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014-93-015

Funded outputs count: 137
Funder award ID: 014-93-015
OpenAlex ID: G300339986
A genome-wide meta-analysis of actinic keratosis identifies 12 novel loci and overlap with keratinocyte carcinoma and pigmentation
2026 · Christina M. W. Eecen, Christopher D. George, et al. · Communications Biology
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Cross‐ancestry polygenic risk scores enhance Alzheimer's disease risk prediction in multiethnic cohorts
2026 · Meri Okorie, Caroline Jonson, et al. · Alzheimer s & Dementia · 5
Genetic architecture and cross-platform validation of apolipoprotein A-IV concentrations
2026 · Adriana Koller, Florian Schnitzer, et al. · Genome biology
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
2026 · Nora I. Strom, Brad Verhulst, et al. · Nature Genetics · 28
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Interactive Effects of Telomere Length and Genetic Variants on Alzheimer Disease Risk Across Multiple Ancestral Populations
2025 · Zainab Khurshid, Tong Tong, et al. · medRxiv · 1
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Exploring the genetics of airflow limitation in lung function across the lifespan – a polygenic risk score study
2024 · Natalia Hernandez-Pacheco, Anna Kilanowski, et al. · EClinicalMedicine · 20
Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling
2024 · Nora I. Strom, Brad Verhulst, et al. · medRxiv · 27
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Towards Personalized TSH Reference Ranges: A Genetic and Population-Based Approach in Three Independent Cohorts
2024 · Aleksander Kuś, Aleksander Kuś, et al. · Thyroid · 11
Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia
2024 · Muralidharan Sargurupremraj, Aicha Soumaré, et al. · JAMA Network Open · 21
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Genetic variants for head size share genes and pathways with cancer
2024 · Maria J. Knol, Raymond A. Poot, et al. · Cell Reports Medicine · 10
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Early‐onset Alzheimer's disease explained by polygenic risk of late‐onset disease?
2023 · William G. Mantyh, J. Nicholas Cochran, et al. · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 13
Investigation of the independent role of a rare APOE variant (L28P; APOE*4Pittsburgh) in late-onset Alzheimer disease
2022 · KangHsien Fan, Lily Francis, et al. · Neurobiology of Aging · 21
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A comparative study of structural variant calling strategies using the Alzheimer’s Disease Sequencing Project’s whole genome family data
2022 · John S. Malamon, John J. Farrell, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1
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Genetic variants associated with longitudinal changes in brain structure across the lifespan
2022 · Rachel M. Brouwer, Marieke Klein, et al. · Nature Neuroscience · 227
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Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping
2022 · Michael E. Belloy, Sarah J. Eger, et al. · Alzheimer s Research & Therapy · 22
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Toll-Like Receptor 1 Locus Re-examined in a Genome-Wide Association Study Update on Anti–Helicobacter pylori IgG Titers
2022 · Suk Yee Lam, Michiel C. Mommersteeg, et al. · Gastroenterology · 25
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Genetic architecture of orbital telorism
2021 · Maria J Knol, Mikolaj A Pawlak, et al. · Human Molecular Genetics · 9
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Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project
2021 · Wan-Ping Lee, Albert A. Tucci, et al. · Frontiers in Genetics · 13
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Investigating the genetic and environmental basis of head micromovements during MRI
2021 · Frauke Beyer, Katrin Horn, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
2021 · Janel O. Johnson, Ruth Chia, et al. · JAMA Neurology · 82
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An Association Test of the Spatial Distribution of Rare Missense Variants within Protein Structures Improves Statistical Power of Sequencing Studies
2021 · Bowen Jin, John A. Capra, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 2
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A comparison of genotyping arrays
2021 · Joost A. M. Verlouw, Eva Clemens, et al. · European Journal of Human Genetics · 87
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A Machine Learning Method to Identify Genetic Variants Potentially Associated With Alzheimer’s Disease
2021 · Bradley Monk, Andrei Rajkovic, et al. · Frontiers in Genetics · 16
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Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
2020 · Julie Hahn, Yi-Ping Fu, et al. · PLoS ONE · 9
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Genome-wide association study identifies 48 common genetic variants associated with handedness
2020 · Gabriel Cuellar-Partida, Joyce Y. Tung, et al. · Nature Human Behaviour · 159
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