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Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer

American journal of human genetics, 2012-10, Vol.91 (4), p.754-759

2012

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Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia

American journal of human genetics, 2012-11, Vol.91 (5), p.906-911

2012

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Tazarotene 0.015% Cream as a Potential Topical Agent for Management of Ichthyosis in Dorfman-Chanarin Syndrome

Acta dermato-venereologica, 2019-03, Vol.99 (3), p.345-346

2019

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Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss

Journal of dermatological science, 2013-11, Vol.72 (2), p.186-188

2013

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Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance

Journal of investigative dermatology, 2012-09, Vol.132 (9), p.2192-2197

2012

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Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata

Journal of investigative dermatology, 2018-03, Vol.138 (3), p.549-556

2018

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Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2

Experimental dermatology, 2017-06, Vol.26 (6), p.536-541

2017

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A controlled trial of photodynamic therapy of actinic keratosis comparing different red light sources

EJD. European journal of dermatology, 2014-05, Vol.24 (3), p.335-341

2014

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A Case of Ankyloblepharon-ectodermal Defects-cleft Lip/Palate-syndrome with Choanal Atresia and Skin Erosions: Phenotypic Variability of TP63-related Disorders

Acta dermato-venereologica, 2019-01, Vol.99 (1), p.111-112

2019

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Neonatal blue light phototherapy increases café-au-lait macules in preschool children

European journal of pediatrics, 2014-11, Vol.173 (11), p.1519-1525

2014

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Genetic Variants in CTLA4 Are Strongly Associated with Alopecia Areata

Journal of investigative dermatology, 2011-05, Vol.131 (5), p.1169-1172

2011

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Immunochip-Based Analysis: High-Density Genotyping of Immune-Related Loci Sheds Further Light on the Autoimmune Genetic Architecture of Alopecia Areata

Journal of investigative dermatology, 2015-03, Vol.135 (3), p.919-921

2015

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Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability

Acta dermato-venereologica, 2016-01, Vol.96 (4), p.468-472

2016

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Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss

Archives of Dermatological Research, 2014-05, Vol.306 (4), p.413-418

2014

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Engineered antibodies: new possibilities for brain PET?

European journal of nuclear medicine and molecular imaging, 2019-12, Vol.46 (13), p.2848-2858

2019

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Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified

Experimental dermatology, 2012-05, Vol.21 (5), p.390-393

2012

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Time trends in tumour thickness vary in subgroups: analysis of 6475 patients by age, tumour site and melanoma subtype

Melanoma research, 2009-02, Vol.19 (1), p.24-30

2009

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Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss

Archives of Dermatological Research, 2013-04, Vol.305 (3), p.249-253

2013

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Concomitant Manifestation of Pili Annulati and Alopecia Areata: Coincidental Rather than True Association

Acta dermato-venereologica, 2011-06, Vol.91 (4), p.459-462

2011

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A Gene Locus Responsible for the Familial Hair Shaft Abnormality Pili Annulati Maps to Chromosome 12q24.32–24.33

Journal of investigative dermatology, 2004-12, Vol.123 (6), p.1073-1077

2004

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Pili Annulati: A Report of 2 American Families

Cutis (New York, N.Y.), 2013-05, Vol.91 (5), p.254-257

2013

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Genomewide analysis of copy number variants in alopecia areata in a C entral E uropean cohort reveals association with MCHR 2

Experimental dermatology, 2017-06, Vol.26 (6), p.536-541

2017

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Recurrent pyoderma in Kindler syndrome

Hautarzt, 2018-10, Vol.69 (Suppl 1), p.16-18

2018

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Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL 13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance

Journal of investigative dermatology, 2012, Vol.132 (9), p.2192-2197

2012

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Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer

Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia

Tazarotene 0.015% Cream as a Potential Topical Agent for Management of Ichthyosis in Dorfman-Chanarin Syndrome

Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss

Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance

Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata

Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2

A controlled trial of photodynamic therapy of actinic keratosis comparing different red light sources

A Case of Ankyloblepharon-ectodermal Defects-cleft Lip/Palate-syndrome with Choanal Atresia and Skin Erosions: Phenotypic Variability of TP63-related Disorders

Neonatal blue light phototherapy increases café-au-lait macules in preschool children

Genetic Variants in CTLA4 Are Strongly Associated with Alopecia Areata

Immunochip-Based Analysis: High-Density Genotyping of Immune-Related Loci Sheds Further Light on the Autoimmune Genetic Architecture of Alopecia Areata

Eight Novel Mutations Confirm the Role of AAGAB in Punctate Palmoplantar Keratoderma Type 1 (Buschke-Fischer-Brauer) and Show Broad Phenotypic Variability

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss

Engineered antibodies: new possibilities for brain PET?

Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified

Time trends in tumour thickness vary in subgroups: analysis of 6475 patients by age, tumour site and melanoma subtype

Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss

Concomitant Manifestation of Pili Annulati and Alopecia Areata: Coincidental Rather than True Association

A Gene Locus Responsible for the Familial Hair Shaft Abnormality Pili Annulati Maps to Chromosome 12q24.32–24.33

Pili Annulati: A Report of 2 American Families

Genomewide analysis of copy number variants in alopecia areata in a C entral E uropean cohort reveals association with MCHR 2

Recurrent pyoderma in Kindler syndrome

Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL 13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance

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