Search Results - Peter Lichtner

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  1. 1
    An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14

    An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14 by Peter Lichtner

    Published 2000
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  2. 2
    The impact of genetic relationship information on genomic breeding values in German Holstein cattle

    The impact of genetic relationship information on genomic breeding values in German Holstein cattle by David Habier, Jens Tetens, Franz R. Seefried, Peter Lichtner, Georg Thaller

    Published 2010
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  3. 3
    A One Base Pair Deletion in the Canine ATP13A2 Gene Causes Exon Skipping and Late-Onset Neuronal Ceroid Lipofuscinosis in the Tibetan Terrier

    A One Base Pair Deletion in the Canine ATP13A2 Gene Causes Exon Skipping and Late-Onset Neuronal Ceroid Lipofuscinosis in the Tibetan Terrier by Anne Wöhlke, U. Philipp, Patricia Bock, Andreas Beineke, Peter Lichtner, Thomas Meitinger, O. Distl

    Published 2011
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  4. 4
    Genetic Variation in Soluble Epoxide Hydrolase ( <i>EPHX2</i> ) Is Associated With an Increased Risk of Ischemic Stroke in White Europeans

    Genetic Variation in Soluble Epoxide Hydrolase ( <i>EPHX2</i> ) Is Associated With an Increased Risk of Ischemic Stroke in White Europeans by Andreas Gschwendtner, Stephan Ripke, Tobias Freilinger, Peter Lichtner, Bertram Müller‐Myhsok, H.‐Erich Wichmann, Thomas Meitinger, Martin Dichgans

    Published 2008
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  5. 5
    Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

    Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk by Andrea Rivera, Sheila Fisher, Lars G. Fritsche, Claudia N. Keilhauer, Peter Lichtner, Thomas Meitinger, Bernhard H. F. Weber

    Published 2005
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  6. 6
    Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*

    Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease* by Daniela Berg, Katherine J. Schweitzer, Petra Leitner, Alexander Zimprich, Peter Lichtner, Petra Belcredi, Theresa Brüssel, Claudia Schulte, Sylvia Maaß, Thomas Nägele, Zbigniew K. Wszołek, Thomas Gasser

    Published 2005
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  7. 7
    Length Polymorphisms in Heme Oxygenase-1 and AKI after Cardiac Surgery

    Length Polymorphisms in Heme Oxygenase-1 and AKI after Cardiac Surgery by David E. Leaf, Simon C. Body, Jochen D. Muehlschlegel, Gearoid M. McMahon, Peter Lichtner, Charles D. Collard, Stanton K. Shernan, Amanda A. Fox, Sushrut S. Waikar

    Published 2016
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  8. 8
    Human skin-resident host T cells can persist long term after allogeneic stem cell transplantation and maintain recirculation potential

    Human skin-resident host T cells can persist long term after allogeneic stem cell transplantation and maintain recirculation potential by Gustavo Pereira de Almeida, Peter Lichtner, Gertrud Eckstein, Tonio Brinkschmidt, Chang-Feng Chu, Shan Sun, Julian Reinhard, Sophia C. Mädler, Markus Kloeppel, Mareike Verbeek, Christina E. Zielinski

    Published 2022
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  9. 9
    Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)

    Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2) by Simone Schuffenhauer, Peter Lichtner, Popak Peykar-Derakhshandeh, Jan Murken, O Haas, Elke Back, G. Wolff, Bernhard Zabel, Ingeborg Barišić, Anita Rauch, Zvi Borochowitz, Bruno Dallapiccola, Mark Ross, Thomas Meitinger

    Published 1998
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  10. 10
    Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3

    Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3 by Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Gertrud Eckstein, Yardena Tenenbaum‐Rakover, Janine Wagenstaller, Dov Tiosano, Ruth Gershoni‐Baruch, Norbert Albers, Peter Lichtner, Dirk Schnabel, Ze’ev Hochberg, Tim M. Strom

    Published 2006
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  11. 11
    Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy

    Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy by Juliane Ramser, Mary Ellen Ahearn, C Lenski, Kemal O. Yariz, Heide Hellebrand, Michael von Rhein, Robin D. Clark, Rita K. Schmutzler, Peter Lichtner, Eric P. Hoffman, Alfons Meindl, Lisa Baumbach‐Reardon

    Published 2008
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  12. 12
    Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer

    Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer by Kathrin Giehl, Gertrud Eckstein, Sandra M. Pasternack, Silke Praetzel‐Wunder, Thomas Ruzicka, Peter Lichtner, K. Seidl, Mike A. Rogers, Elisabeth Graf, Lutz Langbein, Markus Braun‐Falco, Regina C. Betz, Tim M. Strom

    Published 2012
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  13. 13
    Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis

    Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis by Rubén Fernández‐Santiago, S. Hoenig, Peter Lichtner, Anne‐Dorte Sperfeld, Manu Sharma, Daniela Berg, Oliver Weichenrieder, Thomas Illig, K. Eger, Thomas Meyer, Johanna Anneser, Christoph Münch, Stephan Zierz, Thomas Gasser, Albert C. Ludolph

    Published 2009
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  14. 14
    Recessive Mutations in the α3 (VI) Collagen Gene COL6A3 Cause Early-Onset Isolated Dystonia

    Recessive Mutations in the α3 (VI) Collagen Gene COL6A3 Cause Early-Onset Isolated Dystonia by Michael Zech, Daniel D. Lam, Ludmila Francescatto, Barbara Schormair, Aaro V. Salminen, Angela Jochim, Thomas Wieland, Peter Lichtner, Annette Peters, Christian Gieger, Hanns Lochmüller, Tim M. Strom, Bernhard Haslinger, Nicholas Katsanis, Juliane Winkelmann

    Published 2015
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  15. 15
    Polymorphisms at<i>PRSS1–PRSS2</i>and<i>CLDN2–MORC4</i>loci associate with alcoholic and non-alcoholic chronic pancreatitis in a European replication study

    Polymorphisms at<i>PRSS1–PRSS2</i>and<i>CLDN2–MORC4</i>loci associate with alcoholic and non-alcoholic chronic pancreatitis in a European replication study by Monique Derikx, Péter Kovács, Markus Scholz, Emmanuelle Masson, Jian‐Min Chen, Claudia Ruffert, Peter Lichtner, René H. M. te Morsche, Giulia Martina Cavestro, Claude Férec, Joost P.H. Drenth, Heiko Witt, Jonas Rosendahl

    Published 2014
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  16. 16
    Ghrelin Receptor Gene: Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Short Normal Stature

    Ghrelin Receptor Gene: Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Sh... by Haijun Wang, Frank Geller, Astrid Dempfle, Nadine Schäuble, Susann Friedel, Peter Lichtner, Francisco Fontenla-Horro, Stefan A. Wudy, Sandra Hagemann, Ludwig Gortner, Klaus Huse, Helmut Remschmidt, Thomas Bettecken, Thomas Meitinger, H. Schäfer, Johannes Hebebrand, Anke Hinney

    Published 2004
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  17. 17
    Prevalence, Spectrum, and Functional Characterization of Melanocortin-4 Receptor Gene Mutations in a Representative Population-Based Sample and Obese Adults from Germany

    Prevalence, Spectrum, and Functional Characterization of Melanocortin-4 Receptor Gene Mutations in a Representative Population-Based Sample and Obese Adults from Germany by Anke Hinney, Thomas Bettecken, Patrick Tarnow, Harald Brumm, Kathrin Reichwald, Peter Lichtner, André Scherag, Thuy Trang Nguyen, Pia Schlumberger, Winfried Rief, Caren Vollmert, Thomas Illig, H‐Erich Wichmann, H. Schäfer, Matthias Platzer, Heike Biebermann, Thomas Meitinger, Johannes Hebebrand

    Published 2006
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  18. 18
    Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations

    Linkage Disequilibrium Patterns and tagSNP Transferability among European Populations by Jakob C. Mueller, Elin Lõhmussaar, Reedik Mägi, Maido Remm, Thomas Bettecken, Peter Lichtner, Saskia Biskup, Thomas Illig, Arne Pfeufer, Jan Luedemann, Stefan Schreiber, Peter P. Pramstaller, Irene Pichler, Giovanni Romeo, Anthony Gaddi, A. Testa, Heinz‐Erich Wichmann, Andres Metspalu, Thomas Meitinger

    Published 2005
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  19. 19
    Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13

    Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13 by David Kemlink, Giuseppe Plazzi, Roberto Vetrugno, Federica Provini, Olli Polo, Karin Stiasny‐Kolster, Wolfgang H. Oertel, Soňa Nevšímalová, Karel Šonka, Birgit Högl, Birgit Frauscher, Georgios M. Hadjigeorgiou, Peter P. Pramstaller, Peter Lichtner, Thomas Meitinger, Bertram Müller-Myshok, Juliane Winkelmann, Pasquale Montagna

    Published 2008
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  20. 20
    MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease

    MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease by Barbara Schormair, Jens Plag, Maria Kaffe, Nicholas J. Gross, Darina Czamara, W. Samtleben, Peter Lichtner, Andreas Ströhle, Ioannis Stefanidis, A. Vainas, Efthimios Dardiotis, Giorgos K. Sakkas, Christian Gieger, Bertram Müller‐Myhsok, Thomas Meitinger, U. Heemann, Georgios M. Hadjigeorgiou, Konrad Oexle, Juliane Winkelmann

    Published 2011
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