List of works - Ewa Zietkiewicz

Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification.

scientific article

Standardized nomenclature for Alu repeats

scientific article

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm

scientific article

Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era

scientific article (publication date: 11 January 1995)

Genetic structure of the ancestral population of modern humans

scientific article published in August 1998

Nuclear DNA diversity in worldwide distributed human populations

scientific article published on December 1997

Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees

scientific article

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

scientific article

Translational readthrough potential of natural termination codons in eucaryotes--The impact of RNA sequence

scientific article (publication date: 2015)

Recent advances in primary ciliary dyskinesia genetics.

scientific article

The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim

scientific article published in September 1997

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients

scientific article published on 20 March 2012

Evolution of secondary structure in the family of 7SL-like RNAs

scientific article published on 01 November 1994

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies.

scientific article published on 25 November 2015

Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity

scientific article

RPGR mutations might cause reduced orientation of respiratory cilia

scientific article published on 6 August 2012

Mosaic evolution of rodent B1 elements

scientific article

Current genetic methodologies in the identification of disaster victims and in forensic analysis

scientific article published on 15 October 2011

Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy

scientific article (publication date: July 1999)

Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec

scientific article published on 10 May 2005

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes

scientific article

Is selection responsible for the low level of variation in the last intron of the ZFY locus?

scientific article

A young Alu subfamily amplified independently in human and African great apes lineages

scientific article

Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR

scientific article published on September 1992

Monophyletic origin of Alu elements in primates

scientific article published on August 1998

Advances in therapeutic use of a drug-stimulated translational readthrough of premature termination codons.

scientific article published on 29 May 2018

Archaic lineages in the history of modern humans

scientific article (publication date: October 2000)

Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes.

scientific article

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects

scientific article (publication date: 6 February 2007)

Phylogenetic affinities of tarsier in the context of primate Alu repeats

scientific article published in February 1999

Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors.

scientific article

Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).

scientific article

Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contacts.

scientific article published in April 2004

Are CpG sites mutation hot spots in the dystrophin gene?

article

Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.

scientific article

Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients

scientific article

Identification of chrysanthemum cultivars and stability of DNA fingerprint patterns

scientific article published on 01 August 1995

Cytogenetic perspective of ageing and longevity in men and women

scientific article published on January 2009

Phylogenetic analysis of a reported complementary DNA sequence

scholarly article

In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases

scientific article published on 02 December 2010

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q

article

CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients

scientific article (publication date: 2014)

Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus

scientific article published on 01 June 1992

ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia

scientific article published on 29 January 2016

Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.

scientific article published on 18 July 2016

Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24-25.

scientific article published in January 2006

CFAP300: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking

scientific article published on 01 October 2019

Overall informativity, OI, in DNA polymorphisms revealed by inter-Alu PCR: detection of genomic rearrangements

scientific article published on 01 September 1996

Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism

scientific article published on 01 January 1992

EurEAs_Gplex--A new SNaPshot assay for continental population discrimination and gender identification

scientific article published on 19 October 2015

List of works by Ewa Zietkiewicz

Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification.

Standardized nomenclature for Alu repeats

DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm

Ubiquitous mammalian-wide interspersed repeats (MIRs) are molecular fossils from the mesozoic era

Genetic structure of the ancestral population of modern humans

Nuclear DNA diversity in worldwide distributed human populations

Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees

Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

Translational readthrough potential of natural termination codons in eucaryotes--The impact of RNA sequence

Recent advances in primary ciliary dyskinesia genetics.

The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients

Evolution of secondary structure in the family of 7SL-like RNAs

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies.

Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern human diversity

RPGR mutations might cause reduced orientation of respiratory cilia

Mosaic evolution of rodent B1 elements

Current genetic methodologies in the identification of disaster victims and in forensic analysis

Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogy

Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes

Is selection responsible for the low level of variation in the last intron of the ZFY locus?

A young Alu subfamily amplified independently in human and African great apes lineages

Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR

Monophyletic origin of Alu elements in primates

Advances in therapeutic use of a drug-stimulated translational readthrough of premature termination codons.

Archaic lineages in the history of modern humans

Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes.

Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects

Phylogenetic affinities of tarsier in the context of primate Alu repeats

Correlation between the level of cytogenetic aberrations in cultured human lymphocytes and the age and gender of donors.

Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD).

Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contacts.

Are CpG sites mutation hot spots in the dystrophin gene?

Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia.

Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients

Identification of chrysanthemum cultivars and stability of DNA fingerprint patterns

Cytogenetic perspective of ageing and longevity in men and women

Phylogenetic analysis of a reported complementary DNA sequence

In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q

CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients

Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus

ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia

Association of germline genetic variants in RFC, IL15 and VDR genes with minimal residual disease in pediatric B-cell precursor ALL.

Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24-25.

CFAP300: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking

Overall informativity, OI, in DNA polymorphisms revealed by inter-Alu PCR: detection of genomic rearrangements

Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism

EurEAs_Gplex--A new SNaPshot assay for continental population discrimination and gender identification