| Year |
Citation |
Score |
| 2015 |
Cooper NJ, Shtir CJ, Smyth DJ, Guo H, Swafford AD, Zanda M, Hurles ME, Walker NM, Plagnol V, Cooper JD, Howson JM, Burren OS, Onengut-Gumuscu S, Rich SS, Todd JA. Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes. Human Molecular Genetics. 24: 1774-90. PMID 25424174 DOI: 10.1093/Hmg/Ddu581 |
0.463 |
|
| 2014 |
Zanda M, Onengut-Gumuscu S, Walker N, Shtir C, Gallo D, Wallace C, Smyth D, Todd JA, Hurles ME, Plagnol V, Rich SS. A genome-wide assessment of the role of untagged copy number variants in type 1 diabetes. Plos Genetics. 10: e1004367. PMID 24875393 DOI: 10.1371/Journal.Pgen.1004367 |
0.469 |
|
| 2012 |
Loo SK, Shtir C, Doyle AE, Mick E, McGough JJ, McCracken J, Biederman J, Smalley SL, Cantor RM, Faraone SV, Nelson SF. Genome-wide association study of intelligence: additive effects of novel brain expressed genes. Journal of the American Academy of Child and Adolescent Psychiatry. 51: 432-440.e2. PMID 22449649 DOI: 10.1016/J.Jaac.2012.01.006 |
0.425 |
|
| 2012 |
Williams NM, Franke B, Mick E, Anney RJ, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, ... ... Shtir C, et al. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. The American Journal of Psychiatry. 169: 195-204. PMID 22420048 DOI: 10.1176/Appi.Ajp.2011.11060822 |
0.353 |
|
| 2012 |
Hunt KA, Smyth DJ, Balschun T, Ban M, Mistry V, Ahmad T, Anand V, Barrett JC, Bhaw-Rosun L, Bockett NA, Brand OJ, Brouwer E, Concannon P, Cooper JD, Dias KR, ... ... Shtir C, et al. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nature Genetics. 44: 3-5. PMID 22200769 DOI: 10.1038/Ng.1037 |
0.32 |
|
| 2012 |
Elia J, Glessner JT, Wang K, Takahashi N, Shtir CJ, Hadley D, Sleiman PM, Zhang H, Kim CE, Robison R, Lyon GJ, Flory JH, Bradfield JP, Imielinski M, Hou C, et al. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics. 44: 78-84. PMID 22138692 DOI: 10.1038/Ng.1013 |
0.335 |
|
| 2011 |
Mazhar K, Varma R, Choudhury F, McKean-Cowdin R, Shtir CJ, Azen SP. Severity of diabetic retinopathy and health-related quality of life: the Los Angeles Latino Eye Study. Ophthalmology. 118: 649-55. PMID 21035872 DOI: 10.1016/J.Ophtha.2010.08.003 |
0.378 |
|
| 2009 |
Shtir C, Pique-Regi R, Siegmund K, Morrison J, Schumacher F, Marjoram P. Copy number variation in the Framingham Heart Study. Bmc Proceedings. 3: S133. PMID 20018000 DOI: 10.1186/1753-6561-3-S7-S133 |
0.477 |
|
| 2009 |
Shtir CJ, Marjoram P, Azen S, Conti DV, Le Marchand L, Haiman CA, Varma R. Variation in genetic admixture and population structure among Latinos: the Los Angeles Latino eye study (LALES). Bmc Genetics. 10: 71. PMID 19903357 DOI: 10.1186/1471-2156-10-71 |
0.464 |
|
| 2008 |
Francis BA, Varma R, Chopra V, Lai MY, Shtir C, Azen SP. Intraocular pressure, central corneal thickness, and prevalence of open-angle glaucoma: the Los Angeles Latino Eye Study. American Journal of Ophthalmology. 146: 741-6. PMID 18672218 DOI: 10.1016/J.Ajo.2008.05.048 |
0.347 |
|
| 2007 |
Shtir C, Nagakawa IS, Duren WL, Conneely KN, Scott LJ, Silander K, Valle TT, Tuomilehto J, Buchanan TA, Bergman RN, Collins FS, Boehnke M, Watanabe RM. Subsets of Finns with high HDL to total cholesterol ratio show evidence for linkage to type 2 diabetes on chromosome 6q. Human Heredity. 63: 17-25. PMID 17179727 DOI: 10.1159/000097927 |
0.343 |
|
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