Hautärztin - Allergologin - Andrologin

Dr. med. 

Sandra Hanneken
Praxis Empoderm


Patiententraining
Individualberatung
Schulung

Individualberatung - Patiententraining - Schulung

Dr. med. Sandra Hanneken

Praxis Empoderm

Hautärztin - Allergologin - Andrologin

Dr. med. 

Sandra Hanneken
Praxis Empoderm


Neurodermitischulung


Neurodermitisschulung

Dr. med. Sandra Hanneken

Praxis Empoderm

Hautärztin - Allergologin - Andrologin

Dr. med. 

Sandra Hanneken
Praxis Empoderm


Berufsdermatologin


Zertifizierte Berufsdermatologin

Dr. med. Sandra Hanneken

Praxis Empoderm

Hautärztin - Allergologin - Andrologin

Dr. med. 

Sandra Hanneken
Praxis Empoderm


Ernährungsmedizin


Ernährungsmedizin

Dr. med. Sandra Hanneken

Praxis Empoderm

Hautärztin - Allergologin - Andrologin

Dr. med. 

Sandra Hanneken
Praxis Empoderm


Kinderwunschberatung


Kinderwunschberatung

Dr. med. Sandra Hanneken

Praxis Empoderm

Hautärztin - Allergologin - Andrologin

Publikationsliste

Parren LJMT, Baron JM, Joussen 5, Marquardt Y, Hanneken S, van Steensel MAM, Steijlen PM, van Geel M2,Frank J (2018) J Eur Acad Dermatol Venereol. 2018 CYLD mutations differentially affect splicing and mRNA decay in Brooke-Spiegler syndrome. Feb 25. doi: 10.1111/jdv.14889. [Epub ahead of print]

Fischer, J, Degenhardt, F, Hofmann, A, Redler, S, Basmanav, F, Heilmann-Heimbach, S, Hanneken, S, Giehl, K, Wolff, H, Moebus, S. , Kruse, R, Lutz, G, Blaumeiser, B, Böhm, M, Garcia Bartels, N, Blume-Peytavi, U, Pethukova, L, Christiano, A, Nöthen, M, Betz, R (2017) Genome-wide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2. Exp Dermatol Jun;26(6):536-541.

Redler S, Angisch M, Heilmann S, Wolf S, Barth S, Basmanav BF, Giehl KA, Hanneken S, Eigelshoven S, Mangold E, Kruse R, Blaumeiser B, Böhm M, Knapp M, Garcia Bartels N, Lutz G, Wolff H, Blume-Peytavi U, Nöthen MM, Becker T, Betz RC (2015) Immunochip-based analysis: high-density genotyping of immune-related loci sheds further light on the autoimmune genetic architecture of alopecia areata. J Invest Dermatol 135(3):919-21.

Basmanav FB, Fritz G, Lestringant GG, Pachat D, Hoffjan S, Fischer J, Wehner M, Wolf S, Thiele H, Altmüller J, Pulimood SA, Rütten A, Kruse R, Hanneken S, Frank J, Danda S, Bygum A, Betz RC (2015) Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura. J Invest Dermatol 135(2):615-8.

Verma S, Pasternack SM, Rütten A, Ruzicka T, Betz RC, Hanneken S (2014) The First Report of KRT5 Mutation Underlying Acantholytic Dowling-Degos Disease with Mottled Hypopigmentation in an Indian Family. Indian J Dermatol 59(5):476-80.

Basmanav FB, Oprisoreanu AM, Pasternack SM, Thiele H, Fritz G, Wenzel J, Größer L, Wehner M, Wolf S, Fagerberg C, Bygum A, Altmüller J, Rütten A, Parmentier L, El Shabrawi-Caelen L, Hafner C, Nürnberg P, Kruse R, Schoch S, Hanneken S, Betz RC (2014) Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease. Am J Hum Genet 2;94(1):135-43

Redler S, Dobson K, Drichel D, Heilmann S, Wolf S, Brockschmidt FF, Tazi-Ahnini R, Birch P, Teßmann P, Giehl KA, Kruse R, Lutz G, Garcia Bartels N, Hanneken S, Wolff H, Böhm M, Becker T, Blume-Peytavi U, Nöthen MM, Messenger AG, Betz RC (2013) Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss. J Dermatol Sci 72(2):186-8.

Nuwaihyd R, Redler S, Heilmann S, Drichel D, Wolf S, Birch P, Dobson K, Lutz G, Giehl KA, Kruse R, Tazi-Ahnini R, Hanneken S, Böhm M, Miesel A, Fischer T, Wolff H, Becker T, Garcia-Bartels N, Blume-Peytavi U, Nöthen MM, Messenger AG, Betz RC (2014) Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss. Arch Dermatol Res 306(4):413-8.

Forstbauer LM, Brockschmidt FF, Moskvina V, Herold C, Redler S, Herzog A, Hillmer AM, Meesters C, Heilmann S, Albert F, Alblas M, Hanneken S, Eigelshoven S, Giehl KA, Jagielska D, Blume-Peytavi U, Garcia Bartels N, Kuhn J, Hennies HC, Goebeler M, Jung A, Peitsch WK, Kortüm AK, Moll I, Kruse R, Lutz G, Wolff H, Blaumeiser B, Böhm M, Kirov G, Becker T, Nöthen MM, Betz RC (2012) Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata. Eur J Hum Genet 20(3):326-32.

Heilmann S, Brockschmidt FF, Hillmer AM, Hanneken S, Eigelshoven S, Ludwig KU, Herold C, Mangold E, Becker T, Kruse R, Knapp M, Nöthen MM (2013) Evidence for a polygenic contribution to androgenetic alopecia. Br J Dermatol 169(4):927-30.

Mahmoudi H, Redler S, Birch P, Drichel D, Dobson K, Tazi-Ahnini R, Teßmann P, Giehl KA, Kruse R, Lutz G, Hanneken S, Wolff H, Blume-Peytavi U, Becker T, Nöthen MM, Messenger AG, Böhm M, Betz RC (2013) Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss. Arch Dermatol Res 305(3):249-53.

Bafteh PR, Siegesmund M, Hanneken S, Neumann NJ (2012) Protective effects of β-carotene and melanin against protoporphyrine IX-induced phototoxicity in the photo hen's egg test. Photodermatol Photoimmunol Photomed 28(1):12-6.

Redler S, Albert F, Brockschmidt FF, Herold C, Hanneken S, Eigelshoven S, Giehl KA, Kruse R, Lutz G, Wolff H, Blaumeiser B, Böhm M, Becker T, Nöthen MM, Betz RC (2012) Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata. Br J Dermatol 167(6):1360-5.

Braun SA, Hanneken S, Reifenberger J, Helbig D, Frank J (2012) [Hereditary cutaneous leiomyomatosis]. Hautarzt 63(4):276-8.

Lichte V, Hanneken S, Gerber PA, van Geel M, Frank J. (2012) [Facial papules and pneumothoraces. Birt-Hogg-Dubé syndrome]. Hautarzt 63(10):762-5.

Jagielska D, Redler S, Brockschmidt FF, Herold C, Pasternack SM, Garcia Bartels N, Hanneken S, Eigelshoven S, Refke M, Barth S, Giehl KA, Kruse R, Lutz G, Wolff H, Blaumeiser B, Böhm M, Blume-Peytavi U, Becker T, Nöthen MM, Betz RC (2012) Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance. J Invest Dermatol 132(9):2192-7.

Braun SA, Helbig D, Frank J, Hanneken S (2012) [Eruptive melanocytic nevi during azathioprine therapy in myasthenia gravis]. Hautarzt 63(10):756-9.

Katugampola RP, Anstey AV, Finlay AY, Whatley S, Woolf J, Mason N, Deybach JC, Puy H, Ged C, de Verneuil H, Hanneken S, Minder E, Schneider-Yin X, Badminton MN (2012) A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases. Br J Dermatol 167(4):888-900.

Katugampola RP, Badminton MN, Finlay AY, Whatley S, Woolf J, Mason N, Deybach JC, Puy H, Ged C, de Verneuil H, Hanneken S, Minder E, Schneider-Yin X, Anstey AV (2012) Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases. Br J Dermatol 167(4):901-13.

Hoff NP, Reifenberger J, Schulte KW, Hanneken S (2012) [Epithelioid sarcoma of the right hand]. Hautarzt 63(4):278-82.

Li R, Brockschmidt FF, Kiefer AK, Stefansson H, Nyholt DR, Song K, Vermeulen SH, Kanoni S, Glass D, Medland SE, Dimitriou M, Waterworth D, Tung JY, Geller F, Heilmann S, Hillmer AM, Bataille V, Eigelshoven S, Hanneken S, Moebus S, Herold C, den Heijer M, Montgomery GW, Deloukas P, Eriksson N, Heath AC, Becker T, Sulem P, Mangino M, Vollenweider P, Spector TD, Dedoussis G, Martin NG, Kiemeney LA, Mooser V, Stefansson K, Hinds DA, Nöthen MM, Richards JB (2012) Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genet 8(5)

Meinhard Schiller, Claus-Detlev Klemke, Andreas Arnold, Nina Booken, Sandra Hanneken, Erhard Hölzle, Martin Kaatz, Thomas Schwarz, Michael Weichenthal , Uwe Hillen (2011) S1 Leitlinie - extrakorporale Photopherese. AWMF Register Nummer 013/072

John KK, Brockschmidt FF, Redler S, Herold C, Hanneken S, Eigelshoven S, Giehl KA, De Weert J, Lutz G, Kruse R, Wolff H, Blaumeiser B, Böhm M, Becker T, Nöthen MM, Betz RC (2011) Genetic variants in CTLA4 are strongly associated with alopecia areata. J Invest Dermatol 131(5):1169-72.

Brockschmidt FF, Heilmann S, Ellis JA, Eigelshoven S, Hanneken S, Herold C, Moebus S, Alblas MA, Lippke B, Kluck N, Priebe L, Degenhardt FA, Jamra RA, Meesters C, Jöckel KH, Erbel R, Harrap S, Schumacher J, Fröhlich H, Kruse R, Hillmer AM, Becker T, Nöthen MM (2011) Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness. Br J Dermatol 165(6):1293-302.

Hanneken S, Rütten A, Eigelshoven S, Braun-Falco M, Pasternack SM, Ruzicka T, Nöthen MM, Betz RC, Kruse R (2011) [Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients]. Hautarzt 62(11):842-51.

Kochs C, Bockmann A, Hanneken S, Neumann NJ (2011) [Scleredema diabeticorum: successful treatment with UVA-1 phototherapy]. Hautarzt 62(4):255-7.

Braun SA, Albrecht P, Methner A, Hanneken S. (2011) POEMS syndrome. An interdisciplinary clinical challenge. Hautarzt 62(10):722-5.

Redler S, Kruse R, Eigelshoven S, Hanneken S, Refke M, Wen Y, Zhang X, Cichon S, Betz RC, Nöthen MM (2010) Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report. J Am Acad Dermatol 64(4):e45-50

Redler S, Brockschmidt FF, Forstbauer L, Giehl KA, Herold C, Eigelshoven S, Hanneken S, de Weert J, Lutz G, Wolff H, Kruse R, Blaumeiser B, Böhm M, Becker T, Nöthen MM, Betz RC (2010) The TRAF/C5 locus confers risk for familial and severe alopecia areata. Br J Dermatol 162 (4): 866-869.

Mota R, Reifenberger J, Hanneken S, Mühlenstädt E (2010) [Classical and atypical presentations of Galli-Galli disease]. Hautarzt 61(4):284-6.

Hanneken S, Rütten A, Pasternack SM, Eigelshoven S, El Shabrawi-Caelen L, Wenzel J, Braun-Falco M, Ruzicka T, Nöthen MM, Kruse R, Betz RC (2010) Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. Br J Dermatol 163(1):197-200.

Brockschmidt FF, Hillmer AM, Eigelshoven S, Hanneken S, Heilmann S, Barth S, Herold C, Becker T, Kruse R, Nöthen MM (2010) Fine mapping of the human AR/EDA2R locus in androgenetic alopecia. Br J Dermatol 162(4):899-903.

Hanneken S, Siegesmund M, Bolsen K, Gardlo K, Neumann NJ (2010) The prognostic value of cord blood analysis in erythropoietic protoporphyria:
The ‘Duesseldorf Cord Blood Study’. Photoderm Photoimmunol Photomed 26(1):7-9.

Hoff NP, Akanay-Diesel S, Pippirs U, Schulte KW, Hanneken S (2009) [Cutaneous side effects of hydroxyurea tretament for polycythemia vera.] Hautarzt 60(10):783-7.

Hoff NP, Hanneken S (2009) Nebenwirkungen einer Hydroxyurea-Therapie an der Haut. Campanile 2/2009:2-3.

Kochs C, Mühlenstädt E, Neumann NJ, Hanneken S (2009) [Solarium-induced pseudoporphyria and variegate porphyria as rare differential diagnoses of porphyria cutanea tarda.] Hautarzt 60(10):790-3.

Hanneken S, Kürten V, Hörnke M, Neumann NJ (2009) Metastatic colon cancer triggering an acute attack of variegate porphyria. Int J Colorectal Dis 24:127-8.

Akanay-Diesel S, Richter J, Schneider M, Schulte KW, Reifenberger J, Hanneken S (2009) [Shulman’s syndrome (eosinophilic fasciitis)]. Hautarzt 60(4):278-81

Wessendorf U, Hanneken S, Haust M, Neumann NJ (2009) [Fixed solar urticaria with delayed onset]. J Am Acad Dermatol 60(4):695-7.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM (2008) Susceptibility variants for male-pattern baldness on chromosome 20p11. Nat Genet 40(11):1279-81.

Hanneken S, Wessendorf U, Neumann NJ (2008) Photodynamic onycholysis: first report of photo-onycholysis after photodynamic therapy. Clin Exp Dermatol 33(5):659-60.

Antal AS, Hanneken S, Neumann NJ, Hengge UR (2008) [Considerable variation in the range of time for complications to appear after tattoos.] Hautarzt 59(10):769-71.

Kochs C, Hanneken S, Schulte KW, Reifenberger J (2008) [Treatment of carcinoma in situ of erythema ab igne with photodynamic therapy] Hautarzt 59(10):777-9.

Hanneken S, Schulte KW, Neumann NJ (2008) [Photodynamic therapy of granuloma annulare.] Hautarzt 59(4):283-5.

Hillmer AM, Flaquer A, Hanneken S, Eigelshoven S, Kortüm AK, Brockschmidt FF, Golla A, Metzen C, Thiele H, Kolberg S, Reinartz R, Betz RC, Ruzicka T, Hennies HC, Kruse R and Nöthen MM (2008) Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26. Am J Hum Genet 82(3):737-43.

Betz R, König K, Flaquer A, Redler S, Eigelhoven S, Kortüm AK, Hanneken S, Hillmer A, Tüting T, Lambert J, De Weert J, Kruse R, Lutz G, Blaumeiser B, Nöthen MM (2008) The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata. Br J Dermatol 158(2):389-91.

Betz R, Pforr J, Flaquer A, Redler S, Hanneken S, Eigelhoven S, Kortüm AK, Tüting T, Lambert J, De Weert J, Hillmer A, Schmael C, Wienker T, Kruse R, Lutz G, Blaumeiser B, Nöthen MM (2007) 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. J Invest Dermatol 127(11):2539-43.

Planko L, Böhse K, Höfeld J, Betz R, Hanneken S, Eigelshoven S, Kruse R, Nöthen M, Magin T (2007) Identification of a keratin-associated protein with a putative role in vesicle transport. Eur J Cell Biol 86(11-12):827-39.

Schafer N, Blaumeiser B, Becker T, Freudenberg-Hua Y, Hanneken S, Eigelshoven S, Schmael C, Lambert J, De Weert J, Kruse R, Nothen MM, Betz RC (2006) Investigation of the functional variant c.-169T>C of the Fc receptorlike 3 (FCRL3) gene in alopecia areata. Int J Immunogenet 33(6):393-5.

Hanneken S, Reifenberger J, Homey B (2006) [Double-lip and blepharochalasis: Ascher syndrome in a 13 year-old female patient.] Hautarzt 57(10):903-4.

Ritzmann S, Kruse R, Rauch L, Hanneken S, Ruzicka T, Neumann NJ (2006) Thelalgia in man – successful treatment with botulinum toxin. Arch Dermatol 142(9):1242-3.

Entz P, Blaumeiser B, Betz R, Lambert J, Seymons K, Eigelshoven S, Hanneken S, Kruse R, Nurnberg P, Nagy M, Nöthen MM (2006) Investigation of the HLA-DRB1 locus in alopecia areata. Eur J Dermatol 16(4):363-7.

Pforr J, Blaumeiser B, Becker T, Freudenberg-Hua Y, Hanneken S, Eigelshoven S, Cuyt I, De Weert J, Lambert J, Kruse R, Nöthen MM & Betz RC (2006) Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata. Tissue Antigens 68:58-61.

Blaumeiser B, van der Goot I, Fimmers R, Hanneken S, Ritzmann S, Seymons K, Betz RC, Ruzicka T, Wienker TF, De Weert J, Lambert J, Kruse R, Nöthen MM (2006) Familial aggregation of alopecia areata. J Am Acad Dermatol 54(4):627-32.

Hanneken S, Kürten V, Reifenberger J, Ruzicka T, Neumann NJ (2006) [Erythropoetic protoporphyria in childhood.] Hautarzt 57(4):318-20.

Kuhn A, Hanneken S, Megahed M, Ruzicka T, Neumann NJ (2006) [Extreme photosensitivity since childhood.] Hautarzt 57 (1):56-8.

Betz RC, Planko L, Eigelshoven S, Hanneken S, Pasternack SM, Bussow H, Bogaert KV, Wenzel J, Braun-Falco M, Rütten A, Rogers MA, Ruzicka T, Nöthen MM, Magin TM, Kruse R. (2006) Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease. Am J Hum Genet 78(3):510-9.

Ritzmann S, Hanneken S, Neumann NJ, Ruzicka T, Kruse R (2006) Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's Syndrome). Dermatology 212(1):84-7.

Hanneken S, Hodzic-Avdagic N, Neumann NJ, Ruzicka T, Bruch-Gerharz D (2005) [Postpartum persistent herpes gestationis. A therapeutic challenge]
Hautarzt 56(10):961-3.

Hillmer AM, Hanneken S, Ritzmann S, Becker T, Freudenberg J, Brockschmidt FF, Flaquer A, Freudenberg-Hua Y, Jamra RA, Metzen C, Heyn U, Schweiger N, Betz RC, Blaumeiser B, Hampe J, Schreiber S, Schulze TG, Hennies HC, Schumacher J, Propping P, Ruzicka T, Cichon S, Wienker TF, Kruse R, Nöthen MM. (2005) Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia. Am J Hum Genet 77(1):140-148.

Hanneken S, Sterzinger AA, Schulte KW, Reifenberger J (2005) [Photodynamic therapy for a nevoid basal cell carcinoma syndrome.] Hautarzt 56:363-4.

Neumann NJ, Hanneken S, Ruzicka T, Lehmann P (2004) Phototoxicity of exogenous protoporphyrin IX and δ-aminolevulinic acid in the photo hen’s egg test. Photoderm Photoimmunol Photomed 20:224-9.

Gardlo K, Hanneken S, Ruzicka T, Neumann NJ (2004) [Photodynamic therapy of cutaneous leishmaniasis. A promising new therapeutic modality.] Hautarzt 5(4):381-3.

Neumann NJ, Hanneken S, Ruzicka T, Schulte KW (2004) [Special emergencies in dermatology]. Hautarzt 55(6):512-8.

Hanneken S, Kruse R, Dall P, Ruzicka T, Neumann NJ (2004) Unilateral pseudogynecomastia: a novel work-related disease. Ann Intern Med 140 (6):W28.

Kruse R, Schuppe HC, Malms J, Hanneken S, Ruzicka T, Neumann NJ (2003) Anti-inflammatory and varicozele treatment in non-obstructive azoospermia. Andrologia 35: 217-9.

Hanneken S, Ritzmann S, Nöthen MM, Kruse R (2003) Androgenetische Alopezie: Aktuelle Aspekte eines vertrauten Phänotyps. Hautarzt 54(8):703-12.

Hanneken S, Kruse R, Schulte KW, Ruzicka, T, Neumann, NJ (2002) [Der diagnostische Stellenwert von Nagelveränderungen für die allgemeinmedizinische Praxis.] Z Allg. Med 78:547-51.

Hanneken S, Kruse R, Dall P, Ruzicka T, Neumann NJ (2002) Unilaterale Pseudogynäkomastie. Z Hautkr 76:445-61.

Asadullah K , Friedrich M , Hanneken S, Rohrbach C, Audring H, Vergopoulos A, Ebeling M, Döcke WD, Volk HD, Sterry W (2001) Effects of systemic interleukin-10 therapy on psoriatic skin lesions: Histologic, immunhistologic and molecular biology findings. J Invest Dermatol 116(5):721-27.

Asadullah K, Haeußler-Quade A, Gellrich S, Hanneken S, Hansen-Hagge TE, Döcke WD, Volk HD, Sterry W (2000) IL-15 and IL-16 overexpression in cutaneous T-cell lymphomas: stage-dependent increase in mycosis fungoides progression. Exp Dermatol 9:248-51.