Andreas Hermann
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Explore the profile of Andreas Hermann including associated specialties, affiliations and a list of published articles.
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Articles
323
Citations
4294
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Recent Articles
1.
Sona C, Yeh Y, Li Y, Liu X, Ghosh A, Hinte L, et al.
Sci Signal
. 2025 Feb;
18(875):eadl6745.
PMID: 39999211
Proper formation of the complex neurovascular unit (NVU) along with the blood-brain barrier is critical for building and sustaining a healthy, functioning central nervous system. The RNA binding protein argonaute2...
2.
Ranieri U, Bellin C, Conway L, Gaal R, Loveday J, Hermann A, et al.
Commun Chem
. 2025 Feb;
8(1):57.
PMID: 39994378
No abstract available.
3.
Shuttleworth H, Kuzovnikov M, Conway L, Hu H, Gallego-Parra S, Osmond I, et al.
Angew Chem Int Ed Engl
. 2025 Feb;
:e202422710.
PMID: 39968800
Carbon, nitrogen, and hydrogen are among the most abundant elements in the solar system, and our understanding of their interactions is fundamental to prebiotic chemistry. CH4 and N2 are the...
4.
Teipel S, Hoffmann H, Storch A, Hermann A, Dyrba M, Schumacher J
Brain Commun
. 2024 Dec;
6(6):fcae382.
PMID: 39713239
The brain-age gap, i.e. the difference between the brain age estimated from structural MRI data and the chronological age of an individual, has been proposed as a summary measure of...
5.
Peikert K, Spranger A, Miltenberger-Miltenyi G, Glass H, Falkenburger B, Klose C, et al.
Mov Disord
. 2024 Dec;
PMID: 39665525
Background: VPS13A disease is an ultra-rare disorder caused by loss of function mutations in VPS13A characterized by striatal degeneration and by red blood cell (RBC) acanthocytosis. VPS13A is a bridge-like...
6.
Rudolph J, Rueckel J, Dopfert J, Ling W, Opalka J, Brem C, et al.
Alzheimers Dement (Amst)
. 2024 Dec;
16(4):e70037.
PMID: 39665087
Introduction: This study evaluates the clinical value of a deep learning-based artificial intelligence (AI) system that performs rapid brain volumetry with automatic lobe segmentation and age- and sex-adjusted percentile comparisons....
7.
Zimyanin V, Dash B, Grossmann D, Simolka T, Glass H, Verma R, et al.
bioRxiv
. 2024 Nov;
PMID: 39605661
Mutations in the gene ( ) are among the most frequently occurring genetic forms of amyotrophic lateral sclerosis (ALS). Early pathogenesis of -ALS involves impaired DNA damage response and axonal...
8.
Dash B, Freischmidt A, Helferich A, Ludolph A, Andersen P, Weishaupt J, et al.
Front Cell Neurosci
. 2024 Nov;
18:1457704.
PMID: 39588282
Amyotrophic lateral sclerosis (ALS) is a fatal, adult-onset disease marked by a progressive degeneration of motor neurons (MNs) present in the spinal cord, brain stem and motor cortex. Death in...
9.
Hoe R, Zhao Y, Ong H, Tay K, Tan N, Khor M, et al.
Neurol Genet
. 2024 Nov;
10(6):e200207.
PMID: 39588054
Objectives: Chorea-acanthocytosis is an autosomal recessively inherited condition caused by loss-of-function pathogenic variants in . We identified a novel synonymous exonic variant leading to abnormal mRNA splicing in a patient...
10.
Marqueno T, Osmond I, Kuzovnikov M, Shuttleworth H, Gallego-Parra S, Gregoryanz E, et al.
Inorg Chem
. 2024 Oct;
63(45):21734-21741.
PMID: 39480973
The Na-W-H and Na-Re-H ternary systems were studied in a diamond anvil cell through X-ray diffraction and Raman spectroscopy, supported by density functional theory and molecular dynamics calculations. NaWH can...