Jannine D Cody
Overview
Explore the profile of Jannine D Cody including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
44
Citations
466
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Larson C, ODonnell L, Soileau B, Van Riper M, Stark D, Hale D, et al.
J Genet Couns
. 2023 Oct;
33(5):1070-1081.
PMID: 37882415
Siblings of individuals with disabilities hold a pivotal and sometimes unappreciated position in the lives of their brother or sister. We sought to understand the unique challenges and opportunities in...
2.
Mehl J, Gelfond J, Carey J, Cody J
Am J Med Genet A
. 2023 Oct;
194(2):279-287.
PMID: 37822198
Mortality in individuals with trisomy 18 has significantly decreased over the past 20 years, but there is scant literature addressing the prognosis and cause of death in individuals with trisomy...
3.
4.
Moreira A, Das H, Hasi-Zogaj M, Soileau B, Hill A, Bruder J, et al.
Am J Med Genet A
. 2019 Jan;
179(3):417-422.
PMID: 30637922
Tetrasomy 18p is a rare chromosomal abnormality, resulting from an additional iso-chromosome composed of two copies of the short arm. It is characterized by craniofacial abnormalities, neuromuscular dysfunction, and developmental...
5.
Cody J, Heard P, Rupert D, Hasi-Zogaj M, Hill A, Sebold C, et al.
Hum Genet
. 2018 Nov;
137(11-12):961-970.
PMID: 30448861
In 2009, we described the first generation of the chromosome 18 gene dosage maps. This tool included the annotation of each gene as well as each phenotype associated region. The...
6.
Cody J, Hasi-Zogaj M, Heard P, Hill A, Rupert D, Sebold C, et al.
Mol Genet Genomic Med
. 2018 Apr;
6(3):416-421.
PMID: 29603904
Background: The Chromosome 18 Clinical Research Center has created a pediatrician-friendly virtual resource center for managing patients with chromosome 18 abnormalities. To date, children with rare chromosome abnormalities have been...
7.
Balog J, Goossens R, Lemmers R, Straasheijm K, van der Vliet P, van den Heuvel A, et al.
J Med Genet
. 2018 Mar;
55(7):469-478.
PMID: 29563141
Background: 18p deletion syndrome is a rare disorder caused by partial or full monosomy of the short arm of chromosome 18. Clinical symptoms caused by 18p hemizygosity include cognitive impairment,...
8.
Hennig K, Fass D, Zhao W, Sheridan S, Fu T, Erdin S, et al.
Mol Neuropsychiatry
. 2017 Sep;
3(1):53-71.
PMID: 28879201
Genetic variation within the transcription factor locus can cause the intellectual disability and developmental disorder Pitt-Hopkins syndrome (PTHS), whereas single-nucleotide polymorphisms within noncoding regions are associated with schizophrenia. These genetic...
9.
Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, et al.
Am J Med Genet C Semin Med Genet
. 2015 Aug;
169(3):251-64.
PMID: 26250845
Since 18p- was first described in 1963, much progress has been made in our understanding of this classic deletion condition. We have been able to establish a fairly complete picture...
10.
Cody J, Sebold C, Heard P, Carter E, Soileau B, Hasi-Zogaj M, et al.
Am J Med Genet C Semin Med Genet
. 2015 Aug;
169(3):265-80.
PMID: 26235940
Providing clinically relevant prognoses and treatment information for people with a chromsome18q deletion is particularly challenging because every unrelated person has a unique region of hemizygosity. The hemizygous region can...