Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
28675 | 201 | 19.4 | 63% |
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 |
28675 | 1 | 3 HYDROXYISOBUTYRATE DEHYDROGENASE//ECHS1//3 HYDROXYISOBUTYRIC ACID | 201 |
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 | 3 HYDROXYISOBUTYRATE DEHYDROGENASE | authKW | 883879 | 4% | 73% | 8 |
2 | ECHS1 | authKW | 607666 | 3% | 67% | 6 |
3 | 3 HYDROXYISOBUTYRIC ACID | authKW | 455753 | 1% | 100% | 3 |
4 | HIBCH | authKW | 455753 | 1% | 100% | 3 |
5 | SERINE DEHYDROGENASE | authKW | 455753 | 1% | 100% | 3 |
6 | LACTONOHYDROLASE | authKW | 345262 | 2% | 45% | 5 |
7 | 3 HYDROXYISOBUTYRIC ACIDURIA | authKW | 303835 | 1% | 100% | 2 |
8 | D BETA HYDROXYISOBUTYRIC ACID | authKW | 303835 | 1% | 100% | 2 |
9 | D LACTONOHYDROLASE | authKW | 303835 | 1% | 100% | 2 |
10 | D PANTONOHYDROLASE | authKW | 303835 | 1% | 100% | 2 |
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 | Biotechnology & Applied Microbiology | 654 | 25% | 0% | 50 |
2 | Biochemistry & Molecular Biology | 262 | 32% | 0% | 65 |
3 | Chemistry, Applied | 138 | 8% | 0% | 17 |
4 | Food Science & Technology | 122 | 10% | 0% | 20 |
5 | Genetics & Heredity | 122 | 11% | 0% | 23 |
6 | Engineering, Chemical | 109 | 11% | 0% | 22 |
7 | Medicine, Research & Experimental | 90 | 9% | 0% | 18 |
8 | Crystallography | 52 | 5% | 0% | 10 |
9 | Biochemical Research Methods | 37 | 5% | 0% | 11 |
10 | Endocrinology & Metabolism | 30 | 6% | 0% | 12 |
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 | PROD DEV HIGASHI KU | 202555 | 1% | 67% | 2 |
2 | BIO OURCE SCI PL MICROBIOL | 151918 | 0% | 100% | 1 |
3 | BIO OURCE SCI PL MICROBIOL NANKO KU | 151918 | 0% | 100% | 1 |
4 | CENT 311 SAKURAI SHIMAMOTO | 151918 | 0% | 100% | 1 |
5 | DRUG CHILD HEALTH NEUROFARBA | 151918 | 0% | 100% | 1 |
6 | EMIL ERLENMEYER FORUM | 151918 | 0% | 100% | 1 |
7 | HEAD GENET METAB DIS | 151918 | 0% | 100% | 1 |
8 | HEAD OFF CYUO KU | 151918 | 0% | 100% | 1 |
9 | HOSP NEUROL SURG | 151918 | 0% | 100% | 1 |
10 | SOZIALPADIATR ZENTRUM NEUROPADIATRIE | 151918 | 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 | BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY | 1807 | 6% | 0% | 12 |
2 | JOURNAL OF FERMENTATION TECHNOLOGY | 1676 | 1% | 0% | 3 |
3 | JOURNAL OF INHERITED METABOLIC DISEASE | 1636 | 3% | 0% | 7 |
4 | CRYSTAL ENGINEERING | 1517 | 0% | 1% | 1 |
5 | ORPHANET JOURNAL OF RARE DISEASES | 1226 | 1% | 0% | 3 |
6 | KAGAKU KOGAKU RONBUNSHU | 1216 | 3% | 0% | 6 |
7 | MOLECULAR GENETICS AND METABOLISM | 773 | 2% | 0% | 4 |
8 | JOURNAL OF INCLUSION PHENOMENA AND MOLECULAR RECOGNITION IN CHEMISTRY | 758 | 1% | 0% | 2 |
9 | CANCER MEDICINE | 680 | 1% | 0% | 2 |
10 | APPLIED MICROBIOLOGY AND BIOTECHNOLOGY | 527 | 3% | 0% | 7 |
Author Key Words |
Rank | Term | Chi square | Shr. of publ. in class containing term |
Class's shr. of term's tot. occurrences |
#P with term in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | 3 HYDROXYISOBUTYRATE DEHYDROGENASE | 883879 | 4% | 73% | 8 | Search 3+HYDROXYISOBUTYRATE+DEHYDROGENASE | Search 3+HYDROXYISOBUTYRATE+DEHYDROGENASE |
2 | ECHS1 | 607666 | 3% | 67% | 6 | Search ECHS1 | Search ECHS1 |
3 | 3 HYDROXYISOBUTYRIC ACID | 455753 | 1% | 100% | 3 | Search 3+HYDROXYISOBUTYRIC+ACID | Search 3+HYDROXYISOBUTYRIC+ACID |
4 | HIBCH | 455753 | 1% | 100% | 3 | Search HIBCH | Search HIBCH |
5 | SERINE DEHYDROGENASE | 455753 | 1% | 100% | 3 | Search SERINE+DEHYDROGENASE | Search SERINE+DEHYDROGENASE |
6 | LACTONOHYDROLASE | 345262 | 2% | 45% | 5 | Search LACTONOHYDROLASE | Search LACTONOHYDROLASE |
7 | 3 HYDROXYISOBUTYRIC ACIDURIA | 303835 | 1% | 100% | 2 | Search 3+HYDROXYISOBUTYRIC+ACIDURIA | Search 3+HYDROXYISOBUTYRIC+ACIDURIA |
8 | D BETA HYDROXYISOBUTYRIC ACID | 303835 | 1% | 100% | 2 | Search D+BETA+HYDROXYISOBUTYRIC+ACID | Search D+BETA+HYDROXYISOBUTYRIC+ACID |
9 | D LACTONOHYDROLASE | 303835 | 1% | 100% | 2 | Search D+LACTONOHYDROLASE | Search D+LACTONOHYDROLASE |
10 | D PANTONOHYDROLASE | 303835 | 1% | 100% | 2 | Search D+PANTONOHYDROLASE | Search D+PANTONOHYDROLASE |
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 | WANDERS, RJA , DURAN, M , LOUPATTY, FJ , (2012) ENZYMOLOGY OF THE BRANCHED-CHAIN AMINO ACID OXIDATION DISORDERS: THE VALINE PATHWAY.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 35. ISSUE 1. P. 5-12 | 20 | 56% | 19 |
2 | SASS, JO , WALTER, M , SHIELD, JPH , ATHERTON, AM , GARG, U , SCOTT, D , WOODS, CG , SMITH, LD , (2012) 3-HYDROXYISOBUTYRATE ACIDURIA AND MUTATIONS IN THE ALDH6A1 GENE CODING FOR METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 35. ISSUE 3. P. 437 -442 | 14 | 74% | 9 |
3 | MARCADIER, JL , SMITH, AM , POHL, D , SCHWARTZENTRUBER, J , AL-DIRBASHI, OY , MAJEWSKI, J , FERDINANDUSSE, S , WANDERS, RJA , BULMAN, DE , BOYCOTT, KM , ET AL (2013) MUTATIONS IN ALDH6A1 ENCODING METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE ARE ASSOCIATED WITH DYSMYELINATION AND TRANSIENT METHYLMALONIC ACIDURIA.ORPHANET JOURNAL OF RARE DISEASES. VOL. 8. ISSUE . P. - | 12 | 71% | 4 |
4 | TCHIGVINTSEV, A , SINGER, A , BROWN, G , FLICK, R , EVDOKIMOVA, E , TAN, KM , GONZALEZ, CF , SAVCHENKO, A , YAKUNIN, AF , (2012) BIOCHEMICAL AND STRUCTURAL STUDIES OF UNCHARACTERIZED PROTEIN PA0743 FROM PSEUDOMONAS AERUGINOSA REVEALED NAD(+)-DEPENDENT L-SERINE DEHYDROGENASE.JOURNAL OF BIOLOGICAL CHEMISTRY. VOL. 287. ISSUE 3. P. 1874 -1883 | 19 | 44% | 9 |
5 | PETERS, H , FERDINANDUSSE, S , RUITER, JP , WANDERS, RJA , BONEH, A , PITT, J , (2015) METABOLITE STUDIES IN HIBCH AND ECHS1 DEFECTS: IMPLICATIONS FOR SCREENING.MOLECULAR GENETICS AND METABOLISM. VOL. 115. ISSUE 4. P. 168 -173 | 12 | 63% | 4 |
6 | SCHOTTMANN, G , SARPONG, A , LORENZ, C , WEINHOLD, N , GILL, E , TESCHNER, L , FERDINANDUSSE, S , WANDERS, RJA , PRIGIONE, A , SCHUELKE, M , (2016) A MOVEMENT DISORDER WITH DYSTONIA AND ATAXIA CAUSED BY A MUTATION IN THE HIBCH GENE.MOVEMENT DISORDERS. VOL. 31. ISSUE 11. P. 1733 -1739 | 11 | 69% | 0 |
7 | HONDA, K , KATAOKA, M , SHIMIZU, S , (2002) ENZYMATIC PREPARATION OF D-BETA-ACETYLTHIOISOBUTYRIC ACID AND CETRAXATE HYDROCHLORIDE USING A STEREO- AND/OR REGIOSELECTIVE HYDROLASE, 3,4-DIHYDROCOUMARIN HYDROLASE FROM ACINETOBACTER CALCOACETICUS.APPLIED MICROBIOLOGY AND BIOTECHNOLOGY. VOL. 60. ISSUE 3. P. 288-292 | 13 | 72% | 7 |
8 | LOUPATTY, FJ , VAN DER STEEN, A , IJLST, L , RUITER, JPN , OFMAN, R , BAUMGARTNER, MR , BALLHAUSEN, D , YAMAGUCHI, S , DURAN, M , WANDERS, RJA , (2006) CLINICAL, BIOCHEMICAL, AND MOLECULAR FINDINGS IN THREE PATIENTS WITH 3-HYDROXYISOBUTYRIC ACIDURIA.MOLECULAR GENETICS AND METABOLISM. VOL. 87. ISSUE 3. P. 243-248 | 10 | 77% | 10 |
9 | NAIR, P , HAMZEH, AR , MOHAMED, M , MALIK, EM , AL-ALI, MT , BASTAKI, F , (2016) NOVEL ECHS1 MUTATION IN AN EMIRATI NEONATE WITH SEVERE METABOLIC ACIDOSIS.METABOLIC BRAIN DISEASE. VOL. 31. ISSUE 5. P. 1189 -1192 | 7 | 88% | 0 |
10 | YAMADA, K , AIBA, K , KITAURA, Y , KONDO, Y , NOMURA, N , NAKAMURA, Y , FUKUSHI, D , MURAYAMA, K , SHIMOMURA, Y , PITT, J , ET AL (2015) CLINICAL, BIOCHEMICAL AND METABOLIC CHARACTERISATION OF A MILD FORM OF HUMAN SHORT-CHAIN ENOYL-COA HYDRATASE DEFICIENCY: SIGNIFICANCE OF INCREASED N-ACETYL-S-(2-CARBOXYPROPYL) CYSTEINE EXCRETION.JOURNAL OF MEDICAL GENETICS. VOL. 52. ISSUE 10. P. 691 -698 | 10 | 56% | 4 |
Classes with closest relation at Level 1 |