Kirk Wilhelmsen - Publications

Affiliations: 
Biomedical Engineering University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Genetics

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 Seyerle AA, Sitlani CM, Noordam R, Gogarten SM, Li J, Li X, Evans DS, Sun F, Laaksonen MA, Isaacs A, Kristiansson K, Highland HM, Stewart JD, Harris TB, Trompet S, ... ... Wilhelmsen K, et al. Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology. The Pharmacogenomics Journal. PMID 28719597 DOI: 10.1038/Tpj.2017.10  0.314
2017 Vora NL, Powell B, Brandt A, Strande N, Hardisty E, Gilmore K, Foreman AKM, Wilhelmsen K, Bizon C, Reilly J, Owen P, Powell CM, Skinner D, Rini C, Lyerly AD, et al. Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28518170 DOI: 10.1038/Gim.2017.33  0.323
2016 Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, ... ... Wilhelmsen K, et al. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. American Journal of Human Genetics. PMID 27181682 DOI: 10.1016/J.Ajhg.2016.04.011  0.31
2014 Fan Z, Greenwood R, Felix AC, Shiloh-Malawsky Y, Tennison M, Roche M, Crooks K, Weck K, Wilhelmsen K, Berg J, Evans J. GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia. Journal of Neurology. 261: 622-4. PMID 24509643 DOI: 10.1007/S00415-014-7265-3  0.311
2013 Szigeti K, Lal D, Li Y, Doody RS, Wilhelmsen K, Yan L, Liu S, Ma C. Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 33: 517-23. PMID 23202439 DOI: 10.3233/Jad-2012-121285  0.354
2012 Szigeti K, Li Y, Shaw C, Sheffer I, Sule N, Powell S, Zaidi N, Lupski J, Wilhelmsen K, Doody R. Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease Alzheimers & Dementia. 8: 672. DOI: 10.1016/J.Jalz.2012.05.1817  0.357
2011 Shaw CA, Li Y, Wiszniewska J, Chasse S, Zaidi SN, Jin W, Dawson B, Wilhelmsen K, Lupski JR, Belmont JW, Doody RS, Szigeti K. Olfactory copy number association with age at onset of Alzheimer disease. Neurology. 76: 1302-9. PMID 21482944 DOI: 10.1212/Wnl.0B013E3182166Df5  0.331
2011 Wilhelmsen K, Chasse S, Griffin N, Diaz-Arrastia R, Barber R, Royall D, O'Bryant S, Doody R, Fairchild T, Rosenberg RN, Adams P, Reisch J. P2-088: Genome-Wide association scan replication for biomarker endophenotypes of Alzheimer's disease Alzheimer's & Dementia. 7: S335-S336. DOI: 10.1016/J.Jalz.2011.05.978  0.329
2011 O'Bryant S, Guanghua X, Robert B, Hall J, Doody R, Reisch J, Royall D, Adams P, Wilhelmsen K, Fairchild T, Diaz-Arrastia R. A Serum protein-based algorithm for the detection of Alzheimer's disease Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.1944  0.306
2005 Schuckit MA, Wilhelmsen K, Smith TL, Feiler HS, Lind P, Lange LA, Kalmijn J. Autosomal linkage analysis for the level of response to alcohol. Alcoholism, Clinical and Experimental Research. 29: 1976-82. PMID 16340454 DOI: 10.1097/01.Alc.0000187598.82921.27  0.304
1997 Wilhelmsen K, Mirel D, Marder K, Bernstein M, Naini A, Leal SM, Cote LJ, Tang MX, Freyer G, Graziano J, Mayeux R. Is there a genetic susceptibility locus for Parkinson's disease on chromosome 22q13? Annals of Neurology. 41: 813-7. PMID 9189044 DOI: 10.1002/Ana.410410619  0.33
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