Mark J. Berger

Genetics · 2016–2019

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 Mark J. Berger trusts overall

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

  1. James Y. Zou

Papers from Mark J. Berger's perspective

Ordered by how strongly the researchers Mark J. Berger 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. Analysis of protein-coding genetic variation in 60,706 humans
  7. Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.
  8. Faculty Opinions recommendation of Targeted capture and massively parallel sequencing of 12 human exomes.
  9. ACMG clinical laboratory standards for next-generation sequencing (Genetics in Medicine)
  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