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

Year Number of Results
1990 2
1991 1
1992 2
1993 3
1994 1
1995 2
1996 1
1997 3
1998 3
1999 4
2000 5
2001 6
2002 15
2003 9
2004 7
2005 5
2006 8
2007 9
2008 6
2009 11
2010 6
2011 9
2012 11
2013 6
2014 13
2015 18
2016 10
2017 6
2018 6
2019 8
2020 5
2021 7
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191 results
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Page 1
Single cell dissection of plasma cell heterogeneity in symptomatic and asymptomatic myeloma.
Ledergor G, Weiner A, Zada M, Wang SY, Cohen YC, Gatt ME, Snir N, Magen H, Koren-Michowitz M, Herzog-Tzarfati K, Keren-Shaul H, Bornstein C, Rotkopf R, Yofe I, David E, Yellapantula V, Kay S, Salai M, Ben Yehuda D, Nagler A, Shvidel L, Orr-Urtreger A, Halpern KB, Itzkovitz S, Landgren O, San-Miguel J, Paiva B, Keats JJ, Papaemmanuil E, Avivi I, Barbash GI, Tanay A, Amit I. Ledergor G, et al. Among authors: orr urtreger a. Nat Med. 2018 Dec;24(12):1867-1876. doi: 10.1038/s41591-018-0269-2. Epub 2018 Dec 6. Nat Med. 2018. PMID: 30523328
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, Eblan MJ, Fahn S, Farrer MJ, Fung HC, Gan-Or Z, Gasser T, Gershoni-Baruch R, Giladi N, Griffith A, Gurevich T, Januario C, Kropp P, Lang AE, Lee-Chen GJ, Lesage S, Marder K, Mata IF, Mirelman A, Mitsui J, Mizuta I, Nicoletti G, Oliveira C, Ottman R, Orr-Urtreger A, Pereira LV, Quattrone A, Rogaeva E, Rolfs A, Rosenbaum H, Rozenberg R, Samii A, Samaddar T, Schulte C, Sharma M, Singleton A, Spitz M, Tan EK, Tayebi N, Toda T, Troiano AR, Tsuji S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG. Sidransky E, et al. Among authors: orr urtreger a. N Engl J Med. 2009 Oct 22;361(17):1651-61. doi: 10.1056/NEJMoa0901281. N Engl J Med. 2009. PMID: 19846850 Free PMC article.
Advances in the genetics of Parkinson's disease.
Rosner S, Giladi N, Orr-Urtreger A. Rosner S, et al. Among authors: orr urtreger a. Acta Pharmacol Sin. 2008 Jan;29(1):21-34. doi: 10.1111/j.1745-7254.2008.00731.x. Acta Pharmacol Sin. 2008. PMID: 18158863 Review.
A novel mutation in TARDBP segregates with amyotrophic lateral sclerosis in a large family with early onset and fast progression.
Goldstein O, Kedmi M, Gana-Weisz M, Nefussy B, Vainer B, Fainmesser Y, Drory VE, Orr-Urtreger A. Goldstein O, et al. Among authors: orr urtreger a. Amyotroph Lateral Scler Frontotemporal Degener. 2020 May;21(3-4):280-285. doi: 10.1080/21678421.2020.1747496. Epub 2020 Apr 7. Amyotroph Lateral Scler Frontotemporal Degener. 2020. PMID: 32253937
Tossing and Turning in Bed: Nocturnal Movements in Parkinson's Disease.
Mirelman A, Hillel I, Rochester L, Del Din S, Bloem BR, Avanzino L, Nieuwboer A, Maidan I, Herman T, Thaler A, Gurevich T, Kestenbaum M, Orr-Urtreger A, Brys M, Cedarbaum JM, Giladi N, Hausdorff JM. Mirelman A, et al. Among authors: orr urtreger a. Mov Disord. 2020 Jun;35(6):959-968. doi: 10.1002/mds.28006. Epub 2020 Feb 20. Mov Disord. 2020. PMID: 32080891
Genetic testing in Israel: an overview.
Rosner G, Rosner S, Orr-Urtreger A. Rosner G, et al. Among authors: orr urtreger a. Annu Rev Genomics Hum Genet. 2009;10:175-92. doi: 10.1146/annurev.genom.030308.111406. Annu Rev Genomics Hum Genet. 2009. PMID: 19453249 Review.
Progression in the LRRK2-Asssociated Parkinson Disease Population.
Saunders-Pullman R, Mirelman A, Alcalay RN, Wang C, Ortega RA, Raymond D, Mejia-Santana H, Orbe-Reilly M, Johannes BA, Thaler A, Ozelius L, Orr-Urtreger A, Marder KS, Giladi N, Bressman SB; LRRK2 Ashkenazi Jewish Consortium. Saunders-Pullman R, et al. Among authors: orr urtreger a. JAMA Neurol. 2018 Mar 1;75(3):312-319. doi: 10.1001/jamaneurol.2017.4019. JAMA Neurol. 2018. PMID: 29309488 Free PMC article.
New genetic principles.
Yaron Y, Orr-Urtreger A. Yaron Y, et al. Among authors: orr urtreger a. Clin Obstet Gynecol. 2002 Sep;45(3):593-604; discussion 730-2. doi: 10.1097/00003081-200209000-00004. Clin Obstet Gynecol. 2002. PMID: 12370600 Review. No abstract available.
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, Follett J, Farrer MJ, Trinh J, Gasser T, Goldwurm S, Gustavsson E, Klein C, Lang AE, Langston JW, Latourelle J, Lynch T, Marder K, Marras C, Martin ER, McLean CY, Mejia-Santana H, Molho E, Myers RH, Nuytemans K, Ozelius L, Payami H, Raymond D, Rogaeva E, Rogers MP, Ross OA, Samii A, Saunders-Pullman R, Schüle B, Schulte C, Scott WK, Tanner C, Tolosa E, Tomkins JE, Vilas D, Trojanowski JQ; 23andMe Research Team, Uitti R, Vance JM, Visanji NP, Wszolek ZK, Zabetian CP, Mirelman A, Giladi N, Orr Urtreger A, Cannon P, Fiske B, Foroud T. Lai D, et al. Among authors: orr urtreger a. Ann Neurol. 2021 Jul;90(1):76-88. doi: 10.1002/ana.26094. Epub 2021 May 17. Ann Neurol. 2021. PMID: 33938021 Free PMC article.
191 results
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