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Larissa Arning

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Articles 93
Citations 1296
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Recent Articles
1.
Findlay Black H, Kay C, Dawson J, Bortnick S, Javier K, Xia Q, et al.
Genet Med Open . 2024 Dec; 2:101882. PMID: 39669608
Purpose: In Huntington disease (HD), synonymous variants causing loss or duplication of the interrupting CAA codon in the CAG repeat modify disease onset. These variants are undetectable during HD genetic...
2.
Dawson J, Kay C, Findlay Black H, Bortnick S, Javier K, Xia Q, et al.
Genet Med . 2024 Aug; 26(11):101239. PMID: 39140258
Purpose: To determine the frequency and clinical impact of loss-of-interruption (LOI) and duplication-of-interruption modifier variants of the HTT CAG and CCG repeat in a cohort of individuals with Huntington disease...
3.
Arning L, Nguyen H
Med Genet . 2024 Jun; 33(4):293-300. PMID: 38835439
The causative mutation for Huntington disease (HD), an expanded trinucleotide repeat sequence in the first exon of the huntingtin gene () is naturally polymorphic and inevitably associated with disease symptoms...
4.
Dalene Skarping K, Arning L, Petersen A, Nguyen H, Gebre-Medhin S
Sci Rep . 2024 Feb; 14(1):4300. PMID: 38383663
DNA mismatch repair (MMR) is thought to contribute to the onset and progression of Huntington disease (HD) by promoting somatic expansion of the pathogenic CAG nucleotide repeat in the huntingtin...
5.
Fisse A, Schafer E, Hieke A, Schroder M, Klimas R, Brunger J, et al.
Eur J Neurol . 2024 Jan; 31(4):e16205. PMID: 38205888
Background And Purpose: Chronic inflammatory demyelinating polyneuropathy (CIDP) is an autoimmune disease with humoral and cellular autoimmunity causing demyelination of peripheral nerves, commonly treated with intravenous immunoglobulins (IVIg). The neonatal...
6.
Genc E, Metzen D, Fraenz C, Schluter C, Voelkle M, Arning L, et al.
Hum Brain Mapp . 2023 Apr; 44(8):3359-3376. PMID: 37013679
Intelligence is highly heritable. Genome-wide association studies (GWAS) have shown that thousands of alleles contribute to variation in intelligence with small effect sizes. Polygenic scores (PGS), which combine these effects...
7.
Emons B, Arning L, Makulla V, Suchy M, Tsikas D, Lucke T, et al.
Ann Gen Psychiatry . 2023 Mar; 22(1):11. PMID: 36932421
Background: The serotonergic and the endocannabinoid system are involved in the etiology of depression. Depressive patients exhibit low serotonergic activity and decreased level of the endocannabinoids anandamide (AEA) and 2-arachidonylglycerol...
8.
Ocklenburg S, Metzen D, Schluter C, Fraenz C, Arning L, Streit F, et al.
Brain Struct Funct . 2021 Jul; 227(2):515-527. PMID: 34235564
Handedness is the most widely investigated motor preference in humans. The genetics of handedness and especially the link between genetic variation, brain structure, and right-left preference have not been investigated...
9.
Genc E, Schluter C, Fraenz C, Arning L, Metzen D, Nguyen H, et al.
Mol Neurobiol . 2021 May; 58(8):4145-4156. PMID: 33954905
Intelligence is a highly polygenic trait and genome-wide association studies (GWAS) have identified thousands of DNA variants contributing with small effects. Polygenic scores (PGS) can aggregate those effects for trait...
10.
Packheiser J, Schmitz J, Arning L, Beste C, Gunturkun O, Ocklenburg S
Sci Rep . 2020 Nov; 10(1):20050. PMID: 33184306
An amendment to this paper has been published and can be accessed via a link at the top of the paper.