A novel multiplex analysis of filaggrin polymorphisms

A novel multiplex analysis of filaggrin polymorphisms: A universally applicable method for genotyping

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

A novel multiplex analysis of filaggrin polymorphisms : A universally applicable method for genotyping. / Meldgaard, Michael; Szecsi, Pal B; Carlsen, Berit C; Thyssen, Jacob P; Johansen, Jeanne D; Menné, Torkil; Stender, Steen.

In: Clinica Chimica Acta, Vol. 413, No. 19-20, 2012, p. 1488-92.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Meldgaard, M, Szecsi, PB, Carlsen, BC, Thyssen, JP, Johansen, JD, Menné, T & Stender, S 2012, 'A novel multiplex analysis of filaggrin polymorphisms: A universally applicable method for genotyping', Clinica Chimica Acta, vol. 413, no. 19-20, pp. 1488-92. https://doi.org/10.1016/j.cca.2012.06.014

APA

Meldgaard, M., Szecsi, P. B., Carlsen, B. C., Thyssen, J. P., Johansen, J. D., Menné, T., & Stender, S. (2012). A novel multiplex analysis of filaggrin polymorphisms: A universally applicable method for genotyping. Clinica Chimica Acta, 413(19-20), 1488-92. https://doi.org/10.1016/j.cca.2012.06.014

Vancouver

Meldgaard M, Szecsi PB, Carlsen BC, Thyssen JP, Johansen JD, Menné T et al. A novel multiplex analysis of filaggrin polymorphisms: A universally applicable method for genotyping. Clinica Chimica Acta. 2012;413(19-20):1488-92. https://doi.org/10.1016/j.cca.2012.06.014

Author

Meldgaard, Michael ; Szecsi, Pal B ; Carlsen, Berit C ; Thyssen, Jacob P ; Johansen, Jeanne D ; Menné, Torkil ; Stender, Steen. / A novel multiplex analysis of filaggrin polymorphisms : A universally applicable method for genotyping. In: Clinica Chimica Acta. 2012 ; Vol. 413, No. 19-20. pp. 1488-92.

Bibtex

@article{6560c00d416c4f8a817ebfaecdc7e467,

title = "A novel multiplex analysis of filaggrin polymorphisms: A universally applicable method for genotyping",

abstract = "The filaggrin protein is expressed as profilaggrin mainly in stratum granulosum cells of the epidermis. The profilaggrin gene codes for 10-12 filaggrin repeats. The filaggrin protein is important for skin barrier function. Filaggrin deficiency due to functional null-polymorphisms affects 8-10% of the people in Northern Europe and is a strong risk factor for several diseases. Here, we describe a novel method for efficient, multiplexed genotyping of variations in the profilaggrin gene.",

author = "Michael Meldgaard and Szecsi, {Pal B} and Carlsen, {Berit C} and Thyssen, {Jacob P} and Johansen, {Jeanne D} and Torkil Menn{\'e} and Steen Stender",

year = "2012",

doi = "10.1016/j.cca.2012.06.014",

language = "English",

volume = "413",

pages = "1488--92",

journal = "Clinica Chimica Acta",

issn = "0009-8981",

publisher = "Elsevier",

number = "19-20",

}

RIS

TY - JOUR

T1 - A novel multiplex analysis of filaggrin polymorphisms

T2 - A universally applicable method for genotyping

AU - Meldgaard, Michael

AU - Szecsi, Pal B

AU - Carlsen, Berit C

AU - Thyssen, Jacob P

AU - Johansen, Jeanne D

AU - Menné, Torkil

AU - Stender, Steen

PY - 2012

Y1 - 2012

N2 - The filaggrin protein is expressed as profilaggrin mainly in stratum granulosum cells of the epidermis. The profilaggrin gene codes for 10-12 filaggrin repeats. The filaggrin protein is important for skin barrier function. Filaggrin deficiency due to functional null-polymorphisms affects 8-10% of the people in Northern Europe and is a strong risk factor for several diseases. Here, we describe a novel method for efficient, multiplexed genotyping of variations in the profilaggrin gene.

AB - The filaggrin protein is expressed as profilaggrin mainly in stratum granulosum cells of the epidermis. The profilaggrin gene codes for 10-12 filaggrin repeats. The filaggrin protein is important for skin barrier function. Filaggrin deficiency due to functional null-polymorphisms affects 8-10% of the people in Northern Europe and is a strong risk factor for several diseases. Here, we describe a novel method for efficient, multiplexed genotyping of variations in the profilaggrin gene.

U2 - 10.1016/j.cca.2012.06.014

DO - 10.1016/j.cca.2012.06.014

M3 - Journal article

C2 - 22705401

VL - 413

SP - 1488

EP - 1492

JO - Clinica Chimica Acta

JF - Clinica Chimica Acta

SN - 0009-8981

IS - 19-20

ER -

ID: 40165585