| Year |
Citation |
Score |
| 2024 |
Ferrell M, Wang Z, Anderson JT, Li XS, Witkowski M, DiDonato JA, Hilser JR, Hartiala JA, Haghikia A, Cajka T, Fiehn O, Sangwan N, Demuth I, König M, Steinhagen-Thiessen E, et al. Publisher Correction: A terminal metabolite of niacin promotes vascular inflammation and contributes to cardiovascular disease risk. Nature Medicine. PMID 38448791 DOI: 10.1038/s41591-024-02899-7 |
0.537 |
|
| 2024 |
Ferrell M, Wang Z, Anderson JT, Li XS, Witkowski M, DiDonato JA, Hilser JR, Hartiala JA, Haghikia A, Cajka T, Fiehn O, Sangwan N, Demuth I, König M, Steinhagen-Thiessen E, et al. A terminal metabolite of niacin promotes vascular inflammation and contributes to cardiovascular disease risk. Nature Medicine. 30: 424-434. PMID 38374343 DOI: 10.1038/s41591-023-02793-8 |
0.565 |
|
| 2024 |
Sakano Y, Sakano K, Hurrell BP, Helou DG, Shafiei-Jahani P, Kazemi MH, Li X, Shen S, Hilser JR, Hartiala JA, Allayee H, Barbers R, Akbari O. Blocking CD226 regulates ILC2 effector function and alleviates airway hyperreactivity. The Journal of Allergy and Clinical Immunology. PMID 38244725 DOI: 10.1016/j.jaci.2024.01.003 |
0.462 |
|
| 2023 |
Biswas S, Hilser JR, Woodward NC, Wang Z, Gukasyan J, Nemet I, Schwartzman WS, Huang P, Han Y, Fouladian Z, Charugundla S, Spencer NJ, Pan C, Tang WHW, Lusis AJ, ... ... Hartiala JA, et al. Effect of Genetic and Dietary Perturbation of Glycine Metabolism on Atherosclerosis in Humans and Mice. Medrxiv : the Preprint Server For Health Sciences. PMID 38168321 DOI: 10.1101/2023.12.08.23299748 |
0.595 |
|
| 2022 |
Hilser JR, Hartiala JA, Sriprasert I, Kono N, Cai Z, Karim R, DeYoung J, Mack WJ, Hodis HN, Allayee H. Effect of menopausal hormone therapy on methylation levels in early and late postmenopausal women. Clinical Epigenetics. 14: 90. PMID 35850911 DOI: 10.1186/s13148-022-01311-w |
0.471 |
|
| 2022 |
Schillemans T, Tragante V, Maitusong B, Gigante B, Cresci S, Laguzzi F, Vikström M, Richards M, Pilbrow A, Cameron V, Foco L, Doughty RN, Kuukasjärvi P, Allayee H, Hartiala JA, et al. Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis. Frontiers in Physiology. 13: 909870. PMID 35812313 DOI: 10.3389/fphys.2022.909870 |
0.6 |
|
| 2022 |
Schmidt KA, Jones RB, Rios C, Corona Y, Berger PK, Plows JF, Alderete TL, Fogel J, Hampson H, Hartiala JA, Cai Z, Allayee H, Nayak KS, Sinatra FR, Harlan G, et al. Clinical Intervention to Reduce Dietary Sugar does not Impact Liver Fat in Latino Youth, Regardless of PNPLA3 Genotype: A Randomized Controlled Trial. The Journal of Nutrition. PMID 35218194 DOI: 10.1093/jn/nxac046 |
0.504 |
|
| 2021 |
Hartiala JA, Hilser JR, Biswas S, Lusis AJ, Allayee H. Gene-Environment Interactions for Cardiovascular Disease. Current Atherosclerosis Reports. 23: 75. PMID 34648097 DOI: 10.1007/s11883-021-00974-9 |
0.544 |
|
| 2021 |
Schunk SJ, Kleber ME, März W, Pang S, Zewinger S, Triem S, Ege P, Reichert MC, Krawczyk M, Weber SN, Jaumann I, Schmit D, Sarakpi T, Wagenpfeil S, Kramann R, ... ... Hartiala JA, et al. Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality. European Heart Journal. PMID 33748830 DOI: 10.1093/eurheartj/ehab107 |
0.546 |
|
| 2021 |
Hilser JR, Han Y, Biswas S, Gukasyan J, Cai Z, Zhu R, Tang WHW, Deb A, Lusis AJ, Hartiala JA, Allayee H. Association of serum HDL cholesterol and apolipoprotein A1 levels with risk of severe SARS-CoV-2 infection. Journal of Lipid Research. 100061. PMID 33667465 DOI: 10.1016/j.jlr.2021.100061 |
0.562 |
|
| 2021 |
Hartiala JA, Han Y, Jia Q, Hilser JR, Huang P, Gukasyan J, Schwartzman WS, Cai Z, Biswas S, Trégouët DA, Smith NL, Seldin M, et al. Genome-wide analysis identifies novel susceptibility loci for myocardial infarction. European Heart Journal. PMID 33532862 DOI: 10.1093/eurheartj/ehaa1040 |
0.565 |
|
| 2020 |
Mahmoodi BK, Tragante V, Kleber ME, Holmes MV, Schmidt AF, McCubrey RO, Howe LJ, Direk K, Allayee H, Baranova EV, Braund PS, Delgado GE, Eriksson N, Gijsberts CM, Gong Y, ... Hartiala J, et al. Association of Factor V Leiden with Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data. Circulation. PMID 32654539 DOI: 10.1161/Circulationaha.119.045526 |
0.604 |
|
| 2020 |
Han Y, Jia Q, Jahani PS, Hurrell BP, Pan C, Huang P, Gukasyan J, Woodward NC, Eskin E, Gilliland FD, Akbari O, Hartiala JA, Allayee H. Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma. Nature Communications. 11: 1776. PMID 32296059 DOI: 10.1038/S41467-020-15649-3 |
0.582 |
|
| 2019 |
Maazi H, Hartiala JA, Suzuki Y, Crow AL, Shafiei Jahani P, Lam J, Patel N, Rigas D, Han Y, Huang P, Eskin E, Lusis AJ, Gilliland FD, Akbari O, Allayee H. A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity. Plos Genetics. 15: e1008528. PMID 31869344 DOI: 10.1371/Journal.Pgen.1008528 |
0.591 |
|
| 2019 |
Jia Q, Han Y, Huang P, Woodward NC, Gukasyan J, Kettunen J, Ala-Korpela M, Anufrieva O, Wang Q, Perola M, Raitakari O, Lehtimäki T, Viikari J, Järvelin MR, Boehnke M, ... ... Hartiala JA, et al. Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. Journal of the American Heart Association. 8: e011922. PMID 31070104 DOI: 10.1161/Jaha.119.011922 |
0.666 |
|
| 2019 |
Patel RS, Schmidt AF, Tragante V, McCubrey RO, Holmes MV, Howe LJ, Direk K, Åkerblom A, Leander K, Virani SS, Kaminski KA, Muehlschlegel JD, Dubé MP, Allayee H, Almgren P, ... ... Hartiala J, et al. Association of Chromosome 9p21 with Subsequent Coronary Heart Disease Events: A GENIUS-CHD Study of Individual Participant Data. Circulation. Genomic and Precision Medicine. PMID 30897348 DOI: 10.1161/CIRCGEN.119.002471 |
0.586 |
|
| 2019 |
Patel R, Tragante V, Schmidt AF, McCubrey RO, Holmes MV, Howe LJ, Direk K, Åkerblom A, Leander K, Virani SS, Kaminski KA, Muehlschlegel JD, Allayee H, Almgren P, Alver M, ... ... Hartiala J, et al. Subsequent Event Risk in Individuals with Established Coronary Heart Disease: Design and Rationale of the GENIUS-CHD Consortium. Circulation. Genomic and Precision Medicine. PMID 30896328 DOI: 10.1161/CIRCGEN.119.002470 |
0.585 |
|
| 2019 |
Woodward NC, Crow AL, Zhang Y, Epstein S, Hartiala J, Johnson R, Kocalis H, Saffari A, Sankaranarayanan I, Akbari O, Ramanathan G, Araujo JA, Finch CE, Bouret SG, Sioutas C, et al. Exposure to Nanoscale Particulate Matter from Gestation to Adulthood Impairs Metabolic Homeostasis in Mice. Scientific Reports. 9: 1816. PMID 30755631 DOI: 10.1038/S41598-018-37704-2 |
0.538 |
|
| 2018 |
Li XS, Wang Z, Cajka T, Buffa JA, Nemet I, Hurd AG, Gu X, Skye SM, Roberts AB, Wu Y, Li L, Shahen CJ, Wagner MA, Hartiala JA, Kerby RL, et al. Untargeted metabolomics identifies trimethyllysine, a TMAO-producing nutrient precursor, as a predictor of incident cardiovascular disease risk. Jci Insight. 3. PMID 29563342 DOI: 10.1172/Jci.Insight.99096 |
0.607 |
|
| 2018 |
Barrington WT, Salvador AC, Hartiala JA, De Caterina R, Kohlmeier M, Martinez JA, Kreutzer CB, Heber D, Lusis AJ, Li Z, Allayee H. Proceedings of the 11th Congress of the International Society of Nutrigenetics and Nutrigenomics (ISNN 2017). Journal of Nutrigenetics and Nutrigenomics. 10: 155-162. PMID 29339647 DOI: 10.1159/000485799 |
0.541 |
|
| 2017 |
Zewinger S, Kleber ME, Tragante V, McCubrey RO, Schmidt AF, Direk K, Laufs U, Werner C, Koenig W, Rothenbacher D, Mons U, Breitling LP, Brenner H, Jennings RT, Petrakis I, ... ... Hartiala JA, et al. Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study. The Lancet. Diabetes & Endocrinology. PMID 28566218 DOI: 10.1016/S2213-8587(17)30096-7 |
0.633 |
|
| 2017 |
Saleheen D, Zhao W, Young R, Nelson CP, Ho WK, Ferguson JF, Rasheed A, Ou K, Nurnberg ST, Bauer RC, Goel A, Do R, Stewart AFR, Hartiala J, Zhang W, et al. Loss of Cardio-Protective Effects at the ADAMTS7 Locus Due to Gene-Smoking Interactions. Circulation. PMID 28461624 DOI: 10.1161/Circulationaha.116.022069 |
0.599 |
|
| 2017 |
Hartiala J, Schwartzman WS, Gabbay J, Ghazalpour A, Bennett BJ, Allayee H. The Genetic Architecture of Coronary Artery Disease: Current Knowledge and Future Opportunities. Current Atherosclerosis Reports. 19: 6. PMID 28130654 DOI: 10.1007/S11883-017-0641-6 |
0.586 |
|
| 2016 |
Salehi P, Myint A, Kim YJ, Ge MX, Lavinsky J, Ho MK, Crow AL, Cruz C, Monges-Hernadez M, Wang J, Hartiala J, Zhang LI, Allayee H, Lusis AJ, Ohyama T, et al. Genome-Wide Association Analysis Identifies Dcc as an Essential Factor in the Innervation of the Peripheral Vestibular System in Inbred Mice. Journal of the Association For Research in Otolaryngology : Jaro. PMID 27539716 DOI: 10.1007/S10162-016-0578-4 |
0.581 |
|
| 2016 |
Hartiala J, Breton CV, Tang WH, Lurmann F, Hazen SL, Gilliland FD, Allayee H. Ambient Air Pollution Is Associated With the Severity of Coronary Atherosclerosis and Incident Myocardial Infarction in Patients Undergoing Elective Cardiac Evaluation. Journal of the American Heart Association. 5. PMID 27468926 DOI: 10.1161/Jaha.116.003947 |
0.577 |
|
| 2016 |
Hartiala JA, Tang WH, Wang Z, Crow AL, Stewart AF, Roberts R, McPherson R, Erdmann J, Willenborg C, Hazen SL, Allayee H. Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease. Nature Communications. 7: 10558. PMID 26822151 DOI: 10.1038/Ncomms10558 |
0.65 |
|
| 2015 |
Kato N, Loh M, Takeuchi F, Verweij N, Wang X, Zhang W, Kelly TN, Saleheen D, Lehne B, Mateo Leach I, Drong AW, Abbott J, Wahl S, Tan ST, Scott WR, ... ... Hartiala J, et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nature Genetics. 47: 1282-93. PMID 26390057 DOI: 10.1038/Ng.3405 |
0.581 |
|
| 2015 |
Crow AL, Ohmen J, Wang J, Lavinsky J, Hartiala J, Li Q, Li X, Salehide P, Eskin E, Pan C, Lusis AJ, Allayee H, Friedman RA. The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency Specific Genetic Determinants. G3 (Bethesda, Md.). PMID 26342000 DOI: 10.1534/G3.115.021592 |
0.59 |
|
| 2015 |
Schmidt RJ, Hansen RL, Hartiala J, Allayee H, Sconberg JL, Schmidt LC, Volk HE, Tassone F. Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE Study. Early Human Development. 91: 483-489. PMID 26073892 DOI: 10.1016/J.Earlhumdev.2015.05.008 |
0.592 |
|
| 2015 |
Zhou X, Crow AL, Hartiala J, Spindler TJ, Ghazalpour A, Barsky LW, Bennett BB, Parks BW, Eskin E, Jain R, Epstein JA, Lusis AJ, Adams GB, Allayee H. The Genetic Landscape of Hematopoietic Stem Cell Frequency in Mice. Stem Cell Reports. PMID 26050929 DOI: 10.1016/J.Stemcr.2015.05.008 |
0.585 |
|
| 2015 |
Jeong S, Patel N, Edlund CK, Hartiala J, Hazelett DJ, Itakura T, Wu PC, Avery RL, Davis JL, Flynn HW, Lalwani G, Puliafito CA, Wafapoor H, Hijikata M, Keicho N, et al. Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension. Investigative Ophthalmology & Visual Science. 56: 2737-48. PMID 25813999 DOI: 10.1167/Iovs.14-14803 |
0.551 |
|
| 2015 |
Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, ... ... Hartiala J, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 518: 102-6. PMID 25487149 DOI: 10.1038/Nature13917 |
0.595 |
|
| 2014 |
Ren J, Xiang AH, Trigo E, Takayanagi M, Beale E, Lawrence JM, Hartiala J, Richey JM, Allayee H, Buchanan TA, Watanabe RM. Genetic variation in MTNR1B is associated with gestational diabetes mellitus and contributes only to the absolute level of beta cell compensation in Mexican Americans. Diabetologia. 57: 1391-9. PMID 24728128 DOI: 10.1007/S00125-014-3239-3 |
0.556 |
|
| 2014 |
Hartiala J, Bennett BJ, Tang WH, Wang Z, Stewart AF, Roberts R, McPherson R, Lusis AJ, Hazen SL, Allayee H. Comparative genome-wide association studies in mice and humans for trimethylamine N-oxide, a proatherogenic metabolite of choline and L-carnitine. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 1307-13. PMID 24675659 DOI: 10.1161/Atvbaha.114.303252 |
0.59 |
|
| 2014 |
Biancolella M, Fortini BK, Tring S, Plummer SJ, Mendoza-Fandino GA, Hartiala J, Hitchler MJ, Yan C, Schumacher FR, Conti DV, Edlund CK, Noushmehr H, Coetzee SG, Bresalier RS, Ahnen DJ, et al. Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1. Human Molecular Genetics. 23: 2198-209. PMID 24256810 DOI: 10.1093/Hmg/Ddt584 |
0.351 |
|
| 2013 |
Walker RW, Sinatra F, Hartiala J, Weigensberg M, Spruijt-Metz D, Alderete TL, Goran MI, Allayee H. Genetic and clinical markers of elevated liver fat content in overweight and obese Hispanic children. Obesity (Silver Spring, Md.). 21: E790-7. PMID 23804528 DOI: 10.1002/Oby.20523 |
0.575 |
|
| 2013 |
Reiner AP, Hartiala J, Zeller T, Bis JC, Dupuis J, Fornage M, Baumert J, Kleber ME, Wild PS, Baldus S, Bielinski SJ, Fontes JD, Illig T, Keating BJ, Lange LA, et al. Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Human Molecular Genetics. 22: 3381-93. PMID 23620142 DOI: 10.1093/Hmg/Ddt189 |
0.635 |
|
| 2013 |
Zhou G, Marathe GK, Hartiala J, Hazen SL, Allayee H, Tang WH, McIntyre TM. Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2). The Journal of Biological Chemistry. 288: 11940-8. PMID 23508960 DOI: 10.1074/Jbc.M112.427674 |
0.567 |
|
| 2013 |
Chan K, Patel RS, Newcombe P, Nelson CP, Qasim A, Epstein SE, Burnett S, Vaccarino VL, Zafari AM, Shah SH, Anderson JL, Carlquist JF, Hartiala J, Allayee H, Hinohara K, et al. Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. Journal of the American College of Cardiology. 61: 957-70. PMID 23352782 DOI: 10.1016/J.Jacc.2012.10.051 |
0.597 |
|
| 2013 |
Chan K, Patel RS, Newcombe P, Nelson CP, Qasim A, Epstein SE, Burnett S, Vaccarino VL, Zafari AM, Shah SH, Anderson JL, Carlquist JF, Hartiala J, Allayee H, Hinohara K, et al. 126 CHROMOSOME 9P21 LOCUS AND ANGIOGRAPHIC CORONARY ARTERY DISEASE BURDEN: A COLLABORATIVE META-ANALYSIS Heart. 99: A75.1-A75. DOI: 10.1136/Heartjnl-2013-304019.126 |
0.639 |
|
| 2012 |
van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, ... ... Hartiala J, et al. Seventy-five genetic loci influencing the human red blood cell. Nature. 492: 369-75. PMID 23222517 DOI: 10.1038/Nature11677 |
0.593 |
|
| 2012 |
Tang WH, Hartiala J, Fan Y, Wu Y, Stewart AF, Erdmann J, Kathiresan S, Roberts R, McPherson R, Allayee H, Hazen SL. Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk. Arteriosclerosis, Thrombosis, and Vascular Biology. 32: 2803-12. PMID 22982463 DOI: 10.1161/Atvbaha.112.253930 |
0.592 |
|
| 2012 |
Patel RS, Sun YV, Hartiala J, Veledar E, Su S, Sher S, Liu YX, Rahman A, Patel R, Rab ST, Vaccarino V, Zafari AM, Samady H, Tang WH, Allayee H, et al. Association of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography. Circulation. Cardiovascular Genetics. 5: 441-9. PMID 22767652 DOI: 10.1161/Circgenetics.111.960229 |
0.642 |
|
| 2012 |
Schmidt RJ, Tancredi DJ, Ozonoff S, Hansen RL, Hartiala J, Allayee H, Schmidt LC, Tassone F, Hertz-Picciotto I. Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study. The American Journal of Clinical Nutrition. 96: 80-9. PMID 22648721 DOI: 10.3945/Ajcn.110.004416 |
0.571 |
|
| 2012 |
Hartiala J, Gilliam E, Vikman S, Campos H, Allayee H. Association of PLA2G4A with myocardial infarction is modulated by dietary PUFAs. The American Journal of Clinical Nutrition. 95: 959-65. PMID 22378731 DOI: 10.3945/Ajcn.111.032094 |
0.615 |
|
| 2012 |
Tang WH, Wu Y, Hartiala J, Fan Y, Stewart AF, Roberts R, McPherson R, Fox PL, Allayee H, Hazen SL. Clinical and genetic association of serum ceruloplasmin with cardiovascular risk. Arteriosclerosis, Thrombosis, and Vascular Biology. 32: 516-22. PMID 22075249 DOI: 10.1161/Atvbaha.111.237040 |
0.606 |
|
| 2011 |
Gieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U, Goodall AH, Labrune Y, Lopez LM, Mägi R, Meacham S, Okada Y, Pirastu N, ... ... Hartiala J, et al. New gene functions in megakaryopoiesis and platelet formation. Nature. 480: 201-8. PMID 22139419 DOI: 10.1038/Nature10659 |
0.567 |
|
| 2011 |
Schmidt RJ, Hansen RL, Hartiala J, Allayee H, Schmidt LC, Tancredi DJ, Tassone F, Hertz-Picciotto I. Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism. Epidemiology (Cambridge, Mass.). 22: 476-85. PMID 21610500 DOI: 10.1097/Ede.0B013E31821D0E30 |
0.599 |
|
| 2011 |
Mendoza-Fandino GA, Gee JM, Ben-Dor S, Gonzalez-Quevedo C, Lee K, Kobayashi Y, Hartiala J, Myers RM, Leal SM, Allayee H, Patel PI. A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia. Clinical Genetics. 80: 265-72. PMID 21443745 DOI: 10.1111/J.1399-0004.2010.01529.X |
0.544 |
|
| 2011 |
Lettre G, Palmer CD, Young T, Ejebe KG, Allayee H, Benjamin EJ, Bennett F, Bowden DW, Chakravarti A, Dreisbach A, Farlow DN, Folsom AR, Fornage M, Forrester T, Fox E, ... ... Hartiala J, et al. Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Plos Genetics. 7: e1001300. PMID 21347282 DOI: 10.1371/Journal.Pgen.1001300 |
0.644 |
|
| 2011 |
Stephensen CB, Armstrong P, Newman JW, Pedersen TL, Legault J, Schuster GU, Kelley D, Vikman S, Hartiala J, Nassir R, Seldin MF, Allayee H. ALOX5 gene variants affect eicosanoid production and response to fish oil supplementation. Journal of Lipid Research. 52: 991-1003. PMID 21296957 DOI: 10.1194/Jlr.P012864 |
0.581 |
|
| 2011 |
Hartiala J, Li D, Conti DV, Vikman S, Patel Y, Tang WH, Brennan ML, Newman JW, Stephensen CB, Armstrong P, Hazen SL, Allayee H. Genetic contribution of the leukotriene pathway to coronary artery disease. Human Genetics. 129: 617-27. PMID 21293878 DOI: 10.1007/S00439-011-0963-3 |
0.647 |
|
| 2011 |
Qi L, Ma J, Qi Q, Hartiala J, Allayee H, Campos H. Genetic risk score and risk of myocardial infarction in Hispanics. Circulation. 123: 374-80. PMID 21242481 DOI: 10.1161/Circulationaha.110.976613 |
0.64 |
|
| 2010 |
Nicholls SJ, Tang WH, Scoffone H, Brennan DM, Hartiala J, Allayee H, Hazen SL. Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy. Journal of Lipid Research. 51: 3055-61. PMID 20601648 DOI: 10.1194/Jlr.M008961 |
0.58 |
|
| 2009 |
Li X, Shu YH, Xiang AH, Trigo E, Kuusisto J, Hartiala J, Swift AJ, Kawakubo M, Stringham HM, Bonnycastle LL, Lawrence JM, Laakso M, Allayee H, Buchanan TA, Watanabe RM. Additive effects of genetic variation in GCK and G6PC2 on insulin secretion and fasting glucose. Diabetes. 58: 2946-53. PMID 19741163 DOI: 10.2337/Db09-0228 |
0.53 |
|
| 2009 |
Vikman S, Brena RM, Armstrong P, Hartiala J, Stephensen CB, Allayee H. Functional analysis of 5-lipoxygenase promoter repeat variants. Human Molecular Genetics. 18: 4521-9. PMID 19717473 DOI: 10.1093/Hmg/Ddp414 |
0.583 |
|
| 2009 |
Shu YH, Hartiala J, Xiang AH, Trigo E, Lawrence JM, Allayee H, Buchanan TA, Bottini N, Watanabe RM. Evidence for sex-specific associations between variation in acid phosphatase locus 1 (ACP1) and insulin sensitivity in Mexican-Americans. The Journal of Clinical Endocrinology and Metabolism. 94: 4094-102. PMID 19622628 DOI: 10.1210/Jc.2008-2751 |
0.535 |
|
| 2009 |
Li X, Allayee H, Xiang AH, Trigo E, Hartiala J, Lawrence JM, Buchanan TA, Watanabe RM. Variation in IGF2BP2 interacts with adiposity to alter insulin sensitivity in Mexican Americans. Obesity (Silver Spring, Md.). 17: 729-36. PMID 19148120 DOI: 10.1038/Oby.2008.593 |
0.59 |
|
| 2009 |
Orrú V, Tsai SJ, Rueda B, Fiorillo E, Stanford SM, Dasgupta J, Hartiala J, Zhao L, Ortego-Centeno N, D'Alfonso S, Arnett FC, Wu H, Gonzalez-Gay MA, Tsao BP, et al. A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus. Human Molecular Genetics. 18: 569-79. PMID 18981062 DOI: 10.1093/Hmg/Ddn363 |
0.592 |
|
| 2008 |
Allayee H, Baylin A, Hartiala J, Wijesuriya H, Mehrabian M, Lusis AJ, Campos H. Nutrigenetic association of the 5-lipoxygenase gene with myocardial infarction. The American Journal of Clinical Nutrition. 88: 934-40. PMID 18842779 DOI: 10.1093/Ajcn/88.4.934 |
0.6 |
|
| 2008 |
Mehrabian M, Schulthess FT, Nebohacova M, Castellani LW, Zhou Z, Hartiala J, Oberholzer J, Lusis AJ, Maedler K, Allayee H. Identification of ALOX5 as a gene regulating adiposity and pancreatic function. Diabetologia. 51: 978-88. PMID 18421434 DOI: 10.1007/S00125-008-1002-3 |
0.571 |
|
| 2008 |
Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, et al. Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease. Human Genetics. 123: 399-408. PMID 18369664 DOI: 10.1007/S00439-008-0489-5 |
0.646 |
|
| 2008 |
Chang AJ, Kline MM, Currie Y, Perez MO, Hartiala J, Wijesuriya H, Buchanan TA, Watanabe RM, Allayee H. Allgrove syndrome in a Mexican American family is caused by an ancestral mutation derived from North Africa. Clinical Genetics. 73: 385-7. PMID 18261130 DOI: 10.1111/J.1399-0004.2008.00965.X |
0.516 |
|
| 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 |
0.586 |
|
| 2007 |
Allayee H, Hartiala J, Lee W, Mehrabian M, Irvin CG, Conti DV, Lima JJ. The effect of montelukast and low-dose theophylline on cardiovascular disease risk factors in asthmatics. Chest. 132: 868-74. PMID 17646220 DOI: 10.1378/Chest.07-0831 |
0.582 |
|
| 2007 |
Watanabe RM, Allayee H, Xiang AH, Trigo E, Hartiala J, Lawrence JM, Buchanan TA. Transcription factor 7-like 2 (TCF7L2) is associated with gestational diabetes mellitus and interacts with adiposity to alter insulin secretion in Mexican Americans. Diabetes. 56: 1481-5. PMID 17317761 DOI: 10.2337/Db06-1682 |
0.548 |
|
| 2007 |
Mendoza G, Pemberton TJ, Lee K, Scarel-Caminaga R, Mehrian-Shai R, Gonzalez-Quevedo C, Ninis V, Hartiala J, Allayee H, Snead ML, Leal SM, Line SR, Patel PI. A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Human Genetics. 120: 653-62. PMID 17024372 DOI: 10.1007/S00439-006-0246-6 |
0.576 |
|
| 2006 |
Tymchuk CN, Hartiala J, Patel PI, Mehrabian M, Allayee H. Nonconventional genetic risk factors for cardiovascular disease. Current Atherosclerosis Reports. 8: 184-92. PMID 16640955 DOI: 10.1007/s11883-006-0072-2 |
0.604 |
|
| 2003 |
Carvajal-Carmona LG, Ophoff R, Hartiala J, Molina J, Leon P, Ospina J, Bedoya G, Freimer N, Ruiz-Linares A. Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica. Human Genetics. 112: 534-541. PMID 12601469 DOI: 10.1007/S00439-002-0899-8 |
0.322 |
|
| 2002 |
Jartti L, Ronnemaa T, Kaprio J, Jarvisalo MJ, Toikka JO, Marniemi J, Hammar N, Alfredsson L, Saraste M, Hartiala J, Koskenvuo M, Raitakari OT. Population-Based Twin Study of the Effects of Migration From Finland to Sweden on Endothelial Function and Intima-Media Thickness Arteriosclerosis, Thrombosis, and Vascular Biology. 22: 832-837. PMID 12006398 DOI: 10.1161/01.Atv.0000013313.70875.A7 |
0.328 |
|
| 2002 |
Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. American Journal of Human Genetics. 70: 652-62. PMID 11836652 DOI: 10.1086/339078 |
0.312 |
|
| 1999 |
Pajukanta P, Terwilliger JD, Perola M, Hiekkalinna T, Nuotio I, Ellonen P, Parkkonen M, Hartiala J, Ylitalo K, Pihlajamäki J, Porkka K, Laakso M, Viikari J, Ehnholm C, Taskinen MR, et al. Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. American Journal of Human Genetics. 64: 1453-63. PMID 10205279 DOI: 10.1086/302365 |
0.33 |
|
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