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Zeynep Baskurt, Ph.D. - Publications

Affiliations: 
2014 Statistics University of Toronto, Toronto, ON, Canada 
Area:
Statistics
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10 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 Baskurt Z, Mastromatteo S, Gong J, Wintle RF, Scherer SW, Strug LJ. VikNGS: A C ++ Variant Integration Kit for Next Generation Sequencing Association Analysis. Bioinformatics (Oxford, England). PMID 31580400 DOI: 10.1093/Bioinformatics/Btz716  0.53
2019 Gong J, Wang F, Xiao B, Panjwani N, Lin F, Keenan K, Avolio J, Esmaeili M, Zhang L, He G, Soave D, Mastromatteo S, Baskurt Z, Kim S, O'Neal WK, et al. Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci. Plos Genetics. 15: e1008007. PMID 30807572 DOI: 10.1371/Journal.Pgen.1008007  0.552
2018 Baskurt Z, Strug LJ. Genetic association analysis with pedigrees: Direct inference using the composite likelihood ratio. Genetic Epidemiology. PMID 30221395 DOI: 10.1002/Gepi.22153  0.561
2018 Panjwani N, Xiao B, Xu L, Gong J, Keenan K, Lin F, He G, Baskurt Z, Kim S, Zhang L, Esmaeili M, Blackman S, Scherer SW, Corvol H, Drumm M, et al. Improving imputation in disease-relevant regions: lessons from cystic fibrosis. Npj Genomic Medicine. 3: 8. PMID 29581887 DOI: 10.1038/S41525-018-0047-6  0.564
2018 Al-Labadi L, Baskurt Z, Evans M. Statistical Reasoning: Choosing and Checking the Ingredients, Inferences Based on a Measure of Statistical Evidence with Some Applications Entropy. 20: 289. DOI: 10.3390/E20040289  0.3
2012 Strug LJ, Addis L, Chiang T, Baskurt Z, Li W, Clarke T, Hardison H, Kugler SL, Mandelbaum DE, Novotny EJ, Wolf SM, Pal DK. The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy. Plos One. 7: e40696. PMID 22815793 DOI: 10.1371/Journal.Pone.0040696  0.557
2011 Hodge SE, Baskurt Z, Strug LJ. Using parametric multipoint lods and mods for linkage analysis requires a shift in statistical thinking. Human Heredity. 72: 264-75. PMID 22189469 DOI: 10.1159/000331463  0.575
2011 Hodge SE, Baskurt Z, Strug LJ, Greenberg DA, Vieland VJ, Huang Y, Seok S, Burian J, Catalyurek U, O’Connell J, Segre A, Valentine-Cooper W, Bailey-Wilson JE, Wilson AF, Devoto M, et al. Contents Vol. 72, 2011 Human Heredity. 72. DOI: 10.1159/000334420  0.471
2009 Clarke T, Baskurt Z, Strug LJ, Pal DK. Evidence of shared genetic risk factors for migraine and rolandic epilepsy. Epilepsia. 50: 2428-33. PMID 19674062 DOI: 10.1111/J.1528-1167.2009.02240.X  0.542
2009 Strug LJ, Clarke T, Chiang T, Chien M, Baskurt Z, Li W, Dorfman R, Bali B, Wirrell E, Kugler SL, Mandelbaum DE, Wolf SM, McGoldrick P, Hardison H, Novotny EJ, et al. Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4). European Journal of Human Genetics : Ejhg. 17: 1171-81. PMID 19172991 DOI: 10.1038/Ejhg.2008.267  0.554
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