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Publications

Global, regional, and national burden of stroke and its risk factors, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021.

Global, regional, and national burden of stroke and its risk factors, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021. The Lancet. Neurology. 2024;23(10):973-1003. doi:10.1016/S1474-4422(24)00369-7

The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point Mutations.

Weinstock JS, Chaudhry SA, Ioannou M, et al. The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point Mutations. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.08.22.24312319

Non-canonical Wnt signaling triggered by WNT2B drives adrenal aldosterone production.

Borges KS, Little DW, Magalhães T de A, et al. Non-canonical Wnt signaling triggered by WNT2B drives adrenal aldosterone production. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.08.23.609423

Descriptives and genetic correlates of eating disorder diagnostic transitions and presumed remission in the Danish registry.

Abdulkadir M, Larsen JT, Clausen L, et al. Descriptives and genetic correlates of eating disorder diagnostic transitions and presumed remission in the Danish registry. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.09.05.24313142

A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner.

Boltz TA, Chu BB, Liao C, et al. A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner. bioRxiv : the preprint server for biology. 2024. doi:10.1101/2024.09.06.611689

Inter-organ cross-talk in human cancer cachexia revealed by spatial metabolomics.

Sun N, Krauss T, Seeliger C, et al. Inter-organ cross-talk in human cancer cachexia revealed by spatial metabolomics. Metabolism: clinical and experimental. 2024:156034. doi:10.1016/j.metabol.2024.156034

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder.

Blackburn PR, Ebstein F, Hsieh TC, et al. Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder. Annals of neurology. 2024. doi:10.1002/ana.27077

Molecular basis of TMED9 oligomerization and entrapment of misfolded protein cargo in the early secretory pathway.

Xiao L, Pi X, Goss AC, et al. Molecular basis of TMED9 oligomerization and entrapment of misfolded protein cargo in the early secretory pathway. Science advances. 2024;10(38):eadp2221. doi:10.1126/sciadv.adp2221

Biological Insights from Schizophrenia-associated Loci in Ancestral Populations.

Bigdeli TB, Chatzinakos C, Bendl J, et al. Biological Insights from Schizophrenia-associated Loci in Ancestral Populations. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.08.27.24312631

Biological Insights from Schizophrenia-associated Loci in Ancestral Populations.

Bigdeli TB, Chatzinakos C, Bendl J, et al. Biological Insights from Schizophrenia-associated Loci in Ancestral Populations. medRxiv : the preprint server for health sciences. 2024. doi:10.1101/2024.08.27.24312631