Pawel Stankiewicz

Genetics · 2002–2010

A researcher in the Science corpus: 5 papers; trusts 3 researchers and is trusted by 7 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 55 citations into it; #1,872 of 6,854 by trust here, #1,064 by citations
• Molecular Biology — 37 citations into it
• Plant Science — 30 citations into it; #2,089 of 8,232 by trust here, #2,434 by citations

Whom Pawel Stankiewicz trusts overall

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

1. J. R. Lupski
2. D. Kleinjan

Who trusts Pawel Stankiewicz overall

1. J. R. Lupski
2. Edwin H. Cook Jr.
3. N. Hunter
4. W. Gu
5. Feng Zhang
6. Elizabeth T. Cirulli
7. H. Zoghbi
8. Stephen W. Scherer
9. P. Hastings

Papers from Pawel Stankiewicz's perspective

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

1. Large-Scale Copy Number Polymorphism in the Human Genome (Science)
2. Global variation in copy number in the human genome (Nature)
3. The Influence of CCL3L1 Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility (Science)
4. A common inversion under selection in Europeans (Nature Genetics)
5. Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes (New England Journal of Medicine)
6. Segmental duplications and copy-number variation in the human genome. (American Journal of Human Genetics)
7. Long-range control of gene expression: emerging mechanisms and disruption in disease. (American Journal of Human Genetics)
8. Detection of large-scale variation in the human genome (Nature Genetics)
9. Genome architecture, rearrangements and genomic disorders. (Trends in Genetics)
10. Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes (PLoS Genetics)

Their papers

• Structural variation in the human genome and its role in disease. (2010) — 1,226 citations
• Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy (2010) — 783 citations
• Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities (2008) — 606 citations
• Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes (2005) — 601 citations
• Genome architecture, rearrangements and genomic disorders. (2002) — 961 citations