W. Küster

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Cytogenetic effects during extracorporeal photopheresis treatment of two patients with cutaneous T-cell lymphoma

G. Plewig, U. Peterseim, W. Küster, 2004, Archives of Dermatological Research.

Mutation spectrum and functional analysis of epidermis‐type lipoxygenases in patients with autosomal recessive congenital ichthyosis

H. Hennies, K. Eckl, H. Traupe, 2005, Human mutation.

Birt-Hogg-Dubé syndrome: germline mutation in the (C)8 mononucleotide tract of the BHD gene in a German patient.

T. Sauerbruch, R. Kruse, A. Rütten, 2005, Acta dermato-venereologica.

Lipid Composition of Outer Stratum corneum in Hereditary Palmoplantar Keratodermas

H. Hamm, H. Traupe, B. Melnik, 2003, Dermatology.

n-alkanes in the skin.

G. Plewig, B. Melnik, W. Küster, 1991, Archives of dermatology.

Autosomal dominant lamellar ichthyosis exhibits an abnormal scale lipid pattern

G. Plewig, H. Traupe, B. Melnik, 1989, Clinical genetics.

Improving Sun Protection Behaviour in Children: Study Design and Baseline Results of a Randomized Trial in Italian Elementary Schools

J. Utikal, C. Klemke, T. Waldmann, 2003, Dermatology.

Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients

T. Wienker, A. Reis, K. Reich, 2005, Journal of Medical Genetics.

Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.

H. Hennies, A. Reis, D. Mischke, 1995, Human molecular genetics.

A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case.

W. Küster, B. Korge, F. B. Müller, 1999, The Journal of investigative dermatology.

Novel K5 and K14 mutations in German patients with the Weber-Cockayne variant of epidermolysis bullosa simplex.

L. Bruckner-Tuderman, W. Küster, B. Korge, 1998, The Journal of investigative dermatology.

GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - EITHER 180-KD BULLOUS PEMPHIGOID ANTIGEN (BP180) OR LAMININ-5 IS DEFICIENT

A. Sonnenberg, M. Meurer, H. Scheffer, 1995 .

Efficacy of Urea Therapy in Children with Ichthyosis

K. Bohnsack, F. Rippke, H. Traupe, 1998, Dermatology.

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Matti Pirinen, Christian Gieger, Peter Donnelly, 2012 .

The inheritance of common baldness: two B or not two B?

R. Happle, W. Küster, 1984, Journal of the American Academy of Dermatology.

A family study of atopic dermatitis

W. Sterry, E. Christophers, W. Küster, 2004, Archives of Dermatological Research.

Neurotological and Neuroanatomical Changes in the Connexin-26-Related HID/KID Syndrome

H. Hennies, D. Basta, A. Ernst, 2006, Audiology and Neurotology.

Three novel homozygous point mutations and a new polymorphism in the COL17A1 gene: relation to biological and clinical phenotypes of junctional epidermolysis bullosa.

J. Uitto, L. Pulkkinen, A. Mauviel, 1997, American journal of human genetics.

Novel mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.

R. Spritz, P. Itin, W. Küster, 1993, The Journal of investigative dermatology.

CHILD syndrome in a boy.

R. Happle, S. Orlow, I. Effendy, 1996, American journal of medical genetics.

Linear lichen planopilaris of the face.

G. Plewig, P. Kind, E. Hölzle, 1989, Journal of the American Academy of Dermatology.

Progressive erythrokeratodermia and cochlear hearing impairment. A case report and review of the literature.

A. Lamprecht, W. Küster, T. Goecke, 1988, International journal of pediatric otorhinolaryngology.

HID and KID syndromes are associated with the same connexin 26 mutation

H. Hennies, R. Happle, M. Geel, 2002, The British journal of dermatology.

Nevus psiloliparus: A Distinct Fatty Tissue Nevus

R. Happle, W. Küster, 1998, Dermatology.

The CHILD nevus: a distinct skin disorder.

R. Happle, W. Küster, H. Mittag, 1995, Dermatology.

A new family with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.

S. Emmert, M. Zutt, W. Küster, 2003, Journal of the American Academy of Dermatology.

[Clinical aspects and genetics of congenital skin defects].

H. Traupe, W. Küster, 1988, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12–q21

K. Sperling, A. Reis, W. Küster, 1992, Human Genetics.

Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation

H. Hennies, A. Reis, W. Küster, 2002, Archives of Dermatological Research.

Localisation of gene for the naevoid basal-cell carcinoma syndrome

R. Wegner, J. Burger, M. Kuklík, 1992, The Lancet.

Clustering of COL7A1 mutations in exon 73: implications for mutation analysis in dystrophic epidermolysis bullosa.

L. Bruckner-Tuderman, W. Küster, H. Schumann, 1999, The Journal of investigative dermatology.

Transient bullous dermolysis of the newborn associated with compound heterozygosity for recessive and dominant COL7A1 mutations.

M. Raghunath, L. Bruckner-Tuderman, W. Küster, 1998, The Journal of investigative dermatology.

Localization of parathyroid tumors by computed tomography.

H. Imhof, B. Niederle, R. Willvonseder, 1980, The New England journal of medicine.

[Acne inversa. Pathogenesis and genetics].

G. Plewig, W. Küster, O. Rödder-Wehrmann, 1991, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency.

A. Sonnenberg, M. Meurer, L. Bruckner-Tuderman, 1996, Archives of dermatology.

Letters to Dermatology

D. Margolis, L. Thomas, R. Dummer, 1998, Dermatology.

Chapter 32. Genetic Hypomelanoses: Localized Hypopigmentation

R. Happle, J. Nordlund, J. Bolognia, 2007 .

Lack of genetic association of the three more common polymorphisms of CARD15 with psoriatic arthritis and psoriasis in a German cohort

A. Reis, R. Kelsch, J. Lascorz, 2004, Annals of the rheumatic diseases.

Lack of genetic association of the interleukin-4 receptor single-nucleotide polymorphisms I50V and Q551R with erosive disease in psoriatic arthritis.

A. Reis, J. Lascorz, H. Burkhardt, 2006, Arthritis and rheumatism.

Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis.

V. Wiebe, H. Hennies, A. Reis, 1998, American journal of human genetics.

Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: a new genodermatosis?

R. Happle, P. Frossard, W. Küster, 1998, American journal of medical genetics.

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

D. Kelsell, H. Hennies, I. Leigh, 2001, European Journal of Human Genetics.

Systematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgaris.

A. Reis, R. Kelsch, J. Lascorz, 2005, The Journal of investigative dermatology.

Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren‐Larsson syndrome

C. Wadelius, C. Ayuso, C. Kraus, 1998, Human mutation.

Neurocutaneous disorders in children.

R. Happle, W. Küster, 1993, Current opinion in pediatrics.

Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.

H. Hennies, A. Hovnanian, P. Steijlen, 2006, Human molecular genetics.

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21

T. Wienker, U. Wahn, Young-Ae Lee, 2000, Nature Genetics.

[Perifollicular fibroma of the skin and colonic polyps: Hornstein-Knickenberg syndrome].

R. Happle, W. Küster, A. Schachtschabel, 1996, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

Muckle–Wells syndrome: clinical and histological skin findings compatible with cold air urticaria in a large kindred

T. Zuberbier, B. Henz, W. Küster, 2004, The British journal of dermatology.

Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly

T. Krieg, L. Bruckner-Tuderman, W. Küster, 2006, Human mutation.

47 patients in 14 families with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.

H. Haenssle, H. Hennies, S. Emmert, 2003, European journal of dermatology : EJD.

The genetics of Crohn disease: complex segregation analysis of a family study with 265 patients with Crohn disease and 5,387 relatives.

F. Majewski, L. Pascoe, W. Küster, 1989, American journal of medical genetics.

Indication for the identity of palmoplantar keratoderma type Unna-Thost with type Vörner. Thost's family revisited 110 years later.

W. Küster, A. Becker, 1992, Acta dermato-venereologica.

Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.

T. Wienker, A. Spurdle, M. Ramsay, 1997, American journal of human genetics.

Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity.

H. Hennies, A. Reis, P. Frossard, 2001, American journal of human genetics.

[Acne inversa. Diagnosis and therapy].

G. Plewig, W. Küster, O. Rödder-Wehrmann, 1991, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

Central nervous system involvement in progressive facial hemiatrophy: further evidence of chronic localised meningoencephalitis

S. Felber, R. Felix, H. Henkes, 1995 .

[Basal cell nevus syndrome with squamous cell carcinoma of the larynx].

G. Plewig, W. Küster, W. Stieler, 1988, Zeitschrift fur Hautkrankheiten.

Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma

H. Hennies, A. Reis, W. Küster, 1994, Human Genetics.

Balneophototherapy – combined treatment of psoriasis vulgaris and atopic dermatitis with salt water baths and artificial ultraviolet radiation

T. Gambichler, P. Altmeyer, K. Hoffmann, 2000, Journal of the European Academy of Dermatology and Venereology : JEADV.

[Varicella pneumonia in a patient with Hodgkin's disease (author's transl)].

W. Küster, L. Wicke, J. Kühböck, 1978, Der Radiologe.

Autosomal dominant inheritance of HID syndrome (hystrix-likeichthyosis with deafness)

R. Happle, W. Küster, A. König, 1997 .

Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts.

T. Wienker, A. Reis, R. Kelsch, 2005, The Journal of investigative dermatology.

Clinical relevance of radiologic examination of the skeleton and bone density measurements in osteoporosis of old age

W. Dorda, R. Willvonseder, G. Seidl, 1981, Skeletal Radiology.

Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis.

T. Wienker, A. Reis, M. Steffens, 2006, The Journal of investigative dermatology.

Deletion of the SLUG (SNAI2) gene results in human piebaldism

B. Korf, R. Spritz, M. Sánchez-Martín, 2003, American journal of medical genetics. Part A.

Prenatal diagnosis of epidermolytic hyperkeratosis by direct gene sequencing.

D. Roop, J. Rothnagel, M. Longley, 1994, The Journal of investigative dermatology.