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Publications by Davids Fridmanis

Next-Generation-Sequencing-Based Identification of Familial Hypercholesterolemia-Related Mutations in Subjects With Increased LDL–C Levels in a Latvian Population

BMC Medical Genetics

Genetics

2015

English

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Identification of TAZ Mutations in Pediatric Patients With Cardiomyopathy by Targeted Next-Generation Sequencing in a Chinese Cohort

Orphanet Journal of Rare Diseases

English

“Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-Like Disease”

Pediatric Rheumatology

English

Analysis of HDL-microRNA Panel in Heterozygous Familial Hypercholesterolemia Subjects With LDL Receptor Null or Defective Mutation

Scientific Reports

Multidisciplinary

2019

English

Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing

Molecular Medicine Reports

English

ApoB Metabolism in Familial Hypercholesterolemia. Inconsistencies With the LDL Receptor Paradigm

Arteriosclerosis and Thrombosis: A Journal of Vascular Biology

1994

English

A Chinese Homozygote of Familial Hypercholesterolemia: Identification of a Novel C263R Mutation in the LDL Receptor Gene

Journal of Human Genetics

Genetics

2001

English

Next Generation Sequencing in Synovial Sarcoma Reveals Novel Gene Mutations

Oncotarget

Oncology

2015

English

Coupling Chemical Mutagenesis to Next Generation Sequencing for the Identification of Drug Resistance Mutations in Leishmania

Nature Communications

English

Identification of Novel GNAS Mutations in Intramuscular Myxoma Using Next-Generation Sequencing With Single-Molecule Tagged Molecular Inversion Probes

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Davids Fridmanis

Next-Generation-Sequencing-Based Identification of Familial Hypercholesterolemia-Related Mutations in Subjects With Increased LDL–C Levels in a Latvian Population

Related publications

Identification of TAZ Mutations in Pediatric Patients With Cardiomyopathy by Targeted Next-Generation Sequencing in a Chinese Cohort

“Next Generation Sequencing Identifies Mutations in GNPTG Gene as a Cause of Familial Form of Scleroderma-Like Disease”

Analysis of HDL-microRNA Panel in Heterozygous Familial Hypercholesterolemia Subjects With LDL Receptor Null or Defective Mutation

Identification of Novel USH2A Mutations in Patients With Autosomal Recessive Retinitis Pigmentosa via Targeted Next‑generation Sequencing

ApoB Metabolism in Familial Hypercholesterolemia. Inconsistencies With the LDL Receptor Paradigm

A Chinese Homozygote of Familial Hypercholesterolemia: Identification of a Novel C263R Mutation in the LDL Receptor Gene

Next Generation Sequencing in Synovial Sarcoma Reveals Novel Gene Mutations

Coupling Chemical Mutagenesis to Next Generation Sequencing for the Identification of Drug Resistance Mutations in Leishmania

Identification of Novel GNAS Mutations in Intramuscular Myxoma Using Next-Generation Sequencing With Single-Molecule Tagged Molecular Inversion Probes