Willard, Huntington F.

X-inactivation profile reveals extensive variability in X-linked gene expression in females

Carrel, L., & Willard, H. F. (2005) · Nature

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 2,097

The DNA sequence of the human X chromosome

Ross, M. T., Grafham, D. V., Coffey, A. J., Scherer, S., McLay, K., Muzny, D., Platzer, M., Howell, G. R., Burrows, C., Bird, C. P., et al. (2005) · Nature

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesChromosomal and Genetic Variations

Cited by 1,129

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Franco, B., Guioli, S., Pragliola, A., Incerti, B., Bardoni, B., Tonlorenzi, R., Carrozzo, R., Maestrini, E., Pieretti, M., Taillon-Miller, P., et al. (1991) · Nature

Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies

Cited by 846

Genomic and personalized medicine: foundations and applications

Ginsburg, G. S., & Willard, H. F. (2009) · Translational Research

Genomics and Rare DiseasesPharmacogenetics and Drug Metabolism

Cited by 637

Heritable Individual-Specific and Allele-Specific Chromatin Signatures in Humans

McDaniell, R., Lee, B.-K., Song, L., Liu, Z., Boyle, A. P., Erdos, M. R., Scott, L. J., Morken, M. A., Kucera, K. S., Battenhouse, A., et al. (2010) · Science

Genomics and Chromatin DynamicsGenetic Associations and Epidemiology

Cited by 308

Clinical outcomes of a genomic screening program for actionable genetic conditions

Buchanan, A. H., Lester Kirchner, H., Schwartz, M. L. B., Kelly, M. A., Schmidlen, T., Jones, L. K., Hallquist, M. L. G., Rocha, H., Betts, M., Schwiter, R., et al. (2020) · Genetics in Medicine

BRCA gene mutations in cancerGenomics and Rare Diseases

Cited by 143