Concepedia

Author

Wolfgang Küster

Heinrich Heine University Düsseldorf

Also Known As

Ständer, Markward, W Küster, W. Kuster, W. Küster, WOLFGANG KÜSTER, Wolfgang Kuster, Wolfgang Küster

131

Publications

3.4K

Citations

35

H-Index

86

Concepts

All Affiliations

Heinrich Heine University DüsseldorfPhilipps University of MarburgUniversity of MünsterMax Delbrück CenterFriedrich-Alexander-Universität Erlangen-Nürnberg
WK

About

Wolfgang Küster is an author at Heinrich Heine University Düsseldorf specializing in medicine, dermatology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

24

30

1.8K

2

Arts

1

1

17

3

Health Sciences

1

1

12

4

Public Health

1

1

21

5

Social Sciences

1

1

18

Wolfgang Küster

×

45

Publications

2.7K

Citations

31

H-Index

YearCitations

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

Youngae Lee, U. Wahn, Rainer Kehrt,

Nature Genetics

2000

266

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

Wolfgang Küster, Rudolf Happle

Journal of the American Academy of Dermatology

1984

203

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

Michel van Geel, Maurice A. M. Van Steensel, Wolfgang Küster,

British Journal of Dermatology

2002

135

Deletion of the SLUG (<i>SNAI2</i>) gene results in human piebaldism

Manuel Sánchez‐Martín, Jesús Pérez‐Losada, Belén González‐Sánchez,

American Journal of Medical Genetics Part A

2003

122

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

Wolfgang Küster, Leigh Pascoe, J Purrmann,

American Journal of Medical Genetics

1989

108

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

DebbieM Hunt, Lisa Rickman, NeilV Whittock,

European Journal of Human Genetics

2001

104

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

Katja‐Martina Eckl, Peter Krieg, Wolfgang Küster,

Human Mutation

2005

104

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

Vinzenz Oji, J. Mazereeuw‐Hautier, Bijan Ahvazi,

Human Molecular Genetics

2006

94

Diagnosis-related frequency of compulsory measures in 10 German psychiatric hospitals and correlates with hospital characteristics

Tilman Steinert, Veronika Martin, Manfred Baur,

Social Psychiatry and Psychiatric Epidemiology

2006

89

Three Novel Homozygous Point Mutations and a New Polymorphism in the COL17A1 Gene: Relation to Biological and Clinical Phenotypes of Junctional Epidermolysis Bullosa

Hauke Schumann, Nadja Hammami-Hauasli, Leena Pulkkinen,

The American Journal of Human Genetics

1997

81

Page 1