Allison R Bialas
Overview
Explore the profile of Allison R Bialas including associated specialties, affiliations and a list of published articles.
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10
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5093
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Recent Articles
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Sekar A, Bialas A, de Rivera H, Davis A, Hammond T, Kamitaki N, et al.
Nature
. 2021 Dec;
601(7892):E4-E5.
PMID: 34912127
No abstract available.
3.
Dodge J, Jensen E, Yu J, Sardi S, Bialas A, Taksir T, et al.
J Neurosci
. 2020 Oct;
40(47):9137-9147.
PMID: 33051352
Amyotrophic lateral sclerosis (ALS) is a fatal neuromuscular disease characterized by motor neuron (MN) death. Lipid dysregulation manifests during disease; however, it is unclear whether lipid homeostasis is adversely affected...
4.
Bialas A, Presumey J, Das A, van der Poel C, Lapchak P, Mesin L, et al.
Nature
. 2020 Feb;
578(7793):177.
PMID: 32025017
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
5.
Presumey J, Bialas A, Carroll M
Adv Immunol
. 2017 Aug;
135:53-79.
PMID: 28826529
Recent discoveries implicate the classical complement cascade in normal brain development and in disease. Complement proteins C1q, C3, and C4 participate in synapse elimination, tagging inappropriate synaptic connections between neurons...
6.
Bialas A, Presumey J, Das A, van der Poel C, Lapchak P, Mesin L, et al.
Nature
. 2017 Jun;
546(7659):539-543.
PMID: 28614301
Systemic lupus erythematosus (SLE) is an incurable autoimmune disease characterized by autoantibody deposition in tissues such as kidney, skin and lungs. Notably, up to 75% of patients with SLE experience...
7.
Sekar A, Bialas A, de Rivera H, Davis A, Hammond T, Kamitaki N, et al.
Nature
. 2016 Jan;
530(7589):177-83.
PMID: 26814963
Schizophrenia is a heritable brain illness with unknown pathogenic mechanisms. Schizophrenia's strongest genetic association at a population level involves variation in the major histocompatibility complex (MHC) locus, but the genes...
8.
Macosko E, Basu A, Satija R, Nemesh J, Shekhar K, Goldman M, et al.
Cell
. 2015 May;
161(5):1202-1214.
PMID: 26000488
Cells, the basic units of biological structure and function, vary broadly in type and state. Single-cell genomics can characterize cell identity and function, but limitations of ease and scale have...
9.
Giera S, Deng Y, Luo R, Ackerman S, Mogha A, Monk K, et al.
Nat Commun
. 2015 Jan;
6:6121.
PMID: 25607655
Mutations in GPR56, a member of the adhesion G protein-coupled receptor family, cause a human brain malformation called bilateral frontoparietal polymicrogyria (BFPP). Magnetic resonance imaging (MRI) of BFPP brains reveals...
10.
Bialas A, Stevens B
Nat Neurosci
. 2013 Oct;
16(12):1773-82.
PMID: 24162655
Immune molecules, including complement proteins C1q and C3, have emerged as critical mediators of synaptic refinement and plasticity. Complement localizes to synapses and refines the developing visual system through C3-dependent...