Wang Y - Search Results

1

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

Clark LN, Wang Y, Karlins E, Saito L, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Clark LN, et al. Among authors: wang y. Neurology. 2006 Nov 28;67(10):1786-91. doi: 10.1212/01.wnl.0000244345.49809.36. Epub 2006 Oct 18. Neurology. 2006. PMID: 17050822

2

Case-control study of the parkin gene in early-onset Parkinson disease.

Clark LN, Afridi S, Karlins E, Wang Y, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Clark LN, et al. Among authors: wang y. Arch Neurol. 2006 Apr;63(4):548-52. doi: 10.1001/archneur.63.4.548. Arch Neurol. 2006. PMID: 16606767 Free article.

3

A method for estimating penetrance from families sampled for linkage analysis.

Wang Y, Ottman R, Rabinowitz D. Wang Y, et al. Biometrics. 2006 Dec;62(4):1081-8. doi: 10.1111/j.1541-0420.2006.00614.x. Biometrics. 2006. PMID: 17156282 Free PMC article.

4

A screening assessment of cognitive impairment in patients with ALS.

Gordon PH, Wang Y, Doorish C, Lewis M, Battista V, Mitsumoto H, Marder K. Gordon PH, et al. Among authors: wang y. Amyotroph Lateral Scler. 2007 Dec;8(6):362-5. doi: 10.1080/17482960701500817. Epub 2007 Jul 30. Amyotroph Lateral Scler. 2007. PMID: 17852014

5

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease.

Clark LN, Ross BM, Wang Y, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Clark LN, et al. Among authors: wang y. Neurology. 2007 Sep 18;69(12):1270-7. doi: 10.1212/01.wnl.0000276989.17578.02. Neurology. 2007. PMID: 17875915 Free PMC article.

6

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method.

Wang Y, Clark LN, Louis ED, Mejia-Santana H, Harris J, Cote LJ, Waters C, Andrews H, Ford B, Frucht S, Fahn S, Ottman R, Rabinowitz D, Marder K. Wang Y, et al. Arch Neurol. 2008 Apr;65(4):467-74. doi: 10.1001/archneur.65.4.467. Arch Neurol. 2008. PMID: 18413468 Free PMC article.

7

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.

Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R. Poduri A, et al. Among authors: wang y. Neurology. 2009 Oct 20;73(16):1264-72. doi: 10.1212/WNL.0b013e3181bd10d3. Neurology. 2009. PMID: 19841378 Free PMC article.

8

Predicting Disease Onset from Mutation Status Using Proband and Relative Data with Applications to Huntington's Disease.

Chen T, Wang Y, Ma Y, Marder K, Langbehn DR. Chen T, et al. Among authors: wang y. J Probab Stat. 2012 Jan 1;2012:375935. doi: 10.1155/2012/375935. J Probab Stat. 2012. PMID: 23476655 Free PMC article.

9

Targeted Local Support Vector Machine for Age-Dependent Classification.

Chen T, Wang Y, Chen H, Marder K, Zeng D. Chen T, et al. Among authors: wang y. J Am Stat Assoc. 2014 Sep 1;109(507):1174-1187. doi: 10.1080/01621459.2014.881743. J Am Stat Assoc. 2014. PMID: 25284918 Free PMC article.

10

COMBINING ISOTONIC REGRESSION AND EM ALGORITHM TO PREDICT GENETIC RISK UNDER MONOTONICITY CONSTRAINT.

Qin J, Garcia TP, Ma Y, Tang MX, Marder K, Wang Y. Qin J, et al. Among authors: wang y. Ann Appl Stat. 2014;8(2):1182-1208. doi: 10.1214/14-AOAS730. Ann Appl Stat. 2014. PMID: 25404955 Free PMC article.

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