Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
17020 | 622 | 29.8 | 76% |
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 |
17020 | 1 | GLUTARIC ACIDURIA TYPE I//GLUTARIC ACIDURIA TYPE 1//L 2 HYDROXYGLUTARIC ACIDURIA | 622 |
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 | GLUTARIC ACIDURIA TYPE I | authKW | 2066086 | 7% | 96% | 44 |
2 | GLUTARIC ACIDURIA TYPE 1 | authKW | 1821151 | 6% | 95% | 39 |
3 | L 2 HYDROXYGLUTARIC ACIDURIA | authKW | 1772180 | 6% | 95% | 38 |
4 | GLUTARYL COA DEHYDROGENASE | authKW | 1154423 | 4% | 87% | 27 |
5 | GLUTARIC ACIDEMIA TYPE I | authKW | 1082045 | 4% | 96% | 23 |
6 | GLUTARIC ACIDURIA | authKW | 927460 | 4% | 82% | 23 |
7 | 3 HYDROXYGLUTARIC ACID | authKW | 788181 | 3% | 94% | 17 |
8 | D 2 HYDROXYGLUTARIC ACIDURIA | authKW | 628358 | 3% | 80% | 16 |
9 | GLUTARYL COA DEHYDROGENASE DEFICIENCY | authKW | 592596 | 2% | 93% | 13 |
10 | GLUTARIC ACID | authKW | 546362 | 5% | 35% | 32 |
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 | 3702 | 32% | 0% | 202 |
2 | Medicine, Research & Experimental | 3311 | 28% | 0% | 172 |
3 | Endocrinology & Metabolism | 2687 | 26% | 0% | 161 |
4 | Pediatrics | 1865 | 19% | 0% | 121 |
5 | Clinical Neurology | 1370 | 21% | 0% | 133 |
6 | Neurosciences | 238 | 14% | 0% | 85 |
7 | Neuroimaging | 154 | 2% | 0% | 13 |
8 | Radiology, Nuclear Medicine & Medical Imaging | 73 | 5% | 0% | 34 |
9 | Medical Laboratory Technology | 63 | 2% | 0% | 12 |
10 | Biochemistry & Molecular Biology | 18 | 9% | 0% | 59 |
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 | NEUROPEDIAT METAB DIS | 104716 | 1% | 27% | 8 |
2 | ESTUDIO SELECT | 98182 | 0% | 100% | 2 |
3 | WELBIO PHYSIOL CHEM | 98182 | 0% | 100% | 2 |
4 | INBORN METAB DIS | 82178 | 2% | 14% | 12 |
5 | CANADA CHAIR DEV NEUROPATHOL | 65453 | 0% | 67% | 2 |
6 | SEKT ANGEBORENE STOFFWECHSELERKRANKUNGEN | 65453 | 0% | 67% | 2 |
7 | WELBIO DE DUVE | 65453 | 0% | 67% | 2 |
8 | METAB ENDOCRINE DIS | 64174 | 3% | 7% | 19 |
9 | CLEMENTE ESTABLE | 63114 | 0% | 43% | 3 |
10 | ABT KLIN CHEM PADIAT | 49091 | 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 | 146177 | 19% | 3% | 116 |
2 | MOLECULAR GENETICS AND METABOLISM | 14133 | 5% | 1% | 30 |
3 | NEUROPEDIATRICS | 2910 | 2% | 1% | 11 |
4 | BRAIN & DEVELOPMENT | 2267 | 2% | 0% | 13 |
5 | METABOLIC BRAIN DISEASE | 1684 | 1% | 0% | 7 |
6 | AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS | 1618 | 1% | 1% | 4 |
7 | NEUROLOGIA | 1510 | 1% | 1% | 6 |
8 | EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY | 1104 | 1% | 0% | 5 |
9 | JOURNAL OF CHILD NEUROLOGY | 805 | 1% | 0% | 9 |
10 | PEDIATRIC RADIOLOGY | 716 | 2% | 0% | 10 |
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 | BOY, N , MUHLHAUSEN, C , MAIER, EM , HERINGER, J , ASSMANN, B , BURGARD, P , DIXON, M , FLEISSNER, S , GREENBERG, CR , HARTING, I , ET AL (2017) PROPOSED RECOMMENDATIONS FOR DIAGNOSING AND MANAGING INDIVIDUALS WITH GLUTARIC ACIDURIA TYPE I: SECOND REVISION.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 40. ISSUE 1. P. 75 -101 | 102 | 73% | 0 |
2 | JAFARI, P , BRAISSANT, O , BONAFE, L , BALLHAUSEN, D , (2011) THE UNSOLVED PUZZLE OF NEUROPATHOGENESIS IN GLUTARIC ACIDURIA TYPE I.MOLECULAR GENETICS AND METABOLISM. VOL. 104. ISSUE 4. P. 425-437 | 81 | 76% | 21 |
3 | KOLKER, S , CHRISTENSEN, E , LEONARD, JV , GREENBERG, CR , BONEH, A , BURLINA, AB , BURLINA, AP , DIXON, M , DURAN, M , CAZORLA, AG , ET AL (2011) DIAGNOSIS AND MANAGEMENT OF GLUTARIC ACIDURIA TYPE I - REVISED RECOMMENDATIONS.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 34. ISSUE 3. P. 677 -694 | 65 | 79% | 63 |
4 | KRANENDIJK, M , STRUYS, EA , SALOMONS, GS , VAN DER KNAAP, MS , JAKOBS, C , (2012) PROGRESS IN UNDERSTANDING 2-HYDROXYGLUTARIC ACIDURIAS.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 35. ISSUE 4. P. 571-587 | 59 | 75% | 60 |
5 | KOLKER, S , CHRISTENSEN, E , LEONARD, JV , GREENBERG, CR , BURLINA, AB , BURLINA, AP , DIXON, M , DURAN, M , GOODMAN, SI , KOELLER, DM , ET AL (2007) GUIDELINE FOR THE DIAGNOSIS AND MANAGEMENT OF GLUTARYL-COA DEHYDROGENASE DEFICIENCY (GLUTARIC ACIDURIA TYPE I).JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 30. ISSUE 1. P. 5-22 | 54 | 89% | 67 |
6 | SAUER, SW , OPP, S , KOMATSUZAKI, S , BLANK, AE , MITTELBRONN, M , BURGARD, P , KOELLER, DM , OKUN, JG , KOLKER, S , (2015) MULTIFACTORIAL MODULATION OF SUSCEPTIBILITY TO L-LYSINE IN AN ANIMAL MODEL OF GLUTARIC ACIDURIA TYPE I.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1852. ISSUE 5. P. 768 -777 | 48 | 75% | 0 |
7 | TIAN, FY , FU, X , GAO, JZ , YING, YQ , HOU, L , LIANG, Y , NING, Q , LUO, XP , (2014) GLUTARIC ACID-MEDIATED APOPTOSIS IN PRIMARY STRIATAL NEURONS.BIOMED RESEARCH INTERNATIONAL. VOL. . ISSUE . P. - | 37 | 97% | 1 |
8 | HARTING, I , BOY, N , HERINGER, J , SEITZ, A , BENDSZUS, M , POUWELS, PJW , KOLKER, S , (2015) H-1-MRS IN GLUTARIC ACIDURIA TYPE 1: IMPACT OF BIOCHEMICAL PHENOTYPE AND AGE ON THE CEREBRAL ACCUMULATION OF NEUROTOXIC METABOLITES.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 38. ISSUE 5. P. 829 -838 | 38 | 84% | 4 |
9 | SAUER, SW , (2007) BIOCHEMISTRY AND BIOENERGETICS OF GLUTARYL-COA DEHYDROGENASE DEFICIENCY.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 30. ISSUE 5. P. 673-680 | 53 | 75% | 7 |
10 | MIKHAILOVA, SV , ZAKHAROVA, EY , BOBYLOVA, MY , IL'INA, ES , BANIN, AV , RASSKAZCHIKOVA, IV , BAIDAKOVA, GV , SHEKHTER, OV , BRYUSOVA, IB , VOLKOVA, GI , ET AL (2007) GLUTARIC ACIDURIA TYPE 1: CLINICAL PRESENTATIONS, DIAGNOSTICS AND TREATMENT.ZHURNAL NEVROLOGII I PSIKHIATRII IMENI S S KORSAKOVA. VOL. 107. ISSUE 10. P. 4-12 | 42 | 95% | 0 |
Classes with closest relation at Level 1 |