Dan Pinkel

Genetics · 2000–2006

A researcher in the Science corpus: 13 papers; trusts 4 researchers and is trusted by 8 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 34 citations into it; #1,614 of 6,854 by trust here, #684 by citations
• Molecular Biology — 27 citations into it; #4,926 of 17,773 by trust here, #1,972 by citations
• Plant Science — 20 citations into it; #1,965 of 8,232 by trust here, #1,490 by citations

Whom Dan Pinkel trusts overall

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

1. Jane Fridlyand
2. Antoine Snijders
3. John P. A. Ioannidis
4. Ajay N. Jain
5. Donna Albertson

Who trusts Dan Pinkel overall

1. F. Mitelman
2. B. Johansson
3. F. Mertens
4. Chandra Erdman
5. Nancy Ruonan Zhang

Papers from Dan Pinkel's perspective

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

1. Assembly of microarrays for genome-wide measurement of DNA copy number (Nature Genetics)
2. Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling (Nature)
3. Fully automatic quantification of microarray image data. (Genome Research)
4. Molecular portraits of human breast tumours (Nature)
5. A tutorial on hidden Markov models and selected applications in speech recognition
6. Gentleman R: R: A language for data analysis and graphics
7. Chromosome aberrations in solid tumors (Nature Genetics)
8. Prospective identification of tumorigenic breast cancer cells (Proceedings of the National Academy of Sciences of the United States of America)
9. Exploration, normalization, and summaries of high density oligonucleotide array probe level data. (Biostatistics)
10. Diagnosis of multiple cancer types by shrunken centroids of gene expression

Their papers

• Segmental duplications and copy-number variation in the human genome. (2005) — 993 citations
• A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes. (2006) — 3,249 citations
• Distinct sets of genetic alterations in melanoma. (2005) — 2,454 citations
• Fully automatic quantification of microarray image data. (2002) — 363 citations
• Assembly of microarrays for genome-wide measurement of DNA copy number (2001) — 1,027 citations
• A tiling resolution DNA microarray with complete coverage of the human genome (2004) — 672 citations
• Somatic activation of KIT in distinct subtypes of melanoma. (2006) — 1,558 citations
• Array comparative genomic hybridization and its applications in cancer (2005) — 628 citations
• Hidden Markov models approach to the analysis of array CGH data (2004) — 383 citations
• Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome (2006) — 638 citations
• Determinants of BRAF mutations in primary melanomas. (2003) — 678 citations
• Fine-scale structural variation of the human genome (2005) — 1,086 citations
• Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene (2000) — 609 citations