Connection

IRENE NEWSHAM to Male

This is a "connection" page, showing publications IRENE NEWSHAM has written about Male.
Connection Strength

0.072
  1. Structure, function and diversity of the healthy human microbiome. Nature. 2012 Jun 13; 486(7402):207-14.
    View in: PubMed
    Score: 0.012
  2. A framework for human microbiome research. Nature. 2012 Jun 13; 486(7402):215-21.
    View in: PubMed
    Score: 0.012
  3. Alteration of chromosome 9p21 and/or p16 in benign and dysplastic nevi suggests a role in early melanoma progression (United States). Cancer Causes Control. 2002 Sep; 13(7):675-82.
    View in: PubMed
    Score: 0.006
  4. Novel regions of allelic deletion on chromosome 18p in tumors of the lung, brain and breast. Oncogene. 1998 Dec 31; 17(26):3499-505.
    View in: PubMed
    Score: 0.005
  5. PRUNE2 is a human prostate cancer suppressor regulated by the intronic long noncoding RNA PCA3. Proc Natl Acad Sci U S A. 2015 Jul 07; 112(27):8403-8.
    View in: PubMed
    Score: 0.004
  6. The genomes of two key bumblebee species with primitive eusocial organization. Genome Biol. 2015 Apr 24; 16:76.
    View in: PubMed
    Score: 0.004
  7. The first myriapod genome sequence reveals conservative arthropod gene content and genome organisation in the centipede Strigamia maritima. PLoS Biol. 2014 Nov; 12(11):e1002005.
    View in: PubMed
    Score: 0.004
  8. Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circ Cardiovasc Genet. 2014 Jun; 7(3):335-43.
    View in: PubMed
    Score: 0.004
  9. Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor. Genomics. 1994 Feb; 19(3):433-40.
    View in: PubMed
    Score: 0.003
  10. Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron. 2013 Jan 23; 77(2):235-42.
    View in: PubMed
    Score: 0.003
  11. Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria. Am J Med Genet A. 2011 Sep; 155A(9):2071-7.
    View in: PubMed
    Score: 0.003
  12. Whole-genome sequencing for optimized patient management. Sci Transl Med. 2011 Jun 15; 3(87):87re3.
    View in: PubMed
    Score: 0.003
  13. Clear cell ependymoma: a clinicopathologic and radiographic analysis of 10 patients. Cancer. 2003 Nov 15; 98(10):2232-44.
    View in: PubMed
    Score: 0.002
  14. Meningiomas: loss of heterozygosity on chromosome 10 and marker-specific correlations with grade, recurrence, and survival. Clin Cancer Res. 2003 Oct 01; 9(12):4443-51.
    View in: PubMed
    Score: 0.002
  15. Differential involvement of protein 4.1 family members DAL-1 and NF2 in intracranial and intraspinal ependymomas. Mod Pathol. 2002 May; 15(5):526-31.
    View in: PubMed
    Score: 0.002
  16. Aggressive phenotypic and genotypic features in pediatric and NF2-associated meningiomas: a clinicopathologic study of 53 cases. J Neuropathol Exp Neurol. 2001 Oct; 60(10):994-1003.
    View in: PubMed
    Score: 0.001
  17. Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesis. Proc Natl Acad Sci U S A. 1996 Oct 15; 93(21):11757-62.
    View in: PubMed
    Score: 0.001
  18. The t(11;22)(p15.5;q11.23) in a retroperitoneal rhabdoid tumor also includes a regional deletion distal to CRYBB2 on 22q. Genes Chromosomes Cancer. 1995 Jul; 13(3):145-50.
    View in: PubMed
    Score: 0.001
  19. A new highly polymorphic DNA restriction site marker in the 5' region of the human tyrosine hydroxylase gene (TH) detecting loss of heterozygosity in human embryonal rhabdomyosarcoma. Hum Genet. 1994 Mar; 93(3):349-50.
    View in: PubMed
    Score: 0.001
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.