K. McCallum
Molecular Biology · 2013–2016
A researcher in the Science corpus: 2 papers; trusts 7 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 21 citations into it; #14,189 of 17,773 by trust here, #11,207 by citations
Whom K. McCallum trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts K. McCallum overall
Papers from K. McCallum's perspective
Ordered by how strongly the researchers K. McCallum trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- Quantifying heterogeneity in a meta‐analysis (Statistics in Medicine)
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (Nature)
- A general framework for estimating the relative pathogenicity of human genetic variants
- FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism (Cell)
- Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper
- Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. (The Lancet)
- Exome sequencing as a tool for Mendelian disease gene discovery
- Sequencing technologies — the next generation (Nature reviews genetics)
- Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome (Nature Genetics)
Their papers
- A SPECTRAL APPROACH INTEGRATING FUNCTIONAL GENOMIC ANNOTATIONS FOR CODING AND NONCODING VARIANTS (2016) — 572 citations
- Variation in the Heritability of Educational Attainment: An International Meta-Analysis (2013) — 311 citations