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203 results

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Page 1
System size effects on gyrokinetic turbulence.
McMillan BF, Lapillonne X, Brunner S, Villard L, Jolliet S, Bottino A, Görler T, Jenko F. McMillan BF, et al. Among authors: villard l. Phys Rev Lett. 2010 Oct 8;105(15):155001. doi: 10.1103/PhysRevLett.105.155001. Epub 2010 Oct 4. Phys Rev Lett. 2010. PMID: 21230913
Role of plasma elongation on turbulent transport in magnetically confined plasmas.
Angelino P, Garbet X, Villard L, Bottino A, Jolliet S, Ghendrih P, Grandgirard V, McMillan BF, Sarazin Y, Dif-Pradalier G, Tran TM. Angelino P, et al. Among authors: villard l. Phys Rev Lett. 2009 May 15;102(19):195002. doi: 10.1103/PhysRevLett.102.195002. Epub 2009 May 12. Phys Rev Lett. 2009. PMID: 19518964
Locality and universality in gyrokinetic turbulence.
Teaca B, Navarro AB, Jenko F, Brunner S, Villard L. Teaca B, et al. Among authors: villard l. Phys Rev Lett. 2012 Dec 7;109(23):235003. doi: 10.1103/PhysRevLett.109.235003. Epub 2012 Dec 5. Phys Rev Lett. 2012. PMID: 23368214
Tokamak equilibria with reversed current density.
Martynov AA, Medvedev SY, Villard L. Martynov AA, et al. Among authors: villard l. Phys Rev Lett. 2003 Aug 22;91(8):085004. doi: 10.1103/PhysRevLett.91.085004. Epub 2003 Aug 21. Phys Rev Lett. 2003. PMID: 14525248
Observation of multiple kinetic Alfvén eigenmodes.
Fasoli A, Lister JB, Sharapov S, Borba D, Deliyanakis N, Gormezano C, Jacquinot J, Jaun A, Holties HA, Huysmans GT, Kerner W, Moret J, Villard L. Fasoli A, et al. Among authors: villard l. Phys Rev Lett. 1996 Feb 12;76(7):1067-1070. doi: 10.1103/PhysRevLett.76.1067. Phys Rev Lett. 1996. PMID: 10061625 No abstract available.
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Sabeh P, Dumas SA, Maios C, Daghar H, Korzeniowski M, Rousseau J, Lines M, Guerin A, Millichap JJ, Landsverk M, Grebe T, Lindstrom K, Strober J, Ait Mouhoub T, Zweier C, Steinraths M, Hebebrand M, Callewaert B, Abou Jamra R, Kautza-Lucht M, Wegler M, Kruszka P, Kumps C, Banne E, Waberski MB, Dieux A, Raible S, Krantz I, Medne L, Pechter K, Villard L, Guerrini R, Bianchini C, Barba C, Mei D, Blanc X, Kallay C, Ranza E, Yang XR, O'Heir E, Donald KA, Murugasen S, Bruwer Z, Calikoglu M, Mathews JM, Lesieur-Sebellin M, Baujat G, Derive N, Pierson TM, Murrell JR, Shillington A, Ormieres C, Rondeau S, Reis A, Fernandez-Jaen A, Au PYB, Sweetser DA, Briere LC, Couque N, Perrin L, Schymick J, Gueguen P, Lefebvre M, Van Andel M, Juusola J, Antonarakis SE, Parker JA, Burnett BG, Campeau PM. Sabeh P, et al. Among authors: villard l. Am J Hum Genet. 2025 Jan 2;112(1):75-86. doi: 10.1016/j.ajhg.2024.11.009. Epub 2024 Dec 24. Am J Hum Genet. 2025. PMID: 39721588
Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders.
Cali E, Quirin T, Rocca C, Efthymiou S, Riva A, Marafi D, Zaki MS, Suri M, Dominguez R, Elbendary HM, Alavi S, Abdel-Hamid MS, Morsy H, Mau-Them FT, Nizon M, Tesner P, Ryba L, Zafar F, Rana N, Saadi NW, Firoozfar Z, Gencpinar P, Unay B, Ustun C, Bruel AL, Coubes C, Stefanich J, Sezer O, Agolini E, Novelli A, Vasco G, Lettori D, Milh M, Villard L, Zeidler S, Opperman H, Strehlow V, Issa MY, El Khassab H, Chand P, Ibrahim S, Nejad-Rashidi A, Miryounesi M, Larki P, Morrison J, Cristian I, Thiffault I, Bertsch NL, Noh GJ, Pappas J, Moran E, Marinakis NM, Traeger-Synodinos J, Hosseini S, Abbaszadegan MR, Caumes R, Vissers LELM, Neshatdoust M, Montazer MZ, El Fahime E, Canavati C, Kamal L, Kanaan M, Askander O, Voinova V, Levchenko O, Haider S, Halbach SS, Maia ER, Mansoor S, Vivek J, Tawde S, Santhosh R Challa V, Gowda VK, Srinivasan VM, Victor LA, Pinero-Banos B, Hague J, Ei-Awady HA, Maria de Miranda Henriques-Souza A, Cheema HA, Anjum MN, Idkaidak S, Alqarajeh F, Atawneh O, Mor-Shaked H, Harel T, Zifarelli G, Bauer P, Kok F, Kitajima JP, Monteiro F, Josahkian J, Lesca G, Chatron N, Ville D, Murphy D, Neul JL, Mullegama SV, Begtrup A, Herman I, Mitani T, Posey JE, Tay CG, Jave… See abstract for full author list ➔ Cali E, et al. Among authors: villard l. Genet Med. 2024 Sep 10:101251. doi: 10.1016/j.gim.2024.101251. Online ahead of print. Genet Med. 2024. PMID: 39275948 Free article.
Clinical and molecular characterization of patients with YWHAG-related epilepsy.
Cetica V, Pisano T, Lesca G, Marafi D, Licchetta L, Riccardi F, Mei D, Chung HB, Bayat A, Balasubramanian M, Lowenstein DH, Endzinienė M, Alotaibi M, Villeneuve N, Jacobs J, Isidor B, Solazzi R, den Hollander NS, Marjanovic D, Rougeot-Jung C, Jung J, Lesieur-Sebellin M, Accogli A, Salpietro V, Saadi NW, Panagiotakaki E, Foiadelli T, Redon S, Tsai MH, Bisulli F, Hammer TB, Lupski JR, Parrini E, Guerrini R; YWHAG Study Group. Cetica V, et al. Epilepsia. 2024 May;65(5):1439-1450. doi: 10.1111/epi.17939. Epub 2024 Mar 16. Epilepsia. 2024. PMID: 38491959
203 results