I Dunham

Author PubWeight™ 290.38‹?›

Top papers

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