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Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

PLoS genetics, 2012-05, Vol.8 (5), p.e1002746-e1002746

2012

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Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

American journal of human genetics, 2006-03, Vol.78 (3), p.510-519

2006

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Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

Journal of investigative dermatology, 2007-11, Vol.127 (11), p.2539-2543

2007

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Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

Journal of the American Academy of Dermatology, 2011-04, Vol.64 (4), p.e45-e50

2011

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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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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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Immediate and delayed hypersensitivity to corticosteroids

Journal der Deutschen Dermatologischen Gesellschaft, 2011-11, Vol.9 (11), p.885-888

2011

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Typ-I- und Typ-IV-Allergie gegenüber Glukokortikosteroiden

Journal der Deutschen Dermatologischen Gesellschaft, 2011-11, Vol.9 (11), p.885-888

2011

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Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26

American journal of human genetics, 2008-03, Vol.82 (3), p.737-743

2008

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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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Identification of a keratin-associated protein with a putative role in vesicle transport

European journal of cell biology, 2007-12, Vol.86 (11), p.827-839

2007

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Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair

Archives of Dermatological Research, 2009-09, Vol.301 (8), p.621-624

2009

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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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Richner–Hanhart Syndrome Detected by Expanded Newborn Screening

Pediatric dermatology, 2008-05, Vol.25 (3), p.378-380

2008

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Periorifizielle und akrale Hautveränderungen nach Abstillen

Monatsschrift Kinderheilkunde, 2007-02, Vol.155 (2), p.176-178

2007

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Waardenburg Syndrome Type I with Heterochromia Iridis and Circumscribed Hypopigmentation of the Skin

Pediatric dermatology, 2009-11, Vol.26 (6), p.759-761

2009

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Investigation of the HLA-DRB1 locus in alopecia areata

EJD. European journal of dermatology, 2006-07, Vol.16 (4), p.363-367

2006

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Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltrates

Folia histochemica et cytobiologica, 2009-01, Vol.47 (1), p.127-130

2009

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Genome-wide Scan and Fine-Mapping Linkage Study of And rogenetic Alopecia Reveals a Locus on Chromosome 3q26

American journal of human genetics, 2008-03, Vol.82 (3), p.737

2008

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Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltrates

Folia histochemica et cytobiologica, 2009-05, Vol.47 (1), p.127-130

2009

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Thelalgia in man: successful treatment with botulinum toxin

Archives of dermatology (1960), 2006-09, Vol.142 (9), p.1242

2006

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Richner-Hanhart Syndrome Detected by Expanded Newborn Screening

Pediatric Dermatology, 2008, Vol.25 (3), p.378-380

2008

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Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report

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

Susceptibility variants for male-pattern baldness on chromosome 20p11

Genetic Variants in CTLA4 Are Strongly Associated with Alopecia Areata

Immediate and delayed hypersensitivity to corticosteroids

Typ-I- und Typ-IV-Allergie gegenüber Glukokortikosteroiden

Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26

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

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

Identification of a keratin-associated protein with a putative role in vesicle transport

Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair

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

Richner–Hanhart Syndrome Detected by Expanded Newborn Screening

Periorifizielle und akrale Hautveränderungen nach Abstillen

Waardenburg Syndrome Type I with Heterochromia Iridis and Circumscribed Hypopigmentation of the Skin

Investigation of the HLA-DRB1 locus in alopecia areata

Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltrates

Genome-wide Scan and Fine-Mapping Linkage Study of And rogenetic Alopecia Reveals a Locus on Chromosome 3q26

Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltrates

Susceptibility variants for male-pattern baldness on chromosome 20p11

Thelalgia in man: successful treatment with botulinum toxin

Richner-Hanhart Syndrome Detected by Expanded Newborn Screening

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