Andre Reis - Dissemin

Papers authored by Andre Reis

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2005 Martin Zenker, Michel Pierson, Philippe Jonveaux, André Reis

Demonstration of two novelLAMB2 mutations in the original Pierson syndrome family reported 42 years ago

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Harald Burkhardt, Ulrike Hüffmeier, Bernd Spriewald, Beate Böhm, Rolf Rau, Stefan Kallert, Ake Engström, Rikard Holmdahl, André Reis

Association between protein tyrosine phosphatase 22 variant R620W in conjunction with the HLA-DRB1 shared epitope and humoral autoimmunity to an immunodominant epitope of cartilage-specific type II collagen in early rheumatoid arthritis

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Arjan P. M. de Brouwer, Hendrikus P. M. Kunst, Alice Krebsova, Karin van Asseldonk, André Reis

, Rik L. Snoeckx, Guy Van Camp

, Cor W. R. J. Cremers, Frans P. M. Cremers, Hannie Kremer

Fine mapping of autosomal dominant nonsyndromic hearing impairmentDFNA21 to chromosome 6p24.1-22.3

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I. M. Adham, M. Gille, A. J. Gamel, A. Reis

, R. Dressel, G. Steding, B. Brand-Saberi, W. Engel

The scoliosis (sco) mouse: a new allele of Pax1

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2004 Ashraf U. Mannan, Elena Roussa, Cornelia Kraus, Micheal Rickmann, Joerg Maenner, Karim Nayernia, Kerstin Krieglstein, Andr� Reis

, Wolfgang Engel

Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse

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Martin Zenker, Tim Tralau, Thomas Lennert, Susanne Pitz, Karlheinz Mark, Henry Madlon, Jörg Dötsch, André Reis

, Horst Müntefering, Luitgard M. Neumann

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndrome: Microcoria-Congenital Nephrosis Syndrome

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Marc Trimborn, Sandra M. Bell, Clive Felix, Yasmin Rashid, Hussain Jafri, Paul D. Griffiths, Luitgard M. Neumann, Alice Krebs, André Reis

, Karl Sperling, Heidemarie Neitzel, Andrew P. Jackson

Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

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H. Seedorf, Mh de Angelis, In N. Springer, E. Grundner-Culemann, Hk-K. Albers, A. Reis

, H. Fuchs, M. Hrabe de Angelis

, Y. Acil, Y. Açil

Amelogenesis Imperfecta in a New Animal Model--a Mutation in Chromosome 5 (human 4q21)

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Hans Christian Hennies, Anita Rauch, Wenke Seifert, Christian Schumi, Elisabeth Moser, Eva Al-Taji, Gholamali Tariverdian, Krystyna H. Chrzanowska, Malgorzata Krajewska-Walasek, Anna Rajab, Roberto Giugliani, Thomas E. Neumann, Katja M. Eckl, Mohsen Karbasiyan, André Reis

and 1 other authors

Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome

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Corinna Berghoff, Martin Berghoff, Alejandro Leal, Bernal Morera, Ramiro Barrantes, André Reis

, Bernhard Neundörfer, Bernd Rautenstrauss, Gerardo Del Valle, Dieter Heuss

Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3

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Martin Zenker, Anita Rauch, Andreas Winterpacht, Andreas Tagariello, Cornelia Kraus, Thomas Rupprecht, Heinrich Sticht, André Reis

A Dual Phenotype of Periventricular Nodular Heterotopia and Frontometaphyseal Dysplasia in One Patient Caused by a Single FLNA Mutation Leading to Two Functionally Different Aberrant Transcripts

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Martin Zenker, Gernot Buheitel, Ralf Rauch, Rainer Koenig, Kirstin Bosse, Wolfram Kress, Hans-Ulrich Tietze, Helmuth-Guenther Doerr, Michael Hofbeck, Helmut Singer, André Reis

, Anita Rauch

Genotype-phenotype correlations in Noonan syndrome

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

A. Junemann, N. Wakili, C. Mardin, Goh Naumann, S. Bleich, K. Henkel, G. Beck, J. Kornhuber, U. Reulbach, B. Rautenstrauss, A. Reis

Prospective case control study on genetic assocation of apolipoprotein epsilon 2 with intraocular pressure

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2003 P. Hensen, C. Windemuth, U. Hüffmeier, F. Rüschendorf, A. Stadelmann, V. Hoppe, D. Fenneker, M. Ständer, M. Schmitt Egenolf

, T. F. Wienker, H. Traupe, A. Reis

Association scan of the novel psoriasis susceptibility region on chromosome 19: Evidence for both susceptible and protective loci

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P. Hensen, K. Asadullah, C. Windemuth, F. Rüschendorf, U. Hüffmeier, M. Ständer, M. Schmitt Egenolf

, T. F. Wienker, A. Reis

, H. Traupe

Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis

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Alejandro Leal, Corinna Berghoff, Martin Berghoff, Gerardo Del Valle, Carlos Contreras, Olga Montoya, Erick Hern�ndez, Ramiro Barrantes, Ursula Schl�tzer-Schrehardt, Bernhard Neund�rfer, Andr� Reis

, Bernd Rautenstrauss, Dieter Heuss

Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero ( MPZ , P0 ) gene causes different phenotypes in homozygous and heterozygous carriers within one family

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This paper is made freely available by the publisher.

Christian T. Thiel, Cornelia Kraus, Anita Rauch, Arif B. Ekici, Bernd Rautenstrauss, André Reis

A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPP

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Gabriela Chavarria Soley, Kristin A. Bosse, David Flikier, Paul Flikier, Jorge Azofeifa, Christian Y. Mardin, Andre Reis

, Karin G. Michels-Rautenstrauss, Bernd W. Rautenstrauss

Primary Congenital Glaucoma: A Novel Single-Nucleotide Deletion and Varying Phenotypic Expression for the 1546???1555dup Mutation in the GLC3A (CYP1B1) Gene in 2 Families of Different Ethnic Origin:

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Kathrin Saar, Frank Geller, F. Rueschendorf, Franz Ruschendorf, André Reis

, Susann Friedel, N. Schaeuble, Nadine Schauble, P. Nuernberg, Peter Nurnberg, Wolfgang Siegfried, Hans-Peter Goldschmidt, H. Schaefer, Helmut Schafer, Andreas Ziegler and 3 other authors

Genome scan for childhood and adolescent obesity in German families

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Karin Michels-Rautenstrauss, Christian Mardin, Nina Wakili, Anselm M. Jünemann, Luis Villalobos, Carlos Mejia, Gabriela Chavarria Soley, Sevinc Özbey, Jorge Azofeifa, Sevinc Ozbey, Gottfried Oh H. Naumann, Andre Reis

, Bernd Rautenstrauss

Novel mutations in the MYOC/GLC1A gene in a large group of glaucoma patients

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Papers authored by Andre Reis