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Connection

Ruth Lininger to Loss of Heterozygosity

This is a "connection" page, showing publications Ruth Lininger has written about Loss of Heterozygosity.
Connection Strength

0.571
  1. Lininger RA, Zhuang Z, Man Y, Park WS, Emmert-Buck M, Tavassoli FA. Loss of heterozygosity is detected at chromosomes 1p35-36 (NB), 3p25 (VHL), 16p13 (TSC2/PKD1), and 17p13 (TP53) in microdissected apocrine carcinomas of the breast. Mod Pathol. 1999 Dec; 12(12):1083-9.
    View in: PubMed
    Score: 0.178
  2. Lininger RA, Fujii H, Man YG, Gabrielson E, Tavassoli FA. Comparison of loss heterozygosity in primary and recurrent ductal carcinoma in situ of the breast. Mod Pathol. 1998 Dec; 11(12):1151-9.
    View in: PubMed
    Score: 0.166
  3. Lininger RA, Park WS, Man YG, Pham T, MacGrogan G, Zhuang Z, Tavassoli FA. LOH at 16p13 is a novel chromosomal alteration detected in benign and malignant microdissected papillary neoplasms of the breast. Hum Pathol. 1998 Oct; 29(10):1113-8.
    View in: PubMed
    Score: 0.164
  4. Man YG, Magrane GG, Lininger RA, Shen T, Kuhls E, Bratthauer GL. Morphologically similar epithelial and stromal cells in primary bilateral breast tumors display different genetic profiles: implications for treatment. Appl Immunohistochem Mol Morphol. 2004 Dec; 12(4):305-14.
    View in: PubMed
    Score: 0.063
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.