| Year |
Citation |
Score |
| 2023 |
Peljto AL, Blumhagen RZ, Walts AD, Cardwell J, Powers J, Corte TJ, Dickinson JL, Glaspole I, Moodley YP, Vasakova MK, Bendstrup E, Davidsen JR, Borie R, Crestani B, Dieude P, ... ... Fingerlin TE, et al. Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants. American Journal of Respiratory and Critical Care Medicine. PMID 36602845 DOI: 10.1164/rccm.202207-1331OC |
0.304 |
|
| 2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Fingerlin TE, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.523 |
|
| 2020 |
Moore CM, Jacobson SA, Fingerlin TE. Power and Sample Size Calculations for Genetic Association Studies in the Presence of Genetic Model Misspecification. Human Heredity. 1-16. PMID 32721961 DOI: 10.1159/000508558 |
0.337 |
|
| 2019 |
Allen RJ, Guillen-Guio B, Oldham JM, Ma SF, Dressen A, Paynton ML, Kraven LM, Obeidat M, Li X, Ng M, Braybrooke R, Molina-Molina M, Hobbs BD, Putman RK, Sakornsakolpat P, ... ... Fingerlin TE, et al. Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 31710517 DOI: 10.1164/Rccm.201905-1017Oc |
0.346 |
|
| 2019 |
Mathai SK, Humphries S, Kropski JA, Blackwell TS, Powers J, Walts AD, Markin C, Woodward J, Chung JH, Brown KK, Steele MP, Loyd JE, Schwarz MI, Fingerlin T, Yang IV, et al. variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis. Thorax. PMID 31558622 DOI: 10.1136/Thoraxjnl-2018-212430 |
0.307 |
|
| 2019 |
Hobbs BD, Putman RK, Araki T, Nishino M, Gudmundsson G, Gudnason V, Eiriksdottir G, Zilhao Nogueira NR, Dupuis J, Xu H, O'Connor GT, Manichaikul A, Nguyen J, Podolanczuk AJ, Madahar P, ... ... Fingerlin TE, et al. Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 31339356 DOI: 10.1164/Rccm.201903-0511Oc |
0.431 |
|
| 2019 |
Young KA, Palmer ND, Fingerlin TE, Langefeld CD, Norris JM, Wang N, Xiang AH, Guo X, Williams AH, Chen YI, Taylor KD, Rotter JI, Raffel LJ, Goodarzi MO, Watanabe RM, et al. Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium. Obesity (Silver Spring, Md.). PMID 31219225 DOI: 10.1002/Oby.22527 |
0.308 |
|
| 2019 |
Ryan SM, Fingerlin TE, Mroz M, Barkes B, Hamzeh N, Maier LA, Carlson NE. Radiomic Measures from Chest HRCT Associated with Lung Function in Sarcoidosis. The European Respiratory Journal. PMID 31196947 DOI: 10.1183/13993003.00371-2019 |
0.34 |
|
| 2019 |
Moore C, Blumhagen RZ, Yang IV, Walts A, Powers J, Walker T, Bishop M, Russell P, Vestal B, Cardwell J, Markin CR, Mathai SK, Schwarz MI, Steele MP, Lee J, ... ... Fingerlin TE, et al. Resequencing Study Confirms Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 31034279 DOI: 10.1164/Rccm.201810-1891Oc |
0.365 |
|
| 2019 |
Sakornsakolpat P, Prokopenko D, Lamontagne M, Reeve NF, Guyatt AL, Jackson VE, Shrine N, Qiao D, Bartz TM, Kim DK, Lee MK, Latourelle JC, Li X, Morrow JD, Obeidat M, ... ... Fingerlin TE, et al. Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. Nature Genetics. PMID 30804561 DOI: 10.1038/S41588-018-0342-2 |
0.406 |
|
| 2019 |
Allen R, Guillen-Guio B, Oldham J, Ma S, Dressen A, Paynton M, Kraven L, Obeidat M, Li X, Braybrooke R, Fingerlin T, Hall I, Sayers I, Tobin, Maher T, et al. T1 Meta-analysis of idiopathic pulmonary fibrosis genome-wide analyses identifies three novel genetic signals associated with disease susceptibility Thorax. 74. DOI: 10.1136/Thorax-2019-Btsabstracts2019.1 |
0.418 |
|
| 2018 |
Juge PA, Lee JS, Ebstein E, Furukawa H, Dobrinskikh E, Gazal S, Kannengiesser C, Ottaviani S, Oka S, Tohma S, Tsuchiya N, Rojas-Serrano J, González-Pérez MI, Mejía M, Buendía-Roldán I, ... ... Fingerlin T, et al. MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease. The New England Journal of Medicine. PMID 30345907 DOI: 10.1056/Nejmoa1801562 |
0.321 |
|
| 2018 |
Juge P-, Lee JS, Ebstein E, Furukawa H, Dobrinskikh E, Gazal S, Kannengiesser C, Ottaviani S, Tsuchiya N, Oka S, Tohma S, Rojas-Serrano J, Gonzalez-Perez M-, Mejia M, Buendia-Roldan I, ... ... Fingerlin T, et al. OP0284 Muc5b promoter variant rs35705950 is a risk factor for rheumatoid arthritis – interstitial lung disease Annals of the Rheumatic Diseases. 77: 190-190. DOI: 10.1136/Annrheumdis-2018-Eular.4727 |
0.343 |
|
| 2017 |
Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, ... ... Fingerlin T, et al. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America. PMID 29279374 DOI: 10.1073/Pnas.1705859115 |
0.4 |
|
| 2017 |
Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Fingerlin T, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179 |
0.368 |
|
| 2017 |
Silveira LJ, Strand M, Van Dyke MV, Mroz MM, Faino AV, Dabelea DM, Maier LA, Fingerlin TE. Clinical tool for disease phenotyping in granulomatous lung disease. Plos One. 12: e0188119. PMID 29145499 DOI: 10.1371/Journal.Pone.0188119 |
0.3 |
|
| 2017 |
Allen RJ, Porte J, Braybrooke R, Flores C, Fingerlin TE, Oldham JM, Guillen-Guio B, Ma SF, Okamoto T, John AE, Obeidat M, Yang IV, Henry A, Hubbard RB, Navaratnam V, et al. Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. The Lancet. Respiratory Medicine. PMID 29066090 DOI: 10.1016/S2213-2600(17)30387-9 |
0.411 |
|
| 2017 |
Raghavan S, Zhang W, Yang IV, Lange LA, Lange EM, Fingerlin TE, Dabelea D. Association between gestational diabetes mellitus exposure and childhood adiposity is not substantially explained by offspring genetic risk of obesity. Diabetic Medicine : a Journal of the British Diabetic Association. PMID 29048747 DOI: 10.1111/Dme.13529 |
0.318 |
|
| 2017 |
McIntosh LA, Marion MC, Sudman M, Comeau ME, Becker ML, Bohnsack JF, Fingerlin TE, Griffin TA, Haas JP, Lovell DJ, Maier LA, Nigrovic PA, Prahalad S, Punaro M, Rosé CD, et al. Genome-wide association meta-analysis reveals novel juvenile idiopathic arthritis susceptibility loci. Arthritis & Rheumatology (Hoboken, N.J.). PMID 28719732 DOI: 10.1002/Art.40216 |
0.377 |
|
| 2017 |
Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, Viñuela A, Brown AA, Wu Y, ... ... Fingerlin T, et al. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. PMID 28341696 DOI: 10.2337/Db16-1329 |
0.365 |
|
| 2017 |
Hobbs BD, de Jong K, Lamontagne M, Bossé Y, Shrine N, Artigas MS, Wain LV, Hall IP, Jackson VE, Wyss AB, London SJ, North KE, Franceschini N, Strachan DP, Beaty TH, ... ... Fingerlin TE, et al. Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. Nature Genetics. PMID 28166215 DOI: 10.1038/Ng.3752 |
0.405 |
|
| 2016 |
Lutz SM, Fingerlin TE, Hokanson JE, Lange C. A general approach to testing for pleiotropy with rare and common variants. Genetic Epidemiology. PMID 27900789 DOI: 10.1002/Gepi.22011 |
0.371 |
|
| 2016 |
Kropski JA, Young LR, Cogan JD, Mitchell DB, Lancaster LH, Worrell JA, Markin C, Liu N, Mason WR, Fingerlin TE, Schwartz DA, Lawson WE, Blackwell TS, Phillips Iii JA, Loyd JE. Genetic Evaluation and Testing of Patients and Families with Idiopathic Pulmonary Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 27786550 DOI: 10.1164/Rccm.201609-1820Pp |
0.361 |
|
| 2016 |
Evans CM, Fingerlin TE, Schwarz MI, Lynch D, Kurche J, Warg L, Yang IV, Schwartz DA. Idiopathic Pulmonary Fibrosis: A Genetic Disease That Involves Mucociliary Dysfunction of the Peripheral Airways. Physiological Reviews. 96: 1567-1591. PMID 27630174 DOI: 10.1152/Physrev.00004.2016 |
0.382 |
|
| 2016 |
Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Fingerlin T, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642 |
0.382 |
|
| 2016 |
Fingerlin TE, Zhang W, Yang IV, Ainsworth HC, Russell PH, Blumhagen RZ, Schwarz MI, Brown KK, Steele MP, Loyd JE, Cosgrove GP, Lynch DA, Groshong S, Collard HR, Wolters PJ, et al. Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia. Bmc Genetics. 17: 74. PMID 27266705 DOI: 10.1186/S12863-016-0377-2 |
0.394 |
|
| 2016 |
Palmer ND, Wagenknecht LE, Langefeld CD, Wang N, Buchanan TA, Xiang AH, Allayee H, Bergman RN, Raffel LJ, Ida Chen YD, Haritunians T, Fingerlin T, Goodarzi MO, Taylor KD, Rotter JI, et al. Improved Performance of Dynamic Measures of Insulin Response over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium. Diabetes. PMID 27207554 DOI: 10.2337/Db15-1543 |
0.309 |
|
| 2016 |
Chung JH, Peljto AL, Chawla A, Talbert JL, McKean DF, Rho BH, Fingerlin TE, Schwarz MI, Schwartz DA, Lynch DA. CT Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism. Chest. PMID 26836909 DOI: 10.1016/J.Chest.2015.11.009 |
0.322 |
|
| 2015 |
Mathai SK, Pedersen BS, Smith K, Russell P, Schwarz MI, Brown KK, Steele MP, Loyd JE, Crapo JD, Silverman EK, Nickerson D, Fingerlin TE, Yang IV, Schwartz DA. Desmoplakin (DSP) Variants are Associated with Idiopathic Pulmonary Fibrosis. American Journal of Respiratory and Critical Care Medicine. PMID 26669357 DOI: 10.1164/Rccm.201509-1863Oc |
0.395 |
|
| 2015 |
Yang IV, Fingerlin TE, Evans CM, Schwarz MI, Schwartz DA. MUC5B and Idiopathic Pulmonary Fibrosis. Annals of the American Thoracic Society. 12: S193-9. PMID 26595739 DOI: 10.1513/Annalsats.201503-110Aw |
0.38 |
|
| 2015 |
Fingerlin TE, Hamzeh N, Maier LA. Genetics of Sarcoidosis. Clinics in Chest Medicine. 36: 569-84. PMID 26593134 DOI: 10.1016/J.Ccm.2015.08.002 |
0.346 |
|
| 2015 |
Palmer ND, Goodarzi MO, Langefeld CD, Wang N, Guo X, Taylor KD, Fingerlin TE, Norris JM, Buchanan TA, Xiang AH, Haritunians T, Ziegler JT, Williams AH, Stefanovski D, Cui J, et al. Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium. Diabetes. 64: 1853-66. PMID 25524916 DOI: 10.2337/Db14-0732 |
0.368 |
|
| 2015 |
Peljto AL, Selman M, Kim DS, Murphy E, Tucker L, Pardo A, Lee JS, Ji W, Schwarz MI, Yang IV, Schwartz DA, Fingerlin TE. The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestries. Chest. 147: 460-4. PMID 25275363 DOI: 10.1378/Chest.14-0867 |
0.432 |
|
| 2014 |
Norris JM, Kroehl M, Fingerlin TE, Frederiksen BN, Seifert J, Wong R, Clare-Salzler M, Rewers M. Erythrocyte membrane docosapentaenoic acid levels are associated with islet autoimmunity: the Diabetes Autoimmunity Study in the Young. Diabetologia. 57: 295-304. PMID 24240437 DOI: 10.1007/S00125-013-3106-7 |
0.307 |
|
| 2013 |
Lutz SM, Fingerlin T, Fardo DW. Statistical Approaches to Combine Genetic Association Data. Journal of Biometrics & Biostatistics. 4: 1000166. PMID 24009987 DOI: 10.4172/2155-6180.1000166 |
0.331 |
|
| 2013 |
Frederiksen BN, Kroehl M, Fingerlin TE, Wong R, Steck AK, Rewers M, Norris JM. Association between vitamin D metabolism gene polymorphisms and risk of islet autoimmunity and progression to type 1 diabetes: the diabetes autoimmunity study in the young (DAISY). The Journal of Clinical Endocrinology and Metabolism. 98: E1845-51. PMID 23979957 DOI: 10.1210/Jc.2013-2256 |
0.392 |
|
| 2013 |
Yang IV, Coldren CD, Leach SM, Seibold MA, Murphy E, Lin J, Rosen R, Neidermyer AJ, McKean DF, Groshong SD, Cool C, Cosgrove GP, Lynch DA, Brown KK, Schwarz MI, ... Fingerlin TE, et al. Expression of cilium-associated genes defines novel molecular subtypes of idiopathic pulmonary fibrosis. Thorax. 68: 1114-21. PMID 23783374 DOI: 10.1136/Thoraxjnl-2012-202943 |
0.331 |
|
| 2013 |
Hunninghake GM, Hatabu H, Okajima Y, Gao W, Dupuis J, Latourelle JC, Nishino M, Araki T, Zazueta OE, Kurugol S, Ross JC, San José Estépar R, Murphy E, Steele MP, Loyd JE, ... ... Fingerlin TE, et al. MUC5B promoter polymorphism and interstitial lung abnormalities. The New England Journal of Medicine. 368: 2192-200. PMID 23692170 DOI: 10.1097/01.Sa.0000435633.11233.8A |
0.388 |
|
| 2013 |
Fingerlin TE, Murphy E, Zhang W, Peljto AL, Brown KK, Steele MP, Loyd JE, Cosgrove GP, Lynch D, Groshong S, Collard HR, Wolters PJ, Bradford WZ, Kossen K, Seiwert SD, et al. Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. Nature Genetics. 45: 613-20. PMID 23583980 DOI: 10.1038/Ng.2609 |
0.326 |
|
| 2013 |
Jaiswal M, Urbina EM, Wadwa RP, Talton JW, D'Agostino RB, Hamman RF, Fingerlin TE, Daniels SR, Marcovina SM, Dolan LM, Dabelea D. Reduced heart rate variability is associated with increased arterial stiffness in youth with type 1 diabetes: the SEARCH CVD study. Diabetes Care. 36: 2351-8. PMID 23435158 DOI: 10.2337/Dc12-0923 |
0.318 |
|
| 2013 |
Frederiksen B, Liu E, Romanos J, Steck AK, Yin X, Kroehl M, Fingerlin TE, Erlich H, Eisenbarth GS, Rewers M, Norris JM. Investigation of the vitamin D receptor gene (VDR) and its interaction with protein tyrosine phosphatase, non-receptor type 2 gene (PTPN2) on risk of islet autoimmunity and type 1 diabetes: The Diabetes Autoimmunity Study in the Young (DAISY) Journal of Steroid Biochemistry and Molecular Biology. 133: 51-57. PMID 22960018 DOI: 10.1016/J.Jsbmb.2012.08.012 |
0.382 |
|
| 2013 |
Fingerlin TE, Murphy E, Zhang W, Peljto AL, Brown KK, Steele MP, Loyd JE, Cosgrove GP, Lynch D, Groshong S, Collard HR, Wolters PJ, Bradford WZ, Kossen K, Seiwert SD, et al. Erratum: Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis Nature Genetics. 45: 1409-1409. DOI: 10.1038/Ng1113-1409A |
0.367 |
|
| 2012 |
Silveira LJ, McCanlies EC, Fingerlin TE, Van Dyke MV, Mroz MM, Strand M, Fontenot AP, Bowerman N, Dabelea DM, Schuler CR, Weston A, Maier LA. Chronic beryllium disease, HLA-DPB1, and the DP peptide binding groove. Journal of Immunology (Baltimore, Md. : 1950). 189: 4014-23. PMID 22972925 DOI: 10.4049/Jimmunol.1200798 |
0.338 |
|
| 2012 |
Aschard H, Lutz S, Maus B, Duell EJ, Fingerlin TE, Chatterjee N, Kraft P, Van Steen K. Challenges and opportunities in genome-wide environmental interaction (GWEI) studies. Human Genetics. 131: 1591-613. PMID 22760307 DOI: 10.1007/S00439-012-1192-0 |
0.338 |
|
| 2012 |
Peljto AL, Steele MP, Fingerlin TE, Hinchcliff ME, Murphy E, Podlusky S, Carns M, Schwarz M, Varga J, Schwartz DA. The pulmonary fibrosis-associated MUC5B promoter polymorphism does not influence the development of interstitial pneumonia in systemic sclerosis. Chest. 142: 1584-8. PMID 22576636 DOI: 10.1378/Chest.12-0110 |
0.407 |
|
| 2011 |
Seibold MA, Wise AL, Speer MC, Steele MP, Brown KK, Loyd JE, Fingerlin TE, Zhang W, Gudmundsson G, Groshong SD, Evans CM, Garantziotis S, Adler KB, Dickey BF, du Bois RM, et al. A common MUC5B promoter polymorphism and pulmonary fibrosis. The New England Journal of Medicine. 364: 1503-12. PMID 21506741 DOI: 10.1056/Nejmoa1013660 |
0.311 |
|
| 2011 |
Sinkus ML, Wamboldt MZ, Barton A, Fingerlin TE, Laudenslager ML, Leonard S. The α7 nicotinic acetylcholine receptor and the acute stress response: maternal genotype determines offspring phenotype. Physiology & Behavior. 104: 321-6. PMID 21073885 DOI: 10.1016/J.Physbeh.2010.11.007 |
0.308 |
|
| 2011 |
Monos D, Fingerlin T, Mackiewicz K, Papazoglou A, Rossman M, Rosenman K, Bradfield J, Mroz P, Silveira L, Hakonarson H, Maier L. 19-OR New directions in HLA and disease associations: The search beyond HLAs using genome-wide SNP-genotyping and next generation sequencing Human Immunology. 72: S15. DOI: 10.1016/J.Humimm.2011.07.024 |
0.349 |
|
| 2010 |
Engelman CD, Meyers KJ, Ziegler JT, Taylor KD, Palmer ND, Haffner SM, Fingerlin TE, Wagenknecht LE, Rotter JI, Bowden DW, Langefeld CD, Norris JM. Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study. The Journal of Steroid Biochemistry and Molecular Biology. 122: 186-92. PMID 20600896 DOI: 10.1016/J.Jsbmb.2010.06.013 |
0.659 |
|
| 2010 |
Palmer ND, Langefeld CD, Ziegler JT, Hsu F, Haffner SM, Fingerlin T, Norris JM, Chen YI, Rich SS, Haritunians T, Taylor KD, Bergman RN, Rotter JI, Bowden DW. Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study. Diabetologia. 53: 281-9. PMID 19902172 DOI: 10.1007/S00125-009-1586-2 |
0.322 |
|
| 2010 |
Miller MR, Zhang W, Sibbel SP, Langefeld CD, Bowden DW, Haffner SM, Bergman RN, Norris JM, Fingerlin TE. Variant in the 3' region of the IkappaBalpha gene associated with insulin resistance in Hispanic Americans: The IRAS Family Study. Obesity (Silver Spring, Md.). 18: 555-62. PMID 19798070 DOI: 10.1038/Oby.2009.303 |
0.367 |
|
| 2009 |
Norris JM, Langefeld CD, Talbert ME, Wing MR, Haritunians T, Fingerlin TE, Hanley AJ, Ziegler JT, Taylor KD, Haffner SM, Chen YD, Bowden DW, Wagenknecht LE. Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study. Obesity (Silver Spring, Md.). 17: 1932-41. PMID 19461586 DOI: 10.1038/Oby.2009.143 |
0.402 |
|
| 2008 |
Engelman CD, Fingerlin TE, Langefeld CD, Hicks PJ, Rich SS, Wagenknecht LE, Bowden DW, Norris JM. Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans. The Journal of Clinical Endocrinology and Metabolism. 93: 3381-8. PMID 18593774 DOI: 10.1210/Jc.2007-2702 |
0.304 |
|
| 2008 |
Wasfi YS, Silveira LJ, Jonth A, Hokanson JE, Fingerlin T, Sato H, Parsons CE, Lympany P, Welsh K, du Bois RM, Newman LS, Maier LA. Fas promoter polymorphisms: genetic predisposition to sarcoidosis in African-Americans. Tissue Antigens. 72: 39-48. PMID 18588573 DOI: 10.1111/J.1399-0039.2008.01060.X |
0.392 |
|
| 2008 |
Black MH, Fingerlin TE, Allayee H, Zhang W, Xiang AH, Trigo E, Hartiala J, Lehtinen AB, Haffner SM, Bergman RN, McEachin RC, Kjos SL, Lawrence JM, Buchanan TA, Watanabe RM. Evidence of interaction between PPARG2 and HNF4A contributing to variation in insulin sensitivity in Mexican Americans. Diabetes. 57: 1048-56. PMID 18162503 DOI: 10.2337/Db07-0848 |
0.382 |
|
| 2008 |
Aly TA, Baschal EE, Jahromi MM, Fernando MS, Babu SR, Fingerlin TE, Kretowski A, Erlich HA, Fain PR, Rewers MJ, Eisenbarth GS. Analysis of single nucleotide polymorphisms identifies major type 1A diabetes locus telomeric of the major histocompatibility complex. Diabetes. 57: 770-6. PMID 18065518 DOI: 10.2337/Db07-0900 |
0.357 |
|
| 2008 |
Meng JF, Fingerlin TE. Linear models for analysis of multiple single nucleotide polymorphisms with quantitative traits in unrelated individuals Annales Zoologici Fennici. 45: 429-440. DOI: 10.5735/086.045.0506 |
0.386 |
|
| 2007 |
Langefeld CD, Fingerlin TE. Association methods in human genetics. Methods in Molecular Biology (Clifton, N.J.). 404: 431-60. PMID 18450062 DOI: 10.1007/978-1-59745-530-5_21 |
0.375 |
|
| 2007 |
Nelson TL, Fingerlin TE, Moss L, Barmada MM, Ferrell RE, Norris JM. The PPARgamma Pro12Ala polymorphism is not associated with body mass index or waist circumference among Hispanics from Colorado. Annals of Nutrition & Metabolism. 51: 252-7. PMID 17587797 DOI: 10.1159/000104145 |
0.365 |
|
| 2007 |
Nelson TL, Fingerlin TE, Moss LK, Barmada MM, Ferrell RE, Norris JM. Association of the peroxisome proliferator-activated receptor gamma gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado. Metabolism: Clinical and Experimental. 56: 388-93. PMID 17292728 DOI: 10.1016/J.Metabol.2006.10.022 |
0.353 |
|
| 2006 |
Tsuchiya T, Schwarz PE, Bosque-Plata LD, Geoffrey Hayes M, Dina C, Froguel P, Wayne Towers G, Fischer S, Temelkova-Kurktschiev T, Rietzsch H, Graessler J, Vcelák J, Palyzová D, Selisko T, Bendlová B, ... ... Fingerlin TE, et al. Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Molecular Genetics and Metabolism. 89: 174-84. PMID 16837224 DOI: 10.1016/J.Ymgme.2006.05.013 |
0.383 |
|
| 2004 |
Silander K, Mohlke KL, Scott LJ, Peck EC, Hollstein P, Skol AD, Jackson AU, Deloukas P, Hunt S, Stavrides G, Chines PS, Erdos MR, Narisu N, Conneely KN, Li C, ... Fingerlin TE, et al. Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. Diabetes. 53: 1141-9. PMID 15047633 DOI: 10.2337/Diabetes.53.4.1141 |
0.415 |
|
| 2004 |
Fingerlin TE, Boehnke M, Abecasis GR. Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information. American Journal of Human Genetics. 74: 432-43. PMID 14752704 DOI: 10.1086/381652 |
0.372 |
|
| 2002 |
Mohlke KL, Erdos MR, Scott LJ, Fingerlin TE, Jackson AU, Silander K, Hollstein P, Boehnke M, Collins FS. High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools. Proceedings of the National Academy of Sciences of the United States of America. 99: 16928-33. PMID 12482934 DOI: 10.1073/Pnas.262661399 |
0.336 |
|
| 2002 |
Fingerlin TE, Erdos MR, Watanabe RM, Wiles KR, Stringham HM, Mohlke KL, Silander K, Valle TT, Buchanan TA, Tuomilehto J, Bergman RN, Boehnke M, Collins FS. Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort. Diabetes. 51: 1644-8. PMID 11978669 DOI: 10.2337/Diabetes.51.5.1644 |
0.376 |
|
| 2000 |
Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, et al. The Finland–United States Investigation of Non–Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. II. An Autosomal Genome Scan for Diabetes-Related Quantitative-Trait Loci The American Journal of Human Genetics. 67: 1186-1200. DOI: 10.1016/S0002-9297(07)62949-8 |
0.316 |
|
| 2000 |
Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, Mohlke KL, Silander K, Kohtamäki K, Chines P, Balow J, Birznieks G, Chang J, Eldridge W, ... ... Fingerlin TE, et al. The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. American Journal of Human Genetics. 67: 1174-1185. DOI: 10.1016/S0002-9297(07)62948-6 |
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