Heinonen S - Search Results

1

Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.

Tyrmi JS, Kaartokallio T, Lokki AI, Jääskeläinen T, Kortelainen E, Ruotsalainen S, Karjalainen J, Ripatti S, Kivioja A, Laisk T, Kettunen J, Pouta A, Kivinen K, Kajantie E, Heinonen S, Kere J, Laivuori H; FINNPEC Study Group, FinnGen Project, and the Estonian Biobank Research Team. Tyrmi JS, et al. Among authors: heinonen s. JAMA Cardiol. 2023 Jul 1;8(7):674-683. doi: 10.1001/jamacardio.2023.1312. JAMA Cardiol. 2023. PMID: 37285119 Free PMC article.

2

Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation.

Kallinen J, Heinonen S, Mannermaa A, Ryynänen M. Kallinen J, et al. Among authors: heinonen s. Clin Genet. 2000 Aug;58(2):111-5. doi: 10.1034/j.1399-0004.2000.580204.x. Clin Genet. 2000. PMID: 11005143

3

Apolipoprotein E alleles in women with intrahepatic cholestasis of pregnancy.

Eloranta ML, Heiskanen J, Hiltunen M, Helisalmi S, Mannermaa A, Heinonen S. Eloranta ML, et al. Among authors: heinonen s. Scand J Gastroenterol. 2000 Sep;35(9):966-8. doi: 10.1080/003655200750023048. Scand J Gastroenterol. 2000. PMID: 11063158

4

Antenatal genetic screening for congenital nephrosis.

Kallinen J, Heinonen S, Ryynänen M, Pulkkinen L, Mannermaa A. Kallinen J, et al. Among authors: heinonen s. Prenat Diagn. 2001 Feb;21(2):81-4. doi: 10.1002/1097-0223(200102)21:2<81::aid-pd1>3.0.co;2-8. Prenat Diagn. 2001. PMID: 11241530

5

Apolipoprotein E alleles in women with polycystic ovary syndrome.

Heinonen S, Korhonen S, Hippeläinen M, Hiltunen M, Mannermaa A, Saarikoski S. Heinonen S, et al. Fertil Steril. 2001 May;75(5):878-80. doi: 10.1016/s0015-0282(01)01691-0. Fertil Steril. 2001. PMID: 11334897 Free article.

6

Antenatal gene tests in low-risk pregnancies: molecular screening for aspartylglucosaminuria (AGU) and infantile neuronal ceroid lipofuscinosis (INCL) in Finland.

Kallinen J, Heinonen S, Palotie A, Mannermaa A, Ryynanen M. Kallinen J, et al. Among authors: heinonen s. Prenat Diagn. 2001 May;21(5):409-12. doi: 10.1002/pd.82. Prenat Diagn. 2001. PMID: 11360285

7

Wide scope prenatal diagnosis at Kuopio University Hospital 1997-1998: integration of gene tests and fetal karyotyping.

Kallinen J, Marin K, Heinonen S, Mannermaa A, Palotie A, Ryynänen M. Kallinen J, et al. Among authors: heinonen s. BJOG. 2001 May;108(5):505-9. doi: 10.1111/j.1471-0528.2001.00118.x. BJOG. 2001. PMID: 11368137

8

Maternal susceptibility locus for obstetric cholestasis maps to chromosome region 2p13 in Finnish patients.

Heinonen S, Eloranta ML, Heiskanen J, Punnonen K, Helisalmi S, Mannermaa A, Hiltunen M. Heinonen S, et al. Scand J Gastroenterol. 2001 Jul;36(7):766-70. doi: 10.1080/003655201300192049. Scand J Gastroenterol. 2001. PMID: 11444477

9

Apolipoprotein E alleles in women with pre-eclampsia.

Makkonen N, Heinonen S, Hiltunen M, Helisalmi S, Mannermaa A, Kirkinen P. Makkonen N, et al. Among authors: heinonen s. J Clin Pathol. 2001 Aug;54(8):652-4. doi: 10.1136/jcp.54.8.652. J Clin Pathol. 2001. PMID: 11477126 Free PMC article.

10

Insertion-deletion polymorphism in the gene for angiotensin-converting enzyme is associated with obstetric cholestasis but not with preeclampsia.

Heiskanen JT, Pirskanen MM, Hiltunen MJ, Mannermaa AJ, Punnonen KR, Heinonen ST. Heiskanen JT, et al. Among authors: heinonen st. Am J Obstet Gynecol. 2001 Sep;185(3):600-3. doi: 10.1067/mob.2001.116722. Am J Obstet Gynecol. 2001. PMID: 11568784

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