Lista de obras - Cordula Haas - Dominio Público Uruguay

2,000 Year old β-thalassemia case in Sardinia suggests malaria was endemic by the Roman period.

artículo científico publicado en 2017

A Th1 Response Is Essential for Induction of Crescentic Glomerulonephritis in Mice

scientific article published on 01 January 1999

A collaborative EDNAP exercise on SNaPshot™-based mtDNA control region typing

artículo científico publicado en 2016

A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results.

artículo científico publicado en 2014

A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

artículo científico publicado en 2014

A syndrome resembling human systemic sclerosis (scleroderma) in MRL/lpr mice lacking interferon-gamma (IFN-gamma) receptor (MRL/lprgammaR-/-).

artículo científico publicado en 1999

Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).

artículo científico publicado en 2014

Assigning forensic body fluids to donors in mixed body fluids by targeted RNA/DNA deep sequencing of coding region SNPs

artículo científico publicado en 2020

Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.

artículo científico publicado en 2010

Body Fluid Identification Using mRNA Profiling.

artículo científico publicado en 2016

Body fluid identification and assignment to donors using a targeted mRNA massively parallel sequencing approach - results of a second EUROFORGEN / EDNAP collaborative exercise

artículo científico publicado en 2019

Body fluid identification using a targeted mRNA massively parallel sequencing approach - results of a EUROFORGEN/EDNAP collaborative exercise.

artículo científico publicado en 2018

Capillary Electrophoresis of a Multiplex Reverse Transcription-Polymerase Chain Reaction to Target Messenger RNA Markers for Body Fluid Identification

artículo científico publicado en 2012

Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling

artículo científico publicado en 2018

Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour

artículo científico publicado en 2014

Detection of painted-over traces of blood and seminal fluid

artículo científico publicado en 2018

Development and optimization of a PCR assay for detection of Dobrava and Puumala hantaviruses in Bosnia and Herzegovina.

artículo científico publicado en 2012

Erratum to: Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases

article

Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes

artículo científico publicado en 2018

Failure to induce anti-glomerular basement membrane glomerulonephritis in TNF alpha/beta deficient mice

artículo científico publicado en 1998

Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise.

artículo científico publicado en 2015

Forensic interlaboratory evaluation of the ForFLUID kit for vaginal fluids identification

artículo científico publicado en 2013

Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death

artículo científico publicado en 2019

Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.

artículo científico publicado en 2018

HIrisPlex-S system for eye, hair, and skin color prediction from DNA: Massively parallel sequencing solutions for two common forensically used platforms

artículo científico publicado en 2019

IFN-gamma is essential for the development of autoimmune glomerulonephritis in MRL/Ipr mice

article

IFN-gamma receptor deletion prevents autoantibody production and glomerulonephritis in lupus-prone (NZB x NZW)F1 mice ⬇️

artículo científico publicado el 15 de abril de 1998

Introducing novel type of human DNA markers for forensic tissue identification: DNA copy number variation allows the detection of blood and semen

artículo científico publicado en 2018

Lipopolysaccharide-induced glomerulonephritis develops in the absence of interferon-gamma signaling.

artículo científico publicado en 1996

MHC antigens in interferon γ (IFNγ) receptor deficient mice: IFNγ-independent up-regulation of MHC class II in renal tubules

artículo científico publicado en 1995

Messenger RNA biomarker signatures for forensic body fluid identification revealed by targeted RNA sequencing.

artículo científico publicado en 2018

Microbiome-based body fluid identification of samples exposed to indoor conditions

scientific article published on 11 February 2019

Multidisciplinary Identification of the Controversial Freedom Fighter Jörg Jenatsch, Assassinated 1639 in Chur, Switzerland

artículo científico publicado en 2016

No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians

artículo científico publicado en 2009

Novel taxonomy-independent deep learning microbiome approach allows for accurate classification of different forensically relevant human epithelial materials

scientific article published on 04 April 2019

Ongoing tissue changes in an experimentally mummified human leg

scientific article published on 13 December 2019

Post mortem DNA degradation of human tissue experimentally mummified in salt

artículo científico publicado en 2014

Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.

artículo científico publicado en 2017

Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases

article

Predicting the origin of stains from next generation sequencing mRNA data

artículo científico publicado en 2018

Predicting the origin of stains from whole miRNome massively parallel sequencing data

scientific article published on 15 February 2019

Prevention of crescentic glomerulonephritis induced by anti-glomerular membrane antibody in tumor necrosis factor-deficient mice

artículo científico publicado en 1998

RNA/DNA co-analysis from blood stains--results of a second collaborative EDNAP exercise.

artículo científico publicado en 2011

RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains: results of a fourth and fifth collaborative EDNAP exercise.

artículo científico publicado en 2013

RNA/DNA co-analysis from human saliva and semen stains--results of a third collaborative EDNAP exercise.

artículo científico publicado en 2012

RNA/DNA co-analysis from human skin and contact traces--results of a sixth collaborative EDNAP exercise

artículo científico publicado en 2015

Recovery of Trace DNA on Clothing: A Comparison of Mini-tape Lifting and Three Other Forensic Evidence Collection Techniques.

artículo científico publicado en 2016

Sarcomeric gene mutations in sudden infant death syndrome (SIDS).

artículo científico publicado en 2012

Selection of highly specific and sensitive mRNA biomarkers for the identification of blood

scientific article published on 08 October 2010

Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.

artículo científico publicado en 2016

Sodium/proton exchanger 3 (NHE3) and sudden infant death syndrome (SIDS)

Specific and sensitive mRNA biomarkers for the identification of skin in 'touch DNA' evidence

artículo científico publicado en 2012

The combined inactivation of tumor necrosis factor and interleukin-6 prevents induction of the major acute phase proteins by endotoxin

artículo científico publicado en 1998

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

artículo científico publicado en 2014

Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

Transcription and microbial profiling of body fluids using a massively parallel sequencing approach

artículo científico publicado en 2019

Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians

artículo científico publicado en 2014

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland

article

Y-chromosomal analysis identifies the skeletal remains of Swiss national hero Jörg Jenatsch (1596-1639).

artículo científico publicado en 2013

Y-chromosome STR haplotypes in a population sample from Switzerland (Zurich area).

artículo científico publicado en 2005

[Tracking down the culprit - mRNA profiling for the identification of body fluids]

artículo científico publicado en 2016

mRNA profiling for body fluid identification by reverse transcription endpoint PCR and realtime PCR.

artículo científico publicado en 2008

mRNA profiling for the identification of blood--results of a collaborative EDNAP exercise.

artículo científico publicado en 2010

mRNA profiling using a minimum of five mRNA markers per body fluid and a novel scoring method for body fluid identification

artículo científico publicado en 2012

Lista de obras de Cordula Haas

2,000 Year old β-thalassemia case in Sardinia suggests malaria was endemic by the Roman period.

A Th1 Response Is Essential for Induction of Crescentic Glomerulonephritis in Mice

A collaborative EDNAP exercise on SNaPshot™-based mtDNA control region typing

A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results.

A global analysis of Y-chromosomal haplotype diversity for 23 STR loci

A syndrome resembling human systemic sclerosis (scleroderma) in MRL/lpr mice lacking interferon-gamma (IFN-gamma) receptor (MRL/lprgammaR-/-).

Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).

Assigning forensic body fluids to donors in mixed body fluids by targeted RNA/DNA deep sequencing of coding region SNPs

Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.

Body Fluid Identification Using mRNA Profiling.

Body fluid identification and assignment to donors using a targeted mRNA massively parallel sequencing approach - results of a second EUROFORGEN / EDNAP collaborative exercise

Body fluid identification using a targeted mRNA massively parallel sequencing approach - results of a EUROFORGEN/EDNAP collaborative exercise.

Capillary Electrophoresis of a Multiplex Reverse Transcription-Polymerase Chain Reaction to Target Messenger RNA Markers for Body Fluid Identification

Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling

Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour

Detection of painted-over traces of blood and seminal fluid

Development and optimization of a PCR assay for detection of Dobrava and Puumala hantaviruses in Bosnia and Herzegovina.

Erratum to: Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases

Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes

Failure to induce anti-glomerular basement membrane glomerulonephritis in TNF alpha/beta deficient mice

Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise.

Forensic interlaboratory evaluation of the ForFLUID kit for vaginal fluids identification

Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death

Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.

HIrisPlex-S system for eye, hair, and skin color prediction from DNA: Massively parallel sequencing solutions for two common forensically used platforms

IFN-gamma is essential for the development of autoimmune glomerulonephritis in MRL/Ipr mice

IFN-gamma receptor deletion prevents autoantibody production and glomerulonephritis in lupus-prone (NZB x NZW)F1 mice ⬇️

Introducing novel type of human DNA markers for forensic tissue identification: DNA copy number variation allows the detection of blood and semen

Lipopolysaccharide-induced glomerulonephritis develops in the absence of interferon-gamma signaling.

MHC antigens in interferon γ (IFNγ) receptor deficient mice: IFNγ-independent up-regulation of MHC class II in renal tubules

Messenger RNA biomarker signatures for forensic body fluid identification revealed by targeted RNA sequencing.

Microbiome-based body fluid identification of samples exposed to indoor conditions

Multidisciplinary Identification of the Controversial Freedom Fighter Jörg Jenatsch, Assassinated 1639 in Chur, Switzerland

No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians

Novel taxonomy-independent deep learning microbiome approach allows for accurate classification of different forensically relevant human epithelial materials

Ongoing tissue changes in an experimentally mummified human leg

Post mortem DNA degradation of human tissue experimentally mummified in salt

Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.

Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases

Predicting the origin of stains from next generation sequencing mRNA data

Predicting the origin of stains from whole miRNome massively parallel sequencing data

Prevention of crescentic glomerulonephritis induced by anti-glomerular membrane antibody in tumor necrosis factor-deficient mice

RNA/DNA co-analysis from blood stains--results of a second collaborative EDNAP exercise.

RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains: results of a fourth and fifth collaborative EDNAP exercise.

RNA/DNA co-analysis from human saliva and semen stains--results of a third collaborative EDNAP exercise.

RNA/DNA co-analysis from human skin and contact traces--results of a sixth collaborative EDNAP exercise

Recovery of Trace DNA on Clothing: A Comparison of Mini-tape Lifting and Three Other Forensic Evidence Collection Techniques.

Sarcomeric gene mutations in sudden infant death syndrome (SIDS).

Selection of highly specific and sensitive mRNA biomarkers for the identification of blood

Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.

Sodium/proton exchanger 3 (NHE3) and sudden infant death syndrome (SIDS)

Specific and sensitive mRNA biomarkers for the identification of skin in 'touch DNA' evidence

The combined inactivation of tumor necrosis factor and interleukin-6 prevents induction of the major acute phase proteins by endotoxin

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

Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

Transcription and microbial profiling of body fluids using a massively parallel sequencing approach

Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians

Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland

Y-chromosomal analysis identifies the skeletal remains of Swiss national hero Jörg Jenatsch (1596-1639).

Y-chromosome STR haplotypes in a population sample from Switzerland (Zurich area).

[Tracking down the culprit - mRNA profiling for the identification of body fluids]

mRNA profiling for body fluid identification by reverse transcription endpoint PCR and realtime PCR.

mRNA profiling for the identification of blood--results of a collaborative EDNAP exercise.

mRNA profiling using a minimum of five mRNA markers per body fluid and a novel scoring method for body fluid identification