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Items: 1 to 50 of 261

1.

Facilitating phenotype transfer using a common data model.

Hripcsak G, Shang N, Peissig PL, Rasmussen LV, Liu C, Benoit B, Carroll RJ, Carrell DS, Denny JC, Dikilitas O, Gainer VS, Howell KM, Klann JG, Kullo IJ, Lingren T, Mentch FD, Murphy SN, Natarajan K, Pacheco JA, Wei WQ, Wiley K, Weng C.

J Biomed Inform. 2019 Aug;96:103253. doi: 10.1016/j.jbi.2019.103253. Epub 2019 Jul 17.

PMID:
31325501
2.

GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.

Namjou B, Lingren T, Huang Y, Parameswaran S, Cobb BL, Stanaway IB, Connolly JJ, Mentch FD, Benoit B, Niu X, Wei WQ, Carroll RJ, Pacheco JA, Harley ITW, Divanovic S, Carrell DS, Larson EB, Carey DJ, Verma S, Ritchie MD, Gharavi AG, Murphy S, Williams MS, Crosslin DR, Jarvik GP, Kullo IJ, Hakonarson H, Li R; eMERGE Network, Xanthakos SA, Harley JB.

BMC Med. 2019 Jul 17;17(1):135. doi: 10.1186/s12916-019-1364-z.

3.

Use of Twitter to Promote Awareness of Familial Hypercholesterolemia.

Bangash H, Khan F, He B, Arce M, Kullo IJ.

Circ Genom Precis Med. 2019 Jul;12(7):e002550. doi: 10.1161/CIRCGEN.119.002550. Epub 2019 Jul 15. No abstract available.

PMID:
31306057
4.

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

Edwards TL, Giri A, Hellwege JN, Hartmann KE, Stewart EA, Jeff JM, Bray MJ, Pendergrass SA, Torstenson ES, Keaton JM, Jones SH, Gogoi RP, Kuivaniemi H, Jackson KL, Kho AN, Kullo IJ, McCarty CA, Im HK, Pacheco JA, Pathak J, Williams MS, Tromp G, Kenny EE, Peissig PL, Denny JC, Roden DM, Velez Edwards DR.

Front Genet. 2019 Jun 12;10:511. doi: 10.3389/fgene.2019.00511. eCollection 2019.

5.

Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.

Ahmad F, McNally EM, Ackerman MJ, Baty LC, Day SM, Kullo IJ, Madueme PC, Maron MS, Martinez MW, Salberg L, Taylor MR, Wilcox JE.

Circ Genom Precis Med. 2019 Jun;12(6):e000054. doi: 10.1161/HCG.0000000000000054. Epub 2019 May 23.

PMID:
31117808
6.

Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease-Brief Report.

Safarova MS, Fan X, Austin EE, van Zuydam N, Hopewell J, Schaid DJ, Kullo IJ.

Arterioscler Thromb Vasc Biol. 2019 Jun;39(6):1227-1233. doi: 10.1161/ATVBAHA.118.312128.

PMID:
31070467
7.

DENND5B Regulates Intestinal Triglyceride Absorption and Body Mass.

Gordon SM, Neufeld EB, Yang Z, Pryor M, Freeman LA, Fan X, Kullo IJ, Biesecker LG, Remaley AT.

Sci Rep. 2019 Mar 5;9(1):3597. doi: 10.1038/s41598-019-40296-0.

8.
9.

A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR.

Safarova MS, Satterfield BA, Fan X, Austin EE, Ye Z, Bastarache L, Zheng N, Ritchie MD, Borthwick KM, Williams MS, Larson EB, Scrol A, Jarvik GP, Crosslin DR, Leppig K, Rasmussen-Torvik LJ, Pendergrass SA, Sturm AC, Namjou B, Shah AS, Carroll RJ, Chung WK, Wei WQ, Feng Q, Stein CM, Roden DM, Manolio TA, Schaid DJ, Denny JC, Hebbring SJ, de Andrade M, Kullo IJ.

NPJ Genom Med. 2019 Feb 11;4:3. doi: 10.1038/s41525-019-0078-7. eCollection 2019.

10.

Interleukin-6 Receptor Signaling and Abdominal Aortic Aneurysm Growth Rates.

Paige E, Clément M, Lareyre F, Sweeting M, Raffort J, Grenier C, Finigan A, Harrison J, Peters JE, Sun BB, Butterworth AS, Harrison SC, Bown MJ, Lindholt JS, Badger SA, Kullo IJ, Powell J, Norman PE, Scott DJA, Bailey MA, Rose-John S, Danesh J, Freitag DF, Paul DS, Mallat Z.

Circ Genom Precis Med. 2019 Feb;12(2):e002413. doi: 10.1161/CIRCGEN.118.002413.

11.

Association of Ankle-Brachial Indices With Limb Revascularization or Amputation in Patients With Peripheral Artery Disease.

Moussa Pacha H, Mallipeddi VP, Afzal N, Moon S, Kaggal VC, Kalra M, Oderich GS, Wennberg PW, Rooke TW, Scott CG, Kullo IJ, McBane RD 2nd, Nishimura RA, Chaudhry R, Liu H, Arruda-Olson AM.

JAMA Netw Open. 2018 Dec 7;1(8):e185547. doi: 10.1001/jamanetworkopen.2018.5547.

12.

Should pretest genetic counselling be required for patients pursuing genomic sequencing? Results from a survey of participants in a large genomic implementation study.

Pacyna JE, Radecki Breitkopf C, Jenkins SM, Sutton EJ, Horrow C, Kullo IJ, Sharp RR.

J Med Genet. 2019 May;56(5):317-324. doi: 10.1136/jmedgenet-2018-105577. Epub 2018 Dec 22.

PMID:
30580287
13.

Leveraging the Electronic Health Record to Create an Automated Real-Time Prognostic Tool for Peripheral Arterial Disease.

Arruda-Olson AM, Afzal N, Priya Mallipeddi V, Said A, Moussa Pacha H, Moon S, Chaudhry AP, Scott CG, Bailey KR, Rooke TW, Wennberg PW, Kaggal VC, Oderich GS, Kullo IJ, Nishimura RA, Chaudhry R, Liu H.

J Am Heart Assoc. 2018 Dec 4;7(23):e009680. doi: 10.1161/JAHA.118.009680.

14.

Probing the Virtual Proteome to Identify Novel Disease Biomarkers.

Mosley JD, Benson MD, Smith JG, Melander O, Ngo D, Shaffer CM, Ferguson JF, Herzig MS, McCarty CA, Chute CG, Jarvik GP, Gordon AS, Palmer MR, Crosslin DR, Larson EB, Carrell DS, Kullo IJ, Pacheco JA, Peissig PL, Brilliant MH, Kitchner TE, Linneman JG, Namjou B, Williams MS, Ritchie MD, Borthwick KM, Kiryluk K, Mentch FD, Sleiman PM, Karlson EW, Verma SS, Zhu Y, Vasan RS, Yang Q, Denny JC, Roden DM, Gerszten RE, Wang TJ.

Circulation. 2018 Nov 27;138(22):2469-2481. doi: 10.1161/CIRCULATIONAHA.118.036063.

PMID:
30571344
15.

Developing a Process for Returning Medically Actionable Genomic Variants to Latino Patients in a Federally Qualified Health Center.

Shaibi GQ, Kullo IJ, Singh DP, Sharp RR, De Filippis E, Cuellar I, Hernandez V, Levey S, Radecki Breitkopf C, Olson JE, Cerhan JR, Mandarino LJ, Thibodeau SN, Lindor NM.

Public Health Genomics. 2018;21(1-2):77-84. doi: 10.1159/000494488. Epub 2018 Dec 6.

PMID:
30522109
16.

Patient and Provider Perspectives on a Decision Aid for Familial Hypercholesterolemia.

Farwati M, Kumbamu A, Kochan DC, Kullo IJ.

J Pers Med. 2018 Nov 4;8(4). pii: E35. doi: 10.3390/jpm8040035.

17.

The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results.

Kullo IJ, Olson J, Fan X, Jose M, Safarova M, Radecki Breitkopf C, Winkler E, Kochan DC, Snipes S, Pacyna JE, Carney M, Chute CG, Gupta J, Jose S, Venner E, Murugan M, Jiang Y, Zordok M, Farwati M, Philogene M, Smith E, Shaibi GQ, Caraballo P, Freimuth R, Lindor NM, Sharp R, Thibodeau SN.

Mayo Clin Proc. 2018 Nov;93(11):1600-1610. doi: 10.1016/j.mayocp.2018.06.026.

PMID:
30392543
18.

The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.

Stanaway IB, Hall TO, Rosenthal EA, Palmer M, Naranbhai V, Knevel R, Namjou-Khales B, Carroll RJ, Kiryluk K, Gordon AS, Linder J, Howell KM, Mapes BM, Lin FTJ, Joo YY, Hayes MG, Gharavi AG, Pendergrass SA, Ritchie MD, de Andrade M, Croteau-Chonka DC, Raychaudhuri S, Weiss ST, Lebo M, Amr SS, Carrell D, Larson EB, Chute CG, Rasmussen-Torvik LJ, Roy-Puckelwartz MJ, Sleiman P, Hakonarson H, Li R, Karlson EW, Peterson JF, Kullo IJ, Chisholm R, Denny JC, Jarvik GP; eMERGE Network, Crosslin DR.

Genet Epidemiol. 2019 Feb;43(1):63-81. doi: 10.1002/gepi.22167. Epub 2018 Oct 8.

19.

A Clinical Decision Support Tool for Familial Hypercholesterolemia Based on Physician Input.

Hasnie AA, Kumbamu A, Safarova MS, Caraballo PJ, Kullo IJ.

Mayo Clin Proc Innov Qual Outcomes. 2018 May 24;2(2):103-112. doi: 10.1016/j.mayocpiqo.2018.03.006. eCollection 2018 Jun.

20.

Adverse effects of long-term weight gain on microvascular endothelial function.

Coutinho T, Turner ST, Kullo IJ.

Obes Res Clin Pract. 2018 Sep - Oct;12(5):452-458. doi: 10.1016/j.orcp.2018.06.008. Epub 2018 Jun 28.

PMID:
30224028
21.

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.

Mosley JD, Feng Q, Wells QS, Van Driest SL, Shaffer CM, Edwards TL, Bastarache L, Wei WQ, Davis LK, McCarty CA, Thompson W, Chute CG, Jarvik GP, Gordon AS, Palmer MR, Crosslin DR, Larson EB, Carrell DS, Kullo IJ, Pacheco JA, Peissig PL, Brilliant MH, Linneman JG, Namjou B, Williams MS, Ritchie MD, Borthwick KM, Verma SS, Karnes JH, Weiss ST, Wang TJ, Stein CM, Denny JC, Roden DM.

Nat Commun. 2018 Aug 30;9(1):3522. doi: 10.1038/s41467-018-05624-4.

22.

Design of a Controlled Trial of Cascade Screening for Hypercholesterolemia: The (CASH) Study.

Kullo IJ, Bailey KR.

J Pers Med. 2018 Aug 23;8(3). pii: E27. doi: 10.3390/jpm8030027.

23.

Innovative Informatics Approaches for Peripheral Artery Disease: Current State and Provider Survey of Strategies for Improving Guideline-Based Care.

Chaudhry AP, Afzal N, Abidian MM, Mallipeddi VP, Elayavilli RK, Scott CG, Kullo IJ, Wennberg PW, Pankratz JJ, Liu H, Chaudhry R, Arruda-Olson AM.

Mayo Clin Proc Innov Qual Outcomes. 2018 Jun;2(2):129-136. doi: 10.1016/j.mayocpiqo.2018.02.001.

24.

Higher plasma leptin levels are associated with reduced left ventricular mass and left ventricular diastolic stiffness in black women: insights from the Genetic Epidemiology Network of Arteriopathy (GENOA) study.

Kamimura D, Suzuki T, Wang W, deShazo M, Hall JE, Winniford MD, Kullo IJ, Mosley TH, Butler KR, Hall ME.

Hypertens Res. 2018 Aug;41(8):629-638. doi: 10.1038/s41440-018-0062-0. Epub 2018 Jun 15.

25.

A Network-Biology Informed Computational Drug Repositioning Strategy to Target Disease Risk Trajectories and Comorbidities of Peripheral Artery Disease.

Shameer K, Dow G, Glicksberg BS, Johnson KW, Ze Y, Tomlinson MS, Readhead B, Dudley JT, Kullo IJ.

AMIA Jt Summits Transl Sci Proc. 2018 May 18;2017:108-117. eCollection 2018.

26.

Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.

Aronson S, Babb L, Ames D, Gibbs RA, Venner E, Connelly JJ, Marsolo K, Weng C, Williams MS, Hartzler AL, Liang WH, Ralston JD, Devine EB, Murphy S, Chute CG, Caraballo PJ, Kullo IJ, Freimuth RR, Rasmussen LV, Wehbe FH, Peterson JF, Robinson JR, Wiley K, Overby Taylor C; eMERGE Network EHRI Working Group.

J Am Med Inform Assoc. 2018 Oct 1;25(10):1375-1381. doi: 10.1093/jamia/ocy051.

27.

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.

Wei WQ, Li X, Feng Q, Kubo M, Kullo IJ, Peissig PL, Karlson EW, Jarvik GP, Lee MTM, Shang N, Larson EA, Edwards T, Shaffer CM, Mosley JD, Maeda S, Horikoshi M, Ritchie M, Williams MS, Larson EB, Crosslin DR, Bland ST, Pacheco JA, Rasmussen-Torvik LJ, Cronkite D, Hripcsak G, Cox NJ, Wilke RA, Stein CM, Rotter JI, Momozawa Y, Roden DM, Krauss RM, Denny JC.

Circulation. 2018 Oct 23;138(17):1839-1849. doi: 10.1161/CIRCULATIONAHA.117.031356.

PMID:
29703846
28.

Natural language processing of clinical notes for identification of critical limb ischemia.

Afzal N, Mallipeddi VP, Sohn S, Liu H, Chaudhry R, Scott CG, Kullo IJ, Arruda-Olson AM.

Int J Med Inform. 2018 Mar;111:83-89. doi: 10.1016/j.ijmedinf.2017.12.024. Epub 2017 Dec 28.

29.

Making pretest genomic counseling optional: lessons from the RAVE study.

Sutton EJ, Kullo IJ, Sharp RR.

Genet Med. 2018 Oct;20(10):1157-1158. doi: 10.1038/gim.2017.240. Epub 2018 Feb 1. No abstract available.

30.

Lessening the Burden of Familial Hypercholesterolemia Using Health Information Technology.

Safarova MS, Kullo IJ.

Circ Res. 2018 Jan 5;122(1):26-27. doi: 10.1161/CIRCRESAHA.117.312319. Review. No abstract available.

31.

Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.

Fossey R, Kochan D, Winkler E, Pacyna JE, Olson J, Thibodeau S, Connolly JJ, Harr M, Behr MA, Prows CA, Cobb B, Myers MF, Leslie ND, Namjou-Khales B, Milo Rasouly H, Wynn J, Fedotov A, Chung WK, Gharavi A, Williams JL, Pais L, Holm I, Aufox S, Smith ME, Scrol A, Leppig K, Jarvik GP, Wiesner GL, Li R, Stroud M, Smoller JW, Sharp RR, Kullo IJ.

J Pers Med. 2018 Jan 3;8(1). pii: E2. doi: 10.3390/jpm8010002.

32.

Temporal trends in lipid testing among children and adolescents: A population based study.

Sriram S, St Sauver JL, Jacobson DJ, Fan C, Lynch BA, Cristiani V, Kullo IJ, Lteif AN, Kumar S.

Prev Med Rep. 2017 Nov 8;8:267-272. doi: 10.1016/j.pmedr.2017.11.001. eCollection 2017 Dec.

33.

Health disparities among adult patients with a phenotypic diagnosis of familial hypercholesterolemia in the CASCADE-FH™ patient registry.

Amrock SM, Duell PB, Knickelbine T, Martin SS, O'Brien EC, Watson KE, Mitri J, Kindt I, Shrader P, Baum SJ, Hemphill LC, Ahmed CD, Andersen RL, Kullo IJ, McCann D, Larry JA, Murray MF, Fishberg R, Guyton JR, Wilemon K, Roe MT, Rader DJ, Ballantyne CM, Underberg JA, Thompson P, Duffy D, Linton MF, Shapiro MD, Moriarty PM, Knowles JW, Ahmad ZS.

Atherosclerosis. 2017 Dec;267:19-26. doi: 10.1016/j.atherosclerosis.2017.10.006. Epub 2017 Oct 6.

PMID:
29080546
34.

Burden of hospitalization in clinically diagnosed peripheral artery disease: A community-based study.

Arruda-Olson AM, Moussa Pacha H, Afzal N, Abram S, Lewis BR, Isseh I, Haddad R, Scott CG, Bailey K, Liu H, Rooke TW, Kullo IJ.

Vasc Med. 2018 Feb;23(1):23-31. doi: 10.1177/1358863X17736152. Epub 2017 Oct 25.

35.

Relationship of circulating spexin with markers of cardiovascular disease: a pilot study in adolescents with obesity.

Kumar S, Hossain MJ, Javed A, Kullo IJ, Balagopal PB.

Pediatr Obes. 2018 Jun;13(6):374-380. doi: 10.1111/ijpo.12249. Epub 2017 Oct 10.

36.

Sex differences in associations of cardio-ankle vascular index with left ventricular function and geometry.

Ye Z, Pellikka PA, Kullo IJ.

Vasc Med. 2017 Dec;22(6):465-472. doi: 10.1177/1358863X17725810. Epub 2017 Sep 20.

PMID:
28931350
37.

The association between cigarette smoking and inflammation: The Genetic Epidemiology Network of Arteriopathy (GENOA) study.

Tibuakuu M, Kamimura D, Kianoush S, DeFilippis AP, Al Rifai M, Reynolds LM, White WB, Butler KR, Mosley TH, Turner ST, Kullo IJ, Hall ME, Blaha MJ.

PLoS One. 2017 Sep 18;12(9):e0184914. doi: 10.1371/journal.pone.0184914. eCollection 2017.

38.

Surveillance of Peripheral Arterial Disease Cases Using Natural Language Processing of Clinical Notes.

Afzal N, Sohn S, Scott CG, Liu H, Kullo IJ, Arruda-Olson AM.

AMIA Jt Summits Transl Sci Proc. 2017 Jul 26;2017:28-36. eCollection 2017.

39.

Biomarker-Based Risk Models to Risk Stratify Patients With Stable Coronary Heart Disease.

Omland T, Kullo IJ.

J Am Coll Cardiol. 2017 Aug 15;70(7):827-829. doi: 10.1016/j.jacc.2017.06.051. No abstract available.

40.

Elevated serum osteoprotegerin is associated with increased left ventricular mass index and myocardial stiffness.

Kamimura D, Suzuki T, Furniss AL, Griswold ME, Kullo IJ, Lindsey ML, Winniford MD, Butler KR, Mosley TH, Hall ME.

J Cardiovasc Med (Hagerstown). 2017 Dec;18(12):954-961. doi: 10.2459/JCM.0000000000000549.

41.

Effect of Disclosing Genetic Risk for Coronary Heart Disease on Information Seeking and Sharing: The MI-GENES Study (Myocardial Infarction Genes).

Brown SN, Jouni H, Marroush TS, Kullo IJ.

Circ Cardiovasc Genet. 2017 Aug;10(4). pii: e001613. doi: 10.1161/CIRCGENETICS.116.001613.

42.

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

Holzinger ER, Verma SS, Moore CB, Hall M, De R, Gilbert-Diamond D, Lanktree MB, Pankratz N, Amuzu A, Burt A, Dale C, Dudek S, Furlong CE, Gaunt TR, Kim DS, Riess H, Sivapalaratnam S, Tragante V, van Iperen EPA, Brautbar A, Carrell DS, Crosslin DR, Jarvik GP, Kuivaniemi H, Kullo IJ, Larson EB, Rasmussen-Torvik LJ, Tromp G, Baumert J, Cruickshanks KJ, Farrall M, Hingorani AD, Hovingh GK, Kleber ME, Klein BE, Klein R, Koenig W, Lange LA, Mӓrz W, North KE, Charlotte Onland-Moret N, Reiner AP, Talmud PJ, van der Schouw YT, Wilson JG, Kivimaki M, Kumari M, Moore JH, Drenos F, Asselbergs FW, Keating BJ, Ritchie MD.

BioData Min. 2017 Jul 24;10:25. doi: 10.1186/s13040-017-0145-5. eCollection 2017.

43.

A DAB2IP genotype: sex interaction is associated with abdominal aortic aneurysm expansion.

Ye Z, Austin E, Schaid DJ, Bailey KR, Pellikka PA, Kullo IJ.

J Investig Med. 2017 Oct;65(7):1077-1082. doi: 10.1136/jim-2016-000404. Epub 2017 Jul 11.

PMID:
28698188
44.

Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.

Rasmussen-Torvik LJ, Almoguera B, Doheny KF, Freimuth RR, Gordon AS, Hakonarson H, Hawkins JB, Husami A, Ivacic LC, Kullo IJ, Linderman MD, Manolio TA, Obeng AO, Pellegrino R, Prows CA, Ritchie MD, Smith ME, Stallings SC, Wolf WA, Zhang K, Scott SA.

J Mol Diagn. 2017 Jul;19(4):561-566. doi: 10.1016/j.jmoldx.2017.04.002. Epub 2017 May 11.

45.

Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes.

Mosley JD, Shoemaker MB, Wells QS, Darbar D, Shaffer CM, Edwards TL, Bastarache L, McCarty CA, Thompson W, Chute CG, Jarvik GP, Crosslin DR, Larson EB, Kullo IJ, Pacheco JA, Peissig PL, Brilliant MH, Linneman JG, Witte JS, Denny JC, Roden DM.

Circ Cardiovasc Genet. 2017 Apr;10(2). pii: e001482. doi: 10.1161/CIRCGENETICS.116.001482.

46.

Motivation, Perception, and Treatment Beliefs in the Myocardial Infarction Genes (MI-GENES) Randomized Clinical Trial.

Kattel S, Onyekwelu T, Brown SA, Jouni H, Austin E, Kullo IJ.

J Genet Couns. 2017 Oct;26(5):1153-1161. doi: 10.1007/s10897-017-0092-9. Epub 2017 Apr 6.

PMID:
28386791
47.

Precision Cardiovascular Medicine: State of Genetic Testing.

Giudicessi JR, Kullo IJ, Ackerman MJ.

Mayo Clin Proc. 2017 Apr;92(4):642-662. doi: 10.1016/j.mayocp.2017.01.015. Review.

48.

Genetic Risk, Lifestyle, and Coronary Artery Disease.

Kullo IJ, Fan X, Ding K.

N Engl J Med. 2017 Mar 23;376(12):1192-3. doi: 10.1056/NEJMc1700362. No abstract available.

PMID:
28332385
49.

Genome-wide study of resistant hypertension identified from electronic health records.

Dumitrescu L, Ritchie MD, Denny JC, El Rouby NM, McDonough CW, Bradford Y, Ramirez AH, Bielinski SJ, Basford MA, Chai HS, Peissig P, Carrell D, Pathak J, Rasmussen LV, Wang X, Pacheco JA, Kho AN, Hayes MG, Matsumoto M, Smith ME, Li R, Cooper-DeHoff RM, Kullo IJ, Chute CG, Chisholm RL, Jarvik GP, Larson EB, Carey D, McCarty CA, Williams MS, Roden DM, Bottinger E, Johnson JA, de Andrade M, Crawford DC.

PLoS One. 2017 Feb 21;12(2):e0171745. doi: 10.1371/journal.pone.0171745. eCollection 2017.

50.

Identification of unique venous thromboembolism-susceptibility variants in African-Americans.

Heit JA, Armasu SM, McCauley BM, Kullo IJ, Sicotte H, Pathak J, Chute CG, Gottesman O, Bottinger EP, Denny JC, Roden DM, Li R, Ritchie MD, de Andrade M.

Thromb Haemost. 2017 Apr 3;117(4):758-768. doi: 10.1160/TH16-08-0652. Epub 2017 Feb 16.

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