Aimee McKinney
Overview
Explore the profile of Aimee McKinney including associated specialties, affiliations and a list of published articles.
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8
Citations
40
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0
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Recent Articles
1.
Schieffer K, Moccia A, Bucknor B, Stonerock E, Jayaraman V, Jenkins H, et al.
Cancers (Basel)
. 2023 Sep;
15(17).
PMID: 37686670
Gene fusions are a form of structural rearrangement well established as driver events in pediatric and adult cancers. The identification of such events holds clinical significance in the refinement, prognostication,...
2.
Miller C, Lee K, Pfau R, Reshmi S, Corsmeier D, Hashimoto S, et al.
Cold Spring Harb Mol Case Stud
. 2020 May;
6(3).
PMID: 32371413
Exome sequencing (ES) has become an important tool in pediatric genomic medicine, improving identification of disease-associated variation due to assay breadth. Depth is also afforded by ES, enabling detection of...
3.
Wollison B, Thai E, McKinney A, Ward A, Clapp A, Clinton C, et al.
PLoS One
. 2017 Dec;
12(12):e0188835.
PMID: 29206863
Objectives: Liquid biopsy technologies allow non-invasive tumor profiling for patients with solid tumor malignancies by sequencing circulating tumor DNA. These studies may be useful in risk-stratification, monitoring for relapse, and...
4.
Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy
Santoro S, Hashimoto S, McKinney A, Mosher T, Pyatt R, Reshmi S, et al.
Cytogenet Genome Res
. 2017 Jul;
152(2):105-109.
PMID: 28746920
Maternal uniparental disomy (UPD) 15 is one of the molecular causes of Prader-Willi syndrome (PWS), a multisystem disorder which presents with neonatal hypotonia and feeding difficulty. Current diagnostic algorithms differ...
5.
Kekis M, Deeg C, Hashimoto S, McKinney A, Erdman L, Green-Geer C, et al.
Am J Med Genet A
. 2017 Mar;
173(4):1056-1060.
PMID: 28328127
Intrachromosomal triplications are complex chromosomal rearrangements which arise during meiosis or mitosis and lead to a tetrasomic dose of the affected genomic regions. We describe a female patient harboring an...
6.
Kekis M, Hashimoto S, Deeg C, Calloway I, McKinney A, Shuss C, et al.
Eur J Med Genet
. 2016 Oct;
59(11):569-572.
PMID: 27717910
Constitutional mosaicism for trisomy 3 is extremely rare, with only a few postnatally diagnosed cases reported in the literature. We report a case of constitutional trisomy 3 mosaicism in a...
7.
Repnikova E, Rosenfeld J, Bailes A, Weber C, Erdman L, McKinney A, et al.
Forensic Sci Int Genet
. 2013 Aug;
7(5):475-81.
PMID: 23948316
Short tandem repeat (STR) loci are commonly used in forensic casework, familial analysis for human identification, and for monitoring hematopoietic cell engraftment after bone marrow transplant. Unexpected genetic variation leading...
8.
Alyaqoub F, Pyatt R, Bailes A, Brock A, Deeg C, McKinney A, et al.
Am J Med Genet A
. 2012 Sep;
158A(11):2925-30.
PMID: 22987822
The 12q14 microdeletion syndrome is a rare condition that has previously been characterized by pre- and postnatal growth restriction, proportionate short stature, failure to thrive, developmental delay, and osteopoikilosis. Previously...