檢索結果 - Kerstin U. Ludwig

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  1. 1
    Predicting the pathogenicity of missense variants using features derived from AlphaFold2

    Predicting the pathogenicity of missense variants using features derived from AlphaFold2 由 Axel Schmidt, Sebastian Röner, Karola Mai, Hannah Klinkhammer, Martin Kircher, Kerstin U. Ludwig

    出版 2023
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  2. 2
    The role of <i>Escherichia coli</i> O 157 infections in the classical (enteropathic) haemolytic uraemic syndrome: Results of a Central European, multicentre study

    The role of <i>Escherichia coli</i> O 157 infections in the classical (enteropathic) haemolytic uraemic syndrome: Results of a Central European, multicentre study 由 Martin Bitzan, Kerstin U. Ludwig, M. Klemt, H. König, Jonas Burén, D. E. Müller‐Wiefel

    出版 1993
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  3. 3
    p63 establishes epithelial enhancers at critical craniofacial development genes

    p63 establishes epithelial enhancers at critical craniofacial development genes 由 Enrique Lin-Shiao, Yemin Lan, Julia Welzenbach, Katherine A. Alexander, Zhen Zhang, Michael Knapp, Elisabeth Mangold, Morgan A. Sammons, Kerstin U. Ludwig, Shelley L. Berger

    出版 2019
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  4. 4
    A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients

    A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients 由 Hartmut Engels, Eva Wohlleber, Alexander M. Zink, Juliane Hoyer, Kerstin U. Ludwig, Felix F. Brockschmidt, Dagmar Wieczorek, Ute Moog, Birgit Hellmann-Mersch, Ruthild G. Weber, Lionel Willatt, Martina Kreiß‐Nachtsheim, Helen V. Firth, Anita Rauch

    出版 2009
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  5. 5
    TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19

    TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19 由 Axel Schmidt, Sophia Peters, Alexej Knaus, Hemmen Sabir, Frauke Hamsen, Carlo Maj, Julia Fazaal, Sugirthan Sivalingam, Oleksandr Savchenko, Aakash Mantri, Dirk Holzinger, Ulrich Neudorf, Andreas Müller, Kerstin U. Ludwig, Peter Krawitz, Hartmut Engels, Markus M. Nöthen, Soyhan Bağcı

    出版 2021
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  6. 6
    Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study

    Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study 由 Terri H. Beaty, Margaret A. Taub, Alan F. Scott, Jeffrey C. Murray, Mary L. Marazita, Holger Schwender, Margaret M. Parker, Jacqueline B. Hetmanski, Poojitha Balakrishnan, M. Adela Mansilla, Elisabeth Mangold, Kerstin U. Ludwig, Markus M. Nöethen, Michele Rubini, Nursel Elcioğlu, Ingo Ruczinski

    出版 2013
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  7. 7
    Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation

    Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation 由 Laura Godfrey, Jan Förster, Sven‐Thorsten Liffers, Christopher Schröder, Johannes Köster, Leonie Henschel, Kerstin U. Ludwig, David Lähnemann, Marija Trajkovic‐Arsic, Diana Behrens, Aldo Scarpa, Rita T. Lawlor, Kathrin E. Witzke, Barbara Sitek, Steven A. Johnsen, Sven Rahmann, Bernhard Horsthemke, Michael Zeschnigk, Jens T. Siveke

    出版 2024
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  8. 8
    Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology

    Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology 由 Laurence J Howe, Myoung Keun Lee, Gemma C. Sharp, George Davey Smith, Beaté St Pourcain, John R. Shaffer, Kerstin U. Ludwig, Elisabeth Mangold, Mary L. Marazita, Eleanor Feingold, Alexei I. Zhurov, Evie Stergiakouli, Jonathan Sandy, Stephen Richmond, Seth M. Weinberg, Gibran Hemani, Sarah J. Lewis

    出版 2018
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  9. 9
    Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene

    Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative G... 由 Kerstin U. Ludwig, Syeda Ahmed, Anne C. Böhmer, Nasim Bahram Sangani, Sheryil Varghese, Johanna Klamt, Hannah Schuenke, Pınar Gültepe, Andrea Hofmann, Michele Rubini, Khalid Aldhorae, Régine P.M. Steegers‐Theunissen, Augusto Rojas‐Martínez, Rudolf Reiter, Guntram Borck, Michael Knapp, Mitsushiro Nakatomi, Daniel Graf, Elisabeth Mangold, Heiko Peters

    出版 2016
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  10. 10
    Imputation of Orofacial Clefting Data Identifies Novel Risk Loci and Sheds Light on the Genetic Background of Cleft Lip ± Cleft Palate and Cleft Palate Only.

    Imputation of Orofacial Clefting Data Identifies Novel Risk Loci and Sheds Light on the Genetic Background of Cleft Lip ± Cleft Palate and Cleft Palate Only. 由 Kerstin U. Ludwig, Anne C. Böhmer, John Bowes, Miloš Nikolić, Nina Ishorst, Niki Wyatt, Nigel L. Hammond, Lina Gölz, Frederic Thieme, Sandra Barth, Hannah Schuenke, Johanna Klamt, Malte Spielmann, Khalid Aldhorae, Augusto Rojas-Martı́nez, Markus M. Nöthen, Álvaro Rada-Iglesias, Michael J. Dixon, Michael Knapp, Elisabeth Mangold

    出版 2017
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  11. 11
    DNA methylation mediates genetic liability to non-syndromic cleft lip/palate

    DNA methylation mediates genetic liability to non-syndromic cleft lip/palate 由 Laurence J Howe, Tom G. Richardson, Ryan Arathimos, Lucas Alvizi, Maria-Rita Passos-Bueno, Philip Stanier, Ellen A. Nøhr, Kerstin U. Ludwig, Elisabeth Mangold, Michael Knapp, Evie Stergiakouli, Beaté St Pourcain, George Davey Smith, Jonathan Sandy, Caroline L. Relton, Sarah J. Lewis, Gibran Hemani, Gemma C. Sharp

    出版 2018
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  12. 12
    Evidence for DNA Methylation Mediating Genetic Liability to Non-Syndromic Cleft Lip/Palate

    Evidence for DNA Methylation Mediating Genetic Liability to Non-Syndromic Cleft Lip/Palate 由 Laurence J Howe, Tom G. Richardson, Ryan Arathimos, Lucas Alvizi, Maria Rita Passos‐Bueno, Philip Stanier, Ellen A. Nøhr, Kerstin U. Ludwig, Elisabeth Mangold, Michael Knapp, Evie Stergiakouli, Beaté St Pourcain, George Davey Smith, Jonathan Sandy, Caroline L. Relton, Sarah J. Lewis, Gibran Hemani, Gemma C. Sharp

    出版 2019
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  13. 13
    Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy

    Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy 由 Markus Draaken, Michael Knapp, Tracie Pennimpede, Johanna Magdalena Schmidt, Anne‐Karolin Ebert, Wolfgang Rösch, Raimund Stein, Boris Utsch, Karin Hirsch, Thomas M. Boemers, Elisabeth Mangold, Stefanie Heilmann‐Heimbach, Kerstin U. Ludwig, Ekkehart Jenetzky, Nadine Zwink, Susanne Moebus, Bernhard G. Herrmann, Manuel Mattheisen, Markus M. Nöthen, Michael Ludwig, Heiko Reutter

    出版 2015
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  14. 14
    Genetic determination of human facial morphology: links between cleft-lips and normal variation

    Genetic determination of human facial morphology: links between cleft-lips and normal variation 由 Stefan Böehringer, Fedde van der Lijn, Fan Liu, Manuel Günther, Stella Sinigerova, Stefanie Nowak, Kerstin U. Ludwig, Ruth Herberz, Stefan Klein, Albert Hofman, André G. Uitterlinden, Wiro J. Niessen, Monique M.B. Breteler, Aad van der Lugt, Rolf P. Würtz, Markus M. Nöthen, Bernhard Horsthemke, Dagmar Wieczorek, Elisabeth Mangold, Manfred Kayser

    出版 2011
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  15. 15
    Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

    Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia 由 Alistair T. Pagnamenta, Elena Bacchelli, Maretha Jonge, Ghazala Mirza, Thomas Scerri, Fiorella Minopoli, Andreas G. Chiocchetti, Kerstin U. Ludwig, Per Hoffmann, Silvia Paracchini, Ernesto Lowy, Denise Harold, Jade Chapman, Sabine M. Klauck, Fritz Poustka, Renske H. Houben, Wouter Staal, Roel A. Ophoff, Michael O’Donovan, Julie Williams, Markus M. Nöthen, Gerd Schulte‐Körne, Panos Deloukas, Jiannis Ragoussis, Anthony Bailey, Elena Maestrini, Anthony P. Monaco

    出版 2010
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  16. 16
    FAF1, a Gene that Is Disrupted in Cleft Palate and Has Conserved Function in Zebrafish

    FAF1, a Gene that Is Disrupted in Cleft Palate and Has Conserved Function in Zebrafish 由 Michella Ghassibe‐Sabbagh, Laurence Desmyter, Tobias Langenberg, Filip Claes, Odile Boute, Bénédicte Bayet, P. Pellerin, Karlien Hermans, Liesbeth Backx, M. Adela Mansilla, Sandra R. Imoehl, Stefanie Nowak, Kerstin U. Ludwig, Carlotta Baluardo, Melissa Ferrian, Peter Mossey, Markus M. Nöethen, Mieke Dewerchin, Geneviève François, Nicole Revençu, R Vanwijck, Jacqueline T. Hecht, Elisabeth Mangold, Jeffrey C. Murray, Michele Rubini, Joris Vermeesch, Hélène A. Poirel, Peter Carmeliet, Miikka Vikkula

    出版 2011
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  17. 17
    Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity

    Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity 由 Yanqin Yu, Xianbo Zuo, Miao He, Jinping Gao, Yuchuan Fu, Chuanqi Qin, Liuyan Meng, Wenjun Wang, Yaling Song, Yong Cheng, Fusheng Zhou, Gang Chen, Xiaodong Zheng, Xinhuan Wang, Bo Liang, Zhengwei Zhu, Xiazhou Fu, Yujun Sheng, Jie-Bing Hao, Zhongyin Liu, Hansong Yan, Elisabeth Mangold, Ingo Ruczinski, Jianjun Liu, Mary L. Marazita, Kerstin U. Ludwig, Terri H. Beaty, Xuejun Zhang, Liangdan Sun, Zhuan Bian

    出版 2017
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  18. 18
    Genome-wide Association Study of Alcohol Dependence

    Genome-wide Association Study of Alcohol Dependence 由 Jens Treutlein, Sven Cichon, Monika Ridinger, Norbert Wodarz, Michael B. Soyka, Peter Zill, Wolfgang Maier, Rainald Moessner, Wolfgang Gäebel, Norbert Dahmen, Christoph Fehr, Norbert Scherbaum, Michael Steffens, Kerstin U. Ludwig, Josef Frank, H.-Erich Wichmann, Stefan Schreiber, Nico Dragano, Wolfgang H. Sommer, Fernando Leonardi‐Essmann, Anbarasu Lourdusamy, Peter J. Gebicke‐Haerter, Thomas F. Wienker, Patrick F. Sullivan, Markus M. Nöthen, Falk Kiefer, Rainer Spanagel, Karl Mann, Marcella Rietschel

    出版 2009
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  19. 19
    Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

    Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate 由 Elisabeth Mangold, Anne C. Böhmer, Nina Ishorst, Ann‐Kathrin Hoebel, Pınar Gültepe, Hannah Schuenke, Johanna Klamt, Andrea Hofmann, Lina Gölz, Ruth Raff, Peter Teßmann, Stefanie Nowak, Heiko Reutter, Alexander Hemprich, Thomas Kreusch, Franz‐Josef Kramer, Bert Braumann, Rudolf H. Reich, Gül Schmidt, Andreas Jäger, Rudolf Reiter, Sibylle Brosch, Janis Stavusis, Miho Ishida, Rimante Seselgyte, Gudrun E. Moore, Markus M. Nöthen, Guntram Borck, Khalid Aldhorae, Baiba Lāce, Philip Stanier, Michael Knapp, Kerstin U. Ludwig

    出版 2016
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  20. 20
    Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer Immunotherapy

    Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer Immunotherapy 由 Nicole Glodde, Tobias Bald, Debby van den Boorn-Konijnenberg, Kyohei Nakamura, Jake S. O’Donnell, Sabrina Szczepanski, Maria Brandes, Sarah Eickhoff, Indrajit Das, Naveen Shridhar, Daniel Hinze, Meri Rogava, Tetje C. van der Sluis, Janne Ruotsalainen, Evelyn Gaffal, Jennifer Landsberg, Kerstin U. Ludwig, Christoph Wilhelm, Monika Riek‐Burchardt, Andreas J. Müller, Christoffer Gebhardt, Richard A. Scolyer, Georgina V. Long, Viktor Janzen, Michele W.L. Teng, Wolfgang Kastenmüller, Massimiliano Mazzone, Mark J. Smyth, Thomas Tüting, Michael Hölzel

    出版 2017
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