Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
27062 | 238 | 28.5 | 65% |
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 |
551 | 3 | FABRY DISEASE//GAUCHER DISEASE//LYSOSOMAL STORAGE DISEASE | 18099 |
491 | 2 | GAUCHER DISEASE//LYSOSOMAL STORAGE DISEASE//MUCOPOLYSACCHARIDOSIS | 15457 |
27062 | 1 | ASPARTYLGLUCOSAMINURIA//GLYCOSYLASPARAGINASE//ASPARTYLGLUCOSAMINIDASE | 238 |
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 | ASPARTYLGLUCOSAMINURIA | authKW | 3776168 | 14% | 89% | 33 |
2 | GLYCOSYLASPARAGINASE | authKW | 2105278 | 8% | 86% | 19 |
3 | ASPARTYLGLUCOSAMINIDASE | authKW | 2095554 | 9% | 78% | 21 |
4 | ASPARTYLGLYCOSAMINURIA | authKW | 659826 | 3% | 86% | 6 |
5 | GLYCOPROTEIN DEGRADATION | authKW | 400933 | 2% | 63% | 5 |
6 | ASPARTYLGLUCOSAMINE | authKW | 256600 | 1% | 100% | 2 |
7 | N TERMINAL NUCLEOPHILE | authKW | 230937 | 1% | 60% | 3 |
8 | AAMD ADAPTIVE BEHAVIOR SCALE | authKW | 128300 | 0% | 100% | 1 |
9 | ACTIVE SITE THREONINE | authKW | 128300 | 0% | 100% | 1 |
10 | AGA GENE MUTATION | authKW | 128300 | 0% | 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 | Biochemistry & Molecular Biology | 822 | 49% | 0% | 117 |
2 | Genetics & Heredity | 770 | 24% | 0% | 58 |
3 | Medicine, Research & Experimental | 251 | 13% | 0% | 31 |
4 | Medical Laboratory Technology | 201 | 5% | 0% | 12 |
5 | Biophysics | 198 | 11% | 0% | 27 |
6 | Cell Biology | 54 | 10% | 0% | 23 |
7 | Biochemical Research Methods | 44 | 5% | 0% | 13 |
8 | Endocrinology & Metabolism | 41 | 6% | 0% | 15 |
9 | Pediatrics | 40 | 5% | 0% | 13 |
10 | Biotechnology & Applied Microbiology | 16 | 5% | 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 | FDN GD ANNUNZIO | 128300 | 0% | 100% | 1 |
2 | FINLAND ASTRAZENECA RD | 128300 | 0% | 100% | 1 |
3 | HOSP CHILDREN ADOLESCENTS PAEDIAT NEUROL | 128300 | 0% | 100% | 1 |
4 | JOINT CLIN CHEM | 128300 | 0% | 100% | 1 |
5 | NEWBORN SCREENING FINLAND | 128300 | 0% | 100% | 1 |
6 | PAAJARVI | 102637 | 1% | 40% | 2 |
7 | TURKU SITE | 64149 | 0% | 50% | 1 |
8 | WILLINK BIOCHEM GENET | 64149 | 0% | 50% | 1 |
9 | ABERDEEN OOMYCETES | 42765 | 0% | 33% | 1 |
10 | EXCELLENCE DIS GENET | 42765 | 0% | 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 | 5545 | 6% | 0% | 14 |
2 | ACTA MEDICA POLONA | 1643 | 0% | 1% | 1 |
3 | URBAN MORPHOLOGY | 1058 | 0% | 1% | 1 |
4 | GLYCOBIOLOGY | 717 | 2% | 0% | 4 |
5 | HUMAN MOLECULAR GENETICS | 635 | 3% | 0% | 7 |
6 | CLINICAL CHEMISTRY | 524 | 3% | 0% | 7 |
7 | SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION | 450 | 2% | 0% | 4 |
8 | BIOCHEMICAL JOURNAL | 426 | 4% | 0% | 10 |
9 | ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 407 | 1% | 0% | 2 |
10 | HUMAN GENETICS | 395 | 2% | 0% | 5 |
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 | ASPARTYLGLUCOSAMINURIA | 3776168 | 14% | 89% | 33 | Search ASPARTYLGLUCOSAMINURIA | Search ASPARTYLGLUCOSAMINURIA |
2 | GLYCOSYLASPARAGINASE | 2105278 | 8% | 86% | 19 | Search GLYCOSYLASPARAGINASE | Search GLYCOSYLASPARAGINASE |
3 | ASPARTYLGLUCOSAMINIDASE | 2095554 | 9% | 78% | 21 | Search ASPARTYLGLUCOSAMINIDASE | Search ASPARTYLGLUCOSAMINIDASE |
4 | ASPARTYLGLYCOSAMINURIA | 659826 | 3% | 86% | 6 | Search ASPARTYLGLYCOSAMINURIA | Search ASPARTYLGLYCOSAMINURIA |
5 | GLYCOPROTEIN DEGRADATION | 400933 | 2% | 63% | 5 | Search GLYCOPROTEIN+DEGRADATION | Search GLYCOPROTEIN+DEGRADATION |
6 | ASPARTYLGLUCOSAMINE | 256600 | 1% | 100% | 2 | Search ASPARTYLGLUCOSAMINE | Search ASPARTYLGLUCOSAMINE |
7 | N TERMINAL NUCLEOPHILE | 230937 | 1% | 60% | 3 | Search N+TERMINAL+NUCLEOPHILE | Search N+TERMINAL+NUCLEOPHILE |
8 | AAMD ADAPTIVE BEHAVIOR SCALE | 128300 | 0% | 100% | 1 | Search AAMD+ADAPTIVE+BEHAVIOR+SCALE | Search AAMD+ADAPTIVE+BEHAVIOR+SCALE |
9 | ACTIVE SITE THREONINE | 128300 | 0% | 100% | 1 | Search ACTIVE+SITE+THREONINE | Search ACTIVE+SITE+THREONINE |
10 | AGA GENE MUTATION | 128300 | 0% | 100% | 1 | Search AGA+GENE+MUTATION | Search AGA+GENE+MUTATION |
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 | ARVIO, M , MONONEN, I , (2016) ASPARTYLGLYCOSAMINURIA: A REVIEW.ORPHANET JOURNAL OF RARE DISEASES. VOL. 11. ISSUE . P. - | 53 | 90% | 0 |
2 | ARONSON, NN , (1999) ASPARTYLGLYCOSAMINURIA: BIOCHEMISTRY AND MOLECULAR BIOLOGY.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1455. ISSUE 2-3. P. 139 -154 | 60 | 80% | 18 |
3 | OPLADEN, T , EBINGER, F , ZSCHOCKE, J , SENGUPTA, D , BEN-OMRAN, T , SHAHBECK, N , MOOG, U , FISCHER, C , BURGER, F , HAAS, D , ET AL (2014) ASPARTYLGLUCOSAMINURIA: UNUSUAL NEONATAL PRESENTATION IN QATARI TWINS WITH A NOVEL ASPARTYLGLUCOSAMINIDASE GENE MUTATION AND 3 NEW CASES IN A TURKISH FAMILY.JOURNAL OF CHILD NEUROLOGY. VOL. 29. ISSUE 1. P. 36-42 | 23 | 79% | 3 |
4 | BANNING, A , GULEC, C , ROUVINEN, J , GRAY, SJ , TIKKANEN, R , (2016) IDENTIFICATION OF SMALL MOLECULE COMPOUNDS FOR PHARMACOLOGICAL CHAPERONE THERAPY OF ASPARTYLGLUCOSAMINURIA.SCIENTIFIC REPORTS. VOL. 6. ISSUE . P. - | 27 | 66% | 0 |
5 | SUI, LF , LAKSHMINARASIMHAN, D , PANDE, S , GUO, HC , (2014) STRUCTURAL BASIS OF A POINT MUTATION THAT CAUSES THE GENETIC DISEASE ASPARTYLGLUCOSAMINURIA.STRUCTURE. VOL. 22. ISSUE 12. P. 1855 -1861 | 21 | 75% | 2 |
6 | MONONEN, I , FISHER, KJ , KAARTINEN, V , ARONSON, NN , (1993) ASPARTYLGLYCOSAMINURIA - PROTEIN CHEMISTRY AND MOLECULAR-BIOLOGY OF THE MOST COMMON LYSOSOMAL STORAGE DISORDER OF GLYCOPROTEIN DEGRADATION.FASEB JOURNAL. VOL. 7. ISSUE 13. P. 1247-1256 | 41 | 67% | 29 |
7 | ARVIO, P , ARVIO, M , KERO, M , PIRINEN, S , LUKINMAA, PL , (1999) OVERGROWTH OF ORAL MUCOSA AND FACIAL SKIN, A NOVEL FEATURE OF ASPARTYLGLUCOSAMINURIA.JOURNAL OF MEDICAL GENETICS. VOL. 36. ISSUE 5. P. 398 -404 | 24 | 83% | 9 |
8 | HARKKE, S , LAINE, M , JALANKO, A , (2003) ASPARTYTGTUCOSAMINIDASE (AGA) IS EFFICIENTLY PRODUCED AND ENDOCYTOSED BY GLIAL CELLS: IMPLICATION FOR THE THERAPY OF A LYSOSOMAL STORAGE DISORDER.JOURNAL OF GENE MEDICINE. VOL. 5. ISSUE 6. P. 472-482 | 25 | 69% | 6 |
9 | SAARELA, J , LAINE, M , OINONEN, C , VON SCHANTZ, C , JALANKO, A , ROUVINEN, J , PELTONEN, L , (2001) MOLECULAR PATHOGENESIS OF A DISEASE: STRUCTURAL CONSEQUENCES OF ASPARTYLGLUCOSAMINURIA MUTATIONS.HUMAN MOLECULAR GENETICS. VOL. 10. ISSUE 9. P. 983 -995 | 23 | 74% | 21 |
10 | RISLEY, JM , HUANG, DH , KAYLOR, JJ , MALIK, JJ , XIA, YQ , YORK, WM , (2001) GLYCOSYLASPARAGINASE ACTIVITY REQUIRES THE ALPHA-CARBOXYL GROUP, BUT NOT THE ALPHA-AMINO GROUP, ON N-4-(2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-L-ASPARAGINE.ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS. VOL. 391. ISSUE 2. P. 165 -170 | 25 | 63% | 5 |
Classes with closest relation at Level 1 |