Louise ODonnell
Overview
Explore the profile of Louise ODonnell including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
170
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0
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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.
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...
3.
Olvera R, Glahn D, ODonnell L, Bearden C, Soares J, Winkler A, et al.
J Clin Med
. 2015 Aug;
3(2):416-31.
PMID: 26237382
Background: There is increasing evidence that bipolar disorder (BD) and conduct disorder (CD) are co-occurring disorders. Magnetic resonance imaging has revealed differences in the structure and function of the frontal...
4.
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...
5.
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...
6.
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....
7.
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...
8.
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...
9.
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...
10.
Schillerstrom J, Sanchez-Reilly S, ODonnell L
Acad Psychiatry
. 2012 Jul;
36(3):188-90.
PMID: 22751819
Objective: The purpose of this study was to explore the educational potential for a collaboration between palliative medicine and psychiatry designed to improve first-year medical students' knowledge and comfort with...