| Year |
Citation |
Score |
| 2021 |
Arthur VL, Li Z, Cao R, Oetting WS, Israni AK, Jacobson PA, Ritchie MD, Guan W, Chen J. A Multi-Marker Test for Analyzing Paired Genetic Data in Transplantation. Frontiers in Genetics. 12: 745773. PMID 34721531 DOI: 10.3389/fgene.2021.745773 |
0.313 |
|
| 2020 |
Nguyen TT, Pearson RA, Mohamed ME, Schladt DP, Berglund D, Rivers Z, Skaar DJ, Wu B, Guan W, van Setten J, Keating BJ, Dorr C, Remmel RP, Matas AJ, Mannon RB, ... ... Oetting WS, et al. Pharmacogenomics in kidney transplant recipients and potential for integration into practice. Journal of Clinical Pharmacy and Therapeutics. PMID 32662547 DOI: 10.1111/Jcpt.13223 |
0.341 |
|
| 2019 |
Mohamed ME, Schladt DP, Guan W, Wu B, van Setten J, Keating B, Iklé D, Remmel RP, Dorr CR, Mannon RB, Matas AJ, Israni AK, Oetting WS, Jacobson PA. Tacrolimus Troughs and Genetic Determinants of Metabolism in Kidney Transplant Recipients: A comparison of four ancestry groups. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. PMID 30953600 DOI: 10.1111/Ajt.15385 |
0.369 |
|
| 2019 |
Stapleton CP, Heinzel A, Guan W, van der Most PJ, van Setten J, Lord GM, Keating BJ, Israni AK, de Borst MH, Bakker SJL, Snieder H, Weale ME, Delaney F, Hernandez-Fuentes MP, Reindl-Schwaighofer R, ... ... Oetting WS, et al. The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. PMID 30920136 DOI: 10.1111/Ajt.15326 |
0.395 |
|
| 2019 |
Oetting WS, Wu B, Schladt DP, Guan W, van Setten J, Keating BJ, Iklé D, Remmel RP, Dorr CR, Mannon RB, Matas AJ, Israni AK, Jacobson PA. Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. Transplantation. PMID 30801552 DOI: 10.1097/Tp.0000000000002625 |
0.392 |
|
| 2019 |
Oetting WS, Schladt DP, Dorr CR, Wu B, Guan W, Remmel RP, Iklé D, Mannon RB, Matas AJ, Israni AK, Jacobson PA. Analysis of 75 Candidate SNPs Associated with Acute Rejection in Kidney Transplant Recipients: Validation of rs2910164 in MicroRNA MIR146A. Transplantation. PMID 30801535 DOI: 10.1097/Tp.0000000000002659 |
0.41 |
|
| 2018 |
Dorr CR, Wu B, Remmel RP, Muthusamy A, Schladt DP, Abrahante JE, Guan W, Mannon RB, Matas AJ, Oetting WS, Jacobson PA, Israni AK. Identification of genetic variants associated with tacrolimus metabolism in kidney transplant recipients by extreme phenotype sampling and next generation sequencing. The Pharmacogenomics Journal. PMID 30442921 DOI: 10.1038/S41397-018-0063-Z |
0.428 |
|
| 2018 |
Wu JF, Muthusamy A, Al-Ghalith GA, Knights D, Guo B, Wu B, Remmel RP, Schladt DP, Alegre ML, Oetting WS, Jacobson PA, Israni AK. Urinary Microbiome Associated with Chronic Allograft Dysfunction in Kidney Transplant Recipients. Clinical Transplantation. e13436. PMID 30372560 DOI: 10.1111/Ctr.13436 |
0.32 |
|
| 2018 |
Seibert SR, Schladt DP, Wu B, Guan W, Dorr C, Remmel RP, Matas AJ, Mannon RB, Israni AK, Oetting WS, Jacobson PA. Tacrolimus Trough and Dose Intra-Patient Variability and CYP3A5 Genotype: Effects on Acute Rejection and Graft Failure in European American and African American Kidney Transplant Recipients. Clinical Transplantation. e13424. PMID 30318646 DOI: 10.1111/Ctr.13424 |
0.344 |
|
| 2018 |
Scheibner A, Remmel R, Schladt D, Oetting W, Guan W, Wu B, Dorr C, Israni A, Jacobson PA. Tacrolimus Elimination in Four Patients with a CYP3A5*3/*3 CYP3A4*22/*22 Genotype. Pharmacotherapy. PMID 29804290 DOI: 10.1002/Phar.2131 |
0.362 |
|
| 2018 |
Snoek R, van Setten J, Keating BJ, Israni AK, Jacobson PA, Oetting WS, Matas AJ, Mannon RB, Zhang Z, Zhang W, Hao K, Murphy B, Reindl-Schwaighofer R, Heinzl A, Oberbauer R, et al. (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD. Journal of the American Society of Nephrology : Jasn. PMID 29654215 DOI: 10.1681/Asn.2017111200 |
0.364 |
|
| 2018 |
Oetting WS, Wu B, Schladt DP, Guan W, Remmel RP, Dorr C, Mannon RB, Matas AJ, Israni AK, Jacobson PA. Attempted validation of 44 reported SNPs associated with tacrolimus troughs in a cohort of kidney allograft recipients. Pharmacogenomics. PMID 29318894 DOI: 10.2217/Pgs-2017-0187 |
0.375 |
|
| 2018 |
Israni AK, Jacobson PA, Guan W, Dorr CR, van Setten J, de Borst MH, Stapleton CP, Phelan PJ, Conlon PJ, Birdwell KA, Reindl-Schwaighofer R, Heinzel A, Bakker SJ, Cavelleri G, Oetting WS, et al. Genome-Wide Association Meta-Analysis for Acute Rejection of Kidney Transplants Transplantation. 102: S27. DOI: 10.1097/01.Tp.0000542576.73240.16 |
0.361 |
|
| 2017 |
Oetting WS, Béroud C, Brenner SE, Greenblatt MS, Karchin R, Mooney SD. Methods and tools for assessing the impact of genetic variations: The 2017 annual scientific meeting of the Human Genome Variation Society. Human Mutation. PMID 29282786 DOI: 10.1002/Humu.23393 |
0.301 |
|
| 2017 |
Oetting WS, Wu B, Schladt DP, Guan W, Remmel RP, Mannon RB, Matas AJ, Israni AK, Jacobson PA. Genome-wide association study identifies the common variants in CYP3A4 and CYP3A5 responsible for variation in tacrolimus trough concentration in Caucasian kidney transplant recipients. The Pharmacogenomics Journal. PMID 29160300 DOI: 10.1038/Tpj.2017.49 |
0.432 |
|
| 2017 |
Oetting WS, Dorr C, Remmel RP, Matas AJ, Israni AK, Jacobson PA. Concepts of Genomics in Kidney Transplantation. Current Transplantation Reports. 4: 116-123. PMID 29123971 DOI: 10.1007/S40472-017-0153-X |
0.364 |
|
| 2017 |
Dorr CR, Oetting WS, Jacobson PA, Israni AK. Genetics of Acute Rejection after Kidney Transplantation. Transplant International : Official Journal of the European Society For Organ Transplantation. PMID 29030886 DOI: 10.1111/Tri.13084 |
0.385 |
|
| 2016 |
Oetting WS, Jacobson PA, Israni AK. Validation is Critical for GWAS-based Associations. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. PMID 27640398 DOI: 10.1111/Ajt.14051 |
0.379 |
|
| 2016 |
Oetting WS, Brookes AJ, Béroud C, Taschner PE. Clinical Interpretation of Variants from Next-Generation Sequencing: The 2016 Scientific Meeting of the Human Genome Variation Society. Human Mutation. 37: 1110-3. PMID 27492570 DOI: 10.1002/Humu.23059 |
0.32 |
|
| 2016 |
Oetting WS, Brenner SE, Brookes AJ, Greenblatt MS, Hart RK, Karchin R, Sunyaev SR, Taschner PE. Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation Society. Human Mutation. PMID 26791113 DOI: 10.1002/Humu.22958 |
0.363 |
|
| 2015 |
Sanghavi K, Brundage RC, Miller MB, Schladt DP, Israni AK, Guan W, Oetting WS, Mannon RB, Remmel RP, Matas AJ, Jacobson PA. Genotype-guided tacrolimus dosing in African-American kidney transplant recipients. The Pharmacogenomics Journal. PMID 26667830 DOI: 10.1038/Tpj.2015.87 |
0.347 |
|
| 2015 |
Oetting WS, Schladt DP, Guan W, Miller MB, Remmel RP, Dorr C, Sanghavi K, Mannon RB, Herrera B, Matas AJ, Salomon DR, Kwok PY, Keating BJ, Israni AK, Jacobson PA, et al. Genomewide Association Study of Tacrolimus Concentrations in African American Kidney Transplant Recipients Identifies Multiple CYP3A5 Alleles. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. PMID 26485092 DOI: 10.1111/Ajt.13495 |
0.42 |
|
| 2015 |
Kalman LV, Agúndez JA, Appell ML, Black JL, Bell GC, Boukouvala S, Bruckner C, Bruford E, Bruckner C, Caudle K, Coulthard S, Daly AK, Del Tredici AL, den Dunnen JT, Drozda K, ... ... Oetting WS, et al. Pharmacogenetic Allele Nomenclature: International Workgroup Recommendations for Test Result Reporting. Clinical Pharmacology and Therapeutics. PMID 26479518 DOI: 10.1002/Cpt.280 |
0.323 |
|
| 2015 |
Keating BJ, Setten Jv, Jacobson PA, Holmes MV, Verma SS, Chandrupatla HR, Nair N, Gao H, Li YR, Chang B, Wong C, Phillips R, Cole BS, Mukhtar E, Zhang W, ... ... Oetting WS, et al. Design and Implementation of the International Genetics and Translational Research in Transplantation Network Transplantation. 99: 2401-2412. PMID 26479416 DOI: 10.1097/Tp.0000000000000913 |
0.367 |
|
| 2015 |
Li YR, van Setten J, Verma SS, Lu Y, Holmes MV, Gao H, Lek M, Nair N, Chandrupatla H, Chang B, Karczewski KJ, Wong C, Mohebnasab M, Mukhtar E, Phillips R, ... ... Oetting WS, et al. Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies. Genome Medicine. 7: 90. PMID 26423053 DOI: 10.1186/S13073-015-0211-X |
0.404 |
|
| 2015 |
Pulk RA, Schladt DS, Oetting WS, Guan W, Israni AK, Matas AJ, Remmel RP, Jacobson PA. Multigene predictors of tacrolimus exposure in kidney transplant recipients. Pharmacogenomics. 16: 841-54. PMID 26067485 DOI: 10.2217/Pgs.15.42 |
0.359 |
|
| 2015 |
Dorr C, Wu B, Guan W, Muthusamy A, Sanghavi K, Schladt DP, Maltzman JS, Scherer SE, Brott MJ, Matas AJ, Jacobson PA, Oetting WS, Israni AK. Differentially expressed gene transcripts using RNA sequencing from the blood of immunosuppressed kidney allograft recipients. Plos One. 10: e0125045. PMID 25946140 DOI: 10.1371/Journal.Pone.0125045 |
0.339 |
|
| 2015 |
Oetting WS, Greenblatt MS, Brookes AJ, Karchin R, Mooney SD. Germline & somatic mosaicism: the 2014 annual scientific meeting of the Human Genome Variation Society. Human Mutation. 36: 390-3. PMID 25597405 DOI: 10.1002/Humu.22757 |
0.312 |
|
| 2015 |
Oetting WS. The Ultimate Guide to DMD Variants Human Mutation. 36. DOI: 10.1002/Humu.22780 |
0.326 |
|
| 2014 |
Vrieze SI, Malone SM, Vaidyanathan U, Kwong A, Kang HM, Zhan X, Flickinger M, Irons D, Jun G, Locke AE, Pistis G, Porcu E, Levy S, Myers RM, Oetting W, et al. In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Psychophysiology. 51: 1309-20. PMID 25387710 DOI: 10.1111/Psyp.12350 |
0.371 |
|
| 2014 |
Wu J, Lin R, Huang J, Guan W, Oetting WS, Sriramarao P, Blumenthal MN. Functional Fcgamma receptor polymorphisms are associated with human allergy. Plos One. 9: e89196. PMID 24586589 DOI: 10.1371/Journal.Pone.0089196 |
0.335 |
|
| 2014 |
Oetting WS, Guan W, Schladt DP, Wildebush WA, Becker J, Thyagarajan B, Jacobson PA, Matas AJ, Israni AK. Telomere length of recipients and living kidney donors and chronic graft dysfunction in kidney transplants. Transplantation. 97: 325-9. PMID 24492422 DOI: 10.1097/01.Tp.0000436705.87898.88 |
0.336 |
|
| 2014 |
Stanley CM, Sunyaev SR, Greenblatt MS, Oetting WS. Clinically relevant variants - identifying, collecting, interpreting, and disseminating: the 2013 annual scientific meeting of the Human Genome Variation Society. Human Mutation. 35: 505-10. PMID 24470180 DOI: 10.1002/Humu.22516 |
0.347 |
|
| 2014 |
Pulk R, Schladt D, Guan W, Oetting W, Israni A, Matas A, Jacobson P. Multi-Gene Pharmacogenomics of Tacrolimus Troughs in Kidney Transplant Recipients.: Abstract# A518 Transplantation. 98: 890. DOI: 10.1097/00007890-201407151-03041 |
0.326 |
|
| 2014 |
Keating B, Nair N, Holmes M, Oetting W, Jacobson P, Israni A, Shaked A. Concept, Design and Implementation of a Sedicated Genome-Wide Transplant SNP Array With > 780,000 Markers. Transplantation. 98: 889. DOI: 10.1097/00007890-201407151-03038 |
0.336 |
|
| 2013 |
Ellard S, Patrinos GP, Oetting WS. Clinical applications of next-generation sequencing: the 2013 human genome variation society scientific meeting. Human Mutation. 34: 1583-7. PMID 23956188 DOI: 10.1002/Humu.22400 |
0.326 |
|
| 2013 |
McGue M, Zhang Y, Miller MB, Basu S, Vrieze S, Hicks B, Malone S, Oetting WS, Iacono WG. A genome-wide association study of behavioral disinhibition. Behavior Genetics. 43: 363-73. PMID 23942779 DOI: 10.1007/S10519-013-9606-X |
0.371 |
|
| 2013 |
Israni AK, Riad SM, Leduc R, Oetting WS, Guan W, Schladt D, Matas AJ, Jacobson PA. Tacrolimus trough levels after month 3 as a predictor of acute rejection following kidney transplantation: a lesson learned from DeKAF Genomics. Transplant International : Official Journal of the European Society For Organ Transplantation. 26: 982-9. PMID 23879408 DOI: 10.1111/Tri.12155 |
0.325 |
|
| 2013 |
Oetting WS, Robinson PN, Greenblatt MS, Cotton RG, Beck T, Carey JC, Doelken SC, Girdea M, Groza T, Hamilton CM, Hamosh A, Kerner B, MacArthur JA, Maglott DR, Mons B, et al. Getting ready for the Human Phenome Project: the 2012 forum of the Human Variome Project. Human Mutation. 34: 661-6. PMID 23401191 DOI: 10.1002/Humu.22293 |
0.344 |
|
| 2013 |
Israni AK, Leduc R, Jacobson PA, Wildebush W, Guan W, Schladt D, Matas AJ, Oetting WS. Inflammation in the setting of chronic allograft dysfunction post-kidney transplant: phenotype and genotype. Clinical Transplantation. 27: 348-58. PMID 23350966 DOI: 10.1111/Ctr.12074 |
0.389 |
|
| 2012 |
Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M. The Minnesota Center for Twin and Family Research genome-wide association study. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 15: 767-74. PMID 23363460 DOI: 10.1017/Thg.2012.62 |
0.33 |
|
| 2012 |
Oetting WS, Guan W, Schladt DP, Leduc RE, Jacobson PA, Matas AJ, Chinnakotla S, Schröppel B, Murphy BT, Israni AK. Donor polymorphisms of toll-like receptor 4 associated with graft failure in liver transplant recipients. Liver Transplantation : Official Publication of the American Association For the Study of Liver Diseases and the International Liver Transplantation Society. 18: 1399-405. PMID 22987288 DOI: 10.1002/Lt.23549 |
0.364 |
|
| 2012 |
Fang G, Haznadar M, Wang W, Yu H, Steinbach M, Church TR, Oetting WS, Van Ness B, Kumar V. High-order SNP combinations associated with complex diseases: efficient discovery, statistical power and functional interactions. Plos One. 7: e33531. PMID 22536319 DOI: 10.1371/Journal.Pone.0033531 |
0.352 |
|
| 2012 |
Jacobson PA, Schladt D, Israni A, Oetting WS, Lin YC, Leduc R, Guan W, Lamba V, Matas AJ. Genetic and clinical determinants of early, acute calcineurin inhibitor-related nephrotoxicity: results from a kidney transplant consortium. Transplantation. 93: 624-31. PMID 22334041 DOI: 10.1097/Tp.0B013E3182461288 |
0.347 |
|
| 2012 |
Oetting WS. Exome and genome analysis as a tool for disease identification and treatment: the 2011 Human Genome Variation Society scientific meeting. Human Mutation. 33: 586-90. PMID 22213110 DOI: 10.1002/Humu.22018 |
0.355 |
|
| 2012 |
Oetting WS, Zhu Y, Brott MJ, Matas AJ, Cordner GK, Pan W. Validation of genetic variants associated with early acute rejection in kidney allograft transplantation. Clinical Transplantation. 26: 418-23. PMID 21919968 DOI: 10.1111/J.1399-0012.2011.01522.X |
0.431 |
|
| 2012 |
Jacobson PA, Schladt D, Oetting WS, Leduc R, Guan W, Matas AJ, Lamba V, Mannon RB, Julian BA, Israni A. Reply to "genetic determinants of mycophenolate-related anemia and leukopenia after transplantation" Transplantation. 93: e41-e42. DOI: 10.1097/Tp.0B013E3182529Bdf |
0.342 |
|
| 2011 |
Oetting WS, Schladt DP, Leduc RE, Jacobson PA, Guan W, Matas AJ, Israni A. Validation of single nucleotide polymorphisms associated with acute rejection in kidney transplant recipients using a large multi-center cohort. Transplant International : Official Journal of the European Society For Organ Transplantation. 24: 1231-8. PMID 21955043 DOI: 10.1111/J.1432-2277.2011.01359.X |
0.433 |
|
| 2011 |
Dalgleish R, Oetting WS, Auerbach AD, Beckmann JS, Cambon-Thomsen A, Devereau A, Greenblatt MS, Patrinos GP, Taylor GR, Vihinen M, Brookes AJ. Clarity and claims in variation/mutation databasing. Nature Biotechnology. 29: 790-2; author reply . PMID 21904316 DOI: 10.1038/Nbt.1961 |
0.311 |
|
| 2011 |
Passey C, Birnbaum AK, Brundage RC, Oetting WS, Israni AK, Jacobson PA. Dosing equation for tacrolimus using genetic variants and clinical factors. British Journal of Clinical Pharmacology. 72: 948-57. PMID 21671989 DOI: 10.1111/J.1365-2125.2011.04039.X |
0.324 |
|
| 2011 |
Oetting WS. Exploring the functional consequences of genomic variation: the 2010 Human Genome Variation Society Scientific Meeting. Human Mutation. 32: 486-90. PMID 21412951 DOI: 10.1002/Humu.21443 |
0.345 |
|
| 2011 |
Jacobson PA, Oetting WS, Brearley AM, Leduc R, Guan W, Schladt D, Matas AJ, Lamba V, Julian BA, Mannon RB, Israni A. Novel polymorphisms associated with tacrolimus trough concentrations: results from a multicenter kidney transplant consortium. Transplantation. 91: 300-8. PMID 21206424 DOI: 10.1097/Tp.0B013E318200E991 |
0.346 |
|
| 2011 |
Jacobson PA, Schladt D, Oetting WS, Leduc R, Guan W, Matas AJ, Lamba V, Mannon RB, Julian BA, Israni A. Genetic determinants of mycophenolate-related anemia and leukopenia after transplantation. Transplantation. 91: 309-16. PMID 21107304 DOI: 10.1097/Tp.0B013E318200E971 |
0.32 |
|
| 2011 |
Oetting WS. Sequencing the human genome: Gateway to personalized medicine or the new eugenics? Theology and Science. 9: 181-191. DOI: 10.1080/14746700.2011.563582 |
0.321 |
|
| 2010 |
Israni A, Leduc R, Holmes J, Jacobson PA, Lamba V, Guan W, Schladt D, Chen J, Matas AJ, Oetting WS. Single-nucleotide polymorphisms, acute rejection, and severity of tubulitis in kidney transplantation, accounting for center-to-center variation. Transplantation. 90: 1401-8. PMID 21085059 DOI: 10.1097/Tp.0B013E3182000085 |
0.405 |
|
| 2010 |
Oetting WS. Impact of next generation sequencing: the 2009 Human Genome Variation Society Scientific Meeting. Human Mutation. 31: 500-3. PMID 20127974 DOI: 10.1002/Humu.21210 |
0.347 |
|
| 2010 |
Oetting WS. Identifying functional promoter SNPs using allelic imbalance. Human Mutation. 31: v. PMID 20024938 DOI: 10.1002/Humu.21174 |
0.311 |
|
| 2010 |
Israni A, Leduc R, Jacobson P, Schladt D, Guan W, Oetting W, Matas A. CLINICAL FACTORS AND SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CHRONIC ALLOGRAFT DYSFUNCTION POST-KIDNEY TRANSPLANT Transplantation Journal. 90: 246. DOI: 10.1097/00007890-201007272-00466 |
0.357 |
|
| 2010 |
Israni A, Leduc R, Jacobson P, Schladt D, Guan W, Oetting W, Matas A. SINGLE NUCLEOTIDE POLYMORPHISM ASSOCIATED WITH SEVERITY OF ACUTE REJECTION ON KIDNEY ALLOGRAFT BIOPSIES Transplantation Journal. 90: 244. DOI: 10.1097/00007890-201007272-00461 |
0.351 |
|
| 2009 |
He H, Oetting WS, Brott MJ, Basu S. Power of multifactor dimensionality reduction and penalized logistic regression for detecting gene-gene interaction in a case-control study. Bmc Medical Genetics. 10: 127. PMID 19961594 DOI: 10.1186/1471-2350-10-127 |
0.319 |
|
| 2009 |
Kaput J, Cotton RG, Hardman L, Watson M, Al Aqeel AI, Al-Aama JY, Al-Mulla F, Alonso S, Aretz S, Auerbach AD, Bapat B, Bernstein IT, Bhak J, Bleoo SL, Blöcker H, ... ... Oetting WS, et al. Planning the human variome project: the Spain report. Human Mutation. 30: 496-510. PMID 19306394 DOI: 10.1002/Humu.20972 |
0.342 |
|
| 2009 |
Oetting WS. Clinical genetics & human genome variation: the 2008 Human Genome Variation Society scientific meeting. Human Mutation. 30: 852-6. PMID 19260058 DOI: 10.1002/Humu.20987 |
0.4 |
|
| 2009 |
Oetting WS, Pietsch J, Brott MJ, Savage S, Fryer JP, Summers CG, King RA. The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism. American Journal of Medical Genetics. Part A. 149: 466-9. PMID 19208379 DOI: 10.1002/Ajmg.A.32654 |
0.414 |
|
| 2009 |
Akkina SK, Zhang Y, Nelsestuen GL, Oetting WS, Ibrahlm HN. Temporal stability of the urinary proteome after kidney transplant: more sensitive than protein composition? Journal of Proteome Research. 8: 94-103. PMID 19012427 DOI: 10.1021/Pr800646J |
0.311 |
|
| 2008 |
Johnson LA, Oetting WS, Basu S, Prausa S, Matas A, Jacobson PA. Pharmacogenetic effect of the UGT polymorphisms on mycophenolate is modified by calcineurin inhibitors. European Journal of Clinical Pharmacology. 64: 1047-56. PMID 18568343 DOI: 10.1007/S00228-008-0501-Y |
0.3 |
|
| 2008 |
Oetting WS. Large scale DNA sequencing: new challenges emerge--the 2007 Human Genome Variation Society scientific meeting. Human Mutation. 29: 765-8. PMID 18348287 DOI: 10.1002/Humu.20729 |
0.351 |
|
| 2007 |
Reilly C, Miller MB, Liu Y, Oetting WS, King R, Blumenthal M. Linkage analysis of a cluster-based quantitative phenotype constructed from pulmonary function test data in 27 multigenerational families with multiple asthmatic members. Human Heredity. 64: 136-45. PMID 17476113 DOI: 10.1159/000101992 |
0.342 |
|
| 2007 |
Chan PA, Duraisamy S, Miller PJ, Newell JA, McBride C, Bond JP, Raevaara T, Ollila S, Nyström M, Grimm AJ, Christodoulou J, Oetting WS, Greenblatt MS. Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR). Human Mutation. 28: 683-93. PMID 17370310 DOI: 10.1002/Humu.20492 |
0.373 |
|
| 2007 |
Oetting WS. The 2006 Human Genome Variation Society scientific meeting. Human Mutation. 28: 517-21. PMID 17357128 DOI: 10.1002/Humu.20489 |
0.38 |
|
| 2007 |
Long J, Oetting WS, Xinjing W, Luo X, Tomblyn M, Weisdorf D, Jacobson P. Pharmacogenetics of Mycophenolate Mofetil in Patients Undergoing Hematopoietic Cell Transplantation (HCT). Blood. 110: 3010-3010. DOI: 10.1182/Blood.V110.11.3010.3010 |
0.349 |
|
| 2005 |
Oetting WS, Garrett SS, Brott M, King RA. P gene mutations associated with oculocutaneous albinism type II (OCA2). Human Mutation. 25: 323. PMID 15712365 DOI: 10.1002/Humu.9318 |
0.343 |
|
| 2004 |
Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, et al. X-linked high myopia associated with cone dysfunction. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 897-908. PMID 15197065 DOI: 10.1001/Archopht.122.6.897 |
0.342 |
|
| 2004 |
Blumenthal MN, Ober C, Beaty TH, Bleecker ER, Langefeld CD, King RA, Lester L, Cox N, Barnes K, Togias A, Mathias R, Meyers DA, Oetting W, Rich SS. Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA). Genes and Immunity. 5: 226-31. PMID 15029235 DOI: 10.1038/Sj.Gene.6364063 |
0.306 |
|
| 2004 |
Blumenthal MN, Langefeld CD, Beaty TH, Bleecker ER, Ober C, Lester L, Lange E, Barnes KC, Wolf R, King RA, Solway J, Oetting W, Meyers DA, Rich SS. A genome-wide search for allergic response (atopy) genes in three ethnic groups: Collaborative Study on the Genetics of Asthma. Human Genetics. 114: 157-64. PMID 14586638 DOI: 10.1007/S00439-003-1030-5 |
0.312 |
|
| 2004 |
King RA, Pietsch J, Brott MJ, Savage S, Fryer JP, Summers CG, Oetting WS. The R402Q mutation of the Tyrosinase Gene: Lack of Association with oculocutaneous albinism type 1 (OCA1). Pigment Cell Research. 17: 427-427. DOI: 10.1111/J.1600-0749.2004.00175_4.X |
0.35 |
|
| 2003 |
Fryer JP, Oetting WS, King RA. Identification and characterization of a DNase hypersensitive region of the human tyrosinase gene. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 16: 679-84. PMID 14629726 DOI: 10.1046/J.1600-0749.2003.00099.X |
0.354 |
|
| 2003 |
King RA, Pietsch J, Fryer JP, Savage S, Brott MJ, Russell-Eggitt I, Summers CG, Oetting WS. Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype. Human Genetics. 113: 502-13. PMID 13680365 DOI: 10.1007/S00439-003-0998-1 |
0.374 |
|
| 2003 |
King RA, Willaert RK, Schmidt RM, Pietsch J, Savage S, Brott MJ, Fryer JP, Summers CG, Oetting WS. MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2). American Journal of Human Genetics. 73: 638-45. PMID 12876664 DOI: 10.1086/377569 |
0.388 |
|
| 2003 |
Oetting WS, Fryer JP, Shriram S, King RA. Oculocutaneous albinism type 1: the last 100 years. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 16: 307-11. PMID 12753405 DOI: 10.1034/J.1600-0749.2003.00045.X |
0.382 |
|
| 2002 |
Oetting WS. New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene. Human Mutation. 19: 85-92. PMID 11793467 DOI: 10.1002/Humu.10034 |
0.359 |
|
| 2001 |
Mathias RA, Freidhoff LR, Blumenthal MN, Meyers DA, Lester L, King R, Xu JF, Solway J, Barnes KC, Pierce J, Stine OC, Togias A, Oetting W, Marshik PL, Hetmanski JB, et al. Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families. Genetic Epidemiology. 20: 340-55. PMID 11255243 DOI: 10.1002/Gepi.5 |
0.342 |
|
| 2000 |
Oetting WS. The tyrosinase gene and oculocutaneous albinism type 1 (OCA1): A model for understanding the molecular biology of melanin formation. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 13: 320-5. PMID 11041207 DOI: 10.1034/J.1600-0749.2000.130503.X |
0.343 |
|
| 1999 |
Tripathi RK, Flanders DJ, Young TL, Oetting WS, Ramaiah A, King RA, Boissy RE, Nordlund JJ. Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluation. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 12: 187-92. PMID 10385915 DOI: 10.1111/J.1600-0749.1999.Tb00512.X |
0.389 |
|
| 1999 |
Oetting WS, King RA. Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism. Human Mutation. 13: 99-115. PMID 10094567 DOI: 10.1002/(Sici)1098-1004(1999)13:2<99::Aid-Humu2>3.0.Co;2-C |
0.357 |
|
| 1999 |
Wildenberg SC, Fryer JP, Oetting WS, King RA. Three novel polymorphisms in the gene responsible for the Hermansky‐Pudlak syndrome Human Mutation. 13: 174-174. DOI: 10.1002/(Sici)1098-1004(1999)13:2<174::Aid-Humu23>3.0.Co;2-S |
0.313 |
|
| 1998 |
Oetting WS, Fryer JP, King RA. Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. Online. Human Mutation. 12: 433-4. PMID 10671066 DOI: 10.1002/(Sici)1098-1004(1998)12:6<433::Aid-Humu14>3.0.Co;2-G |
0.334 |
|
| 1998 |
Wildenberg SC, Fryer JP, Gardner JM, Oetting WS, Brilliant MH, King RA. Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico. The Journal of Investigative Dermatology. 110: 777-81. PMID 9579545 DOI: 10.1046/J.1523-1747.1998.00183.X |
0.332 |
|
| 1995 |
Wildenberg SC, King RA, Oetting WS. Detection of a Tsp509I polymorphism in the 3' UTR of the human tyrosinase related protein-1 (TYRP) gene. Human Genetics. 95: 247. PMID 7860080 DOI: 10.1007/Bf00209417 |
0.329 |
|
| 1994 |
Oetting WS, Fryer JP, Oofuji Y, Middendorf LR, Brumbaugh JA, Summers CG, King RA. Analysis of tyrosinase gene mutations using direct automated infrared fluorescence DNA sequencing of amplified exons. Electrophoresis. 15: 159-64. PMID 8026428 DOI: 10.1002/Elps.1150150127 |
0.329 |
|
| 1994 |
Oetting WS, King RA. Molecular basis of oculocutaneous albinism. The Journal of Investigative Dermatology. 103: 131S-136S. PMID 7963676 DOI: 10.1038/Jid.1994.24 |
0.378 |
|
| 1994 |
Oetting WS, King RA. Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1). Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 7: 285-90. PMID 7886000 DOI: 10.1111/J.1600-0749.1994.Tb00629.X |
0.307 |
|
| 1993 |
Oetting WS, King RA. Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene. Human Mutation. 2: 1-6. PMID 8477259 DOI: 10.1002/Humu.1380020102 |
0.399 |
|
| 1993 |
Oetting WS, Stine OC, Townsend D, King RA. Evolution of the tyrosinase related gene (TYRL) in primates. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 6: 171-7. PMID 8234203 DOI: 10.1111/J.1600-0749.1993.Tb00597.X |
0.323 |
|
| 1992 |
Oetting WS, King RA. Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism. Human Genetics. 90: 258-62. PMID 1487241 DOI: 10.1007/Bf00220074 |
0.333 |
|
| 1992 |
King RA, Oetting WS. Molecular basis of type IA (tyrosinase negative) oculocutaneous albinism. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 249-53. PMID 1409426 DOI: 10.1111/J.1600-0749.1990.Tb00380.X |
0.332 |
|
| 1992 |
Oetting WS, King RA. Analysis of mutations in the copper B binding region associated with type I (tyrosinase-related) oculocutaneous albinism. Pigment Cell Research / Sponsored by the European Society For Pigment Cell Research and the International Pigment Cell Society. 5: 274-8. PMID 1292009 DOI: 10.1111/J.1600-0749.1992.Tb00549.X |
0.312 |
|
| 1991 |
King RA, Townsend D, Oetting W, Gail Summers C, Olds DP, White JG, Spritz RA. Temperature-sensitive tyrosinase associated with peripheral pigmentation in oculocutaneous albinism Journal of Clinical Investigation. 87: 1046-1053. PMID 1900307 DOI: 10.1172/Jci115064 |
0.33 |
|
| 1991 |
Oetting WS, Handoko HY, Mentink MM, Paller AS, White JG, King RA. Molecular analysis of an extended family with type IA (tyrosinase-negative) oculocutaneous Albinism Journal of Investigative Dermatology. 97: 15-19. PMID 1676041 DOI: 10.1111/1523-1747.Ep12477808 |
0.349 |
|
| 1986 |
Brumbaugh JA, Oetting WS. What Can We Learn from Chick Embryo Melanocytes Bioscience. 36: 381-387. DOI: 10.2307/1310260 |
0.327 |
|
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