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Publications 2008

Alef,T., Torres,S., Eckl,K.M., Kolberg,S., Hausser,I., Metze,D., Lestringant,G.G., and Hennies,H.C. (2008). Analysis of 3D skin models mimicking a syndrome of ichthyosis, follicular atrophoderma, and hypotrichosis. J Invest Dermatol. 128 Suppl., 759.

Aufenvenne,K., Oji,V., Walker,T., Hennies,H., Bruckner,P., and Trouper,H. (2008). Transglutamiase-1 and bathing suit ichthyosis: Molecular analysis of gene/environment interactions. J Invest Dermatol. 128 Suppl., 704.

Bergmann,C., Fliegauf,M., Brüchle,N.O., Frank,V., Olbrich,H., Kirschner,J., Schermer,B., Schmedding,I., Kispert,A., Kränzlin,B., Nürnberg,G., Becker,C., Grimm,T., Girschick,G., Lynch,S.A., Kelehan,P., Senderek,J., Neuhaus,T.J., Stallmach,T., Zentgraf,H., Nürnberg,P., Gretz,N., Lo,C., Lienkamp,S., Schäfer,T., Walz,G., Benzing,T., Zerres,K., and Omran,H. (2008). Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. Am J Hum Genet. 82, 959-970.

Boulouiz,R., Li,Y., Soualhine,H., Abidi,O., Chafik,A., Nürnberg,G., Becker,C., Nürnberg,P., Kubisch,C., Wollnik,B., and Barakat,A. (2008). A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family. Am J Med Genet A. 146A, 3086-3089.

Bruck,H., Schwerdtfeger,T., Leineweber,K., Toliat,M.R., Kribben,A., Philipp,T., and Brodde,O.E. (2008). Functional importance of alpha 2CDel-adrenoceptor polymorphism in Caucasians under conditions of increased and reduced sympathetic activity. J Hypertens. 26 Suppl., S129.

Budde,B.S., Namavar,Y., Barth,P.G., Poll-The,B., Nürnberg,G., Becker,C., van Ruissen,F., Weterman,M.A., Fluiter,K., te,B.E., Aronica,E., van der Knaap,M.S., Höhne,W., Toliat,M.R., Crow,Y.J., Steinling,M., Voit,T., Roelenso,F., Brussel,W., Brockmann,K., Kyllerman,M., Boltshauser,E., Hammersen,G., Willemsen,M., Basel-Vanagaite,L., Krägeloh-Mann,I., de Vries,L.S., Sztriha,L., Muntoni,F., Ferrie,C.D., Battini,R., Hennekam,R.C., Grillo,E., Beemer,F.A., Stoets,L.M., Wollnik,B., Wollnik,B., Nürnberg,P., Nürnberg,P., and Baas,F. (2008). tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nat Genet. 40, 1113-1118.

Douysset,G., Sander,T., Gouriou,J., and Nutbrown,R. (2008). Comparison of air kerma standards of LNE-LNHB and NPL for 192Ir HDR brachytherapy sources: EUROMET project no 814. Phys Med Biol. 53, N85-N97.

Ebermann,I., Elsayed,S.M., bdel-Ghaffar,T.Y., Nürnberg,G., Nürnberg,P., Elsobky,E., and Bolz,H.J. (2008). Double homozygosity for mutations of AGL and SCN9A mimicking neurohepatopathy syndrome. Neurology. 70, 2343-2344.

Eckl,K.M., Torres,S., Alef,T., and Hennies,H.C. (2008). 3D skin models and keratinisation disorders: who mimics whom? J Invest Dermatol. 128 Suppl., 737.

Eitel,I., Behrendt,F., Schindler,K., Kivelitz,D., Gutberlet,M., Schuler,G., and Thiele,H. (2008). Differential diagnosis of suspected apical ballooning syndrome using contrast-enhanced magnetic resonance imaging. Eur Heart J. 29, 2651-2659.

Everett,K., Chioza,B., Aicardi,J., Aschauer,H., Brouwer,O., Callenbach,P., Covanis,A., Dulac,O., Eeg-Olofsson,O., Feucht,M., Friis,M., Goutieres,F., Guerrini,R., Heils,A., Kjeldsen,M., Lehesjoki,A.E., Makoff,A., Nabbout,R., Olsson,I., Sander,T., Siren,A., McKeigue,P., Robinson,R., Taske,N., Rees,M., and Gardiner,M. (2008). Linkage and association analysis of CACNG3 in childhood absence epilepsy (vol 15, pg 463, 2007). Eur J Hum Genet. 16, 659-660.

Frank,V., den Hollander,A.I., Brüchle,N.O., Zonneveld,M.N., Nürnberg,G., Becker,C., Du Bois,G., Kendziorra,H., Roosing,S., Senderek,J., Nürnberg,P., Cremers,F.P., Zerres,K., and Bergmann,C. (2008). Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome. Hum Mutat. 29, 45-52.

Franke,A., Fischer,A., Till,A., Lu,T.T., Becker,C., Muller-Quernheim,J., Wittig,M., Herrmann,A., Balschun,T.C., Hofmann,S., Nurnberg,P., Hampe,J., Krawczak,M., Schurmann,M., Rosenstiel,P.C., Nebel,A., and Schreiber,S. (2008). A combined analysis of genome-wide scans for sarcoidosis and Crohn disease identifies a common susceptibility locus. Gastroenterology. 134 Suppl., A522.

Franke,A., Fischer,A., Nothnagel,M., Becker,C., Grabe,N., Till,A., Lu,T., Müller-Quernheim,J., Wittig,M., Hermann,A., Balschun,T., Hofmann,S., Niemiec,R., Schulz,S., Hampe,J., Nikolaus,S., Nürnberg,P., Krawczak,M., Schürmann,M., Rosenstiel,P., Nebel,A., and Schreiber,S. (2008). Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. Gastroenterology. 135, 1207-1215.

Frommolt,P., Thomas,R.K., and Thomas,R.K. (2008). Standardized high-throughput evaluation of cell-based compound screens. BMC Bioinformatics. 9, 475.

Fürst,R., Bubik,M.F., Bihari,P., Mayer,B.A., Khandoga,A.G., Hoffmann,F., Rehberg,M., Krombach,F., Zahler,S., and Vollmar,A.M. (2008). Atrial natriuretic peptide protects against histamine-induced endothelial barrier dysfunction in vivo. Mol Pharmacol. 74, 1-8.

Fürst,R., Zahler,S., and Vollmar,A.M. (2008). Dexamethasone-induced expression of endothelial mitogen-activated protein kinase phosphatase-1 involves activation of the transcription factors activator protein-1 and 3',5'-cyclic adenosine 5'-monophosphate response element-binding protein and the genera. Endocrinology. 149, 3635-3642.

Geier,C., Gehmlich,K., Ehler,E., Hassfeld,S., Perrot,A., Hayess,K., Cardim,N., Wenzel,K., Erdmann,B., Krackhardt,F., Posch,M.G., Osterziel,K.J., Bublak,A., Naegele,H., Scheffold,T., Dietz,R., Chien,K.R., Spuler,S., Furst,D.O., Nurnberg,P., and Ozcelik,C. (2008). Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy (vol 17, pg 2753, 2008). Hum Mol Genet. 17, 3436.

Geier,C., Gehmlich,K., Ehler,E., Hassfeld,S., Perrot,A., Hayess,K., Cardim,N., Wenzel,K., Erdmann,B., Krackhardt,F., Posch,M.G., Osterziel,K.J., Bublak,A., Nägele,H., Scheffold,T., Dietz,R., Chien,K.R., Spuler,S., Fürst,D.O., Nürnberg,P., and Ozcelik,C. (2008). Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy. Hum Mol Genet. 17, 2753-2765.

Haenssle,H.A., Finkenrath,A., Hausser,I., Oji,V., Traupe,H., Hennies,H.C., Neumann,C., and Emmert,S. (2008). Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosis. Clin Exp Dermatol. 33, 578-581.

Hennies,H.C., Kornak,U., Zhang,H., Egerer,J., Zhang,X., Seifert,W., Kühnisch,J., Budde,B., Nätebus,M., Brancati,F., Wilcox,W.R., Müller,D., Kaplan,P.B., Rajab,A., Zampino,G., Fodale,V., Dallapiccola,B., Newman,W., Metcalfe,K., Clayton-Smith,J., Tassabehji,M., Steinmann,B., Barr,F.A., Nürnberg,P., Nürnberg,P., Nürnberg,P., Wieacker,P., and Mundlos,S. (2008). Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. Nat Genet. 40, 1410-1412.

Hennies,H.C., Kurtenbach,J., Natebus,M., de Juane,S., Traupe,H., Preil,M.L., Kieg,P., Sprecher,E., and Eckl,K.M. (2008). Inactivating mutations in autosomal recessive congenital ichthyosis: extended allelic heterogeneity for mutations in ALOX12B and recurrent mutations in ALOXE3. J Invest Dermatol. 128 Suppl., 758.

Hiernaut,J.P., Wiss,T., Colle,J.Y., Thiele,H., Walker,C.T., Goll,W., and Konings,R.J.M. (2008). Fission product release and microstructure changes during laboratory annealing of a very high burn-up fuel specimen. J NUCL MATER. 377, 313-324.

Hillmer,A.M., Flaquer,A., Hanneken,S., Eigelshoven,S., Kortüm,A.K., Brockschmidt,F.F., Golla,A., Metzen,C., Thiele,H., Kolberg,S., Reinartz,R., Betz,R.C., Ruzicka,T., Hennies,H.C., Hennies,H.C., Kruse,R., and Nöthen,M.M. (2008). Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26. Am J Hum Genet. 82, 737-743.

Huyghe,J.R., Van Laer,L., Hendrickx,J.J., Fransen,E., Demeester,K., Topsakal,V., Kunst,S., Manninen,M., Jensen,M., Bonaconsa,A., Mazzoli,M., Baur,M., Hannula,S., Mäki-Torkko,E., Espeso,A., Van Eyken,E., Flaquer,A., Becker,C., Stephens,D., Sorri,M., Orzan,E., Bille,M., Parving,A., Pyykkö,I., Cremers,C.W., Kremer,H., Van de Heyning,P.H., Wienker,T.F., Nürnberg,P., Nürnberg,P., Pfister,M., and Van Camp,G. (2008). Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. Am J Hum Genet. 83, 401-407.

Janke,D., Mehralivand,S., Strand,D., Gödtel-Armbrust,U., Habermeier,A., Gradhand,U., Fischer,C., Toliat,M.R., Fritz,P., Zanger,U.M., Schwab,M., Fromm,M.F., Nürnberg,P., Wojnowski,L., Closs,E.I., and Lang,T. (2008). 6-mercaptopurine and 9-(2-phosphonyl-methoxyethyl) adenine (PMEA) transport altered by two missense mutations in the drug transporter gene ABCC4. Hum Mutat. 29, 659-669.

Kayser,M., Lao,O., Saar,K., Brauer,S., Wang,X., Nürnberg,P., Trent,R.J., and Stoneking,M. (2008). Genome-wide analysis indicates more Asian than Melanesian ancestry of Polynesians. Am J Hum Genet. 82, 194-198.

Kloeckener-Gruissem,B., Vandekerckhove,K., Nürnberg,G., Neidhardt,J., Zeitz,C., Nürnberg,P., Schipper,I., and Berger,W. (2008). Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria. Am J Hum Genet. 82, 772-779.

Kocher,M., Frommolt,P., Frommolt,P., Borberg,S.K., Rühl,U., Steingräber,M., Niewald,M., Staar,S., Stuschke,M., Becker,G., Fischedick,A.R., Herfarth,K., Grauthoff,H., and Müller,R.P. (2008). Randomized Study of Postoperative Radiotherapy and Simultaneous Temozolomide without Adjuvant Chemotherapy for Glioblastoma. Strahlenther Onkol. 184, 572-579.

Kornak,U., Reynders,E., Dimopoulou,A., van Reeuwijk,J., Fischer,B., Rajab,A., Budde,B., Nürnberg,P., Foulquier,F., ARCL Debré-type Study Group, Lefeber,D., Urban,Z., Gruenewald,S., Annaert,W., Brunner,H.G., van Bokhoven,H., Wevers,R., Morava,E., Matthijs,G., Van Maldergem,L., and Mundlos,S. (2008). Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2. Nat Genet. 40, 32-34.

Kuhl,A., Melberg,A., Meinl,E., Nürnberg,G., Nürnberg,P., Kehrer-Sawatzki,H., and Jenne,D.E. (2008). Myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7: corroboration and narrowing of the critical region on 10q22.3. Eur J Hum Genet. 16, 367-373.

Lang,U.E., Bajbouj,M., Sander,T., and Gallinat,J. (2008). Gender-dependent association of the functional catechol-o-methyltransferase Val158Met genotype with sensation seeking personality trait (vol 32, pg 1950, 2007). Neuropsychopharmacology. 33, 1216.

Lang,U.E., Hellweg,R., Bajbouj,M., Gaus,V., Sander,T., and Gallinat,J. (2008). Gender-dependent association of a functional NGF polymorphism with anxiety-related personality traits. Pharmacopsychiatry. 41, 196-199.

Lao,O., Lu,T.T., Nothnagel,M., Junge,O., Freitag-Wolf,S., Caliebe,A., Balascakova,M., Bertranpetit,J., Bindoff,L.A., Comas,D., Holmlund,G., Kouvatsi,A., Macek,M., Mollet,I., Parson,W., Palo,J., Ploski,R., Sajantila,A., Tagliabracci,A., Gether,U., Werge,T., Rivadeneira,F., Hofman,A., Uitterlinden,A.G., Gieger,C., Wichmann,H.E., Rüther,A., Schreiber,S., Becker,C., Nürnberg,P., Nelson,M.R., Krawczak,M., and Kayser,M. (2008). Correlation between genetic and geographic structure in Europe. Curr Biol. 18, 1241-1248.

Lembcke,A., Thiele,H., Lachnitt,A., Enzweiler,C.N., Wagner,M., Hein,P.A., Eddicks,S., and Kivelitz,D.E. (2008). Precision of forty slice spiral computed tomography for quantifying aortic valve stenosis: comparison with echocardiography and validation against cardiac catheterization. Invest Radiol. 43, 719-728.

Lohoff,F.W., Lautenschlager,M., Mohr,J., Ferraro,T.N., Sander,T., and Gallinat,J. (2008). Association between variation in the vesicular monoamine transporter 1 gene on chromosome 8p and anxiety-related personality traits. Neurosci Lett. 434, 41-45.

Lugassy,J., Hennies,H.C., Indelman,M., Khamaysi,Z., Bergman,R., and Sprecher,E. (2008). Rapid detection of homozygous mutations in congenital recessive ichthyosis. Arch Dermatol Res. 300, 81-85.

Machner,B., Sprenger,A., Kompf,D., Sander,T., Heide,W., and Kimmig,H. (2008). Virtual model of homonymous hemianopia reveals visual search disorders in patients with unilateral occipital stroke. J Neurol. 255 Suppl., 747.

Machner,B., Neppert,B., Paulsen,M., Hofmann,C., Sander,T., and Helmchen,C. (2008). Pseudotumour cerebri as a reversible side-effect of all-trans retinoic acid treatment in acute promyelocytic leukaemia. J Neurol. 255 Suppl., 862.

Machner,B., Neppert,B., Paulsen,M., Hofmann,C., Sander,T., and Helmchen,C. (2008). Pseudotumor cerebri as a reversible side effect of all-trans retinoic acid treatment in acute promyelocytic leukaemia. Eur J Neurol. 15, e68-e69.

Mackert,B.M., Leistner,S., Sander,T., Liebert,A., Wabnitz,H., Burghoff,M., Trahms,L., Macdonald,R., and Curio,G. (2008). Dynamics of cortical neurovascular coupling analyzed by simultaneous DC-magnetoencephalography and time-resolved near-infrared spectroscopy. Neuroimage. 39, 979-986.

Märschenz,S., Brinckmann,A., Nürnberg,P., Krüger,D.H., Günther,S., and Meisel,H. (2008). Co-replication analyses of naturally occurring defective hepatitis B virus variants with wild-type. Virology. 372, 247-259.

Mezger,M., Steffens,M., Semmler,C., Arlt,E.M., Zimmer,M., Kristjanson,G.I., Wienker,T.F., Toliat,M.R., Kessler,T., Einsele,H., and Loeffler,J. (2008). Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation. Clin Microbiol Infect. 14, 228-234.

Mezger,M., Steffens,M., Beyer,M., Manger,C., Eberle,J., Toliat,M.R., Wienker,T.F., Ljungman,P., Hebart,H., Dornbusch,H.J., Einsele,H., and Loeffler,J. (2008). Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cells. Blood. 111, 534-536.

Mohr,C., Leyendecker,S., Mangels,I., Machner,B., Sander,T., and Helmchen,C. (2008). Central representation of cold-evoked pain relief in capsaicin induced pain: an event-related fMRI study. Pain. 139, 416-430.

Möller,I., Michel,K., Frech,N., Burger,M., Pfeifer,D., Frommolt,P., Veelken,H., and Thomas-Kaskel,A.K. (2008). Dendritic cell maturation with poly(I:C)-based versus PGE2-based cytokine combinations results in differential functional characteristics relevant to clinical application. J Immunother. 31, 506-519.

Muller,C., Schmidt,E., Traupe,H., Hansser,I., Hennies,H.C., Oji,V., Brocker,E.B., and Hamm,H. (2008). Severe transglutaminase-1-negative lamellar ichthyosis in a 9-year-old boy. J Invest Dermatol. 128, 3.

Müller-Ehmsen,J., Braun,D., Schneider,T., Pfister,R., Worm,N., Wielckens,K., Scheid,C., Frommolt,P., Frommolt,P., and Flesch,M. (2008). Decreased number of circulating progenitor cells in obesity: beneficial effects of weight reduction. Eur Heart J. 29, 1560-1568.

Nagel,I.E., Chicherio,C., Li,S.C., von Oertzen,T., Sander,T., Villringer,A., Heekeren,H.R., Bäckman,L., and Lindenberger,U. (2008). Human aging magnifies genetic effects on executive functioning and working memory. Front Hum Neurosci. 2, 1.

Neidhardt,J., Glaus,E., Lorenz,B., Netzer,C., Li,Y., Schambeck,M., Wittmer,M., Feil,S., Kirschner-Schwabe,R., Rosenberg,T., Cremers,F.P., Bergen,A.A., Barthelmes,D., Baraki,H., Schmid,F., Tanner,G., Fleischhauer,J., Orth,U., Becker,C., Wegscheider,E., Nürnberg,G., Nürnberg,P., Bolz,H.J., Gal,A., and Berger,W. (2008). Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing. Mol Vis. 14, 1081-1093.

Neubauer,B.A., Waldegger,S., Heinzinger,J., Hahn,A., Kurlemann,G., Fiedler,B., Eberhard,F., Muhle,H., Stephani,U., Garkisch,S., Eeg-Olofsson,O., Müller,U., and Sander,T. (2008). KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes. Neurology. 71, 177-183.

Noll,L., Peterson,F.C., Hayes,P.L., Volkman,B.F., and Sander,T. (2008). Heterodimer formation of the myeloid zinc finger 1 SCAN domain and association with promyelocytic leukemia nuclear bodies. Leuk Res. 32, 1582-1592.

Nürnberg,G., Jacobi,F.K., Broghammer,M., Becker,C., Blin,N., Nürnberg,P., Stephani,U., and Pusch,C.M. (2008). Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping. Int J Mol Med. 21, 429-438.

Opgen-Rhein,C., Neuhaus,A.H., Urbanek,C., Hahn,E., Sander,T., and Dettling,M. (2008). Executive attention in schizophrenic males and the impact of COMT Val108/158Met genotype on performance on the attention network test. Schizophr Bull. 34, 1231-1239.

Pasternack,S.M., von Kügelgen,I., Aboud,K.A., Lee,Y.A., Rüschendorf,F., Voss,K., Hillmer,A.M., Molderings,G.J., Franz,T., Ramirez,A., Nürnberg,P., Nöthen,M.M., and Betz,R.C. (2008). G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. Nat Genet. 40, 329-334.

Peterson,D.B., Sander,T., Kaul,S., Wakim,B.T., Halligan,B., Twigger,S., Pritchard,K.A., Oldham,K.T., and Ou,J.S. (2008). Comparative proteomic analysis of PAI-1 and TNF-alpha-derived endothelial microparticles. Proteomics. 8, 2430-2446.

Puk,O., Löster,J., Dalke,C., Soewarto,D., Fuchs,H., Budde,B., Nürnberg,P., Wolf,E., de Angelis,M.H., and Graw,J. (2008). Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype. Invest Ophthalmol Vis Sci. 49, 1525-1532.

Qureischie,H., Heun,R., Lütjohann,D., Popp,J., Jessen,F., Ledschbor-Frahnert,C., Thiele,H., Maier,W., Hentschel,F., Kelemen,P., and Kölsch,H. (2008). CETP polymorphisms influence cholesterol metabolism but not Alzheimer's disease risk. Brain Res. 1232, 1-6.

Racz,I., Schürmann,B., Karpushova,A., Reuter,M., Cichon,S., Montag,C., Fürst,R., Schütz,C., Franke,P.E., Strohmaier,J., Wienker,T.F., Terenius,L., Osby,U., Gunnar,A., Maier,W., Bilkei-Gorzó,A., Nöthen,M., and Zimmer,A. (2008). The opioid peptides enkephalin and beta-endorphin in alcohol dependence. Biol Psychiatry. 64, 989-997.

Rajab,A., Kornak,U., Budde,B.S., Hoffmann,K., Jaeken,J., Nürnberg,P., and Mundlos,S. (2008). Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman. Am J Med Genet A. 146A, 965-976.

Rutsch,F., Crisponi,L., Meloni,A., Toliat,M.R., Nurnberg,G., Hohne,W., Nurnberg,P., and Crisponi,G. (2008). Mutations in CRLF1 cause Crisponi syndrome and cold-induced sweating. Eur J Pediatr. 167, 373.

Sander,T., Sprenger,A., Machner,B., Rambold,H., and Helmchen,C. (2008). Disjunctive saccades during smooth pursuit eye movements in ocular myasthenia gravis. J Neurol. 255, 1094-1096.

Sanggaard,K.M., Kjaer,K.W., Eiberg,H., Nürnberg,G., Nürnberg,P., Hoffman,K., Jensen,H., Sørum,C., Rendtorff,N.D., and Tranebjaerg,L. (2008). A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family. Am J Med Genet A. 146A, 1017-1025.

Sauermann,U., Stahl-Hennig,C., Altmuller,J., Nurnberg,P., Fritzer,E., Krawczak,M., Siddiqui,R., and Platzer,M. (2008). Chromosomal regions determine disease progression in simian immunodeficiency virus (SIV)-infected rhesus macaques: results from a genome wide screening study. Tissue Antigens. 71, O28.

Sauermann,U., Siddiqui,R., Suh,Y.S., Platzer,M., Leuchte,N., Meyer,H., Mätz-Rensing,K., Stoiber,H., Nürnberg,P., Hunsmann,G., Stahl-Hennig,C., and Krawczak,M. (2008). Mhc class I haplotypes associated with survival time in simian immunodeficiency virus (SIV)-infected rhesus macaques. Genes Immun. 9, 69-80.

Schmack,K., Schlagenhauf,F., Sterzer,P., Wrase,J., Beck,A., Dembler,T., Kalus,P., Puls,I., Sander,T., Heinz,A., and Gallinat,J. (2008). Catechol-O-methyltransferase val158met genotype influences neural processing of reward anticipation. Neuroimage. 42, 1631-1638.

Stuhrmann,M., Hennies,H.C., Bukhari,I.A., Brakensiek,K., Nürnberg,G., Nürnberg,G., Becker,C., Huebener,J., Miranda,M.C., Frye-Boukhriss,H., Knothe,S., Schmidtke,J., and El-Harith,E.H. (2008). Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23. Clin Genet. 73, 566-572.

Tang,B., Sander,T., Craven,K.B., Hempelmann,A., and Escayg,A. (2008). Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy. Neurobiol Dis. 29, 59-70.

Thiele,H., Schindler,K., Friedenberger,J., Eitel,I., Fürnau,G., Grebe,E., Erbs,S., Linke,A., Möbius-Winkler,S., Kivelitz,D., and Schuler,G. (2008). Intracoronary compared with intravenous bolus abciximab application in patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention: the randomized Leipzig immediate percutaneous coronary intervention abciximab IV. Circulation. 118, 49-57.

Tossios,P., Krausgrill,B., Schmidt,M., Fischer,T., Halbach,M., Fries,J.W., Fahnenstich,S., Frommolt,P., Frommolt,P., Heppelmann,I., Schmidt,A., Schomäcker,K., Fischer,J.H., Bloch,W., Mehlhorn,U., Schwinger,R.H., and Müller-Ehmsen,J. (2008). Role of balloon occlusion for mononuclear bone marrow cell deposition after intracoronary injection in pigs with reperfused myocardial infarction. Eur Heart J. 29, 1911-1921.

von Korff,M., Freyss,J., and Sander,T. (2008). Flexophore, a new versatile 3D pharmacophore descriptor that considers molecular flexibility. J Chem Inf Model. 48, 797-810.

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