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Bernhard Horsthemke

1985–2024 年に発表

97
論文数
18,832
被引用数
79
h 指数
97
i10 指数

被引用数

Bernhard Horsthemke の年別被引用数1984 年: 被引用 6 件1985 年: 被引用 1 件1986 年: 被引用 3 件1987 年: 被引用 4 件1988 年: 被引用 8 件1989 年: 被引用 12 件1990 年: 被引用 8 件1991 年: 被引用 11 件1992 年: 被引用 8 件1993 年: 被引用 36 件1994 年: 被引用 48 件1995 年: 被引用 49 件1996 年: 被引用 96 件1997 年: 被引用 160 件1998 年: 被引用 124 件1999 年: 被引用 171 件2000 年: 被引用 167 件2001 年: 被引用 202 件2002 年: 被引用 133 件2003 年: 被引用 169 件2004 年: 被引用 144 件2005 年: 被引用 174 件2006 年: 被引用 148 件2007 年: 被引用 125 件2008 年: 被引用 135 件2009 年: 被引用 126 件2010 年: 被引用 170 件2011 年: 被引用 146 件2012 年: 被引用 143 件2013 年: 被引用 125 件2014 年: 被引用 146 件2015 年: 被引用 111 件2016 年: 被引用 135 件2017 年: 被引用 136 件2018 年: 被引用 137 件2019 年: 被引用 383 件2020 年: 被引用 370 件2021 年: 被引用 363 件2022 年: 被引用 261 件2023 年: 被引用 169 件2024 年: 被引用 273 件2025 年: 被引用 85 件2026 年: 被引用 1 件

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 1,785 件、この内訳の 26.8%イギリス: 引用元論文 626 件、この内訳の 9.4%ドイツ: 引用元論文 558 件、この内訳の 8.4%中国: 引用元論文 350 件、この内訳の 5.2%カナダ: 引用元論文 298 件、この内訳の 4.5%フランス: 引用元論文 296 件、この内訳の 4.4%オランダ: 引用元論文 283 件、この内訳の 4.2%イタリア: 引用元論文 237 件、この内訳の 3.6%オーストラリア: 引用元論文 198 件、この内訳の 3%日本: 引用元論文 192 件、この内訳の 2.9%スペイン: 引用元論文 177 件、この内訳の 2.6%ベルギー: 引用元論文 105 件、この内訳の 1.6%
0%26.8%その他 23.4%

機関

分野

  • Biochemistry, Genetics and Molecular Biology63.9%
  • Medicine28.9%
  • Neuroscience2.8%
  • Immunology and Microbiology1.2%
  • Computer Science0.8%
  • Agricultural and Biological Sciences0.8%
  • その他1.6%

トピック

  • Epigenetics and DNA Methylation10.1%
  • Genetic Syndromes and Imprinting7.8%
  • RNA modifications and cancer4.3%
  • Prenatal Screening and Diagnostics4.1%
  • Ocular Oncology and Treatments3.6%
  • Genetics and Neurodevelopmental Disorders2.6%
  • その他67.5%

共著者

全論文

検索で開く
  1. The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery

    著者: H.G. Stunnenberg, Sergio Abrignani, David J. Adams, Melanie de Almeida, Lucia Altucci, Viren Amin, Ido Amit, Stylianos E. Antonarakis, Samuel Aparício, Takahiro Arima, Laura Arrigoni, Rob J.W. Arts, Vahid Asnafi, Manel Esteller, Jae‐Bum Bae, Kevin Baßler, Stephan Beck, Benjamin E. Berkman, B Bernstein, Mikhail Bilenky, Adrian Bird, Christoph Bock, Bernhard O. Boehm, Guillaume Bourque, Charles E. Breeze, Benedikt Brors, David Bujold, Oliver S. Burren, Marion J.G. Bussemakers, Adam S. Butterworth, Elı́as Campo, Enrique Carrillo de Santa Pau, Lisa H. Chadwick, Kui Ming Chan, Wei Chen, Tom H. Cheung, Luca Chiapperino, Nak Hyen Choi, Ho‐Ryun Chung, Laura Clarke, Joseph M. Connors, Philippe Cronet, John Danesh, Manolis Dermitzakis, Gerard Drewes, Pawel Durek, Stephanie O. M. Dyke, Tomasz Dyląg, Connie J. Eaves, Peter Ebert, Roland Eils, Jürgen Eils, Catherine Ennis, Tariq Enver, Elise A. Feingold, Bärbel Felder, Anne C. Ferguson‐Smith, Jude Fitzgibbon, Paul Flicek, Roger Foo, Peter Fraser, Mattia Frontini, Eileen E. M. Furlong, Sitanshu Gakkhar, Nina Gasparoni, Gilles Gasparoni, Daniel H. Geschwind, Petar Glažar, Thomas Graf, Frank Grosveld, Xin‐Yuan Guan, Roderic Guigó, Marta Gut, Alf Hamann, Bok-Ghee Han, R. Alan Harris, Simon Heath, Kristian Helin, Jan G. Hengstler, Alireza Heravi‐Moussavi, Karl Herrup, Steven Hill, Jason A. Hilton, Benjamin C. Hitz, Bernhard Horsthemke, Ming Hu, Jooyeon Hwang, Nancy Y. Ip, Takashi Ito, Biola M. Javierre, Sasa Jenko, Thomas Jenuwein, Yann Joly, Steven J.M. Jones, Yae Kanai, Hee Gyung Kang, Aly Karsan, Alexandra K. Kiemer, Song Cheol Kim, Bong-Jo Kim ほか 130 名 - Cell 2016 被引用: 566

  2. Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

    著者: Marcel Martin, Lars Maßhöfer, Petra Temming, Sven Rahmann, Claudia H.D. Metz, Norbert Bornfeld, Johannes van de Nes, Ludger Klein‐Hitpaß, Alan G. Hinnebusch, Bernhard Horsthemke, Dietmar Lohmann, Michael Zeschnigk - Nature Genetics 2013 被引用: 533

  3. A critical view on transgenerational epigenetic inheritance in humans

    著者: Bernhard Horsthemke - Nature Communications 2018 被引用: 345

  4. Angelman syndrome — insights into a rare neurogenetic disorder

    著者: Karin Buiting, Charles A. Williams, Bernhard Horsthemke - Nature Reviews Neurology 2016 被引用: 400

  5. Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

    著者: Valerie Greger, Eberhard Passarge, Wolfgang H�pping, Elmar P. Messmer, Bernhard Horsthemke - Human Genetics 1989 被引用: 566

  6. Prognostic implications of monosomy 3 in uveal melanoma

    著者: N Bornfeld, Gabriele Prescher, R Becher, H Hirche, K-H Jöckel, Bernhard Horsthemke - The Lancet 1996 被引用: 766

  7. Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans

    著者: Louise E Docherty, Faisal I. Rezwan, Rebecca Poole, Claire Turner, Emma Kivuva, Eamonn R. Maher, Sarah Smithson, Julian Hamilton‐Shield, Michał Patalan, Maria Giżewska, Jarosław Peregud‐Pogorzelski, Jasmin Beygo, Karin Buiting, Bernhard Horsthemke, Lukas Soellner, Matthias Begemann, Thomas Eggermann, Emma L. Baple, Sahar Mansour, I. Karen Temple, Deborah Mackay - Nature Communications 2015 被引用: 204

  8. Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

    著者: Elsa Leitão, Christopher Schröder, Ilaria Parenti, Carine Dalle, Agnès Rastetter, Theresa Kühnel, Alma Kuechler, Sabine Kaya, Bénédicte Gérard, Élise Schaefer, Caroline Nava, Nathalie Drouot, Camille Engel, Juliette Piard, Bénédicte Duban‐Bedu, Laurent Villard, Alexander P.A. Stegmann, Els K. Vanhoutte, Job A.J. Verdonschot, Frank J. Kaiser, Frédéric Tran Mau‐Them, Marcello Scala, Pasquale Striano, Suzanna G.M. Frints, Emanuela Argilli, Elliott H. Sherr, Fikret Elder, Julien Buratti, Boris Keren, Cyril Mignot, Delphine Héron, Jean‐Louis Mandel, Jozef Gécz, Vera M. Kalscheuer, Bernhard Horsthemke, Amélie Piton, Christel Depienne - Nature Communications 2022 被引用: 45

  9. N6-Adenosine Methylation in MiRNAs

    著者: Tea Berulava, Sven Rahmann, Katrin Rademacher, L. Klein‐Hitpass, Bernhard Horsthemke - PLoS ONE 2015 被引用: 142

  10. Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

    著者: Rahel T. Florian, Florian Kraft, Elsa Leitão, Sabine Kaya, Stephan Klebe, Éloi Magnin, Anne‐Fleur van Rootselaar, Julien Buratti, Theresa Kühnel, Christopher Schröder, Sebastian Gießelmann, Nikolai Tschernoster, Janine Altmueller, Anaide Lamiral, Boris Keren, Caroline Nava, Delphine Bouteiller, Sylvie Forlani, Ludmila Jornéa, Regina Kubica, Tao Ye, Damien Plassard, Bernard Jost, Vincent Meyer, Jean‐François Deleuze, Yannick Delpu, Mario Davide Maria Avarello, Lisanne S. Vijfhuizen, Gabrielle Rudolf, Édouard Hirsch, Thessa Kroes, Philipp S. Reif, Felix Rosenow, Christos Ganos, Marie Vidailhet, Lionel Thivard, Alexandre Mathieu, Thomas Bourgeron, Ingo Kurth, Haloom Rafehi, Laura Steenpaß, Bernhard Horsthemke, Samuel F. Berkovic, Francesca Bisulli, Francesco Brancati, Laura Canafoglia, Giorgio Casari, Renzo Guerrini, Hiroyuki Ishiura, Laura Licchetta, Davide Mei, Tommaso Pippucci, Lynette G. Sadleir, Ingrid E. Scheffer, Pasquale Striano, Paolo Tinuper, Shoji Tsuji, Federico Zara, Éric Leguern, Karl Martin Klein, Pierre Labauge, Mark F. Bennett, Melanie Bahlo, Jozef Gécz, Mark Corbett, Marina A.J. Tijssen, Arn M. J. M. van den Maagdenberg, Christel Depienne - Nature Communications 2019 被引用: 170

  11. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

    著者: Jérôme Cavaillé, Karin Buiting, Martin Kiefmann, Marc Lalande, Camilynn I. Brannan, Bernhard Horsthemke, Jean‐Pierre Bachellerie, Jürgen Brosius, Alexander Hüttenhofer - National Academy of Sciences, Proceedings of the National Academy of Sciences 2000 被引用: 597

  12. A germ cell‐specific ageing pattern in otherwise healthy men

    著者: Sandra Laurentino, Jann‐Frederik Cremers, Bernhard Horsthemke, Frank Tüttelmann, K. Czeloth, Michael Zitzmann, Eva Pohl, Sven Rahmann, Christopher Schröder, Sven Berres, Klaus Redmann, Claudia Krallmann, Stefan Schlatt, Sabine Kliesch, Jörg Gromoll - Aging Cell 2020 被引用: 60

  13. Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

    著者: Andreas Poplinski, Frank Tüttelmann, Deniz Kanber, Bernhard Horsthemke, Jörg Gromoll - International Journal of Andrology 2009 被引用: 235

  14. Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I

    著者: Parastoo Momeni, Gernot Glöckner, Olaf Schmidt, D. von Holtum, Beate Albrecht, Gabriele Gillessen-Kaesbach, Raoul C. M. Hennekam, Peter Meinecke, Bernhard Zabel, André Rosenthal, Bernhard Horsthemke, Hermann‐Josef Lüdecke - Nature Genetics 2000 被引用: 374

  15. A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

    著者: Deniz Kanber, Jacques C. Giltay, Dagmar Wieczorek, Corinna Zogel, Ron Hochstenbach, Almuth Caliebe, Alma Kuechler, Bernhard Horsthemke, Karin Buiting - European Journal of Human Genetics 2008 被引用: 136

  16. The obesity-associated SNPs in intron 1 of the FTO gene affect primary transcript levels

    著者: Tea Berulava, Bernhard Horsthemke - European Journal of Human Genetics 2010 被引用: 198

  17. Mechanisms of imprinting of the Prader–Willi/Angelman region

    著者: Bernhard Horsthemke, Joseph Wagstaff - American Journal of Medical Genetics Part A 2008 被引用: 321

  18. Epigenetic dynamics of monocyte-to-macrophage differentiation

    著者: Stefan Wallner, Christopher Schröder, Elsa Leitão, Tea Berulava, Claudia Haak, Daniela Beißer, Sven Rahmann, Andreas S. Richter, Thomas Manke, Ulrike Bönisch, Laura Arrigoni, Sebastian Fröhler, Filippos Klironomos, Wei Chen, Nikolaus Rajewsky, Fabian Müller, Peter Ebert, Thomas Lengauer, Matthias Barann, Philip Rosenstiel, Gilles Gasparoni, Karl Nordström, Jörn Walter, Benedikt Brors, Gideon Zipprich, Bärbel Felder, Ludger Klein‐Hitpaß, Corinna Attenberger, Gerd Schmitz, Bernhard Horsthemke - Epigenetics & Chromatin 2016 被引用: 96

  19. Lasp1 regulates adherens junction dynamics and fibroblast transformation in destructive arthritis

    著者: Denise Beckmann, Anja Römer-Hillmann, Annika Krause, Uwe Hansen, Corinna Wehmeyer, Johanna Intemann, David J. J. de Gorter, Berno Dankbar, Jan Hillen, Marianne Heitzmann, Isabell Begemann, Milos Galic, Toni Weinhage, Dirk Foell, Rizi Ai, Joachim Kremerskothen, Hans P. Kiener, Sylvia Müller, Thomas Kamradt, Christopher Schröder, Elsa Leitão, Bernhard Horsthemke, Philip Rosenstiel, Karl Nordström, Gilles Gasparoni, Nina Gasparoni, Jörn Walter, Na Li, Xinyi Yang, Ho‐Ryun Chung, Hermann Pavenstädt, Nico Lindemann, Hans‐Joachim Schnittler, Wei Wang, Gary S. Firestein, Thomas Pap, Adelheid Korb‐Pap - Nature Communications 2021 被引用: 30

  20. Early-set POMC methylation variability is accompanied by increased risk for obesity and is addressable by MC4R agonist treatment

    著者: Lara Lechner, Robert Opitz, Matt J. Silver, Philipp Krabusch, Andrew M. Prentice, Martha S. Field, Harald Stachelscheid, Elsa Leitão, Christopher Schröder, Valeria Fernández Vallone, Bernhard Horsthemke, Karl‐Heinz Jöckel, Börge Schmidt, Markus M. Nöthen, Per Hoffmann, Stefan Herms, Patrick W. Kleyn, Matthias Megges, Ulrike Blume‐Peytavi, Katja Weiß, Knut Mai, Oliver Blankenstein, Benedikt Obermayer, Susanna Wiegand, Peter Kühnen - Science Translational Medicine 2023 被引用: 17

  21. Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects

    著者: Gerald F. Cox, Joachim Bürger, Va Lip, Ulrike Mau, Karl Sperling, Bai‐Lin Wu, Bernhard Horsthemke - The American Journal of Human Genetics 2002 被引用: 705

  22. Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

    著者: Stefanie Birnbaum, Kerstin U. Ludwig, Heiko Reutter, Stefan Herms, Michael Steffens, Michele Rubini, Carlotta Baluardo, Melissa Ferrian, Nilma Almeida de Assis, Margrieta A Alblas, Sandra Barth, Jan Freudenberg, Carola Lauster, Gül Schmidt, Martin Scheer, Bert Braumann, Stefaan Bergé, Rudolf H. Reich, Franziska Schiefke, Alexander Hemprich, Simone Pötzsch, Régine P.M. Steegers‐Theunissen, Bernd Pötzsch, Susanne Moebus, Bernhard Horsthemke, Franz‐Josef Kramer, Thomas F. Wienker, Peter Mossey, Peter Propping, Sven Cichon, Per Hoffmann, Michael Knapp, Markus M. Nöthen, Elisabeth Mangold - Nature Genetics 2009 被引用: 479

  23. A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

    著者: Eugene M. Rinchik, Scott J. Bultman, Bernhard Horsthemke, Seung‐Taek Lee, Kathleen M. Strunk, Richard A. Spritz, Karen M. Avidano, M T Jong, Robert D. Nicholls - Nature 1993 被引用: 415

  24. Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

    著者: Tohru Ohta, Todd A. Gray, Peter K. Rogan, Karin Buiting, James M. Gabriel, Shinji Saitoh, Bethi Muralidhar, B. Bilienska, Małgorzata Krajewska‐Walasek, Daniel J. Driscoll, Bernhard Horsthemke, Merlin G. Butler, Robert D. Nicholls - The American Journal of Human Genetics 1999 被引用: 276