BerniceAAllittoMD

PubMed

• 402 citations
  Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens
  Elaine A Sugarman, Narasimhan Nagan, Hui Zhu, Viatcheslav R. Akmaev, Zhaoqing Zhou, Elizabeth M. Rohlfs, Kerry Flynn, Brant C. Hendrickson, Thomas Scholl, Deborah Alex...> ;European Journal of Human Genetics. 2012 Jan 1
• 55 citations
  Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population
  Elizabeth M. Rohlfs, Zhaoqing Zhou, Ruth A. Heim, Narasimhan Nagan, Lynne S Rosenblum, Kerry Flynn, Thomas Scholl, Viatcheslav R. Akmaev, D. Alexa Sirko-Osadsa, Bernic...> ;Clinical Chemistry. 2011 Jun 1
• 117 citations
  Differences in SMN1 allele frequencies among ethnic groups within North America
  Brant C. Hendrickson, Colin Donohoe, Viatcheslav R. Akmaev, Elaine A Sugarman, Paul Labrousse, Leonid Boguslavskiy, Kerry Flynn, Elizabeth M. Rohlfs, Andrew M. Walker,...> ;Journal of Medical Genetics. 2009 Sep 1
• 60 citations
  CFTR mutation distribution among U.S. Hispanic and African American individuals: evaluation in cystic fibrosis patient and carrier screening populations.
  Elaine A Sugarman, Elizabeth M. Rohlfs, Lawrence M. Silverman, Bernice A Allitto> ;Genetics in Medicine. 2004 Sep 1
• 88 citations
  Standards and Guidelines for CFTR Mutation Testing
  Carolyn Sue Richards, Linda A. Bradley, Jean A. Amos, Bernice A Allitto, Wayne W. Grody, Anne Maddalena, Matthew McGinnis, Thomas W. Prior, Bradley W. Popovich, Michae...> ;Genetics in Medicine. 2002 Sep 1
• 63 citations
  The I148T CFTR allele occurs on multiple haplotypes: a complex allele is associated with cystic fibrosis.
  Elizabeth M. Rohlfs, Zhaoqing Zhou, Elaine A Sugarman, Ruth A. Heim, Rhonda G. Pace, Michael R. Knowles, Lawrence M. Silverman, Bernice A Allitto> ;Genetics in Medicine. 2002 Sep 1
• 81 citations
  Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel.
  Ruth A. Heim, Elaine A Sugarman, Bernice A Allitto> ;Genetics in Medicine. 2001 May 1
• 33 citations
  Cystic fibrosis and chromosome abnormalities associated with echogenic fetal bowel.
  Beth M Berlin, Mary E. Norton, Elaine A Sugarman, Judith Tsipis, Bernice A Allitto> ;Obstetrics and Gynecology. 1999 Jul 1
• 2 citations
  Fetal echogenic bowel and a dilated loop of bowel associated with cystic fibrosis (CF mutations ΔF508 and 2183AA→G
  Peggy W. Rush, Subodh Vats, Bernice A Allitto, Faisal Qureshi, Gerald L. Feldman> ;Prenatal Diagnosis. 1998 Jun 1
• Clinical molecular genetic testing.
  Brzustowicz, L. M., Allitto, B. A.> ;J Am Med Womens Assoc. 1997
• Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
  Brzustowicz, L. M., Allitto, B. A., Matseoane, D., Theve, R., Michaud, L., Chatkupt, S., Sugarman, E., Penchaszadeh, G. K., Suslak, L., Koenigsberger, M. R.> ;Am J Hum Genet. 1994 Mar
• Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington''s disease region of chromosome 4.
  Allitto, B. A., McClatchey, A. I., Barnes, G., Altherr, M., Wasmuth, J., Frischauf, A. M., MacDonald, M. E., Gusella, J.> ;Mol Cell Probes. 1992 Dec
• The Huntington''s disease candidate region exhibits many different haplotypes.
  MacDonald, M. E., Novelletto, A., Lin, C., Tagle, D., Barnes, G., Bates, G., Taylor, S., Allitto, B., Altherr, M., Myers, R.> ;Nat Genet. 1992 May
• Detection by PCR of the VNTR polymorphism at D4S95.
  Allitto, B. A., Horn, G. T., Altherr, M. R., Richards, B., McClatchey, A. I., Wasmuth, J. J., Gusella, J. F.> ;Nucleic Acids Res. 1991 Jul 25
• Increased recombination adjacent to the Huntington disease-linked D4S10 marker.
  Allitto, B. A., MacDonald, M. E., Bucan, M., Richards, J., Romano, D., Whaley, W. L., Falcone, B., Ianazzi, J., Wexler, N. S., Wasmuth, J. J.> ;Genomics. 1991 Jan
• Mapping of cosmid clones in Huntington's disease region of chromosome 4.
  Whaley, W. L., Bates, G. P., Novelletto, A., Sedlacek, Z., Cheng, S., Romano, D., Ormondroyd, E., Allitto, B., Lin, C., Youngman, S.> ;Somat Cell Mol Genet. 1991 Jan
• A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.
  Bates, G. P., MacDonald, M. E., Baxendale, S., Sedlacek, Z., Youngman, S., Romano, D., Whaley, W. L., Allitto, B. A., Poustka, A., Gusella, J. F.> ;Am J Hum Genet. 1990 Apr
• Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation.
  Bu?an, M., Zimmer, M., Whaley, W. L., Poustka, A., Youngman, S., Allitto, B. A., Ormondroyd, E., Smith, B., Pohl, T. M., MacDonald, M.> ;Genomics. 1990 Jan
• Clustering of multiallele DNA markers near the Huntington''s disease gene.
  MacDonald, M. E., Cheng, S. V., Zimmer, M., Haines, J. L., Poustka, A., Allitto, B., Smith, B., Whaley, W. L., Romano, D. M., Jagadeesh, J.> ;J Clin Invest. 1989 Sep
• Recombination events suggest potential sites for the Huntington's disease gene.
  MacDonald, M. E., Haines, J. L., Zimmer, M., Cheng, S. V., Youngman, S., Whaley, W. L., Wexler, N., Bucan, M., Allitto, B. A., Smith, B.> ;Neuron. 1989 Aug
• A DNA segment encoding two genes very tightly linked to Huntington''s disease.
  Gilliam, T. C., Bucan, M., MacDonald, M. E., Zimmer, M., Haines, J. L., Cheng, S. V., Pohl, T. M., Meyers, R. H., Whaley, W. L., Allitto, B. A.> ;Science. 1987 Nov 13
• 10 citations
  A family of DNA sequences is reproducibly rearranged in the somatic nucleus of Tetrahymena
  Bernice A. Allitto, Kathleen M. Karrer> ;Nucleic Acids Research. 1986 Oct 1
• 4 citations
  Quantitation of immunoglobulins in the effusions of human ovarian epithelial neoplasms
  William H. Kutteh, Stanley A. Gall, George J. Doellgast, Bernice A. Allitto, Jeffrey R. Dawson> ;American Journal of Obstetrics and Gynecology. 1984 Sep 1
• 21 citations
  Micronucleus-specific DNA sequences in an amicronucleate mutant of Tetrahymena☆
  Kathleen M. Karrer, Susan Stein-Gavens, Bernice A. Allitto> ;Developmental Biology. 1984 Sep 1
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