S Bort

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

S Bort, Eva Nelis, Vincent Timmerman et al. · Human Genetics · 1997 · 137 citations

Mutational Analysis, Mendelian Disorder, Genetic Disorder +7

Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis

Francesc Palau, Ann Löfgren, Peter De Jonghe et al. · Human Molecular Genetics · 1993 · 128 citations

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

Philip C. Bennett, Ricardo Segurado, Ian Jones et al. · Molecular Psychiatry · 2002 · 72 citations · Full text

Psychiatry, Genetics, Psychiatric Genetics +8

Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22

David Lambert, Fiona Middle, Marian L. Hamshere et al. · Molecular Psychiatry · 2005 · 60 citations

Chromosomes 6Q16–q21, Psychiatry, Genetic Disorder +14

An Integrated Physical and Gene Map of Human Distal Chromosome 17q24–Proximal 17q25 Encompassing Multiple Disease Loci

Linda M. Kalikin, Roberta Ann V. George, Marcel P. Keller et al. · Genomics · 1999 · 28 citations

Chromosome Dynamics, Integrated Physical, Multiple Disease Loci +12