Saarela T - Search Results

1

Genetic testing for familial hypercholesterolemia in a Finnish cohort of patients with premature coronary artery disease and elevated LDL-C levels.

Jokiniitty A, Eskola M, Metso S, Bogsrud M, Huhtala H, Saarela T. Jokiniitty A, et al. Among authors: saarela t. Front Cardiovasc Med. 2024 Jul 26;11:1433042. doi: 10.3389/fcvm.2024.1433042. eCollection 2024. Front Cardiovasc Med. 2024. PMID: 39131706 Free PMC article.

2

Preeclampsia and androgen receptor gene CAG repeat length: results from both children and women.

Saarela T, Jääskeläinen J, Tenhola S, Voutilainen R, Heinonen S. Saarela T, et al. J Assist Reprod Genet. 2005 Aug;22(7-8):269-75. doi: 10.1007/s10815-005-5349-9. J Assist Reprod Genet. 2005. PMID: 16195823

3

Increased Risk of Preeclampsia in Women With a Genetic Predisposition to Elevated Blood Pressure.

Kivioja A, Toivonen E, Tyrmi J, Ruotsalainen S, Ripatti S, Huhtala H, Jääskeläinen T, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Saarela T, Laivuori H. Kivioja A, et al. Among authors: saarela t. Hypertension. 2022 Sep;79(9):2008-2015. doi: 10.1161/HYPERTENSIONAHA.122.18996. Epub 2022 Jul 7. Hypertension. 2022. PMID: 35862124 Free PMC article.

4

Role of an automated screening tool for familial hypercholesterolemia in patients with premature coronary artery disease.

Jokiniitty A, Eskola M, Saarela T, Huhtala H, Metso S. Jokiniitty A, et al. Among authors: saarela t. Atheroscler Plus. 2022 Jan 6;48:1-7. doi: 10.1016/j.athplu.2022.01.001. eCollection 2022 Apr. Atheroscler Plus. 2022. PMID: 36644564 Free PMC article.

5

Genetic testing and new variants in diagnosis of congenital ichthyoses.

Salo M, Kimpimäki T, Huhtala H, Saarela T. Salo M, et al. Among authors: saarela t. Mol Genet Genomic Med. 2024 Aug;12(8):e70000. doi: 10.1002/mgg3.70000. Mol Genet Genomic Med. 2024. PMID: 39189679 Free PMC article.

6

Associations of polygenic risk scores for preeclampsia and blood pressure with hypertensive disorders of pregnancy.

Nurkkala J, Kauko A, FinnGen, Laivuori H, Saarela T, Tyrmi JS, Vaura F, Cheng S, Bello NA, Aittokallio J, Niiranen T. Nurkkala J, et al. Among authors: saarela t. J Hypertens. 2023 Mar 1;41(3):380-387. doi: 10.1097/HJH.0000000000003336. Epub 2022 Dec 16. J Hypertens. 2023. PMID: 36947680 Free PMC article.

7

Plasma cell membrane glycoprotein-1 K121Q polymorphism in preeclampsia.

Saarela T, Hiltunen M, Helisalmi S, Heinonen S, Laakso M. Saarela T, et al. Gynecol Obstet Invest. 2006;61(3):124-7. doi: 10.1159/000089482. Epub 2005 Nov 2. Gynecol Obstet Invest. 2006. PMID: 16272817

8

Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype.

Schultz R, Elenius V, Lukkarinen H, Saarela T. Schultz R, et al. Among authors: saarela t. BMC Med Genet. 2020 Nov 26;21(1):237. doi: 10.1186/s12881-020-01171-2. BMC Med Genet. 2020. PMID: 33243178 Free PMC article.

9

Tumour necrosis factor-alpha gene haplotype is associated with pre-eclampsia.

Saarela T, Hiltunen M, Helisalmi S, Heinonen S, Laakso M. Saarela T, et al. Mol Hum Reprod. 2005 Jun;11(6):437-40. doi: 10.1093/molehr/gah182. Epub 2005 May 18. Mol Hum Reprod. 2005. PMID: 15901845

10

Polymorphisms of interleukin-6, hepatic lipase and calpain-10 genes, and preeclampsia.

Saarela T, Hiltunen M, Helisalmi S, Heinonen S, Laakso M. Saarela T, et al. Eur J Obstet Gynecol Reprod Biol. 2006 Sep-Oct;128(1-2):175-9. doi: 10.1016/j.ejogrb.2005.12.015. Epub 2006 Jan 20. Eur J Obstet Gynecol Reprod Biol. 2006. PMID: 16427731

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