DavidR.WittMD

PubMed

• 21 citations
  Prevalence of Spontaneous Clearance of Hepatitis C Virus Infection Doubled From 1998 to 2017
  Suk I. Seo, Michael J. Silverberg, Leo B. Hurley, Joanna Ready, Varun Saxena, David R. Witt, C. Bradley Hare, Jamila H. Champsi, Daniel G. Korn, Mary Patricia Pauly, S...> ;Clinical Gastroenterology and Hepatology. 2020 Feb 1
• 19 citations
  A successful program preventing nonventilator hospital-acquired pneumonia in a large hospital system.
  Cristine C Lacerna, Donna Patey, Lawrence Block, Sejal Naik, Yulia Kevorkova, Jessica Galin, Melanie Parker, Robin Betts, Stephen Parodi, David R. Witt> ;Infection Control and Hospital Epidemiology. 2020 Jan 15
• 47 citations
  Disparities in Initiation of Direct-Acting Antiviral Agents for Hepatitis C Virus Infection in an Insured Population.
  Marcus, J. L., Marcus, J. L., Marcus, J. L., Marcus, J. L., Marcus, J. L., Hurley, L. B., Hurley, L. B., Hurley, L. B., Hurley, L. B., Hurley, L. B., Chamberland, S., ...> ;Public health reports (Washington, D.C. : 1974). 2018 May 12
• 16 citations
  Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis
  Ganka Douglas, Joanna Wiszniewska, Mark H. Lipson, David R. Witt, Taryn McDowell, Mara Sifry-Platt, Michio Hirano, William J. Craigen, Lee-Jun C. Wong> ;Journal of Human Genetics. 2011 Oct 20
• 11 citations
  Identification of copy number variants associated with BPES-like phenotypes.
  Antoinet C.J. Gijsbers, Barbara D'haene, Yvonne Hilhorst-Hofstee, Marcel M.A.M. Mannens, Beate Albrecht, Joerg Seidel, David R. Witt, Melissa K. Maisenbacher, Bart Loe...> ;Human Genetics. 2008 Oct 25
• 21 citations
  Partial deletion of the short arm of chromosome 3 (3p25----3pter). Further delineation of the clinical phenotype.
  David R. Witt, Brian Biedermann, Judith G. Hall> ;Clinical Genetics. 2008 Jun 28
• 71 citations
  Growth curves for height in Noonan syndrome.
  David R. Witt, B. Keena, Judith G. Hall, Judith Allanson> ;Clinical Genetics. 2008 Apr 23
• 238 citations
  Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.
  David P. Kelsell, Elizabeth E. Norgett, H Unsworth, Muy-Teck Teh, Thomas Cullup, Charles A. Mein, Patricia J.C. Dopping-Hepenstal, Beverly A. Dale, Gianluca Tadini, Ph...> ;American Journal of Human Genetics. 2005 May 1
• 315 citations
  Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel
  Michael S. Watson, Garry R. Cutting, Robert J. Desnick, Deborah A. Driscoll, Katherine W. Klinger, Michael T. Mennuti, Glenn E. Palomaki, Bradley W. Popovich, Victoria...> ;Genetics in Medicine. 2004 Sep 1
• 8 citations
  Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: three additional cases.
  Alison M. Elliott, Elizabeth R. Roeder, David R. Witt, David L. Rimoin, Ralph S. Lachman> ;American Journal of Medical Genetics. 2000 Dec 18
• 17 citations
  Issues in implementing prenatal screening for cystic fibrosis: results of a working conference.
  James E. Haddow, Linda A. Bradley, Glenn E. Palomaki, Richard A. Doherty, Barbara A. Bernhardt, David J. H. Brock, Brian Cheuvront, George C. Cunningham, Alan E. Donne...> ;Genetics in Medicine. 1999 May 1
• 42 citations
  Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients
  Barbara J. Trask, Heather C Mefford, Ger van den Engh, Hillary Massa, Ramesh C. Juyal, Lorraine Potocki, Brenda Finucane, Dianne N. Abuelo, David R. Witt, Ellen Mageni...> ;Human Genetics. 1996 Nov 7
• 292 citations
  Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
  Laura E. Warner, Max J. Hilz, Stanley H. Appel, James M. Killian, Edwin H. Kolodny, George Karpati, Stirling Carpenter, Gordon V. Watters, Calvin Wheeler, David R. Wit...> ;Neuron. 1996 Sep 1
• 68 citations
  Cystic fibrosis heterozygote screening in 5,161 pregnant women.
  David R. Witt, C Schaefer, P Hallam, S Wi, B Blumberg, A Fishbach, J Holtzman, S Kornfeld, R Lee, L Nemzer, R Palmer> ;American Journal of Human Genetics. 1996 Apr 1
• 34 citations
  Desbuquois syndrome: Clinical, radiographic, and morphologic characterization
  M. Shohat, Ralph S. Lachman, Helen E. Gruber, Y. E. Hsia, M S Golbus, David R. Witt, Bodell A, Christine R. Bryke, Hogge Wa, David L. Rimoin> ;American Journal of Medical Genetics. 1994 Aug 1
• 344 citations
  A mutation in CFTR produces different phenotypes depending on chromosomal background
  S. Kiesewetter, Milan Macek, C. Davis, Sheila Curristin, Chin-Shyan Chu, C. Graham, A. E. Shrimpton, S. M. Cashman, Lap-Chee Tsui, J. Mickle, Jean A. Amos, W. E. Highs...> ;Nature Genetics. 1993 Nov 1
• 323 citations
  Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs
  Brenda Richards, Joel Skoletsky, Anthony P. Shuber, Rosemary Balfour, Robert C Stern, Henry L. Dorkin, Richard B. Parad, David R. Witt, Katherine W. Klinger> ;Human Molecular Genetics. 1993 Feb 1
• 51 citations
  Bleeding diathesis in Noonan syndrome: A common association
  David R. Witt, Bardbara C. McGillivray, Judith Allanson, H. E. Hughes, William E. Hathaway, Alvin Zipursky, Judith G. Hall, John M. Opitz, James F. Reynolds> ;American Journal of Medical Genetics. 1988 Oct 1
• 110 citations
  Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature
  David R. Witt, H. E. Hoyme, J. Zonana, David K. Manchester, J. P. Fryns, J. G. Stevenson, Cynthia J. Curry, Judith G. Hall> ;American Journal of Medical Genetics. 1987 Aug 1
• 2 citations
  Hypergonadotropic hypogonadism with congestive cardiomyopathy.
  David R. Witt, Vazken M. Der Kaloustian> ;American Journal of Medical Genetics. 1987 Apr 1
• 36 citations
  Arrested epidermal morphogenesis in three newborn infants with a fatal genetic disorder (restrictive dermopathy).
  Karen A. Holbrook, Beverly A. Dale, David R. Witt, Michael R. Hayden, Helga V. Toriello> ;The Journal of Investigative Dermatology. 1987 Mar 1
• 6 citations
  Abnormal keratinization in restrictive dermopathy.
  Beverly A. Dale, Karen A. Holbrook, David R. Witt, Helge V. Toriello> ;Current Problems in Dermatology. 1987 Jan 1
• 2 citations
  Approach to multiple congenital anomaly syndromes.
  David R. Witt, Judith G. Hall> ;Seminars in Perinatology. 1985 Apr 1
• 70 citations
  Restrictive dermopathy: A newly recognized autosomal recessive skin dysplasia
  David R. Witt, Michael R. Hayden, Holbrook Ka, Beverly A. Dale, Virginia J. Baldwin, Glenn Taylor> ;American Journal of Medical Genetics. 1986 Aug 1
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