PubRank

K Kontula

Author PubWeight™ 121.57‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein. N Engl J Med 1995 3.54
2 Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 2001 3.34
3 A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E. Genomics 1990 2.95
4 Increased risk of acute myocardial infarction in carriers of the hemochromatosis gene Cys282Tyr mutation : a prospective cohort study in men in eastern Finland. Circulation 1999 2.29
5 Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study. Neurology 2001 1.98
6 CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease. Gut 2003 1.87
7 Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. J Am Coll Cardiol 1999 1.68
8 Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects. J Am Coll Cardiol 1999 1.59
9 Telomere length and cardiovascular risk in hypertensive patients with left ventricular hypertrophy: the LIFE study. J Hum Hypertens 2011 1.56
10 APOE epsilon4 does not predict mortality, cognitive decline, or dementia in the oldest old. Neurology 2000 1.51
11 Neonatal diagnosis of familial hypercholesterolemia in newborns born to a parent with a molecularly defined heterozygous familial hypercholesterolemia. Arterioscler Thromb Vasc Biol 1997 1.45
12 You may live to the age of more than 100 years even if you are homozygous for a haemochromatosis gene mutation. Eur J Clin Invest 2003 1.41
13 A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics. J Am Coll Cardiol 2001 1.39
14 Binding of progestins to the glucocorticoid receptor. Correlation to their glucocorticoid-like effects on in vitro functions of human mononuclear leukocytes. Biochem Pharmacol 1983 1.36
15 Common candidate gene variants are associated with QT interval duration in the general population. J Intern Med 2009 1.35
16 Primary structure of human insulin-like growth factor-binding protein/placental protein 12 and tissue-specific expression of its mRNA. FEBS Lett 1988 1.29
17 Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease. Neurology 1997 1.23
18 A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia. Proc Natl Acad Sci U S A 1994 1.20
19 Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings. J Hypertens 2000 1.19
20 Aging and genetic variation of plasma apolipoproteins. Relative loss of the apolipoprotein E4 phenotype in centenarians. Arterioscler Thromb 1994 1.11
21 Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24. J Clin Endocrinol Metab 2000 1.11
22 Lack of association of apolipoprotein E allele epsilon 4 with late-onset Alzheimer's disease among Finnish centenarians. Neurology 1995 1.11
23 Familial hypercholesterolemia in the Finnish north Karelia. A molecular, clinical, and genealogical study. Arterioscler Thromb Vasc Biol 1997 1.10
24 Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study. BMJ 2000 1.10
25 Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension. Hypertension 1999 1.08
26 Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population. Tissue Antigens 2012 1.05
27 Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects. Hum Mutat 2000 1.02
28 The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finland. J Clin Invest 1992 1.00
29 Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defective phenotype. J Clin Invest 1989 1.00
30 Female sex steroid receptor status in primary and metastatic breast carcinoma and its relationship to serum steroid peptide hormone levels. Int J Cancer 1980 1.00
31 Plasma concentrations and receptor binding of RU 486 and its metabolites in humans. J Steroid Biochem 1987 0.99
32 Progesterone-binding proteins: in vitro binding and biological activity of different steroidal ligands. Acta Endocrinol (Copenh) 1975 0.99
33 Leptin concentration in cord blood correlates with intrauterine growth. J Clin Endocrinol Metab 1997 0.99
34 Genetic association of alpha2-macroglobulin with Alzheimer's disease in a Finnish elderly population. Ann Neurol 1999 0.99
35 Familial and sporadic inflammatory bowel disease: comparison of clinical features and serological markers in a genetically homogeneous population. Scand J Gastroenterol 2002 0.98
36 Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns. J Am Coll Cardiol 2000 0.98
37 Direct sequencing of affinity-captured amplified human DNA application to the detection of apolipoprotein E polymorphism. FEBS Lett 1989 0.96
38 Evaluation of QT interval duration and dispersion and proposed clinical criteria in diagnosis of long QT syndrome in patients with a genetically uniform type of LQT1. J Am Coll Cardiol 1998 0.96
39 Female sex steroid receptors in normal, hyperplastic and carcinomatous endometrium. The relationship to serum steroid hormones and gonadotropins and changes during medroxyprogesterone acetate administration. Int J Cancer 1979 0.96
40 Response of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndrome. Heart 2001 0.95
41 Melanocortin-3-receptor gene variants in morbid obesity. Int J Obes Relat Metab Disord 2003 0.95
42 Polymorphisms of the apolipoprotein and angiotensin converting enzyme genes in young North Karelian patients with coronary heart disease. Hum Genet 1994 0.94
43 Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes. J Am Coll Cardiol 1999 0.94
44 Oestrogen-induced progesterone receptor in human uterus. J Steroid Biochem 1976 0.92
45 Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences. Finnish FH-group. Ann Med 2001 0.92
46 DNA polymorphisms of apolipoprotein A-I/C-III and insulin genes in familial hypertriglyceridemia and coronary heart disease. Atherosclerosis 1987 0.91
47 Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol. Atherosclerosis 1990 0.91
48 677 C-->T polymorphism of the methylenetetrahydrofolate reductase gene and preeclampsia. Obstet Gynecol 2000 0.90
49 Common polymorphism of the vitamin D receptor gene is associated with variation of peak bone mass in young finns. Calcif Tissue Int 1996 0.88
50 APOE alleles in Alzheimer's disease and vascular dementia in a population aged 85+. Neurobiol Aging 1996 0.87
51 Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21. Eur J Hum Genet 2001 0.87
52 Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhood blood pressure. Am J Hypertens 1999 0.86
53 Identification of a deletion in the LDL receptor gene. A Finnish type of mutation. FEBS Lett 1988 0.86
54 Does apolipoprotein E influence learning and memory in the nondemented oldest old? Int Psychogeriatr 2001 0.86
55 Deletion of exon 15 of the LDL receptor gene is associated with a mild form of familial hypercholesterolemia. FH-Espoo. Arterioscler Thromb 1993 0.86
56 The beta-adrenergic system in man: physiological and pathophysiological response. Regulation of receptor density and functioning. Scand J Clin Lab Invest Suppl 1990 0.85
57 Polymorphisms of the gene encoding cholesterol ester transfer protein and serum lipoprotein levels in subjects with and without coronary heart disease. Hum Genet 1991 0.85
58 Glucocorticoid receptors in adrenocorticoid disorders. J Clin Endocrinol Metab 1980 0.85
59 Prevalence of familial hypercholesterolemia among young north Karelian patients with coronary heart disease: a study based on diagnosis by polymerase chain reaction. J Lipid Res 1993 0.85
60 A single-base substitution in exon 6 of the androgen receptor gene causing complete androgen insensitivity: the mutated receptor fails to transactivate but binds to DNA in vitro. Hum Mol Genet 1993 0.84
61 Polymorphism of the beta 3-adrenergic receptor gene in morbid obesity. Int J Obes Relat Metab Disord 1996 0.84
62 Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study. Ann Med 2001 0.84
63 Markers for the gene ob and serum leptin levels in human morbid obesity. Hum Genet 1997 0.84
64 Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred. Hum Mutat 1998 0.84
65 XbaI and c/g polymorphisms of the apolipoprotein B gene locus are associated with serum cholesterol and LDL-cholesterol levels in Finland. Atherosclerosis 1988 0.84
66 Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over. Neurosci Lett 2000 0.84
67 Diagnosis of heterozygous familial hypercholesterolemia. DNA analysis complements clinical examination and analysis of serum lipid levels. Arterioscler Thromb 1992 0.84
68 Relation of collagen type I alpha 1 (COLIA 1) and vitamin D receptor genotypes to bone mass, turnover, and fractures in early postmenopausal women and to hip fractures in elderly people. Eur J Intern Med 2001 0.83
69 Serum low density lipoprotein cholesterol level and cholesterol absorption efficiency are influenced by apolipoprotein B and E polymorphism and by the FH-Helsinki mutation of the low density lipoprotein receptor gene in familial hypercholesterolemia. Arterioscler Thromb 1991 0.83
70 Apolipoprotein A-IFin. Dominantly inherited hypoalphalipoproteinemia due to a single base substitution in the apolipoprotein A-I gene. Arterioscler Thromb Vasc Biol 1997 0.83
71 Progesterone-binding protein in human myometrium. Binding site concentration in relation to endogenous progesterone and estradiol-17beta levels. J Steroid Biochem 1979 0.83
72 Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men. Forensic Sci Int 1999 0.82
73 Polymorphisms of the genes encoding apoproteins A-I, B, C-III, and E and LDL receptor, and cholesterol and LDL metabolism during increased cholesterol intake. Common alleles of the apoprotein E gene show the greatest regulatory impact. Arterioscler Thromb Vasc Biol 1997 0.82
74 Reduced level of cellular glucocorticoid receptors in patients with anorexia nervosa. Horm Metab Res 1982 0.82
75 The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12-p13 and description of a DNA polymorphism. Hum Genet 1989 0.82
76 Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients. Genes Immun 2012 0.82
77 The common pentanucleotide polymorphism of the 3'-untranslated region of the leptin receptor gene is associated with serum insulin levels and the risk of type 2 diabetes in non-diabetic men: a prospective case-control study. J Intern Med 2000 0.82
78 Genetic risk factors and ischaemic cerebrovascular disease: role of common variation of the genes encoding apolipoproteins and angiotensin-converting enzyme. Ann Med 1998 0.82
79 Effect of acute ethanol intake on thromboxane and prostacyclin in human. Life Sci 1982 0.81
80 DNA polymorphisms of the apolipoprotein B and A-I/C-III genes are associated with variations of serum low density lipoprotein cholesterol level in childhood. J Lipid Res 1991 0.81
81 Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5% of cases with very low serum HDL cholesterol levels. Arterioscler Thromb Vasc Biol 1998 0.81
82 Association of seropositivity for Chlamydia pneumoniae and coronary artery disease in heterozygous familial hypercholesterolaemia. Lancet 1999 0.81
83 Effect of the antimalarial drug halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A. Am J Cardiol 2001 0.81
84 Apolipoprotein A-IFIN (Leu159-->Arg) mutation affects lecithin cholesterol acyltransferase activation and subclass distribution of HDL but not cholesterol efflux from fibroblasts. Arterioscler Thromb Vasc Biol 1997 0.81
85 Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease. Scand J Gastroenterol 1999 0.80
86 A common pentanucleotide polymorphism of the 3'-untranslated part of the leptin receptor gene generates a putative stem-loop motif in the mRNA and is associated with serum insulin levels in obese individuals. Int J Obes Relat Metab Disord 1998 0.80
87 Progesterone receptor and regulation of progestin action in mammalian tissues. Med Biol 1978 0.80
88 Glucocorticoid receptors and glucocorticoid sensitivity of human leukemic cells. Int J Cancer 1980 0.80
89 Functional polymorphism in IL12B promoter site is associated with ulcerative colitis. Inflamm Bowel Dis 2011 0.80
90 Reduction of lymphocytic beta-adrenoceptor level in chronic alcoholics and rapid reversal after ethanol withdrawal. Eur J Clin Invest 1990 0.79
91 Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment. J Intern Med 1995 0.79
92 Vitamin D receptor polymorphism and treatment of psoriasis with calcipotriol. Br J Dermatol 1997 0.79
93 A novel point mutation (Pro84-->Ser) of the low density lipoprotein receptor gene in a family with moderate hypercholesterolemia. Clin Genet 1997 0.79
94 Familial moderate hypercholesterolemia caused by Asp235-->Glu mutation of the LDL receptor gene and co-occurrence of a de novo deletion of the LDL receptor gene in the same family. Arterioscler Thromb Vasc Biol 1997 0.79
95 Glucocorticoid receptors and responsiveness of normal and neoplastic human adrenal cortex. J Clin Endocrinol Metab 1985 0.78
96 Prevalence of factor V Leiden in young adults with retinal vein occlusion. Thromb Haemost 1997 0.78
97 Stanol ester margarine alone and with simvastatin lowers serum cholesterol in families with familial hypercholesterolemia caused by the FH-North Karelia mutation. Arterioscler Thromb Vasc Biol 2000 0.78
98 Molecular characterization of minor gene rearrangements in Finnish patients with heterozygous familial hypercholesterolemia: identification of two common missense mutations (Gly823-->Asp and Leu380-->His) and eight rare mutations of the LDL receptor gene. Am J Hum Genet 1995 0.78
99 Lipoproteins and their genetic variation in subjects with and without angiographically verified coronary artery disease. Arterioscler Thromb 1992 0.78
100 Cytochemical demonstration of estrogen binding sites in breast cancer by estradiol covalently linked to horseradish peroxidase. Eur J Cancer Clin Oncol 1985 0.78
101 Cholesterol absorption and metabolism and LDL kinetics in healthy men with different apoprotein E phenotypes and apoprotein B Xba I and LDL receptor Pvu II genotypes. Arterioscler Thromb Vasc Biol 1995 0.78
102 Lack of correlation between the glucocorticoid receptor density and the in vitro growth-inhibitory effect of dexamethasone in human leukemia cell lines. J Recept Res 1980 0.78
103 Functional analysis of the C(-188)A polymorphism of the human leptin promoter. Hum Genet 1998 0.77
104 No evidence for linkage between familial hypertriglyceridemia and apolipoprotein B, apolipoprotein C-III or lipoprotein lipase genes. Hum Genet 1994 0.77
105 Genetic polymorphism of the apolipoprotein B gene locus influences serum LDL cholesterol level in familial hypercholesterolemia. Hum Genet 1989 0.77
106 Glucocorticoid receptors in hairy-cell leukemia. Int J Cancer 1982 0.77
107 Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects. Int J Obes Relat Metab Disord 1997 0.77
108 Steroid binding properties of estradiol receptors in human breast cancer. Med Biol 1975 0.77
109 Propranolol attenuates exercise-induced increment in human lymphocytic beta-adrenergic receptors. Scand J Clin Lab Invest 1988 0.77
110 DNA polymorphisms of apolipoprotein B and AI/CIII genes and response to gemfibrozil treatment. Clin Pharmacol Ther 1991 0.77
111 Serum progesterone, estradiol, and estriol before and during induced labor. Am J Obstet Gynecol 1980 0.77
112 Progestin receptors in human tissues: concentrations and binding kinetics. J Steroid Biochem 1977 0.77
113 Effect of propranolol and pindolol on the up-regulation of lymphocytic beta adrenoceptors during acute submaximal physical exercise. A placebo-controlled double-blind study. J Cardiovasc Pharmacol 1990 0.77
114 Genetic polymorphism of platelet glycoprotein IIIa in patients with acute myocardial infarction and acute ischaemic stroke. J Cardiovasc Risk 1999 0.77
115 Variability gene effects of DNA polymorphisms at the apo B, apo A I/C III and apo E loci on serum lipids: the Cardiovascular Risk in Young Finns Study. Clin Genet 1994 0.77
116 Apolipoprotein E, cognitive function, and dementia in a general population aged 85 years and over. Int Psychogeriatr 2000 0.77
117 No evidence for mutations of the leptin or leptin receptor genes in women with polycystic ovary syndrome. Mol Hum Reprod 2000 0.76
118 A history of stressful life events, prolonged mental stress and arrhythmic events in inherited long QT syndrome. Heart 2010 0.76
119 Physical exercise after alcohol intake: effect on plasma catecholamines and lymphocytic beta-adrenergic receptors. Alcohol Clin Exp Res 1991 0.76
120 A novel amino acid substitution (His183-->Gln) in exon 5 of the lipoprotein lipase gene results in loss of catalytic activity: phenotypic expression of the mutant gene in a heterozygous state. J Lipid Res 1994 0.76
121 Human granulosa cells contain insulin-like growth factor-binding protein (IGF BP-1) mRNA. Clin Endocrinol (Oxf) 1990 0.76
122 Association of apolipoprotein E and B polymorphisms with serum lipids. Ann Med 1991 0.76
123 Beta-adrenergic receptors of human lymphocytes in physically active and immobilized subjects: characterization by a polyethylene glycol precipitation assay. Scand J Clin Lab Invest 1987 0.76
124 Steroid induced osteoporosis. BMJ 1992 0.75
125 Work stress and the long QT syndrome: high job strain and effort-reward imbalance at work associated with arrhythmic risk in the long QT syndrome. J Occup Environ Med 2013 0.75
126 Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency. Arterioscler Thromb Vasc Biol 1995 0.75
127 [What is known about genetic factors behind chronic inflammatory bowel diseases?]. Duodecim 2000 0.75
128 [Genes and cholesterol]. Duodecim 1988 0.75
129 HFE haemochromatosis gene mutations in liver transplant patients. Scand J Gastroenterol 2001 0.75
130 High-dose folic acid treatment for red-cell aplasia. Lancet 1995 0.75
131 Screening for a prevalent LDL receptor mutation in patients with severe hypercholesterolaemia. Hum Genet 1991 0.75
132 [The family of lipoprotein receptors is growing]. Duodecim 1995 0.75
133 [Principles and problems of drug therapy in pregnancy]. Duodecim 1986 0.75
134 [Thromboembolic complications during pregnancy]. Duodecim 1988 0.75
135 Response of the beta-adrenergic system to maximal dynamic exercise in congestive heart failure secondary to idiopathic dilated cardiomyopathy. Am J Cardiol 1989 0.75
136 Development of Cushing's disease in a patient with anorexia nervosa. J Endocrinol Invest 1984 0.75
137 Lymphocytic beta-adrenergic receptors in X-linked muscular dystrophy. J Neurol Sci 1989 0.75
138 [Recent genetic association in Alzheimer's disease]. Duodecim 1996 0.75
139 [Research on Finnish genes]. Duodecim 1994 0.75
140 Review article: mechanism of action of female sex steroids. Acta Obstet Gynecol Scand Suppl 1976 0.75
141 [SETTI-Study and antioxidants--more questions than answers]. Duodecim 1994 0.75
142 Partial purification and characterization of progesterone-binding protein from pregnant guinea pig uterus. Biochem Biophys Res Commun 1972 0.75
143 Ligand specificity of progesterone-binding proteins in guinea pig and sheep. J Steroid Biochem 1974 0.75
144 Molecular genetics of familial hypercholesterolemia. Adv Exp Med Biol 1991 0.75
145 [Steroid hormone receptors and endocrine treatment of breast cancer]. Duodecim 1977 0.75
146 [Familial hypercholesterolemia--from gene defect to cholesterol accumulation]. Duodecim 1992 0.75
147 Deletions of the low density lipoprotein receptor gene underlying familial hypercholesterolaemia: screening by polymerase chain reaction using pooled DNA and blood samples. Mol Cell Probes 1997 0.75
148 Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs. Eur J Hum Genet 1999 0.75
149 [Adrenergic receptors]. Duodecim 1989 0.75
150 Arg 506 Gln factor V mutation (factor V Leiden) in patients with familial hypercholesterolaemia. Thromb Haemost 1996 0.75
151 Amenorrhea with low normal thyroid function and thyroxine treatment. Int J Gynaecol Obstet 1980 0.75
152 [DNA and its message in disease]. Duodecim 1986 0.75
153 DNA, hyperlipidaemias and atherosclerosis. Ann Clin Res 1986 0.75
154 A novel deletion/inversion mutation in the low-density lipoprotein receptor gene as a cause of heterozygous familial hypercholesterolemia. Hum Mutat 1996 0.75
155 [Genetic background and DNA diagnostics of hemochromatosis]. Duodecim 1998 0.75
156 Progesterone-binding proteins from endometrium and myometrium of sheep uterus: a comparative study. Acta Endocrinol (Copenh) 1975 0.75
157 [Hereditary polymorphic ventricular tachycardia as a cause of syncopes and sudden cardiac deaths]. Duodecim 2000 0.75
158 A novel polymorphism of apolipoprotein A-IV is the result of an asparagine to serine substitution at residue 127. Biochim Biophys Acta 1992 0.75
159 [Genes, HDL cholesterol and risk of coronary artery disease]. Duodecim 1999 0.75
160 Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses: a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia. Mol Cell Probes 1999 0.75
161 [Anonymous but irreplaceable experts in scientific journals]. Duodecim 1993 0.75
162 Aseptic necrosis of the femoral head during pregnancy. Obstet Gynecol 1988 0.75
163 Use of polymerase chain reaction to detect heterozygous familial hypercholesterolemia. Clin Chem 1990 0.75
164 Effect of acute ethanol intake and hangover on the levels of plasma and urinary catecholamines and lymphocytic beta-adrenergic receptors. Alcohol Clin Exp Res 1989 0.75
165 CARD15 frameshift mutation in patients with CROHN disease is associated with immune dysregulation. Scand J Gastroenterol 2004 0.75
166 Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene. Hum Genet 1995 0.75
167 Progesterone-binding protein in human myometrium. Influence of metal ions on binding. J Clin Endocrinol Metab 1974 0.75
168 [Mode of action of steroid hormones]. Duodecim 1976 0.75
169 Glucocorticoid receptors and their role in human disease. Ann Clin Res 1980 0.75
170 [Lipoproteins, genetic factors and Finnish coronary heart disease]. Duodecim 1991 0.75
171 Glucocorticoid receptors in human polymorphonuclear and mononuclear leucocytes. Concentrations and binding characteristics. Scand J Haematol 1981 0.75