Concepedia

Nikki Liburd

NL

Statistics

Publications

3

Citations

729

H-Index

3

Active since

2000

Affiliations

Centre of Excellence in Molecular Biology(Current)

National Institute on Deafness and Other Communication Disorders

University of the Punjab

Nikki Liburd is an author at Centre of Excellence in Molecular Biology specializing in genetics, human genetics, and cochlear disorders.

Publications per year

2000–2001

3

Publications

3

Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

Edward R. Wilcox, Quianna Burton, Sadaf Naz et al. · Cell · 2001 · 440 citations · Full text

, , +7

Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

Nikki Liburd, Manju Ghosh, Saima Riazuddin et al. · Human Genetics · 2001 · 148 citations · Full text

, , +9

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

Saima Riazuddin, Caley M. Castelein, Zubair M. Ahmed et al. · Nature Genetics · 2000 · 141 citations

, , +8

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