List of works - Tarjinder Singh

ASD and ADHD have a similar burden of rare protein-truncating variants

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

scientific article published on 25 November 2019

Characterization of expression quantitative trait loci in the human colon

scientific article published on February 2015

Contribution of retrotransposition to developmental disorders

scientific article published on 11 October 2019

De novo variants in neurodevelopmental disorders with epilepsy

scientific article published on 25 June 2018

Development and characterization of 10 microsatellite markers in Sagina nodosa (Caryophyllaceae)

scientific article

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

scientific article published in August 2016

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations

scientific article published on 13 January 2020

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer

scientific article published on 10 February 2015

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania

scientific article

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Pdx1 maintains β cell identity and function by repressing an α cell program

scientific article published on February 2014

Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. ⬇️

scientific article published in December 2017

Rare coding variants in ten genes confer substantial risk for schizophrenia

article

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

scientific article

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

scientific article published on 26 June 2017

The genetic architecture and evolution of the human skeletal form

scientific article published on 20 July 2023

List of works by Tarjinder Singh

ASD and ADHD have a similar burden of rare protein-truncating variants

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Characterization of expression quantitative trait loci in the human colon

Contribution of retrotransposition to developmental disorders

De novo variants in neurodevelopmental disorders with epilepsy

Development and characterization of 10 microsatellite markers in Sagina nodosa (Caryophyllaceae)

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer

Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

Pdx1 maintains β cell identity and function by repressing an α cell program

Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. ⬇️

Rare coding variants in ten genes confer substantial risk for schizophrenia

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

The genetic architecture and evolution of the human skeletal form