, Arvid
2019.
On the relationship between the heritability and the attributable fraction.
Human Genetics,
Vol. 138,
Issue. 4,
p.
425.
Liu, Zheng-Yu
Liu, Fen
Cao, Yan
Peng, Shao-Liang
Pan, Hong-Wei
Hong, Xiu-Qin
and
Zheng, Peng-Fei
2023.
ACSL1, CH25H, GPCPD1, and PLA2G12A as the potential lipid-related diagnostic biomarkers of acute myocardial infarction.
Aging,