| 45 EXOME SEQUENCING OF 25,000 SCHIZOPHRENIA CASES IMPLICATES 10 RISK GENES, AND PROVIDES INSIGHT INTO SHARED AND DISTINCT GENETIC RISK AND BIOLOGY WITH OTHER NEURODEVELOPMENTAL … T Singh, B Neale, M Daly European Neuropsychopharmacology 29, S84, 2019 | | 2019 |
| 54EXOME SEQUENCING OF 23,851 CASES IMPLICATES NOVEL RISK GENES AND PROVIDES INSIGHTS INTO THE GENETIC ARCHITECTURE OF SCHIZOPHRENIA T Singh, B Neale, M Daly, SCHEMA Consortium European Neuropsychopharmacology 29, S1098, 2019 | 2 | 2019 |
| 56. GENOTYPE-PHENOTYPE ANALYSES IN 10,000 INDIVIDUALS WITH PSYCHOSIS HIGHLIGHTS COMPLEX ROLE OF ULTRA-RARE CODING VARIANTS AND COMMON POLYGENIC RISK IN PRESENTATION AND ETIOLOGY T Singh, M Daly, B Neale, A Palotie European Neuropsychopharmacology 51, e70-e71, 2021 | | 2021 |
| A Comparative Study of Therapeutic Efficacy between Intralesional Steroids and Cryotherapy in the Management of Keloids BP Kumar, M Shahana, GNR Netha, KB Kumar, TR Singh, CHR Mohan | | |
| A META-ANALYSIS OF> 16,000 EXOMES REVEALS A DOMINANT, HIGHLY PENETRANT SUBTYPE OF SCHIZOPHRENIA COMORBID WITH INTELLECTUAL DISABILITY T Singh, J Barrett EUROPEAN NEUROPSYCHOPHARMACOLOGY 27, S275-S275, 2017 | | 2017 |
| 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 |
| Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications,(2018), 9, 1 … B Snijders, J Rousseau, J Twist, S Ehresmann, M Takaku, H Venselaar, ... Nature Communications, 2019 | | 2019 |
| Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants FK Satterstrom, RK Walters, T Singh, EM Wigdor, F Lescai, D Demontis, ... Nature neuroscience 22 (12), 1961-1965, 2019 | 204 | 2019 |
| BASIC AND TRANSLATIONAL-PANCREAS T Gao, D Zhou, C Yang, T Singh, A Penzo-Mendez, R Maddipati, ... GASTROENTEROLOGY 144 (7), 1543-U380, 2013 | | 2013 |
| Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia KM Gorman, E Meyer, D Grozeva, E Spinelli, A McTague, A Sanchis-Juan, ... The American Journal of Human Genetics 104 (5), 948-956, 2019 | 59 | 2019 |
| Characterization of expression quantitative trait loci in the human colon T Singh, AP Levine, PJ Smith, AM Smith, AW Segal, JC Barrett Inflammatory bowel diseases 21 (2), 251-256, 2015 | 32 | 2015 |
| Characterization of six CaMKIIα variants found in patients with schizophrenia CN Brown, SG Cook, HF Allen, KC Crosby, T Singh, SJ Coultrap, ... Iscience 24 (10), 2021 | 10 | 2021 |
| CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018) LS Blok, J Rousseau, J Twist, S Ehresmann, M Takaku, H Venselaar, ... Nature Communications 10 (1), 883-, 2019 | 1 | 2019 |
| 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 |
| 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 |
| Contribution of retrotransposition to developmental disorders EJ Gardner, E Prigmore, G Gallone, P Danecek, KE Samocha, ... Nature Communications 10 (1), 4630, 2019 | 64 | 2019 |
| De novo variants in neurodevelopmental disorders with epilepsy HO Heyne, T Singh, H Stamberger, R Abou Jamra, H Caglayan, D Craiu, ... Nature genetics 50 (7), 1048-1053, 2018 | 264 | 2018 |
| 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 |
| Deogratius Soka, Bruno Mmbando, Evarist Msaki, Iris Kolder, Swee Lay Thein, et al. Genome wide association study of fetal hemoglobin in sickle cell anemia in tanzania SN Mtatiro, T Singh, H Rooks, J Mgaya, H Mariki PloS one 9 (11), e111464, 2014 | 2 | 2014 |
| Development and characterization of 10 microsatellite markers in Sagina nodosa (Caryophyllaceae) T Singh, J Edwards, LS Maroja Applications in plant sciences 2 (1), 1300064, 2014 | 2 | 2014 |
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
