Author

S. Boyle

Observed institutions: King's College London, Western General Hospital, MRC Human Genetics Unit

OpenAlex ID: A5076461968

The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells

2001 · S. Boyle · Human Molecular Genetics · 717

Re-modelling of nuclear architecture in quiescent and senescent human fibroblasts

2000 · J.M. Bridger, S. Boyle, et al. · Current Biology · 278

Chromosomal Localization in Mouse and Human of the Vasoactive Intestinal Peptide Receptor Type 2 Gene: A Possible Contributor to the Holoprosencephaly 3 Phenotype

1996 · M. Mackay, J. Fantes, et al. · Genomics · 45

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11) (q42.2;q21), associated with schizophrenia

2008 · W.J. Muir, C.M. Gosden, et al. · Cytogenetics and Cell Genetics · 27

Dual Y-chromosome Painting and Immunofluorescence Staining of Archival Human Liver Transplant Biopsies

2001 · S. R. Dundas, S. Boyle, et al. · Journal of Histochemistry & Cytochemistry · 16

Condensation behaviour of the human X chromosome in male germ cells and Sertoli cells examined by fluorescencein situ hybridization

1994 · S. Kofman-Alfaro, R. M. Speed, et al. · Chromosome Research · 9

A Sequence-Ready 3-Mb PAC Contig Covering 16 Breakpoints of the Wilms Tumor/Anirida Region of Human Chromosome 11p13

1998 · A. Niederführ, H. Hummerich, et al. · Genomics · 8

Automatic aberration scoring using whole chromosome F. I. S. H

1993 · Jim Piper, Rachel Bayley, et al. · OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · 1

Works count: 9

Citation count: 1,101

H-index: 7

I10-index: 5