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Diana L. Abbott, Ph.D. - Publications

Affiliations: 
Statistical Genetics University of Iowa, Iowa City, IA 
Area:
eyeblink conditioning
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11 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
2017 Tompson SW, Johnson C, Abbott D, Bakall B, Soler V, Yanovitch TL, Whisenhunt KN, Klemm T, Rozen S, Stone EM, Johnson M, Young TL. Reduced penetrance in a large Caucasian pedigree with Stickler syndrome. Ophthalmic Genetics. 1-8. PMID 28095098 DOI: 10.1080/13816810.2016.1275018  0.394
2013 Hinckley JD, Abbott D, Burns TL, Heiman M, Shapiro AD, Wang K, Di Paola J. Quantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits. Molecular Genetics & Genomic Medicine. 1: 131-141. PMID 24058921 DOI: 10.1002/Mgg3.16  0.552
2012 Abbott D, Li YJ, Guggenheim JA, Metlapally R, Malecaze F, Calvas P, Rosenberg T, Paget S, Zayats T, Mackey DA, Feng S, Young TL. An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error. Molecular Vision. 18: 720-9. PMID 22509102  0.401
2010 Gbadegesin R, Lavin P, Janssens L, Bartkowiak B, Homstad A, Wu G, Bowling B, Eckel J, Potocky C, Abbott D, Conlon P, Scott WK, Howell D, Hauser E, Winn MP. A new locus for familial FSGS on chromosome 2p. Journal of the American Society of Nephrology : Jasn. 21: 1390-7. PMID 20616172 DOI: 10.1681/Asn.2009101046  0.506
2010 Metlapally R, Ki CS, Li YJ, Tran-Viet KN, Abbott D, Malecaze F, Calvas P, Mackey DA, Rosenberg T, Paget S, Guggenheim JA, Young TL. Genetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohort. Investigative Ophthalmology & Visual Science. 51: 4476-9. PMID 20435602 DOI: 10.1167/Iovs.09-4912  0.436
2009 Yanovitch T, Li YJ, Metlapally R, Abbott D, Viet KN, Young TL. Hepatocyte growth factor and myopia: genetic association analyses in a Caucasian population. Molecular Vision. 15: 1028-35. PMID 19471602  0.342
2009 Metlapally R, Li YJ, Tran-Viet KN, Abbott D, Czaja GR, Malecaze F, Calvas P, Mackey D, Rosenberg T, Paget S, Zayats T, Owen MJ, Guggenheim JA, Young TL. COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus. Investigative Ophthalmology & Visual Science. 50: 4080-6. PMID 19387081 DOI: 10.1167/Iovs.08-3346  0.479
2009 Li YJ, Guggenheim JA, Bulusu A, Metlapally R, Abbott D, Malecaze F, Calvas P, Rosenberg T, Paget S, Creer RC, Kirov G, Owen MJ, Zhao B, White T, Mackey DA, et al. An international collaborative family-based whole-genome linkage scan for high-grade myopia. Investigative Ophthalmology & Visual Science. 50: 3116-27. PMID 19324860 DOI: 10.1167/Iovs.08-2781  0.469
2008 Wang K, Abbott D. A principal components regression approach to multilocus genetic association studies. Genetic Epidemiology. 32: 108-18. PMID 17849491 DOI: 10.1002/Gepi.20266  0.44
2007 Di Paola J, Wagner K, Nixon B, Kline J, Shapiro A, Abbott D, Burns T, Wang K. An Association Study of Candidate Modifier Genes in a Large Pedigree with Von Willebrand Disease. Blood. 110: 2135-2135. DOI: 10.1182/Blood.V110.11.2135.2135  0.552
2007 Abbott D, Wang K, Shapiro A, Burns T, Di Paola J. Genome Wide Scan of Complete Blood Count (CBC) Measures Suggests Strong Linkage of Red Blood Cell (RBC) Count to Chromosome 4q25. Blood. 110: 1729-1729. DOI: 10.1182/Blood.V110.11.1729.1729  0.57
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