A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation

Parametric and nonparametric linkage analysis: a unified multipoint approach.

Leonid Kruglyak, Mark J. Daly, Mary Pat Reeve-Daly et al. · PubMed · 1996 · 2.9K citations · Full text

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

Genetic Analysis, Linkage Disequilibrium, Genotype-phenotype Association +14

KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

Christian Kubisch, Björn C. Schroeder, Thomas Friedrich et al. · Cell · 1999 · 862 citations · Full text

Genetic epidemiological studies of early‐onset deafness in the U.S. school‐age population

Mary L. Marazita, Lynn Ploughman, Brenda W. Rawlings et al. · American Journal of Medical Genetics · 1993 · 456 citations

Genetic Epidemiological Studies, Pediatric Otolaryngology, Early‐onset Deafness +13

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

Jia-Hui Xia, Chunyu Liu, Bei-sha Tang et al. · Nature Genetics · 1998 · 422 citations

Auditory Processing, Developmental Biology, Health Sciences +13