Siobhan M. Dolan

Publication List Details

Period

2008 - 2009

Number

7

Co-Authors

Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases (2009)

Khoury, Muin J., Bertram, Lars, Boffetta, Paolo, Butterworth, Adam S., Chanock, Stephen J., Dolan, Siobhan M., ...

Genome-wide association studies (GWAS) have led to a rapid increase in available data on common genetic variants and phenotypes and numerous discoveries of new loci associated with susceptibility to...

GAPscreener: An automatic tool for screening human genetic association literature in PubMed using the support vector machine technique (2008)

Yu, Wei, Clyne, Melinda, Dolan, Siobhan M, Yesupriya, Ajay, Wulf, Anja, Liu, Tiebin, ...

Abstract Background Synthesis of data from published human genetic association studies is a critical step in the translation of human genome discoveries into health applications. Although genetic...

Assessment of cumulative evidence on genetic associations: interim guidelines (2008)

Ioannidis, John PA, Boffetta, Paolo, Little, Julian, O’Brien, Thomas R, Uitterlinden, Andre G, Vineis, Paolo, ...

Established guidelines for causal inference in epidemiological studies may be inappropriate for genetic associations. A consensus process was used to develop guidance criteria for assessing...

BioMed Central (2008)

Bmc Bioinformatics, Wei Yu, Melinda Clyne, Siobhan M Dolan, Ajay Yesupriya, Anja Wulf, ...

Software GAPscreener: An automatic tool for screening human genetic association literature in PubMed using the support vector machine technique

Newborn Screening: Complexities in Universal Genetic Testing

Green, Nancy S., Dolan, Siobhan M., Murray, Thomas H.

Newborn screening (NBS)—in which each newborn infant is screened for up to 50 specific metabolic disorders for early detection and intervention—is the first program of populationwide genetic...

Genome-Wide Association Studies, Field Synopses, and the Development of the Knowledge Base on Genetic Variation and Human Diseases

Khoury, Muin J., Bertram, Lars, Boffetta, Paolo, Butterworth, Adam S., Chanock, Stephen J., Dolan, Siobhan M., ...

Genome-wide association studies (GWAS) have led to a rapid increase in available data on common genetic variants and phenotypes and numerous discoveries of new loci associated with susceptibility to...