Huntington F. Willard

According to our database, Huntington F. Willard authored at least 5 papers between 1997 and 2014.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2014

Genomic Characterization of Large Heterochromatic Gaps in the Human Genome Assembly.

Nicolas Altemose, Karen H. Miga, Mauro Maggioni, Huntington F. Willard

PLoS Comput. Biol., 2014

2009

A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine.

Kensaku Kawamoto, David F. Lobach, Huntington F. Willard, Geoffrey S. Ginsburg

BMC Medical Informatics Decis. Mak., 2009

2006

Evidence of Influence of Genomic DNA Sequence on Human X Chromosome Inactivation.

Zhong Wang, Huntington F. Willard, Sayan Mukherjee, Terrence S. Furey

PLoS Comput. Biol., 2006

2001

Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome.

Brian P. Chadwick, Cory M. Valley, Huntington F. Willard

Nucleic Acids Res., 2001

1997

Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation.

Brian D. Hendrich, Robert M. Plenge, Huntington F. Willard

Nucleic Acids Res., 1997