2013 - Member of the National Academy of Sciences
2009 - William Allan Award, the American Society of Human Genetics
2008 - Fellow of the American Academy of Arts and Sciences
2005 - Fellow of the American Association for the Advancement of Science (AAAS)
Genetics and Medical genetics are two areas of study in which Huntington F. Willard engages in interdisciplinary research. Huntington F. Willard conducted interdisciplinary study in his works that combined Medical genetics and Genetics. While working on this project, Huntington F. Willard studies both Gene and Computational biology. His work often combines Computational biology and Gene studies. In his works, he undertakes multidisciplinary study on Soil science and Miami. Miami and Soil science are two areas of study in which he engages in interdisciplinary research. He brings together Chromosome 22 and Human genome to produce work in his papers. While working on this project, he studies both Human genome and Chromosome 22. Huntington F. Willard connects X chromosome with Chromosome in his study.
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Report of the committee on the genetic constitution of the X chromosome
K E Davies;J L Mandel;A P Monaco;R L Nussbaum.
Cytogenetic and Genome Research (1988)
A first-generation X-inactivation profile of the human X chromosome
Laura Carrel;Amy A. Cottle;Karrie C. Goglin;Huntington F. Willard.
Proceedings of the National Academy of Sciences of the United States of America (1999)
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation.
Carolyn J. Brown;Huntington F. Willard.
The interleukin-2 receptor γ chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1
Jennifer M. Puck;Suzanne M. Deschenes;Joanne C. Porter;Amalla S. Dutra.
Human Molecular Genetics (1993)
Isolation and characterization of a major tandem repeat family from the human X chromosome
Huntington F. Willard;Kirby D. Smith;Joanne Sutherland.
Nucleic Acids Research (1983)
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.
E Bakker;N Goor;K Wrogemann;L.M Kunkel.
The Lancet (1985)
Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome.
J S Waye;H F Willard.
Molecular and Cellular Biology (1986)
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation.
Plenge Rm;Hendrich Bd;Schwartz C;Arena Jf.
Nature Genetics (1997)
Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome
Brian P. Chadwick;Huntington F. Willard.
Proceedings of the National Academy of Sciences of the United States of America (2004)
Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques.
M.H. Skolnick;H.F. Willard;L.A. Menlove.
Cytogenetic and Genome Research (1982)
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