PubRank

S Ingvarsson

Author PubWeight™ 46.13‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients. Cancer Res 1996 2.43
2 Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13. Cancer Res 1995 2.14
3 Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations. Cancer Res 1997 2.03
4 Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc Natl Acad Sci U S A 1988 1.76
5 Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype. Am J Hum Genet 1996 1.75
6 Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival. Br J Cancer 1999 1.71
7 Mapping loss of heterozygosity at chromosome 13q: loss at 13q12-q13 is associated with breast tumour progression and poor prognosis. Eur J Cancer 1998 1.28
8 Altered expression of E-cadherin in breast cancer. patterns, mechanisms and clinical significance. Eur J Cancer 2000 1.14
9 Identification of a novel splice-site mutation of the BRCA1 gene in two breast cancer families: screening reveals low frequency in Icelandic breast cancer patients. Hum Mutat 1998 1.05
10 Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations. Br J Cancer 1995 1.04
11 Chromosome alterations and E-cadherin gene mutations in human lobular breast cancer. Br J Cancer 1999 1.04
12 High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancer. Eur J Cancer 2002 1.00
13 Loss of heterozygosity at chromosome 7q in human breast cancer: association with clinical variables. Anticancer Res 1997 0.94
14 Alterations of E-cadherin and beta-catenin in gastric cancer. BMC Cancer 2001 0.94
15 The effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequences. Int J Oncol 2000 0.94
16 Replication error in colorectal carcinoma: association with loss of heterozygosity at mismatch repair loci and clinicopathological variables. Anticancer Res 1999 0.93
17 Immature B cells in bone marrow express Fas/FasL. Scand J Immunol 2000 0.92
18 Multiple chromosomal rearrangements in a spontaneously arising t(6;7) rat immunocytoma juxtapose c-myc and immunoglobulin heavy chain sequences. Proc Natl Acad Sci U S A 1986 0.91
19 Drosophila homolog of the murine Int-1 protooncogene. Proc Natl Acad Sci U S A 1988 0.89
20 Gene localization on sorted chromosomes: definitive evidence on the relative positioning of genes participating in the mouse plasmacytoma-associated typical translocation. Proc Natl Acad Sci U S A 1985 0.87
21 Amplification of c-myc and pvt-1 homologous sequences in acute nonlymphatic leukemia. Leuk Res 1988 0.86
22 Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer trait. Clin Genet 1995 0.84
23 Nucleotide sequence of the rat Bmyc gene. Oncogene 1989 0.84
24 Loss of heterozygosity on chromosome 9 in human breast cancer: association with clinical variables and genetic changes at other chromosome regions. Int J Cancer 1995 0.83
25 Human interdigitating dendritic cells induce isotype switching and IL-13-dependent IgM production in CD40-activated naive B cells. J Immunol 2000 0.83
26 Loss of heterozygosity on chromosome arm 3p in nasopharyngeal carcinoma. Genes Chromosomes Cancer 1996 0.82
27 Similarities and differences in the regulation of N-myc and c-myc genes in murine embryonal carcinoma cells. Exp Cell Res 1987 0.82
28 High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers. Oncogene 1998 0.82
29 High frequency of LOH at chromosome 18q in human breast cancer: association with high S-phase fraction and low progesterone receptor content. Anticancer Res 1998 0.81
30 Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice. Proc Natl Acad Sci U S A 2001 0.81
31 Chromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomes. Genomics 1991 0.81
32 A gene near the D3F15S2 site on 3p is expressed in normal human kidney but not or only at a severely reduced level in 11 of 15 primary renal cell carcinomas (RCC). Oncogene 1990 0.80
33 Differences in c-myc and pvt-1 amplification in SEWA sarcoma sublines selected for adherent or non-adherent growth. Int J Cancer 1990 0.79
34 Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer. J Med Genet 2000 0.78
35 Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3. Hum Genet 1995 0.78
36 Analysis of the fragile histidine triad (FHIT) gene in lobular breast cancer. Eur J Cancer 2000 0.78
37 Specific polypeptide differences in normal versus malignant human breast tissues by two-dimensional electrophoresis. Breast Cancer Res Treat 1987 0.78
38 Rapid polarization of Th2 cells during induction of antigen-specific IgE antibodies in vitro. Clin Exp Allergy 2000 0.78
39 Characterization of specific IgE response in vitro against protein and drug allergens using atopic and normal donors. Allergy 2002 0.77
40 Replication error in human breast cancer: comparison with clinical variables and family history of cancer. Oncol Rep 1999 0.77
41 Elevated expression of c-myc and N-myc produces distinct changes in nuclear fine structure and chromatin organization. Oncogene 1988 0.77
42 Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2. Eur J Cancer 1998 0.76
43 Urinary system tumours in a family. Eur J Cancer 1993 0.76
44 Chromosomal assignment of five cancer-associated rat genes: two thyroid hormone receptor (ERBA) genes, two ERBB genes and the retinoblastoma gene. Oncogene 1991 0.76
45 Isoenzyme pattern and subcellular localization of hexokinases in human breast cancer and nonpathological breast tissue. Int J Cancer 1984 0.75
46 CD40 employs p38 MAP kinase in IgE isotype switching. Biochem Biophys Res Commun 2001 0.75
47 Mapping of chromosome-3 alterations in human breast-cancer using microsatellite PCR markers - correlation with clinical-variables. Int J Oncol 1995 0.75
48 The most frequently lost allelic site in human renal cell carcinoma (D3F15S2) on the short arm of chromosome 3 has homologous sequences on rat chromosome 8. Cytogenet Cell Genet 1991 0.75
49 c-myc activation in spontaneous rat immunocytomas containing a 6;7 chromosomal translocation. Curr Top Microbiol Immunol 1986 0.75
50 Loss of heterozygosity at chromosome 1p in human breast cancer. Int J Oncol 1996 0.75
51 Loss of heterozygosity at chromosome 6q correlates with tumor progression and patient survival. Int J Oncol 1995 0.75
52 Recombinant plasmid expressing the entire coding region of the Bmyc putative protein. J Clin Lab Immunol 1990 0.75
53 Catabolite repressive effects of 5-thio-D-glucose on Saccharomyces cerevisiae. J Gen Microbiol 1986 0.75