16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy Get access

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GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics Open Access

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Genome-wide meta-analysis of common variant differences between men and women Open Access

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Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension Get access

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Genome-wide association study identifies two loci strongly affecting transferrin glycosylation Get access

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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study Open Access

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Two trans-acting eQTLs modulate the penetrance of PRPF31 mutations Get access

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Human–mouse differences in the embryonic expression patterns of developmental control genes and disease genes Get access

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Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development Get access

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An α-Tectorin Gene Defect Causes a Newly Identified Autosomal Recessive Form of Sensorineural Pre-Lingual Non-Syndromic Deafness, DFNB21 Get access

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A Susceptibility Locus for Early-Onset Non-Insulin Dependent (Type 2) Diabetes Mellitus Maps to Chromosome 20q, Proximal to the Phosphoenolpyruvate Carboxykinase Gene Get access

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Genetic studies and molecular structures: the dystrophin associated complex Get access

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Mapping a gene (SRN1) to chromosome 1q25–q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis Get access

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A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene Get access

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Dinucleotide repeat at the D15S129 locus Get access

A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites Get access

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Dinucleotide repeat polymorphism at the locus D15S222 Get access

Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy Get access

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