A decreasing gradient of 374F allele frequencies in the skin pigmentation gene SLC45A2, from the north of West Europe to North Africa.

Characterization of the biological processes shaping the genetic structure of the Italian population. BMC Genet (2015) 0.77

The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population. PLoS One (2014) 0.76

Demographic events and evolutionary forces shaping European genetic diversity. Cold Spring Harb Perspect Biol (2014) 0.75

Vitamin D status and risk for malignant cutaneous melanoma: recent advances. Eur J Cancer Prev (2017) 0.75

Extreme mtDNA homogeneity in continental Asian populations. Am J Phys Anthropol (2002) 1.47

Multiplex amplified product-length polymorphism analysis of 36 mitochondrial single-nucleotide polymorphisms for haplogrouping of East Asian populations. Electrophoresis (2005) 1.06

De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy. Hum Mutat (2013) 0.98

Caucasian-specific allele in non-synonymous single nucleotide polymorphisms of the gene encoding deoxyribonuclease I-like 3, potentially relevant to autoimmunity, produces an inactive enzyme. Clin Chim Acta (2009) 0.96

Association of functional gene polymorphisms of matrix metalloproteinase (MMP)-1, MMP-3 and MMP-9 with the progression of chronic liver disease. J Gastroenterol Hepatol (2005) 0.94

The genotypes of IL-1 beta and MMP-3 are associated with the prognosis of HCV-related hepatocellular carcinoma. Intern Med (2010) 0.90

The 35delG mutation in the connexin 26 gene (GJB2) associated with congenital deafness: European carrier frequencies and evidence for its origin in ancient Greece. Genet Test (2005) 0.90

North African Berber and Arab influences in the western Mediterranean revealed by Y-chromosome DNA haplotypes. Hum Biol (2006) 0.88

Three Japanese Patients with Beta-Ketothiolase Deficiency Who Share a Mutation, c.431A>C (H144P) in ACAT1 : Subtle Abnormality in Urinary Organic Acid Analysis and Blood Acylcarnitine Analysis Using Tandem Mass Spectrometry. JIMD Rep (2011) 0.87

Population distribution of the methionine allele at the PRNP codon 129 polymorphism in Europe and the Middle East. Hum Biol (2008) 0.87

Impact of ionizing radiation on the life cycle of Saccharomyces cerevisiae Ty1 retrotransposon. Yeast (2005) 0.86

Global analysis of single nucleotide polymorphisms in the exons of human deoxyribonuclease I-like 1 and 2 genes. Electrophoresis (2010) 0.83

Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects. Genet Test (2008) 0.83

Genetic variants associated with arsenic metabolism within human arsenic (+3 oxidation state) methyltransferase show wide variation across multiple populations. Arch Toxicol (2010) 0.82

Genetic and expression analysis of all non-synonymous single nucleotide polymorphisms in the human deoxyribonuclease I-like 1 and 2 genes. Electrophoresis (2010) 0.82

Forensic species identification based on size variation of mitochondrial DNA hypervariable regions. Int J Legal Med (2008) 0.81

Three single nucleotide polymorphisms leading to non-synonymous amino acid substitution in the human ribonuclease 2 and angiogenin genes exhibit markedly less genetic heterogeneity in six populations. Cell Biochem Funct (2008) 0.80

The association of MMP-1, -3 and -9 genotypes with the prognosis of HCV-related hepatocellular carcinoma patients. Res Commun Mol Pathol Pharmacol (2005) 0.80

Genetic and expression analysis of all 7 non-synonymous single nucleotide polymorphisms in the human deoxyribonuclease II gene, with potential relevance to autoimmunity. Clin Chim Acta (2009) 0.79

Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I. J Inherit Metab Dis (2011) 0.78

Monozygotic twins discordant for Klippel-Feil syndrome. Pediatr Neurol (2006) 0.78

Complete mitochondrial DNA sequence of a tadpole shrimp (Triops cancriformis) and analysis of museum samples. Electrophoresis (2002) 0.78

Variation of interleukin 8 -251 A>T polymorphism in worldwide populations and intra-ethnic differences in Japanese populations. Clin Chim Acta (2006) 0.77

The population distribution of the Met allele at the PRNP129 polymorphism (a high risk factor for Creutzfeldt-Jakob disease) in various regions of France and in West Europe. Infect Genet Evol (2005) 0.77

Simultaneous determination of seven informative Y chromosome SNPs to differentiate East Asian, European, and African populations. Leg Med (Tokyo) (2011) 0.77

Near fixation of 374l allele frequencies of the skin pigmentation gene SLC45A2 in Africa. Biochem Genet (2013) 0.77

Simultaneous genotyping of 11 non-synonymous SNPs in the 4 glutathione peroxidase genes using the multiplex single base extension method. Clin Chim Acta (2008) 0.77

Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia. Brain Dev (2003) 0.76

Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's disease. Genet Test (2006) 0.76

Recent progress in mitochondrial DNA analysis. Leg Med (Tokyo) (2005) 0.76

Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2. Electrophoresis (2011) 0.76

Design and synthesis of APTCs (aminopyrrolidinetricarboxylic acids): identification of a new group III metabotropic glutamate receptor selective agonist. Bioorg Med Chem Lett (2006) 0.76

Allele frequencies of a SNP and a 27-bp deletion that are the determinant of earwax type in the ABCC11 gene. Leg Med (Tokyo) (2007) 0.75

Nonsynonymous single-nucleotide polymorphisms of the human apoptosis-related endonuclease--DNA fragmentation factor beta polypeptide, endonuclease G, and Flap endonuclease-1--genes show a low degree of genetic heterogeneity. DNA Cell Biol (2011) 0.75

Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene. J Forensic Sci (2003) 0.75

Y-chromosome DNA haplotype XI in Eastern Europe. Hum Biol (2003) 0.75

Global genetic analysis of all single nucleotide polymorphisms in exons of the human deoxyribonuclease I-like 3 gene and their effect on its catalytic activity. Electrophoresis (2011) 0.75

Origin and evolution of gene for prolactin-induced protein. Gene (2006) 0.75

Cutis laxa with frontoparietal cortical malformation: a novel type of congenital disorder of glycosylation. Eur J Paediatr Neurol (2008) 0.75

Population genetics of 17 Y-chromosomal STR loci in Japanese. Forensic Sci Int Genet (2008) 0.75

A novel 56-bp variable tandem repeat polymorphism in the human deoxyribonuclease I gene and its population data. Leg Med (Tokyo) (2004) 0.75

Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution. Leg Med (Tokyo) (2012) 0.75

Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1. Leg Med (Tokyo) (2006) 0.75

Allele frequencies and haplotypes for 28 Y-STRs in Ovambo population. Leg Med (Tokyo) (2009) 0.75

Y-chromosome DNA haplotypes in Jews: comparisons with Lebanese and Palestinians. Genet Test (2003) 0.75

Development of genotyping methods for single nucleotide polymorphism in the human pancreatic ribonuclease gene (RNASE1) and their application to population studies. Biochem Genet (2008) 0.75

[Y-chromosome haplotypes in Corsica]. C R Biol (2002) 0.75