Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome von Ü. Basmanav, F. Buket, Cau, Laura, Tafazzoli, Aylar, Méchin, Marie-Claire, Wolf, Sabrina, Romano, Maria Teresa, Valentin, Frederic, Wiegmann, Henning, Huchenq, Anne, Kandil, Rima, Garcia Bartels, Natalie, Kilic, Arzu, George, Susannah, Ralser, Damian J., Bergner, Stefan, Ferguson, David J.P., Oprisoreanu, Ana-Maria, Wehner, Maria, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Swan, Daniel, Houniet, Darren, Büchner, Aline, Weibel, Lisa, Wagner, Nicola, Grimalt, Ramon, Bygum, Anette, Serre, Guy, Blume-Peytavi, Ulrike, Sprecher, Eli, Schoch, Susanne, Oji, Vinzenz, Hamm, Henning, Farrant, Paul, Simon, Michel, Betz, Regina C.

Volltext

Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa von Ralser, Damian J, Basmanav, F Buket Ü, Tafazzoli, Aylar, Wititsuwannakul, Jade, Delker, Sarah, Danda, Sumita, Thiele, Holger, Wolf, Sabrina, Busch, Michélle, Pulimood, Susanne A, Altmüller, Janine, Nürnberg, Peter, Lacombe, Didier, Hillen, Uwe, Wenzel, Jörg, Frank, Jorge, Odermatt, Benjamin, Betz, Regina C

Volltext

Sequential growth factor delivery from complexed microspheres for bone tissue engineering von Buket Basmanav, F, Kose, Gamze T, Hasirci, Vasif

Volltext

Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2 von Schlaweck, Annika E, Tazi-Ahnini, Rachid, Ü Basmanav, F Buket, Mohungoo, Javed, Pasternack-Ziach, Sandra M, Mattheisen, Manuel, Oprisoreanu, Ana-Maria, Humbatova, Aytaj, Wolf, Sabrina, Messenger, Andrew, Betz, Regina C

Volltext

Pathogenicity of POFUT1 in Dowling-Degos Disease: Additional Mutations and Clinical Overlap with Reticulate Acropigmentation of Kitamura von Buket Basmanav, F., Fritz, Günter, Lestringant, Gilles G., Pachat, Divya, Hoffjan, Sabine, Fischer, Johannes, Wehner, Maria, Wolf, Sabrina, Thiele, Holger, Altmüller, Janine, Pulimood, Susanne A., Rütten, Arno, Kruse, Roland, Hanneken, Sandra, Frank, Jorge, Danda, Sumita, Bygum, Anette, Betz, Regina C.

Volltext

Intercellular transfer of plasmid DNA between in vitro cultured HEK293 cells following transient transfection von Gerdes, Christoph, Basmanav, F. Buket

Volltext

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia von Forstner, Andreas J., MD, Basmanav, F. Buket, MSc, Mattheisen, Manuel, MD, GROUP Investigators, MSc, Böhmer, Anne C., PhD, Hollegaard, Mads V., BAS, Janson, Esther, MSc, Strengman, Eric, MSc, Priebe, Lutz, MD, Degenhardt, Franziska, PhD, Hoffmann, Per, MSc, Herms, Stefan, MD, Maier, Wolfgang, MD, Mössner, Rainald, MD, Rujescu, Dan, PhD, Ophoff, Roel A., PhD, Moebus, Susanne, MD, DMSc, Mortensen, Preben B., MD, PhD, Børglum, Anders D., MD, DSc, Hougaard, David M., MSc, Frank, Josef, PhD, Witt, Stephanie H., MD, Rietschel, Marcella, PhD, Zimmer, Andreas, MD, Nöthen, Markus M., PhD, Miró, Xavier, PhD, Cichon, Sven

Volltext

First East Asian case of uncombable hair syndrome von Li, Ye, Xiong, Xing, Cesarato, Nicole, Wehner, Maria, Basmanav, F. Buket, Betz, Regina C.

Volltext

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients von Mühleisen, Thomas W, Basmanav, F. Buket, Forstner, Andreas J, Mattheisen, Manuel, Priebe, Lutz, Herms, Stefan, Breuer, Rene, Moebus, Susanne, Nenadic, Igor, Sauer, Heinrich, Mössner, Rainald, Maier, Wolfgang, Rujescu, Dan, Ludwig, Michael, Rietschel, Marcella, Nöthen, Markus M, Cichon, Sven

Volltext

Recent advances in the genetics of alopecia areata von Buket Basmanav, F., Betz, Regina C.

Volltext

A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family von Xiong, Xing, Uddin, Syed Ashraf, Munir, Sobia, Cesarato, Nicole, Thiele, Holger, Hassan, Noor, Kumar, Surjeet, Rehman, Fazal Ur, Naeem, Muhammad, Wali, Abdul, Basit, Sulman, Basmanav, F Buket, Ayub, Muhammad, Betz, Regina C

Volltext

Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2 von Fischer, Johannes, Degenhardt, Franziska, Hofmann, Andrea, Redler, Silke, Basmanav, F. Buket, Heilmann‐Heimbach, Stefanie, Hanneken, Sandra, Giehl, Kathrin A., Wolff, Hans, Moebus, Susanne, Kruse, Roland, Lutz, Gerhard, Blaumeiser, Bettina, Böhm, Markus, Garcia Bartels, Natalie, Blume‐Peytavi, Ulrike, Petukhova, Lynn, Christiano, Angela M., Nöthen, Markus M., Betz, Regina C.

Volltext

Investigation of the role of TCF4 rare sequence variants in schizophrenia von Basmanav, F. Buket, Forstner, Andreas J., Fier, Heide, Herms, Stefan, Meier, Sandra, Degenhardt, Franziska, Hoffmann, Per, Barth, Sandra, Fricker, Nadine, Strohmaier, Jana, Witt, Stephanie H., Ludwig, Michael, Schmael, Christine, Moebus, Susanne, Maier, Wolfgang, Mössner, Rainald, Rujescu, Dan, Rietschel, Marcella, Lange, Christoph, Nöthen, Markus M., Cichon, Sven

Volltext

Immunochip-Based Analysis: High-Density Genotyping of Immune-Related Loci Sheds Further Light on the Autoimmune Genetic Architecture of Alopecia Areata von Redler, Silke, Angisch, Marina, Heilmann, Stefanie, Wolf, Sabrina, Barth, Sandra, Basmanav, Buket F., Giehl, Kathrin A., Hanneken, Sandra, Eigelshoven, Sibylle, Mangold, Elisabeth, Kruse, Roland, Blaumeiser, Bettina, Böhm, Markus, Knapp, Michael, Garcia Bartels, Natalie, Lutz, Gerhard, Wolff, Hans, Blume-Peytavi, Ulrike, Nöthen, Markus M., Becker, Tim, Betz, Regina C.

Volltext

Erster ostasiatischer Fall des Syndroms der unkämmbaren Haare von Li, Ye, Xiong, Xing, Cesarato, Nicole, Wehner, Maria, Basmanav, F. Buket, Betz, Regina C.

Volltext

Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss von Cesarato, Nicole, Schwieger-Briel, Agnes, Gossmann, Yasmina, Henne, Sabrina K, Hillmann, Kathrin, Frommherz, Leonie H, Wehner, Maria, Xiong, Xing, Thiele, Holger, Oji, Vinzenz, Milani, Donatella, Tantcheva-Poor, Iliana, Giehl, Kathrin, Fölster-Holst, Regina, Teichler, Anne, Braeckmans, Delphine, Hoeger, Peter H, Jones, Gabriela, Frank, Jorge, Weibel, Lisa, Blume-Peytavi, Ulrike, Hamm, Henning, Nöthen, Markus M, Geyer, Matthias, Heilmann-Heimbach, Stefanie, Basmanav, F Buket, Betz, Regina C

Volltext

Mutations in three genes encoding proteins involved in hair shaft formation cause uncombable hair syndrome von Ü Basmanav, F Buket, Cau, Laura, Tafazzoli, Aylar, Büchner, Aline, Weibel, Lisa

Volltext

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene von Luo, X-j, Li, M, Huang, L, Steinberg, S, Mattheisen, M, Liang, G, Donohoe, G, Shi, Y, Chen, C, Yue, W, Alkelai, A, Lerer, B, Li, Z, Yi, Q, Rietschel, M, Cichon, S, Collier, D A, Tosato, S, Suvisaari, J, Rujescu, Dan, Golimbet, V, Silagadze, T, Durmishi, N, Milovancevic, M P, Stefansson, H, Schulze, T G, Nöthen, M M, Chen, C, Lyne, R, Morris, D W, Gill, M, Corvin, A, Zhang, D, Dong, Q, Moyzis, R K, Stefansson, K, Sigurdsson, E, Hu, F, Su, B, Gan, L

Volltext

First East Asian case of uncombable hair syndrome von Li, Ye, Xiong, Xing, Cesarato, Nicole, Wehner, Maria, Basmanav, F. Buket, Betz, Regina C.

Volltext

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe von Rietschel, M, Mattheisen, M, Degenhardt, F, Mühleisen, T W, Kirsch, P, Esslinger, C, Herms, S, Demontis, D, Steffens, M, Strohmaier, J, Haenisch, B, Breuer, R, Czerski, P M, Giegling, I, Strengman, E, Schmael, C, Mors, O, Mortensen, P B, Hougaard, D M, Ørntoft, T, Kapelski, P, Priebe, L, Basmanav, F B, Forstner, A J, Hoffmann, P, Meier, S, Nikitopoulos, J, Moebus, S, Alexander, M, Mössner, R, Wichmann, H-E, Schreiber, S, Rivandeneira, F, Hofman, A, Uitterlinden, A G, Wienker, T F, Schumacher, J, Hauser, J, Maier, W, Cantor, R M, Erk, S, Schulze, T G, Craddock, N, Owen, M J, O'Donovan, M C, Børglum, A D, Rujescu, D, Walter, H, Meyer-Lindenberg, A, Nöthen, M M, Ophoff, R A, Cichon, S

Volltext