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Evidence of gene–gene interaction in hidradenitis suppurativa: a nationwide registry study of Danish twins

British journal of dermatology (1951), 2022-01, Vol.186 (1), p.78-85

2022

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RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

Nature communications, 2020-11, Vol.11 (1), p.5816-5816, Article 5816

2020

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Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twins

European journal of clinical microbiology & infectious diseases, 2013-10, Vol.32 (10), p.1321-1326

2013

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Characterization of vascular structures and skin bruises using hyperspectral imaging, image analysis and diffusion theory

Journal of biophotonics, 2010-01, Vol.3 (1-2), p.53-65

2010

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Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening

Human mutation, 2003-05, Vol.21 (5), p.455-465

2003

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Mutations in the HERG K +-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

The American journal of cardiology, 2005-02, Vol.95 (3), p.433-434

2005

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T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome

Heart rhythm, 2004-09, Vol.1 (3), p.285-292

2004

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Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

European journal of human genetics : EJHG, 2004-08, Vol.12 (8), p.673-677

2004

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Prediction of milk/plasma concentration ratio of drugs

The Annals of pharmacotherapy, 2003-09, Vol.37 (9), p.1299-1306

2003

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Coordination of TGFβ/BMP signaling is associated with the primary cilium

Cilia (London), 2015-07, Vol.4 (S1), p.P17-P17, Article P17

2015

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High‐throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

Human mutation, 2003-02, Vol.21 (2), p.116-122

2003

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Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients

Biochemical and biophysical research communications, 2007-03, Vol.354 (3), p.776-782

2007

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High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device

Electrophoresis, 2005-05, Vol.26 (9), p.1834-1842

2005

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Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

Clinical chemistry (Baltimore, Md.), 2001-08, Vol.47 (8), p.1390-1395

2001

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One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region

European journal of human genetics : EJHG, 2005-02, Vol.13 (2), p.161-165

2005

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Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac β-myosin gene mutations

Cardiovascular research, 2003-02, Vol.57 (2), p.347-357

2003

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High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

Human mutation, 1999, Vol.13 (4), p.318-327

1999

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Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

American journal of medical genetics, 2005-01, Vol.132A (3), p.324-328

2005

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Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen

Human genetics, 2000-11, Vol.107 (5), p.499-503

2000

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Genome-wide Gene Expression Profiling of SCID Mice with T-cell-mediated Colitis

Scandinavian journal of immunology, 2009-05, Vol.69 (5), p.437-446

2009

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Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease

American journal of medical genetics. Part A, 2006-03, Vol.140A (5), p.427-433

2006

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Matrix isolation mid- and far-infrared spectra of sulfuric acid and deuterated sulfuric acid vapors

Journal of molecular structure, 1999-10, Vol.509 (1-3), p.35-47

1999

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Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current ( I TO,f), are not a frequent cause of long QT syndrome

Clinica chimica acta, 2005, Vol.351 (1), p.95-100

2005

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Transforming growth factor beta (TGFβ) signaling is regulated at the pocket region of primary cilia

Cilia (London), 2012-11, Vol.1 (S1), p.O23-O23, Article O23

2012

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GLI1 is involved in cell cycle regulation and proliferation of NT2 embryonal carcinoma stem cells

DNA and cell biology, 2008-05, Vol.27 (5), p.251-256

2008

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Evidence of gene–gene interaction in hidradenitis suppurativa: a nationwide registry study of Danish twins

RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twins

Characterization of vascular structures and skin bruises using hyperspectral imaging, image analysis and diffusion theory

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening

Mutations in the HERG K +-ion channel: A novel link between long QT syndrome and sudden infant death syndrome

T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

Prediction of milk/plasma concentration ratio of drugs

Coordination of TGFβ/BMP signaling is associated with the primary cilium

High‐throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method

Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients

High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac β-myosin gene mutations

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen

Genome-wide Gene Expression Profiling of SCID Mice with T-cell-mediated Colitis

Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease

Matrix isolation mid- and far-infrared spectra of sulfuric acid and deuterated sulfuric acid vapors

Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current ( I TO,f), are not a frequent cause of long QT syndrome

Transforming growth factor beta (TGFβ) signaling is regulated at the pocket region of primary cilia

GLI1 is involved in cell cycle regulation and proliferation of NT2 embryonal carcinoma stem cells

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