H.F. Willard

Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17

David Barker, E Wright, K. Nguyen et al. · Science · 1987 · 695 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

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

Kinya Otsu, H.F. Willard, Veena Khanna et al. · Journal of Biological Chemistry · 1990 · 617 citations · Full text

Cardiac Muscle, Muscle Function, Ca2+ Release Channel +20

PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

Egbert Bakker, Nicole Goor, Klaus Wrogemann et al. · The Lancet · 1985 · 376 citations

Pediatrics, Diagnosis, Degenerative Disease +4

Chromosome-specific subsets of human alpha satellite DNA: Analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat

H.F. Willard, John S. Waye · Journal of Molecular Evolution · 1987 · 199 citations

Medicine, Genetics, Evolutionary Biology +9

Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease.

Robert G. Korneluk, Don J. Mahuran, Kuldeep Neote et al. · Journal of Biological Chemistry · 1986 · 177 citations · Full text