Anders D Borglum
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Explore the profile of Anders D Borglum including associated specialties, affiliations and a list of published articles.
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239
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16725
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Recent Articles
1.
Kaas M, Chofflet N, Bicer D, Skeldal S, Duan J, Feller B, et al.
bioRxiv
. 2025 Mar;
PMID: 40027832
The leukocyte common antigen related receptor (LAR) is a member of the LAR receptor protein tyrosine phosphatase (RPTP) family of synaptic adhesion molecules that contribute to the proper alignment and...
2.
Gu Y, Maria-Stauffer E, Bedford S, Romero-Garcia R, Grove J, Borglum A, et al.
Mol Psychiatry
. 2025 Feb;
PMID: 39994426
Genetic variants linked to autism are thought to change cognition and behaviour by altering the structure and function of the brain. Although a substantial body of literature has identified structural...
3.
Kweon H, Burik C, Ning Y, Ahlskog R, Xia C, Abner E, et al.
Nat Hum Behav
. 2025 Jan;
PMID: 39875632
We conducted a genome-wide association study on income among individuals of European descent (N = 668,288) to investigate the relationship between socio-economic status and health disparities. We identified 162 genomic...
4.
OConnell K, Koromina M, van der Veen T, Boltz T, David F, Yang J, et al.
Nature
. 2025 Jan;
PMID: 39843750
Bipolar disorder is a leading contributor to the global burden of disease. Despite high heritability (60-80%), the majority of the underlying genetic determinants remain unknown. We analysed data from participants...
5.
Montalbano S, Dybdahl Krebs M, Rosengren A, Vaez M, Georgii Hellberg K, Mortensen P, et al.
NPJ Genom Med
. 2024 Dec;
9(1):67.
PMID: 39695155
The NRXN1 locus is a hotspot for non-recurrent copy number variants and exon-disrupting NRXN1 deletions have been associated with increased risk of neurodevelopmental disorders in case-control studies. However, corresponding population-based...
6.
Voloudakis G, Therrien K, Tomasi S, Rajagopal V, Choi S, Demontis D, et al.
Nat Hum Behav
. 2024 Dec;
PMID: 39658624
Polygenic scores (PGS) enable the exploration of pleiotropic effects and genomic dissection of complex traits. Here, in 421,889 individuals with European ancestry from the Million Veteran Program and UK Biobank,...
7.
Christiansen G, Petersen L, Chatwin H, Yilmaz Z, Schendel D, Bulik C, et al.
Mol Psychiatry
. 2024 Nov;
PMID: 39543370
Eating disorders (EDs) commonly co-occur with other psychiatric and neurodevelopmental disorders including attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD); however, the pattern of family history and genetic overlap among...
8.
Vaez M, Montalbano S, Waples R, Dybdahl Krebs M, Georgii Hellberg K, Gadin J, et al.
medRxiv
. 2024 Oct;
PMID: 39398991
The impact of rare recurrent copy number variants (rCNVs) and polygenic background attributed to common variants, on the risk of psychiatric disorders is well-established in separate studies. However, it remains...
9.
Strom N, Halvorsen M, Grove J, Asbjornsdottir B, Ludvigsson P, Thorarensen O, et al.
Biol Psychiatry
. 2024 Oct;
97(7):743-752.
PMID: 39389409
Background: Despite the significant personal and societal burden of tic disorders (TDs), treatment outcomes remain modest, necessitating a deeper understanding of their etiology. Family history is the biggest known risk...
10.
Akter H, Rahaman M, Eshaque T, Mohamed N, Islam A, Morshed M, et al.
Genet Med
. 2024 Sep;
27(1):101282.
PMID: 39342494
Purpose: The genetic underpinning of neurodevelopmental disorders (NDDs) in diverse ethnic populations, especially those with high rates of consanguinity, remains largely unexplored. Here, we aim to elucidate genomic insight from...