I. Mašindová

发表

Admixture Mapping Identifies an Amerindian Ancestry Locus Associated with Albuminuria in Hispanics in the United States.

D. Levy, S. Redline, T. Thornton, 2017, Journal of the American Society of Nephrology : JASN.

Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report

M. Skopkova, D. Gašperíková, D. Danis, 2019, BMC Medical Genetics.

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss

D. Gašperíková, S. Riazuddin, Z. Ahmed, 2015, Human Genetics.

Novel variants in EDNRB gene in waardenburg syndrome type II and SOX10 gene in PCWH syndrome.

M. Skopkova, D. Gašperíková, D. Danis, 2020, International journal of pediatric otorhinolaryngology.

Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies.

D. Gašperíková, J. Stanik, I. Klimeš, 2012, Endocrine regulations.

Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

D. Gašperíková, I. Klimeš, I. Mašindová, 2014, Acta oto-laryngologica.

A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians

C. Bogardus, R. Hanson, S. Kobes, 2017, Diabetes.

MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin

D. Gašperíková, S. Riazuddin, Z. Ahmed, 2015, PloS one.

Prevalence of DFNB1 mutations among cochlear implant users in Slovakia and its clinical implications

D. Gašperíková, I. Klimeš, I. Mašindová, 2014, European Archives of Oto-Rhino-Laryngology.

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss

D. Gašperíková, S. Riazuddin, Z. Ahmed, 2015, Human Genetics.