List of works - Jesper Petersen

(GT)n Repeat Polymorphism in Heme Oxygenase-1 (HO-1) Correlates with Clinical Outcome after Myeloablative or Nonmyeloablative Allogeneic Hematopoietic Cell Transplantation

scientific article

A novel homozygous GFI1B variant in 2 sisters with thrombocytopenia and severe bleeding tendency

scientific article published on 07 July 2020

Detection of mutations in the beta-globin gene by colorimetric staining of DNA microarrays visualized by a flatbed scanner

scientific article published on 07 September 2006

Detection of mutations using microarrays of poly(C)10-poly(T)10 modified DNA probes immobilized on agarose films

scientific article published on 23 March 2006

Genotyping of mutations in the beta-globin gene using allele specific hybridization.

scientific article published in January 2009

Haemoglobinopathia Ypsilanti - A rare, but important differential diagnosis to polycythaemia vera

scientific article published on 9 October 2013

Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies.

scientific article published on 03 June 2009

Microfludic device for creating ionic strength gradients over DNA microarrays for efficient DNA melting studies and assay development

scientific article

Microfluidic DNA microarrays in PMMA chips: streamlined fabrication via simultaneous DNA immobilization and bonding activation by brief UV exposure

scientific article published on 01 August 2010

Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.

scientific article

Prevalence of Congenital Hemolytic Disorders in Denmark, 2000-2016

scientific article published on 21 May 2020

Prevalence of glucose-6-phosphate dehydrogenase deficiency and diagnostic challenges in 1500 immigrants in Denmark examined for haemoglobinopathies.

scientific article published on 30 April 2015

Progression of JAK2-mutant polycythemia vera to CALR-mutant myelofibrosis severely impacts on disease phenotype and response to therapy

scientific article published on 01 July 2019

Severe G6PD Deficiency Due to a New Missense Mutation in an Infant of Northern European Descent.

scientific article published on 16 October 2015

Target preparation for genotyping specific genes or gene segments.

scientific article published in January 2009

The MainSTREAM component platform: a holistic approach to microfluidic system design

scientific article

Thrombosis in Hb Taybe [codons 38/39 (-ACC) (α1)]

scientific article published on 01 January 2012

Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays

scientific article

List of works by Jesper Petersen

(GT)n Repeat Polymorphism in Heme Oxygenase-1 (HO-1) Correlates with Clinical Outcome after Myeloablative or Nonmyeloablative Allogeneic Hematopoietic Cell Transplantation

A novel homozygous GFI1B variant in 2 sisters with thrombocytopenia and severe bleeding tendency

Detection of mutations in the beta-globin gene by colorimetric staining of DNA microarrays visualized by a flatbed scanner

Detection of mutations using microarrays of poly(C)10-poly(T)10 modified DNA probes immobilized on agarose films

Genotyping of mutations in the beta-globin gene using allele specific hybridization.

Haemoglobinopathia Ypsilanti - A rare, but important differential diagnosis to polycythaemia vera

Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies.

Microfludic device for creating ionic strength gradients over DNA microarrays for efficient DNA melting studies and assay development

Microfluidic DNA microarrays in PMMA chips: streamlined fabrication via simultaneous DNA immobilization and bonding activation by brief UV exposure

Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.

Prevalence of Congenital Hemolytic Disorders in Denmark, 2000-2016

Prevalence of glucose-6-phosphate dehydrogenase deficiency and diagnostic challenges in 1500 immigrants in Denmark examined for haemoglobinopathies.

Progression of JAK2-mutant polycythemia vera to CALR-mutant myelofibrosis severely impacts on disease phenotype and response to therapy

Severe G6PD Deficiency Due to a New Missense Mutation in an Infant of Northern European Descent.

Target preparation for genotyping specific genes or gene segments.

The MainSTREAM component platform: a holistic approach to microfluidic system design

Thrombosis in Hb Taybe [codons 38/39 (-ACC) (α1)]

Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays