Harendra Guturu

Genetics · 2016–2021

A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Whom Harendra Guturu trusts

Their strongest outbound trust, strongest first, inferred from their citations.

  1. James Y. Zou (in Genetics)

Papers from Harendra Guturu's perspective

Ordered by how strongly the researchers Harendra Guturu trusts endorse each paper. Same corpus, a different order for every researcher.

  1. A method and server for predicting damaging missense mutations
  2. Exome sequencing identifies the cause of a Mendelian disorder (Nature Genetics)
  3. The UCSC genome browser and associated tools (Briefings Bioinform.)
  4. The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
  5. Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders (Journal of the American Medical Association (JAMA))
  6. Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.
  7. Analysis of protein-coding genetic variation in 60,706 humans
  8. ACMG clinical laboratory standards for next-generation sequencing (Genetics in Medicine)
  9. Faculty Opinions recommendation of Targeted capture and massively parallel sequencing of 12 human exomes.
  10. Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular…

Their papers