F. S. Collins

Molecular Biology · 2000–2019

A researcher in the Science corpus: 57 papers; trusts 6 researchers and is trusted by 13 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 541 citations into it; #5,334 of 17,773 by trust here, #63 by citations
• Genetics — 531 citations into it; #2,696 of 6,854 by trust here, #29 by citations
• Immunology — 48 citations into it
• Public Health, Environmental and Occupational Health — 44 citations into it; #2,230 of 2,368 by trust here, #273 by citations
• Oncology — 25 citations into it
• Hematology — 11 citations into it
• Spectroscopy — 8 citations into it

Whom F. S. Collins trusts overall

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

1. Brian J. Druker
2. David Reich
3. Matthias Mann
4. Eric S. Lander
5. D. Selkoe
6. D. Lockhart
7. Joel Hirschhorn

Who trusts F. S. Collins overall

1. Sudhir Kumar
2. Torsten Schwede
3. Alan J. Filipski
4. Jay Shendure
5. S. Dunbar
6. Lin Liu
7. William R. Hersh
8. John P. A. Ioannidis
9. Koichiro Tamura
10. Martha L. Bulyk

Papers from F. S. Collins's perspective

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

1. Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
2. SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations (Nature Genetics)
3. Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol (Science)
4. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. (New England Journal of Medicine)
5. A global reference for human genetic variation
6. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
7. A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
8. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
9. 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)
10. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)

Their papers

• Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (2009) — 4,227 citations
• A vision for the future of genomics research (2003) — 1,818 citations
• Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
• Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) — 2,140 citations
• The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (2004) — 602 citations
• A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
• The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) — 2,411 citations
• Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
• Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations
• The Genome Sequence of the Malaria Mosquito Anopheles gambiae (2002) — 2,077 citations
• The Human Genome Project: Lessons from Large-Scale Biology (2003) — 1,177 citations
• Implications of the Human Genome Project for medical science. (2001) — 750 citations
• Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS). (2005) — 522 citations
• VectorBase: an updated bioinformatics resource for invertebrate vectors and other organisms related with human diseases (2014) — 567 citations
• International network of cancer genome projects (2010) — 2,229 citations
• Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
• Short interfering RNAs can induce unexpected and divergent changes in the levels of untargeted proteins in mammalian cells (2004) — 636 citations
• Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants (2013) — 661 citations
• Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) — 7,050 citations
• The path to personalized medicine. (2010) — 957 citations