Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Initial sequencing and analysis of the human genome.
|
Nature
|
2001
|
212.86
|
2
|
A gene map of the human genome.
|
Science
|
1996
|
14.32
|
3
|
A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome.
|
Nat Genet
|
2000
|
4.78
|
4
|
The DNA sequence and analysis of human chromosome 6.
|
Nature
|
2003
|
4.75
|
5
|
An SNP map of human chromosome 22.
|
Nature
|
2000
|
2.99
|
6
|
Rapid assessment of S. cerevisiae mating type by PCR.
|
Trends Genet
|
1990
|
2.75
|
7
|
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy.
|
Nat Genet
|
1998
|
2.51
|
8
|
A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence.
|
Genome Res
|
2001
|
2.49
|
9
|
The DNA sequence and biological annotation of human chromosome 1.
|
Nature
|
2006
|
2.42
|
10
|
Human major histocompatibility complex contains genes for the major heat shock protein HSP70.
|
Proc Natl Acad Sci U S A
|
1989
|
2.34
|
11
|
Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.
|
Am J Hum Genet
|
1995
|
2.19
|
12
|
The extent of linkage disequilibrium in four populations with distinct demographic histories.
|
Am J Hum Genet
|
2000
|
2.03
|
13
|
Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia.
|
EMBO J
|
1987
|
2.00
|
14
|
Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region.
|
EMBO J
|
1989
|
1.97
|
15
|
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease.
|
Hum Mol Genet
|
1993
|
1.76
|
16
|
The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X.
|
Nature
|
2001
|
1.63
|
17
|
Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH.
|
Oncogene
|
2006
|
1.40
|
18
|
Psoriasis upregulated phorbolin-1 shares structural but not functional similarity to the mRNA-editing protein apobec-1.
|
J Invest Dermatol
|
1999
|
1.37
|
19
|
The DNA sequence and analysis of human chromosome 13.
|
Nature
|
2004
|
1.33
|
20
|
Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.
|
Lancet
|
1992
|
1.31
|
21
|
The organization of the gamma-glutamyl transferase genes and other low copy repeats in human chromosome 22q11.
|
Genome Res
|
1997
|
1.31
|
22
|
A bacterial artificial chromosome-based framework contig map of human chromosome 22q.
|
Proc Natl Acad Sci U S A
|
1996
|
1.30
|
23
|
RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer.
|
Oncogene
|
2006
|
1.25
|
24
|
Organization of the human immunoglobulin lambda light-chain locus on chromosome 22q11.2.
|
Hum Mol Genet
|
1995
|
1.24
|
25
|
The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family.
|
Proc Natl Acad Sci U S A
|
1999
|
1.23
|
26
|
DNA sequence and analysis of human chromosome 9.
|
Nature
|
2004
|
1.21
|
27
|
Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q.
|
J Med Genet
|
1999
|
1.13
|
28
|
Characterization of a second human clathrin heavy chain polypeptide gene (CLH-22) from chromosome 22q11.
|
Hum Mol Genet
|
1996
|
1.09
|
29
|
SAM: a system for iteratively building marker maps.
|
Comput Appl Biosci
|
1995
|
1.07
|
30
|
A sequence-based integrated map of chromosome 22.
|
Genome Res
|
2001
|
1.04
|
31
|
Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma gene.
|
Hum Mol Genet
|
1994
|
1.02
|
32
|
The development and application of automated gridding for efficient screening of yeast and bacterial ordered libraries.
|
Genomics
|
1992
|
1.01
|
33
|
From long range mapping to sequence-ready contigs on human chromosome 6.
|
DNA Seq
|
1997
|
0.93
|
34
|
beta-1,3-Glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation.
|
Mol Psychiatry
|
2003
|
0.92
|
35
|
Characterization of the human synaptogyrin gene family.
|
Hum Genet
|
1998
|
0.91
|
36
|
Mechanism of spreading of the highly related neurofibromatosis type 1 (NF1) pseudogenes on chromosomes 2, 14 and 22.
|
Eur J Hum Genet
|
2000
|
0.88
|
37
|
Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12.
|
Hum Mol Genet
|
1993
|
0.87
|
38
|
Fine-mapping, genomic organization, and transcript analysis of the human ubiquitin-conjugating enzyme gene UBE2L3.
|
Genomics
|
1998
|
0.85
|
39
|
Mapping and complex expression pattern of the human NPAP60L nucleoporin gene.
|
Cytogenet Cell Genet
|
1999
|
0.85
|
40
|
A YAC contig spanning the ataxia-telangiectasia locus (groups A and C) at 11q22-q23.
|
Genomics
|
1994
|
0.82
|
41
|
Mapping human chromosomes.
|
Curr Opin Genet Dev
|
1995
|
0.81
|
42
|
Polymorphism of the human complement component C4.
|
Exp Clin Immunogenet
|
1990
|
0.81
|
43
|
Physical mapping of chromosome 6: a strategy for the rapid generation of sequence-ready contigs.
|
DNA Seq
|
1996
|
0.80
|
44
|
Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human.
|
Mamm Genome
|
1999
|
0.79
|
45
|
A panel of human chromosome 22-specific sequence tagged sites.
|
Genomics
|
1992
|
0.79
|
46
|
Identification and characterization of NF1-related loci on human chromosomes 22, 14 and 2.
|
Hum Genet
|
1996
|
0.77
|
47
|
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresis.
|
Hum Genet
|
1990
|
0.77
|
48
|
An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin.
|
Genomics
|
2000
|
0.77
|
49
|
Generation of alphoid DNA probes for fluorescence in situ hybridization (FISH) using the polymerase chain reaction.
|
Methods Mol Biol
|
1994
|
0.77
|
50
|
Molecular mapping of the HLA class II region in HLA-DR3 associated idiopathic membranous nephropathy.
|
Kidney Int Suppl
|
1993
|
0.76
|
51
|
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification.
|
Genomics
|
1992
|
0.76
|
52
|
A random STS strategy for construction of YAC contigs spanning defined chromosomal regions.
|
Genomics
|
1992
|
0.76
|
53
|
Data disclosure in the human genome project.
|
Mol Med Today
|
1998
|
0.75
|
54
|
Genetic mapping of 14 short tandem repeat polymorphisms on human chromosome 22.
|
Hum Genet
|
1994
|
0.75
|
55
|
Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.
|
Immunodeficiency
|
1993
|
0.75
|
56
|
Molecular mapping of the HLA-linked complement genes and the RCA linkage group.
|
Exp Clin Immunogenet
|
1988
|
0.75
|
57
|
YAC library storage and transport.
|
Methods Mol Biol
|
1996
|
0.75
|
58
|
Lessons from the sequence of human chromosome 22.
|
Ernst Schering Res Found Workshop
|
2002
|
0.75
|
59
|
YAC library screening. I. Preparation of hybridization filters and PCRpools.
|
Methods Mol Biol
|
1996
|
0.75
|
60
|
The Chromosome 6 database at the Sanger Centre.
|
DNA Seq
|
1997
|
0.75
|
61
|
Third single chromosome 6 workshop: meeting report.
|
DNA Seq
|
1997
|
0.75
|
62
|
DNA rescue by the vectorette method.
|
Methods Mol Biol
|
1996
|
0.75
|
63
|
A molecular cytogenetic clone resource for chromosome 22.
|
Chromosome Res
|
1999
|
0.75
|
64
|
YAC library screening. II. Hybridization and PCR-based screening protocols.
|
Methods Mol Biol
|
1996
|
0.75
|
65
|
Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.
|
Genomics
|
1995
|
0.75
|
66
|
Report of the Fourth International Chromosome 6 Workshop 1999. 10-12 June 1999. Cambridge, UK. Abstracts.
|
Cytogenet Cell Genet
|
2000
|
0.75
|