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2009
Giehl,K.A.; Rogers,M.A.; Radivojkov,M.; Tosti,A.; De Berker,D.A.R.; Weinlich,G.; Schmuth,M.; Ruzicka,T.; Eckstein,G.N., Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysis, British Journal of Dermatology 160, 527-533, 2009.

Yu,Z.; Gordon,S.W.; Nixon,A.J.; Bawden,C.S.; Rogers,M.A.; Wildermoth,J.E.; Maqbool,N.J.; Pearson,A.J., Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles, Differentiation 77, 307-316, 2009.

2008
Rogers M.A., Langbein L, Praetzel-Wunder S., Giehl K., Characterization and expression analysis of the hair keratin associated protein KAP26.1, British Journal of Dermatology 159, 715-729, 2008.

2007
Rogers M.A., Winter H., Langbein L., Wollschläger A., Praezel-Wunder S., Schweizer J., Isolation, characterization and expression analysis of human KAP24.1, a cuticular hair keratin associated protein (KAP) with unusual amino acid composition and repeat structure, Journal of Investigative Dermatology 127, 1197-1204, 2007.

Langbein L., Rogers M.A., Praetzel-Wunder S., Boeckler D., Schirmacher P., The novel keratins K39 and K40 are the latest expressed type I hair keratins: completion of the human hair keratin catalog, Journal of Investigative Dermatology 127, 1532-1535 2007.

Schweizer J., Langbein L., Rogers M.A., Winter H., Hair follicle-specific keratins and their diseases, Experimental Cell Research 313, 2010-2020, 2007.

2006
Betz R.C., Planko L., Eigelshoven S., Hanneken S., Pasternack S., Büssow H., Van den Bogaert K., Braun-Falco M., Rütten A., Rogers M.A., Ruzicka T., Nöthen M.M., Magin T.M., Kruse R. Loss of function mutations in the keratin 5 gene lead to Dowling-Degos disease, American Journal of Human Genetics 78, 510-519, 2006.

Parry D.A.D., Smith T.A., Rogers M.A., Schweizer J. Human hair keratin associated proteins: Sequence regularities and structural implications, Journal of Structural Biology, 155, 361-369, 2006.

Schweizer J., Bowden P.E., Coulombe P.A., Langbein L., Lane E.B., Magin T., Maltais L., Omary M.B., Parry D.A.D, Rogers M.A., Wright M.W., The new consensus nomenclature for mammalian keratins. Journal of Cell Biology 174, 169-174, 2006.

Langbein L., Rogers M.A., Praezel-Wunder S., Schirrmacher P., Schweizer J., K25irs1, K25irs2, K25irs3, K25irs4 represent the type I inner root sheath (IRS) keratins of the human hair follicle. Journal of Investigative Dermatology 126, 2377-2386, 2006.
Rogers M.A., Langbein L., Praetzel S., Winter H., Schweizer J. Human hair keratin associated proteins (KAPs), International Review of Cytology 251, 209-263, 2006.

2005
Rogers M.A., Edler L., Winter H., Langbein L., Beckmann I., Schweizer J. Characterization of new members of the human type II keratin gene family and a general evaluation of the keratin gene domain on chromosome 12q13.13, Journal of Investigative Dermatology 124, 536-544, 2005.

Langbein L., Rogers M.A., Praetzel S., Cribier B., Peltre B., Gassler N., Schweizer J. Characterization of a novel human type II epithelial keratin K1b, specifically expressed in eccrine sweat glands, Journal of Investigative Dermatology 125, 428-444, 2005.

Rogers M., Schweizer J., Human KAP genes, only the half of it? Extensive size polymorphisms in hair keratin-associated protein genes, Journal of Investigative Dermatology 124, VII-IX, 2005.

2004
Winter H., Schissel D., Parry D.A.D., Smith T.A., Liovic M., Lane E.B., Edler L. Langbein L., Jave-Suarez L.F., Rogers M.A., Wilde J., Peters G.., Schweizer J. An unusual Ala12Thr polymorphism in the 1A -helical segment of the companion layer-specific keratin K6hf is a risk factor for the common hair disorder pseudofolliculitis barbae, Journal of Investigative Dermatology 122, 652-657, 2004.

Rogers M.A., Langbein L., Winter H., Beckmann I., Praetzel S., Schweizer J. Hair keratin associated proteins (KAPs): Characterization of a second high sulfur KAP gene domain on human chromosome 21, Journal of Investigative Dermatology 122, 147-158, 2004.

Rogers M.A., Winter H., Langbein L., Bleiler R., Schweizer J. The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain, Differentiation 72, 527-540, 2004.

Jave-Suarez L., Langbein L., Winter H., Praetzel S., Rogers M., Schweizer J. Androgen regulation of the human hair follicle: The type I hair keratin hHa7 is a direct target gene in hair follicle trichocytes, Journal of Investigative Dermatology 122, 555-564, 2004.

Langbein L., Spring H., Rogers M.A., Praetzel S., Schweizer J., Hair keratins and hair follicle-specific epithelial keratins, In: Methods in Cell Biology 78, 413-451, 2004.

2003
Langbein L., Rogers M.A., Praetzel S, Winter H., Schweizer J. K6irs1, 2, 3, and 4 represent the inner root sheath (IRS)-specific type II epithelial keratins of the human hair follicle, Journal of Investigative Dermatology 120, 512-522, 2003.

Shimomura Y., Aoki N., Rogers M.A., Langbein L., Schweizer J., Ito M. Characterization of human keratin associated protein 1 family members, Journal of Investigative Dermatology Symposium Proceedings 8: 96-99, 2003.

Rogers, M., Keratins and keratin diseases, In: Nature Encyclopaedia of the Human Genome, Volume 3; Editor D.N. Cooper; Nature Publishing-Group, London, New York, Tokyo; 606-610, 2003.

2002
Jave-Suarez L., Winter H., Langbein L., Rogers M.A., Schweizer J., HOXC13 regulates the expression of human hair keratin genes, Journal of Biological Chemistry: 272: 3718-2726, 2002.

Langbein L., Rogers M.A., Praetzel S., Aoki N., Winter H., Schweizer J., A novel epithelial keratin, hK6irs1, is expressed differentially in all layers of the inner root sheath, including specialized Huxley cells (Flugelzellen) of the human hair follicle, Journal of Investigative Dermatology 118: 789-799,2002.

Rogers M.A., Langbein L., Winter, H., Ehmann, C., Praetzel S., Schweizer J., Characterization of a first domain of human high glycine-tyrosine and high sulfur keratin associated protein (KAP) genes on chromosome 21q22.1, Journal of Biological Chemistry 277, 48993-49002, 2002.

Shimomura Y., Aoki N., Schweizer J., Langbein L, Rogers M.A., Winter H., Ito M., Polymorphisms in the human high sulfur hair keratin associated protein, KAP1, gene family, Journal of Biological Chemistry 277: 45493-45501, 2002.

Shimomura Y., Aoki N., Rogers M.A., Langbein L., Schweizer J., Ito M., Identification of hKAP1.6 and hKAP1.7, two novel human high sulfur keratin–associated proteins (KAPs) expressed in the hair follicle cortex., Journal of Investigative Dermatology 118: 226-231, 2002.

2001
Aoki N., Sawada S., Rogers M.A., Schweizer J., Shimomura Y., Tsujimoto T., Ito K., Ito M., A novel type II cytokeratin, mK6irs, is expressed in the Huxley and Henle layers of the mouse inner root sheath, Journal of Investigative Dermatology 116: 359-365. 2001.

Winter H., Langbein L., Krawczak M., Cooper,D.N., Jave-Suarez L.F., Rogers M.A., Praetzel S., Heid P.J., Schweizer J., Human type I hair keratin pseudogene hHaA has functional orthologs in the chimpanzee and gorilla: Evidence for recent inactivation of the human gene after the Pan-Homo divergence, Human Genetics 38: 37-42, 2001.

Rogers M.A., Langbein L., Winter H., Ehmann C., Praetzel S., Schweizer J., Characterization of a cluster of human high/ ultrahigh sulfur keratin associated protein (KAP) genes imbedded in the type I keratin gene domain on chromosome 17q12-21, Journal of Biological Chemistry: 276: 19440-19451, 2001.

Langbein,L.; Rogers,M.A.; Winter,H.; Praetzel,S.; Schweizer,J. The catalog of human hair keratins. II. expression of the six type II members in the hair follicle and the combined catalog of human type I and II keratins, Journal of Biological Chemistry 276: 35123-35132, 2001

2000
Winter H., Vabres P., Larregue M., Rogers M.A., Schweizer J., A novel missense mutation, A118E, in the helix initiation motif of the type II hair cortex keratin hHb6, causing Monilethrix, Human Heredity 50: 322-324, 2000.

Rogers M.A., Winter H., Langbein L., Wolf C., Schweizer J., Characterization of a 300 kb region of human DNA containing a domain of type II hair keratin genes, Journal of Investigative Dermatology 114: 464-472, 2000.

1999
Winter H., Clark R.D., Tarras-Wahlberg C., Rogers M.A., Schweizer J., Monilethrix: A novel mutation, E402K, in the helix termination motif and the first causative muatations, N114D, in the helix initiation motif of the type II hair keratin hHb6, Journal of Investigative Dermatology 113: 263-266, 1999.

Langbein L, Rogers M.A., Winter H., Praetzel S., Beckhaus U., Rackwitz H.-J., Schweizer J. , The catalog of human hair keratins: I. Expression of the nine type I members in the hair follicle, Journal of Biological Chemistry 274: 19874-19884, 1999.

1998
Winter H., Labreze C., Chapalain V., Surleve-Bazeille J.E., Mercier M., Rogers M.A., Taieb A., Schweizer J., A variable monilethrix phenotype associated with a novel mutation, Glu392Lys, in the helix termination motif of the type II hair keratin hHb1, Journal of Investigative Dermatology 111:169-172, 1998.

Rogers M.A., Winter H., Wolf C., Heck M., Schweizer J., Characterization of a 190-kilobase pair domain of human type I hair keratin genes, Journal of Biological Chemistry 273: 26683-26691, 1998.

Winter H., Langbein L, Jakobs M., Rogers M.A. Schweizer J., A novel human type II epithelial cytokeratin, K6hf, specifically expressed in the companion layer of the anagen hair follicle, Journal of Investigative Dermatology 111: 955-962, 1998.

1997
Winter H., Rogers M.A:, Langbein L., Stevens H.P., Leigh I.M., Labreze C., Roul S., Taieb, A., Krieg T., Schweizer J., Mutation in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix, Nature Genetics 16, 372-374, 1997.

Winter H., Rogers M.A., Gebhardt M., Wollina U., Boxall L., Chitayat D., Babul-Hirji R., Stevens H.P., Zlotogorski A., Schweizer J., A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix. Human Genetics 101: 165-169, 1997.

Winter, H., Hofman I., Langbein L., Rogers M.A., Schweizer J., A splice site mutation in the gene of the human type I hair keratin hHa1 results in the expression of a tailless keratin isoform, Journal of Biological Chemistry 272: 32345-32352, 1997.

Rogers M.A., Langbein L, Präetzel S., Moll I., Krieg T., Winter H., Schweizer J., Sequencing and differential expression of three type II human hair keratins, Differentiation 61: 187-194, 1997.

1996
Winter H., Rogers M.A., Mahr B., Cremer M., Krieg T., Navsaria H.A., Leigh I.M., Schweizer J., The region coding for the helix termination motif and the adjacent intron 6 of the human type I hair keratin gene hHa2 contains three natural, closely spaced polymorphic sites, Journal of Investigative Dermatology 106: 544-548, 1996.

Rogers M.A., Winter H., Langbein L., Krieg T., Schweizer J., Genomic characterization of the human type I cuticular hair keratin hHa2 and identification of an adjacent novel type I hair keratin gene hHa5, Journal of Investigative Dermatology 107: 633-638, 1996.

1995
Royer-Pokora B., Rogers M., Zhu T.H., Schneider S., Loos U., Bolitz U., The TTG-2/RBTN2 T-cell oncogene encodes two alternative transcripts from two promoters: The distal promoter is removed by most 11p13 translocations in acute T cell leukaemias (T-ALL), Oncogene 10: 1353-1360, 1995.

Rogers M.A., Schweizer J., Krieg T., Winter H., A novel human type I hair keratin gene: Evidence for two keratin hHa3 isoforms, Molecular Biology Reports 20: 155-161, 1995.

Fink P., Rogers M.A., Korge B., Winter H., Schweizer J., A cDNA encoding the human type I hair keratin hHa1, Biochemica et Biophysica Acta 1264: 12-14, 1995

Rogers M.A., Nischt R., Korge B., Krieg T., Fink TM, Lichter P., Winter H., Schweizer J. Sequence data and chromsomal localization of human type I and type II hair keratin genes, Experimental Cell Research 220: 357-362, 1995.

Daniel L.W., Civoli F., Rogers M.A., Smitherman P.K., Raju P.A., Roederer, M. ET-18-0CH3 inhibits nuclear factor-kappa ß activation by 12-0-tetradecanoylphorbol-13-acetate but not by tumor necrosis factor- or interleukin 1-, Cancer Research 55: 4844-4849, 1995.

1987-1990
Rogers M., Berestecky J., Hossain M.Z., Guo H., Nicholson B.J., Kadle R.O., Bertram J.S., Retinoid-enhanced gap junctional communication is achieved by increased levels of connexin43 mRNA and protein, Molecular Carcinogenesis 3: 335-343, 1990.

Fürstenberger G., Rogers M., Schnapke R., Hoefler P., Marks F., Stimulatory role of transforming growth factors in multistage skin carcinogenesis: Possible explanation for the tumor-inducing effects of wounding in initiated mouse skin, International Journal of Cancer 43: 915-921, 1989.

Geschwendt M., Fürstenberger G., Rose-John S., Rogers M., Kittstein W., Pettit G.R., Harald C.L., Marks F., Bryostatin 1, an activator of protein kinase C, mimics as well as inhibits biological effects of phorbol ester TPA in vivo and in vitro, Carcinogenesis 9: 555-562, 1988.

Rogers M., Fürstenberger G., Marks F., Bauer G., Hoefler P. EIF-Epstein-Barr-Virus Inducing Factor, a factor with TGF-ß activity is a convertogenic agent (stage I tumor promoter) in mouse skin in vivo In: Progress in Cancer Research and Therapy Vol 35: F. Bresciana, R.J.B. King, M.E. Lippman (eds), Raven Press Ltd., New York, 254-257, 1988.

Marks F., Fürstenberger G., Geschwendt M., Rogers M., Schurich B., Kaina B., Bauer G. The wound response as a key element for an understanding of multistage carcinogenesis in skin, In: Chemical Carcinogenesis: F. Feoug (ed.), Plenum Press, New York, 217-232, 1988.

Fürstenberger G., Rogers M., Faberman J., Ganss M., Richter H., Marks F., Effects of the phorbol ester TPA and of the ionophore A-23187 on phospholipase A2 and C activities in the mouse epidermal cell line HEL-30, Cancer Research and Clinical Oncology 113: 310-318, 1987.