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

Year Number of Results
1950 1
1951 1
1970 2
1972 2
1979 2
1980 1
1981 1
1982 4
1983 3
1984 2
1985 2
1986 3
1987 3
1988 2
1989 6
1990 6
1991 5
1992 7
1993 8
1994 2
1995 4
1996 2
1997 4
1998 7
1999 2
2000 5
2001 2
2002 3
2003 4
2004 6
2005 6
2006 6
2007 7
2008 7
2009 5
2010 13
2011 12
2012 11
2013 15
2014 14
2015 24
2016 16
2017 18
2018 11
2019 12
2020 19
2021 17
2022 14
2023 11
2024 18
2025 13
2026 10

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341 results

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Page 1
Did you mean brosseau s[au] (70 results)?
APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
Lanoiselée HM, Nicolas G, Wallon D, Rovelet-Lecrux A, Lacour M, Rousseau S, Richard AC, Pasquier F, Rollin-Sillaire A, Martinaud O, Quillard-Muraine M, de la Sayette V, Boutoleau-Bretonniere C, Etcharry-Bouyx F, Chauviré V, Sarazin M, le Ber I, Epelbaum S, Jonveaux T, Rouaud O, Ceccaldi M, Félician O, Godefroy O, Formaglio M, Croisile B, Auriacombe S, Chamard L, Vincent JL, Sauvée M, Marelli-Tosi C, Gabelle A, Ozsancak C, Pariente J, Paquet C, Hannequin D, Campion D; collaborators of the CNR-MAJ project. Lanoiselée HM, et al. Among authors: rousseau s. PLoS Med. 2017 Mar 28;14(3):e1002270. doi: 10.1371/journal.pmed.1002270. eCollection 2017 Mar. PLoS Med. 2017. PMID: 28350801 Free PMC article.
Domain mapping of disease mutations reveals pathogenic SORL1 variants in Alzheimer's disease.
Andersen OM, de Waal MWJ, Monti G, Tesi N, Jensen AMG, de Geus C, van Spaendonk R, Vogel M, Ahmad S, Amin N, Amouyel P, Beecham GW, Bellenguez C, Berr C, Bis JC, Boland A, Bossù P, Bouwman F, Bras J, Charbonnier C, Clarimon J, Cruchaga C, Daniele A, Dartigues JF, Debette S, Deleuze JF, Denning N, DeStefano AL, Dols-Icardo O, van Duijn CM, Farrer LA, Fernández MV, van der Flier WM, Fox NC, Galimberti D, Genin E, Gille JJP, Grenier-Boley B, Grozeva D, Guen YL, Guerreiro R, Haines JL, Holmes C, Hummerich H, Arfan Ikram M, Kamran Ikram M, Kawalia A, Kraaij R, Lambert JC, Lathrop M, Lemstra AW, Lleó A, Myers RM, Mannens MMAM, Marshall R, Martin ER, Masullo C, Mayeux R, Mead S, Mecocci P, Meggy A, Mol MO, Nacmias B, Naj AC, Napolioni V, Nicholas Cochran J, Nicolas G, Pasquier F, Pastor P, Pericak-Vance MA, Pijnenburg YAL, Piras F, Quenez O, Ramirez A, Raybould R, Redon R, Reinders MJT, Richard AC, Riedel-Heller SG, Rivadeneira F, van Rooij JGJ, Rousseau S, Ryan NS, Sanchez-Juan P, Schellenberg GD, Scheltens P, Schott JM, Seshadri S, Sie D, Sims R, Sistermans EA, Sorbi S, van Swieten JC, Tijms B, Uitterlinden AG, Visser PJ, Wagner M, Wallon D, Wang LS, Williams J, Yokoyama JS, Zar… See abstract for full author list ➔ Andersen OM, et al. Among authors: rousseau s. Mol Neurodegener. 2025 Dec 1;20(1):122. doi: 10.1186/s13024-025-00907-z. Mol Neurodegener. 2025. PMID: 41327266 Free PMC article.
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, Beecham GW, Berr C, Bis JC, Boland A, Bossù P, Bouwman F, Bras J, Campion D, Cochran JN, Daniele A, Dartigues JF, Debette S, Deleuze JF, Denning N, DeStefano AL, Farrer LA, Fernández MV, Fox NC, Galimberti D, Genin E, Gille JJP, Le Guen Y, Guerreiro R, Haines JL, Holmes C, Ikram MA, Ikram MK, Jansen IE, Kraaij R, Lathrop M, Lemstra AW, Lleó A, Luckcuck L, Mannens MMAM, Marshall R, Martin ER, Masullo C, Mayeux R, Mecocci P, Meggy A, Mol MO, Morgan K, Myers RM, Nacmias B, Naj AC, Napolioni V, Pasquier F, Pastor P, Pericak-Vance MA, Raybould R, Redon R, Reinders MJT, Richard AC, Riedel-Heller SG, Rivadeneira F, Rousseau S, Ryan NS, Saad S, Sanchez-Juan P, Schellenberg GD, Scheltens P, Schott JM, Seripa D, Seshadri S, Sie D, Sistermans EA, Sorbi S, van Spaendonk R, Spalletta G, Tesi N, Tijms B, Uitterlinden AG, van der Lee SJ, Visser PJ, Wagner M, Wallon D, Wang LS, Zarea A, Clarimon J, van Swieten JC, Greicius MD, Yokoyama JS, Cruchaga C, Hardy J, Ramirez A, Mead S, van der Flier WM, van Duijn CM, W… See abstract for full author list ➔ Holstege H, et al. Among authors: rousseau s. Nat Genet. 2022 Dec;54(12):1786-1794. doi: 10.1038/s41588-022-01208-7. Epub 2022 Nov 21. Nat Genet. 2022. PMID: 36411364 Free PMC article.
Seasonal affective disorder.
Lurie SJ, Gawinski B, Pierce D, Rousseau SJ. Lurie SJ, et al. Among authors: rousseau sj. Am Fam Physician. 2006 Nov 1;74(9):1521-4. Am Fam Physician. 2006. PMID: 17111890 Free article. Review.
[Fatal rickettsiosis].
Raoult D, Kohler JL, Gallais H, De Micco P, Rousseau S, Casanova P. Raoult D, et al. Among authors: rousseau s. Nouv Presse Med. 1982 Feb 20;11(8):607. Nouv Presse Med. 1982. PMID: 7071000 French. No abstract available.
Myocardial Immune Cells: The Basis of Cardiac Immunology.
Cohen CD, Rousseau ST, Bermea KC, Bhalodia A, Lovell JP, Zita MD, Čiháková D, Adamo L. Cohen CD, et al. Among authors: rousseau st. J Immunol. 2023 May 1;210(9):1198-1207. doi: 10.4049/jimmunol.2200924. J Immunol. 2023. PMID: 37068299 Free PMC article.
The Role of B Cells in Cardiomyopathy and Heart Failure.
Bermea K, Bhalodia A, Huff A, Rousseau S, Adamo L. Bermea K, et al. Among authors: rousseau s. Curr Cardiol Rep. 2022 Aug;24(8):935-946. doi: 10.1007/s11886-022-01722-4. Epub 2022 Jun 11. Curr Cardiol Rep. 2022. PMID: 35689723 Free PMC article. Review.
ABCA7 rare variants and Alzheimer disease risk.
Le Guennec K, Nicolas G, Quenez O, Charbonnier C, Wallon D, Bellenguez C, Grenier-Boley B, Rousseau S, Richard AC, Rovelet-Lecrux A, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, Deleuze JF, Amouyel P, Munter HM, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues JF, Pasquier F, Rollin-Sillaire A, Génin E, Lambert JC, Hannequin D, Campion D; CNR-MAJ collaborators. Le Guennec K, et al. Among authors: rousseau s. Neurology. 2016 Jun 7;86(23):2134-7. doi: 10.1212/WNL.0000000000002627. Epub 2016 Apr 1. Neurology. 2016. PMID: 27037229 Free PMC article.
341 results