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Lenka Piherová | Researchclopedia

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Lenka Piherová

Charles University ORCID

38

Works

579

Citations

12

h-index

14

i10-index

Research Topics

Cardiomyopathy and Myosin Studies Cardiovascular Function and Risk Factors Genomics and Rare Diseases

Affiliations

Charles University2005–2026

Instituto Politécnico da Guarda2023–2023

University Hospital Plzen2023–2023

Institute of Clinical and Experimental Medicine2013–2013

Centrum kardiovaskulární a transplantační chirurgie2023–2023

Top Works

Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness

Stanislav Kmoch,Jacek Majewski,et al.

201594 citations

Congenital heart defects research

Cardiovascular Effects of Exercise

Mutations in ANTXR1 Cause GAPO Syndrome

Viktor Stránecký,Alexander Hoischen,et al.

201392 citations

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6

Hana Hartmannová,Lenka Piherová,et al.

201679 citations

Oligonucleotide-based microarray: A new improvement in microarray detection of plant viruses

Dagmar Bystřická,Ondřej Lenz,et al.

200566 citations

Isolated X-Linked Hypertrophic Cardiomyopathy Caused by a Novel Mutation of the Four-and-a-Half LIM Domain 1 Gene

Hana Hartmannová,Miloš Kubánek,et al.

201346 citations

Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction

Miloš Kubánek,Tereza Schimerová,et al.

202041 citations

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency

Alena Čížková,Viktor Stránecký,et al.

200827 citations

Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy

Najim Lahrouchi,Alex V. Postma,et al.

202127 citations

Pigmentary retinopathy can indicate the presence of pathogenic <i>LAMP2</i> variants even in somatic mosaic carriers with no additional signs of Danon disease

Bohdan Kousal,Filip Majer,et al.

202018 citations