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

Year Number of Results
1978 1
1979 3
1980 2
1981 1
1982 1
1983 1
1987 1
1988 2
1989 1
1990 4
1991 4
1992 6
1993 1
1994 3
1995 2
1996 1
1997 2
2000 4
2001 4
2002 2
2003 3
2004 1
2005 6
2006 3
2007 7
2008 10
2009 13
2010 10
2011 20
2012 26
2013 19
2014 11
2015 24
2016 27
2017 12
2018 19
2019 14
2020 16
2021 10
2022 15
2023 13
2024 6

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294 results

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Page 1
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS.
Hop PJ, Zwamborn RAJ, Hannon E, Shireby GL, Nabais MF, Walker EM, van Rheenen W, van Vugt JJFA, Dekker AM, Westeneng HJ, Tazelaar GHP, van Eijk KR, Moisse M, Baird D, Al Khleifat A, Iacoangeli A, Ticozzi N, Ratti A, Cooper-Knock J, Morrison KE, Shaw PJ, Basak AN, Chiò A, Calvo A, Moglia C, Canosa A, Brunetti M, Grassano M, Gotkine M, Lerner Y, Zabari M, Vourc'h P, Corcia P, Couratier P, Mora Pardina JS, Salas T, Dion P, Ross JP, Henderson RD, Mathers S, McCombe PA, Needham M, Nicholson G, Rowe DB, Pamphlett R, Mather KA, Sachdev PS, Furlong S, Garton FC, Henders AK, Lin T, Ngo ST, Steyn FJ, Wallace L, Williams KL; BIOS Consortium; Brain MEND Consortium; Neto MM, Cauchi RJ, Blair IP, Kiernan MC, Drory V, Povedano M, de Carvalho M, Pinto S, Weber M, Rouleau GA, Silani V, Landers JE, Shaw CE, Andersen PM, McRae AF, van Es MA, Pasterkamp RJ, Wray NR, McLaughlin RL, Hardiman O, Kenna KP, Tsai E, Runz H, Al-Chalabi A, van den Berg LH, Van Damme P, Mill J, Veldink JH. Hop PJ, et al. Among authors: dion p. Sci Transl Med. 2022 Feb 23;14(633):eabj0264. doi: 10.1126/scitranslmed.abj0264. Epub 2022 Feb 23. Sci Transl Med. 2022. PMID: 35196023 Free PMC article.
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker AM, Gawor K, Westeneng HJ, Tazelaar GHP, van Eijk KR, Kooyman M, Byrne RP, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, Ticozzi N, Cooper-Knock J, Smith BN, Gromicho M, Chandran S, Pal S, Morrison KE, Shaw PJ, Hardy J, Orrell RW, Sendtner M, Meyer T, Başak N, van der Kooi AJ, Ratti A, Fogh I, Gellera C, Lauria G, Corti S, Cereda C, Sproviero D, D'Alfonso S, Sorarù G, Siciliano G, Filosto M, Padovani A, Chiò A, Calvo A, Moglia C, Brunetti M, Canosa A, Grassano M, Beghi E, Pupillo E, Logroscino G, Nefussy B, Osmanovic A, Nordin A, Lerner Y, Zabari M, Gotkine M, Baloh RH, Bell S, Vourc'h P, Corcia P, Couratier P, Millecamps S, Meininger V, Salachas F, Mora Pardina JS, Assialioui A, Rojas-García R, Dion PA, Ross JP, Ludolph AC, Weishaupt JH, Brenner D, Freischmidt A, Bensimon G, Brice A, Durr A, Payan CAM, Saker-Delye S, Wood NW, Topp S, Rademakers R, Tittmann L, Lieb W, Franke A, Ripke S, Braun A, Kraft J, Whiteman DC, Olsen CM, Uitterlinden AG, Hofman A, Rietschel … See abstract for full author list ➔ van Rheenen W, et al. Among authors: dion pa. Nat Genet. 2021 Dec;53(12):1636-1648. doi: 10.1038/s41588-021-00973-1. Epub 2021 Dec 6. Nat Genet. 2021. PMID: 34873335 Free PMC article.
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Cirulli ET, Lasseigne BN, Petrovski S, Sapp PC, Dion PA, Leblond CS, Couthouis J, Lu YF, Wang Q, Krueger BJ, Ren Z, Keebler J, Han Y, Levy SE, Boone BE, Wimbish JR, Waite LL, Jones AL, Carulli JP, Day-Williams AG, Staropoli JF, Xin WW, Chesi A, Raphael AR, McKenna-Yasek D, Cady J, Vianney de Jong JM, Kenna KP, Smith BN, Topp S, Miller J, Gkazi A; FALS Sequencing Consortium; Al-Chalabi A, van den Berg LH, Veldink J, Silani V, Ticozzi N, Shaw CE, Baloh RH, Appel S, Simpson E, Lagier-Tourenne C, Pulst SM, Gibson S, Trojanowski JQ, Elman L, McCluskey L, Grossman M, Shneider NA, Chung WK, Ravits JM, Glass JD, Sims KB, Van Deerlin VM, Maniatis T, Hayes SD, Ordureau A, Swarup S, Landers J, Baas F, Allen AS, Bedlack RS, Harper JW, Gitler AD, Rouleau GA, Brown R, Harms MB, Cooper GM, Harris T, Myers RM, Goldstein DB. Cirulli ET, et al. Among authors: dion pa. Science. 2015 Mar 27;347(6229):1436-41. doi: 10.1126/science.aaa3650. Epub 2015 Feb 19. Science. 2015. PMID: 25700176 Free PMC article.
Genetics of Intracranial Aneurysms.
Zhou S, Dion PA, Rouleau GA. Zhou S, et al. Among authors: dion pa. Stroke. 2018 Mar;49(3):780-787. doi: 10.1161/STROKEAHA.117.018152. Epub 2018 Feb 6. Stroke. 2018. PMID: 29437983 Review. No abstract available.
"1:1".
Ho AM, Dion PW, Ng CS, Cheung CW, Yeung JH, Critchley LA. Ho AM, et al. Among authors: dion pw. Resuscitation. 2011 May;82(5):627-8. doi: 10.1016/j.resuscitation.2010.12.022. Epub 2011 Feb 24. Resuscitation. 2011. PMID: 21353363 No abstract available.
ALS: Recent Developments from Genetics Studies.
Therrien M, Dion PA, Rouleau GA. Therrien M, et al. Among authors: dion pa. Curr Neurol Neurosci Rep. 2016 Jun;16(6):59. doi: 10.1007/s11910-016-0658-1. Curr Neurol Neurosci Rep. 2016. PMID: 27113253 Review.
Molecular aspects of hereditary spastic paraplegia.
Noreau A, Dion PA, Rouleau GA. Noreau A, et al. Among authors: dion pa. Exp Cell Res. 2014 Jul 1;325(1):18-26. doi: 10.1016/j.yexcr.2014.02.021. Epub 2014 Mar 11. Exp Cell Res. 2014. PMID: 24631291 Review.
Genomic analysis identifies risk factors in restless legs syndrome.
Akçimen F, Chia R, Saez-Atienzar S, Ruffo P, Rasheed M, Ross JP, Liao C, Ray A, Dion PA, Scholz SW, Rouleau GA, Traynor BJ. Akçimen F, et al. Among authors: dion pa. medRxiv [Preprint]. 2023 Dec 20:2023.12.19.23300211. doi: 10.1101/2023.12.19.23300211. medRxiv. 2023. PMID: 38168192 Free PMC article. Preprint.
An Open Letter to Health Canada.
Papp K, Albrecht L, Barber K, Bourcier M, Dion PL, Freiman A, Gooderham M, Guenther L, Gulliver W, Hong CH, Lynde C, Poulin Y, Siddha S, Toole J, Toth D, Vender R, Wasel N, Wiseman M. Papp K, et al. Among authors: dion pl. J Cutan Med Surg. 2017 May/Jun;21(3):195-196. doi: 10.1177/1203475417704642. J Cutan Med Surg. 2017. PMID: 28903599 No abstract available.
294 results