|
1
|
A gene map of the human genome.
|
Science
|
1996
|
14.32
|
|
2
|
A physical map of 30,000 human genes.
|
Science
|
1998
|
12.43
|
|
3
|
A combined linkage-physical map of the human genome.
|
Am J Hum Genet
|
2004
|
4.60
|
|
4
|
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22.
|
Hum Mol Genet
|
1994
|
2.83
|
|
5
|
The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery.
|
Genet Epidemiol
|
2011
|
2.54
|
|
6
|
A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4.
|
Proc Natl Acad Sci U S A
|
2001
|
2.42
|
|
7
|
Age-related macular degeneration. Clinical features in a large family and linkage to chromosome 1q.
|
Arch Ophthalmol
|
1998
|
2.19
|
|
8
|
NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees.
|
Am J Med Genet
|
1998
|
2.09
|
|
9
|
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
|
Nat Genet
|
1993
|
1.73
|
|
10
|
MAP-O-MAT: internet-based linkage mapping.
|
Bioinformatics
|
2004
|
1.35
|
|
11
|
Genome-wide search for schizophrenia susceptibility loci: the NIMH Genetics Initiative and Millennium Consortium.
|
Am J Med Genet
|
1998
|
1.26
|
|
12
|
A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM.
|
Genomics
|
1993
|
1.26
|
|
13
|
Power loss for multiallelic transmission/disequilibrium test when errors introduced: GAW11 simulated data.
|
Genet Epidemiol
|
1999
|
1.10
|
|
14
|
Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study.
|
Hum Reprod
|
2013
|
1.03
|
|
15
|
An integrated transcript map of human chromosome 1p35-p36.
|
Genomics
|
1997
|
1.03
|
|
16
|
Report of the second international workshop on human chromosome 1 mapping 1995.
|
Cytogenet Cell Genet
|
1996
|
1.03
|
|
17
|
A comparison of two algorithms, MultiMap and gene mapping system, for automated construction of genetic linkage maps.
|
Genet Epidemiol
|
1999
|
1.00
|
|
18
|
Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994.
|
Cytogenet Cell Genet
|
1994
|
0.99
|
|
19
|
Loss of heterozygosity for chromosome 14q in neuroblastoma.
|
Med Pediatr Oncol
|
2001
|
0.97
|
|
20
|
Detailed molecular analysis of 1p36 in neuroblastoma.
|
Med Pediatr Oncol
|
2001
|
0.91
|
|
21
|
Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13.
|
Pediatr Res
|
1994
|
0.91
|
|
22
|
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods.
|
Hum Genet
|
1995
|
0.87
|
|
23
|
An integrated genetic linkage map of the laboratory rat.
|
Mamm Genome
|
1998
|
0.86
|
|
24
|
A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2.
|
Hum Mol Genet
|
1995
|
0.85
|
|
25
|
Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.
|
Am J Hum Genet
|
1995
|
0.85
|
|
26
|
A radiation hybrid map of 95 STSs spanning human chromosome 13q.
|
Genomics
|
1995
|
0.84
|
|
27
|
Report and abstracts of the Third International Workshop on Human Chromosome 13 Mapping. Tarrytown, New York, October 29-31, 1995.
|
Cytogenet Cell Genet
|
1996
|
0.78
|
|
28
|
A comprehensive view of human chromosome 1.
|
Genome Res
|
1999
|
0.77
|
|
29
|
Report of the fifth international workshop on human chromosome 1 mapping 1999.
|
Cytogenet Cell Genet
|
1999
|
0.76
|
|
30
|
Report and abstracts of the third international workshop on human chromosome 1 mapping 1997.
|
Cytogenet Cell Genet
|
1997
|
0.76
|
|
31
|
Genomic mapping and mapping databases.
|
Methods Biochem Anal
|
2001
|
0.75
|
|
32
|
Chromosome 13 and chromosome 2 (CA)n polymorphisms.
|
Hum Mol Genet
|
1994
|
0.75
|