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
11.
ODonnell L, Soileau B, Sebold C, Gelfond J, Hale D, Cody J
Am J Med Genet A
. 2015 Apr;
167(7):1474-82.
PMID: 25900901
Our purpose was to describe intellectual and behavioral characteristics of persons with tetrasomy 18p. This is a more detailed investigation into the cognitive and behavioral characteristics of our previously reported...
12.
Lemmers R, van den Boogaard M, van der Vliet P, Donlin-Smith C, Nations S, Ruivenkamp C, et al.
Hum Mutat
. 2015 Mar;
36(7):679-83.
PMID: 25820463
Facioscapulohumeral muscular dystrophy (FSHD) is most often associated with variegated expression in somatic cells of the normally repressed DUX4 gene within the D4Z4-repeat array. The most common form, FSHD1, is...
13.
Sebold C, Soileau B, Heard P, Carter E, ODonnell L, Hale D, et al.
Am J Med Genet A
. 2015 Jan;
167A(2):313-23.
PMID: 25586871
Deletions of the short arm of chromosome 18 have been well-described in case reports. However, the utility of these descriptions in clinical practice is limited by varied and imprecise breakpoints....
14.
Soileau B, Hasi M, Sebold C, Hill A, ODonnell L, Hale D, et al.
J Genet Couns
. 2014 Nov;
24(4):663-74.
PMID: 25403900
The identification of an underlying chromosome abnormality frequently marks the endpoint of a diagnostic odyssey. However, families are frequently left with more questions than answers as they consider their child's...
15.
Carter E, Heard P, Hasi M, Soileau B, Sebold C, Hale D, et al.
Am J Med Genet A
. 2014 Oct;
167A(1):54-63.
PMID: 25339348
Ring chromosome 18 is a rare condition which has predominantly been described by case reports and small case series. We assessed a cohort of 30 individuals with ring 18 using...
16.
Perry B, Cody J
Laryngoscope
. 2014 Jun;
124(11):2606-9.
PMID: 24912803
Objectives/hypothesis: To fully describe the otologic features seen in individuals with deletions of the distal long arm of chromosome 18 (distal 18q-). Study Design: Cross-sectional/observational. Methods: More than 200 individuals...
17.
Perry B, Sebold C, Hasi M, Heard P, Carter E, Hill A, et al.
Otol Neurotol
. 2014 Mar;
35(5):782-6.
PMID: 24662633
Objective: The objective of this study was to characterize hearing loss in individuals with deletions of distal chromsome18q and to identify the smallest region of overlap of their deletions, thereby...
18.
Hermetz K, Newman S, Conneely K, Martin C, Ballif B, Shaffer L, et al.
PLoS Genet
. 2014 Feb;
10(1):e1004139.
PMID: 24497845
Inverted duplications are a common type of copy number variation (CNV) in germline and somatic genomes. Large duplications that include many genes can lead to both neurodevelopmental phenotypes in children...
19.
Cody J, Hasi M, Soileau B, Heard P, Carter E, Sebold C, et al.
Hum Genet
. 2013 Oct;
133(2):199-209.
PMID: 24092497
Although constitutional chromosome abnormalities have been recognized since the 1960s, clinical characterization and development of treatment options have been hampered by their obvious genetic complexity and relative rarity. Additionally, deletions...
20.
Daviss W, ODonnell L, Soileau B, Heard P, Carter E, Pliszka S, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2013 Sep;
162B(8):879-88.
PMID: 24006251
We examined 36 participants at least 4 years old with hemizygous distal deletions of the long arm of Chromosome 18 (18q-) for histories of mood disorders and to characterize these...