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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 4
1991 4
1992 1
1993 8
1994 5
1995 6
1996 11
1997 9
1998 11
1999 8
2000 6
2001 8
2002 5
2003 10
2004 8
2005 13
2006 12
2007 8
2008 11
2009 12
2010 19
2011 16
2012 16
2013 13
2014 9
2015 13
2016 12
2017 10
2018 12
2019 17
2020 18
2021 12
2022 11
2023 12
2024 9

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311 results

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Page 1
CFTR-France, a national relational patient database for sharing genetic and phenotypic data associated with rare CFTR variants.
Claustres M, Thèze C, des Georges M, Baux D, Girodon E, Bienvenu T, Audrezet MP, Dugueperoux I, Férec C, Lalau G, Pagin A, Kitzis A, Thoreau V, Gaston V, Bieth E, Malinge MC, Reboul MP, Fergelot P, Lemonnier L, Mekki C, Fanen P, Bergougnoux A, Sasorith S, Raynal C, Bareil C. Claustres M, et al. Among authors: bienvenu t. Hum Mutat. 2017 Oct;38(10):1297-1315. doi: 10.1002/humu.23276. Epub 2017 Jun 28. Hum Mutat. 2017. PMID: 28603918
Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
Aref-Eshghi E, Kerkhof J, Pedro VP; Groupe DI France; Barat-Houari M, Ruiz-Pallares N, Andrau JC, Lacombe D, Van-Gils J, Fergelot P, Dubourg C, Cormier-Daire V, Rondeau S, Lecoquierre F, Saugier-Veber P, Nicolas G, Lesca G, Chatron N, Sanlaville D, Vitobello A, Faivre L, Thauvin-Robinet C, Laumonnier F, Raynaud M, Alders M, Mannens M, Henneman P, Hennekam RC, Velasco G, Francastel C, Ulveling D, Ciolfi A, Pizzi S, Tartaglia M, Heide S, Héron D, Mignot C, Keren B, Whalen S, Afenjar A, Bienvenu T, Campeau PM, Rousseau J, Levy MA, Brick L, Kozenko M, Balci TB, Siu VM, Stuart A, Kadour M, Masters J, Takano K, Kleefstra T, de Leeuw N, Field M, Shaw M, Gecz J, Ainsworth PJ, Lin H, Rodenhiser DI, Friez MJ, Tedder M, Lee JA, DuPont BR, Stevenson RE, Skinner SA, Schwartz CE, Genevieve D, Sadikovic B. Aref-Eshghi E, et al. Among authors: bienvenu t. Am J Hum Genet. 2020 Mar 5;106(3):356-370. doi: 10.1016/j.ajhg.2020.01.019. Epub 2020 Feb 27. Am J Hum Genet. 2020. PMID: 32109418 Free PMC article.
Rheumatoid arthritis-associated bronchiectasis.
Puéchal X, Bienvenu T, Dusser D. Puéchal X, et al. Among authors: bienvenu t. Lancet. 2019 May 18;393(10185):2035-2036. doi: 10.1016/S0140-6736(19)30020-0. Lancet. 2019. PMID: 31106745 No abstract available.
Frontal sinuses and human evolution.
Balzeau A, Albessard-Ball L, Kubicka AM, Filippo A, Beaudet A, Santos E, Bienvenu T, Arsuaga JL, Bartsiokas A, Berger L, Bermúdez de Castro JM, Brunet M, Carlson KJ, Daura J, Gorgoulis VG, Grine FE, Harvati K, Hawks J, Herries A, Hublin JJ, Hui J, Ives R, Joordens JA, Kaifu Y, Kouloukoussa M, Léger B, Lordkipanidze D, Margvelashvili A, Martin J, Martinón-Torres M, May H, Mounier A, du Plessis A, Rae T, Röding C, Sanz M, Semal P, Stratford D, Stringer C, Tawane M, Temming H, Tsoukala E, Zilhão J, Zipfel B, Buck LT. Balzeau A, et al. Among authors: bienvenu t. Sci Adv. 2022 Oct 21;8(42):eabp9767. doi: 10.1126/sciadv.abp9767. Epub 2022 Oct 21. Sci Adv. 2022. PMID: 36269821 Free PMC article.
Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
Aref-Eshghi E, Kerkhof J, Pedro VP, France GD, Barat-Houari M, Ruiz-Pallares N, Andrau JC, Lacombe D, Van-Gils J, Fergelot P, Dubourg C, Cormier-Daire V, Rondeau S, Lecoquierre F, Saugier-Veber P, Nicolas G, Lesca G, Chatron N, Sanlaville D, Vitobello A, Faivre L, Thauvin-Robinet C, Laumonnier F, Raynaud M, Alders M, Mannens M, Henneman P, Hennekam RC, Velasco G, Francastel C, Ulveling D, Ciolfi A, Pizzi S, Tartaglia M, Heide S, Héron D, Mignot C, Keren B, Whalen S, Afenjar A, Bienvenu T, Campeau PM, Rousseau J, Levy MA, Brick L, Kozenko M, Balci TB, Siu VM, Stuart A, Kadour M, Masters J, Takano K, Kleefstra T, de Leeuw N, Field M, Shaw M, Gecz J, Ainsworth PJ, Lin H, Rodenhiser DI, Friez MJ, Tedder M, Lee JA, DuPont BR, Stevenson RE, Skinner SA, Schwartz CE, Genevieve D, Sadikovic B. Aref-Eshghi E, et al. Among authors: bienvenu t. Am J Hum Genet. 2021 Jun 3;108(6):1161-1163. doi: 10.1016/j.ajhg.2021.04.022. Am J Hum Genet. 2021. PMID: 34087165 Free PMC article. No abstract available.
The primitive brain of early Homo.
Ponce de León MS, Bienvenu T, Marom A, Engel S, Tafforeau P, Alatorre Warren JL, Lordkipanidze D, Kurniawan I, Murti DB, Suriyanto RA, Koesbardiati T, Zollikofer CPE. Ponce de León MS, et al. Among authors: bienvenu t. Science. 2021 Apr 9;372(6538):165-171. doi: 10.1126/science.aaz0032. Science. 2021. PMID: 33833119
[Genetics of complex and syndromic palmoplantar keratoderma].
Sperelakis-Beedham B, Lopez M, Girodon E, Hickman G, Bourrat E, Bienvenu T. Sperelakis-Beedham B, et al. Among authors: bienvenu t. Ann Biol Clin (Paris). 2021 Dec 1;79(6):551-565. doi: 10.1684/abc.2021.1688. Ann Biol Clin (Paris). 2021. PMID: 34961738 Review. French.
Tremor-like subcortical myoclonus in STXBP1 encephalopathy.
Loussouarn A, Doummar D, Beaugendre Y, Bienvenu T, Charles P, Depienne C, Dorison N, Heide S, Héron D, Ioos C, Keren B, Métreau J, Mochel F, Moutard ML, Ravelli C, Apartis E, Mignot C. Loussouarn A, et al. Among authors: bienvenu t. Eur J Paediatr Neurol. 2021 Sep;34:62-66. doi: 10.1016/j.ejpn.2021.06.005. Epub 2021 Jul 3. Eur J Paediatr Neurol. 2021. PMID: 34392114
311 results