Megan T Cho
Overview
Explore the profile of Megan T Cho including associated specialties, affiliations and a list of published articles.
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91
Citations
3400
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Recent Articles
1.
Martin C, Sarlos K, Logan C, Thakur R, Parry D, Bizard A, et al.
Am J Hum Genet
. 2024 May;
111(5):996.
PMID: 38701747
No abstract available.
2.
Cho M, Davis C, Lowe C, Flynn M, Jamal L, Bajaj K, et al.
J Genet Couns
. 2024 Feb;
33(1):118-123.
PMID: 38351603
Educational use of clinical simulation is a way for students to immerse themselves within a realistic yet safe and structured environment as they practice clinical skills. It is widely used...
3.
Higgs E, Wain K, Wynn J, Cho M, Higgins S, Blaisdell D, et al.
J Genet Couns
. 2022 Nov;
32(2):315-324.
PMID: 36385723
Genetic counselors strive to provide high-quality genetic services. To do so, it is essential to define quality in genetic counseling and identify opportunities for improvement. This Professional Issues article provides...
4.
Guerrini R, Mei D, Kerti-Szigeti K, Pepe S, Koenig M, Von Allmen G, et al.
Brain
. 2022 Jun;
145(8):2687-2703.
PMID: 35675510
Vacuolar-type H+-ATPase (V-ATPase) is a multimeric complex present in a variety of cellular membranes that acts as an ATP-dependent proton pump and plays a key role in pH homeostasis and...
5.
Liu S, Aldinger K, Cheng C, Kiyama T, Dave M, McNamara H, et al.
Mol Cell
. 2021 Nov;
81(22):4757.
PMID: 34798045
No abstract available.
6.
Liu S, Aldinger K, Cheng C, Kiyama T, Dave M, McNamara H, et al.
Mol Cell
. 2021 Oct;
81(22):4663-4676.e8.
PMID: 34637754
The heterogeneous family of complexes comprising Polycomb repressive complex 1 (PRC1) is instrumental for establishing facultative heterochromatin that is repressive to transcription. However, two PRC1 species, ncPRC1.3 and ncPRC1.5, are...
7.
Mohassel P, Donkervoort S, Lone M, Nalls M, Gable K, Gupta S, et al.
Nat Med
. 2021 Jun;
27(7):1197-1204.
PMID: 34059824
Amyotrophic lateral sclerosis (ALS) is a progressive, neurodegenerative disease of the lower and upper motor neurons with sporadic or hereditary occurrence. Age of onset, pattern of motor neuron degeneration and...
8.
Bryant L, Li D, Cox S, Marchione D, Joiner E, Wilson K, et al.
Sci Adv
. 2020 Dec;
6(49).
PMID: 33268356
Although somatic mutations in Histone 3.3 (H3.3) are well-studied drivers of oncogenesis, the role of germline mutations remains unreported. We analyze 46 patients bearing de novo germline mutations in histone...
9.
Senter L, Austin J, Carey M, Cho M, Harris S, Linnenbringer E, et al.
J Genet Couns
. 2020 Sep;
29(6):884-887.
PMID: 32969094
To help advance research critical to the achievement of the National Society of Genetic Counselors' (NSGC) strategic objectives, coordination and prioritization of society resources are needed. NSGC convened a task...
10.
Schmidt J, Pizzino A, Nicholl J, Foley A, Wang Y, Rosenfeld J, et al.
Am J Med Genet A
. 2020 Jun;
182(8):1906-1912.
PMID: 32573057
Leukodystrophies are a heterogeneous group of heritable disorders characterized by abnormal brain white matter signal on magnetic resonance imaging (MRI) and primary involvement of the cellular components of myelin. Previous...