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S. Hanneken · SciRah

Researcher profile · Semantic Scholar

S. Hanneken

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S. Hanneken — researcher profile on SciRah

h-index: 27
Works: 62
Citations: 2,449

Most-cited papers

Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.
R. Betz, Laura Planko, S. Eigelshoven, S. Hanneken +11 more
2006American Journal of Human Genetics284 citations Open access
Semantic Scholar
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
A. Hillmer, S. Hanneken, S. Ritzmann, T. Becker +21 more
2005American Journal of Human Genetics235 citations Open access
Semantic Scholar
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.
F. Basmanav, A. Oprişoreanu, Sandra M. Pasternack, H. Thiele +17 more
2014American Journal of Human Genetics153 citations Open access
Semantic Scholar
Susceptibility variants for male-pattern baldness on chromosome 20p11
A. Hillmer, F. F. Brockschmidt, S. Hanneken, S. Eigelshoven +23 more
2008Nature Genetics132 citations
Semantic Scholar
Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance.
Dagny Jagielska, S. Redler, F. F. Brockschmidt, C. Herold +16 more
2012Journal of Investigative Dermatology130 citations Open access
Semantic Scholar
Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
Rui Li, F. F. Brockschmidt, A. Kiefer, H. Stefánsson +35 more
2012PLoS Genetics117 citations Open access
Semantic Scholar
Familial aggregation of alopecia areata.
B. Blaumeiser, Ineke van der Goot, R. Fimmers, S. Hanneken +9 more
2006Journal of American Academy of Dermatology115 citations
Semantic Scholar
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.
R. Betz, J. Pforr, Antònia Flaquer, S. Redler +13 more
2007Journal of Investigative Dermatology102 citations Open access
Semantic Scholar
Congenital erythropoietic porphyria: a single‐observer clinical study of 29 cases
R. Katugampola, M. Badminton, A. Finlay, S. Whatley +10 more
2012British Journal of Dermatology80 citations Open access
Semantic Scholar
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.
A. Hillmer, Antònia Flaquer, S. Hanneken, S. Eigelshoven +12 more
2008American Journal of Human Genetics74 citations Open access
Semantic Scholar
A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases
R. Katugampola, A. Anstey, A. Finlay, S. Whatley +10 more
2012British Journal of Dermatology71 citations
Semantic Scholar
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male‐pattern baldness
F. F. Brockschmidt, S. Heilmann, J. Ellis, S. Eigelshoven +19 more
2011British Journal of Dermatology63 citations Open access
Semantic Scholar
Systematic mutation screening of KRT5 supports the hypothesis that Galli–Galli disease is a variant of Dowling–Degos disease
S. Hanneken, A. Rütten, Sandra M. Pasternack, S. Eigelshoven +7 more
2010British Journal of Dermatology60 citations
Semantic Scholar
IL‐15 and IL‐16 overexpression in cutaneous T‐cell lymphomas: stage‐dependent increase in mycosis fungoides progression
K. Asadullah, A. Haeussler-Quade, S. Gellrich, S. Hanneken +4 more
2000Experimental Dermatology57 citations
Semantic Scholar
Identification of a keratin-associated protein with a putative role in vesicle transport.
Laura Planko, Karsten Böhse, J. Höhfeld, R. Betz +5 more
2007European Journal of Cell Biology55 citations
Semantic Scholar
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata
L. Forstbauer, F. F. Brockschmidt, V. Moskvina, C. Herold +29 more
2011European Journal of Human Genetics49 citations Open access
Semantic Scholar
Genetic variants in CTLA4 are strongly associated with alopecia areata.
Karsten K.-G. John, F. F. Brockschmidt, S. Redler, C. Herold +12 more
2011Journal of Investigative Dermatology48 citations Open access
Semantic Scholar
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata
S. Eigelshoven, K. König, Antònia Flaquer, S. Redler +11 more
2007British Journal of Dermatology48 citations
Semantic Scholar
Evidence for a polygenic contribution to androgenetic alopecia
S. Heilmann, F. F. Brockschmidt, A. M. Hillmer, S. Hanneken +8 more
2013British Journal of Dermatology43 citations
Semantic Scholar
Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata
S. Redler, F. Albert, F. F. Brockschmidt, C. Herold +11 more
2012British Journal of Dermatology39 citations
Semantic Scholar
Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura.
F. Buket Basmanav, G. Fritz, G. Lestringant, Divya Pachat +14 more
2015Journal of Investigative Dermatology34 citations Open access
Semantic Scholar
Investigation of the HLA-DRB1 locus in alopecia areata.
Patricia Entz, B. Blaumeiser, R. Betz, J. Lambert +7 more
2006EJD. European journal of dermatology34 citations
Semantic Scholar
Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss.
S. Redler, K. Dobson, D. Drichel, S. Heilmann +17 more
2013Journal of dermatological science (Amsterdam)32 citations
Semantic Scholar
Fine mapping of the human AR/EDA2R locus in androgenetic alopecia
F. F. Brockschmidt, A. Hillmer, S. Eigelshoven, S. Hanneken +6 more
2009British Journal of Dermatology31 citations
Semantic Scholar
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.
J. Pforr, Bettina Blaumeiser, T. Becker, Yun Freudenberg-Hua +8 more
2006Tissue Antigens29 citations
Semantic Scholar
[Photodynamic therapy of cutaneous leishmaniasis. A promising new therapeutic modality].
K. Gardlo, S. Hanneken, T. Ruzicka, N. Neumann
2004Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete28 citations
Semantic Scholar
Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
Rima Nuwaihyd, S. Redler, S. Heilmann, D. Drichel +18 more
2014Archives of Dermatological Research27 citations
Semantic Scholar
Androgenetische Alopezie
S. Hanneken, S. Ritzmann, M. Nöthen, Rudolf Kruse
2003Der Hautarzt27 citations
Semantic Scholar
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2
J. Fischer, F. Degenhardt, A. Hofmann, S. Redler +16 more
2017Experimental Dermatology26 citations Open access
Semantic Scholar
Morbus Galli-Galli
S. Hanneken, A. Rütten, S. Eigelshoven, M. Braun-Falco +5 more
2011Der Hautarzt23 citations
Semantic Scholar
Type 2 Segmental Manifestation of Cutaneous Leiomyomatosis in Four Unrelated Women with Additional Uterine Leiomyomas (Reed’s Syndrome)
S. Ritzmann, S. Hanneken, N. Neumann, T. Ruzicka +1 more
2005Dermatology21 citations
Semantic Scholar
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.
S. Redler, R. Kruse, S. Eigelshoven, S. Hanneken +6 more
2011Journal of American Academy of Dermatology20 citations
Semantic Scholar
The TRAF1/C5 locus confers risk for familial and severe alopecia areata
S. Redler, F. F. Brockschmidt, L. Forstbauer, K. Giehl +12 more
2009British Journal of Dermatology18 citations
Semantic Scholar
Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL
G. Biolcati, S. Hanneken, E. Minder, N. Neumann +4 more
2021Journal of Patient-Reported Outcomes14 citations Open access
Semantic Scholar
The First Report of KRT5 Mutation Underlying Acantholytic Dowling-Degos Disease with Mottled Hypopigmentation in an Indian Family
S. Verma, Sandra M. Pasternack, A. Rütten, T. Ruzicka +2 more
2014Indian Journal of Dermatology14 citations Open access
Semantic Scholar
Fixed solar urticaria with delayed onset.
U. Wessendorf, S. Hanneken, M. Haust, N. Neumann
2009Journal of American Academy of Dermatology14 citations
Semantic Scholar
Immunochip-based analysis: high-density genotyping of immune-related loci sheds further light on the autoimmune genetic architecture of alopecia areata.
S. Redler, Marina Angisch, S. Heilmann, S. Wolf +17 more
2015Journal of Investigative Dermatology12 citations Open access
Semantic Scholar
Photodynamic onycholysis: first report of photo‐onycholysis after photodynamic therapy
S. Hanneken, Ulf Wessendorf, N. J. Neumann
2008Clincal and Experimental Dermatology12 citations
Semantic Scholar
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
H. Mahmoudi, S. Redler, P. Birch, D. Drichel +14 more
2013Archives of Dermatological Research9 citations
Semantic Scholar
Thelalgia in man: successful treatment with botulinum toxin.
S. Eigelshoven, R. Kruse, L. Rauch, S. Hanneken +2 more
2006Archives of Dermatology6 citations
Semantic Scholar
[Androgenetic alopecia. Current aspects of a common phenotype].
S. Hanneken, S. Ritzmann, M. Nöthen, R. Kruse
2003Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete6 citations
Semantic Scholar
Protective effects of β‐carotene and melanin against protoporphyrine IX‐induced phototoxicity in the photo hen's egg test
Pascal R. Bafteh, M. Siegesmund, S. Hanneken, N. Neumann
2012Photodermatology, Photoimmunology & Photomedicine5 citations
Semantic Scholar
The prognostic value of cord blood analysis in erythropoietic protoporphyria: the ‘Duesseldorf Cord Blood Study’
S. Hanneken, M. Siegesmund, K. Bolsen, K. Gardlo +1 more
2010Photodermatology, Photoimmunology & Photomedicine5 citations
Semantic Scholar
Investigation of the functional variant c.‐169T > C of the Fc receptor‐like 3 (FCRL3) gene in alopecia areata
N. Schäfer, Bettina Blaumeiser, T. Becker, Yun Freudenberg-Hua +8 more
2006International Journal of Immunogenetics5 citations
Semantic Scholar
Correction to: Validation of a novel patient reported tool to assess the impact of treatment in erythropoietic protoporphyria: the EPP-QoL
G. Biolcati, S. Hanneken, E. Minder, N. Neumann +4 more
2021Journal of Patient-Reported Outcomes4 citations Open access
Semantic Scholar
A randomized phase III trial of afamelanotide (Scenesse®), an agonistic alpha-melanocyte-stimulating hormone (MSH) analogue in the treatment of protoporphyria-induced phototoxicity.
G. Biolcati, D. J.C., S. Hanneken, P. Wilson +11 more
20114 citations
Semantic Scholar
[Treatment of carcinoma in situ of erythema ab igne with photodynamic therapy].
C. Kochs, S. Hanneken, K. Schulte, J. Reifenberger
2008Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete4 citations
Semantic Scholar
Phototoxicity of exogenous protoporphyrin IX and δ‐aminolevulinic acid in the photo hen's egg test
N. Neumann, S. Hanneken, T. Ruzicka, P. Lehmann
2004Photodermatology, Photoimmunology & Photomedicine4 citations
Semantic Scholar
Metastatic colon cancer triggering an acute attack of variegate porphyria
S. Hanneken, V. Kuerten, M. Hoernke, Norbert J. Neumann
2008International Journal of Colorectal Disease3 citations
Semantic Scholar
Doppellippe und Blepharochalasis
S. Hanneken, J. Reifenberger, B. Homey
2006Der Hautarzt3 citations
Semantic Scholar

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M. Nöthen×28
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M. Nöthen — researcher profile on SciRah
S. Eigelshoven×22
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S. Eigelshoven — researcher profile on SciRah
R. Kruse×21
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R. Kruse — researcher profile on SciRah
R. Betz×19
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R. Betz — researcher profile on SciRah

F. F. Brockschmidt

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F. F. Brockschmidt — researcher profile on SciRah

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S. Redler — researcher profile on SciRah

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G. Lutz — researcher profile on SciRah

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T. Becker — researcher profile on SciRah

B. Blaumeiser×11

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B. Blaumeiser — researcher profile on SciRah

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Rudolf Kruse×10

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T. Ruzicka — researcher profile on SciRah