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Items: 1 to 20 of 101

1.

G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation.

Weinsheimer S, Brettman AD, Pawlikowska L, Wu DC, Mancuso MR, Kuhnert F, Lawton MT, Sidney S, Zaroff JG, McCulloch CE, Young WL, Kuo C, Kim H.

Transl Stroke Res. 2012 Dec;3(4):418-27. doi: 10.1007/s12975-012-0202-9. Epub 2012 Aug 14.

2.

Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations.

Mikhak B, Weinsheimer S, Pawlikowska L, Poon A, Kwok PY, Lawton MT, Chen Y, Zaroff JG, Sidney S, McCulloch CE, Young WL, Kim H.

Cerebrovasc Dis. 2011;31(4):338-45. doi: 10.1159/000322601. Epub 2011 Jan 7.

3.

EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations.

Weinsheimer S, Kim H, Pawlikowska L, Chen Y, Lawton MT, Sidney S, Kwok PY, McCulloch CE, Young WL.

Circ Cardiovasc Genet. 2009 Oct;2(5):476-82. doi: 10.1161/CIRCGENETICS.109.883595. Epub 2009 Aug 22.

4.

Common variants in interleukin-1-Beta gene are associated with intracranial hemorrhage and susceptibility to brain arteriovenous malformation.

Kim H, Hysi PG, Pawlikowska L, Poon A, Burchard EG, Zaroff JG, Sidney S, Ko NU, Achrol AS, Lawton MT, McCulloch CE, Kwok PY, Young WL.

Cerebrovasc Dis. 2009;27(2):176-82. doi: 10.1159/000185609. Epub 2008 Dec 18.

5.

Genome-wide association study of sporadic brain arteriovenous malformations.

Weinsheimer S, Bendjilali N, Nelson J, Guo DE, Zaroff JG, Sidney S, McCulloch CE, Al-Shahi Salman R, Berg JN, Koeleman BP, Simon M, Bostroem A, Fontanella M, Sturiale CL, Pola R, Puca A, Lawton MT, Young WL, Pawlikowska L, Klijn CJ, Kim H; GEN-AVM Consortium..

J Neurol Neurosurg Psychiatry. 2016 Sep;87(9):916-23. doi: 10.1136/jnnp-2015-312272. Epub 2016 Jan 27.

PMID:
26818729
6.

Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms.

Bendjilali N, Nelson J, Weinsheimer S, Sidney S, Zaroff JG, Hetts SW, Segal M, Pawlikowska L, McCulloch CE, Young WL, Kim H.

J Neurol Neurosurg Psychiatry. 2014 Nov;85(11):1280-3. doi: 10.1136/jnnp-2013-306461. Epub 2014 Apr 28.

7.

Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis.

Kremer PH, Koeleman BP, Rinkel GJ, Diekstra FP, van den Berg LH, Veldink JH, Klijn CJ.

J Neurol Neurosurg Psychiatry. 2016 Jul;87(7):693-6. doi: 10.1136/jnnp-2014-310094. Epub 2015 Aug 13.

PMID:
26272027
8.

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

Fei Q, Wu Z, Wang H, Zhou X, Wang N, Ding Y, Wang Y, Qiu G.

Spine (Phila Pa 1976). 2010 Apr 20;35(9):983-8. doi: 10.1097/BRS.0b013e3181bc963c.

PMID:
20228709
9.

Polymorphisms in genes involved in inflammatory and angiogenic pathways and the risk of hemorrhagic presentation of brain arteriovenous malformations.

Pawlikowska L, Tran MN, Achrol AS, McCulloch CE, Ha C, Lind DL, Hashimoto T, Zaroff J, Lawton MT, Marchuk DA, Kwok PY, Young WL; UCSF BAVM Study Project..

Stroke. 2004 Oct;35(10):2294-300. Epub 2004 Aug 26.

10.

Susceptible gene single nucleotide polymorphism and hemorrhage risk in patients with brain arteriovenous malformation.

Jiang N, Li X, Qi T, Guo S, Liang F, Huang Z.

J Clin Neurosci. 2011 Sep;18(9):1279-81. doi: 10.1016/j.jocn.2011.02.010. Epub 2011 Jul 6.

PMID:
21737283
11.

Polymorphisms of the vascular endothelial growth factor A gene and susceptibility to sporadic brain arteriovenous malformation in a Chinese population.

Chen H, Gu Y, Wu W, Chen D, Li P, Fan W, Lu D, Zhao F, Qiao N, Qiu H, Fu C, Mao Y, Zhao Y.

J Clin Neurosci. 2011 Apr;18(4):549-53. doi: 10.1016/j.jocn.2010.08.025. Epub 2011 Feb 12.

PMID:
21316969
12.

A haplotype analysis of HER-2 gene polymorphisms: association with breast cancer risk, HER-2 protein expression in the tumor, and disease recurrence in Korea.

Han W, Kang D, Lee JE, Park IA, Choi JY, Lee KM, Bae JY, Kim S, Shin ES, Lee JE, Shin HJ, Kim SW, Kim SW, Noh DY.

Clin Cancer Res. 2005 Jul 1;11(13):4775-8.

13.

The rs522616 polymorphism in the matrix metalloproteinase-3 (MMP-3) gene is associated with sporadic brain arteriovenous malformation in a Chinese population.

Zhao Y, Li P, Fan W, Chen D, Gu Y, Lu D, Zhao F, Hu J, Fu C, Chen X, Zhou L, Mao Y.

J Clin Neurosci. 2010 Dec;17(12):1568-72. doi: 10.1016/j.jocn.2010.04.023. Epub 2010 Sep 6.

PMID:
20822909
14.

Tumor necrosis factor-alpha-238G>A promoter polymorphism is associated with increased risk of new hemorrhage in the natural course of patients with brain arteriovenous malformations.

Achrol AS, Pawlikowska L, McCulloch CE, Poon KY, Ha C, Zaroff JG, Johnston SC, Lee C, Lawton MT, Sidney S, Marchuk DA, Kwok PY, Young WL; UCSF BAVM Study Project..

Stroke. 2006 Jan;37(1):231-4. Epub 2005 Dec 1.

15.

The rs9509 polymorphism of MMP-9 is associated with risk of hemorrhage in brain arteriovenous malformations.

Sun B, Qiu H, Zhao F, Qiao N, Fan W, Lu D, Chen H, Hu J, Fu C, Zhou L, Gu Y, Zhao Y, Mao Y.

J Clin Neurosci. 2012 Sep;19(9):1287-90. doi: 10.1016/j.jocn.2011.09.036. Epub 2012 Jul 15.

PMID:
22796276
16.

Replication Study of Polymorphisms Associated With Brain Arteriovenous Malformation in a Population From South of Brazil.

Franciscatto AC, Ludwig FS, Matte US, Mota S, Stefani MA.

Cureus. 2016 Feb 24;8(2):e508. doi: 10.7759/cureus.508.

17.

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.

Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva L, Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, Corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N, O'Donovan MC, Owen MJ.

Mol Psychiatry. 2010 Nov;15(11):1101-11. doi: 10.1038/mp.2009.96. Epub 2009 Sep 29.

PMID:
19786960
18.

Association of RAC1 Gene Polymorphisms with Primary End-Stage Renal Disease in Chinese Renal Recipients.

Liu Y, Zhou J, Luo X, Yang C, Zhang Y, Shi S.

PLoS One. 2016 Feb 3;11(2):e0148270. doi: 10.1371/journal.pone.0148270. eCollection 2016.

19.

The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.

Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I.

Int Clin Psychopharmacol. 2010 Jul;25(4):218-27. doi: 10.1097/YIC.0b013e328338b884.

PMID:
20531207
20.

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