H. Tabor
Genetics · 2001–2015
A researcher in the Science corpus: 6 papers; trusts 5 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 63 citations into it
- Molecular Biology — 53 citations into it
Whom H. Tabor trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Pauline Crystal Ng
- Daniel Chasman
- Shamil R. Sunyaev
- Steven Henikoff
- Rhys M. Adams
- N. Risch
- V. Ramensky
- Lon R. Cardon
Who trusts H. Tabor overall
Papers from H. Tabor's perspective
Ordered by how strongly the researchers H. Tabor trusts endorse each paper. Same corpus, a different order for every researcher.
- Prediction of deleterious human alleles.
- A method and server for predicting damaging missense mutations
- Accounting for human polymorphisms predicted to affect protein function. (Genome Research)
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
- Searching for genetic determinants in the new millennium (Nature)
- Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation.
- Listening to silence and understanding nonsense: exonic mutations that affect splicing (Nature reviews genetics)
- Molecular portraits of human breast tumours (Nature)
- Most rare missense alleles are deleterious in humans: implications for complex disease and association studies. (American Journal of Human Genetics)
- Analysis of gene expression profiles in normal and neoplastic ovarian tissue samples identifies candidate molecular markers of epithelial ovarian cancer. (Proceedings of the National Academy of Sciences of the United States of America)
Their papers
- Exome sequencing identifies the cause of a Mendelian disorder (2009) — 2,093 citations
- Candidate-gene approaches for studying complex genetic traits: practical considerations (2002) — 1,155 citations
- The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. (2015) — 611 citations
- Exome sequencing as a tool for Mendelian disease gene discovery (2011) — 1,755 citations
- Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome (2010) — 1,398 citations
- Older women with diabetes have an increased risk of fracture: a prospective study. (2001) — 818 citations