Publications by authors named "Jannine D Cody"

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Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings.
Catherine Cody Larson, Louise O'Donnell, Bridgette Soileau, Marcia Van Riper, Debra Stark, Jannine D Cody

J Genet Couns· October 2024

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Causes of death in individuals with trisomy 18 after the first year of life.
Justin M Mehl, Jonathan Gelfond, John C Carey, Jannine D Cody

Am J Med Genet A· February 2024

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The Consequences of Abnormal Gene Dosage: Lessons from Chromosome 18.
Jannine DeMars Cody

Trends Genet· October 2020

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Re-evaluation of the classification system for the clinical interpretation of genomic copy number variation.
Jannine D Cody

Genet Med· January 2020

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Abnormal bone mineral content and density in people with tetrasomy 18p.
Alvaro Moreira, Hrishikesh Das, Minire Hasi-Zogaj, Bridgette Soileau, Annice Hill, Jannine D Cody

Am J Med Genet A· March 2019

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Chromosome 18 gene dosage map 2.0.
Jannine D Cody, Patricia Heard, David Rupert, Minire Hasi-Zogaj, Annice Hill

Hum Genet· December 2018

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Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.
Judit Balog, Remko Goossens, Richard J L F Lemmers, Kirsten R Straasheijm, Patrick J van der Vliet, Jannine D Cody

J Med Genet· July 2018

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The Chromosome 18 Clinical Resource Center.
Jannine D Cody, Minire Hasi-Zogaj, Patricia Heard, Annice Hill, David Rupert

Mol Genet Genomic Med· May 2018

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WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene .
Krista M Hennig, Daniel M Fass, Wen-Ning Zhao, Steven D Sheridan, Ting Fu, Jannine D Cody

Mol Neuropsychiatry· July 2017

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Consequences of chromsome18q deletions.
Jannine D Cody, Courtney Sebold, Patricia Heard, Erika Carter, Bridgette Soileau

Am J Med Genet C Semin Med Genet· September 2015

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A review of 18p deletions.
Minire Hasi-Zogaj, Courtney Sebold, Patricia Heard, Erika Carter, Bridgette Soileau, Jannine D Cody

Am J Med Genet C Semin Med Genet· September 2015

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Making chromosome abnormalities treatable conditions.
Jannine DeMars Cody, Daniel Esten Hale

Am J Med Genet C Semin Med Genet· September 2015

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Adults with Chromosome 18 Abnormalities.
Bridgette Soileau, Minire Hasi, Courtney Sebold, Annice Hill, Louise O'Donnell, Jannine D Cody

J Genet Couns· August 2015

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Hemizygosity for SMCHD1 in Facioscapulohumeral Muscular Dystrophy Type 2: Consequences for 18p Deletion Syndrome.
Richard J L F Lemmers, Marlinde L van den Boogaard, Patrick J van der Vliet, Colleen M Donlin-Smith, Sharon P Nations, Jannine D Cody

Hum Mutat· July 2015

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Tetrasomy 18p: report of cognitive and behavioral characteristics.
Louise O'Donnell, Bridgette T Soileau, Courtney Sebold, Jonathan Gelfond, Daniel E Hale, Jannine D Cody

Am J Med Genet A· July 2015

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Whole arm deletions of 18p: medical and developmental effects.
Courtney Sebold, Bridgette Soileau, Patricia Heard, Erika Carter, Louise O'Donnell, Jannine D Cody

Am J Med Genet A· February 2015

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Ring 18 molecular assessment and clinical consequences.
Erika Carter, Patricia Heard, Minire Hasi, Bridgette Soileau, Courtney Sebold, Jannine D Cody

Am J Med Genet A· January 2015

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Otologic characteristics of individuals with deletions of distal 18q.
Brian P Perry, Jannine D Cody

Laryngoscope· November 2014

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Sensorineural hearing loss in people with deletions of 18q: hearing in 18q-.
Brian P Perry, Courtney Sebold, Minire Hasi, Patricia Heard, Erika Carter, Jannine D Cody

Otol Neurotol· June 2014

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Establishing a reference group for distal 18q-: clinical description and molecular basis.
Jannine D Cody, Minire Hasi, Bridgette Soileau, Patricia Heard, Erika Carter

Hum Genet· February 2014

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Large inverted duplications in the human genome form via a fold-back mechanism.
Karen E Hermetz, Scott Newman, Karen N Conneely, Christa L Martin, Blake C Ballif, Jannine D Cody

PLoS Genet· January 2014

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Mood disorders in individuals with distal 18q deletions.
William B Daviss, Louise O'Donnell, Bridgette T Soileau, Patricia Heard, Erika Carter, Jannine D Cody

Am J Med Genet B Neuropsychiatr Genet· December 2013

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Differential expression analysis with global network adjustment.
Jonathan A Gelfond, Joseph G Ibrahim, Mayetri Gupta, Ming-Hui Chen, Jannine D Cody

BMC Bioinformatics· August 2013

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An evaluation tool for collaborative clinical research centers.
Robin Tragus, Jannine D Cody

Clin Transl Sci· June 2013

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A recurrent translocation is mediated by homologous recombination between HERV-H elements.
Karen E Hermetz, Urvashi Surti, Jannine D Cody, M Katharine Rudd

Mol Cytogenet· January 2012

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