about
Development and characterization of 10 microsatellite markers in Sagina nodosa (Caryophyllaceae)Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancerPdx1 maintains β cell identity and function by repressing an α cell program.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.Characterization of expression quantitative trait loci in the human colon.Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing.De novo variants in neurodevelopmental disorders with epilepsyASD and ADHD have a similar burden of rare protein-truncating variantsNovel genes for autism implicate both excitatory and inhibitory cell lineages in riskContribution of retrotransposition to developmental disordersAutism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variantsExome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations
P50
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P50
description
researcher ORCID ID = 0000-0003-0601-6815
@en
wetenschapper
@nl
name
Tarjinder Singh
@ast
Tarjinder Singh
@en
Tarjinder Singh
@es
Tarjinder Singh
@nl
type
label
Tarjinder Singh
@ast
Tarjinder Singh
@en
Tarjinder Singh
@es
Tarjinder Singh
@nl
prefLabel
Tarjinder Singh
@ast
Tarjinder Singh
@en
Tarjinder Singh
@es
Tarjinder Singh
@nl
P106
P21
P31
P496
0000-0003-0601-6815