Publications
Textbook
Graw, J.: Genetik (begr. von W. Hennig), 4. Auflage Springer-Verlag, Heidelberg (2006)
5. Auflage, Springer-Verlag, Heidelberg (2010)
details
Scientific Publications
2011 2010 2009 2008 2007 2006
2011
Churchill, A., Graw, J.: Clinical and Experimental Advances in Congenital and Paediatric Cataracts. Phil. Transact. Royal Soc. Ser. B. 366, 2011, 1234-1249.
Fuchs, H., Gailus-Durner, V., Adler, T., …Puk, O., …Graw, J., … Hrabé de Angelis, M.: Mouse Phenotyping. Methods. 53, 2011, 120-135.
Graw, J.: Confirmation of single nucleotide mutations. In: Gene Discovery for Disease Models; Ed.: Gu, W.; John Wiley & Sons; 2011, 391-402.
Puk, O., Ahmad, N., Wagner, S., Hrabé de Angelis, Graw, J.: First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts. Invest. Ophthalmol. Vis. Sci. 2011 Jan 6. [Epub ahead of print]
2010
Dames, P., Puff, R., Weise, M., Parhofer, K.G., Göke, B., Götz, M., Graw, J., Favor, J., Lechner, A.: Relative roles of the different Pax6 domains for pancreatic alpha-cell development. BMC Dev. Biol. 10, 2010, 39.
Graw, J.: Eye Development. Curr. Top. Dev. Biol. 90C, 2010, 343-386.
Morgan, H., Beck, T., Blake, A., Gates, H., Adams, N., Debouzy, G., Leblanc, S., Lengger, C., Maier, H., Melvin, D., Meziane, H., Richardson, D., Wells, S., White, J., Wood, J., The EUMODIC Consortium* (*Graw, J. is member of the EUMODIC Consortium), Hrabé de Angelis, M., Brown, S.D.M, Hancock, J.M., Mallon, A.-M.: EuroPhenome: a repository for high-throughput mouse phenotyping data. Nucl. Acids Res. 38, 2010, D577-D585.
Rosemann, M., Ivashkevich, A., Favor, J., Dalke, C., Hölter, S.M., Becker, L., Rácz, I., Bolle, I., Klempt, M., Rathkolb, B., Kalaydjiev, S., Adler, T., Aguilar, A., Hans, W., Horsch, M., Rozman, J., Calzada-Wack, J., Kunder, S., Gailus-Durner, V., Fuchs, H., Naton, B., Schulz, H., Beckers, J., Busch, D.H., Burbach, J.P.H., Smidt, M.P., Quintanilla-Martinez; L., Esposito, I., Klopstock, T., Klingenspor, M., Ollert, M., Wolf, E., Wurst, W., Zimmer, A., Hrabé de Angelis, M., Atkinson, M., Heinzmann, U., Graw, J.: Microphthalmia, Parkinsonism and enhanced nociception in Pitx3416insG mice. Mamm. Genome, 21, 2010, 13-27.
Roshan, M., Vijaya, P.H., Lavanya, R.G., Shama P. K., Santhiya, S.T., Graw, J., Gopinath, P.M., Satyamoorthy, K.: A novel human CRYGD mutation in a juvenile autosomal dominant cataract. Mol. Vis. 16, 2010, 887-896.
Santhiya, S.T., Kumar, G.S., Sudhakar, P., Gupta, N., Klopp, N., Illig, T., Söker, T., Groth, M., Platzer, M., Gopinath, P.M., Graw, J.: Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms. Mol Vis. 16, 2010, 1837-1847.
Shyla, A., Hölzlwimmer, G., Calzada-Wack, J., Bink, K., Tischenko, O., Guilly, M.N., Chevillard, S., Samson, E., Graw J., Atkinson, M.J., Pellegata, N.S.: Allelic loss of chromosomes 8 and 19 in MENX-associated rat pheochromocytoma. Int. J. Cancer, 126, 2010, 2362-2372.
2009
Ainsbury, E.A., Bouffler, S.D., Dörr, W., Graw, J., Muirhead, C., Edwards, A.A., Cooper, J.: Radiation cataractogenesis – a review of recent studies. Rad. Res. 172, 2009, 1-9.
Bazhin, A.V., Dalke, C., Willner, N., Abschütz, O., Wildberger, H.G.H., Philippov, P.P., Dummer, R., Graw, J., Hrabé de Angelis, M., Schadendorf, D., Umansky, V., Eichmüller, S.B.: Cancer-retina antigens as potential paraneoplastic antigens in melanoma-associated retinopathy. Int. J. Cancer 124, 2009, 140-149.
Enard, W., Gehre, S., Hammerschmidt, K., Hölter, S.M., Blass, T., Somel, M., Brückner, M.K., Schreiweis, S., Winter, C., Sohr, R., Becker, L., Wiebe, V., Nickel, B., Giger, T., Müller, U., Groszer, M., Adler, T., Aguilar, A., Bolle, I., Calzada-Wack, J., Dalke, C., Ehrhardt, N., Favor, J., Fuchs, H., Gailus-Durner, V., Hans, W., Hölzlwimmer, G., Javaheri, A., Kalaydjiev, S., Kallnik, M., Kling, E., Kunder, S., Moßbrugger, I., Naton, B., Racz, I., Rathkolb, B., Rozman, J., Schrewe, A., Busch, D.H., Graw, J., Ivandic, B., Klingenspor, M., Klopstock, T., Ollert, M., Quintanilla-Martinez, L., Schulz, H., Wolf, E., Wurst, W, Zimmer, A, Fisher, S.E., Morgenstern, R., Arendt, T., Hrabé de Angelis, M, Fischer, J., Schwarz, J., Pääbo, S.: A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell 137, 2009, 961-967.
Fuchs, H., Gailus-Durner, V., Adler, T., Pimentel, J.A., Becker, L., Bolle, I., Brielmeier, M., Calzada-Wack, J., Dalke, C., Ehrhardt, N., Fasnacht, N., Ferwagner, B., Frischmann, U., Hans, W., Hölter, S.M., Hölzlwimmer, G., Horsch, M., Javaheri, A., Kallnik, M., Kling, E., Lengger, C., Maier, H., Mossbrugger, I., Mörth, C., Naton, B., Nöth, U., Pasche, B., Prehn, C., Przemeck, G., Puk, O., Racz, I., Rathkolb, B., Rozman, J., Schäble, K., Schreiner, R., Schrewe, A., Sina, C., Steinkamp, R., Thiele, F., Willershäuser, M., Zeh, R., Adamski, J., Busch, D.H., Beckers, J., Behrendt, H., Daniel, H., Esposito, I., Favor, J., Graw, J., Heldmaier, G., Höfler, H., Ivandic, B., Katus, H., Klingenspor, M., Klopstock, T., Lengeling, A., Mempel, M., Müller, W., Neschen, S., Ollert, M., Quintanilla-Martinez, L., Rosenstiel, P., Schmidt, J., Schreiber, S., Schughart, K., Schulz, H., Wolf, E., Wurst, W., Zimmer, A., Hrabé de Angelis, M.: The German Mouse Clinic: a platform for systemic phenotype analysis of mouse models. Curr. Pharm. Biotechnol. 10, 2009, 236-243.
Gailus-Durner, V., Fuchs, H., Adler, T., Aguilar Pimentel, A., Becker, L., Bolle, I., Calzada-Wack, J., Dalke, C., Ehrhardt, N., Ferwagner, B., Hans, W., Hölter, S.M., Hölzlwimmer, G., Horsch, M., Javaheri, A., Kallnik, M., Kling, E., Lengger, C., Mörth, C., Mossbrugger, I., Naton, B., Prehn, C., Puk, O., Rathkolb, B., Rozman, J., Schrewe, A., Thiele, F., Adamski, J., Aigner, B., Behrendt, H., Busch, D.H., Favor, J., Graw, J., Heldmaier, G., Ivandic, B., Katus, H., Klingenspor, M., Klopstock, T., Kremmer, E., Ollert, M., Quintanilla-Martinez, L., Schulz, H., Wolf, E., Wurst, W., Hrabé de Angelis, M.: Systemic first-line phenotyping. Methods Mol Biol. 530, 2009, 463-509.
Graw, J.: Mouse Models for Cataracts. J. Genet. 88, 2009, 469-486.
Graw, J., Schmidt, W., Minogue, P.J., Rodriguez, J., Tong, J.J., Klopp, N., Illig, T., Ebihara, L., Berthoud, V.M., Beyer, E.C.: The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation. Mol. Vis. 14, 2009, 1881-1885.
Puk, O., Dalke, C., Calzada-Wack, J., Ahmad, N., Klaften, M., Wagner, S., Hrabé de Angelis, M., Graw, J.: Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse. Invest. Ophthalmol. Vis. Sci. 50, 2009, 5653-5661.
Puk, O., Esposito, I., Söker, T., Löster, J., Budde, B., Nürnberg, P., Michel-Soewarto, D., Fuchs, H., Wolf, E., Hrabé de Angelis, M., Graw, J.: A new Fgf10 mutation in the mouse leads to atrophy of the Harderian gland and slit-eye phenotype in heterozygotes: A novel model for dry-eye disease? Invest. Ophthalmol. Vis. Sci. 50, 2009, 4311-4318.
2008
Söker, T., Dalke, C., Puk, O., Floss, T., Becker, L., Bolle, I., Favor, J., Hans, W., Hölter, S.M., Horsch, M., Kallnik, M., Kling, E., Mörth, C., Schrewe, A., Stigloher, C., Topp, S., Gailus-Durner, V., Naton, B., Beckers, J., Fuchs, H., Ivandic, B., Klopstock, T., Schulz, H., Wolf, E., Wurst, W., Bally-Cuif, L., Hrabé de Angelis, M., Graw, J.: Pleiotropic effects in Eya3 knockout mice. BMC Dev. Biol. 8, 2008, 118 (doi:10.1186/1471-213X-8-118).
Puk, O., Dalke, C., Hrabé de Angelis, M., Graw, J.: Variation of the response to the optokinetic drum among various strains of mice. Front. Biosci. 13, 2008, 6269-6275.
Hölter, S.M., Dalke, C., Kallnik, M., Becker, L., Horsch, M., Schrewe, A., Favor, J., Klopstock, T., Beckers, J., Ivandic, B., Gailus-Durner, V., Fuchs, H., Hrabé de Angelis, M., Graw, J., Wurst, W.: Sighted C3H” mice – a tool for analyzing the influence of vision on mouse behaviour? Front. Biosci. 13, 2008, 5810-5823.
Graw, J.: Cataract Genetics. In: Eye, Retina and Visual System of the Mouse. Eds.: Chalupa, L.M. and Williams, R.; MIT-Press, Cambridge, MD/USA, 2008, 493-504.
Schmidt, W., Klopp, N., Illig, T., Graw, J.: A novel GJA8 mutation causing a recessive triangular cataract. Mol. Vis. 14, 2008, 851-856.
Oliver Puk, Jana Löster, Claudia Dalke, Dian Soewarto, Helmut Fuchs, Birgit Budde, Peter Nürnberg, Eckhard Wolf, Martin Hrabé de Angelis, and Jochen Graw
Mutation in a Novel Connexin-like Gene (Gjf1) in the Mouse Affects Early Lens Development and Causes a Variable Small-Eye Phenotype. 2008 49: 1525-1532
Koustav Ganguly, Jack Favor, Angelika Neuhäuser-Klaus, Rodica Sandulache, Oliver Puk, Johannes Beckers, Marion Horsch, Sandra Schädler, Daniela Vogt Weisenhorn, Wolfgang Wurst, and Jochen Graw
Novel Allele of Crybb2 in the Mouse and Its Expression in the Brain. 2008 49: 1533-1541.
2007
Silke Pauli, Torben Söker, Norman Klopp, Thomas Illig, Wolfgang Engel, Jochen Graw: Mutation analysis in a German family identified a new cataractcausing allele in the CRYBB2 gene. Molecular Vision 2007; 13:962-7
2006
Berber, E., Fidanci, I.D., Ün, C., El-Maarri, O., Aktuglu, G., Gürgey, A., Celkan, T., Meral, A., Oldenburg, J., Graw, J., Akar, N., Caglayan, H.: Sequencing of the factor 8 (F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand’s disease type 2N. Haemophilia 12, 2006, 398-400.
Billingsley, G., Santhiya, S.T., Paterson, A.D., Ogata, K., Wodak, S., Hosseini, S.M., Manisastry, S.M., Vijayalakshmi, P., Gopinath, P.M., Graw, J., Héon, E.: CRYBA4, a novel human cataract gene, is also involved in microphthalmia. Am. J. Hum. Genet. 79, 2006, 702-709
Dalke, C., Puk, O., Neuhäuser-Klaus, A., Favor, J., Graw, J.: Eye Disorders. In: Standards of Mouse Model Phenotyping (Hrsg.: Hrabé de Angelis, M., Chambon, P., Brown, S.). Wiley-VCH, Weinheim, 2006, 283-309.
El-Maarri, O., Singer, H., Klein, C., Watzka, M., Herbiniaux, U., Brackmann, H.H., Schröder, J., Graw, J., Müller, C.R., Schramm, W., Schwaab, R., Haaf, T., Hanfland, P., Oldenburg, J.: Lack of F8 mRNA: a novel mechanism leading to hemophilia A. Blood 107, 2006, 2759-2765.
Graw, J., Klopp, N., Illig, T., Preising, M.N., Lorenz, B.: Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P. Graefe's Arch. Clin. Exp. Ophthalmol. 244, 2006, 912-919.
Pellegata, N.S., Quintanilla-Martinez, L., Siggelkow, H., Samson, E., Bink, K., Höfler, H., Graw, J., Atkinson, M.: Germline mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and man. Proc. Natl. Acad. Sci. USA 103, 2006, 15558-15563.
Puk, O., Dalke, C., Favor, J., Hrabé de Angelis, M., Graw, J.: Variations of eye size parameters among different strains of mice. Mamm. Genome 17, 2006, 851-857.
Santhiya, S.T., Söker, T., Klopp, N., Illig, T., Prakash, M.V.S., Selvaraj, B., Gopinath, P.M., Graw, J.: Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family. Mol. Vis. 12, 2006, 768-773.