Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
19487 | 503 | 27.7 | 49% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
5 | 4 | CHEMISTRY, ORGANIC//CHEMISTRY, INORGANIC & NUCLEAR//CHEMISTRY, MULTIDISCIPLINARY | 1745167 |
239 | 3 | LIPASE//JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC//BIOCATALYSIS | 47598 |
2176 | 2 | LIPASE//UPR 9025//COLIPASE | 4953 |
19487 | 1 | LYSOSOMAL ACID LIPASE//CHOLESTERYL ESTER STORAGE DISEASE//WOLMAN DISEASE | 503 |
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 | LYSOSOMAL ACID LIPASE | authKW | 2352584 | 9% | 82% | 47 |
2 | CHOLESTERYL ESTER STORAGE DISEASE | authKW | 2065668 | 7% | 97% | 35 |
3 | WOLMAN DISEASE | authKW | 1992231 | 8% | 86% | 38 |
4 | CHOLESTEROL ESTER STORAGE DISEASE | authKW | 667759 | 2% | 100% | 11 |
5 | LYSOSOMAL ACID LIPASE DEFICIENCY | authKW | 667759 | 2% | 100% | 11 |
6 | ACID LIPASE | authKW | 303517 | 2% | 50% | 10 |
7 | CHOLESTERYL ESTER STORAGE DISEASE CESD | authKW | 242822 | 1% | 100% | 4 |
8 | LAL DEFICIENCY | authKW | 242822 | 1% | 100% | 4 |
9 | LYSOSOMAL ACID LIPASE LAL DEFICIENCY | authKW | 182116 | 1% | 100% | 3 |
10 | WOLMAN | authKW | 182116 | 1% | 100% | 3 |
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 | Biochemistry & Molecular Biology | 709 | 33% | 0% | 168 |
2 | Medicine, Research & Experimental | 486 | 13% | 0% | 63 |
3 | Genetics & Heredity | 403 | 13% | 0% | 65 |
4 | Biophysics | 283 | 10% | 0% | 48 |
5 | Nutrition & Dietetics | 259 | 7% | 0% | 33 |
6 | Medical Laboratory Technology | 229 | 4% | 0% | 19 |
7 | Gastroenterology & Hepatology | 213 | 7% | 0% | 35 |
8 | Pathology | 207 | 6% | 0% | 32 |
9 | Pediatrics | 186 | 8% | 0% | 38 |
10 | Endocrinology & Metabolism | 129 | 7% | 0% | 37 |
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 | ARTERIOSCLEROSIS SPECIALIZED | 121411 | 0% | 100% | 2 |
2 | IU SIMON CANC | 94835 | 2% | 16% | 10 |
3 | MED HLTH SCI NUTR | 80939 | 0% | 67% | 2 |
4 | ABT AUXOL | 60705 | 0% | 100% | 1 |
5 | BASIC MED SCI MOL LIFE SCI | 60705 | 0% | 100% | 1 |
6 | CARDIOL EOS | 60705 | 0% | 100% | 1 |
7 | CORE CLIN PATHOL | 60705 | 0% | 100% | 1 |
8 | EDINBURGH SICK CHILDRENS NHS TRUST | 60705 | 0% | 100% | 1 |
9 | ENDOCRINOL METAB JPK | 60705 | 0% | 100% | 1 |
10 | ENFANTS MALADES IMAGINE | 60705 | 0% | 100% | 1 |
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 INHERITED METABOLIC DISEASE | 3412 | 3% | 0% | 16 |
2 | BIOMEDICINE EXPRESS | 2126 | 0% | 2% | 2 |
3 | ENZYME | 2003 | 1% | 1% | 5 |
4 | LIPIDS | 2001 | 3% | 0% | 14 |
5 | BIOCHIMICA ET BIOPHYSICA ACTA | 2000 | 6% | 0% | 31 |
6 | JOURNAL OF LIPID RESEARCH | 1804 | 3% | 0% | 16 |
7 | MOLECULAR GENETICS AND METABOLISM | 1562 | 2% | 0% | 9 |
8 | BIOCHEMICAL MEDICINE | 1063 | 1% | 1% | 3 |
9 | NUTRITION AND METABOLISM | 1063 | 0% | 2% | 1 |
10 | VOPROSY MEDITSINSKOI KHIMII | 939 | 1% | 0% | 6 |
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 | BERNSTEIN, DL , HULKOVA, H , BIALER, MG , DESNICK, RJ , (2013) CHOLESTERYL ESTER STORAGE DISEASE: REVIEW OF THE FINDINGS IN 135 REPORTED PATIENTS WITH AN UNDERDIAGNOSED DISEASE.JOURNAL OF HEPATOLOGY. VOL. 58. ISSUE 6. P. 1230-1243 | 80 | 90% | 46 |
2 | REYNOLDS, T , (2013) CHOLESTERYL ESTER STORAGE DISEASE: A RARE AND POSSIBLY TREATABLE CAUSE OF PREMATURE VASCULAR DISEASE AND CIRRHOSIS.JOURNAL OF CLINICAL PATHOLOGY. VOL. 66. ISSUE 11. P. 918-923 | 63 | 93% | 7 |
3 | REINER, Z , GUARDAMAGNA, O , NAIR, D , SORAN, H , HOVINGH, K , BERTOLINI, S , JONES, S , CORIC, M , CALANDRA, S , HAMILTON, J , ET AL (2014) LYSOSOMAL ACID LIPASE DEFICIENCY - AN UNDER-RECOGNIZED CAUSE OF DYSLIPIDAEMIA AND LIVER DYSFUNCTION.ATHEROSCLEROSIS. VOL. 235. ISSUE 1. P. 21 -30 | 42 | 66% | 32 |
4 | PORTO, AF , (2014) LYSOSOMAL ACID LIPASE DEFICIENCY: DIAGNOSIS AND TREATMENT OF WOLMAN AND CHOLESTERYL ESTER STORAGE DISEASES.PEDIATRIC ENDOCRINOLOGY REVIEWS PER. VOL. 12. ISSUE . P. 125 -132 | 33 | 89% | 5 |
5 | CHATRATH, H , KEILIN, S , ATTAR, BM , (2009) CHOLESTEROL ESTER STORAGE DISEASE (CESD) DIAGNOSED IN AN ASYMPTOMATIC ADULT.DIGESTIVE DISEASES AND SCIENCES. VOL. 54. ISSUE 1. P. 168 -173 | 28 | 100% | 6 |
6 | FASANO, T , PISCIOTTA, L , BOCCHI, L , GUARDAMAGNA, O , ASSANDRO, P , RABACCHI, C , ZANONI, P , FILOCAMO, M , BERTOLINI, S , CALANDRA, S , (2012) LYSOSOMAL LIPASE DEFICIENCY: MOLECULAR CHARACTERIZATION OF ELEVEN PATIENTS WITH WOLMAN OR CHOLESTERYL ESTER STORAGE DISEASE.MOLECULAR GENETICS AND METABOLISM. VOL. 105. ISSUE 3. P. 450 -456 | 23 | 96% | 8 |
7 | SCOTT, SA , LIU, B , NAZARENKO, I , MARTIS, S , KOZLITINA, J , YANG, Y , RAMIREZ, C , KASAI, Y , HYATT, T , PETER, I , ET AL (2013) FREQUENCY OF THE CHOLESTERYL ESTER STORAGE DISEASE COMMON LIPA E8SJM MUTATION (C.894G > A) IN VARIOUS RACIAL AND ETHNIC GROUPS.HEPATOLOGY. VOL. 58. ISSUE 3. P. 958-965 | 27 | 75% | 14 |
8 | KURANOBU, N , MURAKAMI, J , OKAMOTO, K , NISHIMURA, R , MURAYAMA, K , TAKAMURA, A , UMEDA, T , ETO, Y , KANZAKI, S , (2016) CHOLESTEROL ESTER STORAGE DISEASE WITH A NOVEL LIPA MUTATION (L264P) THAT PRESENTED MASSIVE HEPATOMEGALY: A CASE REPORT.HEPATOLOGY RESEARCH. VOL. 46. ISSUE 5. P. 477 -482 | 20 | 95% | 0 |
9 | PATON, DM , (2016) SEBELIPASE ALFA: ENZYMATIC REPLACEMENT TREATMENT FOR LYSOSOMAL ACID LIPASE DEFICIENCY.DRUGS OF TODAY. VOL. 52. ISSUE 5. P. 287 -293 | 17 | 100% | 1 |
10 | RAJAMOHAN, F , REYES, AR , RUANGSIRILUK, W , HOTH, LR , HAN, S , CASPERS, N , TU, MH , WARD, J , KURUMBAIL, RG , (2015) EXPRESSION AND FUNCTIONAL CHARACTERIZATION OF HUMAN LYSOSOMAL ACID LIPASE GENE (LIPA) MUTATION RESPONSIBLE FOR CHOLESTERYL ESTER STORAGE DISEASE (CESD) PHENOTYPE.PROTEIN EXPRESSION AND PURIFICATION. VOL. 110. ISSUE . P. 22 -29 | 22 | 81% | 0 |
Classes with closest relation at Level 1 |