WilliamPAllenMD

PubMed

• Dysregulations of sonic hedgehog signaling in MED12-related X-linked intellectual disability disorders.
  Srivastava, S.,Niranjan, T.,May, M. M.,Tarpey, P.,Allen, W.,Hackett, A.,Jouk, P. S.,Raymond, L.,Briault, S.,Skinner, C.,Toutain, A.,Gecz, J.,Heath, W.,Stevenson, R. E....> ;Mol Genet Genomic Med. 1900 Jan 01
• Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
  Roessler, E., Du, Y., Mullor, J.L., Casas, E., Allen, W.P., Gillessen-Kaesbach, G., Roeder, E.R., Ming, J.E., Ruiz i Altaba, A., Muenke, M.> ;Proc Natl Acad Sci U S A. 2003 Nov 11
• Equal Employment Opportunities Commission issues new interim enforcement guidance on Americans with Disabilities Act.
  Ostrer H, Allen W> ;Am. J. Hum. Genet.. 1993-08-01
• Anticipating unfair uses of genetic information.
  Allen W, Ostrer H> ;Am. J. Hum. Genet.. 1993-07-01
• Insurance and genetic testing: where are we now?
  Ostrer H, Allen W, Crandall LA, Moseley RE, Dewar MA, Nye D, McCrary SV> ;Am. J. Hum. Genet.. 1993-03-01
• Pathogenic diversity of Epstein-Barr virus.
  Spring SB, Schluederberg A, Allen WP, Gruber J> ;J. Natl. Cancer Inst.. 1989-01-04
• 32 citations
  Concept Review of Genital Herpes Vaccines
  William P. Allen, Fred Rapp> ;The Journal of Infectious Diseases. 1982 Mar 1
• Metallothionein protects against the cytotoxic and DNA-damaging effects of nitric oxide.
  Schwarz, M. A., Lazo, J. S., Yalowich, J. C., Allen, W. P., Whitmore, M., Bergonia, H. A., Tzeng, E., Billiar, T. R., Robbins, P. D., Lancaster, J. R.> ;Proc Natl Acad Sci U S A. 1995 May 9
• Prospects for human papillomavirus vaccines and immunotherapies.
  Schreier, A. A., Allen, W. P., Laughlin, C., Gruber, J.> ;J Natl Cancer Inst. 1988 Aug 17
• The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.
  Berg, J. N., Gallione, C. J., Stenzel, T. T., Johnson, D. W., Allen, W. P., Schwartz, C. E., Jackson, C. E., Porteous, M. E., Marchuk, D. A.> ;Am J Hum Genet. 1997 Jul
• Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.
  Schell, U., Wienberg, J., Köhler, A., Bray-Ward, P., Ward, D. E., Wilson, W. G., Allen, W. P., Lebel, R. R., Sawyer, J. R., Campbell, P. L., Aughton, D. J., Punnett, H...> ;Hum Mol Genet. 1996 Feb
• Haploinsufficiency of MBD5 associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures.
  Williams, S. R., Mullegama, S. V., Rosenfeld, J. A., Dagli, A. I., Hatchwell, E., Allen, W. P., Williams, C. A., Elsea, S. H.> ;Eur J Hum Genet. 2010 Apr 01
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