Rena J Vanzo

Summary

Publications

  1. doi request reprint Familial KANK1 deletion that does not follow expected imprinting pattern
    Rena J Vanzo
    Lineagen, Inc, 423 Wakara Way, Ste 200, Salt Lake City, UT 84108, United States
    Eur J Med Genet 56:256-9. 2013
  2. pmc Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders
    Karen S Ho
    Lineagen, Inc, Salt Lake City, UT 84109, USA
    Int J Mol Sci 17:. 2016
  3. doi request reprint Mosaic deletion of 20pter due to rescue by somatic recombination
    Megan M Martin
    Lineagen, Inc, Salt Lake City, Utah
    Am J Med Genet A 170:243-8. 2016
  4. pmc Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome
    Karen S Ho
    Lineagen, Inc, Salt Lake City, Utah, USA
    J Med Genet 53:256-63. 2016
  5. doi request reprint Clinical utility of chromosomal microarray analysis of DNA from buccal cells: detection of mosaicism in three patients
    Mallory R Sdano
    Genetic Counselor, Lineagen, Inc, 2677 E Parleys, Way Salt Lake City, UT, 84109, USA
    J Genet Couns 23:922-7. 2014

Collaborators

  • Sarah T South
  • Merlin G Butler
  • Megan M Martin
  • Karen S Ho
  • Mallory R Sdano
  • Adrianne L Baxter
  • Charles H Hensel
  • Aparna Prasad
  • Amanda Lortz
  • John C Carey
  • Amy Calhoun
  • Andreas Peiffer
  • E Robert Wassman
  • Hope Twede
  • CHRISTOPHE G LAMBERT
  • Agatino Battaglia
  • Alan F Rope
  • Erin E Baldwin
  • Hutton Kearney
  • William P Allen

Detail Information

Publications5

  1. doi request reprint Familial KANK1 deletion that does not follow expected imprinting pattern
    Rena J Vanzo
    Lineagen, Inc, 423 Wakara Way, Ste 200, Salt Lake City, UT 84108, United States
    Eur J Med Genet 56:256-9. 2013
    ....
  2. pmc Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders
    Karen S Ho
    Lineagen, Inc, Salt Lake City, UT 84109, USA
    Int J Mol Sci 17:. 2016
    ..We note discrete differences in the most common recurrent CNVs found in individuals with or without a diagnosis of ASD...
  3. doi request reprint Mosaic deletion of 20pter due to rescue by somatic recombination
    Megan M Martin
    Lineagen, Inc, Salt Lake City, Utah
    Am J Med Genet A 170:243-8. 2016
    ....
  4. pmc Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome
    Karen S Ho
    Lineagen, Inc, Salt Lake City, Utah, USA
    J Med Genet 53:256-63. 2016
    ..3 region. Seizures are frequently, but not always, associated with WHS. We hypothesised that the size and location of the deleted region may correlate with seizure presentation...
  5. doi request reprint Clinical utility of chromosomal microarray analysis of DNA from buccal cells: detection of mosaicism in three patients
    Mallory R Sdano
    Genetic Counselor, Lineagen, Inc, 2677 E Parleys, Way Salt Lake City, UT, 84109, USA
    J Genet Couns 23:922-7. 2014
    ..We also present practice implications for genetic counselors, including clinic workflow changes and counseling approaches based on increasing use of buccal samples. ..