The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Proposed nomenclature of apoE isoproteins, apoE genotypes, and phenotypes
Open accessAbstract
Children's Hospital Medical Center/Harvard Medical School, Boston, MA 021 15,' Institut fur Humangenetik und Genetische Poliklinik der Philipps-Universitat Marburg, Bahnhofstrasse 7A, West Germany,' Gladstone Foundation Laboratories, San Francisco, CA 94 140; Cardiovascular Research Institute, University of California, San Francisco, CA 941 43; Health Science Center, University of Texas, Dallas, T X 74235,5 Lipid Research Center, Washington University School of Medicine, St. Louis, M O 63110; Harborview Medical Center, Seattle, WA 98104; and Columbia College of Physicians and Surgeons, New York, NY 10032*
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In the citing paper
“The two genotypes combine into six common APOE genotypes, ε22, ε32, ε42, ε33, ε43 and ε44, corresponding to six plasma apoE phenotypes: apoE22, apoE32, apoE42, apoE33, apoE43 and apoE44 [14].”
From Plasma levels of apolipoprotein E, APOE genotype and risk of dementia and ischemic heart disease: A review (2016) · cites this paper as [14]
In the citing paper
“There are three common APOE alleles in the general population defined as: APOE ɛ2, APOE ɛ3, and APOE ɛ4 [2].”
From Discovery of a Missense Mutation (Q222K) of the APOE Gene from the Australian Imaging, Biomarker and Lifestyle Study (2023) · cites this paper as [2]
In the citing paper
“Apolipoprotein E (apoE) is one of the key apolipoproteins in blood lipid transport.”
From Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features (2025) · cites this paper as [1]
In the citing paper
“It has the following features: high hydrophobicity, the ability to bind to the low-density-lipoprotein (LDL) receptor and related receptors, production in various tissues throughout the body, acting as a central apoprotein of cerebrospinal fluid lipoproteins, having three major isoforms (apoE2, apoE3, and apoE4) that vary in their function and susceptibility to genetic mutations1).”
From Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features (2025) · cites this paper as [1]
In the citing paper
“It has the following features: high hydrophobicity, the ability to bind to the low-density-lipoprotein (LDL) receptor and related receptors, production in various tissues throughout the body, acting as a central apoprotein of cerebrospinal fluid lipoproteins, having three major isoforms (apoE2, apoE3, and apoE4) that vary in their function and susceptibility to genetic mutations1).”
From Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features (2025) · cites this paper as [1]
In the citing paper
“It has the following features: high hydrophobicity, the ability to bind to the low-density-lipoprotein (LDL) receptor and related receptors, production in various tissues throughout the body, acting as a central apoprotein of cerebrospinal fluid lipoproteins, having three major isoforms (apoE2, apoE3, and apoE4) that vary in their function and susceptibility to genetic mutations1).”
From Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features (2025) · cites this paper as [1]
In the citing paper
“It has the following features: high hydrophobicity, the ability to bind to the low-density-lipoprotein (LDL) receptor and related receptors, production in various tissues throughout the body, acting as a central apoprotein of cerebrospinal fluid lipoproteins, having three major isoforms (apoE2, apoE3, and apoE4) that vary in their function and susceptibility to genetic mutations1).”
From Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features (2025) · cites this paper as [1]
In the citing paper
“It has the following features: high hydrophobicity, the ability to bind to the low-density-lipoprotein (LDL) receptor and related receptors, production in various tissues throughout the body, acting as a central apoprotein of cerebrospinal fluid lipoproteins, having three major isoforms (apoE2, apoE3, and apoE4) that vary in their function and susceptibility to genetic mutations1).”
From Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features (2025) · cites this paper as [1]
Citations
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Self-citation
Research works printed but not linked: 2
- Utermann, G., A. Steinmetz, and W. Weber. 1982. Polymorphism of human apolipoprotein E: genetic control and gene frequencies. Am. J. Hum. Genet. In press.
- Sherrill, 1980, Addition of E-apoprotein to cholesterol-rich fluorescent lipid dispersion increases liver recognition and uptake, Circulation., 62, 44
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Simple micromethods for determination of isoforms of apolipoproteins.
Harake, B. (1991) · Scholarship at UWindsor (University of Windsor)
Genetic Risk Factors for Complex Forms of Alzheimer’s Disease
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Issa, M. H. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.9.2018.tde-02022018-101833
Estrogen Receptor β Regulates Brain Signaling Involved in Depression
Chhibber, A. (2016) · KU ScholarWorks (The University of Kansas)
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Suehiro, T., Yoshida, K., TAKAMATSU, K., Kawada, M., Hisatake, K., Yasuoka, N., Kishino, W., Shigetoshi, U. G. A., Mizutani, Y., Yamano, T., et al. (1986) · The Journal of Japan Atherosclerosis Society · doi:10.5551/jat1973.14.3_743
Lipoproteins, apoprotein A-1 containing particles and the development of atherosclerosis
Vallance, D. T. (1993) · UCL Discovery (University College London)
Strattan, L. E. (2021) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2021.097
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김은영, 서기우, 김정은, Cho, E., 이왕수, 김치정, & 이갑석 (2009)
Apo D and Apo E Levels in Autism Spectrum DisordersPreprint
Esnafoğlu, E., & Cırrık, S. (2021) · Research Square · doi:10.21203/rs.3.rs-562010/v1
Carrasquillo, M. M., Bu, G., & Nielsen, H. M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-7309-1_2
Chen, Q., Chen, L., Wang, T., & Kang, D. (2022) · Research Square · doi:10.21203/rs.3.rs-1456007/v1
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An Erroneous Apolipoprotein E-3 Band in High Density Lipoprotein Fractions
Rawlings, A. V., & Deegan, T. (1988) · Springer eBooks · doi:10.1007/978-94-009-1259-5_13
Havekes, L. M., Klasen, E. C., & Utermann, G. (1986) · Springer eBooks · doi:10.1007/978-1-4615-9474-1_26
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Batista, J. E. D. S., da Silva, V. S., & Klamt, F. (2023) · doi:10.22533/at.ed.4552309054
Anacardium occidentale L. (ANACARDIACEAE): ANTIBACTERIAL AND ANTIBIOTIC POTENTIATING ACTIVITY
Ulisses, V. R. D. A., Costa, A. R., Coutinho, H. D. M., Pereira, R. L. S., dos Santos, C. A. L., Teles, B. R. D. S., dos Santos, L. B., Silva, L. V., Almeida‐Bezerra, J. W., de Oliveira, M. G., et al. (2023) · doi:10.22533/at.ed.4552309056
de Castro, V. F., Cabral, L. M., & Hoffmann, L. (2023) · doi:10.22533/at.ed.4552309051
la Fuente, A. O. R., Heredia-Rojas, J. A., Rebollar-Téllez, E. A., Noguera-Díaz, P. A., Martínez, P. C. C., & Heredia-Rodríguez, O. (2023) · doi:10.22533/at.ed.4552309055
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Apolipoprotein E Polymorphism And It’s Lifestyle Impact
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APOE, Pesticides, Environmental Pollutants, and Epigenetics
Biosca-Brull, J., Colomina, M. T., Cabré, M., & Guardia-Escote, L. (2025) · Springer eBooks · doi:10.1007/978-3-031-52641-1_50-1
Genetic Dyslipoproteinemias Associated with Coronary Atherosclerosis
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Behavioral Aspects of Apolipoprotein E Knockout Mice
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Olfactory Behavior in ApoE Knockout Mice
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ApoE and COVID-19 Risk and Long-Term Burden
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ApoE and COVID-19 Risk and Long-Term Burden
Tavares-Júnior, J. W. L., Ciurleo, G. C. V., Oriá, R. B., & Braga‐Neto, P. (2026) · Springer eBooks · doi:10.1007/978-3-031-96089-5_56
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Wenhua, Y., Wenjing, M., Yan, D., Fei, L., Chen, J., Xia, T., Guan, Y., Xin, L., Huang, Y., Guo, Y., et al. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1934307
Characterization of genes involved in the metabolism of atherogenic lipoproteins in the mouse
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Metadata
- Authors
- Zannis, V. I., Breslow, J. L., Utermann, G., Mahley, R. W., Weisgraber, K. H., Havel, R. J., Goldstein, J. L., Brown, M. S., Schonfeld, G., Hazzard, W. R., & Blum, C.
- Affiliations
- Harvard University (US)
- Venue
- Journal of Lipid Research
- Publisher
- Elsevier BV
- Published
- 1982-08
- Volume
- 23
- Issue
- 6
- Pages
- 911-914
- ISSN
- 0022-2275 (ISSN-L)
- OpenAlex
- W1770880387
- Cited by
- 436
- References
- 31
- Citations by year
- 2026: 9 · 2025: 14 · 2024: 5 · 2023: 15 · 2022: 8 · 2021: 12 · 2020: 4 · 2019: 4 · 2018: 7 · 2017: 7 · 2016: 9 · 2015: 12 · 2014: 15 · 2013: 11 · 2012: 11
- FWCI
- 25.83
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Lipid Research (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipoproteins and Cardiovascular Health
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Keywords
- apolipoprotein E, APOE genotype, nomenclature, genetic variants, lipoprotein metabolism
- MeSH terms
- Apolipoproteins, Apolipoproteins E, Genotype, Humans, Terminology as Topic, Phenotype
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