☰

Jinko Graham - Publications

Affiliations: 
Simon Fraser University, Burnaby, British Columbia, Canada 
Area:
Statistics, Genetics, Mathematics
Tree Info Similar researchers PubMed Report error

32 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Nieuwoudt C, Brooks-Wilson A, Graham J. SimRVSequences: an R package to simulate genetic sequence data for pedigrees. Bioinformatics (Oxford, England). PMID 31764964 DOI: 10.1093/Bioinformatics/Btz881  0.321
2018 Karunarathna CB, Graham J. Using Gene Genealogies to Localize Rare Variants Associated with Complex Traits in Diploid Populations. Human Heredity. 83: 30-39. PMID 29763929 DOI: 10.1159/000486854  0.34
2017 Szefer E, Lu D, Nathoo F, Beg MF, Graham J. Multivariate association between single-nucleotide polymorphisms in Alzgene linkage regions and structural changes in the brain: discovery, refinement and validation. Statistical Applications in Genetics and Molecular Biology. PMID 29091582 DOI: 10.1515/Sagmb-2016-0077  0.404
2017 Greenlaw K, Szefer E, Graham J, Lesperance M, Nathoo FS. A Bayesian Group Sparse Multi-Task Regression Model for Imaging Genetics. Bioinformatics (Oxford, England). PMID 28419235 DOI: 10.1093/Bioinformatics/Btx215  0.342
2016 Burkett KM, McNeney B, Graham J. Sampletrees and Rsampletrees: sampling gene genealogies conditional on SNP genotype data. Bioinformatics (Oxford, England). PMID 26787665 DOI: 10.1093/Bioinformatics/Btv763  0.706
2014 Burkett KM, McNeney B, Graham J, Greenwood CM. Using gene genealogies to detect rare variants associated with complex traits. Human Heredity. 78: 117-30. PMID 25138120 DOI: 10.1159/000363443  0.712
2014 Shin JH, Infante-Rivard C, McNeney B, Graham J. A data-smoothing approach to explore and test gene-environment interaction in case-parent trios. Statistical Applications in Genetics and Molecular Biology. 13: 159-71. PMID 24413219 DOI: 10.1515/sagmb-2013-0023  0.492
2014 Burkett KM, McNeney B, Graham J, Greenwood CMT, Drichel D, Herold C, Lacour A, Ramirez A, Jessen F, Maier W, Noethen MM, Leber M, Vaitsiakhovich T, Becker T, McDonald MN, et al. Contents Vol. 78, 2014 Human Heredity. 78. DOI: 10.1159/000369520  0.651
2013 Burkett KM, Greenwood CM, McNeney B, Graham J. Gene genealogies for genetic association mapping, with application to Crohn's disease. Frontiers in Genetics. 4: 260. PMID 24348515 DOI: 10.3389/Fgene.2013.00260  0.73
2013 Lubieniecka JM, Graham J, Heffner D, Mottus R, Reid R, Hogge D, Grigliatti TA, Riggs WK. A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor. Frontiers in Genetics. 4: 231. PMID 24273552 DOI: 10.3389/Fgene.2013.00231  0.401
2013 Burkett KM, McNeney B, Graham J. Markov chain Monte Carlo sampling of gene genealogies conditional on unphased SNP genotype data. Statistical Applications in Genetics and Molecular Biology. 12: 559-81. PMID 23962961 DOI: 10.1515/Sagmb-2012-0011  0.715
2013 Yazdanpanah M, Chen C, Graham J. Secondary analysis of publicly available data reveals superoxide and oxygen radical pathways are enriched for associations between type 2 diabetes and low-frequency variants. Annals of Human Genetics. 77: 472-81. PMID 23941231 DOI: 10.1111/Ahg.12035  0.35
2013 Lubieniecka JM, Liu J, Graham J, Heffner D, Reid R, Hogge D, Grigliatti TA, Riggs WK. Single-nucleotide polymorphisms in reductase genes are not associated with response to daunorubicin-based remission induction. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 22: 1918-20. PMID 23880735 DOI: 10.1158/1055-9965.Epi-13-0671  0.382
2013 Nembot-Simo A, Graham J, McNeney B. CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals. Source Code For Biology and Medicine. 8: 5. PMID 23384435 DOI: 10.1186/1751-0473-8-5  0.374
2012 Gyllenberg A, Asad S, Piehl F, Swanberg M, Padyukov L, Van Yserloo B, Rutledge EA, McNeney B, Graham J, Orho-Melander M, Lindholm E, Graff C, Forsell C, Akesson K, Landin-Olsson M, et al. Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes. Genes and Immunity. 13: 632-40. PMID 23052709 DOI: 10.1038/Gene.2012.44  0.398
2012 Lubieniecka JM, Liu J, Heffner D, Graham J, Reid R, Hogge D, Grigliatti TA, Riggs WK. Single-nucleotide polymorphisms in aldo-keto and carbonyl reductase genes are not associated with acute cardiotoxicity after daunorubicin chemotherapy. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 21: 2118-20. PMID 23001242 DOI: 10.1158/1055-9965.Epi-12-1037  0.359
2012 Shin JH, Infante-Rivard C, Graham J, McNeney B. Adjusting for spurious gene-by-environment interaction using case-parent triads. Statistical Applications in Genetics and Molecular Biology. 11. PMID 22499696 DOI: 10.2202/1544-6115.1714  0.537
2011 Qu C, Schuetz JM, Min JE, Leach S, Daley D, Spinelli JJ, Brooks-Wilson A, Graham J. Cost-effective prediction of gender-labeling errors and estimation of gender-labeling error rates in candidate-gene association studies. Frontiers in Genetics. 2: 31. PMID 22303327 DOI: 10.3389/Fgene.2011.00031  0.367
2010 Shin JH, McNeney B, Graham J. On the use of allelic transmission rates for assessing gene-by-environment interaction in case-parent trios. Annals of Human Genetics. 74: 439-51. PMID 20649530 DOI: 10.1111/J.1469-1809.2010.00599.X  0.514
2007 Shin JH, Janer M, McNeney B, Blay S, Deutsch K, Sanjeevi CB, Kockum I, Lernmark A, Graham J, Arnqvist H, Björck E, Eriksson J, Nyström L, et al. IA-2 autoantibodies in incident type I diabetes patients are associated with a polyadenylation signal polymorphism in GIMAP5. Genes and Immunity. 8: 503-12. PMID 17641683 DOI: 10.1038/Sj.Gene.6364413  0.535
2007 Bekris LM, Shephard C, Janer M, Graham J, McNeney B, Shin J, Zarghami M, Griffith W, Farin F, Kavanagh TJ, Lernmark A. Glutamate cysteine ligase catalytic subunit promoter polymorphisms and associations with type 1 diabetes age-at-onset and GAD65 autoantibody levels. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. 115: 221-8. PMID 17479437 DOI: 10.1055/S-2007-970574  0.555
2007 Shin JH, McNeney B, Graham J. Case-control inference of interaction between genetic and nongenetic risk factors under assumptions on their distribution. Statistical Applications in Genetics and Molecular Biology. 6: Article13. PMID 17474879 DOI: 10.2202/1544-6115.1270  0.563
2007 Zamar D, McNeney B, Graham J. elrm: Software Implementing Exact-like Inference for Logistic Regression Models Journal of Statistical Software. 21. DOI: 10.18637/Jss.V021.I03  0.302
2006 Burkett K, Graham J, McNeney B. hapassoc: Software for Likelihood Inference of Trait Associations with SNP Haplotypes and Other Attributes Journal of Statistical Software. 16. DOI: 10.18637/Jss.V016.I02  0.737
2006 Shin J, Blay S, Graham J, McNeney B. LDheatmap: AnRFunction for Graphical Display of Pairwise Linkage Disequilibria Between Single Nucleotide Polymorphisms Journal of Statistical Software. 16. DOI: 10.18637/Jss.V016.C03  0.518
2005 Burkett KM, Ghadessi M, McNeney B, Graham J, Daley D. A comparison of five methods for selecting tagging single-nucleotide polymorphisms. Bmc Genetics. 6: S71. PMID 16451685 DOI: 10.1186/1471-2156-6-S1-S71  0.719
2005 Valdes AM, Thomson G, Graham J, Zarghami M, McNeney B, Kockum I, Smith A, Lathrop M, Steenkiste AR, Dorman JS, Noble JA, Hansen JA, Pugliese A, Lernmark A. D6S265*15 marks a DRB1*15, DQB1*0602 haplotype associated with attenuated protection from type 1 diabetes mellitus Diabetologia. 48: 2540-2543. PMID 16320082 DOI: 10.1007/S00125-005-0011-8  0.349
2004 Burkett K, McNeney B, Graham J. A note on inference of trait associations with SNP haplotypes and other attributes in generalized linear models. Human Heredity. 57: 200-6. PMID 15583426 DOI: 10.1159/000081447  0.711
2004 Burkett K, McNeney B, Graham J, Ott J, Burmester JK, Suarez BK, Lin JH, Jin CH, Miller RD, Zhang K, Salzman SA, Reding DJ, Catalona WJ, Harris EC, Nelsen AJ, et al. Contents Vol. 57, 2004 Human Heredity. 57: 231. DOI: 10.1159/000082515  0.651
2004 Burkett K, McNeney B, Graham J, Ott J, Burmester JK, Suarez BK, Lin JH, Jin CH, Miller RD, Zhang K, Salzman SA, Reding DJ, Catalona WJ, Harris EC, Nelsen AJ, et al. Subject Index Vol. 57, 2004 Human Heredity. 57: 230. DOI: 10.1159/000082514  0.641
2002 Graham J, Hagopian WA, Kockum I, Li LS, Sanjeevi CB, Lowe RM, Schaefer JB, Zarghami M, Day HL, Landin-Olsson M, Palmer JP, Janer-Villanueva M, Hood L, Sundkvist G, Lernmark A, et al. Genetic effects on age-dependent onset and islet cell autoantibody markers in type 1 diabetes. Diabetes. 51: 1346-55. PMID 11978629 DOI: 10.2337/Diabetes.51.5.1346  0.307
2000 Lowe RM, Graham J, Sund G, Kockum I, Landin-Olsson M, Schaefer JB, Törn C, Lernmark A, Dahlquist G. The length of the CTLA-4 microsatellite (AT)N-repeat affects the risk for type 1 diabetes. Diabetes Incidence in Sweden Study Group. Autoimmunity. 32: 173-80. PMID 11092697 DOI: 10.3109/08916930008994090  0.34
Show low-probability matches.