H.F. Willard

Biochemistry, Genetics and Molecular Biology · Life Sciences

28h-index6.0kcitations325works0.02yr avg
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Research Topics

Molecular Biology Techniques and Applications(20), Chromosomal and Genetic Variations(12), Genomic variations and chromosomal abnormalities(10), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities(9), Genomics and Chromatin Dynamics(6)

Publications117 total

Evolution and function of alpha satellite DNA
Pathologie Biologie·2001· 2 cited
An XIST promoter mutation modifies skewed X inactivation in a family segregating an X-linked mental retardation syndrome
1997
Chromosome manipulation: a systematic approach toward understanding human chromosome structure and function.
Proceedings of the National Academy of Sciences·1996· 21 citedOpen Access
Heritability of X chromosome--inactivation phenotype in a large family.
PubMed·1996· 176 citedOpen Access
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure.
The Journal of Cell Biology·1996· 794 citedOpen Access
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
PubMed·1996· 76 cited
Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals
Human Molecular Genetics·1995· 80 cited
An X-linked homologue of the autosomal inprinted gene ZNF127 escapes X inactivation
The American Journal of Human Genetics·1994
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
PubMed·1994· 75 cited
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia
Human Molecular Genetics·1994· 75 cited
Absence of the X1st gene from the late replicating isodicentric X chromosome in myelodysplasia
Leukemia Research·1994
Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin.
Molecular and Cellular Biology·1993· 76 citedOpen Access
2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the <i>RPS4X, PHKA1, XIST</i> and <i>DXS128E</i> genes
Human Molecular Genetics·1993· 53 cited
Epigenetic and Chromosomal Control of Gene Expression: Molecular and Genetic Analysis of X Chromosome Inactivation
Cold Spring Harbor Symposia on Quantitative Biology·1993· 54 cited
Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.
PubMed·1992· 28 cited
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM.
Europe PMC (PubMed Central)·1992· 36 citedOpen Access
Genome maps III
1992· 1 cited
Editorial Notice
Cytogenetic and Genome Research·1992Open Access
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study
Blood·1991· 116 citedOpen Access
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study
Blood·1991· 7 citedOpen Access
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Frequent Co-authors

K. Kidd(28), P.L. Pearson(23), P.J. McAlpine(20), K.K. Kidd(20), J.-L. Mandel(19), A.J. Pakstis(17), M.H. Skolnick(17), Claude Boucheix(15), R.C. Douté(14), N. Van Cong(13), T.B. Shows(13), P. Pearson(12), P. Pearson(11), Robert Miller(11), P.M. Conneally(9), P.A. Lalley(8), G.R. Sutherland(7), D.R. Cox(7), T.B. Shows(6), J.F. Gusella(6)