Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature
JAMRA, Rami Abou, PHILIPPE, Orianne, MUNNICH, Arnold, STROM, Tim M, REIS, Andre, COLLEAUX, Laurence, RAAS-ROTHSCHILD, Annick, ECK, Sebastian H, GRAF, Elisabeth, BUCHERT, Rebecca, BORCK, Guntram, EKICI, Arif, BROCKSCHMIDT, Felix F, NÖTHEN, Markus M
Published in American journal of human genetics (10.06.2011)
Published in American journal of human genetics (10.06.2011)
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Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
Hillmer, Axel M., Hanneken, Sandra, Ritzmann, Sibylle, Becker, Tim, Freudenberg, Jan, Brockschmidt, Felix F., Flaquer, Antonia, Freudenberg-Hua, Yun, Jamra, Rami Abou, Metzen, Christine, Heyn, Uwe, Schweiger, Nadine, Betz, Regina C., Blaumeiser, Bettina, Hampe, Jochen, Schreiber, Stefan, Schulze, Thomas G., Hennies, Hans Christian, Schumacher, Johannes, Propping, Peter, Ruzicka, Thomas, Cichon, Sven, Wienker, Thomas F., Kruse, Roland, Nöthen, Markus M.
Published in American journal of human genetics (01.07.2005)
Published in American journal of human genetics (01.07.2005)
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Journal Article
Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology
Heilmann, Stefanie, Kiefer, Amy K., Fricker, Nadine, Drichel, Dmitriy, Hillmer, Axel M., Herold, Christine, Tung, Joyce Y., Eriksson, Nicholas, Redler, Silke, Betz, Regina C., Li, Rui, Kárason, Ari, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Dedoussis, George, Martin, Nicholas G., Kiemeney, Lambertus A., Mooser, Vincent, Stefansson, Kari, Brent Richards, J., Becker, Tim, Brockschmidt, Felix F., Hinds, David A., Nöthen, Markus M.
Published in Journal of investigative dermatology (01.06.2013)
Published in Journal of investigative dermatology (01.06.2013)
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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children
ROESKE, D, LUDWIG, K. U, MÜLLER-MYHSOK, B, NÖTHEN, M. M, SCHULTE-KÖRNE, G, NEUHOFF, N, BECKER, J, BARTLING, J, BRUDER, J, BROCKSCHMIDT, F. F, WARNKE, A, REMSCHMIDT, H, HOFFMANN, P
Published in Molecular psychiatry (01.01.2011)
Published in Molecular psychiatry (01.01.2011)
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Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
Redler, S., Brockschmidt, F.F., Tazi-Ahnini, R., Drichel, D., Birch, M.P., Dobson, K., Giehl, K.A., Herms, S., Refke, M., Kluck, N., Kruse, R., Lutz, G., Wolff, H., Böhm, M., Becker, T., Nöthen, M.M., Messenger, A.G., Betz, R.C.
Published in British journal of dermatology (1951) (01.06.2012)
Published in British journal of dermatology (1951) (01.06.2012)
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Evidence for a polygenic contribution to androgenetic alopecia
Heilmann, S., Brockschmidt, F.F., Hillmer, A.M., Hanneken, S., Eigelshoven, S., Ludwig, K.U., Herold, C., Mangold, E., Becker, T., Kruse, R., Knapp, M., Nöthen, M.M.
Published in British journal of dermatology (1951) (01.10.2013)
Published in British journal of dermatology (1951) (01.10.2013)
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Journal Article
Investigation of selected cytokine genes suggests that IL2RA and the TNF/LTA locus are risk factors for severe alopecia areata
Redler, S., Albert, F., Brockschmidt, F.F., Herold, C., Hanneken, S., Eigelshoven, S., Giehl, K.A., Kruse, R., Lutz, G., Wolff, H., Blaumeiser, B., Böhm, M., Becker, T., Nöthen, M.M., Betz, R.C.
Published in British journal of dermatology (1951) (01.12.2012)
Published in British journal of dermatology (1951) (01.12.2012)
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Journal Article
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
Brockschmidt, F.F., Heilmann, S., Ellis, J.A., Eigelshoven, S., Hanneken, S., Herold, C., Moebus, S., Alblas, M.A., Lippke, B., Kluck, N., Priebe, L., Degenhardt, F.A., Jamra, R.A., Meesters, C., Jöckel, K.-H., Erbel, R., Harrap, S., Schumacher, J., Fröhlich, H., Kruse, R., Hillmer, A.M., Becker, T., Nöthen, M.M.
Published in British journal of dermatology (1951) (01.12.2011)
Published in British journal of dermatology (1951) (01.12.2011)
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Journal Article
Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti
Debrah, Linda Batsa, Albers, Anna, Debrah, Alexander Yaw, Brockschmidt, Felix F, Becker, Tim, Herold, Christine, Hofmann, Andrea, Osei-Mensah, Jubin, Mubarik, Yusif, Fröhlich, Holger, Hoerauf, Achim, Pfarr, Kenneth
Published in Human genomics (09.11.2017)
Published in Human genomics (09.11.2017)
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Journal Article
Fine mapping of the human AR/EDA2R locus in androgenetic alopecia
Brockschmidt, F.F., Hillmer, A.M., Eigelshoven, S., Hanneken, S., Heilmann, S., Barth, S., Herold, C., Becker, T., Kruse, R., Nöthen, M.M.
Published in British journal of dermatology (1951) (01.04.2010)
Published in British journal of dermatology (1951) (01.04.2010)
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Journal Article
No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
Heilmann, S., Nyholt, D.R., Brockschmidt, F.F., Hillmer, A.M., Herold, C., Becker, T., Martin, N.G., Nöthen, M.M.
Published in British journal of dermatology (1951) (01.07.2013)
Published in British journal of dermatology (1951) (01.07.2013)
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Journal Article
Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
Hillmer, Axel M., Flaquer, Antonia, Hanneken, Sandra, Eigelshoven, Sibylle, Kortüm, Anne-Katrin, Brockschmidt, Felix F., Golla, Astrid, Metzen, Christine, Thiele, Holger, Kolberg, Susanne, Reinartz, Roman, Betz, Regina C., Ruzicka, Thomas, Hennies, Hans Christian, Kruse, Roland, Nöthen, Markus M.
Published in American journal of human genetics (01.03.2008)
Published in American journal of human genetics (01.03.2008)
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Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples
Le Hellard, S, Mühleisen, T W, Djurovic, S, Fernø, J, Ouriaghi, Z, Mattheisen, M, Vasilescu, C, Raeder, M B, Hansen, T, Strohmaier, J, Georgi, A, Brockschmidt, F F, Melle, I, Nenadic, I, Sauer, H, Rietschel, M, Nöthen, M M, Werge, T, Andreassen, O A, Cichon, S, Steen, V M
Published in Molecular psychiatry (01.05.2010)
Published in Molecular psychiatry (01.05.2010)
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Journal Article
The TRAF1/C5 locus confers risk for familial and severe alopecia areata
Redler, S., Brockschmidt, F.F., Forstbauer, L., Giehl, K.A., Herold, C., Eigelshoven, S., Hanneken, S., De Weert, J., Lutz, G., Wolff, H., Kruse, R., Blaumeiser, B., Böhm, M., Becker, T., Nöthen, M.M., Betz, R.C.
Published in British journal of dermatology (1951) (01.04.2010)
Published in British journal of dermatology (1951) (01.04.2010)
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Journal Article
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li, Rui, Brockschmidt, Felix F, Kiefer, Amy K, Stefansson, Hreinn, Nyholt, Dale R, Song, Kijoung, Vermeulen, Sita H, Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E, Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y, Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M, Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W, Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C, Becker, Tim, Sulem, Patrick, Mangino, Massimo, Vollenweider, Peter, Spector, Tim D, Dedoussis, George, Martin, Nicholas G, Kiemeney, Lambertus A, Mooser, Vincent, Stefansson, Kari, Hinds, David A, Nöthen, Markus M, Richards, J Brent
Published in PLoS genetics (01.05.2012)
Published in PLoS genetics (01.05.2012)
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Journal Article
Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
Redler, Silke, Dobson, Kathy, Drichel, Dmitriy, Heilmann, Stefanie, Wolf, Sabrina, Brockschmidt, Felix F, Tazi-Ahnini, Rachid, Birch, Pattie, Teßmann, Peter, Giehl, Kathrin A, Kruse, Roland, Lutz, Gerhard, Garcia Bartels, Natalie, Hanneken, Sandra, Wolff, Hans, Böhm, Markus, Becker, Tim, Blume-Peytavi, Ulrike, Nöthen, Markus M, Messenger, Andrew G, Betz, Regina C
Published in Journal of dermatological science (01.11.2013)
Published in Journal of dermatological science (01.11.2013)
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A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients
ENGELS, Hartmut, WOHLLEBER, Eva, WILLATT, Lionel, KREISS-NACHTSHEIM, Martina, FIRTH, Helen V, RAUCH, Anita, ZINK, Alexander, HOYER, Juliane, LUDWIG, Kerstin U, BROCKSCHMIDT, Felix F, WIECZOREK, Dagmar, MOOG, Ute, HELLMANN-MERSCH, Birgit, WEBER, Ruthild G
Published in European journal of human genetics : EJHG (01.12.2009)
Published in European journal of human genetics : EJHG (01.12.2009)
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Journal Article
Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
Redler, S., Birch, M.P., Drichel, D., Dobson, K., Brockschmidt, F.F., Tazi-Ahnini, R., Giehl, K.A., Kluck, N., Kruse, R., Lutz, G., Wolff, H., Becker, T., Nöthen, M.M., Messenger, A.G., Betz, R.C.
Published in British journal of dermatology (1951) (01.09.2011)
Published in British journal of dermatology (1951) (01.09.2011)
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Journal Article
INTERSNP: genome-wide interaction analysis guided by a priori information
Herold, Christine, Steffens, Michael, Brockschmidt, Felix F., Baur, Max P., Becker, Tim
Published in Bioinformatics (15.12.2009)
Published in Bioinformatics (15.12.2009)
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