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Olaf Rieß

1993–2025 年に発表

別表記
Olaf Riess
160
論文数
23,927
被引用数
82
h 指数
148
i10 指数

被引用数

Olaf Rieß の年別被引用数1967 年: 被引用 7 件1981 年: 被引用 1 件1982 年: 被引用 6 件1984 年: 被引用 6 件1985 年: 被引用 4 件1986 年: 被引用 1 件1987 年: 被引用 6 件1988 年: 被引用 2 件1989 年: 被引用 4 件1990 年: 被引用 3 件1991 年: 被引用 3 件1992 年: 被引用 3 件1993 年: 被引用 2 件1994 年: 被引用 5 件1995 年: 被引用 1 件1996 年: 被引用 5 件1997 年: 被引用 23 件1998 年: 被引用 36 件1999 年: 被引用 59 件2000 年: 被引用 106 件2001 年: 被引用 119 件2002 年: 被引用 119 件2003 年: 被引用 150 件2004 年: 被引用 177 件2005 年: 被引用 138 件2006 年: 被引用 154 件2007 年: 被引用 148 件2008 年: 被引用 199 件2009 年: 被引用 214 件2010 年: 被引用 243 件2011 年: 被引用 356 件2012 年: 被引用 295 件2013 年: 被引用 309 件2014 年: 被引用 315 件2015 年: 被引用 269 件2016 年: 被引用 219 件2017 年: 被引用 262 件2018 年: 被引用 232 件2019 年: 被引用 661 件2020 年: 被引用 655 件2021 年: 被引用 817 件2022 年: 被引用 710 件2023 年: 被引用 594 件2024 年: 被引用 756 件2025 年: 被引用 405 件2026 年: 被引用 32 件1968〜1980 年は被引用が無いため表示していません1983 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 3,155 件、この内訳の 22.3%ドイツ: 引用元論文 1,276 件、この内訳の 9%イギリス: 引用元論文 1,124 件、この内訳の 8%中国: 引用元論文 953 件、この内訳の 6.8%イタリア: 引用元論文 695 件、この内訳の 4.9%フランス: 引用元論文 579 件、この内訳の 4.1%カナダ: 引用元論文 494 件、この内訳の 3.5%オーストラリア: 引用元論文 457 件、この内訳の 3.2%オランダ: 引用元論文 455 件、この内訳の 3.2%日本: 引用元論文 422 件、この内訳の 3%スペイン: 引用元論文 397 件、この内訳の 2.8%スイス: 引用元論文 284 件、この内訳の 2%
0%22.3%その他 27.2%

機関

分野

  • Medicine49.4%
  • Biochemistry, Genetics and Molecular Biology23.9%
  • Neuroscience18.1%
  • Computer Science4.7%
  • Immunology and Microbiology0.9%
  • Nursing0.7%
  • その他2.3%

トピック

  • Parkinson's Disease Mechanisms and Treatments13.4%
  • Genetic Neurodegenerative Diseases5.7%
  • Alzheimer's disease research and treatments4.4%
  • Neurological disorders and treatments4%
  • Mitochondrial Function and Pathology3.8%
  • Nuclear Receptors and Signaling3.3%
  • その他65.4%

共著者

全論文

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  1. Swarm Learning for decentralized and confidential clinical machine learning

    著者: Stefanie Warnat‐Herresthal, Hartmut Schultze, Krishnaprasad Lingadahalli Shastry, Sathyanarayanan Manamohan, Saikat Mukherjee, Vishesh Garg, Ravi Sarveswara, Kristian Händler, Peter Pickkers, N. Ahmad Aziz, Sofia Ira Ktena, Florian Tran, Michael Bitzer, Stephan Ossowski, Nicolas Casadei, Christian Herr, Daniel Petersheim, Uta Behrends, Fabian Kern, Tobias Fehlmann, Philipp Schommers, Clara Lehmann, Max Augustin, Jan Rybniker, Janine Altmüller, Neha Mishra, Joana P. Bernardes, Benjamin Krämer, Lorenzo Bonaguro, Jonas Schulte-Schrepping, Elena De Domenico, Christian Siever, Michael Kraut, Milind Y. Desai, Bruno Monnet, Maria Saridaki, Charles Siegel, Anna Drews, Melanie Nuesch-Germano, Heidi Theis, Jan Heyckendorf, Stefan Schreiber, Sarah Kim-Hellmuth, COVID-19 Aachen Study (COVAS), Paul Balfanz, Thomas Eggermann, Peter Boor, Ralf Hausmann, Hannah Kuhn, Susanne Isfort, Julia Stingl, Günther Schmalzing, Christiane Kühl, Rainer Röhrig, Gernot Marx, Stefan Uhlig, Edgar Dahl, Dirk Müller‐Wieland, Michael Dreher, Nikolaus Marx, Jacob Nattermann, Dirk Skowasch, Ingo Kurth, Andreas Keller, Robert Bals, Peter Nürnberg, Olaf Rieß, Philip Rosenstiel, Mihai G. Netea, Fabian J. Theis, Sach Mukherjee, Michael Backes, Anna C. Aschenbrenner, Thomas Ulas, Deutsche COVID-19 Omics Initiative (DeCOI), Angel Angelov, Alexander Bartholomäus, Anke Becker, Daniela Bezdan, Conny Blumert, Ezio Bonifacio, Peer Bork, Boyke Bunk, Helmut Blum, Thomas Clavel, Maria Colomé‐Tatché, Markus Cornberg, Inti Alberto De La Rosa Velázquez, Andreas Diefenbach, Alexander Dilthey, Nicole Fischer, Konrad U. Förstner, Sören Franzenburg, Julia-Stefanie Frick, Gisela Gabernet, Julien Gagneur, Tina Ganzenmueller, Marie Gauder, Janina Geißert, Alexander Goesmann ほか 81 名 - Nature 2021 被引用: 880

  2. AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease

    著者: Rejko Krüger, W. Kuhn, Thomas Müller, Dirk Woitalla, Manuel B. Graeber, Sigfried Kösel, H. Przuntek, Jörg T. Epplen, Lüdger Schöls, Olaf Rieß - Nature Genetics 1998 被引用: 3,885

  3. Genome-wide association study reveals genetic risk underlying Parkinson's disease

    著者: Javier Simón‐Sánchez, Claudia Schulte, José Brás, Manu Sharma, J. Raphael Gibbs, Daniela Berg, Coro Paisán-Ruı́z, Peter Lichtner, Sonja W. Scholz, Dena Hernández, Rejko Krüger, Monica Federoff, Christine Klein, Alison Goate, Joel S. Perlmutter, Michael von Bonin, Michael A. Nalls, Thomas Illig, Christian Gieger, Henry Houlden, Michael Steffens, Michael S. Okun, Brad A. Racette, Mark Cookson, Kelly D. Foote, Hubert H. Fernandez, Bryan J. Traynor, Stefan Schreiber, Sampath Arepalli, Ryan R. Zonozi, Katrina Gwinn, Marcel van der Brug, Grisel Lopez, Stephen J. Chanock, Arthur Schatzkin, Yikyung Park, Albert R. Hollenbeck, Jianjun Gao, Xuemei Huang, Nick W Wood, Delia Lorenz, Günther Deuschl, Honglei Chen, Olaf Rieß, John Hardy, Andrew Singleton, Thomas Gasser - Nature Genetics 2009 被引用: 1,954

  4. Evidence for bidirectional and trans-synaptic parasympathetic and sympathetic propagation of alpha-synuclein in rats

    著者: Nathalie Van Den Berge, Nelson Ferreira, Hjalte Gram, Trine Werenberg Mikkelsen, Aage Kristian Olsen Alstrup, Nicolas Casadei, Tsung‐Pin Pai, Olaf Rieß, Jens Randel Nyengaard, Gültekin Tamgüney, Poul Henning Jensen, Per Borghammer - Acta Neuropathologica 2019 被引用: 303

  5. Glycation potentiates α-synuclein-associated neurodegeneration in synucleinopathies

    著者: Hugo Vicente Miranda, Éva M. Szegő, Luís M. A. Oliveira, Carlo Breda, Ekrem Darendelioğlu, Rita Machado de Oliveira, Diana G. Ferreira, Marcos António Gomes, Ruth Rott, Márcia Santos Duarte de Oliveira, Francesca Munari, Francisco J. Enguita, Tânia Simões, Eva Rodrigues, Michael Heinrich, Ivo C. Martins, Irina Zamolo, Olaf Rieß, Carlos Cordeiro, Ana Ponces-Freire, Hilal A. Lashuel, Nuno C. Santos, Luı́sa V. Lopes, Wei Xiang, Thomas M. Jovin, Deborah Penque, Simone Engelender, Markus Zweckstetter, Jochen Klucken, Flaviano Giorgini, Alexandre Quintas, Tiago F. Outeiro - Brain 2017 被引用: 225

  6. Recommendations for whole genome sequencing in diagnostics for rare diseases

    著者: Erika Souche, Sergi Beltrán, Erwin Brosens, John W. Belmont, Magdalena Fossum, Olaf Rieß, Christian Gilissen, Amin Ardeshirdavani, Gunnar Houge, Mariëlle van Gijn, Jill Clayton‐Smith, Matthis Synofzik, Nicole de Leeuw, Zandra C. Deans, Yasemin Dincer, Sebastian Eck, Saskia van der Crabben, Meena Balasubramanian, Holm Graeßner, Marc Sturm, Helen V. Firth, Alessandra Ferlini, Rima Nabbout, Elfride De Baere, Thomas Liehr, Milan Maçek, Gert Matthijs, Hans Scheffer, Peter Bauer, Helger G. Yntema, Marjan M. Weiss - European Journal of Human Genetics 2022 被引用: 125

  7. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

    著者: Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Richarda M. de Voer, Steven Laurie, Leslie Matalonga, Christian Gilissen, Stephan Ossowski, Peter A.C. ’t Hoen, Antonio Vitobello, Julia M. Schulze‐Hentrich, Olaf Rieß, Han G. Brunner, Anthony J. Brookes, Ana Rath, Gisèle Bonne, Gulcin Gumus, Alain Verloès, Nicoline Hoogerbrugge, Teresinha Evangelista, Tina Harmuth, Morris A. Swertz, Dylan Spalding, Alexander Hoischen, Sergi Beltrán, Holm Graeßner, T. Haack, Birte Zurek, Kornelia Ellwanger, German Demidov, Marc Sturm, Christoph Keßler, Melanie Wayand, Carlo Wilke, Andreas Traschütz, Lüdger Schöls, Holger Hengel, Peter Heutink, Han G. Brunner, Hans Scheffer, Wouter Steyaert, Karolis Sablauskas, Richarda M. de Voer, Erik-Jan Kamsteeg, Bart van de Warrenburg, Nienke van Os, Iris te Paske, Erik Janssen, Elke de Boer, Marloes Steehouwer, Burcu Yaldız, Tjitske Kleefstra, Colin Veal, Spencer Gibson, Marc Wadsley, Mehdi Mehtarizadeh, Umar Riaz, Greg Warren, Farid Yavari Dizjikan, Thomas Shorter, Volker Straub, C. Marini Bettolo, Sabine Specht, Jill Clayton‐Smith, Siddharth Banka, Elizabeth Alexander, Adam Jackson, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Anne‐Sophie Denommé‐Pichon, Yannis Duffourd, Émilie Tisserant, Ange‐Line Bruel, Christine Peyron, Aurore Pélissier, Sergi Beltrán, Marta Gut, Steven Laurie, Davide Piscia, Leslie Matalonga, Anastasios Papakonstantinou, Gemma Bullich, Alberto Corvò, Carles García, Marcos Fernandez-Callejo, Carles Hernandéz-Ferrer, Daniel Picó, Ida Paramonov, Hanns Lochmüller, Gulcin Gumus, Virginie Bros‐Facer, Marc Hanauer, Annie Olry, David Lagorce, Svitlana Havrylenko, Katia Izem ほか 123 名 - European Journal of Human Genetics 2021 被引用: 103

  8. Blunting neuroinflammation with resolvin D1 prevents early pathology in a rat model of Parkinson’s disease

    著者: Paraskevi Krashia, Alberto Cordella, Annalisa Nobili, Livia La Barbera, Mauro Federici, Alessandro Leuti, Federica Campanelli, Giuseppina Natale, Gioia Marino, Valeria Calabrese, Francescangelo Vedele, Veronica Ghiglieri, Barbara Picconi, Giulia Di Lazzaro, Tommaso Schirinzi, Giulia Maria Sancesario, Nicolas Casadei, Olaf Rieß, Sergio Bernardini, Antonio Pisani, Paolo Calabresi, Maria Teresa Viscomi, Charles N. Serhan, Valerio Chiurchiù, Marcello D’Amelio, Nicola Biagio Mercuri - Nature Communications 2019 被引用: 181

  9. Alpha-synuclein research: defining strategic moves in the battle against Parkinson’s disease

    著者: Luís M. A. Oliveira, Thomas Gasser, Robert H. Edwards, Markus Zweckstetter, Ronald Melki, Leonidas Stefanis, Hilal A. Lashuel, David Sulzer, Kostas Vekrellis, Glenda M. Halliday, Julianna J. Tomlinson, Michael G. Schlossmacher, Poul Henning Jensen, Julia M. Schulze‐Hentrich, Olaf Rieß, Warren D. Hirst, Omar M. A. El‐Agnaf, Brit Mollenhauer, Peter T. Lansbury, Tiago F. Outeiro - npj Parkinson s Disease 2021 被引用: 178

  10. The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases

    著者: Steven Laurie, Davide Piscia, Leslie Matalonga, Alberto Corvò, Carles García, Marcos Fernández-Callejo, Carles Hernandéz-Ferrer, Cristina Luengo, Anastasios Papakonstantinou, Joan Protassio, Inés Martínez, Daniel Picó, Rachel Thompson, Raúl Tonda, Mónica Bayés, Gemma Bullich, Jordi Camps, Ida Paramonov, Jean-Rémi Trotta, Ángel Alonso, Marcella Attimonelli, Christophe Béroud, Virginie Bros‐Facer, Orion J. Buske, Andrés Cañada, José M. Fernández, Mats Hansson, Rita Horváth, Julius O.B. Jacobsen, Rajaram Kaliyaperumal, Séverine Lair, Luana Licata, Pedro Lopes, Estrella López‐Martín, Deborah Mascalzoni, Lucía Monaco, Luis Pérez Jurado, Manuel Posada de la Paz, Jordi Rambla, Ana Rath, Olaf Rieß, Peter N. Robinson, Damian Smedley, Dylan Spalding, Peter A.C. ’t Hoen, Ana Töpf, Irina Zaharieva, Holm Graeßner, Marta Gut, Hanns Lochmüller, Sergi Beltrán - Human Mutation 2022 被引用: 62

  11. Reduced Basal Autophagy and Impaired Mitochondrial Dynamics Due to Loss of Parkinson's Disease-Associated Protein DJ-1

    著者: Guido Krebiehl, Sabine Ruckerbauer, Lena F. Burbulla, Nicole Kieper, Brigitte Maurer, Jens Waak, Hartwig Wolburg, Zemfira Gizatullina, Frank N. Gellerich, Dirk Woitalla, Olaf Rieß, Philipp J. Kahle, Tassula Proikas‐Cezanne, Rejko Krüger - PLoS ONE 2010 被引用: 378

  12. A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next Frontiers

    著者: Kym M. Boycott, Taila Hartley, Leslie G. Biesecker, Richard A. Gibbs, A. Micheil Innes, Olaf Rieß, John W. Belmont, Sally L. Dunwoodie, Nebojša Jojić, Timo Lassmann, Deborah Mackay, I. Karen Temple, Axel Visel, Gareth Baynam - Cell 2019 被引用: 189

  13. Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases

    著者: Nicole Weisschuh, Pascale Mazzola, Theresia Zuleger, Karin Schaeferhoff, Laura Kühlewein, Friederike Kortüm, Dennis Witt, Alexandra Liebmann, Ruth Falb, Lisa Pohl, Milda Reith, Lara G. Stühn, Miriam Bertrand, Amelie J. Müller, Nicolas Casadei, Olga Kelemen, Carina Kelbsch, Christoph Kernstock, Paul Richter, Françoise Sadler, German Demidov, Leon Schütz, Jakob Admard, Marc Sturm, Ute Grasshoff, Felix Tonagel, T. Heinrich, Fadi Nasser, Bernd Wissinger, Stephan Ossowski, Susanne Kohl, Olaf Rieß, Katarína Štingl, Tobias B. Haack - Journal of Medical Genetics 2023 被引用: 66

  14. Analysis of blood-based gene expression in idiopathic Parkinson disease

    著者: Ron Shamir, Christine Klein, David Amar, Eva-Juliane Vollstedt, Michael von Bonin, Marija Usenovic, Yvette C. Wong, Aleš Maver, Sven Poths, Hershel M. Safer, Jean‐Christophe Corvol, Suzanne Lesage, Ofer Lavi, Günther Deuschl, Gregor Kuhlenbäeumer, Heike Pawlack, Igor Ulitsky, Meike Kasten, Olaf Rieß, Alexis Brice, Borut Peterlin, Dimitri Krainc - Neurology 2017 被引用: 151

  15. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

    著者: Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato, Andreas Dufke, Kirsten Cremer, Maja Hempel, Denise Horn, Juliane Hoyer, Pascal Joset, Albrecht Röpke, Ute Moog, Angelika Rieß, Christian T. Thiel, Andreas Tzschach, Antje Wiesener, Eva Wohlleber, Christiane Zweier, Arif B. Ekici, Alexander M. Zink, Andreas Rump, Christa Meisinger, Harald Grallert, Heinrich Sticht, Annette Schenck, Hartmut Engels, Gudrun Rappold, Evelin Schröck, Peter Wieacker, Olaf Rieß, Thomas Meitinger, André Reis, Tim M. Strom - The Lancet 2012 被引用: 1,065

  16. 14-3-3 proteins in the nervous system

    著者: Daniela Berg, Carsten Holzmann, Olaf Rieß - Nature reviews. Neuroscience 2003 被引用: 625

  17. Multi-omics discovery of exome-derived neoantigens in hepatocellular carcinoma

    著者: Markus Löffler, Christopher Mohr, Leon Bichmann, Lena Katharina Freudenmann, Mathias Walzer, Christopher Schroeder, Nico Trautwein, Franz J. Hilke, Raphael S. Zinser, Lena Mühlenbruch, Daniel J. Kowalewski, Heiko Schuster, Marc Sturm, Jakob Matthes, Olaf Rieß, Stefan Czemmel, Sven Nahnsen, Ingmar Königsrainer, Karolin Thiel, Silvio Nadalin, Stefan Beckert, Hans Bösmüller, Falko Fend, Ana Velić, Boris Maček, Sebastian P. Haen, Luigi Buonaguro, Oliver Kohlbacher, Stefan Stevanović, Alfred Königsrainer, Hans‐Georg Rammensee - Genome Medicine 2019 被引用: 179

  18. α-Synuclein in Parkinson’s disease: causal or bystander?

    著者: Peter Riederer, Daniela Berg, Nicolas Casadei, Fubo Cheng, Joseph Claßen, Christian Dresel, Wolfgang H. Jost, Rejko Krüger, Thomas Müller, Heinz Reichmann, Olaf Rieß, Alexander Storch, Sabrina Strobel, Thilo van Eimeren, Hans‐Ullrich Völker, Jürgen Winkler, Konstanze F. Winklhofer, Ullrich Wüllner, Friederike Zunke, Camelia‐Maria Monoranu - Journal of Neural Transmission 2019 被引用: 114

  19. Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

    著者: Karsten M. Strauss, L. Miguel Martins, Hélène Plun‐Favreau, Frank P. Marx, Sabine Kautzmann, Daniela Berg, Thomas Gasser, Zbginiew Wszolek, Thomas Müller, Antje Bornemann, Hartwig Wolburg, Julian Downward, Olaf Rieß, Jörg B. Schulz, Rejko Krüger - Human Molecular Genetics 2005 被引用: 566

  20. Cholesterol Defect Is Marked across Multiple Rodent Models of Huntington's Disease and Is Manifest in Astrocytes

    著者: Marta Valenza, Valerio Leoni, Joanna M. Karasinska, Lara Petricca, Jianjia Fan, Jeffrey B. Carroll, Mahmoud A. Pouladi, Elisa Fossale, Huu Phuc Nguyen, Olaf Rieß, Marcy E. MacDonald, Cheryl L. Wellington, Stefano DiDonato, Michael R. Hayden, Elena Cattaneo - Journal of Neuroscience 2010 被引用: 158

  21. Severely impaired hippocampal neurogenesis associates with an early serotonergic deficit in a BAC α-synuclein transgenic rat model of Parkinson's disease

    著者: Zacharias Kohl, Nada Ben Abdallah, Jonathan Vogelgsang, Lucas Tischer, Janina Deusser, Davide Amato, Scott Anderson, Christian P. Müller, Olaf Rieß, Eliezer Masliah, Silke Nuber, Jürgen Winkler - Neurobiology of Disease 2015 被引用: 117

  22. Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients

    著者: Franz J. Hilke, Tobias Sinnberg, Axel Gschwind, Heike Niessner, German Demidov, Teresa Amaral, Stephan Ossowski, Irina Bonzheim, Martin Röcken, Olaf Rieß, Claus Garbe, Christopher Schroeder, Andrea Forschner - Cancers 2020 被引用: 64

  23. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

    著者: Lüdger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Rieß - The Lancet Neurology 2004 被引用: 1,061

  24. Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology

    著者: Tim Ripperger, Stefan Bielack, Arndt Borkhardt, Ines B. Brecht, Birgit Burkhardt, Gabriele Calaminus, Klaus‐Michael Debatin, Hedwig E. Deubzer, Uta Dirksen, Cornelia Eckert, Angelika Eggert, Miriam Erlacher, Gudrun Fleischhack, Michael C. Frühwald, Astrid Gnekow, Gudrun Goehring, Norbert Graf, Helmut Hanenberg, Julia Hauer, Barbara Hero, Simone Hettmer, Katja von Hoff, Martin A. Horstmann, Juliane Hoyer, Thomas Illig, Peter Kaatsch, Roland Kappler, Kornelius Kerl, Thomas Klingebiel, Udo Kontny, Uwe Kordes, Dieter Körholz, Ewa Kościelniak, Christof M. Kramm, Michaela Kuhlen, Andreas E. Kulozik, Britta Lamottke, Ivo Leuschner, Dietmar Lohmann, Andrea Meinhardt, Markus Metzler, Lüder Hinrich Meyer, Olga Moser, Michaela Nathrath, Charlotte M. Niemeyer, R. Nustede, Kristian W. Pajtler, Claudia Paret, Mareike Rasche, Dirk Reinhardt, Olaf Rieß, Alexandra Russo, Stefan Rutkowski, Brigitte Schlegelberger, Dominik T. Schneider, Reinhard Schneppenheim, Martin Schrappe, Christopher Schroeder, Dietrich von Schweinitz, Thorsten Simon, Monika Sparber‐Sauer, Claudia Spix, Martin Stanulla, Doris Steinemann, Brigitte Strahm, Petra Temming, Kathrin Thomay, André O. von Bueren, Peter Vorwerk, Olaf Witt, Marcin W. Włodarski, Willy Wössmann, Martin Zenker, Stefanie Zimmermann, Stefan M. Pfister, Christian P. Kratz - American Journal of Medical Genetics Part A 2017 被引用: 283