litlas
ログインアカウント作成

Miikka Vikkula

1972–2025 年に発表

136
論文数
24,155
被引用数
83
h 指数
128
i10 指数

被引用数

Miikka Vikkula の年別被引用数1955 年: 被引用 1 件1972 年: 被引用 1 件1983 年: 被引用 1 件1984 年: 被引用 1 件1990 年: 被引用 4 件1991 年: 被引用 1 件1992 年: 被引用 2 件1993 年: 被引用 3 件1994 年: 被引用 6 件1995 年: 被引用 11 件1996 年: 被引用 24 件1997 年: 被引用 15 件1998 年: 被引用 49 件1999 年: 被引用 63 件2000 年: 被引用 64 件2001 年: 被引用 75 件2002 年: 被引用 93 件2003 年: 被引用 96 件2004 年: 被引用 137 件2005 年: 被引用 128 件2006 年: 被引用 116 件2007 年: 被引用 139 件2008 年: 被引用 149 件2009 年: 被引用 166 件2010 年: 被引用 236 件2011 年: 被引用 173 件2012 年: 被引用 163 件2013 年: 被引用 223 件2014 年: 被引用 170 件2015 年: 被引用 183 件2016 年: 被引用 194 件2017 年: 被引用 216 件2018 年: 被引用 196 件2019 年: 被引用 551 件2020 年: 被引用 607 件2021 年: 被引用 645 件2022 年: 被引用 412 件2023 年: 被引用 338 件2024 年: 被引用 627 件2025 年: 被引用 230 件2026 年: 被引用 1 件1956〜1971 年は被引用が無いため表示していません1973〜1982 年は被引用が無いため表示していません1985〜1989 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 2,210 件、この内訳の 30.1%イギリス: 引用元論文 519 件、この内訳の 7.1%中国: 引用元論文 448 件、この内訳の 6.1%ドイツ: 引用元論文 371 件、この内訳の 5%フランス: 引用元論文 333 件、この内訳の 4.5%オランダ: 引用元論文 327 件、この内訳の 4.4%ベルギー: 引用元論文 308 件、この内訳の 4.2%カナダ: 引用元論文 274 件、この内訳の 3.7%日本: 引用元論文 272 件、この内訳の 3.7%イタリア: 引用元論文 264 件、この内訳の 3.6%オーストラリア: 引用元論文 219 件、この内訳の 3%スペイン: 引用元論文 183 件、この内訳の 2.5%
0%30.1%その他 22.1%

機関

分野

  • Medicine54.3%
  • Biochemistry, Genetics and Molecular Biology40.4%
  • Neuroscience1.7%
  • Immunology and Microbiology1.6%
  • Engineering0.4%
  • Nursing0.4%
  • その他1.2%

トピック

  • Vascular Malformations and Hemangiomas5.3%
  • Wnt/β-catenin signaling in development and cancer3.6%
  • Lymphatic System and Diseases3.1%
  • Vascular Malformations Diagnosis and Treatment2.9%
  • Bone Metabolism and Diseases2.4%
  • Angiogenesis and VEGF in Cancer2.4%
  • その他80.3%

共著者

全論文

検索で開く
  1. Genetic Basis and Therapies for Vascular Anomalies

    著者: Angela Queisser, Emmanuel Seront, Laurence M. Boon, Miikka Vikkula - Circulation Research 2021 被引用: 230

  2. LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development

    著者: Yaoqin Gong, Roger B. Slee, Naomi Fukai, Georges Rawadi, Sergio Roman‐Roman, Anthony M. Reginato, Hongwei Wang, Tim Cundy, F. H. Glorieux, Dorit Lev, Margaret Zacharin, Konrad Oexle, J. R. Marcelino, W. Suwairi, Shauna Heeger, G. Sabatakos, Suneel Apte, William N. Adkins, Jeremy Allgrove, Mine Arslan‐Kirchner, Jennifer Batch, Peter Beighton, Graeme C. Black, Richard G. Boles, Laurence M. Boon, C Borrone, HG Brunner, Georges F. Carle, Bruno Dallapiccola, Anne De Paepe, B. Floege, M. L. Halfhide, Bryan Hall, Raoul C. M. Hennekam, Tatsuo Hirose, Anneke Jans, Harald Jüppner, Chong Ae Kim, Kim M. Keppler‐Noreuil, A. Kohlschuetter, Didier Lacombe, Marie Lambert, Emmanuelle Lemyre, Tom G.W. Letteboer, Leena Peltonen, Raj Ramesar, Marta Romanengo, Hannu Somer, Elisabeth Steichen‐Gersdorf, B Steinmann, Beth Sullivan, Andrea Superti‐Furga, Walter Swoboda, M. J. van den Boogaard, Wim Van Hul, Miikka Vikkula, Marcela Votruba, Bernhard Zabel, Teresa García, Roland Baron, Bjørn R. Olsen, Matthew L. Warman - Cell 2001 被引用: 2,248

  3. Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies

    著者: Michel Wassef, Francine Blei, Denise M. Adams, Ahmad I. Alomari, Eulàlia Baselga, Alejandro Berenstein, Patricia E. Burrows, Ilona J. Frieden, Maria C. Garzón, Juan Carlos López‐Gutiérrez, David Lord, Sally Mitchel, Julie Powell, Julie Prendiville, Miikka Vikkula - PEDIATRICS 2015 被引用: 1,394

  4. Lymphatic Malformations: Genetics, Mechanisms and Therapeutic Strategies

    著者: Taija Mäkinen, Laurence M. Boon, Miikka Vikkula, Kari Alitalo - Circulation Research 2021 被引用: 226

  5. Somatic Activating PIK3CA Mutations Cause Venous Malformation

    著者: Nisha Limaye, J. Kangas, Antonella Mendola, Catherine Godfraind, Matthieu J. Schlögel, Raphaël Helaers, Lauri Eklund, Laurence M. Boon, Miikka Vikkula - The American Journal of Human Genetics 2015 被引用: 354

  6. Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations

    著者: Nisha Limaye, Vinciane Wouters, Mélanie Uebelhoer, Marjut Tuominen, Riikka Wirkkala, John B. Mulliken, Lauri Eklund, Laurence M. Boon, Miikka Vikkula - Nature Genetics 2008 被引用: 495

  7. Arterial Tortuosity

    著者: Simina Ciurică, Marilucy Lopez‐Sublet, Bart Loeys, I. Radhouani, Nalin Natarajan, Miikka Vikkula, Angela H.E.M. Maas, David Adlam, Alexandre Persu - Hypertension 2019 被引用: 201

  8. Chromosome instability is common in human cleavage-stage embryos

    著者: Evelyne Vanneste, Thierry Voet, Cédric Le Caignec, Michèle Ampe, Peter Könings, Cindy Melotte, Sophie Debrock, Mustapha Amyere, Miikka Vikkula, Frans Schuit, Jean‐Pierre Fryns, Geert Verbeke, Thomas D’Hooghe, Yves Moreau, Joris Vermeesch - Nature Medicine 2009 被引用: 899

  9. Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling

    著者: Mustapha Amyere, Nicole Revençu, Raphaël Helaers, Eleonore Pairet, Eulàlia Baselga, Maria Cordisco, Wendy K. Chung, Josée Dubois, J.‐P. Lacour, Loreto Martorell, J. Mazereeuw‐Hautier, Reed E. Pyeritz, David J. Amor, Annouk Bisdorff, Francine Blei, Hannah Bombei, A. Dompmartin, David G. Brooks, Juliette Dupont, María Antonia González-Enseñat, Ilona J. Frieden, Marion Gérard, Malin Kvarnung, Andrea Hanson‐Kahn, Louanne Hudgins, C. Léauté‐Labrèze, Catherine McCuaïg, Denise W. Metry, P. Parent, C. Paul, Florence Petit, Alice Phan, I. Quéré, Aïcha Salhi, Anne Turner, P. Vabres, Asunción Vicente, Orli Wargon, Shôji Watanabe, Lisa Weibel, Ashley Wilson, Marcia Willing, John B. Mulliken, Laurence M. Boon, Miikka Vikkula - Circulation 2017 被引用: 293

  10. Rapamycin improves TIE2-mutated venous malformation in murine model and human subjects

    著者: Elisa Boscolo, Nisha Limaye, Lan Huang, Kyu-Tae Kang, Julie Soblet, Mélanie Uebelhoer, Antonella Mendola, Marjut Nätynki, Emmanuel Seront, Sophie Dupont, Jennifer Hammer, Catherine Legrand, Carlo Brugnara, Lauri Eklund, Miikka Vikkula, Joyce Bischoff, Laurence M. Boon - Journal of Clinical Investigation 2015 被引用: 240

  11. A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestations

    著者: Guillaume Canaud, Adrienne M. Hammill, Denise M. Adams, Miikka Vikkula, Kim M. Keppler‐Noreuil - Orphanet Journal of Rare Diseases 2021 被引用: 176

  12. Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation

    著者: Inés Martínez‐Corral, Yan Zhang, Milena Petkova, Henrik Ortsäter, Sofie Sjöberg, Sandra D. Castillo, Pascal Brouillard, Louis Libbrecht, Dieter Saur, Mariona Graupera, Kari Alitalo, Laurence M. Boon, Miikka Vikkula, Taija Mäkinen - Nature Communications 2020 被引用: 111

  13. Preliminary results of the European multicentric phase III trial regarding sirolimus in slow-flow vascular malformations

    著者: Emmanuel Seront, An Van Damme, Catherine Legrand, Annouk Bisdorff-Bresson, Philippe Orcel, Thomas Funck‐Brentano, Marie‐Antoinette Sevestre, A. Dompmartin, I. Quéré, Pascal Brouillard, Nicole Revençu, Martina De Bortoli, Frank Hammer, Philippe Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M. Boon - JCI Insight 2023 被引用: 64

  14. Primary lymphoedema

    著者: Pascal Brouillard, Marlys H. Witte, Robert P. Erickson, Robert J. Damstra, Corinne Becker, I. Quéré, Miikka Vikkula - Nature Reviews Disease Primers 2021 被引用: 97

  15. KRAS-driven model of Gorham-Stout disease effectively treated with trametinib

    著者: Nassim Homayun Sepehr, Anna McCarter, Raphaël Helaers, Christine Galant, Laurence M. Boon, Pascal Brouillard, Miikka Vikkula, Michael T. Dellinger - JCI Insight 2021 被引用: 77

  16. Sirolimus is efficacious in treatment for extensive and/or complex slow-flow vascular malformations: a monocentric prospective phase II study

    著者: Jennifer Hammer, Emmanuel Seront, Steven Duez, Sophie Dupont, An Van Damme, Sandra Schmitz, Claire Hoyoux, Caroline Chopinet, Philippe Clapuyt, Frank Hammer, Miikka Vikkula, Laurence M. Boon - Orphanet Journal of Rare Diseases 2018 被引用: 235

  17. New and Emerging Targeted Therapies for Vascular Malformations

    著者: An Van Damme, Emmanuel Seront, Valérie Dekeuleneer, Laurence M. Boon, Miikka Vikkula - American Journal of Clinical Dermatology 2020 被引用: 130

  18. Capillary Malformation–Arteriovenous Malformation, a New Clinical and Genetic Disorder Caused by RASA1 Mutations

    著者: Iiro Eerola, Laurence M. Boon, John B. Mulliken, Patricia E. Burrows, A. Dompmartin, Shôji Watanabe, R Vanwijck, Miikka Vikkula - The American Journal of Human Genetics 2003 被引用: 750

  19. Vascular Dysmorphogenesis Caused by an Activating Mutation in the Receptor Tyrosine Kinase TIE2

    著者: Miikka Vikkula, Laurence M. Boon, Kermit L. Carraway, Jennifer T. Calvert, A. John Diamonti, Boyan C. Goumnerov, Krystyna A. Pasyk, Douglas A. Marchuk, Matthew L. Warman, Lewis C. Cantley, John B. Mulliken, Bjørn R. Olsen - Cell 1996 被引用: 812

  20. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused byRASA1 mutations

    著者: Nicole Revençu, Laurence M. Boon, John B. Mulliken, O Enjolras, Maria Cordisco, Patricia E. Burrows, Philippe Clapuyt, Frank Hammer, Josée Dubois, Eulàlia Baselga, Francesco Brancati, Robin Carder, José Miguel Ceballos Quintal, Bruno Dallapiccola, Gayle Fischer, Ilona J. Frieden, Maria C. Garzón, John Harper, Jennifer Johnson-Patel, Christine Labrèze, Loreto Martorell, Harriet J. Paltiel, Annette Pohl, Julie Prendiville, I. Quéré, Dawn H. Siegel, Enza Maria Valente, Annet van Hagen, Liselot van Hest, Keith K. Vaux, Asunción Vicente, Lisa Weibel, David Chitayat, Miikka Vikkula - Human Mutation 2008 被引用: 430

  21. RASA1Mutations and Associated Phenotypes in 68 Families with Capillary Malformation-Arteriovenous Malformation

    著者: Nicole Revençu, Laurence M. Boon, Antonella Mendola, Maria Cordisco, Josée Dubois, Philippe Clapuyt, Frank Hammer, David J. Amor, Alan D. Irvine, Eulàlia Baselga, A. Dompmartin, Samira Syed, A. Martín‐Santiago, Lesley C. Adès, Felicity Collins, Janine Smith, Sarah A. Sandaradura, Victoria R. Barrio, Patricia E. Burrows, Francine Blei, Mariarosaria Cozzolino, Nicola Brunetti‐Pierri, Asunción Vicente, Marc Abramowicz, Julie Désir, Catheline Vilain, Wendy K. Chung, Ashley Wilson, Carol Gardiner, Yim Dwight, David Lord, Leona Fishman, Cheryl Cytrynbaum, Sarah L. Chamlin, Fred Ghali, Yolanda Gilaberte, Shelagh Joss, María del Carmen Boente, C. Léauté‐Labrèze, Marie-Ange Delrue, Susan Bayliss, Loreto Martorell, Maria-Antonia González-Enseñat, J. Mazereeuw‐Hautier, Brid O’Donnell, D. Bessis, Reed E. Pyeritz, Aïcha Salhi, Oon Tian Tan, Orli Wargon, John B. Mulliken, Miikka Vikkula - Human Mutation 2013 被引用: 292

  22. TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation

    著者: François Foulquier, Mustapha Amyere, Jaak Jaeken, Renate Zeevaert, Els Schollen, Valérie Race, Riet Bammens, Willy Morelle, Claire Rosnoblet, Dominique Legrand, Didier Demaegd, Neil R.M. Buist, David Cheillan, Nathalie Guffon, Pierre Morsomme, Willem Annaert, Hudson H. Freeze, Emile Van Schaftingen, Miikka Vikkula, Gert Matthijs - The American Journal of Human Genetics 2012 被引用: 206

  23. Case report study of thalidomide therapy in 18 patients with severe arteriovenous malformations

    著者: Laurence M. Boon, Valérie Dekeuleneer, Julien Coulie, Liliane Marot, Anne-Christine Bataille, Frank Hammer, Philippe Clapuyt, Anne Jeanjean, A. Dompmartin, Miikka Vikkula - Nature Cardiovascular Research 2022 被引用: 47

  24. Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema

    著者: Alicia B. Byrne, Pascal Brouillard, Drew L. Sutton, Jan Kazenwadel, Saba Montazaribarforoushi, Genevieve A. Secker, Anna Oszmiana, Milena Babic, Kelly L. Betterman, Peter J Brautigan, Melissa White, Sandra Piltz, Paul Q. Thomas, Christopher N Hahn, Matthias Rath, Ute Felbor, Georg-Christoph Korenke, Christopher L. Smith, Kathleen H. Wood, Sarah E. Sheppard, Denise M. Adams, Ariana Kariminejad, Raphaël Helaers, Laurence M. Boon, Nicole Revençu, Lynette Moore, Christopher Barnett, Eric Haan, Peer Arts, Miikka Vikkula, Hamish S. Scott, Natasha L. Harvey - Science Translational Medicine 2022 被引用: 41