Sotabase

Career

· Chair, VCSE Alliance, Nottingham And Nottinghamshire, NHS Nottingham and Nottinghamshire Integrated Care Board2023–
· Professor, Nottingham Trent University2018–
· Associate Professor In Organizational Behaviour, Nottingham Trent University2017–2018
· Senior Lecturer In Organizational Behaviour, Nottingham Trent University2007–2017
· Sessional Lecturer, University of Manchester2001–2006

Publications (19)

Prevalence and architecture of de novo mutations in developmental disorders
Nature · 2017
1,352
cited
Large-scale discovery of novel genetic causes of developmental disorders
Nature · 2014
1,051
cited
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
The Lancet · 2015
731
cited
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Cell Genomics · 2022
220
cited
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.
American Journal of Human Genetics · 2018
219
cited
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
Nature Genetics · 2015
147
cited
A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders
Genome Research · 2014
60
cited
Absence of heterozygosity due to template switching during replicative rearrangements.
American Journal of Human Genetics · 2015
54
cited
Mosaic structural variation in children with developmental disorders
Human Molecular Genetics · 2015
51
cited
Detection of structural mosaicism from targeted and whole-genome sequencing data
bioRxiv · 2016
48
cited
Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study
bioRxiv · 2016
48
cited
Analysis of genetic dominance in the UK Biobank
bioRxiv · 2021
41
cited
Systematic single-variant and gene-based association testing of 3,700 phenotypes in 281,850 UK Biobank exomes
medRxiv · 2021
21
cited
Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data
American Journal of Human Genetics · 2019
9
cited
Attention-deficit/hyperactivity disorder and ischemic stroke: A Mendelian randomization study
International Journal of Stroke · 2022
8
cited
Polygenic Scores and Parental Predictors: An Adult Height Study Based on the United Kingdom Biobank and the Framingham Heart Study
Frontiers in Genetics · 2021
7
cited
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Nature Communications · 2019
3
cited
PERHAPS: Paired-End short Reads-based HAPlotyping from next-generation Sequencing data
Briefings Bioinform. · 2020
3
cited
PAGEANT: personal access to genome and analysis of natural traits
medRxiv · 2021
1
cited
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Daniel A. King | Researcher Profile | Sotabase | Sotabase