Lisa A Cannon-Albright
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Explore the profile of Lisa A Cannon-Albright including associated specialties, affiliations and a list of published articles.
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160
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Recent Articles
1.
Armon C, Cannon-Albright L, Allen-Brady K, Wolfson S
Adv Neurol (Singap)
. 2024 Dec;
3(2).
PMID: 39634155
Alzheimer's disease (AD) is a major cause of dementia. While maternal inheritance has been recognized for late-onset AD (LOAD), risk factors have not been identified consistently on the X chromosome....
2.
Cannon-Albright L, Stevens J, Teerlink C, Facelli J, Allen-Brady K, Welm A
Cancers (Basel)
. 2023 Dec;
15(24).
PMID: 38136396
A significant fraction of breast cancer recurs, with lethal outcome, but specific genetic variants responsible have yet to be identified. Five cousin pairs with recurrent breast cancer from pedigrees with...
3.
Berndt S, Vijai J, Benavente Y, Camp N, Nieters A, Wang Z, et al.
Leukemia
. 2023 Sep;
37(10):2142.
PMID: 37666943
No abstract available.
4.
Oxnard G, Chen R, Pharr J, Koeller D, Bertram A, Dahlberg S, et al.
J Clin Oncol
. 2023 Aug;
41(34):5274-5284.
PMID: 37579253
Purpose: The genomic underpinnings of inherited lung cancer risk are poorly understood. This prospective study characterized the clinical phenotype of patients and families with germline pathogenic variants (PVs). Methods: The...
5.
Cannon-Albright L, Stevens J, Facelli J, Teerlink C, Allen-Brady K, Agarwal N
Cancers (Basel)
. 2023 Apr;
15(7).
PMID: 37046747
There is evidence for contribution of inherited factors to prostate cancer, and more specifically to lethal prostate cancer, but few responsible genes/variants have been identified. We examined genetic sequence data...
6.
Cannon-Albright L, Teerlink C, Stevens J, Facelli J, Carr S, Allen-Brady K, et al.
Int J Cancer
. 2023 Mar;
153(2):364-372.
PMID: 36916144
A unique approach with rare resources was used to identify candidate variants predisposing to familial nonsquamous nonsmall-cell lung cancers (NSNSCLC). We analyzed sequence data from NSNSCLC-affected cousin pairs belonging to...
7.
Valentine D, Teerlink C, Farnham J, Rowe K, Kaddas H, Tschanz J, et al.
Int J Environ Res Public Health
. 2022 Dec;
19(24).
PMID: 36554301
(1) Importance: Alzheimer's disease (AD) is complex and only partially understood. Analyzing the relationship between other more treatable or preventable diseases and AD may help in the prevention and the...
8.
Brockmeyer D, Cheshier S, Stevens J, Facelli J, Rowe K, Heiss J, et al.
J Neurosurg
. 2022 Nov;
139(1):266-274.
PMID: 36433874
Objective: Inherited variants predisposing patients to type 1 or 1.5 Chiari malformation (CM) have been hypothesized but have proven difficult to confirm. The authors used a unique high-risk pedigree population...
9.
Berndt S, Vijai J, Benavente Y, Camp N, Nieters A, Wang Z, et al.
Leukemia
. 2022 Oct;
36(12):2835-2844.
PMID: 36273105
Lymphoma risk is elevated for relatives with common non-Hodgkin lymphoma (NHL) subtypes, suggesting shared genetic susceptibility across subtypes. To evaluate the extent of mutual heritability among NHL subtypes and discover...
10.
Gurgel R, Couldwell W, Patel N, Cannon-Albright L
Otol Neurotol
. 2022 Sep;
43(10):e1157-e1163.
PMID: 36113461
Object: Unlike the autosomal dominant inheritance of neurofibromatosis 2, there are no known inherited risk factors for sporadic, unilateral vestibular schwannoma (VS), which comprise most VS cases. The authors tested...