|
1
|
Genetic structure of human populations.
|
Science
|
2002
|
30.91
|
|
2
|
A human genome diversity cell line panel.
|
Science
|
2002
|
14.11
|
|
3
|
The genetic structure and history of Africans and African Americans.
|
Science
|
2009
|
10.65
|
|
4
|
The genetic structure of Pacific Islanders.
|
PLoS Genet
|
2008
|
3.31
|
|
5
|
Ethnic-difference markers for use in mapping by admixture linkage disequilibrium.
|
Am J Hum Genet
|
2002
|
2.29
|
|
6
|
Low levels of genetic divergence across geographically and linguistically diverse populations from India.
|
PLoS Genet
|
2006
|
2.26
|
|
7
|
A 360-kb interchromosomal duplication of the human HYDIN locus.
|
Genomics
|
2006
|
1.91
|
|
8
|
Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits.
|
Hum Mol Genet
|
2007
|
1.77
|
|
9
|
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family.
|
Am J Hum Genet
|
2004
|
1.72
|
|
10
|
STRP screening sets for the human genome at 5 cM density.
|
BMC Genomics
|
2003
|
1.53
|
|
11
|
Markers that discriminate between European and African ancestry show limited variation within Africa.
|
Hum Genet
|
2002
|
1.27
|
|
12
|
Mutant deoxynucleotide carrier is associated with congenital microcephaly.
|
Nat Genet
|
2002
|
1.25
|
|
13
|
Quantitative trait locus analysis of atherosclerosis in an intercross between C57BL/6 and C3H mice carrying the mutant apolipoprotein E gene.
|
Genetics
|
2005
|
1.24
|
|
14
|
Quantifying the increase in average human heterozygosity due to urbanisation.
|
Eur J Hum Genet
|
2008
|
1.17
|
|
15
|
A novel locus for adolescent idiopathic scoliosis on chromosome 12p.
|
J Orthop Res
|
2009
|
1.13
|
|
16
|
Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects.
|
Eur J Hum Genet
|
2008
|
0.98
|
|
17
|
The Iceland map.
|
Nat Genet
|
2002
|
0.96
|
|
18
|
Linkage disequilibrium between STRPs and SNPs across the human genome.
|
Am J Hum Genet
|
2008
|
0.91
|
|
19
|
Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis.
|
Pediatr Nephrol
|
2002
|
0.85
|
|
20
|
Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders.
|
Hum Mutat
|
2006
|
0.81
|
|
21
|
Read all about it: The Lancet's Paper of the Year, 2003.
|
Lancet
|
2003
|
0.79
|
|
22
|
Channel glass-based detection of human short insertion/deletion polymorphisms by tandem hybridization.
|
Mol Biotechnol
|
2007
|
0.78
|
|
23
|
A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformations.
|
Genet Med
|
2011
|
0.75
|
|
24
|
A comparison of hybridization efficiency between flat glass and channel glass solid supports.
|
Mol Biotechnol
|
2007
|
0.75
|