Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
37064 | 67 | 26.0 | 69% |
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 |
1504 | 2 | CARNITINE//L CARNITINE//TRIMETAZIDINE | 7543 |
37064 | 1 | MALONIC ACIDURIA//MALONYL COA DECARBOXYLASE DEFICIENCY//MALONYL COA DECARBOXYLASE | 67 |
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 | MALONIC ACIDURIA | authKW | 2791507 | 10% | 88% | 7 |
2 | MALONYL COA DECARBOXYLASE DEFICIENCY | authKW | 2734540 | 9% | 100% | 6 |
3 | MALONYL COA DECARBOXYLASE | authKW | 2536364 | 24% | 35% | 16 |
4 | MLYCD | authKW | 1823026 | 6% | 100% | 4 |
5 | TRANSIT IL 2020 | address | 1458420 | 6% | 80% | 4 |
6 | MALONYL COENZYME A DECARBOXYLASE DEFICIENCY | authKW | 911513 | 3% | 100% | 2 |
7 | METAB MODULATOR LTD | address | 911513 | 3% | 100% | 2 |
8 | CARDIOMYOPATHY TREATMENT | authKW | 455757 | 1% | 100% | 1 |
9 | CHEM DISCOVERY BIOL | address | 455757 | 1% | 100% | 1 |
10 | CR CENT HOSP | address | 455757 | 1% | 100% | 1 |
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 | 267 | 27% | 0% | 18 |
2 | Medicine, Research & Experimental | 168 | 19% | 0% | 13 |
3 | Biochemistry & Molecular Biology | 160 | 42% | 0% | 28 |
4 | Endocrinology & Metabolism | 157 | 19% | 0% | 13 |
5 | Biophysics | 102 | 15% | 0% | 10 |
6 | Chemistry, Medicinal | 74 | 10% | 0% | 7 |
7 | Biochemical Research Methods | 40 | 9% | 0% | 6 |
8 | Pediatrics | 37 | 9% | 0% | 6 |
9 | Chemistry, Organic | 11 | 7% | 0% | 5 |
10 | Crystallography | 5 | 3% | 0% | 2 |
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 | TRANSIT IL 2020 | 1458420 | 6% | 80% | 4 |
2 | METAB MODULATOR LTD | 911513 | 3% | 100% | 2 |
3 | CHEM DISCOVERY BIOL | 455757 | 1% | 100% | 1 |
4 | CR CENT HOSP | 455757 | 1% | 100% | 1 |
5 | MED CHEM METAB DISORDERS DRUG METAB PHARMA | 455757 | 1% | 100% | 1 |
6 | VET MED DIOGNOST | 455757 | 1% | 100% | 1 |
7 | MMRL | 364603 | 3% | 40% | 2 |
8 | METAB MODULATORS LTD | 227877 | 1% | 50% | 1 |
9 | METAB DIS CLIN GENET | 151918 | 1% | 33% | 1 |
10 | METAB OFF | 151918 | 1% | 33% | 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 | 8164 | 13% | 0% | 9 |
2 | JOURNAL OF BIOCHEMISTRY AND MOLECULAR BIOLOGY | 1425 | 3% | 0% | 2 |
3 | MOLECULAR GENETICS AND METABOLISM | 1312 | 4% | 0% | 3 |
4 | BRAIN & DEVELOPMENT | 1128 | 4% | 0% | 3 |
5 | BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY | 660 | 1% | 0% | 1 |
6 | EUROPEAN JOURNAL OF PEDIATRICS | 549 | 4% | 0% | 3 |
7 | COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING | 340 | 1% | 0% | 1 |
8 | METABOLIC BRAIN DISEASE | 320 | 1% | 0% | 1 |
9 | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 285 | 6% | 0% | 4 |
10 | ANNALS OF HUMAN GENETICS | 261 | 1% | 0% | 1 |
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 | POLINATI, PP , VALANNE, L , TYNI, T , (2015) MALONYL-COA DECARBOXYLASE DEFICIENCY: LONG-TERM FOLLOW-UP OF A PATIENT NEW CLINICAL FEATURES AND NOVEL MUTATIONS.BRAIN & DEVELOPMENT. VOL. 37. ISSUE 1. P. 107 -113 | 25 | 76% | 3 |
2 | CELATO, A , MITOLA, C , TOLVE, M , GIANNINI, MT , DE LEO, S , CARDUCCI, C , CARDUCCI, C , LEUZZI, V , (2013) A NEW CASE OF MALONIC ACIDURIA WITH A PRESYMPTOMATIC DIAGNOSIS AND AN EARLY TREATMENT.BRAIN & DEVELOPMENT. VOL. 35. ISSUE 7. P. 675-680 | 17 | 89% | 4 |
3 | XUE, JJ , PENG, J , ZHOU, MX , ZHONG, L , YIN, F , LIANG, DS , WU, LQ , (2012) NOVEL COMPOUND HETEROZYGOUS MUTATION OF MLYCD IN A CHINESE PATIENT WITH MALONIC ACIDURIA.MOLECULAR GENETICS AND METABOLISM. VOL. 105. ISSUE 1. P. 79-83 | 17 | 89% | 5 |
4 | LIU, H , TAN, DQ , HAN, LS , YE, J , QIU, WJ , GU, XF , ZHANG, HW , (2016) A NEW CASE OF MALONYL-COA DECARBOXYLASE DEFICIENCY WITH MILD CLINICAL FEATURES.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 170. ISSUE 5. P. 1347 -1351 | 12 | 86% | 0 |
5 | DE WIT, MCY , DE COO, IFM , VERBEEK, E , SCHOT, R , SCHOONDERWOERD, GC , DURAN, M , DE KLERK, JBC , HUIJMANS, JGM , LEQUIN, MH , VERHEIJEN, FW , ET AL (2006) BRAIN ABNORMALITIES IN A CASE OF MALONYL-COA DECARBOXYLASE DEFICIENCY.MOLECULAR GENETICS AND METABOLISM. VOL. 87. ISSUE 2. P. 102-106 | 13 | 68% | 17 |
6 | BAERTLING, F , MAYATEPEK, E , THIMM, E , SCHLUNE, A , KOVACEVIC, A , DISTELMAIER, F , SALOMONS, GS , MEISSNER, T , (2014) MALONIC ACIDURIA: LONG-TERM FOLLOW-UP OF NEW PATIENTS DETECTED BY NEWBORN SCREENING.EUROPEAN JOURNAL OF PEDIATRICS. VOL. 173. ISSUE 12. P. 1719 -1722 | 9 | 82% | 1 |
7 | SURENDRAN, S , SACKSTEDER, KA , GOULD, SJ , COLDWELL, JG , RADY, PL , TYRING, SK , MATALON, R , (2001) MALONYL COA DECARBOXYLASE DEFICIENCY: C TO T TRANSITION IN INTRON 2 OF THE MCD GENE.JOURNAL OF NEUROSCIENCE RESEARCH. VOL. 65. ISSUE 6. P. 591-594 | 12 | 80% | 9 |
8 | MALVAGIA, S , PAPI, L , MORRONE, A , DONATI, MA , CIANI, F , PASQUINI, E , LA MARCA, G , SCHOLTE, HR , GENUARDI, M , ZAMMARCHI, E , (2007) FATAL MALONYL COA DECARBOXYLASE DEFICIENCY DUE TO MATERNAL UNIPARENTAL ISODISOMY OF THE TELOMERIC END OF CHROMOSOME 16.ANNALS OF HUMAN GENETICS. VOL. 71. ISSUE . P. 705-712 | 17 | 44% | 13 |
9 | ALFARES, A , NUNEZ, LD , AL-THIHLI, K , MITCHELL, J , MELANCON, S , ANASTASIO, N , HA, KCH , MAJEWSKI, J , ROSENBLATT, DS , BRAVERMAN, N , (2011) COMBINED MALONIC AND METHYLMALONIC ACIDURIA: EXOME SEQUENCING REVEALS MUTATIONS IN THE ACSF3 GENE IN PATIENTS WITH A NON-CLASSIC PHENOTYPE.JOURNAL OF MEDICAL GENETICS. VOL. 48. ISSUE 9. P. 602 -605 | 13 | 50% | 9 |
10 | SALOMONS, GS , JAKOBS, C , POPE, LL , ERRAMI, A , POTTER, M , NOWACZYK, M , OLPIN, S , MANNING, N , RAIMAN, JAJ , SLADE, T , ET AL (2007) CLINICAL, ENZYMATIC AND MOLECULAR CHARACTERIZATION OF NINE NEW PATIENTS WITH MALONYL-COENZYME A DECARBOXYLASE DEFICIENCY.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 30. ISSUE 1. P. 23-28 | 10 | 71% | 18 |
Classes with closest relation at Level 1 |