| Year |
Citation |
Score |
| 2019 |
Wang Y, Li Y, Hao M, Liu X, Zhang M, Wang J, Xiong M, Shugart YY, Jin L. Robust Reference Powered Association Test of Genome-Wide Association Studies. Frontiers in Genetics. 10: 319. PMID 31024629 DOI: 10.3389/Fgene.2019.00319 |
0.354 |
|
| 2018 |
Guo W, Machado-Vieira R, Mathew S, Murrough JW, Charney DS, Gruenbaum M, Oquendo MA, Kadriu B, Akula N, Henter I, Yuan P, Merikangas K, Drevets W, Furey M, Mann JJ, ... ... Shugart YY, et al. Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression. Translational Psychiatry. 8: 280. PMID 30552317 DOI: 10.1038/S41398-018-0311-7 |
0.316 |
|
| 2017 |
Tang J, Fan Y, Li H, Xiang Q, Zhang DF, Li Z, He Y, Liao Y, Wang Y, He F, Zhang F, Shugart YY, Liu C, Tang Y, Chan RCK, et al. Whole-genome sequencing of monozygotic twins discordant for schizophrenia indicates multiple genetic risk factors for schizophrenia. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 28645778 DOI: 10.1016/J.Jgg.2017.05.005 |
0.366 |
|
| 2017 |
Guo W, Samuels JF, Wang Y, Cao H, Ritter M, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, ... ... Shugart YY, et al. Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 27: 657-666. PMID 28641744 DOI: 10.1016/J.Euroneuro.2017.03.011 |
0.431 |
|
| 2017 |
Ritter ML, Guo W, Samuels JF, Wang Y, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, ... ... Shugart YY, et al. Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Frontiers in Molecular Neuroscience. 10: 83. PMID 28386217 DOI: 10.3389/Fnmol.2017.00083 |
0.341 |
|
| 2016 |
Qin HD, Liao XY, Chen YB, Huang SY, Xue WQ, Li FF, Ge XS, Liu DQ, Cai Q, Long J, Li XZ, Hu YZ, Zhang SD, Zhang LJ, Lehrman B, ... ... Shugart YY, et al. Genomic Characterization of Esophageal Squamous Cell Carcinoma Reveals Critical Genes Underlying Tumorigenesis and Poor Prognosis. American Journal of Human Genetics. 98: 709-727. PMID 27058444 DOI: 10.1016/J.Ajhg.2016.02.021 |
0.326 |
|
| 2016 |
Wang J, Zhao S, Shugart YY, Zhou Z, Jin C, Yuan J, Wang G, Wang D, Cheng Z, Zhang F. No association between ZNF804A rs1344706 and schizophrenia in a case-control study of Han Chinese. Neuroscience Letters. PMID 26934312 DOI: 10.1016/J.Neulet.2016.02.048 |
0.377 |
|
| 2016 |
Tao Y, Gao H, Ackerman B, Guo W, Saffen D, Shugart YY. Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders. Bmc Genomics. 17: 163. PMID 26931105 DOI: 10.1186/S12864-016-2475-Y |
0.417 |
|
| 2015 |
Riddle MA, Maher BS, Wang Y, Grados M, Bienvenu OJ, Goes FS, Cullen B, Murphy DL, Rauch SL, Greenberg BD, Knowles JA, McCracken JT, Pinto A, Piacentini J, Pauls DL, ... ... Shugart YY, et al. OBSESSIVE-COMPULSIVE PERSONALITY DISORDER: EVIDENCE FOR TWO DIMENSIONS. Depression and Anxiety. PMID 26594839 DOI: 10.1002/Da.22452 |
0.324 |
|
| 2015 |
Wang Z, Yang B, Liu Y, Shugart YY, Cheng Z, Jin C, Yuan J, Zhu W, Wang G, Zhang F. Further evidence supporting the association of NKAPL with schizophrenia. Neuroscience Letters. 605: 49-52. PMID 26297123 DOI: 10.1016/J.Neulet.2015.08.023 |
0.39 |
|
| 2015 |
Luo X, Jin C, Zhou Z, Shugart YY, Liu X, Zhang F, Zhang F, Zhu J, Wang Y, Cheng Z. New findings support the association of DISC1 genetic variants with susceptibility to schizophrenia in the Han Chinese population. Psychiatry Research. PMID 26162659 DOI: 10.1016/J.Psychres.2015.05.115 |
0.347 |
|
| 2015 |
Zhang F, Xu Y, Cao H, Jin C, Cheng Z, Wang G, Shugart YY. Mapsnp: an R package to plot a genomic map for single nucleotide polymorphisms. Plos One. 10: e0123609. PMID 25853637 DOI: 10.1371/Journal.Pone.0123609 |
0.355 |
|
| 2015 |
Qin H, Samuels JF, Wang Y, Zhu Y, Grados MA, Riddle MA, Greenberg BD, Knowles JA, Fyer AJ, McCracken JT, Murphy DL, Rasmussen SA, Cullen BA, Piacentini J, Geller D, ... ... Shugart YY, et al. Whole-genome association analysis of treatment response in obsessive-compulsive disorder. Molecular Psychiatry. PMID 25824302 DOI: 10.1038/mp.2015.32 |
0.304 |
|
| 2015 |
Jiang DK, Ma XP, Yu H, Cao G, Ding DL, Chen H, Huang HX, Gao YZ, Wu XP, Long XD, Zhang H, Zhang Y, Gao Y, Chen TY, Ren WH, ... ... Shugart YY, et al. Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. Hepatology (Baltimore, Md.). 62: 118-28. PMID 25802187 DOI: 10.1002/Hep.27794 |
0.373 |
|
| 2015 |
Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Shugart YY, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306 |
0.356 |
|
| 2015 |
Mattheisen M, Samuels JF, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, McLaughlin NC, Nurmi EL, Askland KD, ... ... Shugart YY, et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Molecular Psychiatry. 20: 337-44. PMID 24821223 DOI: 10.1038/mp.2014.43 |
0.312 |
|
| 2014 |
Xu M, Wang HZ, Guo W, Qin H, Shugart YY. Family-based tests applied to extended pedigrees identify rare variants related to hypertension. Bmc Proceedings. 8: S31. PMID 25519318 DOI: 10.1186/1753-6561-8-S1-S31 |
0.368 |
|
| 2014 |
Ahn K, An SS, Shugart YY, Rapoport JL. Common polygenic variation and risk for childhood-onset schizophrenia. Molecular Psychiatry. PMID 25510512 DOI: 10.1038/Mp.2014.158 |
0.352 |
|
| 2014 |
Guo W, Shugart YY. The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees Bmc Genomics. 15. PMID 25070353 DOI: 10.1186/1471-2164-15-632 |
0.376 |
|
| 2014 |
McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Shugart YY, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/J.Jaac.2014.04.022 |
0.337 |
|
| 2014 |
Samuels J, Shugart YY, Wang Y, Grados MA, Bienvenu OJ, Pinto A, Rauch SL, Greenberg BD, Knowles JA, Fyer AJ, Piacentini J, Pauls DL, Cullen B, Rasmussen SA, Stewart SE, et al. Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive-compulsive disorder: Results from the OCD Collaborative Genetics Study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 326-36. PMID 24798771 DOI: 10.1002/Ajmg.B.32235 |
0.362 |
|
| 2014 |
Cao H, Duan J, Lin D, Shugart YY, Calhoun V, Wang YP. Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs Neuroimage. 102: 220-228. PMID 24530838 DOI: 10.1016/J.Neuroimage.2014.01.021 |
0.311 |
|
| 2014 |
Zhang F, Wang G, Shugart YY, Xu Y, Liu C, Wang L, Lu T, Yan H, Ruan Y, Cheng Z, Tian L, Jin C, Yuan J, Wang Z, Zhu W, et al. Association analysis of a functional variant in ATXN2 with schizophrenia. Neuroscience Letters. 562: 24-7. PMID 24333172 DOI: 10.1016/J.Neulet.2013.12.001 |
0.395 |
|
| 2014 |
Ahn K, Gotay N, Andersen TM, Anvari AA, Gochman P, Lee Y, Sanders S, Guha S, Darvasi A, Glessner JT, Hakonarson H, Lencz T, State MW, Shugart YY, Rapoport JL. High rate of disease-related copy number variations in childhood onset schizophrenia. Molecular Psychiatry. 19: 568-72. PMID 23689535 DOI: 10.1038/Mp.2013.59 |
0.369 |
|
| 2013 |
Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... Shugart YY, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864 |
0.424 |
|
| 2013 |
Wang HZ, Qin HD, Guo W, Samuels J, Shugart YY. New insights into the genetic mechanism of IQ in autism spectrum disorders. Frontiers in Genetics. 4: 195. PMID 24151499 DOI: 10.3389/Fgene.2013.00195 |
0.381 |
|
| 2013 |
Xue WQ, Qin HD, Ruan HL, Shugart YY, Jia WH. Quantitative association of tobacco smoking with the risk of nasopharyngeal carcinoma: a comprehensive meta-analysis of studies conducted between 1979 and 2011. American Journal of Epidemiology. 178: 325-38. PMID 23785114 DOI: 10.1093/Aje/Kws479 |
0.312 |
|
| 2013 |
Fan Q, He JF, Wang QR, Cai HB, Sun XG, Zhou XX, Qin HD, Shugart YY, Jia WH. Functional polymorphism in the 5′-UTR of CR2 is associated with susceptibility to nasopharyngeal carcinoma Oncology Reports. 30: 11-16. PMID 23612877 DOI: 10.3892/Or.2013.2421 |
0.368 |
|
| 2013 |
Stewart SE, Mayerfeld C, Arnold PD, Crane JR, O'Dushlaine C, Fagerness JA, Yu D, Scharf JM, Chan E, Kassam F, Moya PR, Wendland JR, Delorme R, Richter MA, Kennedy JL, ... ... Shugart YY, et al. Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 367-79. PMID 23606572 DOI: 10.1002/Ajmg.B.32137 |
0.427 |
|
| 2013 |
Yuan J, Jin C, Qin HD, Wang J, Sha W, Wang M, Zhang Y, Zhang F, Li J, Li J, Yu S, Qi S, Shugart YY. Replication study confirms link between TSPAN18 mutation and schizophrenia in Han Chinese. Plos One. 8: e58785. PMID 23505562 DOI: 10.1371/Journal.Pone.0058785 |
0.395 |
|
| 2013 |
Ruan HL, Qin HD, Shugart YY, Bei JX, Luo FT, Zeng YX, Jia WH. Developing genetic epidemiological models to predict risk for nasopharyngeal carcinoma in high-risk population of China. Plos One. 8: e56128. PMID 23457511 DOI: 10.1371/Journal.Pone.0056128 |
0.358 |
|
| 2013 |
Jiang DK, Sun J, Cao G, Liu Y, Lin D, Gao YZ, Ren WH, Long XD, Zhang H, Ma XP, Wang Z, Jiang W, Chen TY, Gao Y, Sun LD, ... ... Shugart YY, et al. Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. Nature Genetics. 45: 72-5. PMID 23242368 DOI: 10.1038/Ng.2483 |
0.322 |
|
| 2013 |
Alberg AJ, Jorgensen TJ, Ruczinski I, Wheless L, Shugart YY, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Francis L, Alani RM, Smith MW, Strickland PT. DNA repair gene variants in relation to overall cancer risk: a population-based study. Carcinogenesis. 34: 86-92. PMID 23027618 DOI: 10.1093/Carcin/Bgs304 |
0.37 |
|
| 2013 |
Chen DT, Jiang X, Akula N, Shugart YY, Wendland JR, Steele CJ, Kassem L, Park JH, Chatterjee N, Jamain S, Cheng A, Leboyer M, Muglia P, Schulze TG, Cichon S, et al. Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder. Molecular Psychiatry. 18: 195-205. PMID 22182935 DOI: 10.1038/mp.2011.157 |
0.322 |
|
| 2013 |
Su W, Chang K, Shugart YY, Chang Y. Abstract 4838: Exploration of genome-wide two-locus SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility. Cancer Research. 73: 4838-4838. DOI: 10.1158/1538-7445.Am2013-4838 |
0.376 |
|
| 2013 |
Chen DT, Jiang X, Akula N, Shugart YY, Wendland JR, Steele CJM, Kassem L, Park JH, Chatterjee N, Jamain S, Cheng A, Leboyer M, Muglia P, Schulze TG, Cichon S, et al. Erratum: Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder (Molecular Psychiatry (2013) 18 (264-266)) Molecular Psychiatry. 18: 264-266. DOI: 10.1038/Mp.2012.45 |
0.359 |
|
| 2012 |
Shugart YY, Zhu Y, Guo W, Xiong M. Weighted pedigree-based statistics for testing the association of rare variants. Bmc Genomics. 13: 667. PMID 23176082 DOI: 10.1186/1471-2164-13-667 |
0.354 |
|
| 2012 |
Guo W, Shugart YY. Detecting rare variants for quantitative traits using nuclear families Human Heredity. 73: 148-158. PMID 22699804 DOI: 10.1159/000338439 |
0.329 |
|
| 2012 |
Ruczinski I, Jorgensen TJ, Shugart YY, Schaad YB, Kessing B, Hoffman-Bolton J, Helzlsouer KJ, Kao WH, Wheless L, Francis L, Alani RM, Strickland PT, Smith MW, Alberg AJ. A population-based study of DNA repair gene variants in relation to non-melanoma skin cancer as a marker of a cancer-prone phenotype. Carcinogenesis. 33: 1692-8. PMID 22581838 DOI: 10.1093/Carcin/Bgs170 |
0.37 |
|
| 2012 |
Wheless L, Kistner-Griffin E, Jorgensen TJ, Ruczinski I, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Francis L, Shugart YY, Strickland PT, Kao WH, Alani RM, Smith MW, Alberg AJ. A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. The Journal of Investigative Dermatology. 132: 1354-62. PMID 22336945 DOI: 10.1038/Jid.2012.4 |
0.359 |
|
| 2012 |
Nestadt G, Wang Y, Grados MA, Riddle MA, Greenberg BD, Knowles JA, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Piacentini J, Geller D, Pauls D, ... ... Shugart YY, et al. Homeobox genes in obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 53-60. PMID 22095678 DOI: 10.1002/Ajmg.B.32001 |
0.352 |
|
| 2012 |
Ruczinski I, Jorgensen T, Shugart YY, Berthier-Schaad Y, Kessing B, Hoffman-Bolton J, Helzlsouer K, Kao WHL, Wheless L, Francis L, Alani R, Strickland P, Smith M, Alberg AJ. Abstract 2636: Nonmelanoma skin cancer as a marker of a cancer-prone phenotype: Potential role of DNA repair gene variants Cancer Research. 72: 2636-2636. DOI: 10.1158/1538-7445.Am2012-2636 |
0.362 |
|
| 2012 |
Okazaki T, Wang MH, Rawsthorne P, Sargent M, Datta LW, Shugart YY, Bernstein CN, Brant SR. Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohnʼs disease risk in a population-based case-control study: Evidence of gene-gene interactions Inflammatory Bowel Diseases. 18: 1591. DOI: 10.1002/Ibd.23056 |
0.304 |
|
| 2011 |
Akula N, Detera-Wadleigh S, Shugart YY, Nalls M, Steele J, McMahon FJ. Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives. Bmc Proceedings. 5: S76. PMID 22373213 DOI: 10.1186/1753-6561-5-S9-S76 |
0.404 |
|
| 2011 |
Qin HD, Jia WH, Zhang LL, Liu N, Zhou XX, Wang MH, Feng QS, Chen LZ, Zhang Y, Jorgensen TJ, Zeng YX, Shugart YY. Elevated Epstein-Barr virus seroreactivity among unaffected members of families with nasopharyngeal carcinoma. Journal of Medical Virology. 83: 1792-8. PMID 21837797 DOI: 10.1002/Jmv.22121 |
0.314 |
|
| 2011 |
Shen GP, Pan QH, Hong MH, Qin HD, Xu YF, Chen LZ, Feng QS, Jorgensen TJ, Shugart YY, Zeng YX, Jia WH. Human genetic variants of homologous recombination repair genes first found to be associated with Epstein-Barr virus antibody titers in healthy Cantonese. International Journal of Cancer. 129: 1459-66. PMID 21792882 DOI: 10.1002/Ijc.25759 |
0.366 |
|
| 2011 |
Samuels J, Wang Y, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Knowles JA, Piacentini J, Cullen B, Bienvenu OJ, Rasmussen SA, Geller D, ... ... Shugart YY, et al. Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 472-7. PMID 21445956 DOI: 10.1002/Ajmg.B.31184 |
0.416 |
|
| 2011 |
Shugart YY, Wang Y, Jia WH, Zeng YX. GWAS signals across the HLA regions: revealing a clue for common etiology underlying infectious tumors and other immunity diseases Chinese Journal of Cancer. 30: 226-230. PMID 21439243 DOI: 10.5732/Cjc.011.10075 |
0.335 |
|
| 2011 |
Qin HD, Shugart YY, Bei JX, Pan QH, Chen L, Feng QS, Chen LZ, Huang W, Liu JJ, Jorgensen TJ, Zeng YX, Jia WH. Comprehensive pathway-based association study of DNA repair gene variants and the risk of nasopharyngeal carcinoma. Cancer Research. 71: 3000-8. PMID 21368091 DOI: 10.1158/0008-5472.Can-10-0469 |
0.35 |
|
| 2011 |
Li R, Yang Y, An Y, Zhou Y, Liu Y, Yu Q, Lu D, Wang H, Jin L, Zhou W, Qian J, Shugart YY. Genetic polymorphisms in DNA double-strand break repair genes XRCC5, XRCC6 and susceptibility to hepatocellular carcinoma. Carcinogenesis. 32: 530-6. PMID 21304054 DOI: 10.1093/Carcin/Bgr018 |
0.376 |
|
| 2011 |
Li R, Zhao Y, Fan W, Chen H, Chen Y, Liu Y, Chen G, Zhou K, Huang F, Mao Y, Zhou L, Lu D, Shugart YY. Possible association between polymorphisms of human vascular endothelial growth factor A gene and susceptibility to glioma in a Chinese population. International Journal of Cancer. Journal International Du Cancer. 128: 166-75. PMID 20209496 DOI: 10.1002/Ijc.25306 |
0.381 |
|
| 2011 |
Voyiaziakis E, Evgrafov O, Li D, Yoon HJ, Tabares P, Samuels J, Wang Y, Riddle MA, Grados MA, Bienvenu OJ, Shugart YY, Liang KY, Greenberg BD, Rasmussen SA, Murphy DL, et al. Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study. Molecular Psychiatry. 16: 108-20. PMID 19806148 DOI: 10.1038/Mp.2009.100 |
0.35 |
|
| 2010 |
Nicodemus KK, Callicott JH, Higier RG, Luna A, Nixon DC, Lipska BK, Vakkalanka R, Giegling I, Rujescu D, St Clair D, Muglia P, Shugart YY, Weinberger DR. Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging. Human Genetics. 127: 441-52. PMID 20084519 DOI: 10.1007/S00439-009-0782-Y |
0.362 |
|
| 2010 |
Nicodemus KK, Callicott JH, Higier RG, Luna A, Nixon DC, Lipska BK, Vakkalanka R, Giegling I, Rujescu D, Clair DS, Muglia P, Shugart YY, Weinberger D. Erratum: Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: Biological validation with functional neuroimaging (Human Genetics DOI: 10.1007/s00439-009-0782-y)) Human Genetics. 127: 453-454. DOI: 10.1007/S00439-010-0793-8 |
0.314 |
|
| 2009 |
Jia WH, Pan QH, Qin HD, Xu YF, Shen GP, Chen L, Chen LZ, Feng QS, Hong MH, Zeng YX, Shugart YY. A case-control and a family-based association study revealing an association between CYP2E1 polymorphisms and nasopharyngeal carcinoma risk in Cantonese Carcinogenesis. 30: 2031-2036. PMID 19805575 DOI: 10.1093/Carcin/Bgp239 |
0.394 |
|
| 2009 |
Jorgensen TJ, Ruczinski I, Kessing B, Smith MW, Shugart YY, Alberg AJ. Hypothesis-driven candidate gene association studies: practical design and analytical considerations. American Journal of Epidemiology. 170: 986-93. PMID 19762372 DOI: 10.1093/Aje/Kwp242 |
0.354 |
|
| 2009 |
Tse KP, Su WH, Chang KP, Tsang NM, Yu CJ, Tang P, See LC, Hsueh C, Yang ML, Hao SP, Li HY, Wang MH, Liao LP, Chen LC, Lin SR, ... ... Shugart YY, et al. Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. American Journal of Human Genetics. 85: 194-203. PMID 19664746 DOI: 10.1016/J.Ajhg.2009.07.007 |
0.404 |
|
| 2009 |
Lam TK, Ruczinski I, Helzlsouer K, Shugart YY, Li KE, Clipp S, Strickland PT, Alberg AJ. Copy number variants of GSTM1 and GSTT1 in relation to lung cancer risk in a prospective cohort study. Annals of Epidemiology. 19: 546-52. PMID 19394866 DOI: 10.1016/J.Annepidem.2009.03.003 |
0.308 |
|
| 2009 |
Wang MH, Helzlsouer KJ, Smith MW, Hoffman-Bolton JA, Clipp SL, Grinberg V, De Marzo AM, Isaacs WB, Drake CG, Shugart YY, Platz EA. Association of IL10 and other immune response- and obesity-related genes with prostate cancer in CLUE II Prostate. 69: 874-885. PMID 19267370 DOI: 10.1002/Pros.20933 |
0.333 |
|
| 2009 |
Shugart YY, Chen L, Day IN, Lewis SJ, Timpson NJ, Yuan W, Abdollahi MR, Ring SM, Ebrahim S, Golding J, Lawlor DA, Davey-Smith G. Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI. European Journal of Human Genetics : Ejhg. 17: 1050-5. PMID 19209189 DOI: 10.1038/Ejhg.2008.272 |
0.308 |
|
| 2009 |
Shugart YY, Wang Y, Samuels JF, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Hoehn-Saric R, Pinto A, Fyer AJ, Piacentini J, et al. A family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder in 378 families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 886-92. PMID 19152386 DOI: 10.1002/Ajmg.B.30914 |
0.307 |
|
| 2009 |
Li R, Shugart YY, Zhou W, An Y, Yang Y, Zhou Y, Zhang B, Lu D, Wang H, Qian J, Jin L. Common genetic variations of the cytochrome P450 1A1 gene and risk of hepatocellular carcinoma in a Chinese population. European Journal of Cancer (Oxford, England : 1990). 45: 1239-47. PMID 19110417 DOI: 10.1016/J.Ejca.2008.11.007 |
0.343 |
|
| 2009 |
Bienvenu OJ, Wang Y, Shugart YY, Welch JM, Grados MA, Fyer AJ, Rauch SL, McCracken JT, Rasmussen SA, Murphy DL, Cullen B, Valle D, Hoehn-Saric R, Greenberg BD, Pinto A, et al. Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 710-20. PMID 19051237 DOI: 10.1002/Ajmg.B.30897 |
0.302 |
|
| 2008 |
Okazaki T, Wang MH, Rawsthorne P, Sargent M, Datta LW, Shugart YY, Bernstein CN, Brant SR. Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions. Inflammatory Bowel Diseases. 14: 1528-41. PMID 18521914 DOI: 10.1002/Ibd.20512 |
0.37 |
|
| 2008 |
Pinto A, Greenberg BD, Grados MA, Bienvenu OJ, Samuels JF, Murphy DL, Hasler G, Stout RL, Rauch SL, Shugart YY, Pauls DL, Knowles JA, Fyer AJ, McCracken JT, Piacentini J, et al. Further development of YBOCS dimensions in the OCD Collaborative Genetics study: symptoms vs. categories. Psychiatry Research. 160: 83-93. PMID 18514325 DOI: 10.1016/J.Psychres.2007.07.010 |
0.305 |
|
| 2008 |
Liang KY, Wang Y, Shugart YY, Grados M, Fyer AJ, Rauch S, Murphy D, McCracken J, Rasmussen S, Cullen B, Hoehn-Saric R, Greenberg B, Pinto A, Knowles J, Piacentini J, et al. Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive-compulsive disorder with compulsive hoarding. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1000-2. PMID 18286588 DOI: 10.1002/Ajmg.B.30713 |
0.371 |
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| 2008 |
Shugart YY, Silverberg MS, Duerr RH, Taylor KD, Wang MH, Zarfas K, Schumm LP, Bromfield G, Steinhart AH, Griffiths AM, Kane SV, Barmada MM, Rotter JI, Mei L, Bernstein CN, et al. An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29 Genes and Immunity. 9: 161-167. PMID 18246054 DOI: 10.1038/Sj.Gene.6364460 |
0.367 |
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| 2008 |
Chen L, Lawlor DA, Lewis SJ, Yuan W, Abdollahi MR, Timpson NJ, Day IN, Ebrahim S, Smith GD, Shugart YY. Genetic association study of BDNF in depression: finding from two cohort studies and a meta-analysis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 814-21. PMID 18205169 DOI: 10.1002/Ajmg.B.30686 |
0.32 |
|
| 2008 |
Liu Y, Zhou K, Zhang H, Shugart YY, Chen L, Xu Z, Zhong Y, Liu H, Jin L, Wei Q, Huang F, Lu D, Zhou L. Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma Human Mutation. 29: 381-389. PMID 18165945 DOI: 10.1002/Humu.20645 |
0.401 |
|
| 2008 |
Cullen B, Samuels JF, Pinto A, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Greenberg BD, Knowles JA, Piacentini J, Bienvenu OJ, Grados MA, Riddle MA, Rasmussen SA, Pauls DL, ... ... Shugart YY, et al. Demographic and clinical characteristics associated with treatment status in family members with obsessive-compulsive disorder. Depression and Anxiety. 25: 218-24. PMID 17345603 DOI: 10.1002/Da.20293 |
0.303 |
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| 2007 |
Nicodemus KK, Wang W, Shugart YY. Stability of variable importance scores and rankings using statistical learning tools on single-nucleotide polymorphisms and risk factors involved in gene x gene and gene x environment interactions. Bmc Proceedings. 1: S58. PMID 18466558 DOI: 10.1186/1753-6561-1-S1-S58 |
0.366 |
|
| 2007 |
Ziegler A, DeStefano AL, König IR, Bardel C, Brinza D, Bull S, Cai Z, Glaser B, Jiang W, Lee KE, Li CX, Li J, Li X, Majoram P, Meng Y, ... ... Shugart YY, et al. Data mining, neural nets, trees--problems 2 and 3 of Genetic Analysis Workshop 15. Genetic Epidemiology. 31: S51-60. PMID 18046765 DOI: 10.1002/Gepi.20280 |
0.39 |
|
| 2007 |
Shugart YY, Chen L, Li R, Beaty T. Family-based linkage disequilibrium tests using general pedigrees Methods in Molecular Biology. 376: 141-149. PMID 17984543 DOI: 10.1007/978-1-59745-389-9_10 |
0.356 |
|
| 2007 |
He JF, Jia WH, Fan Q, Zhou XX, Qin HD, Shugart YY, Zeng YX. Genetic polymorphisms of TLR3 are associated with Nasopharyngeal carcinoma risk in Cantonese population Bmc Cancer. 7. PMID 17939877 DOI: 10.1186/1471-2407-7-194 |
0.354 |
|
| 2007 |
Daugherty SE, Platz EA, Shugart YY, Fallin MD, Isaacs WB, Chatterjee N, Welch R, Huang WY, Hayes RB. Variants in the alpha-Methylacyl-CoA racemase gene and the association with advanced distal colorectal adenoma. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 16: 1536-42. PMID 17684125 DOI: 10.1158/1055-9965.Epi-07-0117 |
0.354 |
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| 2007 |
Ma H, Xu L, Yuan J, Shao M, Hu Z, Wang F, Wang Y, Yuan W, Qian J, Wang Y, Xun P, Liu H, Chen W, Yang L, Jin G, ... ... Shugart YY, et al. Tagging single nucleotide polymorphisms in excision repair cross-complementing group 1 (ERCC1) and risk of primary lung cancer in a Chinese population. Pharmacogenetics and Genomics. 17: 417-23. PMID 17502833 DOI: 10.1097/01.Fpc.0000239975.77088.17 |
0.308 |
|
| 2007 |
Rioux JD, Xavier RJ, Taylor KD, Silverberg MS, Goyette P, Huett A, Green T, Kuballa P, Barmada MM, Datta LW, Shugart YY, Griffiths AM, Targan SR, Ippoliti AF, Bernard EJ, et al. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. Nature Genetics. 39: 596-604. PMID 17435756 DOI: 10.1038/Ng2032 |
0.355 |
|
| 2007 |
Liu Y, Zhang H, Zhou K, Chen L, Xu Z, Zhong Y, Liu H, Li R, Shugart YY, Wei Q, Jin L, Huang F, Lu D, Zhou L. Tagging SNPs in non-homologous end-joining pathway genes and risk of glioma Carcinogenesis. 28: 1906-1913. PMID 17389609 DOI: 10.1093/Carcin/Bgm073 |
0.393 |
|
| 2007 |
Samuels J, Shugart YY, Grados MA, Willour VL, Bienvenu OJ, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Wang Y, Pinto A, Fyer AJ, Piacentini J, Pauls DL, et al. Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. The American Journal of Psychiatry. 164: 493-9. PMID 17329475 DOI: 10.1176/Ajp.2007.164.3.493 |
0.371 |
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| 2007 |
Yoon DY, Rippel CA, Kobets AJ, Morris CM, Lee JE, Williams PN, Bridges DD, Vandenbergh DJ, Shugart YY, Singer HS. Dopaminergic polymorphisms in Tourette syndrome: association with the DAT gene (SLC6A3). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 605-10. PMID 17171650 DOI: 10.1002/Ajmg.B.30466 |
0.379 |
|
| 2007 |
Nicodemus KK, Luna A, Shugart YY. An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification American Journal of Human Genetics. 80: 178-185. PMID 17160905 DOI: 10.1086/510498 |
0.349 |
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| 2007 |
Brant SR, Wang MH, Rawsthorne P, Sargent M, Datta LW, Nouvet F, Shugart YY, Bernstein CN. A population-based case-control study of CARD15 and other risk factors in Crohn's disease and ulcerative colitis. The American Journal of Gastroenterology. 102: 313-23. PMID 17100976 DOI: 10.1111/J.1572-0241.2006.00926.X |
0.321 |
|
| 2007 |
Hasler G, Pinto A, Greenberg BD, Samuels J, Fyer AJ, Pauls D, Knowles JA, McCracken JT, Piacentini J, Riddle MA, Rauch SL, Rasmussen SA, Willour VL, Grados MA, Cullen B, ... ... Shugart YY, et al. Familiality of factor analysis-derived YBOCS dimensions in OCD-affected sibling pairs from the OCD Collaborative Genetics Study. Biological Psychiatry. 61: 617-25. PMID 17027929 DOI: 10.1016/J.Biopsych.2006.05.040 |
0.355 |
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| 2007 |
Samuels JF, Bienvenu OJ, Pinto A, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Greenberg BD, Knowles JA, Piacentini J, Cannistraro PA, Cullen B, Riddle MA, Rasmussen SA, ... ... Shugart YY, et al. Hoarding in obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. Behaviour Research and Therapy. 45: 673-86. PMID 16824483 DOI: 10.1016/J.Brat.2006.05.008 |
0.343 |
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| 2007 |
Rioux J, Xavier R, Taylor K, Goyette P, Silverberg M, Huett A, Green T, Kuballa P, Barmada M, Datta L, Shugart YY, Jean Bernard E, Mei L, Nicolae D, Steinhart H, et al. Whole Genome Association Identifies Novel Susceptibility Genes for Crohn's Disease and Implicates a Crucial Role for Autophagy Clinical Immunology. 123: S172. DOI: 10.1016/J.Clim.2007.03.131 |
0.323 |
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| 2006 |
Rippel CA, Kobets AJ, Yoon DY, Williams PN, Shugart YY, Bridges DD, Vandenbergh DJ, Singer HS. Norepinephrine transporter polymorphisms in Tourette syndrome with and without attention deficit hyperactivity disorder: no evidence for significant association. Psychiatric Genetics. 16: 179-80. PMID 16969268 DOI: 10.1097/01.Ypg.0000218622.96127.71 |
0.349 |
|
| 2006 |
Doan BQ, Sorant AJ, Frangakis CE, Bailey-Wilson JE, Shugart YY. Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage. European Journal of Human Genetics : Ejhg. 14: 1018-26. PMID 16736037 DOI: 10.1038/Sj.Ejhg.5201650 |
0.355 |
|
| 2006 |
Zhou XX, Jia WH, Shen GP, Qin HD, Yu XJ, Chen LZ, Feng QS, Shugart YY, Zeng YX. Sequence variants in toll-like receptor 10 are associated with nasopharyngeal carcinoma risk Cancer Epidemiology Biomarkers and Prevention. 15: 862-866. PMID 16702361 DOI: 10.1158/1055-9965.Epi-05-0874 |
0.392 |
|
| 2006 |
Samuels JF, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Pinto A, Knowles JA, Piacentini J, Cannistraro PA, Cullen B, Bienvenu OJ, Rasmussen SA, ... ... Shugart YY, et al. The OCD collaborative genetics study: methods and sample description. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 201-7. PMID 16511842 DOI: 10.1002/Ajmg.B.30224 |
0.361 |
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| 2005 |
Wang MH, Guo M, Shugart YY. Application of family-based association testing to assess the genotype-phenotype association involved in complex traits using single-nucleotide polymorphisms. Bmc Genetics. 6: S68. PMID 16451681 DOI: 10.1186/1471-2156-6-S1-S68 |
0.426 |
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| 2005 |
Doan BQ, Frangakis CE, Shugart YY, Bailey-Wilson JE. Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism. Bmc Genetics. 6: S33. PMID 16451643 DOI: 10.1186/1471-2156-6-S1-S33 |
0.357 |
|
| 2005 |
Sheen VL, Jansen A, Chen MH, Parrini E, Morgan T, Ravenscroft R, Ganesh V, Underwood T, Wiley J, Leventer R, Vaid RR, Ruiz DE, Hutchins GM, Menasha J, Willner J, ... ... Shugart YY, et al. Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome. Neurology. 64: 254-62. PMID 15668422 DOI: 10.1212/01.Wnl.0000149512.79621.Df |
0.333 |
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| 2005 |
Vyshkina T, Banisor I, Shugart YY, Leist TP, Kalman B. Genetic variants of Complex I in multiple sclerosis Journal of the Neurological Sciences. 228: 55-64. PMID 15607211 DOI: 10.1016/J.Jns.2004.09.027 |
0.358 |
|
| 2005 |
Vyshkina T, Shugart YY, Birnbaum G, Leist TP, Kalman B. Association of haplotypes in the β-chemokine locus with multiple sclerosis European Journal of Human Genetics. 13: 240-247. PMID 15494740 DOI: 10.1038/Sj.Ejhg.5201295 |
0.341 |
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| 2005 |
Jia WH, Collins A, Zeng YX, Feng BJ, Yu XJ, Huang LX, Feng QS, Huang P, Yao MH, Shugart YY. Complex segregation analysis of nasopharyngeal carcinoma in Guangdong, China: Evidence for a multifactorial mode of inheritance (complex segregation analysis of NPC in China) European Journal of Human Genetics. 13: 248-252. PMID 15483644 DOI: 10.1038/Sj.Ejhg.5201305 |
0.353 |
|
| 2004 |
Vyshkina T, Leist TP, Shugart YY, Kalman B. CD45 (PTPRC) as a candidate gene in multiple sclerosis Multiple Sclerosis. 10: 614-617. PMID 15584483 DOI: 10.1191/1352458504Ms1115Oa |
0.345 |
|
| 2004 |
Brant SR, Shugart YY. Inflammatory bowel disease gene hunting by linkage analysis: Rationale, methodology, and present status of the field Inflammatory Bowel Diseases. 10: 300-311. PMID 15290927 DOI: 10.1097/00054725-200405000-00019 |
0.376 |
|
| 2004 |
Jia WH, Feng BJ, Xu ZL, Zhang XS, Huang P, Huang LX, Yu XJ, Feng QS, Yao MH, Shugart YY, Zeng YX. Familial risk and clustering of nasopharyngeal carcinoma in Guangdong, China. Cancer. 101: 363-9. PMID 15241835 DOI: 10.1002/Cncr.20372 |
0.322 |
|
| 2004 |
Sheen VL, Basel-Vanagaite L, Goodman JR, Scheffer IE, Bodell A, Ganesh VS, Ravenscroft R, Hill RS, Cherry TJ, Shugart YY, Barkovich J, Straussberg R, Walsh CA. Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus. Brain & Development. 26: 326-34. PMID 15165674 DOI: 10.1016/J.Braindev.2003.09.004 |
0.332 |
|
| 2004 |
Shugart YY, Mundorff J, Kilshaw J, Doheny K, Doan B, Wanyee J, Green ED, Drayna D. Results of a Genome-Wide Linkage Scan for Stuttering American Journal of Medical Genetics. 124: 133-135. PMID 14699610 DOI: 10.1002/Ajmg.A.20347 |
0.378 |
|
| 2003 |
Hsu FC, Hetmanski JB, Li L, Markakis D, Jacobs K, Shugart YY. Comparison of significance level at the true location using two linkage approaches: LODPAL and GENEFINDER Bmc Genetics. 4. PMID 14975114 DOI: 10.1186/1471-2156-4-S1-S46 |
0.332 |
|
| 2003 |
Parikh V, Shugart YY, Doheny KF, Zhang J, Li L, Williams J, Hayden D, Craig B, Capo H, Chamblee D, Chen C, Collins M, Dankner S, Fiergang D, Guyton D, et al. A strabismus susceptibility locus on chromosome 7p. Proceedings of the National Academy of Sciences of the United States of America. 100: 12283-8. PMID 14519848 DOI: 10.1073/Pnas.2035118100 |
0.395 |
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| 2003 |
Rajab A, Mochida GH, Hill A, Ganesh V, Bodell A, Riaz A, Grant PE, Shugart YY, Walsh CA. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Neurology. 60: 1664-7. PMID 12771259 DOI: 10.1212/01.Wnl.0000068548.58498.41 |
0.373 |
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| 2003 |
Sheen VL, Topçu M, Berkovic S, Yalnizoglu D, Blatt I, Bodell A, Hill RS, Ganesh VS, Cherry TJ, Shugart YY, Walsh CA. Autosomal recessive form of periventricular heterotopia. Neurology. 60: 1108-12. PMID 12682315 DOI: 10.1212/01.Wnl.0000055898.00349.02 |
0.315 |
|
| 2003 |
Jin Y, Teng W, Ben S, Xiong X, Zhang J, Xu S, Shugart YY, Jin L, Chen J, Huang W. Genome-wide scan of Graves' disease: Evidence for linkage on chromosome 5q31 in Chinese Han pedigrees Journal of Clinical Endocrinology and Metabolism. 88: 1798-1803. PMID 12679476 DOI: 10.1210/Jc.2001-011980 |
0.391 |
|
| 2003 |
Potash JB, Zandi PP, Willour VL, Lan TH, Huo Y, Avramopoulos D, Shugart YY, MacKinnon DF, Simpson SG, McMahon FJ, DePaulo JR, McInnis MG. Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. The American Journal of Psychiatry. 160: 680-6. PMID 12668356 DOI: 10.1176/Appi.Ajp.160.4.680 |
0.349 |
|
| 2002 |
Shugart YY, Feng BJ, Collins A. The power and statistical behaviour of allele-sharing statistics when applied to models with two disease loci. Journal of Genetics. 81: 99-103. PMID 12717038 DOI: 10.1007/Bf02715906 |
0.305 |
|
| 2002 |
Feng BJ, Huang W, Shugart YY, Lee MK, Zhang F, Xia JC, Wang HY, Huang TB, Jian SW, Huang P, Feng QS, Huang LX, Yu XJ, Li D, Chen LZ, et al. Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4. Nature Genetics. 31: 395-9. PMID 12118254 DOI: 10.1038/Ng932 |
0.395 |
|
| 2002 |
Nathanson KL, Shugart YY, Omaruddin R, Szabo C, Goldgar D, Rebbeck TR, Weber BL. CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5q. Human Molecular Genetics. 11: 1327-32. PMID 12019214 DOI: 10.1093/Hmg/11.11.1327 |
0.333 |
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| 2002 |
Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA. An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. American Journal of Human Genetics. 70: 1028-33. PMID 11845408 DOI: 10.1086/339552 |
0.366 |
|
| 2001 |
Shugart YY, Specchia C, Li HH, Doan BQ, Mathias RA, Devoto M. Comparison of sib pair-based approaches for identifying quantitative trait loci underlying asthma in the Busselton families Genetic Epidemiology. 21. PMID 11793669 DOI: 10.1002/Gepi.2001.21.S1.S198 |
0.329 |
|
| 2000 |
Kniazeva M, Traboulsi EI, Yu Z, Stefko ST, Gorin MB, Shugart YY, O'Connell JR, Blaschak CJ, Cutting G, Han M, Zhang K. A new locus for dominant drusen and macular degeneration maps to chromosome 6q14. American Journal of Ophthalmology. 130: 197-202. PMID 11004294 DOI: 10.1016/S0002-9394(00)00585-7 |
0.347 |
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| 2000 |
Rahman N, Teare MD, Seal S, Renard H, Mangion J, Cour C, Thompson D, Shugart Y, Eccles D, Devilee P, Meijers H, Nathanson KL, Neuhausen SL, Weber B, Chang-Claude J, et al. Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22. Oncogene. 19: 4170-4173. PMID 10962578 DOI: 10.1038/Sj.Onc.1203735 |
0.312 |
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| 2000 |
Shugart YY, Hemminki K, Vaittinen P, Kingman A, Dong C. A genetic study of Hodgkin's lymphoma: An estimate of heritability and anticipation based on the familial cancer database in Sweden Human Genetics. 106: 553-556. PMID 10914686 DOI: 10.1007/S004390000291 |
0.343 |
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| 2000 |
Shugart YY, Collins A. Combined segregation and linkage analysis of 59 Hodgkin's disease families indicates the role of HLA determinants European Journal of Human Genetics. 8: 460-463. PMID 10878668 DOI: 10.1038/Sj.Ejhg.5200419 |
0.368 |
|
| 1999 |
Shugart YY, Cour C, Renard H, Lenoir G, Goldgar D, Teare D, Easton D, Rahman N, Gusterton R, Seal S, Barfoot R, Stratton M, Mangion J, Peelen T, Van den Ouweland A, et al. Linkage analysis of 56 multiplex families excludes the Cowden disease gene PTEN as a major contributor to familial breast cancer [3] Journal of Medical Genetics. 36: 720-721. PMID 10507734 DOI: 10.1136/Jmg.36.9.720 |
0.313 |
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| 1998 |
Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. Genomics. 48: 171-7. PMID 9521870 DOI: 10.1006/Geno.1997.5174 |
0.341 |
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| 1997 |
Shugart YY, Goldgar DE. The performance of MIM in comparison with MAPMAKER/SIBS to detect QTLs Genetic Epidemiology. 14: 897-902. PMID 9433597 DOI: 10.1002/(Sici)1098-2272(1997)14:6<897::Aid-Gepi56>3.0.Co;2-H |
0.352 |
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| 1997 |
Bignell GR, Canzian F, Shayeghi M, Stark M, Shugart YY, Biggs P, Mangion J, Hamoudi R, Rosenblatt J, Buu P, Sun S, Stoffer SS, Goldgar DE, Romeo G, Houlston RS, et al. Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer American Journal of Human Genetics. 61: 1123-1130. PMID 9345104 DOI: 10.1086/301610 |
0.342 |
|
| 1994 |
Knowles JA, Shugart Y, Banerjee P, Gilliam TC, Lewis CA, Jacobson SG, Ott J. Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p. Human Molecular Genetics. 3: 1401-3. PMID 7987322 DOI: 10.1093/Hmg/3.8.1401 |
0.356 |
|
| 1994 |
Gabizon R, Rosenman H, Meiner Z, Kahana I, Kahana E, Shugart Y, Ott J, Prusiner SB. Mutation in codon 200 and polymorphism in codon 129 of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 343: 385-90. PMID 7913755 DOI: 10.1098/Rstb.1994.0033 |
0.346 |
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| 1992 |
Wagstaff J, Knoll JH, Glatt KA, Shugart YY, Sommer A, Lalande M. Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression. Nature Genetics. 1: 291-4. PMID 1338769 DOI: 10.1038/Ng0792-291 |
0.301 |
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