Connection

Co-Authors

This is a "connection" page, showing publications co-authored by VICKI D HUFF and LOUISE C STRONG.
Connection Strength

0.625
  1. Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour. J Med Genet. 2016 06; 53(6):385-8.
    View in: PubMed
    Score: 0.133
  2. Re: Familial renal cell carcinoma: hereditary or coincidental? J Urol. 1991 Jul; 146(1):168.
    View in: PubMed
    Score: 0.099
  3. Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation. J Clin Invest. 2011 Jan; 121(1):174-83.
    View in: PubMed
    Score: 0.095
  4. Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors. Cancer Res. 1998 Apr 01; 58(7):1387-90.
    View in: PubMed
    Score: 0.039
  5. Evidence for genetic heterogeneity in familial Wilms' tumor. Cancer Res. 1997 May 15; 57(10):1859-62.
    View in: PubMed
    Score: 0.037
  6. WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences. Am J Hum Genet. 1995 Jan; 56(1):84-90.
    View in: PubMed
    Score: 0.031
  7. Structural analysis of the human nov proto-oncogene and expression in Wilms tumor. Oncogene. 1994 Sep; 9(9):2729-32.
    View in: PubMed
    Score: 0.031
  8. Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. Am J Hum Genet. 1991 May; 48(5):997-1003.
    View in: PubMed
    Score: 0.024
  9. Parental origin of de novo constitutional deletions of chromosomal band 11p13. Am J Hum Genet. 1990 Jul; 47(1):155-60.
    View in: PubMed
    Score: 0.023
  10. A panel of restriction fragment length polymorphisms for chromosomal band 11p13. Hum Genet. 1990 Feb; 84(3):253-7.
    View in: PubMed
    Score: 0.022
  11. Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature. 1988 Nov 24; 336(6197):377-8.
    View in: PubMed
    Score: 0.021
  12. An EcoRI polymorphism associated with a human genomic clone from band 11p13. Nucleic Acids Res. 1987 Sep 25; 15(18):7651.
    View in: PubMed
    Score: 0.019
  13. Mutation in the PAX6 gene in twenty patients with aniridia. Hum Mutat. 2000; 15(4):332-9.
    View in: PubMed
    Score: 0.011
  14. Pleuropulmonary blastoma: a marker for familial disease. J Pediatr. 1996 Feb; 128(2):220-4.
    View in: PubMed
    Score: 0.008
  15. Genetic mosaicism in normal tissues of Wilms' tumour patients. Nat Genet. 1993 Feb; 3(2):127-31.
    View in: PubMed
    Score: 0.007
  16. RNA expression of the WT1 gene in Wilms' tumors in relation to histology. J Natl Cancer Inst. 1992 Feb 05; 84(3):181-7.
    View in: PubMed
    Score: 0.006
  17. Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus. Genomics. 1991 May; 10(1):293-7.
    View in: PubMed
    Score: 0.006
  18. Familial renal cell carcinoma: hereditary or coincidental? J Urol. 1990 Oct; 144(4):849-51.
    View in: PubMed
    Score: 0.006
  19. An XmnI polymorphism detected by a human genomic clone from chromosomal band 11p13 [D11S416]. Nucleic Acids Res. 1990 Feb 11; 18(3):689.
    View in: PubMed
    Score: 0.006
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.