The DOI matches its Crossref record; 85 of the 86 references it cites were found in a registry or an index.
Cardiovascular Disease
Open accessAbstract
ardiovascular disease, including stroke, is the leading cause of illness and death in the United States.There are an estimated 62 million people with cardiovascular disease and 50 million people with hypertension in this country.1 In 2000, approximately 946,000 deaths were attributable to cardiovascular disease, accounting for 39 percent of all deaths in the United States. 2 Epidemiologic studies and randomized clinical trials have provided compelling evidence that coronary heart disease is largely preventable.3 However, there is also reason to believe that there is a heritable component to the disease.In this review, I highlight what we know now about genetic factors in cardiovascular disease.As future genomic discoveries are translated to the care of patients with cardiovascular disease, it is likely that what we can do will change.c lessons learned from monogenic cardiovascular disorders
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“High levels of low density lipoprotein cholesterol are a major risk factor for the development of arteriosclerosis and death from cardiovascular causes (41).”
From Expression of miR-33 from an SREBP2 Intron Inhibits Cholesterol Export and Fatty Acid Oxidation* (2010) · cites this paper as [41]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group (2002) · JAMA: The Journal of the American Medical Association · doi:10.1001/jama.288.23.2981 · Cited by 5,664
Sanguinetti, M. C., Jiang, C., Curran, M. E., & Keating, M. T. (1995) · Cell · doi:10.1016/0092-8674(95)90340-2 · Cited by 2,422
Prevalence of Hypertrophic Cardiomyopathy in a General Population of Young Adults
Maron, B. J., Gardin, J. M., Flack, J. M., Gidding, S. S., Kurosaki, T., & Bild, D. E. (1995) · Circulation · doi:10.1161/01.cir.92.4.785 · Cited by 2,274
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
Chen, Q., Kirsch, G. E., Zhang, D., Brugada, R., Brugada, J., Brugada, P., Potenza, D. R., Moya‐Mitjans, À., Borggrefe, M., BREITHARDT, G. E., et al. (1998) · Nature · doi:10.1038/32675 · Cited by 1,823
Pharmacogenomics — Drug Disposition, Drug Targets, and Side Effects
Evans, W. E., & McLeod, H. L. (2003) · New England Journal of Medicine · doi:10.1056/nejmra020526 · Cited by 1,778
Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel
Sanguinetti, M. C., Curran, M. E., Zou, A., Shen, J., Specter, P. S., Atkinson, D. L., & Keating, M. T. (1996) · Nature · doi:10.1038/384080a0 · Cited by 1,765
Molecular Mechanisms of Human Hypertension
Lifton, R. P., Gharavi, A. G., & Geller, D. S. (2001) · Cell · doi:10.1016/s0092-8674(01)00241-0 · Cited by 1,686
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
Wang, Q. K., Shen, J., Splawski, I., Atkinson, D. L., Li, Z., Robinson, J. L., Moss, A. J., Towbin, J. A., & Keating, M. T. (1995) · Cell · doi:10.1016/0092-8674(95)90359-3 · Cited by 1,682
Berge, K. E., Tian, H., Graf, G. A., Yu, L., Grishin, N. V., Schultz, J. R., Kwiterovich, P. O., Shan, B., Barnes, R., & Hobbs, H. H. (2000) · Science · doi:10.1126/science.290.5497.1771 · Cited by 1,645
KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current
Barhanin, J., Lesage, F., Guillemare, E., Fink, M., Lazdunski, M., & Romey, G. (1996) · Nature · doi:10.1038/384078a0 · Cited by 1,613
Characterization of single-nucleotide polymorphisms in coding regions of human genes
Cargill, M., Altshuler, D., Ireland, J., Sklar, P., Ardlie, K., Patil, N., Lane, C. R., Lim, E. P., Kalyanaraman, N., Nemesh, J., et al. (1999) · Nature Genetics · doi:10.1038/10290 · Cited by 1,547
Human Hypertension Caused by Mutations in WNK Kinases
Wilson, F. H., Disse-Nicodème, S., Choate, K. A., Ishikawa, K., Nelson-Williams, C. J., Desitter, I., Günel, M., Milford, D. V., Lipkin, G. W., Achard, J., et al. (2001) · Science · doi:10.1126/science.1062844 · Cited by 1,466
Geisterfer-Lowrance, A. A. T., Kass, S., Tanigawa, G., Vosberg, H.-P., McKenna, W., Seidman, C. E., & Seidman, J. G. (1990) · Cell · doi:10.1016/0092-8674(90)90274-i · Cited by 1,380
MiRP1 Forms IKr Potassium Channels with HERG and Is Associated with Cardiac Arrhythmia
Abbott, G. W., Sesti, F., Splawski, I., Buck, M. E., Lehmann, M. H., Timothy, K. W., Keating, M. T., & Goldstein, S. A. N. (1999) · Cell · doi:10.1016/s0092-8674(00)80728-x · Cited by 1,353
Shimkets, R. A., Warnock, D. G., Bositis, C. M., Nelson-Williams, C. J., Hansson, J. H., Schambelan, M., Gill, J. R., Ulick, S., Milora, R. V., Findling, J. W., et al. (1994) · Cell · doi:10.1016/0092-8674(94)90250-x · Cited by 1,256
Koster, T., Vandenbroucke, J. P., Rosendaal, F. R., de Ronde, H., Briët, E., & Bertina, R. M. (1993) · The Lancet · doi:10.1016/s0140-6736(05)80081-9 · Cited by 1,236
Spectrum of Mutations in Long-QT Syndrome Genes
Splawski, I., Shen, J., Timothy, K. W., Lehmann, M. H., Priori, S. G., Robinson, J. L., Moss, A. J., Schwartz, P. J., Towbin, J. A., Vincent, G. M., et al. (2000) · Circulation · doi:10.1161/01.cir.102.10.1178 · Cited by 1,231
Simon, D. B., Nelson-Williams, C. J., BIA, M. J., Ellison, D. H., Karet, F. E., Molina, A. M., Vaara, I., Iwata, F., Cushner, H. M., Koolen, M. I., et al. (1996) · Nature Genetics · doi:10.1038/ng0196-24 · Cited by 1,206
Lifton, R. P., Dluhy, R. G., Powers, M., Rich, G. M., Cook, S., Ulick, S., & Lalouel, J.-M. (1992) · Nature · doi:10.1038/355262a0 · Cited by 1,158
Resistance to Activated Protein C as a Basis for Venous Thrombosis
Svensson, P. J., & Dahlbäck, B. (1994) · New England Journal of Medicine · doi:10.1056/nejm199402243300801 · Cited by 1,127
The Genetic Basis for Cardiomyopathy
Seidman, J. G., & Seidman, C. E. (2001) · Cell · doi:10.1016/s0092-8674(01)00242-2 · Cited by 1,050
Weinshilboum, R. M. (2003) · New England Journal of Medicine · doi:10.1056/nejmra020021 · Cited by 1,032
Ridker, P. M., Hennekens, C. H., Lindpaintner, K., Stampfer, M. J., Eisenberg, P. R., & Miletich, J. P. (1995) · New England Journal of Medicine · doi:10.1056/nejm199504063321403 · Cited by 1,031
Molecular and Cellular Mechanisms of Cardiac Arrhythmias
Keating, M. T., & Sanguinetti, M. C. (2001) · Cell · doi:10.1016/s0092-8674(01)00243-4 · Cited by 1,003
Rosendaal, F. R., Koster, T., Vandenbroucke, J. P., & Reitsma, P. H. (1995) · Blood · doi:10.1182/blood.v85.6.1504.bloodjournal8561504 · Cited by 999
Drysdale, C. M., McGraw, D. W., Stack, C. B., Stephens, J. C., Judson, R., Nandabalan, K., Arnold, K., Ruaño, G., & Liggett, S. B. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.19.10483 · Cited by 959
Molecular mechanism for an inherited cardiac arrhythmia
Bennett, P. B., Yazawa, K., Makita, N., & George, A. L. (1995) · Nature · doi:10.1038/376683a0 · Cited by 952
Rosenwald, A., Wright, G. W., Wiestner, A. U., Chan, W. C., Connors, J. M., Campo, E., Gascoyne, R. D., Grogan, T. M., Müller-Hermelink, H. K., Smeland, E. B., et al. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00028-x · Cited by 913
Simon, D. B., Karet, F. E., Hamdan, J. M., Pietro, A. D., Sanjad, S. A., & Lifton, R. P. (1996) · Nature Genetics · doi:10.1038/ng0696-183 · Cited by 902
Finding genes that underlie complex traits.
Glazier, A. M., Nadeau, J. H., & Aitman, T. J. (2002) · Science · doi:10.1126/science.1076641 · Cited by 855
Cooper, R., Cutler, J. A., Desvigne-Nickens, P. M., Fortmann, S. P., Friedman, L., Havlik, R. J., Hogelin, G. C., Marler, J. M., McGovern, P. C., Morosco, G. J., et al. (2000) · Circulation · doi:10.1161/01.cir.102.25.3137 · Cited by 831
Niimura, H., Bachinski, L. L., Sangwatanaroj, S., Watkins, H. C., Chudley, A. E., McKenna, W. J., Kristinsson, A., Roberts, R., Sole, M. J., Maron, B. J., et al. (1998) · New England Journal of Medicine · doi:10.1056/nejm199804303381802 · Cited by 757
Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy
Kamisago, M., Sharma, S. D., DePalma, S. R., Solomon, S., Sharma, P., McDonough, B., Smoot, L., Mullen, M. P., Woolf, P. K., Wigle, E. D., et al. (2000) · New England Journal of Medicine · doi:10.1056/nejm200012073432304 · Cited by 720
Prediction of the Risk of Myocardial Infarction from Polymorphisms in Candidate Genes
Yamada, Y., Izawa, H., Ichihara, S., Takatsu, F., Ishihara, H., Hirayama, H., Sone, T., Tanaka, M., & Yokota, M. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa021445 · Cited by 639
Cardiac conduction defects associate with mutations in SCN5A
Schott, J., Alshinawi, C., Kyndt, F., Probst, V., Hoorntje, T. M., Hulsbeek, M. M. F., Wilde, A. A. M., Escande, D., Mannens, M. M. A. M., & Marec, H. L. (1999) · Nature Genetics · doi:10.1038/12618 · Cited by 634
Gellens, M., George, A. L., Chen, L. Q., Chahine, M., HORN, R. C. V., Barchi, R. L., & Kallen, R. G. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.2.554 · Cited by 628
Garcia, C. K., Wilund, K., Arca, M., Zuliani, G., Fellin, R., Maioli, M., Calandra, S., Bertolini, S., Cossu, F., Grishin, N., et al. (2001) · Science · doi:10.1126/science.1060458 · Cited by 624
Kuivenhoven, J. A., Jukema, J. W., Zwinderman, A. H., de Knijff, P., McPherson, R., Bruschke, A. V. G., Lie, K. I., & Kastelein, J. J. P. (1998) · New England Journal of Medicine · doi:10.1056/nejm199801083380203 · Cited by 623
Hoffmeyer, S. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.050585397 · Cited by 599
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
Kimura, A., Harada, H., Park, J.-E., Nishi, H., Satoh, M., Takahashi, M., Hiroi, S., Sasaoka, T., Ohbuchi, N., Nakamura, T., et al. (1997) · Nature Genetics · doi:10.1038/ng0897-379 · Cited by 576
Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia
Splawski, I., Timothy, K. W., Tateyama, M., Clancy, C. E., Malhotra, A., Beggs, A. H., Cappuccio, F. P., Sagnella, G. A., Kass, R. S., & Keating, M. T. (2002) · Science · doi:10.1126/science.1073569 · Cited by 526
Small, K. M., Wagoner, L. E., Levin, A. M., Kardia, S. L. R., & Liggett, S. B. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa020803 · Cited by 524
A common polymorphism associated with antibiotic-induced cardiac arrhythmia
Sesti, F., Abbott, G. W., Wei, J., Murray, K. T., Saksena, S. V., Schwartz, P. J., Priori, S. G., Roden, D. M., George, A. L., & Goldstein, S. A. N. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.180223197 · Cited by 479
BeadArray ™ Technology: Enabling an Accurate, Cost-Effective Approach to High-Throughput Genotyping
Oliphant, A., Barker, D. L. A., Stuelpnagel, J., & Chee, M. S. (2002) · BioTechniques · doi:10.2144/jun0207 · Cited by 462
Koeleman, B. P. C., Reitsma, P. H., Allaart, C. F., & Bertina, R. M. (1994) · Blood · doi:10.1182/blood.v84.4.1031.1031 · Cited by 442
Anticoagulant protein C pathway defective in majority of thrombophilic patients [see comments]
Griffin, J. H., Evatt, B. L., Wideman, C. S., & Fernandez, J. (1993) · Blood · doi:10.1182/blood.v82.7.1989.1989 · Cited by 415
A sodium-channel mutation causes isolated cardiac conduction disease
Tan, H. L., Bink‐Boelkens, M. T. E., Bezzina, C. R., Viswanathan, P. C., Beaufort‐Krol, G. C. M., van Tintelen, J. P., van den Berg, M. P., Wilde, A. A. M., & Balser, J. R. (2001) · Nature · doi:10.1038/35059090 · Cited by 398
Hansson, J. H., Schild, L., Lu, Y., Wilson, T. A., Gautschi, I., Shimkets, R. A., Nelson-Williams, C. J., Rossier, B. C., & Lifton, R. P. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.25.11495 · Cited by 365
Dishy, V., Sofowora, G. G., Xie, H., Kim, R. B., Byrne, D. W., Stein, C. M., & Wood, A. J. J. (2001) · New England Journal of Medicine · doi:10.1056/nejmoa010819 · Cited by 363
Lifton, R. P., Dluhy, R. G., Powers, M., Rich, G. M., Gutkin, M. C., Fallo, F., Gill, J. R., Feld, L. G., Ganguly, A., Laidlaw, J. C., et al. (1992) · Nature Genetics · doi:10.1038/ng0992-66 · Cited by 329
Sakaeda, T., Nakamura, T., Horinouchi, M., Kakumoto, M., Ohmoto, N., Sakai, T., Morita, Y., Tamura, T., Aoyama, N., Hirai, M., et al. (2001) · Pharmaceutical Research · doi:10.1023/a:1012244520615 · Cited by 322
Yoshida, H., Mitarai, T., Kawamura, T., KITAJIMA, T., Miyazaki, Y., Nagasawa, R., Kawaguchi, Y., Kubo, H., Ichikawa, I., & Sakai, O. (1995) · Journal of Clinical Investigation · doi:10.1172/jci118270 · Cited by 318
Zöller, B., Berntsdotter, A., de Frutos, P. G., & Dahlbäck, B. (1995) · Blood · doi:10.1182/blood.v85.12.3518.bloodjournal85123518 · Cited by 302
Topol, E. J., McCarthy, J. J., Gabriel, S., Moliterno, D. J., Rogers, W. J., Newby, L. K., Freedman, M., Metivier, J., Cannata, R., O’Donnell, C. J., et al. (2001) · Circulation · doi:10.1161/hc4701.100910 · Cited by 282
Goldstein, J. L., & Brown, M. S. (2001) · Science · doi:10.1126/science.1061815 · Cited by 241
Gerdes, L. U., Gerdes, C., Kervinen, K., Savolainen, M. J., Klausen, I. C., HANSEN, P. S., Kesäniemi, Y. A., & Færgeman, O. (2000) · Circulation · doi:10.1161/01.cir.101.12.1366 · Cited by 235
Factor V Leiden (FV R506Q) in Families with Inherited Antithrombin Deficiency
van Boven, H. H., Reitsma, P. H., Rosendaal, F. R., Bayston, T. A., Chowdhury, V., Borg, J. Y., Bauer, K. A., Scharrer, I., Conard, J., & Lane, D. A. (1996) · Thrombosis and Haemostasis · doi:10.1055/s-0038-1650289 · Cited by 227
Fananapazir, L., & Epstein, N. D. (1994) · Circulation · doi:10.1161/01.cir.89.1.22 · Cited by 226
Lechin, M. E., Quiñones, M. A., Omran, A., Hill, R., Yu, Q., Rakowski, H., Wigle, D., Liew, C. C., Sole, M. J., Roberts, R., et al. (1995) · Circulation · doi:10.1161/01.cir.92.7.1808 · Cited by 210
McNamara, D. M., Holubkov, R., Janosko, K. M., Palmer, A., Wang, J. J., MacGowan, G. A., Murali, S., Rosenblum, W. D., London, B., & Feldman, A. M. (2001) · Circulation · doi:10.1161/01.cir.103.12.1644 · Cited by 192
Apolipoprotein E genotype affects plasma lipid response to atorvastatin in a gender specific manner
Pedro‐Botet, J., Schaefer, E. J., Bakker-Arkema, R. G., Black, D. M., Stein, E., Corella, D., & Ordovás, J. M. (2001) · Atherosclerosis · doi:10.1016/s0021-9150(01)00410-5 · Cited by 173
β 2 -Adrenoceptor Polymorphism Determines Vascular Reactivity in Humans
Cockcroft, J. R., Gazis, A., Cross, D. J., Wheatley, A. P., Dewar, J. C., Hall, I. P., & Noon, J. P. (2000) · Hypertension · doi:10.1161/01.hyp.36.3.371 · Cited by 160
Penno, G., Chaturvedi, N., Talmud, P. J., Cotroneo, P., Manto, A., Nannipieri, M., Luong, L. A., & Fuller, J. (1998) · Diabetes · doi:10.2337/diabetes.47.9.1507 · Cited by 160
Homozygous Mutation in Cardiac Troponin T
Ho, C. Y., Lever, H. M., DeSanctis, R. W., Farver, C. F., Seidman, J. G., & Seidman, C. E. (2000) · Circulation · doi:10.1161/01.cir.102.16.1950 · Cited by 150
Prasad, A., Narayanan, S. N., Husain, S., Padder, F. A., Waclawiw, M. A., Epstein, N., & Quyyumi, A. A. (2000) · Circulation · doi:10.1161/01.cir.102.1.35 · Cited by 133
β2-Adrenergic Receptor Pharmacogenetics
Liggett, S. B. (2000) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.161.supplement_2.a1q4-10 · Cited by 130
Lee, A., Krishnasamy, A., Epstein, R. J., & Hong, G. S. (2001) · Nature Genetics · doi:10.1038/87170 · Cited by 126
Zohlnhöfer, D., Klein, C. A., Richter, T., Brandl, R., Murr, A., Nührenberg, T. G., Schömig, A., Baeuerle, P. A., & Neumann, F. (2001) · Circulation · doi:10.1161/01.cir.103.10.1396 · Cited by 125
Left Ventricular Hypertrophy With Exercise and ACE Gene Insertion/Deletion Polymorphism
Myerson, S. G., Montgomery, H., Whittingham, M., Jubb, M., WORLD, M. J., Humphries, S. E., & Pennell, D. J. (2001) · Circulation · doi:10.1161/01.cir.103.2.226 · Cited by 124
Osterop, A. P. R. M., Kofflard, M. J. M., Sandkuijl, L. A., ten Cate, F. J., Krams, R., Schalekamp, M. A. D. H., & Danser, A. H. J. (1998) · Hypertension · doi:10.1161/01.hyp.32.5.825 · Cited by 122
Greengard, J. S., Eichinger, S., Griffin, J. H., & Bauer, K. A. (1994) · New England Journal of Medicine · doi:10.1056/nejm199412083312305 · Cited by 119
Tesson, F., Dufour, C., Moolman, J. C., Carrier, L., Al‐Mahdawi, S., Chojnowska, L., Dubourg, O., Soubrier, F., Brink, P. A., Michel Komajda, N., et al. (1997) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.1996.0332 · Cited by 118
Ortlepp, J. R., Vosberg, H. P., Reith, S., Ohme, F., Mahon, N. G., Schröder, D., Klues, H. G., Hanrath, P., & McKenna, W. J. (2002) · Heart · doi:10.1136/heart.87.3.270 · Cited by 111
Mohlke, K. L., Erdos, M. R., Scott, L. J., Fingerlin, T. E., Jackson, A., Silander, K., Hollstein, P. E., Boehnke, M., & Collins, F. S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.262661399 · Cited by 105
Maron, B. J., Moller, J. H., Seidman, C. E., Vincent, G. M., Dietz, H. C., Moss, A. J., Towbin, J. A., Sondheimer, H. M., Pyeritz, R. E., McGee, G., et al. (1998) · Circulation · doi:10.1161/01.cir.98.14.1460 · Cited by 103
Transcriptome analysis reveals a role of interferon-gamma in human neointima formation.
Zohlnhöfer, D., Richter, T., Neumann, F., Nührenberg, T., Wessely, R., Brandl, R., Murr, A., Klein, C., & Baeuerle, P. (2001) · Molecules and Cells · doi:10.1016/s1097-2765(01)00239-8 · Cited by 99
Stavroulakis, G. A., Makris, T. K., Krespi, P. G., Hatzizacharias, A. N., Gialeraki, A. E., Anastasiadis, G., Triposkiadis, P., & Kyriakidis, M. (2000) · Cardiovascular Drugs and Therapy · doi:10.1023/a:1007820401377 · Cited by 94
Ballantyne, C. M., Herd, J. A., Stein, E. A., Ferlic, L. L., Dunn, J. K., Gotto, A. M., & Marian, A. J. (2000) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(00)00918-9 · Cited by 92
ACE genotype and ACE inhibitors induced renoprotection in chronic proteinuric nephropathies1
Perna, A., (GISEN), F. T. G. I. D. S. E. I. N., Ruggenenti, P. L., Testa, A., Spoto, B., Benini, R., Misefari, V., Remuzzi, G., & Zoccali, C. (2000) · Kidney International · doi:10.1046/j.1523-1755.2000.00818.x · Cited by 91
Stefano, V. D., Martinelli, I., Mannucci, P. M., Paciaroni, K., Rossi, E., Chiusolo, P., Casorelli, I., & Leone, G. G. M. (2001) · British Journal of Haematology · doi:10.1046/j.1365-2141.2001.02827.x · Cited by 90
O’Toole, L., Stewart, M., Padfield, P. L., & Channer, K. S. (1998) · Journal of Cardiovascular Pharmacology · doi:10.1097/00005344-199812000-00017 · Cited by 82
Kohno, M., Yokokawa, K., Minami, M., Kano, H., Yasunari, K., Hanehira, T., & Yoshikawa, J. (1999) · The American Journal of Medicine · doi:10.1016/s0002-9343(99)00067-4 · Cited by 79
Marian, A. J., Safavi, F., Ferlic, L. L., Dunn, J. K., Gotto, A. M., & Ballantyne, C. M. (2000) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(99)00535-5 · Cited by 73
New Concepts in Hypertrophic Cardiomyopathies, Part I
Roberts, R., & Sigwart, U. (2001) · Circulation · doi:10.1161/hc4201.097429 · Cited by 70
Mitsuuchi, Y., Kawamoto, T., Rösler, A., Naiki, Y., Miyahara, K., Toda, K., Kuribayashi, I., Orii, T., Yasuda, K., Miura, K., et al. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)91827-d · Cited by 55
Research works printed but not linked: 3
- Goldstein JL, Hobbs HH, Brown MS. Familial hypercholesterolemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic & molecular bases of inherited disease. 8th ed. Vol. 2. New York: McGraw-Hill, 2001:2863-913.
- Kane JP, Havel RJ. Disorders of the biogenesis and secretion of lipoproteins containing the B apolipoproteins. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic & molecular bases of inherited disease. 8th ed. Vol. 2. New York: McGraw-Hill, 2001:2717-52.
- Seidman CE, Seidman JG. Hypertrophic cardiomyopathy. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic & molecular bases of inherited disease. 8th ed. Vol. 4. New York: McGraw-Hill, 2001:5433-50.
Cited by
Sorted by citations
Cardiovascular Diseases (CVDs)
de la Zerda, A., & Wang, S. X. (2022) · doi:10.1002/9781118910573.ch5 · Cited by 1,281
Nrf2 and Oxidative Stress: A General Overview of Mechanisms and Implications in Human Disease
Ngo, V., & Duennwald, M. L. (2022) · Antioxidants · doi:10.3390/antiox11122345 · Cited by 1,130
A Tale of Coronary Artery Disease and Myocardial Infarction
Nabel, E. G., & Braunwald, E. (2012) · New England Journal of Medicine · doi:10.1056/nejmra1112570 · Cited by 1,024
Self-citationTrends in insulin resistance: insights into mechanisms and therapeutic strategy
Li, M., Chi, X., Wang, Y., Setrerrahmane, S., Xie, W., & Xu, H. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01073-0 · Cited by 939
Oral microbiota in human systematic diseases
Peng, X., Cheng, L., You, Y., Tang, C., Ren, B., Li, Y., Xu, X., & Zhou, X. (2022) · International Journal of Oral Science · doi:10.1038/s41368-022-00163-7 · Cited by 707
Metadata
- Authors
- Nabel, E. G.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Nabel, Elizabeth G.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- Published
- 2003-07-03
- Volume
- 349
- Issue
- 1
- Pages
- 60-72
- ISSN
- 0028-4793 (ISSN-L)
- 1533-4406
- OpenAlex
- W4245959283
- Cited by
- 431
- References
- 86
- Citations by year
- 2026: 11 · 2025: 22 · 2024: 45 · 2023: 37 · 2022: 26 · 2021: 20 · 2020: 9 · 2019: 9 · 2018: 14 · 2017: 10 · 2016: 17 · 2015: 15 · 2014: 19 · 2013: 14 · 2012: 14
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- New England Journal of Medicine (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Risk Factors
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Keywords
- cardiovascular disease, genetic factors, heritability, coronary artery disease, hypertension, stroke, cardiovascular mortality, cardiovascular disease prevention, genomics
- MeSH terms
- Arrhythmias, Cardiac, Cardiovascular Diseases, Coronary Disease, Genetic Testing, Humans, Hypercholesterolemia, Hypertension, Cholesterol, LDL, Mutation, Cardiomyopathies, Polymorphism, Genetic, Thrombosis, Gene Expression Profiling
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review