Harvard Catalyst Profiles

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David N. Louis, M.D.

Co-Author

This page shows the publications co-authored by David Louis and James Gusella.
Connection Strength

0.828
  1. A tiger behind many doors: multiple genetic pathways to malignant glioma. Trends Genet. 1995 Oct; 11(10):412-5.
    View in: PubMed
    Score: 0.165
  2. Neuropathology and molecular genetics of neurofibromatosis 2 and related tumors. Brain Pathol. 1995 Apr; 5(2):163-72.
    View in: PubMed
    Score: 0.160
  3. Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2. J Neuropathol Exp Neurol. 1998 Dec; 57(12):1164-7.
    View in: PubMed
    Score: 0.052
  4. Universal absence of merlin, but not other ERM family members, in schwannomas. Am J Pathol. 1997 Dec; 151(6):1649-54.
    View in: PubMed
    Score: 0.048
  5. NF2 gene analysis distinguishes hemangiopericytoma from meningioma. Am J Pathol. 1995 Nov; 147(5):1450-5.
    View in: PubMed
    Score: 0.042
  6. Cloning of a highly conserved human protein serine-threonine phosphatase gene from the glioma candidate region on chromosome 19q13.3. Genomics. 1995 Sep 20; 29(2):533-6.
    View in: PubMed
    Score: 0.041
  7. Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112. J Neuropathol Exp Neurol. 1995 Sep; 54(5):622-6.
    View in: PubMed
    Score: 0.041
  8. MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p. Hum Mol Genet. 1994 Oct; 3(10):1841-5.
    View in: PubMed
    Score: 0.039
  9. The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC. Cancer Res. 1994 Sep 01; 54(17):4760-3.
    View in: PubMed
    Score: 0.038
  10. Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas. Cancer Res. 1994 Jan 01; 54(1):45-7.
    View in: PubMed
    Score: 0.037
  11. Molecular genetics of pediatric brain stem gliomas. Application of PCR techniques to small and archival brain tumor specimens. J Neuropathol Exp Neurol. 1993 Sep; 52(5):507-15.
    View in: PubMed
    Score: 0.036
  12. Accumulation of wild type p53 protein in human astrocytomas. Cancer Res. 1993 Aug 01; 53(15):3465-7.
    View in: PubMed
    Score: 0.036
  13. Assessing Population Level Genetic Instability via Moving Average. Stat Biosci. 2010 Dec; 2(2):120-136.
    View in: PubMed
    Score: 0.030
  14. Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer. Gastroenterology. 1999 Oct; 117(4):831-7.
    View in: PubMed
    Score: 0.014
  15. The NF2 gene and merlin protein in human osteosarcomas. Neurogenetics. 1998 Dec; 2(1):73-4.
    View in: PubMed
    Score: 0.013
  16. A locus for cerebral cavernous malformations maps to chromosome 7q in two families. Genomics. 1995 Jul 20; 28(2):311-4.
    View in: PubMed
    Score: 0.010
  17. Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma. Am J Pathol. 1995 Apr; 146(4):827-32.
    View in: PubMed
    Score: 0.010
  18. Evidence for subarachnoid spread in the development of multiple meningiomas. Brain Pathol. 1995 Jan; 5(1):11-4.
    View in: PubMed
    Score: 0.010
  19. A RsaI polymorphism in the ERCC2 locus. Hum Mol Genet. 1992 Aug; 1(5):355.
    View in: PubMed
    Score: 0.008
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.