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Items: 1 to 20 of 190

1.

Triggering receptor expressed on myeloid cells 2 variants are rare in Parkinson's disease in a Han Chinese cohort.

Feng SJ, Nie K, Gan R, Huang J, Zhang YW, Wang LM, Zhao JH, Tang HM, Gao L, Zhu RM, Duan ZP, Zhang YH, Wang LJ.

Neurobiol Aging. 2014 Jul;35(7):1780.e11-2. doi: 10.1016/j.neurobiolaging.2014.01.142. Epub 2014 Feb 5.

PMID:
24602511
2.

Triggering receptor expressed on myeloid cells 2 variant is rare in late-onset Alzheimer's disease in Han Chinese individuals.

Yu JT, Jiang T, Wang YL, Wang HF, Zhang W, Hu N, Tan L, Sun L, Tan MS, Zhu XC, Tan L.

Neurobiol Aging. 2014 Apr;35(4):937.e1-3. doi: 10.1016/j.neurobiolaging.2013.10.075. Epub 2013 Oct 11.

PMID:
24184202
3.

Association study of TREM2 polymorphism rs75932628 with leucoaraiosis or Parkinson's disease in the Han Chinese population.

Li Z, Zhong L, Gu L, Huang W, Shi X, Zhang X, An X, Lin Q, Tzeng CM.

BMJ Open. 2016 Jan 12;6(1):e009499. doi: 10.1136/bmjopen-2015-009499.

4.

Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson's disease.

Tan T, Song Z, Yuan L, Xiong W, Deng X, Ni B, Chen Y, Deng H.

Neurosci Lett. 2016 Jan 26;612:189-192. doi: 10.1016/j.neulet.2015.12.029. Epub 2015 Dec 15.

PMID:
26704436
5.

Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population.

Chen Y, Chen X, Guo X, Song W, Cao B, Wei Q, Ou R, Zhao B, Shang HF.

Neurol Sci. 2015 Oct;36(10):1903-6. doi: 10.1007/s10072-015-2279-x. Epub 2015 Jun 10.

PMID:
26058955
6.

A rare coding variant in TREM2 increases risk for Alzheimer's disease in Han Chinese.

Jiang T, Tan L, Chen Q, Tan MS, Zhou JS, Zhu XC, Lu H, Wang HF, Zhang YD, Yu JT.

Neurobiol Aging. 2016 Jun;42:217.e1-3. doi: 10.1016/j.neurobiolaging.2016.02.023. Epub 2016 Mar 3.

PMID:
27067662
7.

Association study of TREM2 polymorphism rs75932628 with late-onset Alzheimer's disease in Chinese Han population.

Ma J, Zhou Y, Xu J, Liu X, Wang Y, Deng Y, Wang G, Xu W, Ren R, Liu X, Zhang Y, Wang C, Tang H, Chen S.

Neurol Res. 2014 Oct;36(10):894-6. doi: 10.1179/1743132814Y.0000000376. Epub 2014 Apr 13.

PMID:
24725293
8.

Lack of association between triggering receptor expressed on myeloid cells 2 polymorphism rs75932628 and late-onset Alzheimer's disease in a Chinese Han population.

Wang P, Guo Q, Zhou Y, Chen K, Xu Y, Ding D, Hong Z, Zhao Q.

Psychiatr Genet. 2018 Feb;28(1):16-18. doi: 10.1097/YPG.0000000000000188.

9.

TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease.

Rayaprolu S, Mullen B, Baker M, Lynch T, Finger E, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Josephs KA, Knopman DS, White CL 3rd, Caselli R, Mackenzie IR, Miller BL, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Younkin SG, Petersen RC, Ertekin-Taner N, Uitti RJ, Meschia JF, Boylan KB, Boeve BF, Graff-Radford NR, Wszolek ZK, Dickson DW, Rademakers R, Ross OA.

Mol Neurodegener. 2013 Jun 21;8:19. doi: 10.1186/1750-1326-8-19.

10.

TREM2 rare variant p.R47H is not associated with Parkinson's disease.

Mengel D, Thelen M, Balzer-Geldsetzer M, Söling C, Bach JP, Schaeffer E, Herold C, Becker T, Liepelt I, Becker J, Riedel-Heller S, Scherer M, Jessen F, Maier W, Dodel R, Ramirez A.

Parkinsonism Relat Disord. 2016 Feb;23:109-11. doi: 10.1016/j.parkreldis.2015.11.026. Epub 2015 Nov 25.

PMID:
26651418
11.

Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China.

Jiao B, Liu X, Tang B, Hou L, Zhou L, Zhang F, Zhou Y, Guo J, Yan X, Shen L.

Neurobiol Aging. 2014 Oct;35(10):2422.e9-2422.e11. doi: 10.1016/j.neurobiolaging.2014.04.025. Epub 2014 May 1.

PMID:
24866402
12.

Assessment of TREM2 rs75932628 association with amyotrophic lateral sclerosis in a Chinese population.

Chen X, Chen Y, Wei Q, Guo X, Cao B, Ou R, Zhao B, Shang HF.

J Neurol Sci. 2015 Aug 15;355(1-2):193-5. doi: 10.1016/j.jns.2015.05.010. Epub 2015 May 16.

PMID:
26026943
13.

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.

Lill CM, Rengmark A, Pihlstrøm L, Fogh I, Shatunov A, Sleiman PM, Wang LS, Liu T, Lassen CF, Meissner E, Alexopoulos P, Calvo A, Chio A, Dizdar N, Faltraco F, Forsgren L, Kirchheiner J, Kurz A, Larsen JP, Liebsch M, Linder J, Morrison KE, Nissbrandt H, Otto M, Pahnke J, Partch A, Restagno G, Rujescu D, Schnack C, Shaw CE, Shaw PJ, Tumani H, Tysnes OB, Valladares O, Silani V, van den Berg LH, van Rheenen W, Veldink JH, Lindenberger U, Steinhagen-Thiessen E; SLAGEN Consortium, Teipel S, Perneczky R, Hakonarson H, Hampel H, von Arnim CAF, Olsen JH, Van Deerlin VM, Al-Chalabi A, Toft M, Ritz B, Bertram L.

Alzheimers Dement. 2015 Dec;11(12):1407-1416. doi: 10.1016/j.jalz.2014.12.009. Epub 2015 Apr 30.

14.

TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.

Ortega-Cubero S, Lorenzo-Betancor O, Lorenzo E, Agúndez JA, Jiménez-Jiménez FJ, Ross OA, Wurster I, Mielke C, Lin JJ, Coria F, Clarimon J, Ezquerra M, Brighina L, Annesi G, Alonso-Navarro H, García-Martin E, Gironell A, Marti MJ, Yueh KC, Wszolek ZK, Sharma M, Berg D, Krüger R, Pastor MA, Pastor P.

Parkinsonism Relat Disord. 2015 Mar;21(3):306-9. doi: 10.1016/j.parkreldis.2014.12.010. Epub 2014 Dec 24.

15.

Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia.

Ruiz A, Dols-Icardo O, Bullido MJ, Pastor P, Rodríguez-Rodríguez E, López de Munain A, de Pancorbo MM, Pérez-Tur J, Alvarez V, Antonell A, López-Arrieta J, Hernández I, Tárraga L, Boada M, Lleó A, Blesa R, Frank-García A, Sastre I, Razquin C, Ortega-Cubero S, Lorenzo E, Sánchez-Juan P, Combarros O, Moreno F, Gorostidi A, Elcoroaristizabal X, Baquero M, Coto E, Sánchez-Valle R, Clarimón J; dementia genetic Spanish consortium (DEGESCO).

Neurobiol Aging. 2014 Feb;35(2):444.e1-4. doi: 10.1016/j.neurobiolaging.2013.08.011. Epub 2013 Sep 13.

PMID:
24041969
16.

TREM2 is associated with the risk of Alzheimer's disease in Spanish population.

Benitez BA, Cooper B, Pastor P, Jin SC, Lorenzo E, Cervantes S, Cruchaga C.

Neurobiol Aging. 2013 Jun;34(6):1711.e15-7. doi: 10.1016/j.neurobiolaging.2012.12.018. Epub 2013 Feb 5.

17.

TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia.

Lattante S, Le Ber I, Camuzat A, Dayan S, Godard C, Van Bortel I, De Septenville A, Ciura S, Brice A, Kabashi E; French Research Network on FTD and FTD-ALS.

Neurobiol Aging. 2013 Oct;34(10):2443.e1-2. doi: 10.1016/j.neurobiolaging.2013.04.030. Epub 2013 Jun 4.

PMID:
23759145
18.

Convergent Genetic and Expression Datasets Highlight TREM2 in Parkinson's Disease Susceptibility.

Liu G, Liu Y, Jiang Q, Jiang Y, Feng R, Zhang L, Chen Z, Li K, Liu J.

Mol Neurobiol. 2016 Sep;53(7):4931-8. doi: 10.1007/s12035-015-9416-7. Epub 2015 Sep 14.

PMID:
26365049
19.

TREM2 R47H variant as a risk factor for early-onset Alzheimer's disease.

Pottier C, Wallon D, Rousseau S, Rovelet-Lecrux A, Richard AC, Rollin-Sillaire A, Frebourg T, Campion D, Hannequin D.

J Alzheimers Dis. 2013;35(1):45-9. doi: 10.3233/JAD-122311.

PMID:
23380991
20.

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls.

Foo JN, Liany H, Tan LC, Au WL, Prakash KM, Liu J, Tan EK.

Neurobiol Aging. 2014 Apr;35(4):935.e1-2. doi: 10.1016/j.neurobiolaging.2013.09.018. Epub 2013 Oct 12.

PMID:
24126164

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