Holger Prokisch
1997–2025 年に発表
- 232
- 論文数
- 37,978
- 被引用数
- 100
- h 指数
- 216
- i10 指数
被引用数
引用元
国・地域
機関
- Harvard University0.8%
- Helmholtz Zentrum München0.7%
- Inserm0.6%
- University College London0.5%
- Technical University of Munich0.5%
- Broad Institute0.5%
- その他96.4%
分野
- Biochemistry, Genetics and Molecular Biology51.6%
- Medicine37.6%
- Neuroscience3.8%
- Immunology and Microbiology1.9%
- Nursing1.2%
- Environmental Science0.8%
- その他3.1%
トピック
- Ferroptosis and cancer prognosis5.6%
- Mitochondrial Function and Pathology4.8%
- RNA modifications and cancer4.3%
- Genetic Associations and Epidemiology4%
- Epigenetics and DNA Methylation3.3%
- Metabolism and Genetic Disorders2.6%
- その他75.4%
共著者
- Thomas Meitinger61
- Tobias B. Haack51
- Tim M. Strom41
- Johannes A. Mayr33
- Robert Kopajtich31
- Peter Freisinger27
- Thomas Klopstock25
- Felix Distelmaier20
- Christian Gieger19
- Daniele Ghezzi18
- Laura S. Kremer18
- Elisabeth Graf17
- Robert W. Taylor17
- Saskia B. Wortmann17
- Christian Herder16
- Katharina Schramm15
- Sarah L. Stenton15
- Annette Peters14
- Arcangela Iuso14
- Lea D. Schlieben14
- René G. Feichtinger14
- Thomas Wieland14
- Uwe Ahting14
- Matias Wagner13
全論文
- ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition
著者: Sebastian Doll, Bettina Proneth, Yulia Y. Tyurina, Elena Panzilius, Sho Kobayashi, Irina Ingold, Martin Irmler, Johannes Beckers, Michaela Aichler, Axel Walch, Holger Prokisch, Dietrich Trümbach, Gaowei Mao, Feng Qu, Hülya Bayır, Joachim Füllekrug, Christina Scheel, Wolfgang Wurst, Joel Schick, Valerian E. Kagan, José Pedro Friedmann Angeli, Marcus Conrad - Nature Chemical Biology 2016 被引用: 4,056
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
著者: Urmo Võsa, Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng, Holger Kirsten, Ashis Saha, Roman Kreuzhuber, Seyhan Yazar, Harm Brugge, Roy Oelen, Dylan H. de Vries, Monique G.P. van der Wijst, Silva Kasela, Natalia Pervjakova, Isabel Alves, Marie-Julie Favé, Mawussé Agbessi, Mark Christiansen, Rick Jansen, Ilkka Seppälä, Tong Lin, Alexander Teumer, Katharina Schramm, Gibran Hemani, Joost Verlouw, Hanieh Yaghootkar, Reyhan Sönmez Flitman, Andrew Brown, Viktorija Kukushkina, Anette Kalnapenkis, Sina Rüeger, Eleonora Porcu, Jaanika Kronberg, Johannes Kettunen, Bernett Lee, Futao Zhang, Ting Qi, José Alquicira-Hernández, Wibowo Arindrarto, Frank Beutner, Peter A.C. ’t Hoen, Joyce B. J. van Meurs, Jenny van Dongen, Maarten van Iterson, Morris A. Swertz, Marc Jan Bonder, Julia Dmitrieva, Mahmoud Elansary, Benjamin P. Fairfax, Michel Georges, Bastiaan T. Heijmans, Alex W. Hewitt, Mika Kähönen, Yungil Kim, Julian C. Knight, Péter Kovács, Knut Krohn, Shuang� Li, Markus Loeffler, Urko M. Marigorta, Hailang Mei, Yukihide Momozawa, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Jonathan K. Pritchard, Olli T. Raitakari, Olaf Rötzschke, P. Eline Slagboom, Coen D.A. Stehouwer, Michael Stümvoll, Patrick Sullivan, Peter A.C. ’t Hoen, Joachim Thiery, Anke Tönjes, Jenny van Dongen, Maarten van Iterson, Jan H. Veldink, Uwe Völker, Robert Warmerdam, Cisca Wijmenga, Morris A. Swertz, Anand Kumar Andiappan, Grant W. Montgomery, Samuli Ripatti, Markus Perola, Zoltán Kutalik, Emmanouil T. Dermitzakis, Sven Bergmann, Timothy M. Frayling, Joyce B. J. van Meurs, Holger Prokisch, Habibul Ahsan, Brandon L. Pierce, Terho Lehtimäki, Dorret I. Boomsma, Bruce M. Psaty ほか 14 名 - Nature Genetics 2021 被引用: 2,182
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes
著者: Angli Xue, Yang Wu, Zhihong Zhu, Futao Zhang, Kathryn E. Kemper, Zhili Zheng, Loïc Yengo, Luke R. Lloyd‐Jones, Julia Sidorenko, Yeda Wu, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Philip Awadalla, Alexis Battle, Frank Beutner, Marc Jan Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, Tõnu Esko, Marie-Julie Favé, Lude Franke, Timothy M. Frayling, Sina A. Gharib, Gregory Gibson, Gibran Hemani, Rick Jansen, Mika Kähönen, Anette Kalnapenkis, Silva Kasela, Johannes Kettunen, Yungil Kim, Holger Kirsten, Péter Kovács, Knut Krohn, Jaanika Kronberg-Guzman, Viktorija Kukushkina, Zoltán Kutalik, Bernett Lee, Terho Lehtimäki, Markus Loeffler, Urko M. Marigorta, Andres Metspalu, Lili Milani, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Markus Perola, Natalia Pervjakova, Brandon L. Pierce, Joseph E. Powell, Holger Prokisch, Bruce M. Psaty, Olli T. Raitakari, Susan M. Ring, Samuli Ripatti, Olaf Rötzschke, Sina Rüeger, Ashis Saha, Markus Scholz, Katharina Schramm, Ilkka Seppälä, Michael Stümvoll, Patrick Sullivan, Alexander Teumer, Joachim Thiery, Tong Lin, Anke Tönjes, Jenny van Dongen, Joyce B. J. van Meurs, Joost Verlouw, Uwe Völker, Urmo Võsa, Hanieh Yaghootkar, Biao Zeng, Allan F. McRae, Peter M. Visscher, Jian Zeng, Jian Yang - Nature Communications 2018 被引用: 1,015
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
著者: Simone Wahl, Alexander Drong, Benjamin Lehne, Marie Loh, William R. Scott, Sonja Kunze, Pei-Chien Tsai, Janina S. Ried, Weihua Zhang, Youwen Yang, Sili Tan, Giovanni Fiorito, Lude Franke, Simonetta Guarrera, Silva Kasela, Jennifer Kriebel, Rebecca C. Richmond, Marco Adamo, Uzma Afzal, Mika Ala‐Korpela, Benedetta Albetti, Ole Ammerpohl, Jane F. Apperley, Marian Beekman, Pier Alberto Bertazzi, S. Lucas Black, Christine Blancher, Marc Jan Bonder, Mario Brosch, Maren Carstensen‐Kirberg, Anton J. M. de Craen, Simon de Lusignan, Abbas Dehghan, Mohamed Elkalaawy, Krista Fischer, Oscar H. Franco, Tom R. Gaunt, Jochen Hampe, Majid Hashemi, Aaron Isaacs, Andrew Jenkinson, Sujeet Jha, Norihiro Kato, Vittorio Krogh, Michael Laffan, Christa Meisinger, Thomas Meitinger, Zuan Yu Mok, Valeria Motta, Hong Kiat Ng, Zacharoula Nikolakopoulou, Georgios Nteliopoulos, Salvatore Panico, Natalia Pervjakova, Holger Prokisch, Wolfgang Rathmann, Michael Roden, Federica Rota, Michelle Ann Rozario, Johanna K. Sandling, Clemens Schafmayer, Katharina Schramm, Reiner Siebert, P. Eline Slagboom, Pasi Soininen, Lisette Stolk, Konstantin Strauch, E Shyong Tai, Letizia Tarantini, Barbara Thorand, Ettje F. Tigchelaar, Rosario Tumino, André G. Uitterlinden, Cornelia M. van Duijn, Joyce B. J. van Meurs, Paolo Vineis, Ananda R. Wickremasinghe, Cisca Wijmenga, Tsun-Po Yang, Wei Yuan, Alexandra Zhernakova, Rachel L. Batterham, George Davey Smith, Panos Deloukas, Bastiaan T. Heijmans, Christian Herder, Albert Hofman, Cecilia M. Lindgren, Lili Milani, Pim van der Harst, Annette Peters, Thomas Illig, Caroline L. Relton, Mélanie Waldenberger, Marjo‐Riitta Järvelin, Valentina Bollati, Richie Soong, Tim D. Spector, James Scott, Mark I. McCarthy ほか 7 名 - Nature 2016 被引用: 1,032
- Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood
著者: Ting Qi, Yang Wu, Jian Zeng, Futao Zhang, Angli Xue, Longda Jiang, Zhihong Zhu, Kathryn E. Kemper, Loïc Yengo, Zhili Zheng, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Philip Awadalla, Alexis Battle, Frank Beutner, Marc Jan Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, Tõnu Esko, Marie-Julie Favé, Lude Franke, Timothy M. Frayling, Sina A. Gharib, Gregory Gibson, Gibran Hemani, Rick Jansen, Mika Kähönen, Anette Kalnapenkis, Silva Kasela, Johannes Kettunen, Yungil Kim, Holger Kirsten, Péter Kovács, Knut Krohn, Jaanika Kronberg-Guzman, Viktorija Kukushkina, Zoltán Kutalik, Bernett Lee, Terho Lehtimäki, Markus Loeffler, Urko M. Marigorta, Andres Metspalu, Lili Milani, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Markus Perola, Natalia Pervjakova, Brandon L. Pierce, Joseph E. Powell, Holger Prokisch, Bruce M. Psaty, Olli T. Raitakari, Susan M. Ring, Samuli Ripatti, Olaf Rötzschke, Sina Rüeger, Ashis Saha, Markus Scholz, Katharina Schramm, Ilkka Seppälä, Michael Stümvoll, Patrick Sullivan, Alexander Teumer, Joachim Thiery, Tong Lin, Anke Tönjes, Jenny van Dongen, Joyce B. J. van Meurs, Joost Verlouw, Uwe Völker, Urmo Võsa, Hanieh Yaghootkar, Biao Zeng, Riccardo E. Marioni, Grant W. Montgomery, Ian J. Deary, Naomi R. Wray, Peter M. Visscher, Allan F. McRae, Jian Yang - Nature Communications 2018 被引用: 466
- OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data
著者: Felix Brechtmann, Christian Mertes, Agnė Matusevičiūtė, Vicente A. Yépez, Žiga Avsec, Maximilian Herzog, Daniel M. Bader, Holger Prokisch, Julien Gagneur - The American Journal of Human Genetics 2018 被引用: 232
- Detection of aberrant gene expression events in RNA sequencing data
著者: Vicente A. Yépez, Christian Mertes, Michaela Müller, Daniela Klaproth-Andrade, Leonhard Wachutka, Laure Frésard, Mirjana Gušić, Ines F. Scheller, Patricia F. Goldberg, Holger Prokisch, Julien Gagneur - Nature Protocols 2021 被引用: 159
- Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
著者: Eleonora Porcu, Sina Rüeger, Kaido Lepik, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Wibowo Arindrarto, Philip Awadalla, Alexis Battle, Frank Beutner, Marc Jan Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, Tõnu Esko, Marie-Julie Favé, Lude Franke, Timothy M. Frayling, Sina A. Gharib, Gregory Gibson, Bastiaan T. Heijmans, Gibran Hemani, Rick Jansen, Mika Kähönen, Anette Kalnapenkis, Silva Kasela, Johannes Kettunen, Yungil Kim, Holger Kirsten, Péter Kovács, Knut Krohn, Jaanika Kronberg-Guzman, Viktorija Kukushkina, Bernett Lee, Terho Lehtimäki, Markus Loeffler, Urko M. Marigorta, Hailang Mei, Lili Milani, Grant W. Montgomery, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Markus Perola, Natalia Pervjakova, Brandon L. Pierce, Joseph E. Powell, Holger Prokisch, Bruce M. Psaty, Olli T. Raitakari, Samuli Ripatti, Olaf Rötzschke, Ashis Saha, Markus Scholz, Katharina Schramm, Ilkka Seppälä, P. Eline Slagboom, Coen D.A. Stehouwer, Michael Stümvoll, Patrick Sullivan, Peter A.C. ’t Hoen, Alexander Teumer, Joachim Thiery, Tong Lin, Anke Tönjes, Jenny van Dongen, Maarten van Iterson, Joyce B. J. van Meurs, Jan H. Veldink, Joost Verlouw, Peter M. Visscher, Uwe Völker, Urmo Võsa, Harm-Jan Westra, Cisca Wijmenga, Hanieh Yaghootkar, Jian Yang, Biao Zeng, Futao Zhang, Wibowo Arindrarto, Marian Beekman, Dorret I. Boomsma, Jan Bot, Joris Deelen, Patrick Deelen, Lude Franke, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Bert A. Hofman, Jouke J. Hottenga, Aaron Isaacs, Marc Jan Bonder, P. Mila Jhamai, Rick Jansen, Szymon M. Kiełbasa, Nico Lakenberg, René Luijk ほか 35 名 - Nature Communications 2019 被引用: 347
- Deficient methylation and formylation of mt-tRNAMet wobble cytosine in a patient carrying mutations in NSUN3
著者: Lindsey Van Haute, Sabine Dietmann, Laura S. Kremer, Shobbir Hussain, Sarah F. Pearce, Christopher A. Powell, Joanna Rorbach, Rebecca Lantaff, Sandra Blanco, Sascha Sauer, Urania Kotzaeridou, Georg F. Hoffmann, Yasin Memari, Anja Kolb‐Kokocinski, Richard Durbin, Johannes A. Mayr, Michaela Frye, Holger Prokisch, Michal Minczuk - Nature Communications 2016 被引用: 255
- Monogenic variants in dystonia: an exome-wide sequencing study
著者: Michael Zech, Robert Jech, Sylvia Boesch, Matěj Škorvánek, Sandrina Weber, Matias Wagner, Chen Zhao, Angela Jochim, Ján Necpál, Yasemin Dincer, Katharina Vill, Felix Distelmaier, Malgorzata Stoklosa, Martin Krenn, Stephan Grunwald, Tobias Bock-Bierbaum, Anna Fečíková, Petra Havránková, Jan Roth, Iva Příhodová, Miriam Adamovičová, Olga Ulmanová, Karel Bechyně, Pavlína Danhofer, Branislav Veselý, Vladimír Haň, Petra Pavelekova, Zuzana Gdovinová, Tobias Mantel, Tobias Meindl, Alexandra Sitzberger, Sebastian Schröder, Astrid Blaschek, Timo Roser, Michaela Bonfert, Edda Haberlandt, Barbara Plecko, Birgit Leineweber, Steffen Berweck, T. Herberhold, Berthold Langguth, Jana Švantnerová, Michal Minár, Gonzalo Alonso Ramos-Rivera, Monica H. Wojcik, Sander Pajusalu, Katrin Õunap, Ulrich A. Schatz, Laura Pölsler, Ivan Milenković, Franco Laccone, Veronika Pilshofer, Roberto Colombo, Steffi Patzer, Arcangela Iuso, Julia Vera, M. Troncoso, Fang Fang, Holger Prokisch, Friederike Wilbert, Matthias Eckenweiler, Elisabeth Graf, Dominik S. Westphal, Korbinian M. Riedhammer, Theresa Brunet, Bader Alhaddad, Riccardo Berutti, Tim M. Strom, Martin Hecht, Matthias Baumann, Marc E. Wolf, Aida Telegrafi, Richard Person, Francisca Millan Zamora, Lindsay B. Henderson, David Weise, Thomas Musacchio, Jens Volkmann, Anna Szuto, Jessica Becker, Kirsten Cremer, Thomas Sycha, Fritz Zimprich, Verena Kraus, Christine Makowski, Pedro Gonzalez‐Alegre, Tanya Bardakjian, Laurie J. Ozelius, Annalisa Vetro, Renzo Guerrini, Esther M. Maier, Ingo Borggraefe, Alice Kuster, Saskia B. Wortmann, Annette Hackenberg, Robert Steinfeld, Birgit Assmann, Christian Staufner, Thomas Opladen, Evžen Růžička ほか 11 名 - The Lancet Neurology 2020 被引用: 214
- Systematic identification of trans eQTLs as putative drivers of known disease associations
著者: Harm-Jan Westra, Marjolein J. Peters, Tōnu Esko, Hanieh Yaghootkar, Claudia Schurmann, Johannes Kettunen, Mark Christiansen, Benjamin P. Fairfax, Katharina Schramm, Joseph E. Powell, Alexandra Zhernakova, Daria V. Zhernakova, Jan H. Veldink, Leonard H. van den Berg, Juha Karjalainen, Sebo Withoff, André G. Uitterlinden, Albert Hofman, Fernando Rivadeneira, Peter A.C. ’t Hoen, Eva Reinmaa, Krista Fischer, Mari Nelis, Lili Milani, David Melzer, Luigi Ferrucci, Andrew Singleton, Dena Hernández, Michael A. Nalls, Georg Homuth, Matthias Nauck, Dörte Radke, Uwe Völker, Markus Perola, Veikko Salomaa, Jennifer A. Brody, Astrid M. Suchy‐Dicey, Sina A. Gharib, Daniel A. Enquobahrie, Thomas Lumley, Grant W. Montgomery, Seiko Makino, Holger Prokisch, Christian Herder, Michael Roden, Harald Grallert, Thomas Meitinger, Konstantin Strauch, Yang Li, Ritsert C. Jansen, Peter M. Visscher, Julian C. Knight, Bruce M. Psaty, Samuli Ripatti, Alexander Teumer, Timothy M. Frayling, Andres Metspalu, Joyce B. J. van Meurs, Lude Franke - Nature Genetics 2013 被引用: 1,769
- Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances
著者: Paul R. H. J. Timmers, Ninon Mounier, Kristi Läll, Krista Fischer, Ning Zheng, Xiao Feng, Andrew D. Bretherick, David W. Clark, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Philip Awadalla, Alexis Battle, MJ Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, Jenny van Dongen, T Esko, Marie-Julie Favé, Lude Franke, T Frayling, Sina A. Gharib, Greg Gibson, G Hemani, Rick Jansen, A Kalnapenkis, Silva Kasela, Jarno L. T. Kettunen, Y Kim, Holger Kirsten, Péter Kovács, Knut Krohn, J Kronberg-Guzman, Viktorija Kukushkina, Zoltán Kutalik, Mika Kähönen, B Lee, Terho Lehtimäki, Markus Loeffler, Urko M. Marigorta, Andres Metspalu, Joyce B. J. van Meurs, Lili Milani, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Markus Perola, Natalia Pervjakova, Brandon L. Pierce, Joseph E. Powell, Holger Prokisch, BM Psaty, Olli Raitakari, Susan M. Ring, Samuli Ripatti, Olaf Rötzschke, Sina Rüeger, A Saha, Markus Scholz, Katharina Schramm, Ilkka Seppälä, Michael Stümvoll, Patrick F. Sullivan, Alexander Teumer, Joachim Thiery, L Tong, Anke Tönjes, Joost Verlouw, Peter M. Visscher, Urmo Võsa, Uwe Völker, Hanieh Yaghootkar, J Yang, Biao Zeng, F Zhang, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Philip Awadalla, A Battle, MJ Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, J van Dongen, T Esko, Marie-Julie Favé, Lude Franke, T Frayling, Sina A. Gharib, G Gibson, G Hemani, Rick Jansen, A Kalnapenkis ほか 55 名 - eLife 2019 被引用: 311
- Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study
著者: John C. Chambers, Marie Loh, Benjamin Lehne, Alexander Drong, Jennifer Kriebel, Valeria Motta, Simone Wahl, Hannah R. Elliott, Federica Rota, William R. Scott, Weihua Zhang, Sian-Tsung Tan, Gianluca Campanella, Marc Chadeau‐Hyam, Loïc Yengo, Rebecca C. Richmond, Martyna Adamowicz‐Brice, Uzma Afzal, Kiymet Bozaoglu, Zuan Yu Mok, Hong Kiat Ng, François Pattou, Holger Prokisch, Michelle Ann Rozario, Letizia Tarantini, James Abbott, Mika Ala‐Korpela, Benedetta Albetti, Ole Ammerpohl, Pier Alberto Bertazzi, Christine Blancher, Robert Caïazzo, John Danesh, Tom R. Gaunt, Simon de Lusignan, Christian Gieger, Thomas Illig, Sujeet Jha, Simon Jones, Jeremy B. M. Jowett, Antti J. Kangas, Anuradhani Kasturiratne, Norihiro Kato, Navaratnam Kotea, Sudhir Kowlessur, Janne Pitkäniemi, Prakash P Punjabi, Danish Saleheen, Clemens Schafmayer, Pasi Soininen, E Shyong Tai, Barbara Thorand, Jaakko Tuomilehto, Ananda R. Wickremasinghe, Soterios Α. Kyrtopoulos, Timothy J. Aitman, Christian Herder, Jochen Hampe, Stéphane Cauchi, Caroline L. Relton, Philippe Froguel, Richie Soong, Paolo Vineis, Marjo‐Riitta Järvelin, James A. Scott, Harald Grallert, Valentina Bollati, Paul Elliott, Mark I. McCarthy, Jaspal S. Kooner - The Lancet Diabetes & Endocrinology 2015 被引用: 544
- Differences between Human Plasma and Serum Metabolite Profiles
著者: Zhonghao Yu, Gabi Kastenmüller, Ying He, Petra Belcredi, Gabriele Möller, Cornelia Prehn, Joaquim Mendes, Simone Wahl, Werner Roemisch‐Margl, Uta Ceglarek, Alexey Polonikov, Norbert Dahmen, Holger Prokisch, Lu Xie, Yixue Li, H-Erich Wichmann, Annette Peters, Florian Kronenberg, Karsten Suhre, Jerzy Adamski, Thomas Illig, Rui Wang‐Sattler - PLoS ONE 2011 被引用: 490
- Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia
著者: Karin Tuschl, Esther Meyer, Leonardo E. Valdivia, Ningning Zhao, Chris Dadswell, Alaa Abdul‐Sada, Christina Hung, Michael A. Simpson, W.K. Chong, Thomas S. Jacques, Randy Woltjer, Simon Eaton, Allison Gregory, Lynn Sanford, Eleanna Kara, Henry Houlden, Stephan M. Cuno, Holger Prokisch, Lorella Valletta, Valeria Tiranti, Rasha Younis, Eamonn Maher, John Spencer, Ania Straatman‐Iwanowska, Paul Gissen, Laila Selim, Guillem Pintos‐Morell, Wifredo Coroleu-Lletget, Shekeeb S. Mohammad, Sangeetha Yoganathan, Russell C. Dale, Maya Thomas, Jason Rihel, Olaf A. Bodamer, Caroline Enns, Susan J. Hayflick, Peter T. Clayton, Philippa B. Mills, Manju A. Kurian, Stephen W. Wilson - Nature Communications 2016 被引用: 323
- Genetics of mitochondrial diseases: Identifying mutations to help diagnosis
著者: Sarah L. Stenton, Holger Prokisch - EBioMedicine 2020 被引用: 267
- Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function
著者: Johann S. Hawe, Rory Wilson, Katharina Schmid, Li Zhou, Lakshmi Narayanan Lakshmanan, Benjamin Lehne, Brigitte Kühnel, William R. Scott, Matthias Wielscher, Yik Weng Yew, Clemens Baumbach, Dominic Paul Lee, Eirini Marouli, Manon Bernard, Liliane Pfeiffer, Pamela R. Matías‐García, Matias Autio, Stéphane Bourgeois, Christian Herder, Ville Karhunen, Thomas Meitinger, Holger Prokisch, Wolfgang Rathmann, Michael Roden, Sylvain Sebért, Jean Shin, Konstantin Strauch, Weihua Zhang, Wilson Lek Wen Tan, Stefanie M. Hauck, Juliane Merl‐Pham, Harald Grallert, Eudes G. V. Barbosa, Kourosh R. Ahmadi, Chrysanthi Ainali, Amy Barrett, Véronique Bataille, Jordana T. Bell, Alfonso Buil, Emmanouil T. Dermitzakis, Antigone S. Dimas, Richard Durbin, Daniel Glass, Elin Grundberg, Neelam Hassanali, Åsa K. Hedman, Catherine Ingle, David A. Knowles, Maria Krestyaninova, Cecilia M. Lindgren, Christopher Lowe, Mark I. McCarthy, Eshwar Meduri, Paola Di Meglio, Josine L. Min, Stephen B. Montgomery, Frank O. Nestlé, Alexandra C. Nica, James Nisbet, Stephen O’Rahilly, Leopold Parts, Simon Potter, Johanna K. Sandling, Magdalena Sekowska, So–Youn Shin, Kerrin S. Small, Nicole Soranzo, Tim D. Spector, Gabriela Surdulescu, Mary E. Travers, Loukia Tsaprouni, Sophia Tsoka, Alicja Wilk, Tsun-Po Yang, Krina T. Zondervan, Thomas Illig, Annette Peters, Tomáš Paus, Zdenka Pausová, Panos Deloukas, Roger Foo, Marjo‐Riitta Järvelin, Jaspal S. Kooner, Marie Loh, Matthias Heinig, Christian Gieger, Mélanie Waldenberger, John C. Chambers - Nature Genetics 2022 被引用: 172
- Aberrant splicing prediction across human tissues
著者: Nils Wagner, Muhammed Hasan Çelik, Florian R. Hölzlwimmer, Christian Mertes, Holger Prokisch, Vicente A. Yépez, Julien Gagneur - Nature Genetics 2023 被引用: 95
- DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases
著者: WHI-EMPC Investigators, Symen Ligthart, CHARGE epigenetics of Coronary Heart Disease, Carola Marzi, Stella Aslibekyan, Michael Mendelson, Karen N. Conneely, Toshiko Tanaka, Elena Colicino, Lindsay L. Waite, Roby Joehanes, Weihua Guan, Jennifer A. Brody, Cathy E. Elks, Riccardo E. Marioni, Min A. Jhun, Golareh Agha, Jan Bressler, Cavin Ward‐Caviness, Brian H. Chen, Tianxiao Huan, Kelly M. Bakulski, Elias Salfati, Giovanni Fiorito, Simone Wahl, Katharina Schramm, Jin Sha, Dena Hernández, Allan C. Just, Jennifer A. Smith, Nona Sotoodehnia, Luke C. Pilling, James S. Pankow, Philip S. Tsao, Chunyu Liu, Wei Zhao, Simonetta Guarrera, Vasiliki Michopoulos, Alicia K. Smith, Marjolein J. Peters, David Melzer, Pantel Vokonas, Myriam Fornage, Holger Prokisch, Joshua C. Bis, Audrey Y. Chu, Christian Herder, Harald Grallert, Chen Yao, Sonia Shah, Allan F. McRae, Honghuang Lin, Steve Horvath, M. Daniele Fallin, Albert Hofman, Nicholas J. Wareham, Kerri L. Wiggins, Andrew P. Feinberg, John M. Starr, Peter M. Visscher, Joanne M. Murabito, Sharon L. R. Kardia, Devin Absher, Elisabeth B. Binder, Andrew B. Singleton, Stefania Bandinelli, Annette Peters, Mélanie Waldenberger, Giuseppe Matullo, Joel Schwartz, Ellen W. Demerath, André G. Uitterlinden, Joyce B. J. van Meurs, Oscar H. Franco, Yii‐Der Ida Chen, Daniel Levy, Stephen T. Turner, Ian J. Deary, Kerry J. Ressler, Josée Dupuis, Luigi Ferrucci, Ken K. Ong, Themistocles L. Assimes, Eric Boerwinkle, Wolfgang Köenig, Donna K. Arnett, Andrea Baccarelli, Emelia J. Benjamin, Abbas Dehghan - Genome biology 2016 被引用: 340
- Detection of aberrant splicing events in RNA-seq data using FRASER
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