Barbara Ploplis

Statistics

Publications

Citations

H-Index

Active since

1992

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

National Institutes of Health

University of the Punjab

Centre of Excellence in Molecular Biology

All India Institute of Medical Sciences

Barbara Ploplis is an author at National Institute on Deafness and Other Communication Disorders specializing in genetics, hearing impairment, and molecular genetics.

Publications per year

1992–2009

Publications

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

Life Sciences, Genetics, Molecular Genetics +7

Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3

Atsushi Watanabe, Kazuhisa Takeda, Barbara Ploplis et al. · Nature Genetics · 1998 · 276 citations

Life Sciences, Genetics, Molecular Genetics +10

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed et al. · The American Journal of Human Genetics · 2009 · 120 citations · Full text

Medicine, Genetics, Molecular Genetics +11

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (<i>dn</i>) locus

Pawan Kumar Jain, Kunihiro Fukushima, Dilip Deshmukh et al. · Human Molecular Genetics · 1995 · 67 citations

Medicine, Genetics, Otolaryngology +8

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Anil K. Lalwani, J. Rodney Brister, Fex J et al. · PubMed · 1994 · 60 citations

Medicine, Audiology, Hearing Science +4

1–5 of 7