Tarjinder Singh
Broad Institute(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Congenital heart defects research
Most-Cited Works
- → Synaptic, transcriptional and chromatin genes disrupted in autism(2014)2,891 cited
- → Rare coding variants in ten genes confer substantial risk for schizophrenia(2022)839 cited
- → Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders(2016)472 cited
- → Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing(2016)464 cited
- → Pdx1 Maintains β Cell Identity and Function by Repressing an α Cell Program(2014)405 cited
- → De novo variants in neurodevelopmental disorders with epilepsy(2018)312 cited
- → Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals(2019)299 cited
- → Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer’s disease mouse models(2022)291 cited
- → Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders(2017)271 cited
- → The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability(2017)245 cited