Associations between the oxytocin receptor gene ( OXTR) and affect, loneliness and intelligence in normal subjects von Lucht, Michael J., Barnow, Sven, Sonnenfeld, Christine, Rosenberger, Albert, Grabe, Hans Joergen, Schroeder, Winnie, Völzke, Henry, Freyberger, Harald J., Herrmann, Falko H., Kroemer, Heyo, Rosskopf, Dieter

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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency von Mariani, Guglielmo, Herrmann, Falko H., Dolce, Alberto, Batorova, Angelika, Etro, Daniela, Peyvandi, Flora, Wulff, Karin, Schved, Jean F., Auerswald, Günter, Ingerslev, Jorgen, Bernardi, Francesco

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Twenty two novel mutations of the factor VII gene in factor VII deficiency von Wulff, Karin, Herrmann, Falko H.

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Decrease of carotid intima-media thickness in patients at risk to cerebral ischemia after supplementation with folic acid, Vitamins B6 and B12 von Till, Uwe, Röhl, Peter, Jentsch, Almut, Till, Heiko, Müller, Andreas, Bellstedt, Klaus, Plonné, Dietmar, Fink, Horst S., Vollandt, Rüdiger, Sliwka, Ulrich, Herrmann, Falko H., Petermann, Henning, Riezler, Reiner

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Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly von Akram Al-Hilali, Karin Wulff, Hikmat Abdel-Razeq, Khalida Abu Saud, Fateh Al-Gaili, Falko H. Herrmann

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Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V von Herrmann, Falko H, Wulff, Karin, Strey, Rüdiger, Siegemund, Annelie, Astermark, Jan, Schulman, Sam

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Haemophilia A in a female caused by coincidence of a Swyer syndrome and a missense mutation in factor VIII gene von Loreth, Ralph M., El-Maarri, Osman, Schröder, Jörg, Budde, Ulrich, Herrmann, Falko H., Oldenburg, Johannes

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Factor V Leiden and the risk of stillbirth in a German population von Völzke, Henry, Grimm, Rita, Robinson, Daniel M., Robinson, Constanze, Kohlmann, Thomas, Schuster, Gudrun, Alte, Dietrich, Herrmann, Falko H., John, Ulrich

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Alcohol Consumption Is Associated with an Interaction between DRD2 Exon 8 A/A Genotype and Self-Directedness in Males von Lucht, Michael, Barnow, Sven, Schroeder, Winnie, Grabe, Hans Joergen, Rosskopf, Dieter, Brummer, Christian, John, Ulrich, Freyberger, Harald J., Herrmann, Falko H.

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Homozygous Factor X gene mutations Gly380Arg and Tyr163delAT are associated with perinatal intracranial hemorrhage von Herrmann, Falko H., Navarette, Marta, Salazar-Sanchez, Lizbeth, Carillo, Juan M., Auerswald, Guenter, Wulff, Karin

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Elemental Composition of Natural Nanoparticles and Fine Colloids in European Forest Stream Waters and Their Role as Phosphorus Carriers von Gottselig, N., Amelung, W., Kirchner, J. W., Bol, R., Eugster, W., Granger, S. J., Hernández‐Crespo, C., Herrmann, F., Keizer, J. J., Korkiakoski, M., Laudon, H., Lehner, I., Löfgren, S., Lohila, A., Macleod, C. J. A., Mölder, M., Müller, C., Nasta, P., Nischwitz, V., Paul‐Limoges, E., Pierret, M. C., Pilegaard, K., Romano, N., Sebastià, M. T., Stähli, M., Voltz, M., Vereecken, H., Siemens, J., Klumpp, E.

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The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patients von Salazar-Sánchez, Lizbeth, Leon, Maria Paz, Cartin, Mayra, Schuster, Gudrun, Wulff, Karin, Schröder, Winnie, Jiménez-Arce, Gerardo, Chacon, Ronald, Herrmann, Falko H.

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Negative perceived paternal parenting is associated with dopamine D2 receptor exon 8 and GABA(A) alpha 6 receptor variants: An explorative study von Lucht, Michael, Barnow, Sven, Schroeder, Winnie, Grabe, Hans Joergen, Finckh, Ulrich, John, Ulrich, Freyberger, Harald J., Herrmann, Falko H.

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Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa Rica von Salazar-Sánchez, Lizbeth, Chaves, Lilliana, Cartin, Mayra, Schuster, Gudrun, Wulff, Karin, Schröder, Winnie, Herrmann, Falko H

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Interaction between factor V Leiden and serum LDL cholesterol increases the risk of atherosclerosis von Völzke, Henry, Wolff, Birger, Grimm, Rita, Robinson, Daniel M., Schuster, Gudrun, Herrmann, Falko H., Motz, Wolfgang, Rettig, Rainer

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Factor V Leiden, Prothrombin Gene G20210A Variant, and Methylenetetrahydrofolate Reductase C677T Genotype in Young Adults With Ischemic Stroke von Lopaciuk, Stanislaw, Bykowska, Ksenia, Kwiecinski, Hubert, Mickielewicz, Anatol, Czlcankawska, Anna, Mendel, Tadeusz, Kuczynska-Zardzewialy, Arletta, Szelagowska, Dorota, Windyga, Jerzy, Schröder, Winnie, Herrmann, Falko H., Jedrzejowska, Hanna

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Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data von Ivaskevicius, Vytautas, Jurgutis, Romualdas, Rost, Simone, Müller, Alexandra, Schmitt, Christoph, Wulff, Karin, Herrmann, Falko H., Müller, Clemens R., Schwaab, Rainer, Oldenburg, Johannes

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The Gly331Ser mutation in factor VII in Europe and the Middle East von Etro, Daniela, Pinotti, Mirko, Wulff, Karin, Marchetti, Giovanna, Rocino, Angiola, Herrmann, Falko H, Bernardi, Francesco

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Das Hämoglobin des Menschen: Struktur, Funktion, Genetik von Herrmann, Falko H

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Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene von HERRMANN, F. H., WULFF, K., AUERSWALD, G., SCHULMAN, S., ASTERMARK, J., BATOROVA, A., KREUZ, W., POLLMANN, H., RUIZ-SAEZ, A., DE BOSCH, N., SALAZAR-SANCHEZ, L.

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