Gordana Raca

Summary

Affiliation: University of Wisconsin
Country: USA

Publications

  1. ncbi Array comparative genomic hybridization analysis in patients with anophthalmia, microphthalmia, and coloboma
    Gordana Raca
    UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, University of Wisconsin Madison, Madison, Wisconsin 53706, USA
    Genet Med 13:437-42. 2011
  2. ncbi Intrachromosomal duplications of 22q11 are not a common cause of isolated coloboma and coloboma with other limited features of cat eye syndrome
    Gordana Raca
    State Laboratory of Hygiene, Madison, Wisconsin 53706, USA
    Am J Med Genet A 146:401-4. 2008
  3. ncbi Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth
    Gordana Raca
    UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, Madison, Wisconsin 53706, USA
    Am J Med Genet A 149:2437-43. 2009
  4. ncbi Phenotype of FOXP2 haploinsufficiency in a mother and son
    Gregory M Rice
    University of Wisconsin Madison, Wisconsin, USA
    Am J Med Genet A 158:174-81. 2012
  5. ncbi Next generation sequencing in research and diagnostics of ocular birth defects
    Gordana Raca
    UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, 465 Henry Mall, Madison, WI 53706, USA
    Mol Genet Metab 100:184-92. 2010
  6. ncbi Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization
    Jennifer J S Laffin
    University of Wisconsin Madison, USA
    Genet Med 14:928-36. 2012
  7. ncbi Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals
    Laura Thorson
    Department of Medical Genetics, University of Wisconsin Madison, Madison, Wisconsin, USA
    Am J Med Genet A 152:904-15. 2010

Collaborators

  • Lisa A Schimmenti
  • Christa Lese Martin
  • Tanya M Bardakjian
  • Kathy J Jakielski
  • Gregory M Rice
  • Jennifer J S Laffin
  • Lawrence D Shriberg
  • Laura Thorson
  • Craig A Jackson
  • Christina M Iyama-Kurtycz
  • Edythe A Strand
  • Sigan L Hartley
  • Rae E Sprague
  • Anne T Heintzelman
  • Jennifer J Laffin
  • Jamie Israel
  • Gregory Rice
  • Amber Artzer
  • Christine Schilz
  • Christine Bryke
  • Suzanne Huber
  • Jennifer Laffin

Detail Information

Publications7

  1. ncbi Array comparative genomic hybridization analysis in patients with anophthalmia, microphthalmia, and coloboma
    Gordana Raca
    UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, University of Wisconsin Madison, Madison, Wisconsin 53706, USA
    Genet Med 13:437-42. 2011
    ..The goal of our study was to determine whether genomic copy number abnormalities (deletions and duplications) affecting genes involved in eye development contributed to the etiology of anophthalmia, microphthalmia, and coloboma...
  2. ncbi Intrachromosomal duplications of 22q11 are not a common cause of isolated coloboma and coloboma with other limited features of cat eye syndrome
    Gordana Raca
    State Laboratory of Hygiene, Madison, Wisconsin 53706, USA
    Am J Med Genet A 146:401-4. 2008
  3. ncbi Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth
    Gordana Raca
    UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, Madison, Wisconsin 53706, USA
    Am J Med Genet A 149:2437-43. 2009
    ..This preliminary study supports the clinical value of aCGH testing in diagnostic evaluation of stillborns with congenital anomalies...
  4. ncbi Phenotype of FOXP2 haploinsufficiency in a mother and son
    Gregory M Rice
    University of Wisconsin Madison, Wisconsin, USA
    Am J Med Genet A 158:174-81. 2012
    ..Better understanding of the behavioral phenotype of FOXP2 disruptions will aid identification of patients, toward an eventual understanding of the pathophysiology of syndromic and nonsyndromic apraxia of speech...
  5. ncbi Next generation sequencing in research and diagnostics of ocular birth defects
    Gordana Raca
    UW Cytogenetic Services, Wisconsin State Laboratory of Hygiene, 465 Henry Mall, Madison, WI 53706, USA
    Mol Genet Metab 100:184-92. 2010
    ....
  6. ncbi Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization
    Jennifer J S Laffin
    University of Wisconsin Madison, USA
    Genet Med 14:928-36. 2012
    ..Childhood apraxia of speech is the speech disorder segregating with a mutation in FOXP2 in a multigenerational London pedigree widely studied for its role in the development of speech-language in humans...
  7. ncbi Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals
    Laura Thorson
    Department of Medical Genetics, University of Wisconsin Madison, Madison, Wisconsin, USA
    Am J Med Genet A 152:904-15. 2010
    ..However, we show that even with detailed molecular characterization, phenotype prediction remains challenging in patients with structural abnormalities of the X chromosome...