Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
2388 | 2263 | 29.5 | 73% |
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 |
389 | 3 | PEROXISOME//CARNITINE//JOURNAL OF INHERITED METABOLIC DISEASE | 30841 |
2144 | 2 | JOURNAL OF INHERITED METABOLIC DISEASE//NEWBORN SCREENING//METHYLMALONIC ACIDEMIA | 5035 |
2388 | 1 | NEWBORN SCREENING//MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY//UNIT MOL MED | 2263 |
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 | NEWBORN SCREENING | authKW | 1092800 | 13% | 27% | 305 |
2 | MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY | authKW | 498904 | 2% | 86% | 43 |
3 | UNIT MOL MED | address | 435627 | 4% | 38% | 86 |
4 | MCAD DEFICIENCY | authKW | 434918 | 2% | 92% | 35 |
5 | INBORN ERRORS OF METABOLISM | authKW | 345210 | 5% | 23% | 112 |
6 | JOURNAL OF INHERITED METABOLIC DISEASE | journal | 294232 | 14% | 7% | 314 |
7 | FATTY ACID OXIDATION DISORDERS | authKW | 253326 | 1% | 72% | 26 |
8 | SHORT CHAIN ACYL COA DEHYDROGENASE DEFICIENCY | authKW | 230064 | 1% | 95% | 18 |
9 | ETHYLMALONIC ENCEPHALOPATHY | authKW | 216612 | 1% | 94% | 17 |
10 | MULTIPLE ACYL COA DEHYDROGENASE DEFICIENCY | authKW | 211752 | 1% | 83% | 19 |
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 | Genetics & Heredity | 13127 | 32% | 0% | 726 |
2 | Pediatrics | 11314 | 25% | 0% | 561 |
3 | Medicine, Research & Experimental | 9715 | 25% | 0% | 565 |
4 | Endocrinology & Metabolism | 6719 | 22% | 0% | 491 |
5 | Medical Laboratory Technology | 4183 | 7% | 0% | 166 |
6 | Medical Ethics | 1002 | 1% | 0% | 30 |
7 | Ethics | 349 | 1% | 0% | 32 |
8 | Clinical Neurology | 291 | 6% | 0% | 147 |
9 | Social Sciences, Biomedical | 102 | 1% | 0% | 24 |
10 | Biochemistry & Molecular Biology | 101 | 10% | 0% | 237 |
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 | UNIT MOL MED | 435627 | 4% | 38% | 86 |
2 | UNITE ETUD MALAD METAB | 69383 | 0% | 86% | 6 |
3 | GENET METAB DIS | 55667 | 3% | 7% | 59 |
4 | KIMBERLY H COURTWRIGHT JOSEPH W SUMMERS ME | 47961 | 0% | 44% | 8 |
5 | GENET SERV BRANCH | 41310 | 0% | 44% | 7 |
6 | NEWBORN SCREENING PROGRAM | 40869 | 0% | 30% | 10 |
7 | INVEST BIOQUIM CLIN PATOL MOL | 40475 | 0% | 100% | 3 |
8 | PUBL HLTH NEWBORN SCREENING STATE BAVARIA | 40475 | 0% | 100% | 3 |
9 | NEW ENGLAND NEWBORN SCREENING PROGRAM | 37343 | 1% | 23% | 12 |
10 | GENET METAB DISEMMA CHILDRENS HOSP | 35975 | 0% | 67% | 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 INHERITED METABOLIC DISEASE | 294232 | 14% | 7% | 314 |
2 | MOLECULAR GENETICS AND METABOLISM | 77564 | 6% | 4% | 134 |
3 | GENETICS IN MEDICINE | 25243 | 2% | 3% | 55 |
4 | PEDIATRIC RESEARCH | 7782 | 3% | 1% | 73 |
5 | PUBLIC HEALTH GENOMICS | 5811 | 1% | 4% | 12 |
6 | EUROPEAN JOURNAL OF PEDIATRICS | 5615 | 2% | 1% | 56 |
7 | JOURNAL OF PEDIATRICS | 4809 | 3% | 1% | 70 |
8 | PEDIATRICS | 4313 | 3% | 0% | 79 |
9 | MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS | 3865 | 0% | 3% | 11 |
10 | CLINICA CHIMICA ACTA | 3359 | 2% | 0% | 53 |
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 | WAJNER, M , AMARAL, AU , (2016) MITOCHONDRIAL DYSFUNCTION IN FATTY ACID OXIDATION DISORDERS: INSIGHTS FROM HUMAN AND ANIMAL STUDIES.BIOSCIENCE REPORTS. VOL. 36. ISSUE . P. - | 88 | 75% | 1 |
2 | GREGERSEN, N , ANDRESEN, BS , CORYDON, M , CORYDON, TJ , OLSEN, RKJ , BOLUND, L , BROSS, P , (2001) MUTATION ANALYSIS IN MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS: EXEMPLIFIED BY ACYL-COA DEHYDROGENASE DEFICIENCIES, WITH SPECIAL FOCUS ON GENOTYPE-PHENOTYPE RELATIONSHIP.HUMAN MUTATION. VOL. 18. ISSUE 3. P. 169 -189 | 99 | 77% | 103 |
3 | HOUTEN, SM , VIOLANTE, S , VENTURA, FV , WANDERS, RJA , (2016) THE BIOCHEMISTRY AND PHYSIOLOGY OF MITOCHONDRIAL FATTY ACID BETA-OXIDATION AND ITS GENETIC DISORDERS.ANNUAL REVIEW OF PHYSIOLOGY, VOL 78. VOL. 78. ISSUE . P. 23 -44 | 72 | 54% | 5 |
4 | NICHOLLS, SG , WILSON, BJ , ETCHEGARY, H , BREHAUT, JC , POTTER, BK , HAYEEMS, R , CHAKRABORTY, P , MILBURN, J , PULLMAN, D , TURNER, L , ET AL (2014) BENEFITS AND BURDENS OF NEWBORN SCREENING: PUBLIC UNDERSTANDING AND DECISION-MAKING.PERSONALIZED MEDICINE. VOL. 11. ISSUE 6. P. 593 -607 | 71 | 72% | 1 |
5 | GREGERSEN, N , ANDRESEN, BS , PEDERSEN, CB , OLSEN, RKJ , CORYDON, TJ , BROSS, P , (2008) MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS-REMAINING CHALLENGES.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 31. ISSUE 5. P. 643-657 | 59 | 87% | 58 |
6 | MAK, CM , LEE, HCH , CHAN, AYW , LAM, CW , (2013) INBORN ERRORS OF METABOLISM AND EXPANDED NEWBORN SCREENING: REVIEW AND UPDATE.CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES. VOL. 50. ISSUE 6. P. 142-162 | 97 | 45% | 15 |
7 | WANDERS, RJA , VREKEN, P , DEN BOER, MEJ , WIJBURG, FA , VAN GENNIP, AH , IJLST, L , (1999) DISORDERS OF MITOCHONDRIAL FATTY ACYL-COA BETA-OXIDATION.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 22. ISSUE 4. P. 442 -487 | 95 | 61% | 136 |
8 | ANDRESEN, BS , LUND, AM , HOUGAARD, DM , CHRISTENSEN, E , GAHRN, B , CHRISTENSEN, M , BROSS, P , VESTED, A , SIMONSEN, H , SKOGSTRAND, K , ET AL (2012) MCAD DEFICIENCY IN DENMARK.MOLECULAR GENETICS AND METABOLISM. VOL. 106. ISSUE 2. P. 175-188 | 47 | 94% | 11 |
9 | BENNETT, MJ , RINALDO, P , STRAUSS, AW , (2000) INBORN ERRORS OF MITOCHONDRIAL FATTY ACID OXIDATION.CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES. VOL. 37. ISSUE 1. P. 1 -44 | 91 | 64% | 60 |
10 | SIM, KG , HAMMOND, J , WILCKEN, B , (2002) STRATEGIES FOR THE DIAGNOSIS OF MITOCHONDRIAL FATTY ACID BETA-OXIDATION DISORDERS.CLINICA CHIMICA ACTA. VOL. 323. ISSUE 1-2. P. 37-58 | 82 | 63% | 52 |
Classes with closest relation at Level 1 |