Thomas D. Als

Biochemistry, Genetics and Molecular Biology · Life Sciences

54h-index25.2kcitations196works12.12yr avg
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Research Topics

Genetic Associations and Epidemiology(70), Genetics and Neurodevelopmental Disorders(29), Attention Deficit Hyperactivity Disorder(19), Autism Spectrum Disorder Research(17), Genomics and Rare Diseases(17)

Publications176 total

Assembly and analysis of 100 full MHC haplotypes from the Danish population
UNC Libraries·2026Open Access
Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease
UNC Libraries·2026Open Access
Identification of common genetic risk variants for autism spectrum disorder
UNC Libraries·2026Open Access
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
UNC Libraries·2026Open Access
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
UNC Libraries·2025Open Access
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
Utrecht University Repository (Utrecht University)·2025Open Access
Genomics yields biological and phenotypic insights into bipolar disorder
Nature·2025· 107 citedOpen Access
Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology
npj Genomic Medicine·2024· 3 citedOpen Access
Polygenic liabilities and treatment trajectories in early-onset depression: a Danish register-based study
Psychological Medicine·2024· 5 citedOpen Access
Sex differences in shared genetic determinants between severe mental disorders and metabolic traits
Psychiatry Research·2024· 3 citedOpen Access
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study
The Journal of Urology·2024· 5 cited
Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants
JAMA Psychiatry·2024· 21 citedOpen Access
Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease
Nature Cardiovascular Research·2024· 39 citedOpen Access
Phenotypic and ancestry-related assortative mating in autism
Molecular Autism·2024· 2 citedOpen Access
Genome-wide association study identifies new loci associated with OCD
2024· 8 citedOpen Access
Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease
Open MIND·2024
Genomics yields biological and phenotypic insights into bipolar disorder
2023· 20 citedOpen Access
INTEGRATIVE GENOMIC AND EPIGENOMIC ANALYSIS OF AUTISM SPECTRUM DISORDER
European Neuropsychopharmacology·2023
81. IDENTIFICATION OF GENETIC FACTORS INFLUENCING EXTERNALIZING AND INTERNALIZING RISK BEHAVIOURS FOR ALCOHOL USE DISORDER
European Neuropsychopharmacology·2023
INTEGRATIVE GENOMIC AND EPIGENOMIC ANALYSIS OF ADHD
European Neuropsychopharmacology·2023
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Frequent Co-authors

Ole Mors(26), Anders D. Børglum(26), Jonas Bybjerg‐Grauholm(25), Jakob Grove(24), Esben Agerbo(21), Marie Bækvad‐Hansen(19), Merete Nordentoft(19), Preben Bo Mortensen(18), Thomas Werge(17), Ditte Demontis(16), David M. Hougaard(16), Manuel Mattheisen(15), Mark J. Daly(13), Stephan Ripke(12), Carsten Bøcker Pedersen(12), Benjamin M. Neale(11), Hreinn Stefánsson(10), Srdjan Djurovic(9), Raymond K. Walters(9), Panos Roussos(9)