Lista de obras -

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting

scientific journal article

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.

artículo científico publicado en 2014

A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?

artículo científico publicado en 2006

A novel mutation in PAX9 causes familial form of molar oligodontia

artículo científico publicado en 2006

Alkaptonuria: a disease with dark brown urine

artículo científico publicado en 2016

An analysis of polymorphisms within the Wnt signaling pathway in relation to ovarian cancer risk in a Polish population.

scientific article published on February 2014

Antibodies to HBV surface antigen in relation to interferon-λ3 in hemodialysis patients

artículo científico publicado en 2016

Antibodies to hepatitis B virus surface antigen and interleukin 12 and interleukin 18 gene polymorphisms in hemodialysis patients ⬇️

artículo científico publicado en 2012

Association between DNMT3L polymorphic variants and the risk of endometriosis-associated infertility.

artículo científico publicado en 2015

Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population.

artículo científico publicado en 2010

Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population

artículo científico publicado en 2015

Association investigation of BACH2 rs3757247 and SOD2 rs4880 polymorphisms with the type 1 diabetes and diabetes long-term complications risk in the Polish population.

artículo científico publicado en 2015

Association of 677C>T polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene with bipolar disorder and schizophrenia.

artículo científico publicado en 2006

Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palate.

artículo científico publicado en 2018

Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population

scientific article published on 06 August 2012

Association of Retinoid X Receptor Alpha Gene Polymorphism with Clinical Course of Chronic Glomerulonephritis.

artículo científico publicado en 2015

Association of aldosterone synthase (CYP11B2) gene -344T/C polymorphism with the risk of primary chronic glomerulonephritis in the Polish population.

artículo científico publicado en 2013

Association of common variants in PAH and LAT1 with non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Polish population.

artículo científico publicado en 2014

Association of rs699947 (-2578 C/A) and rs2010963 (-634 G/C) Single Nucleotide Polymorphisms of the VEGF Gene, VEGF-A and Leptin Serum Level, and Cardiovascular Risk in Patients with Excess Body Mass: A Case-Control Study

scientific article published on 08 February 2020

Association of the interleukin-12 polymorphic variants with the development of antibodies to surface antigen of hepatitis B virus in hemodialysis patients in response to vaccination or infection

artículo científico publicado en 2013

Associations of folate and choline metabolism gene polymorphisms with orofacial clefts

artículo científico publicado en 2010

Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients.

scientific article published on 14 October 2016

Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis

artículo científico publicado en 2006

Calcium-sensing receptor gene (CASR) polymorphisms and CASR transcript level concerning dyslipidemia in hemodialysis patients: a cross-sectional study

scientific article published on 27 November 2019

Circulating Interferon-λ3, Responsiveness to HBV Vaccination, and HBV/HCV Infections in Haemodialysis Patients.

artículo científico publicado en 2017

Clinical aspects of vitamin D-binding protein gene polymorphisms in hemodialysis patients

artículo científico publicado en 2015

Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate

artículo científico publicado en 2017

Contribution of IL12A and IL12B polymorphisms to the risk of cervical cancer

artículo científico publicado en 2012

Correlations of indoleamine 2,3-dioxygenase, interferon-λ3, and anti-HBs antibodies in hemodialysis patients

artículo científico publicado en 2018

DNMT1, DNMT3A and DNMT3B gene variants in relation to ovarian cancer risk in the Polish population

scientific article published on 12 May 2013

De novo EDA mutations: Variable expression in two Egyptian families

artículo científico publicado en 2016

Dissecting the genetic heterogeneity of gastric cancer

ENHO, RXRA, and LXRA polymorphisms and dyslipidaemia, related comorbidities and survival in haemodialysis patients

artículo científico publicado en 2018

EVC gene polymorphisms and risks of isolated hypospadias - a preliminary study.

artículo científico publicado en 2015

Effect of interferon λ3 gene polymorphisms, rs8099917 and rs12979860, on response to hepatitis B virus vaccination and hepatitis B or C virus infections among hemodialysis patients.

artículo científico publicado en 2015

Expression of modified Cry1Ac gene of Bacillus thuringiensis in transgenic tobacco plants.

artículo científico publicado en 2004

Folate and choline metabolism gene variants and development of uterine cervical carcinoma.

artículo científico publicado en 2011

Folate and choline metabolism gene variants in relation to ovarian cancer risk in the Polish population

article

Further Evidence of the Association of the Diacylglycerol Kinase Kappa (DGKK) Gene With Hypospadias

artículo científico publicado en 2018

GREM2 nucleotide variants and the risk of tooth agenesis.

artículo científico publicado en 2017

Genetic polymorphisms of GSTM1 and GSTT1 in mothers of children with isolated cleft lip with or without cleft palate

artículo científico publicado en 2005

Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2014

Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate

artículo científico publicado en 2012

IL4R and IL13 polymorphic variants and development of antibodies to surface antigen of hepatitis B virus in hemodialysis patients in response to HBV vaccination or infection.

artículo científico publicado en 2013

Identification of microdeletions in candidate genes for cleft lip and/or palate

artículo científico publicado en 2009

Interferon-λ3 Gene Polymorphic Variants, rs4803217 and rs12980275, Responsiveness to HBV Vaccine and Outcome of HBV and HCV Exposure in Hemodialyzed Patients

artículo científico publicado en 2021

Interferon‑λ4 gene polymorphisms, circulating interferon λ3, and clinical variables in hemodialysis patients exposed to hepatitis E virus

article

Involvement of 17β-hydroxysteroid dehydrogenase type gene 1 937 A>G polymorphism in infertility in Polish Caucasian women with endometriosis.

artículo científico publicado en 2017

Involvement of adropin and adropin-associated genes in metabolic abnormalities of hemodialysis patients.

artículo científico publicado en 2016

Involvement of vascular endothelial growth factor -460 C/T, +405 G/C and +936 C/T polymorphisms in the development of endometriosis

artículo científico publicado en 2014

Lack of association between metabolic and antioxidant gene polymorphisms (GSTM1, GSTT1, CAT, MnSOD, GPX1) and maternal quitting of smoking in pregnancy--preliminary results

artículo científico publicado en 2009

Lack of association of polymorphic variants of genes encoding zinc transporters with the risk of orofacial cleft-affected pregnancies

artículo científico publicado en 2010

Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population

artículo científico publicado en 2006

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition

artículo científico publicado en 2003

Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development

artículo científico publicado en 2006

No association of monocyte chemoattractant protein-1 -2518 A/G polymorphism with the risk of primary glomerulonephritis in the Polish population

artículo científico publicado en 2011

Novel Candidate Genes for Non-Syndromic Tooth Agenesis Identified Using Targeted Next-Generation Sequencing

artículo científico publicado en 2022

Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.

artículo científico publicado en 2012

Novel PAX9 mutation associated with syndromic tooth agenesis

scientific article published on 13 July 2013

Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia

artículo científico publicado en 2003

Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts.

artículo científico publicado en 2015

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

artículo científico publicado en 2012

Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate

artículo científico publicado en 2014

PAX7 nucleotide variants and the risk of non-syndromic orofacial clefts in the Polish population

artículo científico publicado en 2019

Paraoxonase 1 gene polymorphisms concerning non-insulin-dependent diabetes mellitus nephropathy in hemodialysis patients

artículo científico publicado en 2020

Paraoxonase 1 gene variants concerning cardiovascular mortality in conventional cigarette smokers and non-smokers treated with hemodialysis

artículo científico publicado en 2021

Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the Polish population

scientific article published on 22 October 2011

Polymorphic variants in the dopamine receptor D2 in women with endometriosis-related infertility

artículo científico publicado en 2015

Polymorphic variants in the vitamin D pathway genes and the risk of ovarian cancer among non-carriers of BRCA1/BRCA2 mutations

artículo científico publicado en 2015

Polymorphic variants in vitamin D signaling pathway genes and the risk of endometriosis-associated infertility.

artículo científico publicado en 2015

Polymorphic variants of DNMT3A and the risk of endometriosis.

artículo científico publicado en 2012

Polymorphic variants of folate and choline metabolism genes and the risk of endometriosis-associated infertility

artículo científico publicado en 2011

Polymorphic variants of genes encoding main antioxidant enzymes and the risk of CL/P-affected pregnancies

artículo científico publicado en 2007

Polymorphic variants of genes involved in homocysteine metabolism in celiac disease

artículo científico publicado en 2011

Polymorphic variants of genes related to arginine metabolism and the risk of orofacial clefts.

artículo científico publicado en 2010

Polymorphism rs368234815 of interferon lambda 4 gene and spontaneous clearance of hepatitis C virus in haemodialysis patients: a case-control study

artículo científico publicado en 2021

Polymorphism rs368234815 of interferon-λ4 gene and generation of antibodies to hepatitis B virus surface antigen in extracorporeal dialysis patients

scientific article published on 07 April 2020

Polymorphisms in CHDH gene and the risk of tooth agenesis

artículo científico publicado en 2011

Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.

artículo científico publicado en 2010

Polymorphisms of T helper cell cytokine-associated genes and survival of hemodialysis patients - a prospective study.

artículo científico publicado en 2017

Polymorphisms of Vitamin D Signaling Pathway Genes and Calcium-Sensing Receptor Gene in respect to Survival of Hemodialysis Patients: A Prospective Observational Study

scientific article published on 23 August 2016

Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate.

artículo científico publicado en 2011

Publication ethics of human studies in the light of the Declaration of Helsinki – a mini-review

artículo científico publicado en 2022

Replication study for the association of seven genome- GWAS-identified Loci with susceptibility to ovarian cancer in the Polish population

artículo científico publicado en 2014

Single nucleotide polymorphisms of vitamin D binding protein, vitamin D receptor and retinoid X receptor alpha genes and response to hepatitis B vaccination in renal replacement therapy patients

scientific article published on 22 September 2014

T helper cell‑related cytokine gene polymorphisms and vitamin D pathway gene polymorphisms as predictors of survival probability in patients on renal replacement therapy

artículo científico publicado en 2015

T-cell cytokine gene polymorphisms and vitamin D pathway gene polymorphisms in end-stage renal disease due to type 2 diabetes mellitus nephropathy: comparisons with health status and other main causes of end-stage renal disease.

artículo científico publicado en 2014

The Calcium-Sensing Receptor Gene Polymorphism rs1801725 and Calcium-Related Phenotypes in Hemodialysis Patients.

artículo científico publicado en 2018

The assessment of GWAS - identified polymorphisms associated with infertility risk in Polish women with endometriosis

artículo científico publicado en 2018

Vitamin D receptor gene BsmI and FokI polymorphisms in relation to ovarian cancer risk in the Polish population

artículo científico publicado en 2013

Vitamin D receptor gene BsmI, FokI, ApaI and TaqI polymorphisms and the risk of systemic lupus erythematosus.

artículo científico publicado en 2012

WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies

artículo científico publicado en 2014

Lista de obras de

A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial clefting

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.

A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?

A novel mutation in PAX9 causes familial form of molar oligodontia

Alkaptonuria: a disease with dark brown urine

An analysis of polymorphisms within the Wnt signaling pathway in relation to ovarian cancer risk in a Polish population.

Antibodies to HBV surface antigen in relation to interferon-λ3 in hemodialysis patients

Antibodies to hepatitis B virus surface antigen and interleukin 12 and interleukin 18 gene polymorphisms in hemodialysis patients ⬇️

Association between DNMT3L polymorphic variants and the risk of endometriosis-associated infertility.

Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population.

Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population

Association investigation of BACH2 rs3757247 and SOD2 rs4880 polymorphisms with the type 1 diabetes and diabetes long-term complications risk in the Polish population.

Association of 677C>T polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene with bipolar disorder and schizophrenia.

Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palate.

Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population

Association of Retinoid X Receptor Alpha Gene Polymorphism with Clinical Course of Chronic Glomerulonephritis.

Association of aldosterone synthase (CYP11B2) gene -344T/C polymorphism with the risk of primary chronic glomerulonephritis in the Polish population.

Association of common variants in PAH and LAT1 with non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Polish population.

Association of rs699947 (-2578 C/A) and rs2010963 (-634 G/C) Single Nucleotide Polymorphisms of the VEGF Gene, VEGF-A and Leptin Serum Level, and Cardiovascular Risk in Patients with Excess Body Mass: A Case-Control Study

Association of the interleukin-12 polymorphic variants with the development of antibodies to surface antigen of hepatitis B virus in hemodialysis patients in response to vaccination or infection

Associations of folate and choline metabolism gene polymorphisms with orofacial clefts

Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients.

Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis

Calcium-sensing receptor gene (CASR) polymorphisms and CASR transcript level concerning dyslipidemia in hemodialysis patients: a cross-sectional study

Circulating Interferon-λ3, Responsiveness to HBV Vaccination, and HBV/HCV Infections in Haemodialysis Patients.

Clinical aspects of vitamin D-binding protein gene polymorphisms in hemodialysis patients

Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate

Contribution of IL12A and IL12B polymorphisms to the risk of cervical cancer

Correlations of indoleamine 2,3-dioxygenase, interferon-λ3, and anti-HBs antibodies in hemodialysis patients

DNMT1, DNMT3A and DNMT3B gene variants in relation to ovarian cancer risk in the Polish population

De novo EDA mutations: Variable expression in two Egyptian families

Dissecting the genetic heterogeneity of gastric cancer

ENHO, RXRA, and LXRA polymorphisms and dyslipidaemia, related comorbidities and survival in haemodialysis patients

EVC gene polymorphisms and risks of isolated hypospadias - a preliminary study.

Effect of interferon λ3 gene polymorphisms, rs8099917 and rs12979860, on response to hepatitis B virus vaccination and hepatitis B or C virus infections among hemodialysis patients.

Expression of modified Cry1Ac gene of Bacillus thuringiensis in transgenic tobacco plants.

Folate and choline metabolism gene variants and development of uterine cervical carcinoma.

Folate and choline metabolism gene variants in relation to ovarian cancer risk in the Polish population

Further Evidence of the Association of the Diacylglycerol Kinase Kappa (DGKK) Gene With Hypospadias

GREM2 nucleotide variants and the risk of tooth agenesis.

Genetic polymorphisms of GSTM1 and GSTT1 in mothers of children with isolated cleft lip with or without cleft palate

Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate

Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate

IL4R and IL13 polymorphic variants and development of antibodies to surface antigen of hepatitis B virus in hemodialysis patients in response to HBV vaccination or infection.

Identification of microdeletions in candidate genes for cleft lip and/or palate

Interferon-λ3 Gene Polymorphic Variants, rs4803217 and rs12980275, Responsiveness to HBV Vaccine and Outcome of HBV and HCV Exposure in Hemodialyzed Patients

Interferon‑λ4 gene polymorphisms, circulating interferon λ3, and clinical variables in hemodialysis patients exposed to hepatitis E virus

Involvement of 17β-hydroxysteroid dehydrogenase type gene 1 937 A>G polymorphism in infertility in Polish Caucasian women with endometriosis.

Involvement of adropin and adropin-associated genes in metabolic abnormalities of hemodialysis patients.

Involvement of vascular endothelial growth factor -460 C/T, +405 G/C and +936 C/T polymorphisms in the development of endometriosis

Lack of association between metabolic and antioxidant gene polymorphisms (GSTM1, GSTT1, CAT, MnSOD, GPX1) and maternal quitting of smoking in pregnancy--preliminary results

Lack of association of polymorphic variants of genes encoding zinc transporters with the risk of orofacial cleft-affected pregnancies

Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population

Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition

Natural selection and molecular evolution in primate PAX9 gene, a major determinant of tooth development

No association of monocyte chemoattractant protein-1 -2518 A/G polymorphism with the risk of primary glomerulonephritis in the Polish population

Novel Candidate Genes for Non-Syndromic Tooth Agenesis Identified Using Targeted Next-Generation Sequencing

Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.

Novel PAX9 mutation associated with syndromic tooth agenesis

Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia

Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts.

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate

PAX7 nucleotide variants and the risk of non-syndromic orofacial clefts in the Polish population

Paraoxonase 1 gene polymorphisms concerning non-insulin-dependent diabetes mellitus nephropathy in hemodialysis patients

Paraoxonase 1 gene variants concerning cardiovascular mortality in conventional cigarette smokers and non-smokers treated with hemodialysis

Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the Polish population

Polymorphic variants in the dopamine receptor D2 in women with endometriosis-related infertility

Polymorphic variants in the vitamin D pathway genes and the risk of ovarian cancer among non-carriers of BRCA1/BRCA2 mutations

Polymorphic variants in vitamin D signaling pathway genes and the risk of endometriosis-associated infertility.

Polymorphic variants of DNMT3A and the risk of endometriosis.

Polymorphic variants of folate and choline metabolism genes and the risk of endometriosis-associated infertility

Polymorphic variants of genes encoding main antioxidant enzymes and the risk of CL/P-affected pregnancies

Polymorphic variants of genes involved in homocysteine metabolism in celiac disease

Polymorphic variants of genes related to arginine metabolism and the risk of orofacial clefts.

Polymorphism rs368234815 of interferon lambda 4 gene and spontaneous clearance of hepatitis C virus in haemodialysis patients: a case-control study

Polymorphism rs368234815 of interferon-λ4 gene and generation of antibodies to hepatitis B virus surface antigen in extracorporeal dialysis patients

Polymorphisms in CHDH gene and the risk of tooth agenesis

Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.