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Year Number of Results
1949 1
1991 1
1996 2
1997 1
1999 2
2000 1
2005 1
2006 3
2007 1
2008 2
2009 5
2010 3
2011 8
2012 4
2013 6
2014 3
2015 5
2016 3
2017 1
2019 1
2020 1
2024 0

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Page 1
[Array CGH: why and to whom].
Ferrarini A, Jacquemont S, Popovic MB, Bonafé L, Martinet D. Ferrarini A, et al. Among authors: martinet d. Rev Med Suisse. 2010 Feb 24;6(237):390-2, 394-6. Rev Med Suisse. 2010. PMID: 20383968 French.
A new CRB1 rat mutation links Müller glial cells to retinal telangiectasia.
Zhao M, Andrieu-Soler C, Kowalczuk L, Paz Cortés M, Berdugo M, Dernigoghossian M, Halili F, Jeanny JC, Goldenberg B, Savoldelli M, El Sanharawi M, Naud MC, van Ijcken W, Pescini-Gobert R, Martinet D, Maass A, Wijnholds J, Crisanti P, Rivolta C, Behar-Cohen F. Zhao M, et al. Among authors: martinet d. J Neurosci. 2015 Apr 15;35(15):6093-106. doi: 10.1523/JNEUROSCI.3412-14.2015. J Neurosci. 2015. PMID: 25878282 Free PMC article.
The phenotype of recurrent 10q22q23 deletions and duplications.
van Bon BW, Balciuniene J, Fruhman G, Nagamani SC, Broome DL, Cameron E, Martinet D, Roulet E, Jacquemont S, Beckmann JS, Irons M, Potocki L, Lee B, Cheung SW, Patel A, Bellini M, Selicorni A, Ciccone R, Silengo M, Vetro A, Knoers NV, de Leeuw N, Pfundt R, Wolf B, Jira P, Aradhya S, Stankiewicz P, Brunner HG, Zuffardi O, Selleck SB, Lupski JR, de Vries BB. van Bon BW, et al. Among authors: martinet d. Eur J Hum Genet. 2011 Apr;19(4):400-8. doi: 10.1038/ejhg.2010.211. Epub 2011 Jan 19. Eur J Hum Genet. 2011. PMID: 21248748 Free PMC article.
A single epidermal stem cell strategy for safe ex vivo gene therapy.
Droz-Georget Lathion S, Rochat A, Knott G, Recchia A, Martinet D, Benmohammed S, Grasset N, Zaffalon A, Besuchet Schmutz N, Savioz-Dayer E, Beckmann JS, Rougemont J, Mavilio F, Barrandon Y. Droz-Georget Lathion S, et al. Among authors: martinet d. EMBO Mol Med. 2015 Apr;7(4):380-93. doi: 10.15252/emmm.201404353. EMBO Mol Med. 2015. PMID: 25724200 Free PMC article.
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered.
van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Mühlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH. van der Reijden BA, et al. Among authors: martinet d. Oncogene. 1999 Jan 14;18(2):543-50. doi: 10.1038/sj.onc.1202321. Oncogene. 1999. PMID: 9927211
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
D'Angelo D, Lebon S, Chen Q, Martin-Brevet S, Snyder LG, Hippolyte L, Hanson E, Maillard AM, Faucett WA, Macé A, Pain A, Bernier R, Chawner SJ, David A, Andrieux J, Aylward E, Baujat G, Caldeira I, Conus P, Ferrari C, Forzano F, Gérard M, Goin-Kochel RP, Grant E, Hunter JV, Isidor B, Jacquette A, Jønch AE, Keren B, Lacombe D, Le Caignec C, Martin CL, Männik K, Metspalu A, Mignot C, Mukherjee P, Owen MJ, Passeggeri M, Rooryck-Thambo C, Rosenfeld JA, Spence SJ, Steinman KJ, Tjernagel J, Van Haelst M, Shen Y, Draganski B, Sherr EH, Ledbetter DH, van den Bree MB, Beckmann JS, Spiro JE, Reymond A, Jacquemont S, Chung WK; Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study; 16p11.2 European Consortium; Simons Variation in Individuals Project (VIP) Consortium. D'Angelo D, et al. JAMA Psychiatry. 2016 Jan;73(1):20-30. doi: 10.1001/jamapsychiatry.2015.2123. JAMA Psychiatry. 2016. PMID: 26629640 Free PMC article.
46 results