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» Authors » Mojgan Yazdanpanah

Mojgan Yazdanpanah

Explore the profile of Mojgan Yazdanpanah including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 31
Citations 519
Followers 0
Related Specialties
Cardiology & Vascular Diseases
Genetics
Endocrinology
Top 10 Co-Authors
Eric J G Sijbrands
Cornelia M Van Duijn
Nahid Yazdanpanah
Daniella M Oosterveer
Joep C Defesche
Albert Hofman
John J P Kastelein
Jorie Versmissen
Despoina Manousaki
Jacqueline C M Witteman
Published In
Diabetes
Eur Heart J
Atherosclerosis
Eur J Hum Genet
Nat Genet
Affiliations
Soon will be listed here.
Recent Articles
11.
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach
Versmissen J, Oosterveer D, Yazdanpanah M, Dehghan A, Holm H, Erdman J, et al.
Eur J Hum Genet . 2014 Jun; 23(3):381-7. PMID: 24916650
Mutations in the low-density lipoprotein receptor (LDLR) gene cause familial hypercholesterolemia (FH), a disorder characterized by coronary heart disease (CHD) at young age. We aimed to apply an extreme sampling...
12.
Secondary analysis of publicly available data reveals superoxide and oxygen radical pathways are enriched for associations between type 2 diabetes and low-frequency variants
Yazdanpanah M, Chen C, Graham J
Ann Hum Genet . 2013 Aug; 77(6):472-81. PMID: 23941231
Genome-wide association studies explain at most 5%-10% of the heritable components of type 2 diabetes. Some of the "missing type 2 diabetes heritability" could be explained by low-frequency variants. We...
13.
Low-density lipoprotein receptor mutations generate synthetic genome-wide associations
Oosterveer D, Versmissen J, Defesche J, Sivapalaratnam S, Yazdanpanah M, Mulder M, et al.
Eur J Hum Genet . 2012 Sep; 21(5):563-6. PMID: 22968135
Genome-wide association (GWA) studies have discovered multiple common genetic risk variants related to common diseases. It has been proposed that a number of these signals of common polymorphisms are based...
14.
A frequent variant in the ABCA1 gene is associated with increased coronary heart disease risk and a better response to statin treatment in familial hypercholesterolemia patients
Versmissen J, Oosterveer D, Yazdanpanah M, Mulder M, Dehghan A, Defesche J, et al.
Eur Heart J . 2010 Jul; 32(4):469-75. PMID: 20595220
Aims: Statins are essential for the reduction of risk of coronary heart disease (CHD) in familial hypercholesterolemia (FH). One of many genes influenced by statin treatment is the ATP-binding cassette...
15.
The risk of tendon xanthomas in familial hypercholesterolaemia is influenced by variation in genes of the reverse cholesterol transport pathway and the low-density lipoprotein oxidation pathway
Oosterveer D, Versmissen J, Yazdanpanah M, Defesche J, Kastelein J, Sijbrands E
Eur Heart J . 2009 Dec; 31(8):1007-12. PMID: 20019024
Aims: The presence of tendon xanthomas is a marker of high risk of cardiovascular disease (CVD) among patients with familial hypercholesterolaemia (FH). Therefore, xanthomas and atherosclerosis may result from the...
16.
Genetic variation in the renin-angiotensin system and arterial stiffness. The Rotterdam Study
Sie M, Yazdanpanah M, Mattace-Raso F, Uitterlinden A, Hofman A, Hoeks A, et al.
Clin Exp Hypertens . 2009 Oct; 31(5):389-99. PMID: 19811349
We studied the associations of three renin-angiotensin system polymorphisms, angiotensin-converting enzyme (ACE) I/D, angiotensinogen 235 M/T, and angiotensin II receptor type I 573 C/T, with arterial stiffness. The study was...
17.
The association of the dopamine transporter gene and the dopamine receptor 2 gene with delirium, a meta-analysis
van Munster B, de Rooij S, Yazdanpanah M, Tienari P, Pitkala K, Osse R, et al.
Am J Med Genet B Neuropsychiatr Genet . 2009 Sep; 153B(2):648-655. PMID: 19739106
Delirium is the most common neuropsychiatric syndrome in elderly ill patients. Previously, associations between delirium and the dopamine transporter gene (solute carrier family 6, member 3 (SLC6A3)) and dopamine receptor...
18.
Differences in characteristics and risk of cardiovascular disease in familial hypercholesterolemia patients with and without tendon xanthomas: a systematic review and meta-analysis
Oosterveer D, Versmissen J, Yazdanpanah M, Hamza T, Sijbrands E
Atherosclerosis . 2009 May; 207(2):311-7. PMID: 19439299
Background: Tendon xanthomas are characteristic of familial hypercholesterolemia (FH). It is not clear whether FH patients with xanthomas have higher risk of cardiovascular disease (CVD) than those without xanthomas. The...
19.
5-Lipoxygenase activating protein (ALOX5AP) gene variants associate with the presence of xanthomas in familial hypercholesterolemia
Oosterveer D, Versmissen J, Yazdanpanah M, van der Net J, Defesche J, Kastelein J, et al.
Atherosclerosis . 2009 Apr; 206(1):223-7. PMID: 19361804
Background: Tendon xanthomas are characteristic for familial hypercholesterolemia (FH), and are associated with a higher risk of coronary heart disease (CHD). They often present with local inflammation. Inflammation may therefore...
20.
Genetic polymorphisms in the DRD2, DRD3, and SLC6A3 gene in elderly patients with delirium
van Munster B, Yazdanpanah M, Tanck M, de Rooij S, van de Giessen E, Sijbrands E, et al.
Am J Med Genet B Neuropsychiatr Genet . 2009 Mar; 153B(1):38-45. PMID: 19309018
Dopamine excess appears to be critical in the final common pathway of delirium. The aim of this study was to investigate whether genetic polymorphisms in three dopamine-related genes (the dopamine...