| Antipsychotic medications and sleep problems in patients with schizophrenia E Cederlöf, M Holm, H Taipale, J Tiihonen, A Tanskanen, M Lähteenvuo, ... Schizophrenia Research 267, 230-238, 2024 | | 2024 |
| Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability L Urpa, MI Kurki, E Rahikkala, E Hämäläinen, V Salomaa, J Suvisaari, ... European Journal of Human Genetics 32 (5), 576-583, 2024 | 1 | 2024 |
| Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders A Kämpe, J Suvisaari, M Lähteenvuo, T Singh, A Ahola-Olli, L Urpa, ... Molecular Psychiatry, 1-9, 2024 | | 2024 |
| Enhancement of mediodorsal thalamus rescues aberrant belief dynamics in a mouse model with schizophrenia-associated mutation T Zhou, YY Ho, RX Lee, AB Fath, K He, J Scott, N Bajwa, ND Hartley, ... bioRxiv: the preprint server for biology, 2024 | | 2024 |
| Enhancement of mediodorsal thalamus rescues aberrant belief dynamics in a mouse model with schizophrenia-associated mutation T Zhou, YY Ho, RX Lee, AB Fath, K He, J Scott, N Bajwa, ND Hartley, ... bioRxiv, 2024 | 1 | 2024 |
| The genetic architecture and evolutionary consequences of the human pelvic form L Xu, E Kun, D Pandey, J Wang, M Brasil, T Singh, VM Narasimhan bioRxiv, 2024.05. 02.592256, 2024 | | 2024 |
| W88. PHENOTYPIC AND GENETIC CHARACTERIZATION OF INDIVIDUALS WITH SCHIZOPHRENIA AND HIGH PSYCHIATRIC HOSPITALIZATION BURDEN A Kämpe, J Suvisaari, M Lähteenvuo, E Vartiainen, T Singh, A Ahola-Olli, ... European Neuropsychopharmacology 75, S151-S152, 2023 | | 2023 |
| Deep learning based phenotyping of medical images improves power for gene discovery of complex disease BI Flynn, EM Javan, E Lin, Z Trutner, K Koenig, KO Anighoro, E Kun, ... NPJ Digital Medicine 6 (1), 155, 2023 | 2 | 2023 |
| The genetic architecture and evolution of the human skeletal form E Kun, EM Javan, O Smith, F Gulamali, J de la Fuente, BI Flynn, K Vajrala, ... Science 381 (6655), eadf8009, 2023 | 11 | 2023 |
| The impact of rare protein coding genetic variation on adult cognitive function CY Chen, R Tian, T Ge, M Lam, G Sanchez-Andrade, T Singh, L Urpa, ... Nature Genetics 55 (6), 927-938, 2023 | 18 | 2023 |
| Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia YHH Hsu, G Pintacuda, R Liu, E Nacu, A Kim, K Tsafou, N Petrossian, ... Iscience 26 (5), 2023 | 2 | 2023 |
| Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations D Liu, D Meyer, B Fennessy, C Feng, E Cheng, JS Johnson, YJ Park, ... Nature genetics 55 (3), 369-376, 2023 | 22 | 2023 |
| The genetic architecture of the human skeletal form E Kun, EM Javan, O Smith, F Gulamali, J de la Fuente, BI Flynn, K Vajrala, ... bioRxiv, 2023 | 2 | 2023 |
| Clinical phenotypes of five patients with psychotic disorders carrying rare schizophrenia-associated loss-of-function variants BM Cohen, T Singh, D Öngür, GE Konstantin, ME Gardner Schizophrenia Research 250, 100-103, 2022 | 3 | 2022 |
| Enrichment of Rare, Damaging Variants in Schizophrenia-related Genes in Intellectual Disability Patients with Psychotic Disorders L Urpa, M Kurki, T Singh, E Hamalainen, E Rahikkala, J Moilanen, ... European Neuropsychopharmacology 63, E45-E45, 2022 | | 2022 |
| Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer’s disease mouse models B Dejanovic, T Wu, MC Tsai, D Graykowski, VD Gandham, CM Rose, ... Nature aging 2 (9), 837-850, 2022 | 82 | 2022 |
| The 22q11. 2 region regulates presynaptic gene-products linked to schizophrenia R Nehme, O Pietiläinen, M Artomov, M Tegtmeyer, V Valakh, L Lehtonen, ... Nature Communications 13 (1), 3690, 2022 | 21 | 2022 |
| Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia DS Palmer, DP Howrigan, SB Chapman, R Adolfsson, N Bass, ... Nature genetics 54 (5), 541-547, 2022 | 86 | 2022 |
| Rare coding variants in ten genes confer substantial risk for schizophrenia T Singh, T Poterba, D Curtis, H Akil, M Al Eissa, JD Barchas, N Bass, ... Nature 604 (7906), 509-516, 2022 | 544* | 2022 |
| Rare schizophrenia risk variant burden is conserved in diverse human populations D Liu, D Meyer, B Fennessy, C Feng, E Cheng, JS Johnson, YJ Park, ... medRxiv, 2022.01. 03.22268662, 2022 | 2 | 2022 |
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad Institute在 atgu.mgh.harvard.edu 的电子邮件经过验证
