Published in Nat Genet on April 01, 1994
Signatures of population expansion in microsatellite repeat data. Genetics (1998) 5.76
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Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. Am J Hum Genet (2001) 2.50
The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. Am J Hum Genet (2000) 2.50
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An enhanced linkage map of the sheep genome comprising more than 1000 loci. Genome Res (2001) 1.97
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Single nucleotide polymorphism discovery in rainbow trout by deep sequencing of a reduced representation library. BMC Genomics (2009) 1.81
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An integrated 4249 marker FISH/RH map of the canine genome. BMC Genomics (2004) 1.61
A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet (2006) 1.59
Genome scan for human obesity and linkage to markers in 20q13. Am J Hum Genet (1999) 1.58
Linkage of inflammatory bowel disease to human chromosome 6p. Am J Hum Genet (1999) 1.57
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Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3. Am J Hum Genet (1996) 1.32
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Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease. Gut (2001) 1.23
A first generation integrated map of the rainbow trout genome. BMC Genomics (2011) 1.23
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A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p. Am J Hum Genet (1995) 1.19
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Toward fully automated genotyping: allele assignment, pedigree construction, phase determination, and recombination detection in Duchenne muscular dystrophy. Am J Hum Genet (1994) 1.07
A deer (subfamily Cervinae) genetic linkage map and the evolution of ruminant genomes. Genetics (2002) 1.07
A second generation integrated map of the rainbow trout (Oncorhynchus mykiss) genome: analysis of conserved synteny with model fish genomes. Mar Biotechnol (NY) (2011) 1.06
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination. Am J Hum Genet (1995) 1.05
Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q. Am J Hum Genet (1996) 1.05
A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus). Mamm Genome (2007) 1.04
Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy. Am J Hum Genet (1995) 1.03
Identification of the gene encoding Brain Cell Membrane Protein 1 (BCMP1), a putative four-transmembrane protein distantly related to the Peripheral Myelin Protein 22 / Epithelial Membrane Proteins and the Claudins. BMC Genomics (2001) 1.01
Refining the map and defining flanking markers of the gene for autosomal recessive polycystic kidney disease on chromosome 6p21.1-p12. Am J Hum Genet (1994) 1.00
Exonic SINE insertion in STK38L causes canine early retinal degeneration (erd). Genomics (2010) 1.00
Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22. J Clin Invest (1996) 0.99
First-generation linkage map of the gray, short-tailed opossum, Monodelphis domestica, reveals genome-wide reduction in female recombination rates. Genetics (2004) 0.98
Mapping Loci for fox domestication: deconstruction/reconstruction of a behavioral phenotype. Behav Genet (2010) 0.96
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A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2. Am J Hum Genet (1994) 0.95
Linkage of combined factors V and VIII deficiency to chromosome 18q by homozygosity mapping. J Clin Invest (1997) 0.94
The synaptonemal complex and meiotic recombination in humans: new approaches to old questions. Chromosoma (2006) 0.92
Multilocus analysis for gene-centromere mapping using first polar bodies and secondary oocytes. Genetics (1995) 0.92
Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency. Am J Hum Genet (1996) 0.91
Detection and Validation of QTL Affecting Bacterial Cold Water Disease Resistance in Rainbow Trout Using Restriction-Site Associated DNA Sequencing. PLoS One (2015) 0.91
Mapping and sequencing of the canine NRAMP1 gene and identification of mutations in leishmaniasis-susceptible dogs. Infect Immun (2002) 0.91
Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridization. Hum Genet (1995) 0.90
Loss of heterozygosity on chromosome 22 in ovarian carcinoma is distal to and is not accompanied by mutations in NF2 at 22q12. Br J Cancer (1994) 0.89
Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases. Br J Ophthalmol (1996) 0.89
A genome-wide linkage analysis for reproductive traits in F2 Large White × Meishan cross gilts. Anim Genet (2014) 0.88
Mitochondrial neurogastrointestinal encephalomyopathy syndrome maps to chromosome 22q13.32-qter. Am J Hum Genet (1998) 0.88
Radiation hybrid mapping of cataract genes in the dog. Mol Vis (2006) 0.88
Detection of QTL in rainbow trout affecting survival when challenged with Flavobacterium psychrophilum. Mar Biotechnol (NY) (2013) 0.88
The structural basis of molecular genetic deletions. An integration of classical cytogenetic and molecular analyses in pancreatic adenocarcinoma. Am J Pathol (1997) 0.88
A microsatellite linkage map of striped bass (Morone saxatilis) reveals conserved synteny with the three-spined stickleback (Gasterosteus aculeatus). Mar Biotechnol (NY) (2011) 0.87
Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet (1998) 0.87
Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24. J Med Genet (1995) 0.87
Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuria. Proc Natl Acad Sci U S A (1995) 0.87
A microsatellite-based, physically anchored linkage map for the gray, short-tailed opossum (Monodelphis domestica). Chromosome Res (2007) 0.86
Coat colour in dogs: identification of the merle locus in the Australian shepherd breed. BMC Vet Res (2006) 0.86
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21. Am J Hum Genet (1995) 0.85
Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion. Am J Hum Genet (1996) 0.85
Systematic evaluation of map quality: human chromosome 22. Am J Hum Genet (2002) 0.85
COL9A2 and COL9A3 mutations in canine autosomal recessive oculoskeletal dysplasia. Mamm Genome (2010) 0.84
Autosomal recessive juvenile parkinsonism maps to 6q25.2-q27 in four ethnic groups: detailed genetic mapping of the linked region. Am J Hum Genet (1998) 0.84
A high-resolution comparative map of canine Chromosome 5q14.3-q33 constructed utilizing the 1.5x canine genome sequence. Mamm Genome (2004) 0.82
Pedigree and genotype errors in the Framingham Heart Study. BMC Genet (2003) 0.82
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa. Am J Hum Genet (1996) 0.82
IQCB1 and PDE6B mutations cause similar early onset retinal degenerations in two closely related terrier dog breeds. Invest Ophthalmol Vis Sci (2013) 0.81
Identification of single nucleotide polymorphism markers associated with bacterial cold water disease resistance and spleen size in rainbow trout. Front Genet (2015) 0.79
An alternative to radiation hybrid mapping for large-scale genome analysis in barley. Mol Genet Genomics (2005) 0.79
Radiation hybrid mapping of the canine type I and type IV collagen gene subfamilies. Funct Integr Genomics (2003) 0.78
No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. Am J Hum Genet (1998) 0.78
Quantitative trait loci affecting response to crowding stress in an F(2) generation of rainbow trout produced through phenotypic selection. Mar Biotechnol (NY) (2013) 0.78
Genetic influences on response to novel objects and dimensions of personality in papio baboons. Behav Genet (2015) 0.78
Survey sequencing and radiation hybrid mapping to construct comparative maps. Methods Mol Biol (2008) 0.78
QTL affecting stress response to crowding in a rainbow trout broodstock population. BMC Genet (2012) 0.77
The immunoglobulin heavy-chain variable region in insulin-dependent diabetes mellitus: affected-sib-pair analysis and association studies. Am J Hum Genet (1996) 0.77
A comprehensive view of human chromosome 1. Genome Res (1999) 0.77
Chromosomal mapping of canine-derived BAC clones to the red fox and American mink genomes. J Hered (2009) 0.77
Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders. Mol Vis (2009) 0.76
Enhanced genetic maps from family-based disease studies: population-specific comparisons. BMC Med Genet (2011) 0.76
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