Koenraad Devriendt

1995–2025 年に発表

148
論文数
21,252
被引用数
87
h 指数
145
i10 指数

被引用数

Koenraad Devriendt の年別被引用数1955 年: 被引用 2 件1996 年: 被引用 2 件1997 年: 被引用 2 件1998 年: 被引用 10 件1999 年: 被引用 9 件2000 年: 被引用 31 件2001 年: 被引用 55 件2002 年: 被引用 76 件2003 年: 被引用 76 件2004 年: 被引用 86 件2005 年: 被引用 81 件2006 年: 被引用 90 件2007 年: 被引用 92 件2008 年: 被引用 161 件2009 年: 被引用 199 件2010 年: 被引用 230 件2011 年: 被引用 192 件2012 年: 被引用 204 件2013 年: 被引用 233 件2014 年: 被引用 201 件2015 年: 被引用 220 件2016 年: 被引用 153 件2017 年: 被引用 198 件2018 年: 被引用 181 件2019 年: 被引用 525 件2020 年: 被引用 544 件2021 年: 被引用 581 件2022 年: 被引用 387 件2023 年: 被引用 279 件2024 年: 被引用 449 件2025 年: 被引用 185 件2026 年: 被引用 8 件1956〜1995 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 2,490 件、この内訳の 24.8%イギリス: 引用元論文 897 件、この内訳の 8.9%ドイツ: 引用元論文 626 件、この内訳の 6.2%オランダ: 引用元論文 574 件、この内訳の 5.7%フランス: 引用元論文 505 件、この内訳の 5%カナダ: 引用元論文 497 件、この内訳の 5%イタリア: 引用元論文 478 件、この内訳の 4.8%中国: 引用元論文 432 件、この内訳の 4.3%ベルギー: 引用元論文 394 件、この内訳の 3.9%オーストラリア: 引用元論文 356 件、この内訳の 3.5%スペイン: 引用元論文 246 件、この内訳の 2.5%日本: 引用元論文 208 件、この内訳の 2.1%
0%24.8%その他 23.3%

分野

  • Biochemistry, Genetics and Molecular Biology58.9%
  • Medicine30.1%
  • Neuroscience4.6%
  • Immunology and Microbiology4%
  • Agricultural and Biological Sciences0.7%
  • Computer Science0.3%
  • その他1.4%

トピック

  • Congenital heart defects research6.4%
  • Genomic variations and chromosomal abnormalities6.3%
  • Genomics and Rare Diseases4.2%
  • Genetics and Neurodevelopmental Disorders4.2%
  • Prenatal Screening and Diagnostics2.6%
  • Congenital Heart Disease Studies2.3%
  • その他74%

共著者

全論文

検索で開く
  1. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thierry Billette de Villemeur, Edward Blair, Miriam Bloom, Alberto Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro‐Gago, Anna Cavallini, Cristina Cereda, Kate Chandler, David Chitayat, Abigail E. Collins, Concepción Sierra Córcoles, Nuno Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D’Arrigo, Christian G E L De Goede, Corinne De Laet, Liesbeth M. H. De Waele, Inés María Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Naz Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, P. Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming Lim, Jean‐Pierre Lin, Tarja Linnankivi, Mark T. Mackay, Daphna Marom, Charles Marques Lourenço, Shane McKee, Isabella Moroni, Jenny E.V. Morton, Marie‐Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemí Núñez‐Enamorado, P.J. Oades, Ivana Olivieri, John R. Østergaard, Belén Pérez‐Dueñas, Julie Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez ほか 36 名 - American Journal of Medical Genetics Part A 2015 被引用: 613

  2. Cell-free DNA methylome analysis for early preeclampsia prediction

    著者: , , , , , , , , , , , , , , , , - Nature Medicine 2023 被引用: 83

  3. Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emma Hobson, Kirstin Hoff, Tessa Homfray, Anne-Karin Kahlert, Ami Ketley, Hans-Heiner Kramer, Katherine Lachlan, Anne Katrin Lampe, Jacoba Louw, Ashok Kumar Manickara, Dorin Manase, Karen McCarthy, Kay Metcalfe, Carmel Moore, Ruth Newbury‐Ecob, Seham Osman Babiker Omer, Willem H. Ouwehand, Soo‐Mi Park, Michael Parker, Thomas Pickardt, Martin Pollard, Leema Robert, David J. Roberts, Jennifer Sambrook, Kerry Setchfield, Brigitte Stiller, Chris Thornborough, Okan Toka, Hugh Watkins, Denise Williams, Michael Wright, Seema Mital, Piers E.F. Daubeney, Bernard Keavney, Judith Goodship, Riyadh Mahdi Abu-Sulaiman, Sabine Klaassen, Caroline F. Wright, Helen V. Firth, Jeffrey C. Barrett, Koenraad Devriendt, David Fitzpatrick, J. David Brook, Matthew E. Hurles - Nature Genetics 2016 被引用: 467

  4. Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emeline M. Van Craenenbroeck, Kenji Minatoya, Ritsu Matsukawa, Takuro Tsukube, Noriaki Kubo, Robert M.W. Hofstra, Marie‐José Goumans, Jos A. Bekkers, Jolien W. Roos‐Hesselink, Ingrid M.B.H. van de Laar, Harry C. Dietz, Lut Van Laer, Takayuki Morisaki, Marja W. Wessels, Bart Loeys - Journal of the American College of Cardiology 2015 被引用: 297

  5. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathryn E. Hentges, G.M. Lathrop, Mauro Santibanez‐Koref, Bernard Keavney - Circulation Research 2019 被引用: 198

  6. Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability

    著者: , , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2012 被引用: 271

  7. Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bernard Keavney - The American Journal of Human Genetics 2012 被引用: 338

  8. Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Richard H. Scott, Laurie H. Seaver, Elliott H. Sherr, Miranda Splitt, Helen Stewart, Constance T. R. M. Stumpel, Şehime Gülsün Temel, David D. Weaver, Margo Whiteford, Marc S. Williams, Holly K. Tabor, Joshua D. Smith, Jay Shendure, Deborah A. Nickerson, Michael J. Bamshad - The American Journal of Human Genetics 2014 被引用: 218

  9. PEDIA: prioritization of exome data by image analysis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nechama Haddad, Nurulhuda Hajjir, Yair Hanani, Jakob Hertzberg, Konstanze Hoertnagel, Janelle Howell, Ivan Ivanovski, Angela M. Kaindl, Tom Kamphans, Susanne B. Kamphausen, Catherine Karimov, Hadil Kathom, Anna Keryan, Alexej Knaus, Sebastian Köhler, Uwe Kornak, А. В. Лавров, Maximilian Leitheiser, Gholson J. Lyon, Elisabeth Mangold, Purificación Marín Reina, Antonio Martínez Carrascal, Diana Mitter, Laura Morlán Herrador, Guy Nadav, Markus M. Nöthen, Alfredo Orrico, Claus‐Eric Ott, Kristen Park, Borut Peterlin, Laura Pölsler, Annick Raas‐Rothschild, Linda M. Randolph, Nicole Revençu, Christina Fagerberg, Peter Nick Robinson, Stanislav Rosnev, Sabine Rudnik, Goražd Rudolf, Ulrich A. Schatz, Anna Schossig, Max Schubach, Or Shanoon, Eamonn Sheridan, Pola Smirin‐Yosef, Malte Spielmann, Eun-Kyung Suk, Yves Sznajer, Christian T. Thiel, Gundula Thiel, Alain Verloès, Irena Vrečar, Dagmar Wahl, Ingrid Weber, Korina Winter, Marzena Wiśniewska, Bernd Wollnik, Ming Wai Yeung, Max Zhao, Na Zhu, Johannes Zschocke, Stefan Mundlos, Denise Horn, Peter Krawitz - Genetics in Medicine 2019 被引用: 86

  10. A comprehensive molecular study on Coffin–Siris and Nicolaides–Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gunnar Houge, Esra KAYA KILIÇ, Pelin Özlem Şimşek‐Kiper, Vanesa López‐González, Alma Kuechler, Stanislas Lyonnet, Francesca Mari, Annabella Marozza, Michèle Mathieu Dramard, Barbara Mikat, G Morin, Fanny Morice‐Picard, Ferda Özkınay, Anita Rauch, Alessandra Renieri, Sigrid Tinschert, Gülen Eda Ütine, Catheline Vilain, Rossella Vivarelli, Christiane Zweier, Peter Nürnberg, Sven Rahmann, Joris Vermeesch, Hermann‐Josef Lüdecke, Michael Zeschnigk, Bernd Wollnik - Human Molecular Genetics 2013 被引用: 228

  11. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David S. Winlaw, Shoumo Bhattacharya, Koenraad Devriendt, J. David Brook, Barbara J.M. Mulder, Seema Mital, Alex V. Postma, G.M. Lathrop, Martin Farrall, Judith A. Goodship, Bernard Keavney - Nature Genetics 2013 被引用: 165

  12. Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Koenraad Devriendt, Joris Vermeesch - Genetics in Medicine 2021 被引用: 128

  13. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R. Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I. Salmons, Oanh Tran, Peter Holmans, Antonio F. Pardiñas, James Walters, Wolfram Demaerel, Erik Boot, Nancy J. Butcher, Gregory Costain, Chelsea Lowther, Rens Evers, Thérèse van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koenraad Devriendt, Elfi Vergaelen, Annick Vogels, T. Blaine Crowley, Daniel E. McGinn, Edward Moss, Robert Sharkus, Marta Unolt, Elaine H. Zackai, Monica E. Calkins, Robert S. Gallagher, Ruben C. Gur, Sunny X. Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M. Repetto, Elemi Breetvelt, Sasja N. Duijff, Ania Fiksinski, Hayley Moss, Maria Niarchou, Kieran C. Murphy, Sarah E. Prasad, Eileen Daly, Maria Gudbrandsen, Clodagh M. Murphy, Declan Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria Cristina Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F. Cubells, Opal Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori‐Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider ほか 24 名 - Molecular Psychiatry 2020 被引用: 135

  14. Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies

    著者: , , , , , , , , , , , , , , , , , , , , , , - EClinicalMedicine 2021 被引用: 82

  15. Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Margje Sinnema, Bert B.A. de Vries, Erica H. Gerkes, Rolph Pfundt, Kosuke Izumi, Ian D. Krantz, Zhou L. Xu, Jill R. Murrell, Irene Valenzuela, Ivon Cuscó, Eulàlia Rovira‐Moreno, Yaping Yang, Varoona Bizaoui, Olivier Patat, Laurence Faivre, Frédéric Tran Mau‐Them, Antonio Vitobello, Anne‐Sophie Denommé‐Pichon, Christophe Philippe, Stéphane Bezieau, Benjamin Cogné - Genetics in Medicine 2022 被引用: 51

  16. Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Scott A. LeMaire, Joseph S. Coselli, Michael E. Mitchell, Aoy Tomita‐Mitchell, Siddharth K. Prakash, Karl Stamm, Alexandre F.R. Stewart, Candice K. Silversides, Reiner Siebert, Brigitte Stiller, Jill A. Rosenfeld, Inga Vater, Alex V. Postma, Almuth Caliebe, J. David Brook, Grégor Andelfinger, Matthew E. Hurles, Bernard Thienpont, Lars Allan Larsen, Marc‐Phillip Hitz - PLoS Genetics 2021 被引用: 36

  17. Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Georgina Parkin, Marco Fichera, S Reitano, Mariangela Lo Giudice, Kelly E. Li, Iris Casuga, Adam Broomer, Bernard Conrad, Markus Schwerzmann, Lorenz Räber, Sabina Gallati, Pasquale Striano, Antonietta Coppola, John Tolmie, Edward S. Tobias, Chris J. Lilley, Lluı́s Armengol, Yves Spysschaert, Patrick Verloo, Anja De Coene, Linde Goossens, Geert Mortier, Frank Speleman, Ellen van Binsbergen, Marcel Nelen, Ron Hochstenbach, Martin Poot, Louise Gallagher, Michael Gill, Jon McClellan, Mary‐Claire King, Regina Regan, Cindy Skinner, Roger E. Stevenson, Stylianos E. Antonarakis, Caifu Chen, Xavier Estivill, Björn Menten, Giorgio Gimelli, Susan Gribble, Stuart Schwartz, James S. Sutcliffe, Tom Walsh, Samantha J.L. Knight, Jonathan Sebat, Corrado Romano, Charles E. Schwartz, Joris A. Veltman, Bert B.A. de Vries, Joris Vermeesch, John Barber, Lionel Willatt, May Tassabehji, Evan E. Eichler - New England Journal of Medicine 2008 被引用: 811

  18. GATA3 haplo-insufficiency causes human HDR syndrome

    著者: , , , , , , , , , , , , , , - Nature 2000 被引用: 660

  19. Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome)

    著者: , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2007 被引用: 323

  20. ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Florence Petit, Zornitza Stark, Sylvia Stöckler‐Ipsiroglu, Sigrid Tinschert, Pradeep Vasudevan, Olaya Villa, Susan M. White, Farah Zahir, Adrian S. Woolf, Siddharth Banka - The American Journal of Human Genetics 2017 被引用: 141

  21. Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

    著者: , , , , , , , , , , , , , , , , - Clinical Genetics 2016 被引用: 87

  22. Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group

    著者: , , , , , , , , , , , - Orphanet Journal of Rare Diseases 2022 被引用: 50

  23. X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alison Gardner, Saffron A.G. Willis‐Owen, Chuan Tan, Kathryn Friend, Stefanie Belet, Kees E. P. van Roozendaal, M Jimenez-Pocquet, M.‐P. Moizard, Nathalie Ronce, Ren Sun, Sean O’Keeffe, R Chenna, Alena van Bömmel, Jonathan Göke, Anna Hackett, Michael Field, Louise Christie, Jackie Boyle, Eric Haan, John W. Nelson, Gillian Turner, Gareth Baynam, Gabriele Gillessen‐Kaesbach, Ulrich Müller, Daniela Steinberger, Bartłomiej Budny, Magdalena Badura‐Stronka, Anna Latos‐Bieleńska, Lilian Bomme Ousager, Peter Wieacker, Germán Rodríguez Criado, M.-L. Bondeson, Göran Annerén, Andreas Dufke, Monika Cohen, Lionel Van Maldergem, C. Vincent‐Delorme, Bernard Échenne, Brigitte Simon‐Bouy, Tjitske Kleefstra, Marjolein H. Willemsen, J-P. Fryns, Koenraad Devriendt, Reinhard Ullmann, Martin Vingron, Klaus Wrogemann, Thomas F. Wienker, Andreas Tzschach, Hans van Bokhoven, Jozef Gécz, Thomas J. Jentsch, W. Chen, H‐H Ropers, Vera M. Kalscheuer - Molecular Psychiatry 2015 被引用: 309

  24. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Coman, Carrie Costin, Koenraad Devriendt, Dexin Dong, Annika M. Dries, Tina Duelund Hjortshøj, David A. Dyment, Christine M. Eng, Casie A. Genetti, Siera Grano, Peter Henneman, Delphine Héron, Katrin Hoffmann, Jason Hom, Haowei Du, Maria Iascone, Bertrand Isidor, Irma Järvelä, Julie R. Jones, Boris Keren, Mary Kay Koenig, Jürgen Kohlhase, Seema R. Lalani, Cédric Le Caignec, Andi Lewis, Pengfei Liu, Alysia Kern Lovgren, James R. Lupski, Mike Lyons, Philippe A. Lysy, Melanie Manning, Carlo Marcelis, Scott McLean, Sandra Mercie, Mareike Mertens, Arnaud Molin, Mathilde Nizon, Kimberly Nugent, Susanna Öhman, Melanie O’Leary, Rebecca O. Littlejohn, Florence Petit, Rolph Pfundt, Lorraine Pottocki, Annick Raas‐Rotschild, Kara Ranguin, Nicole Revençu, Jill A. Rosenfeld, Lindsay Rhodes, Fernando Santos Simmaro, Karen Sals, Jolanda Schieving, Isabelle Schrauwen, Janneke Schuurs-Hoeijmakers, Eleanor G. Seaby, Ruth Sheffer, Lot Snijders Blok, Kristina P. Sørensen, Siddharth Srivastava, Zornitza Stark, Radka Stoeva, Chloe Stutterd, Natalie B. Tan, Pernille Mathiesen Tørring, Olivier Vanakker, Liselot van der Laan, Athina Ververi, Pablo Villavicencio‐Lorini, Marie Vincent, Dorothea Wand ほか 11 名 - The American Journal of Human Genetics 2024 被引用: 25