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Mouse and cellular models of KPTN -related disorder implicate mTOR signalling in cognitive and progressive overgrowth phenotypes2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Maria O. Levitin, Lettie E. Rawlins, Gabriela Sánchez-Andrade, Osama A. Arshad, Stephan C. Collins, Stephen J. Sawiak, +35 more
1citations -
Cell-projected Phenotypes Link Transcriptional and Phenotypic Heterogeneity in Alzheimer’s Disease2026 SSRN Electronic Journal preprint Biochemistry, Genetics and Molecular Biology Single-cell and spatial transcriptomics Open access
Riley J. Mangan, Gerard A. Bouland, Tim Schubert, Danish Anwer, Judy Bai, Gülfem Ekiz, +6 more
0citations -
Grey and white matter metrics demonstrate distinct and complementary prediction of differences in cognitive performance in children: Findings from ABCD (N= 11 876)5citations
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Erbb4 deletion from fast-spiking interneurons causes psychosis-relevant neuroimaging phenotypes2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Medicine Schizophrenia research and treatment Open access
Amanda Kiemes, Maria Elisa Serrano Navacerrada, Eugene Kim, Karen Randall, Camilla Simmons, Loreto Rojo Gonzalez, +11 more
1citations -
Genome-wide association study of treatment resistant depression highlights shared biology with metabolic traits2022 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genetic Associations and Epidemiology Open access
Jooeun Kang, Victor Manuel Castro, Michael A. Ripperger, Sanan Venkatesh, David Burstein, Richard Karlsson Linnér, +16 more
3citations -
The MetaboHealth score enhances insulin resistance metabotyping for targeted fat loss through personalized diets: Insights from the PERSON intervention study2024 medRxiv preprint Biochemistry, Genetics and Molecular Biology Metabolomics and Mass Spectrometry Studies Open access
Jordi Morwani‐Mangnani, Fatih A. Bogaards, Alexander Umanets, Gabby B. J. Hul, Anouk Gijbels, Gijs H. Goossens, +5 more
3citations -
Elucidating the clinical and molecular spectrum of SMARCC2 -associated NDD in a cohort of 65 affected individuals2023 medRxiv preprint Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Elisabeth Bosch, Bernt Popp, Esther Güse, Cindy D. Skinner, Pleuntje J. van der Sluijs, Isabelle Maystadt, +64 more
0citations
17 results