A. Guttmacher
Genetics · 2000–2010
A researcher in the Science corpus: 9 papers; trusts 2 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 113 citations into it
- Molecular Biology — 86 citations into it; #14,532 of 17,773 by trust here, #2,960 by citations
Whom A. Guttmacher trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts A. Guttmacher overall
Papers from A. Guttmacher's perspective
Ordered by how strongly the researchers A. Guttmacher trusts endorse each paper. Same corpus, a different order for every researcher.
- The hallmarks of cancer (RNA Biology)
- Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. (New England Journal of Medicine)
- Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome. (New England Journal of Medicine)
- Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. (New England Journal of Medicine)
- A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
- Network dynamics and cell physiology (Nature reviews. Molecular cell biology)
- Complement Factor H Polymorphism in Age-Related Macular Degeneration (Science)
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration (Science)
Their papers
- A vision for the future of genomics research (2003) — 1,818 citations
- International network of cancer genome projects (2010) — 2,229 citations
- Replicating genotype–phenotype associations (2007) — 1,394 citations
- Finding the missing heritability of complex diseases (2009) — 8,360 citations
- International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia (2009) — 1,075 citations
- Finding the missing heritability of complex (2009) — 88 citations
- The family history--more important than ever. (2004) — 508 citations
- Genomic medicine--a primer. (2002) — 614 citations
- Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). (2000) — 1,694 citations