Khalid Shakir
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Nutrition, Genetics, and Disease, Genomics and Phylogenetic Studies
Most-Cited Works
- → Analysis of protein-coding genetic variation in 60,706 humans(2016)10,243 cited
- → From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline(2013)7,119 cited
- → Scaling accurate genetic variant discovery to tens of thousands of samples(2017)2,070 cited
- → Patterns and rates of exonic de novo mutations in autism spectrum disorders(2012)1,788 cited
- → A polygenic burden of rare disruptive mutations in schizophrenia(2014)1,439 cited
- → Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel(2014)452 cited
- → Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes(2014)176 cited
- → Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls(2013)136 cited
- → Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13(2011)105 cited