Maja Bucan
Molecular Biology · 2001–2016
A researcher in the Science corpus: 10 papers; trusts 4 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 85 citations into it; #7,798 of 17,773 by trust here, #4,167 by citations
Whom Maja Bucan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Maja Bucan overall
Papers from Maja Bucan's perspective
Ordered by how strongly the researchers Maja Bucan trusts endorse each paper. Same corpus, a different order for every researcher.
- Large-scale analysis of the human and mouse transcriptomes (Proceedings of the National Academy of Sciences of the United States of America)
- The human genome browser at UCSC.
- Detection of large-scale variation in the human genome (Nature Genetics)
- BLAT--the BLAST-like alignment tool. (Genome Research)
- From genomics to chemical genomics: new developments in KEGG (Nucleic Acids Res.)
- Fine-scale structural variation of the human genome (Nature Genetics)
- Analysis of large-scale gene expression data. (Current Opinion in Immunology)
- EMBOSS: the European Molecular Biology Open Software Suite.
- The UCSC Table Browser data retrieval tool (Nucleic Acids Res.)
- A comparison of normalization methods for high density oligonucleotide array data based on variance and bias (Bioinform.)
Their papers
- A role for AMP-activated protein kinase in contraction- and hypoxia-regulated glucose transport in skeletal muscle. (2001) — 994 citations
- Promoter features related to tissue specificity as measured by Shannon entropy (2005) — 464 citations
- Pathway-based approaches for analysis of genomewide association studies. (2007) — 900 citations
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007) — 1,861 citations
- The Knockout Mouse Project (2004) — 618 citations
- High-throughput discovery of novel developmental phenotypes (2016) — 1,088 citations
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes (2009) — 1,451 citations
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (2009) — 1,008 citations
- Genotype, haplotype and copy-number variation in worldwide human populations (2008) — 881 citations
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements (2007) — 1,398 citations