Published in Ugeskr Laeger on July 31, 2000
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Familial isolated primary hyperparathyroidism. Clin Endocrinol (Oxf) (1994) 1.42
A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3. Mol Psychiatry (2002) 1.34
Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders. Thorax (2008) 1.34
Asthma and atopy - a total genome scan for susceptibility genes. Allergy (2002) 1.28
Power of non-parametric linkage analysis in mapping genes contributing to human longevity in long-lived sib-pairs. Genet Epidemiol (2004) 1.27
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Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene. Hum Mol Genet (1996) 1.17
Linkage relationships and gene order around the locus for X-linked retinoschisis. Am J Hum Genet (1988) 1.15
Refined localization of the gene causing X-linked juvenile retinoschisis. Genomics (1991) 1.15
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Mutational screening and association study of glutamate decarboxylase 1 as a candidate susceptibility gene for bipolar affective disorder and schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2005) 1.11
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Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region. Hum Genet (1991) 1.06
A new HindIII restriction fragment length polymorphism in the hemophilia A locus. Hum Genet (1987) 1.04
An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region. Hum Genet (1987) 1.02
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Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11. Hum Genet (1988) 0.99
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Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia. Clin Genet (2004) 0.97
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Logistic regression models for polymorphic and antagonistic pleiotropic gene action on human aging and longevity. Ann Hum Genet (2003) 0.95
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis. Am J Hum Genet (1991) 0.94
A new locus for Seckel syndrome on chromosome 18p11.31-q11.2. Eur J Hum Genet (2001) 0.94
Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21. Hum Genet (1995) 0.92
Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp. Allergy (2004) 0.91
Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12. Hum Genet (1986) 0.91
Allergic rhinitis--a total genome-scan for susceptibility genes suggests a locus on chromosome 4q24-q27. Eur J Hum Genet (2001) 0.90
Gene expression in epithelial ovarian cancer: a study of intratumor heterogeneity. Int J Gynecol Cancer (2007) 0.90
Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies. J Med Genet (2006) 0.89
A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder. Am J Med Genet B Neuropsychiatr Genet (2005) 0.89
Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with bipolar affective disorder. Mol Psychiatry (2002) 0.89
Association analyses suggest GPR24 as a shared susceptibility gene for bipolar affective disorder and schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2006) 0.88
Assignment of the human cardiac troponin I gene (TNNI3) to chromosome 19q13.4 by radiation hybrid mapping. Cytogenet Cell Genet (1997) 0.88
Assessing genetic association with human survival at multi-allelic loci. Biogerontology (2004) 0.88
Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families. Clin Genet (2006) 0.88
Significant linkage between bipolar affective disorder and chromosome 12q24. Psychiatr Genet (1998) 0.88
Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: correlation between genotype and phenotype. J Invest Dermatol (1999) 0.88
A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba. Am J Med Genet B Neuropsychiatr Genet (2006) 0.86
Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands. Am J Med Genet (2002) 0.86
X-linked retinitis pigmentosa: new map studies of XLRP2, and a possible human centromere effect. Hum Genet (1992) 0.85
The CEPH consortium linkage map of human chromosome 15q. Genomics (1992) 0.84
Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics (1990) 0.84
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Susceptibility loci for bipolar affective disorder on chromosome 18? A review and a study of Danish families. Psychiatr Genet (1997) 0.83
Human ClpP protease: cDNA sequence, tissue-specific expression and chromosomal assignment of the gene. FEBS Lett (1995) 0.83
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases. J Med Genet (2006) 0.83
Possible evidence for a common risk locus for bipolar affective disorder and schizophrenia on chromosome 4p16 in patients from the Faroe Islands. Mol Psychiatry (2004) 0.83
Linkage analysis between manic depressive illness and the region on chromosome 12q involved in Darier's disease. Psychiatr Genet (1994) 0.83
Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2. Am J Hum Genet (1992) 0.82
Dopa decarboxylase genotypes may influence age at onset of schizophrenia. Mol Psychiatry (2001) 0.82
An EcoRI polymorphism for the PLAUR gene. Nucleic Acids Res (1991) 0.82
'Indirect' BRCA1/2 testing: a useful approach in hereditary breast and ovarian cancer families without a living affected relative. Clin Genet (2005) 0.81
Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree. J Clin Endocrinol Metab (2000) 0.81
Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients from the Faroe Islands. Mol Psychiatry (2001) 0.81
Multipoint linkage analysis in Menkes disease. Am J Hum Genet (1992) 0.81
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A longitudinal study of the effect of GSTT1 and GSTM1 gene copy number on survival. Mech Ageing Dev (2006) 0.81
An anonymous single copy X-chromosome clone, pTAK8, identifies a frequent RFLP at Xp11-q12(HGM8 no. DXS146). Nucleic Acids Res (1986) 0.81
Significant linkage to chromosome 12q24.32-q24.33 and identification of SFRS8 as a possible asthma susceptibility gene. Thorax (2006) 0.81
The influence of elongation-factor-Tu . GTP and anticodon-anticodon interactions on the anticodon loop conformation of yeast tRNATyr. Eur J Biochem (1981) 0.80
Refined localization of the human alpha-tropomyosin gene (TPM1) by genetic mapping. Cytogenet Cell Genet (1999) 0.80
A possible locus for manic depressive illness on chromosome 16p13. Psychiatr Genet (1995) 0.80
No linkage and association of atopy to chromosome 16 including the interleukin-4 receptor gene. Allergy (2001) 0.80
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. Am J Med Genet B Neuropsychiatr Genet (2003) 0.79
Photosensitized crosslinking of tRNA to the P-, A- and R-sites of Escherichia coli ribosomes. Biochimie (1982) 0.79
No association between a neuronal nitric oxide synthase (NOS1) gene polymorphism on chromosome 12q24 and bipolar disorder. Am J Med Genet B Neuropsychiatr Genet (2004) 0.79
Two-dimensional DNA typing of human pedigrees: spot pattern characterization and segregation. Genomics (1995) 0.79
An anonymous X-chromosomal clone identifying a frequent RFLP at Xp21-22 (HGM8 provisional no. DXS207). Nucleic Acids Res (1986) 0.78
Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1 alpha subunit. Hum Mol Genet (1994) 0.78
Acute hypoxia induces upregulation of microRNA-210 expression in glioblastoma spheroids. CNS Oncol (2015) 0.78
Cathepsin K gene mutations and 1q21 haplotypes in at patients with pycnodysostosis in an outbred population. Eur J Hum Genet (2000) 0.78
Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder. Mol Psychiatry (1999) 0.78
Linkage analysis between manic-depressive illness and markers on the long arm of chromosome 11. Am J Med Genet (1995) 0.77
A haplotype-based study of lithium responding patients with bipolar affective disorder on the Faroe Islands. Psychiatr Genet (1999) 0.77
Candidate region linkage analysis in twins discordant or concordant for depression symptomatology. Am J Med Genet B Neuropsychiatr Genet (2009) 0.77
Gene diagnosis in X-linked ichthyosis. Arch Dermatol Res (1989) 0.76
Multivariate modelling of endophenotypes associated with the metabolic syndrome in Chinese twins. Diabetologia (2010) 0.76
Support for the possible locus on chromosome 4p16 for bipolar affective disorder. Mol Psychiatry (1998) 0.76
Assignment of the human mitochondrial tryptophanyl-tRNA synthetase (WARS2) to 1p13.3-->p13.1 by radiation hybrid mapping. Cytogenet Cell Genet (1998) 0.76
Three DNA markers for hypophosphataemic rickets. Hum Genet (1992) 0.76
Linkage analysis between manic-depressive illness and the region on chromosome 15q involved in Prader-Willi syndrome, including two GABAA receptor subtype genes. Hum Hered (1994) 0.75
Assignment of the human tryptophanyl-tRNA synthetase gene (WARS) to chromosome 14q32.2 --> q32.32. Cytogenet Cell Genet (1996) 0.75
Assignment of the human skeletal muscle [FC12]a-actin gene (ACTA1) to chromosome 1q42.13-->q42.2 by radiation hybrid mapping. Cytogenet Cell Genet (1998) 0.75
Mapping of 34 minisatellite loci resolved by two-dimensional DNA typing. Cytogenet Cell Genet (1997) 0.75
Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis. Hum Genet (1997) 0.75
Linking genotype to aorto-coronary atherosclerosis: a model using familial hypercholesterolemia and aorto-coronary calcification. Ann Hum Genet (1999) 0.75
Linkage study between manic-depressive illness and chromosome 21. Am J Med Genet (1996) 0.75
Linkage analysis between manic depressive illness and the dopamine beta-hydroxylase gene. Psychiatr Genet (1994) 0.75
Maternal HLA class II allogenotypes are markers for the predisposition to fetal losses in families of women with unexplained recurrent fetal loss. Eur J Immunogenet (1995) 0.75
A functional variant of the serotonin transporter gene in families with bipolar affective disorder. J Affect Disord (1998) 0.75
Two-dimensional DNA typing as a genetic marker system in humans. Cytogenet Cell Genet (1995) 0.75
No evidence of linkage between manic depressive illness and the dopa decarboxylase gene or nearby region on chromosome 7p. Psychiatr Genet (1995) 0.75
The EUROGEM map of human chromosome 15. Eur J Hum Genet (1994) 0.75
A TaqI and a BamHI polymorphism in the COL4A4 gene on chromosome 2q35-37. Clin Genet (1995) 0.75