Huntington F. Willard

发表

Centromeres: the missing link in the development of human artificial chromosomes.

H. Willard, Huntington F. Willard, 1998, Current opinion in genetics & development.

Characterization of a murine gene expressed from the inactive X chromosome

H. Willard, G. Borsani, A. Ballabio, 1991, Nature.

The β-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus

H. Willard, D. Housman, T. Shows, 1986, Nature.

The UTX gene escapes X inactivation in mice and humans.

A. Monaco, H. Willard, L. Carrel, 1998, Human molecular genetics.

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene.

P. Bolton, A. Monaco, H. Willard, 1997, Human molecular genetics.

Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum.

H. Willard, N. Green, K. Otsu, 1990, The Journal of biological chemistry.

Seventh International Workshop on the Fragile X and X-linked Mental Retardation.

H. Willard, C. Schwartz, W. Brown, 1996, American journal of medical genetics.

Regional localization of the TIMP gene on the human X chromosome

H. Willard, K. Davies, B. Williams, 1989, Human Genetics.

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes.

D. Schlessinger, H. Willard, J. Kere, 1995, Genomics.

Patient-Centered Precision Health In A Learning Health Care System: Geisinger's Genomic Medicine Experience.

F. D. Davis, W. Faucett, A. Rahm, 2018, Health affairs.

Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia

H. Willard, G. Annéren, J. Chelly, 1999, European Journal of Human Genetics.

Heritability of X chromosome--inactivation phenotype in a large family.

R. Plenge, L. Bird, A. Naumova, 1996, American journal of human genetics.

Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability.

H. Willard, R. Wevrick, Huntington F. Willard, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Report of the committee on the genetic constitution of the X chromosome.

R. Nussbaum, H. Willard, K. Davies, 1988, Cytogenetics and cell genetics.

The CEPH consortium linkage map of human chromosome 1.

R L White, K H Buetow, J M Lalouel, 1991, Genomics.

Physical and genetic mapping of the human X chromosome centromere: repression of recombination.

H. Willard, M. Mahtani, Huntington F. Willard, 1998, Genome research.

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status.

H. Willard, F. S. French, D. Lubahn, 1992, The Journal of clinical endocrinology and metabolism.

Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays.

H. Willard, R. Wevrick, Huntington F. Willard, 1991, Nucleic acids research.

Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA.

H. Willard, P. Warburton, P E Warburton, 1990, Journal of molecular biology.

Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence.

H. Willard, S. Latt, G. Stetten, 1975, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Xist Rna Paints the Inactive X Chromosome at Interphase: Evidence for a Novel Rna Involved in Nuclear/chromosome Structure Repository Citation

C. Clemson, Huntington F. Willard, John A Mcneil, 2022 .

Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene.

H. Willard, L. Carrel, P. Hunt, 1996, Human molecular genetics.

Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals.

H. Willard, B. Hendrich, Huntington F. Willard, 1995, Human molecular genetics.

Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22.

A. Monaco, J. Weissenbach, D. Schlessinger, 1995, Human molecular genetics.

Mammalian chromosome structure.

C. Tyler-Smith, H. Willard, Huntington F. Willard, 1993, Current opinion in genetics & development.

A novel transmembrane transporter encoded by the XPCT gene in Xq13.2.

H. Willard, L. Carrel, R. Lafreniére, 1994, Human molecular genetics.

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge

Daniel Nilsson, Peter Szolovits, Karen Eilbeck, 2014, Genome Biology.

Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA.

H. Willard, J. Waye, H F Willard, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation.

H. Willard, A. Higgins, N. Dahl, 2000, Genomics.