Kim A Staats
Overview
Explore the profile of Kim A Staats including associated specialties, affiliations and a list of published articles.
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25
Citations
1203
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Recent Articles
1.
Hendricks E, Quihuis A, Hung S, Chang J, Dorjsuren N, Der B, et al.
Cell Rep
. 2023 Aug;
42(8):112983.
PMID: 37590144
Genetic mutations that cause adult-onset neurodegenerative diseases are often expressed during embryonic stages, but it is unclear whether they alter neurodevelopment and how this might influence disease onset. Here, we...
2.
Benatar M, Goutman S, Staats K, Feldman E, Weisskopf M, Talbott E, et al.
J Neurol Neurosurg Psychiatry
. 2023 Jan;
94(5):399-402.
PMID: 36690429
No abstract available.
3.
Staats K, Borchelt D, Tansey M, Wymer J
Mol Neurodegener
. 2022 Jan;
17(1):11.
PMID: 35073950
Amyotrophic Lateral Sclerosis (ALS) is a devastating neurodegenerative disease in which many processes are detected including (neuro)inflammation. Many drugs have been tested for ALS in clinical trials but most have...
4.
Guo W, Vandoorne T, Steyaert J, Staats K, Van Den Bosch L
Brain
. 2020 Mar;
143(6):1651-1673.
PMID: 32206784
Amyotrophic lateral sclerosis is the most common degenerative disorder of motor neurons in adults. As there is no cure, thousands of individuals who are alive at present will succumb to...
5.
Moore S, Alsop E, Lorenzini I, Starr A, Rabichow B, Mendez E, et al.
Acta Neuropathol
. 2019 Sep;
138(5):883-884.
PMID: 31559488
The original article was published erroneously without mentioning the support of the U.S.
6.
Shi Y, Hung S, Rocha G, Lin S, Linares G, Staats K, et al.
JCI Insight
. 2019 Jul;
5.
PMID: 31310593
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease with diverse etiologies. Therefore, the identification of common disease mechanisms and therapeutics targeting these mechanisms could dramatically improve clinical outcomes....
7.
Moore S, Alsop E, Lorenzini I, Starr A, Rabichow B, Mendez E, et al.
Acta Neuropathol
. 2019 Apr;
138(1):49-65.
PMID: 30945056
The hexanucleotide repeat expansion GGGGCC (GC) in the C9orf72 gene is the most common genetic abnormality associated with amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Recent findings suggest that...
8.
Ichida J, Staats K, Davis-Dusenbery B, Clement K, Galloway K, Babos K, et al.
Development
. 2018 Oct;
145(22).
PMID: 30337375
Advances in stem cell science allow the production of different cell types either through the recapitulation of developmental processes, often termed 'directed differentiation', or the forced expression of lineage-specific transcription...
9.
Bento-Abreu A, Jager G, Swinnen B, Rue L, Hendrickx S, Jones A, et al.
Hum Mol Genet
. 2018 Feb;
27(7):1276-1289.
PMID: 29415125
Amyotrophic lateral sclerosis (ALS) is a fatal degenerative motor neuron disorder of which the progression is influenced by several disease-modifying factors. Here, we investigated ELP3, a subunit of the elongator...
10.
Shi Y, Lin S, Staats K, Li Y, Chang W, Hung S, et al.
Nat Med
. 2018 Feb;
24(3):313-325.
PMID: 29400714
An intronic GGGGCC repeat expansion in C9ORF72 is the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD), but the pathogenic mechanism of this repeat remains unclear....