Allison E Ashley-Koch
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Explore the profile of Allison E Ashley-Koch including associated specialties, affiliations and a list of published articles.
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125
Citations
3821
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Recent Articles
1.
Halvorsen M, Garrett M, Cuccaro M, Ashley-Koch A, Crowley J
medRxiv
. 2025 Feb;
PMID: 39974061
Trichotillomania (TTM) is a psychiatric condition in which people feel an overwhelming urge to pull out their hair, resulting in noticeable hair loss and significant distress. Twin, family and candidate...
2.
Ilboudo Y, Brosseau N, Lo K, Belhaj H, Moutereau S, Marshall K, et al.
Hum Mol Genet
. 2025 Jan;
PMID: 39886999
Sickle cell disease (SCD) is the most common monogenic disease in the world and is caused by mutations in the β-globin gene (HBB). Notably, SCD is characterized by extreme clinical...
3.
Shwab E, Man Z, Gingerich D, Gamache J, Garrett M, Serrano G, et al.
bioRxiv
. 2025 Jan;
PMID: 39764045
Introduction: Alzheimer's disease (AD), Dementia with Lewy bodies (DLB), and Parkinson's disease (PD) represent a spectrum of neurodegenerative disorders (NDDs). Here, we performed the first direct comparison of their transcriptomic...
4.
Katrinli S, Wani A, Maihofer A, Ratanatharathorn A, Daskalakis N, Montalvo-Ortiz J, et al.
Genome Med
. 2024 Dec;
16(1):147.
PMID: 39696436
Background: The occurrence of post-traumatic stress disorder (PTSD) following a traumatic event is associated with biological differences that can represent the susceptibility to PTSD, the impact of trauma, or the...
5.
Bourassa K, Dennis P, Patel P, Qin X, Sbarra D, Hauser E, et al.
J Psychiatr Res
. 2024 Nov;
180:500-505.
PMID: 39549463
People with lower levels of social connection are at increased risk for suicidal thoughts and behaviors. This extends to populations at greater risk of death by suicide, including U.S. military...
6.
Bourassa K, Anderson L, Woolson S, Dennis P, Garrett M, Hair L, et al.
medRxiv
. 2024 Nov;
PMID: 39502668
Epigenetic measures of aging derived from DNA methylation are promising biomarkers associated with prospective morbidity and mortality, but require validation in real-world medical settings. Using data from 2,216 post-9/11 veterans,...
7.
Morey R, Zheng Y, Bayly H, Sun D, Garrett M, Gasperi M, et al.
Transl Psychiatry
. 2024 Oct;
14(1):451.
PMID: 39448598
Genetic contributions to human cortical structure manifest pervasive pleiotropy. This pleiotropy may be harnessed to identify unique genetically-informed parcellations of the cortex that are neurobiologically distinct from functional, cytoarchitectural, or...
8.
Sullivan K, Lane M, Cashman M, Miller J, Pavicic M, Walker A, et al.
Commun Biol
. 2024 Oct;
7(1):1360.
PMID: 39433874
Genome-wide association studies (GWAS) identify genetic variants underlying complex traits but are limited by stringent genome-wide significance thresholds. We present GRIN (Gene set Refinement through Interacting Networks), which increases confidence...
9.
Hawkes G, Beaumont R, Li Z, Mandla R, Li X, Albert C, et al.
Nat Commun
. 2024 Oct;
15(1):8549.
PMID: 39362880
The role of rare non-coding variation in complex human phenotypes is still largely unknown. To elucidate the impact of rare variants in regulatory elements, we performed a whole-genome sequencing association...
10.
Garrett M, Le B, Bourassa K, Dennis M, Hatch D, Yang Q, et al.
J Gerontol A Biol Sci Med Sci
. 2024 Sep;
79(11).
PMID: 39297703
Background: Sickle cell disease (SCD) is a chronic medical condition characterized by red blood cell sickling, vaso-occlusion, hemolytic anemia, and subsequently, end-organ damage and reduced survival. Because of this significant...