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Roland Kruse

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Hassnaa Mahmoudi; Andrew G Messenger; Markus M Nöthen; Silke Redler; Rachid Tazi-Ahnini; Peter Teßmann; Hans Wolff; Tim Becker; Pattie Birch; Ulrike Blume-Peytavi; Markus Böhm; Kathy Dobson; Dmitriy Drichel; Kathrin A Giehl; Sandra Hanneken; Roland Kruse; Gerhard Lutz; Regina C Betz
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss.
Sandra M Pasternack; Melanie Refke; Nico Schäfer; Elizabeth Sweeney; Maurice van Steensel; Carlos Ferrándiz; Utz Fischer; Thomas Franz; Alan Fryer; Clemens Grimm; Hans Christian Hennies; Miquel Just; Roland Kruse; Markus M Nöthen; Elham Paknia; Regina C Betz
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.
S Redler; H Wolff; F Albert; Tim Becker; Bettina Blaumeiser; M Böhm; Felix F Brockschmidt; Sibylle Eigelshoven; K A Giehl; Sandra Hanneken; C Herold; Roland Kruse; G Lutz; Markus M Nöthen; Regina C Betz
Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata.

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All Publications

2013: Hassnaa Mahmoudi; Andrew G Messenger; Markus M Nöthen; Silke Redler; Rachid Tazi-Ahnini; Peter Teßmann; Hans Wolff; Tim Becker; Pattie Birch; Ulrike Blume-Peytavi; Markus Böhm; Kathy Dobson; Dmitriy Drichel; Kathrin A Giehl; Sandra Hanneken; Roland Kruse; Gerhard Lutz; Regina C Betz
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss.
Archives of dermatological research 2013;305(3):249-53.
2013: Sandra M Pasternack; Melanie Refke; Nico Schäfer; Elizabeth Sweeney; Maurice van Steensel; Carlos Ferrándiz; Utz Fischer; Thomas Franz; Alan Fryer; Clemens Grimm; Hans Christian Hennies; Miquel Just; Roland Kruse; Markus M Nöthen; Elham Paknia; Regina C Betz
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.
American journal of human genetics 2013;92(1):81-7.
2012: S Redler; H Wolff; F Albert; Tim Becker; Bettina Blaumeiser; M Böhm; Felix F Brockschmidt; Sibylle Eigelshoven; K A Giehl; Sandra Hanneken; C Herold; Roland Kruse; G Lutz; Markus M Nöthen; Regina C Betz
Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata.
The British journal of dermatology 2012;167(6):1360-5.
2012: Dagny Jagielska; Roland Kruse; Gerhard Lutz; Markus M Nöthen; Sandra M Pasternack; Silke Redler; Melanie Refke; Hans Wolff; Bettina Blaumeiser; Ulrike Blume-Peytavi; Markus Böhm; Felix F Brockschmidt; Sibylle Eigelshoven; Natalie Garcia Bartels; Kathrin A Giehl; Sandra Hanneken; Christine Herold; Sandra Barth; Tim Becker; Regina C Betz
Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance.
The Journal of investigative dermatology 2012;132(9):2192-7.
2012: S Redler; M Refke; Rachid Tazi-Ahnini; H Wolff; Tim Becker; M P Birch; M Böhm; Felix F Brockschmidt; K Dobson; D Drichel; K A Giehl; S Herms; Nadine Kluck; Roland Kruse; G Lutz; Andrew G Messenger; Markus M Nöthen; Regina C Betz
Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss.
The British journal of dermatology 2012;166(6):1314-8.
2012: Silke Redler; Melanie Refke; Rachid Tazi-Ahnini; Hans Wolff; Markus M Nöthen; Tim Becker; Regina C Betz; Mary P Birch; Markus Böhm; Felix F Brockschmidt; Kathy Dobson; Dmitriy Drichel; Kathrin A Giehl; Nadine Kluck; Roland Kruse; Gerhard Lutz; Andrew Messenger
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identified.
Experimental dermatology 2012;21(5):390-3.
2011: S Redler; Rachid Tazi-Ahnini; H Wolff; T Becker; M P Birch; Felix F Brockschmidt; K Dobson; D Drichel; K A Giehl; N Kluck; Roland Kruse; G Lutz; Andrew G Messenger; M M Nöthen; Regina C Betz
Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss.
The British journal of dermatology 2011;165(3):703-5.
2011: Karsten K-G John; Felix F Brockschmidt; Silke Redler; Christine Herold; Sandra Hanneken; Sibylle Eigelshoven; Kathrin A Giehl; Jozef De Weert; Gerhard Lutz; Roland Kruse; Hans Wolff; Bettina Blaumeiser; Markus Böhm; Tim Becker; Markus M Nöthen; Regina C Betz
Genetic variants in CTLA4 are strongly associated with alopecia areata.
The Journal of investigative dermatology 2011;131(5):1169-72.
2011: Silke Redler; Roland Kruse; Sibylle Eigelshoven; Sandra Hanneken; Melanie Refke; Yaran Wen; Xue Zhang; Sven Cichon; Regina C Betz; Markus M Nöthen
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;64(4):e45-50.
2010: Felix F Brockschmidt; Axel M Hillmer; Sibylle Eigelshoven; Sandra Hanneken; S Heilmann; S Barth; C Herold; Tim Becker; Roland Kruse; Markus M Nöthen
Fine mapping of the human AR/EDA2R locus in androgenetic alopecia.
The British journal of dermatology 2010;162(4):899-903.
2010: S Redler; Felix F Brockschmidt; L Forstbauer; K A Giehl; C Herold; Sibylle Eigelshoven; Sandra Hanneken; Jozef De Weert; G Lutz; H Wolff; Roland Kruse; Bettina Blaumeiser; M Böhm; Tim Becker; Markus M Nöthen; Regina C Betz
The TRAF1/C5 locus confers risk for familial and severe alopecia areata.
The British journal of dermatology 2010;162(4):866-9.
2009: Sibylle Eigelshoven; Gitta Kameda; Anne-Katrin Kortüm; Simone Hübsch; Wolfgang Angerstein; Preeti Singh; Renate Vöhringer; Timm Goecke; Ertan Mayatepek; Thomas Ruzicka; Gabriele Wildhardt; Thomas Meissner; Roland Kruse
Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skin.
Pediatric dermatology 2009;26(6):759-61.
2009: Sandra M Pasternack; Sundaram Murugusundram; Sibylle Eigelshoven; Melanie Müller; Roland Kruse; Percy Lehmann; Regina C Betz
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.
Archives of dermatological research 2009;301(8):621-4.
2009: Roland Kruse; Sibylle Eigelshoven; Anna Kaiser; Thomas Ruzicka; Norbert J Neumann
Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltrates.
Folia histochemica et cytobiologica / Polish Academy of Sciences, Polish Histochemical and Cytochemical Society 2009;47(1):127-30.
2008: Axel M Hillmer; Felix F Brockschmidt; Sandra Hanneken; Sibylle Eigelshoven; Michael Steffens; Antonia Flaquer; Stefan Herms; Tim Becker; Anne-Katrin Kortüm; Dale R Nyholt; Zhen Zhen Zhao; Grant W Montgomery; Nicholas G Martin; Thomas W Mühleisen; Margrieta A Alblas; Susanne Moebus; Karl-Heinz Jöckel; Martina Bröcker-Preuss; Raimund Erbel; Roman Reinartz; Regina C Betz; Sven Cichon; Peter Propping; Max P Baur; Thomas F Wienker; Roland Kruse; Markus M Nöthen
Susceptibility variants for male-pattern baldness on chromosome 20p11.
Nature genetics 2008;40(11):1279-81.
2008: Peter Arne Gerber; Roland Kruse; Jens Hirchenhain; Jan S Krüssel; Norbert J Neumann
Pregnancy after laser-assisted selection of viable spermatozoa before intracytoplasmatic sperm injection in a couple with male primary cilia dyskinesia.
Fertility and sterility 2008;89(6):1826.e9-12.
2008: Thomas Meissner; Regina Christine Betz; Sandra M Pasternack; Sibylle Eigelshoven; Thomas Ruzicka; Roland Kruse; Gitta Laitenberger; Ertan Mayatepek
Richner-Hanhart syndrome detected by expanded newborn screening.
Pediatric dermatology 2008;25(3):378-80.
2008: Sibylle Eigelshoven; D Löchner-Ernst; C Schneider; Jan S Krüssel; VG Müller-Mattheis; Roland Kruse; Norbert J Neumann
[Sperm retrieval by transrectal electro-ejaculation in primary anorgasmy].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2008;59(4):285-6.
2008: Ulrich Pippirs; Roland Kruse; Daniela Bruch-Gerharz; C-F Eisenberger; W T Knoefel; Klaus W Schulte
[Acne inversa with arm plexus involvement].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2008;59(4):278-80.
2008: Axel M Hillmer; Antonia Flaquer; Sandra Hanneken; Sibylle Eigelshoven; Anne-Katrin Kortüm; Felix F Brockschmidt; Astrid Golla; Christine Metzen; Holger Thiele; Susanne Kolberg; Roman Reinartz; Regina C Betz; Thomas Ruzicka; Hans Christian Hennies; Roland Kruse; Markus M Nöthen
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.
American journal of human genetics 2008;82(3):737-43.
2008: Regina C Betz; K König; Antonia Flaquer; S Redler; Sibylle Eigelshoven; Anne-Katrin Kortüm; Sandra Hanneken; Axel M Hillmer; Thomas Tüting; Julien Lambert; Jozef De Weert; Roland Kruse; G Lutz; Bettina Blaumeiser; Markus M Nöthen
The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata.
The British journal of dermatology 2008;158(2):389-91.
2007: Laura Planko; Karsten Böhse; Jörg Höhfeld; Regina C Betz; Sandra Hanneken; Sibylle Eigelshoven; Roland Kruse; Markus M Nöthen; Thomas M Magin
Identification of a keratin-associated protein with a putative role in vesicle transport.
European journal of cell biology 2007;86(11-12):827-39.
2007: Regina C Betz; Jana Pforr; Antonia Flaquer; Silke Redler; Sandra Hanneken; Sibylle Eigelshoven; Anne-Katrin Kortüm; Thomas Tüting; Julien Lambert; Jozef De Weert; Axel M Hillmer; Christine Schmael; Thomas F Wienker; Roland Kruse; Gerhard Lutz; Bettina Blaumeiser; Markus M Nöthen
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.
The Journal of investigative dermatology 2007;127(11):2539-43.
2007: Daniela Bruch-Gerharz; Roland Kruse
[Meeting of the Department of Dermatology, University of Düsseldorf. Diagnosis: verruca plantaris].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2007;58(10):824, 826.
2007: AS Antal; S Grieb; Bernhard Homey; Ulrich R Hengge; G Schuett; Norbert J Neumann; Roland Kruse
[Paraneoplastic bullous pemphigoid in a man with breast and prostate cancer].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2007;58(10):833-4.
2007: Nermina Hodzic-Avdagic; G Reinerth; Julia Reifenberger; Roland Kruse; Daniela Bruch-Gerharz
[Bullous pemphigoid: first manifestation under a picture of prurigo simplex subacuta].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2007;58(4):290-2.
2007: Rodrigo Mota; Daniela Bruch-Gerharz; Roland Kruse; Ulrich R Hengge
[Disseminated erythema nodosum].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2007;58(4):292-3.
2007: G Reinerth; Daniela Bruch-Gerharz; Roland Kruse; Alf Bernhardt; Klaus W Schulte
[Combination treatment of a cutaneous non-Hodgkin's lymphoma with rituximab and polychemotherapy].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2007;58(4):295-7.
2007: Elisabeth Mangold; Nils Rahner; Nicolaus Friedrichs; Reinhard Buettner; Constanze Pagenstecher; Stefan Aretz; Waltraut Friedl; Thomas Ruzicka; Peter Propping; Arno Rütten; Roland Kruse
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
The British journal of dermatology 2007;156(1):158-62.
2006: Nico Schäfer; Bettina Blaumeiser; Tim Becker; Yun Freudenberg-Hua; Sandra Hanneken; Sibylle Eigelshoven; Christine Schmael; Julien Lambert; Jozef De Weert; Roland Kruse; Markus M Nöthen; Regina C Betz
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 (FCRL3) gene in alopecia areata.
International journal of immunogenetics 2006;33(6):393-5.
2006: Anne-Katrin Kortüm; Stephan Meller; Ulrich R Hengge; Roland Kruse; Julia Reifenberger; Daniela Bruch-Gerharz
[Pityrosporumfolliculitis (malasseziafolliculitis)].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(10):908-9.
2006: G Reinerth; Daniela Bruch-Gerharz; Peter Arne Gerber; Roland Kruse; Norbert J Neumann
[Unilateral laterothoracic exanthema].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(10):909-10.
2006: Sibylle Eigelshoven; Hans-Gerd Lenard; U Orth; Thomas Ruzicka; Roland Kruse
[Anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine-Syndrom)].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(10):911-2.
2006: Sibylle Eigelshoven; Roland Kruse; Lucie Rauch; Sandra Hanneken; Thomas Ruzicka; Norbert J Neumann
Thelalgia in man: successful treatment with botulinum toxin.
Archives of dermatology 2006;142(9):1242-3.
2006: Patricia Entz; Bettina Blaumeiser; Regina C Betz; Julien Lambert; Katia Seymons; Sibylle Eigelshoven; Sandra Hanneken; Roland Kruse; Peter Nürnberg; Marion Nagy; Markus M Nöthen
Investigation of the HLA-DRB1 locus in alopecia areata.
European journal of dermatology : EJD 2006;16(4):363-7.
2006: Jana Pforr; Bettina Blaumeiser; Tim Becker; Yun Freudenberg-Hua; Sandra Hanneken; Sibylle Eigelshoven; I Cuyt; Jozef De Weert; Julien Lambert; Roland Kruse; Markus M Nöthen; Regina C Betz
Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata.
Tissue antigens 2006;68(1):58-61.
2006: Bettina Blaumeiser; Ineke van der Goot; Rolf Fimmers; Sandra Hanneken; Sibylle Ritzmann; Katia Seymons; Regina C Betz; Thomas Ruzicka; Thomas F Wienker; Jozef De Weert; Julien Lambert; Roland Kruse; Markus M Nöthen
Familial aggregation of alopecia areata.
Journal of the American Academy of Dermatology 2006;54(4):627-32.
2006: Virginia Lewerenz; Daniela Bruch-Gerharz; Thomas Ruzicka; Roland Kruse
[Toxic epidermal necrolysis].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(4):322-4.
2006: Anne-Katrin Kortüm; Amanda S Büchau; Birgit Assmann; Thomas Ruzicka; Daniela Bruch-Gerharz; U Orth; Roland Kruse
[Inflammatory stage of incontinentia pigmenti (Bloch-Sulzberger syndrome)].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(4):330-1.
2006: H Dräger; Roland Kruse; Julia Reifenberger; Ulrich Meyer; Klaus W Schulte
[Cylindromatosis].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2006;57(4):332-3.
2006: Regina C Betz; Laura Planko; Sibylle Eigelshoven; Sandra Hanneken; Sandra M Pasternack; Heinrich Bussow; Kris Van Den Bogaert; Joerg Wenzel; Markus Braun-Falco; Arno Rutten; Michael A Rogers; Thomas Ruzicka; Markus M Nöthen; Thomas M Magin; Roland Kruse
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease.
American journal of human genetics 2006;78(3):510-9.
2006: Sibylle Ritzmann; Sandra Hanneken; Norbert J Neumann; Thomas Ruzicka; Roland Kruse
Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's Syndrome).
Dermatology (Basel, Switzerland) 2006;212(1):84-7.
2005: NO Dávalos; A García-Vargas; Jana Pforr; Ingrid Patricia Dávalos; V J Picos-Cárdenas; Diana García-Cruz; Roland Kruse; Luis Figuera; Markus M Nöthen; Regina C Betz
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.
The British journal of dermatology 2005;153(6):1216-9.
2005: Amanda S Büchau; Virginia Lewerenz; Roland Kruse; Norbert J Neumann; Thomas Ruzicka; Julia Reifenberger
[Reactive perforating collagenosis disease].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2005;56(10):963-5.
2005: Virginia Lewerenz; Julia Reifenberger; Thomas Ruzicka; Roland Kruse
[Exanthema in acute HIV disease].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2005;56(10):971-3.
2005: Axel M Hillmer; Sandra Hanneken; Sibylle Ritzmann; Tim Becker; Jan Freudenberg; Felix F Brockschmidt; Antonia Flaquer; Yun Freudenberg-Hua; Rami Abou Jamra; Christine Metzen; Uwe Heyn; Nadine Schweiger; Regina C Betz; Bettina Blaumeiser; Jochen Hampe; Stefan Schreiber; Thomas G. Schulze; Hans Christian Hennies; Johannes Schumacher; Peter Propping; Thomas Ruzicka; Sven Cichon; Thomas F Wienker; Roland Kruse; Markus M Nothen
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
American journal of human genetics 2005;77(1):140-8.
2005: Christof Lamberti; Nadine Schweiger; Wolfgang Hartschuh; Tilman Schulz; Petra Becker-Wegerich; Wolfgang Küster; Arno Rütten; Tilman Sauerbruch; Thomas Ruzicka; Roland Kruse
Birt-Hogg-Dubé syndrome: germline mutation in the (C)8 mononucleotide tract of the BHD gene in a German patient.
Acta dermato-venereologica 2005;85(2):172-3.
2004: Heidi Plettenberg; Suzan Artik; Annegret Kuhn; Mosaad Megahed; Thomas Ruzicka; Roland Kruse
[Purely cutaneous Rosai-Dorfman disease].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2004;55(10):969-71.
2004: Elisabeth Mangold; Constanze Pagenstecher; M Leister; Micaela Mathiak; Arno Rütten; Waltraut Friedl; Peter Propping; T Ruzicka; Roland Kruse
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.
Journal of medical genetics 2004;41(7):567-72.
2004: Roland Kruse; Thomas Ruzicka
DNA mismatch repair and the significance of a sebaceous skin tumor for visceral cancer prevention.
Trends in molecular medicine 2004;10(3):136-41.
2003: Roland Kruse; Hans-Christian Schuppe; J Malms; Sandra Hanneken; Thomas Ruzicka; Norbert J Neumann
Anti-inflammatory and varicocele treatment in nonobstructive azoospermia.
Andrologia 2003;35(4):217-9.
2003: Sandra Hanneken; Sibylle Ritzmann; Markus M Nöthen; Roland Kruse
[Androgenetic alopecia. Current aspects of a common phenotype].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 2003;54(8):703-12.
2003: Etgar Levy-Nissenbaum; Regina C Betz; Moshe Frydman; Michel Simon; Hadas Lahat; Tangiz Bakhan; Boleslaw Goldman; Anette Bygum; Monika Pierick; Axel M Hillmer; Nathalie Jonca; Jaime Toribio; Roland Kruse; Georg Dewald; Sven Cichon; Christian Kubisch; Marina Guerrin; Guy Serre; Markus M Nöthen; Elon Pras
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.
Nature genetics 2003;34(2):151-3.
2003: Roland Kruse; Arno Rütten; Nadine Schweiger; Eva Jakob; Micaela Mathiak; Peter Propping; Elisabeth Mangold; Michele Bisceglia; Thomas Ruzicka
Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias.
The Journal of investigative dermatology 2003;120(5):858-64.
2002: Axel M Hillmer; Roland Kruse; F Macciardi; Uwe Heyn; Regina C Betz; Thomas Ruzicka; Peter Propping; Markus M Nöthen; Sven Cichon
The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach.
The British journal of dermatology 2002;146(4):601-8.
2002: Micaela Mathiak; Arno Rütten; Elisabeth Mangold; Hans-Peter Fischer; Thomas Ruzicka; Waltraut Friedl; Peter Propping; Roland Kruse
Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test.
The American journal of surgical pathology 2002;26(3):338-43.
2002: Christof Lamberti; Matthias Jungck; Michael Laarmann; Michael Knapp; Reiner Caspari; Waltraut Friedl; Tilman Sauerbruch; Peter Propping; Roland Kruse
Arylamine N-acetyltransferase type 2 and glutathione S-transferases M1 and T1 polymorphisms in familial adenomatous polyposis.
Pharmacogenetics 2002;12(1):49-54.
2001: Axel M Hillmer; Roland Kruse; Regina C Betz; Johannes Schumacher; Uwe Heyn; Peter Propping; Markus M Nöthen; Sven Cichon
Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia.
American journal of human genetics 2001;69(1):235-7.
2001: Roland Kruse; Arno Rütten; HR Hosseiny-Malayeri; Michele Bisceglia; Waltraut Friedl; Peter Propping; Thomas Ruzicka; Elisabeth Mangold
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation.
The Journal of investigative dermatology 2001;116(3):463-5.
2000: Sven Cichon; Roland Kruse; Axel M Hillmer; Guido Kukuk; M Anker; K Altland; Michael Knapp; Peter Propping; Markus M Nöthen
A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
The British journal of dermatology 2000;143(4):811-4.
2000: Regina C Betz; YA Lee; Anette Bygum; Flemming Brandrup; A I Bernal; J Toribio; J I Alvarez; Guido Kukuk; H H Ibsen; H B Rasmussen; Thomas F Wienker; A Reis; Peter Propping; Roland Kruse; Sven Cichon; Markus M Nöthen
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
American journal of human genetics 2000;66(6):1979-83.
1999: Roland Kruse; Sven Cichon; M Anker; Axel M Hillmer; Patricio Barros-Núñez; JM Cantú; Evelia Leal; Georg Weinlich; Matthias Schmuth; Peter Fritsch; Thomas Ruzicka; Peter Propping; Markus M Nöthen
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.
The Journal of investigative dermatology 1999;113(6):954-9.
1999: Arno Rütten; Walter Burgdorf; Heino Hügel; Heinz Kutzner; HR Hosseiny-Malayeri; Waltraut Friedl; Peter Propping; Roland Kruse
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study.
The American Journal of dermatopathology 1999;21(5):405-13.
1999: Waltraut Friedl; Roland Kruse; Siegfried Uhlhaas; Manfred Stolte; B Schartmann; Klaus-Michael Keller; Matthias Jungck; M Stern; Steffan Loff; Walter Back; Peter Propping; Dieter E Jenne
Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients.
Genes, chromosomes & cancer 1999;25(4):403-6.
1999: Christof Lamberti; Roland Kruse; C Ruelfs; Reiner Caspari; Yaping Wang; Matthias Jungck; Micaela Mathiak; H R Malayeri; Waltraut Friedl; Tilman Sauerbruch; Peter Propping
Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer.
Gut 1999;44(6):839-43.
1999: Roland Kruse; Siegfried Uhlhaas; Christof Lamberti; Klaus-Michael Keller; C Jackisch; Johannes Steinhard; Gisela Knöpfle; Steffan Loff; Walter Back; Manfred Stolte; Matthias Jungck; Peter Propping; Waltraut Friedl; Dieter E Jenne
Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Mutations in brief no. 227. Online.
Human mutation 1999;13(3):257-8.
1999: Roland Kruse; A Rütten; H R Malayeri; H J Günzl; W Friedl; P Propping
A novel germline mutation in the hMLH1 DNA mismatch repair gene in a patient with an isolated cystic sebaceous tumor.
The Journal of investigative dermatology 1999;112(1):117-8.
1998: Sven Cichon; M Anker; Ina R Vogt; H Rohleder; M Pützstück; Axel M Hillmer; S A Farooq; K S Al-Dhafri; M Ahmad; Sayedul Haque; Marcella Rietschel; Peter Propping; Roland Kruse; Markus M Nöthen
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.
Human molecular genetics 1998;7(11):1671-9.
1998: Roland Kruse; Arno Rütten; Christof Lamberti; HR Hosseiny-Malayeri; Yaping Wang; C Ruelfs; Matthias Jungck; Micaela Mathiak; Thomas Ruzicka; W Hartschuh; M Bisceglia; Waltraut Friedl; Peter Propping
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.
American journal of human genetics 1998;63(1):63-70.
1998: Roland Kruse; M Guttenbach; B Schartmann; Regine Schubert; Hans van der Ven; M Schmid; Peter Propping
Genetic counseling in a patient with XXY/XXXY/XY mosaic Klinefelter's syndrome: estimate of sex chromosome aberrations in sperm before intracytoplasmic sperm injection.
Fertility and sterility 1998;69(3):482-5.
1998: Yaping Wang; Waltraut Friedl; Christof Lamberti; Markus M Nöthen; Roland Kruse; Peter Propping
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among Europeans.
Human heredity 1998;48(2):87-91.
1998: Roland Kruse; Peter Propping
[Skin diseases and genetic instability. II. Genetic dermatoses with genetic instability].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1998;49(2):W153-63.
1998: Markus M Nöthen; Sven Cichon; Ina R Vogt; S Hemmer; Roland Kruse; Michael Knapp; Tobias Höller; Muhammad Faiyaz-Ul-Haque; Sayedul Haque; Peter Propping; M Ahmad; Marcella Rietschel
A gene for universal congenital alopecia maps to chromosome 8p21-22.
American journal of human genetics 1998;62(2):386-90.
1998: Roland Kruse; Peter Propping
[Skin diseases and genetic instability. I: Basic principles of genetic instability].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1998;49(1):65-71.
1997: Yaping Wang; Waltraut Friedl; Christof Lamberti; C Ruelfs; Roland Kruse; Peter Propping
Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue.
Human genetics 1997;100(3-4):362-4.
1997: C Esche; Roland Kruse; C Lamberti; Waltraut Friedl; Peter Propping; Percy Lehmann; Thomas Ruzicka
Muir-Torre syndrome: clinical features and molecular genetic analysis.
The British journal of dermatology 1997;136(6):913-7.
1997: Maria Wehner; L Buschhausen; Christof Lamberti; Roland Kruse; Reiner Caspari; Peter Propping; Waltraut Friedl
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.
Human mutation 1997;10(3):241-4.
1996: Roland Kruse; Christof Lamberti; Yaping Wang; C Ruelfs; A Bruns; C Esche; Percy Lehmann; Thomas Ruzicka; Arno Rütten; Waltraut Friedl; Peter Propping
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
Human genetics 1996;98(6):747-50.