Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
3640 | 1939 | 33.3 | 75% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY | 4064930 |
171 | 3 | MONASCUS//CITRININ//MONASCUS PURPUREUS | 58457 |
1649 | 2 | LIPOPROTEINA//FAMILIAL HYPERCHOLESTEROLEMIA//APOLIPOPROTEINA | 6893 |
3640 | 1 | FAMILIAL HYPERCHOLESTEROLEMIA//FAMILIAL HYPERCHOLESTEROLAEMIA//LOW DENSITY LIPOPROTEIN RECEPTOR | 1939 |
Terms with highest relevance score |
rank | Term | termType | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|---|
1 | FAMILIAL HYPERCHOLESTEROLEMIA | authKW | 4156495 | 27% | 50% | 527 |
2 | FAMILIAL HYPERCHOLESTEROLAEMIA | authKW | 1340126 | 7% | 61% | 139 |
3 | LOW DENSITY LIPOPROTEIN RECEPTOR | authKW | 394959 | 6% | 23% | 111 |
4 | LDL RECEPTOR GENE | authKW | 383005 | 2% | 81% | 30 |
5 | FAMILIAL DEFECTIVE APOLIPOPROTEIN B 100 | authKW | 367045 | 1% | 90% | 26 |
6 | MIPOMERSEN | authKW | 330931 | 2% | 62% | 34 |
7 | LDL RECEPTOR MUTATIONS | authKW | 320370 | 1% | 88% | 23 |
8 | LOW DENSITY LIPOPROTEIN RECEPTOR GENE | authKW | 320370 | 1% | 88% | 23 |
9 | LDL RECEPTOR | authKW | 313032 | 6% | 16% | 121 |
10 | LOMITAPIDE | authKW | 281735 | 1% | 62% | 29 |
Web of Science journal categories |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | Peripheral Vascular Diseases | 9521 | 21% | 0% | 406 |
2 | Cardiac & Cardiovascular System | 8094 | 26% | 0% | 504 |
3 | Genetics & Heredity | 3787 | 19% | 0% | 374 |
4 | Medical Laboratory Technology | 2218 | 6% | 0% | 113 |
5 | Medicine, General & Internal | 938 | 12% | 0% | 225 |
6 | Biochemistry & Molecular Biology | 504 | 17% | 0% | 339 |
7 | Medicine, Research & Experimental | 297 | 6% | 0% | 112 |
8 | Endocrinology & Metabolism | 215 | 5% | 0% | 103 |
9 | Hematology | 59 | 3% | 0% | 49 |
10 | Pharmacology & Pharmacy | 41 | 6% | 0% | 107 |
Address terms |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | LIPID DISORDERS CLIN | 190488 | 2% | 37% | 33 |
2 | CARDIOMETAB SERV | 156530 | 1% | 76% | 13 |
3 | LIPID CLIN | 118013 | 3% | 12% | 64 |
4 | GRP INVEST CARDIOVASC | 115946 | 0% | 82% | 9 |
5 | UNIDADE ID | 111971 | 0% | 89% | 8 |
6 | BRITISH HEART FDN S | 91359 | 2% | 17% | 35 |
7 | LIPID CLIN HEART INCOR | 82374 | 1% | 35% | 15 |
8 | CARDIOVASC GENET | 76009 | 4% | 7% | 73 |
9 | INVEST MOL | 68924 | 1% | 26% | 17 |
10 | MRCC E HEART GRP | 62985 | 0% | 100% | 4 |
Journals |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
---|---|---|---|---|---|
1 | JOURNAL OF CLINICAL LIPIDOLOGY | 90031 | 3% | 9% | 61 |
2 | ATHEROSCLEROSIS | 56986 | 10% | 2% | 196 |
3 | ATHEROSCLEROSIS SUPPLEMENTS | 18384 | 1% | 6% | 18 |
4 | CLINICAL GENETICS | 15959 | 4% | 1% | 72 |
5 | CURRENT OPINION IN LIPIDOLOGY | 12116 | 2% | 2% | 32 |
6 | ARTERIOSCLEROSIS AND THROMBOSIS | 11709 | 1% | 3% | 25 |
7 | CLINICAL LIPIDOLOGY | 10522 | 1% | 4% | 16 |
8 | HUMAN MUTATION | 8698 | 2% | 1% | 47 |
9 | HUMAN GENETICS | 7036 | 3% | 1% | 60 |
10 | JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS | 5610 | 1% | 2% | 20 |
Author Key Words |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Rank | Reference | # ref. in cl. |
Shr. of ref. in cl. |
Citations |
---|---|---|---|---|
1 | JENSEN, HK , (2002) THE MOLECULAR GENETIC BASIS AND DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN DENMARK.DANISH MEDICAL BULLETIN. VOL. 49. ISSUE 4. P. 318-345 | 233 | 67% | 21 |
2 | AUSTIN, MA , HUTTER, CM , ZIMMERN, RL , HUMPHRIES, SE , (2004) GENETIC CAUSES OF MONOGENIC HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA: A HUGE PREVALENCE REVIEW.AMERICAN JOURNAL OF EPIDEMIOLOGY. VOL. 160. ISSUE 5. P. 407 -420 | 87 | 87% | 185 |
3 | DEDOUSSIS, GVZ , SCHMIDT, H , GENSCHEL, J , (2004) LDL-RECEPTOR MUTATIONS IN EUROPE.HUMAN MUTATION. VOL. 24. ISSUE 6. P. 443 -459 | 107 | 81% | 40 |
4 | MEHTA, R , ZUBIRAN, R , MARTAGON, AJ , VAZQUEZ-CARDENAS, A , SEGURA-KATO, Y , TUSIE-LUNA, MT , AGUILAR-SALINAS, CA , (2016) THE PANORAMA OF FAMILIAL HYPERCHOLESTEROLEMIA IN LATIN AMERICA: A SYSTEMATIC REVIEW.JOURNAL OF LIPID RESEARCH. VOL. 57. ISSUE 12. P. 2115 -2129 | 71 | 83% | 0 |
5 | PANG, J , LANSBERG, PJ , WATTS, GF , (2016) INTERNATIONAL DEVELOPMENTS IN THE CARE OF FAMILIAL HYPERCHOLESTEROLEMIA: WHERE NOW AND WHERE TO NEXT?.JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS. VOL. 23. ISSUE 5. P. 505 -519 | 68 | 86% | 0 |
6 | FOODY, JM , VISHWANATH, R , (2016) FAMILIAL HYPERCHOLESTEROLEMIA/AUTOSOMAL DOMINANT HYPERCHOLESTEROLEMIA: MOLECULAR DEFECTS, THE LDL-C CONTINUUM, AND GRADIENTS OF PHENOTYPIC SEVERITY.JOURNAL OF CLINICAL LIPIDOLOGY. VOL. 10. ISSUE 4. P. 970 -986 | 64 | 77% | 1 |
7 | SANTOS, RD , FRAUCHES, TS , CHACRA, APM , (2015) CASCADE SCREENING IN FAMILIAL HYPERCHOLESTEROLEMIA: ADVANCING FORWARD.JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS. VOL. 22. ISSUE 9. P. 869 -880 | 60 | 81% | 3 |
8 | WATTS, GF , GIDDING, S , WIERZBICKI, AS , TOTH, PP , ALONSO, R , BROWN, WV , BRUCKERT, E , DEFESCHE, J , LIN, KK , LIVINGSTON, M , ET AL (2014) INTEGRATED GUIDANCE ON THE CARE OF FAMILIAL HYPERCHOLESTEROLAEMIA FROM THE INTERNATIONAL FH FOUNDATION.INTERNATIONAL JOURNAL OF CARDIOLOGY. VOL. 171. ISSUE 3. P. 309 -325 | 79 | 48% | 44 |
9 | SOUTAR, AK , NAOUMOVA, RP , (2007) MECHANISMS OF DISEASE: GENETIC CAUSES OF FAMILIAL HYPERCHOLESTEROLEMIA.NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE. VOL. 4. ISSUE 4. P. 214-225 | 55 | 73% | 232 |
10 | ANDERSEN, LH , MISEREZ, AR , AHMAD, Z , ANDERSEN, RL , (2016) FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100: A REVIEW.JOURNAL OF CLINICAL LIPIDOLOGY. VOL. 10. ISSUE 6. P. 1297 -1302 | 49 | 94% | 0 |
Classes with closest relation at Level 1 |