|
1
|
Apolipoprotein E, dementia, and cortical deposition of beta-amyloid protein.
|
N Engl J Med
|
1995
|
3.54
|
|
2
|
Prevalence of Alzheimer's disease in very elderly people: a prospective neuropathological study.
|
Neurology
|
2001
|
1.98
|
|
3
|
Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts.
|
J Am Coll Cardiol
|
1999
|
1.68
|
|
4
|
APOE epsilon4 does not predict mortality, cognitive decline, or dementia in the oldest old.
|
Neurology
|
2000
|
1.51
|
|
5
|
A novel mutation of the fibrillin gene causing ectopia lentis.
|
Genomics
|
1994
|
1.36
|
|
6
|
Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings.
|
J Hypertens
|
2000
|
1.19
|
|
7
|
Deficient expression of the gene coding for decorin in a lethal form of Marfan syndrome.
|
J Biol Chem
|
1990
|
1.15
|
|
8
|
An extra cysteine in one of the non-calcium-binding epidermal growth factor-like motifs of the FBN1 polypeptide is connected to a novel variant of Marfan syndrome.
|
J Clin Invest
|
1994
|
1.13
|
|
9
|
Lack of association of apolipoprotein E allele epsilon 4 with late-onset Alzheimer's disease among Finnish centenarians.
|
Neurology
|
1995
|
1.11
|
|
10
|
Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes.
|
J Am Coll Cardiol
|
1999
|
0.94
|
|
11
|
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
|
|
12
|
APOE alleles in Alzheimer's disease and vascular dementia in a population aged 85+.
|
Neurobiol Aging
|
1996
|
0.87
|
|
13
|
Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes.
|
Hum Mutat
|
1998
|
0.87
|
|
14
|
Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhood blood pressure.
|
Am J Hypertens
|
1999
|
0.86
|
|
15
|
Does apolipoprotein E influence learning and memory in the nondemented oldest old?
|
Int Psychogeriatr
|
2001
|
0.86
|
|
16
|
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
|
|
17
|
Markers for the gene ob and serum leptin levels in human morbid obesity.
|
Hum Genet
|
1997
|
0.84
|
|
18
|
Polymorphism of the beta 3-adrenergic receptor gene in morbid obesity.
|
Int J Obes Relat Metab Disord
|
1996
|
0.84
|
|
19
|
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
|
|
20
|
Progestin induction of 17 beta-hydroxysteroid dehydrogenase enzyme protein in the T-47D human breast-cancer cell line.
|
Int J Cancer
|
1990
|
0.82
|
|
21
|
Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndrome.
|
Biochem J
|
1994
|
0.82
|
|
22
|
DNA diagnostics of the Marfan syndrome: application of amplifiable polymorphic markers.
|
Eur J Hum Genet
|
1994
|
0.80
|
|
23
|
Vitamin D receptor polymorphism and treatment of psoriasis with calcipotriol.
|
Br J Dermatol
|
1997
|
0.79
|
|
24
|
Elucidation of the gene defect in Marfan syndrome. Success by two complementary research strategies.
|
FEBS Lett
|
1992
|
0.78
|
|
25
|
Novel polymorphism of the human ob gene promoter in lean and morbidly obese subjects.
|
Int J Obes Relat Metab Disord
|
1997
|
0.77
|
|
26
|
Apolipoprotein E, cognitive function, and dementia in a general population aged 85 years and over.
|
Int Psychogeriatr
|
2000
|
0.77
|
|
27
|
The reality of hand hygiene compliance in two Finnish hospitals based on watching and analysing two hospital reality television series.
|
J Hosp Infect
|
2010
|
0.75
|
|
28
|
Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs.
|
Eur J Hum Genet
|
1999
|
0.75
|
|
29
|
New source for electroweak baryogenesis in the minimal supersymmetric standard model.
|
Phys Rev Lett
|
2000
|
0.75
|
|
30
|
[Genes and hypertension].
|
Duodecim
|
2000
|
0.75
|
|
31
|
[The Marfan syndrome gene is localized].
|
Duodecim
|
1990
|
0.75
|