List of works - Paweł Krajewski

A Role for KIR Gene Variants Other Than KIR2DS1 in Conferring Susceptibility to Psoriasis

article

An association between genetic variation in the glutamatergic system and suicide attempts in alcohol-dependent individuals

scientific article published on 30 May 2017

Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes

scientific article published on 29 January 2020

Analysis of forensically used autosomal short tandem repeat markers in Polish and neighboring populations

scientific article

Analysis of four genes involved in the neurodevelopment shows association of rs4307059 polymorphism in the cadherin 9/10 region with completed suicide

scientific article published on 27 July 2012

Angiotensin-converting enzyme polymorphism and completed suicide: an association in Caucasians and evidence for a link with a method of self-injury

scientific article

Association between FKBP5 Functional Polymorphisms and Completed Suicide

scientific article published on 3 December 2015

Association between tryptophan hydroxylase 2 gene polymorphism and completed suicide

scientific article published on December 2010

Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia

article

Identification and characterization of novel rapidly mutating Y-chromosomal short tandem repeat markers

scientific article published on 24 June 2020

Increased concentration of T-cell receptor rearrangement excision circles (TREC) in peripheral blood in Graves' disease

article published in 2014

Increased concentration of T-cell receptor rearrangement excision circles (TREC) in peripheral blood in Graves' disease

Inverse association between obesity predisposing FTO genotype and completed suicide

scientific article

M34T and V37I mutations inGJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance

scientific article published on 01 November 2007

Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to , and as novel candidates for genes causing human Mendelian disorders

article

No association between MTHFR C677T polymorphism and completed suicide

scientific article published on 14 September 2012

Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy

scientific article published on 28 March 2019

Polymorphism of the oestrogen receptor beta gene (ESR2) is associated with susceptibility to Graves' disease

article

Population carrier rates of pathogenic ARSA gene mutations: is metachromatic leukodystrophy underdiagnosed?

scientific article

Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene

scientific article

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit

scientific article published on 13 July 2020

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

scientific article

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape.

scientific article

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.

scientific article

Toward male individualization with rapidly mutating y-chromosomal short tandem repeats

scientific article

Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications

scientific article published on 14 December 2020

List of works by Paweł Krajewski

A Role for KIR Gene Variants Other Than KIR2DS1 in Conferring Susceptibility to Psoriasis

An association between genetic variation in the glutamatergic system and suicide attempts in alcohol-dependent individuals

Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes

Analysis of forensically used autosomal short tandem repeat markers in Polish and neighboring populations

Analysis of four genes involved in the neurodevelopment shows association of rs4307059 polymorphism in the cadherin 9/10 region with completed suicide

Angiotensin-converting enzyme polymorphism and completed suicide: an association in Caucasians and evidence for a link with a method of self-injury

Association between FKBP5 Functional Polymorphisms and Completed Suicide

Association between tryptophan hydroxylase 2 gene polymorphism and completed suicide

Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia

Identification and characterization of novel rapidly mutating Y-chromosomal short tandem repeat markers

Increased concentration of T-cell receptor rearrangement excision circles (TREC) in peripheral blood in Graves' disease

Increased concentration of T-cell receptor rearrangement excision circles (TREC) in peripheral blood in Graves' disease

Inverse association between obesity predisposing FTO genotype and completed suicide

M34T and V37I mutations inGJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance

Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to , and as novel candidates for genes causing human Mendelian disorders

No association between MTHFR C677T polymorphism and completed suicide

Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy

Polymorphism of the oestrogen receptor beta gene (ESR2) is associated with susceptibility to Graves' disease

Population carrier rates of pathogenic ARSA gene mutations: is metachromatic leukodystrophy underdiagnosed?

Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape

The Role of Recent Admixture in Forming the Contemporary West Eurasian Genomic Landscape.

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.

Toward male individualization with rapidly mutating y-chromosomal short tandem repeats

Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications