Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
2411 | 4184 | 34.0 | 63% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
11 | 4 | NEUROSCIENCES//CLINICAL NEUROLOGY//NEUROL | 1112395 |
124 | 3 | PARKINSONS DISEASE//MOVEMENT DISORDERS//DEEP BRAIN STIMULATION | 67777 |
2411 | 2 | PHENYLKETONURIA//PHENYLALANINE HYDROXYLASE//PKU | 4184 |
2133 | 1 | PHENYLKETONURIA//PKU//HYPERPHENYLALANINEMIA | 2346 |
9156 | 1 | PHENYLALANINE HYDROXYLASE//AROMATIC AMINO ACID HYDROXYLASE//TRYPTOPHAN HYDROXYLASE | 1182 |
16385 | 1 | PHENYLETHANOLAMINE N METHYLTRANSFERASE//TYROSINE HYDROXYLASE//PNMT | 656 |
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 | PHENYLKETONURIA | authKW | 4286734 | 18% | 77% | 765 |
2 | PHENYLALANINE HYDROXYLASE | authKW | 1072463 | 5% | 78% | 189 |
3 | PKU | authKW | 879574 | 3% | 84% | 144 |
4 | HYPERPHENYLALANINEMIA | authKW | 721590 | 3% | 73% | 136 |
5 | MATERNAL PHENYLKETONURIA | authKW | 277948 | 1% | 95% | 40 |
6 | SAPROPTERIN | authKW | 273833 | 1% | 89% | 42 |
7 | TYROSINE HYDROXYLASE | authKW | 258693 | 8% | 10% | 345 |
8 | PHENYLALANINE | authKW | 215776 | 4% | 17% | 176 |
9 | JOURNAL OF INHERITED METABOLIC DISEASE | journal | 161909 | 8% | 7% | 317 |
10 | TETRAHYDROBIOPTERIN | authKW | 151183 | 3% | 16% | 131 |
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 | 11927 | 23% | 0% | 961 |
2 | Endocrinology & Metabolism | 6741 | 16% | 0% | 684 |
3 | Medicine, Research & Experimental | 6672 | 16% | 0% | 658 |
4 | Neurosciences | 5005 | 22% | 0% | 915 |
5 | Pediatrics | 4437 | 12% | 0% | 503 |
6 | Biochemistry & Molecular Biology | 4157 | 29% | 0% | 1210 |
7 | Nutrition & Dietetics | 590 | 4% | 0% | 157 |
8 | Biophysics | 297 | 4% | 0% | 175 |
9 | Medical Laboratory Technology | 154 | 1% | 0% | 53 |
10 | Education, Special | 133 | 1% | 0% | 28 |
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 | UNIDAD ENFERMENDADES METAB | 72962 | 0% | 100% | 10 |
2 | DEBELLE | 55171 | 0% | 69% | 11 |
3 | PKU FOLLOW UP UNIT | 51074 | 0% | 100% | 7 |
4 | PSYCHIAT MOL DEV NEUROBIOL | 51074 | 0% | 100% | 7 |
5 | UNIT DIAG TREATMENT CONGENITAL METAB DIS | 42208 | 0% | 64% | 9 |
6 | SECT METAB DIS | 37437 | 1% | 22% | 23 |
7 | PKU CLIN | 36481 | 0% | 100% | 5 |
8 | BEATRIX CHILDRENS HOSP | 32494 | 2% | 7% | 63 |
9 | PKU | 30597 | 0% | 26% | 16 |
10 | PKU PROGRAM | 30399 | 0% | 83% | 5 |
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 | 161909 | 8% | 7% | 317 |
2 | MOLECULAR GENETICS AND METABOLISM | 103955 | 5% | 7% | 211 |
3 | JOURNAL OF NEUROCHEMISTRY | 17017 | 5% | 1% | 222 |
4 | EUROPEAN JOURNAL OF PEDIATRICS | 10073 | 2% | 1% | 102 |
5 | MOLECULAR BRAIN RESEARCH | 7376 | 2% | 2% | 68 |
6 | SCREENING | 4019 | 0% | 14% | 4 |
7 | HUMAN MUTATION | 3981 | 1% | 1% | 47 |
8 | PTERIDINES | 3027 | 0% | 3% | 13 |
9 | ACTA PAEDIATRICA | 2938 | 1% | 1% | 58 |
10 | HUMAN GENETICS | 2778 | 1% | 1% | 56 |
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 | PHENYLKETONURIA | 4286734 | 18% | 77% | 765 | Search PHENYLKETONURIA | Search PHENYLKETONURIA |
2 | PHENYLALANINE HYDROXYLASE | 1072463 | 5% | 78% | 189 | Search PHENYLALANINE+HYDROXYLASE | Search PHENYLALANINE+HYDROXYLASE |
3 | PKU | 879574 | 3% | 84% | 144 | Search PKU | Search PKU |
4 | HYPERPHENYLALANINEMIA | 721590 | 3% | 73% | 136 | Search HYPERPHENYLALANINEMIA | Search HYPERPHENYLALANINEMIA |
5 | MATERNAL PHENYLKETONURIA | 277948 | 1% | 95% | 40 | Search MATERNAL+PHENYLKETONURIA | Search MATERNAL+PHENYLKETONURIA |
6 | SAPROPTERIN | 273833 | 1% | 89% | 42 | Search SAPROPTERIN | Search SAPROPTERIN |
7 | TYROSINE HYDROXYLASE | 258693 | 8% | 10% | 345 | Search TYROSINE+HYDROXYLASE | Search TYROSINE+HYDROXYLASE |
8 | PHENYLALANINE | 215776 | 4% | 17% | 176 | Search PHENYLALANINE | Search PHENYLALANINE |
9 | TETRAHYDROBIOPTERIN | 151183 | 3% | 16% | 131 | Search TETRAHYDROBIOPTERIN | Search TETRAHYDROBIOPTERIN |
10 | PHENYLKETONURIA PKU | 139693 | 1% | 64% | 30 | Search PHENYLKETONURIA+PKU | Search PHENYLKETONURIA+PKU |
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 | CAMP, KM , PARISI, MA , ACOSTA, PB , BERRY, GT , BILDER, DA , BLAU, N , BODAMER, OA , BROSCO, JP , BROWN, CS , BURLINA, AB , ET AL (2014) PHENYLKETONURIA SCIENTIFIC REVIEW CONFERENCE: STATE OF THE SCIENCE AND FUTURE RESEARCH NEEDS.MOLECULAR GENETICS AND METABOLISM. VOL. 112. ISSUE 2. P. 87 -122 | 239 | 87% | 24 |
2 | TEKIN, I , ROSKOSKI, R , CARKACI-SALLI, N , VRANA, KE , (2014) COMPLEX MOLECULAR REGULATION OF TYROSINE HYDROXYLASE.JOURNAL OF NEURAL TRANSMISSION. VOL. 121. ISSUE 12. P. 1451 -1481 | 203 | 74% | 8 |
3 | ENNS, GM , KOCH, R , BRUMM, V , BLAKELY, E , SUTER, R , JURECKI, E , (2010) SUBOPTIMAL OUTCOMES IN PATIENTS WITH PKU TREATED EARLY WITH DIET ALONE: REVISITING THE EVIDENCE.MOLECULAR GENETICS AND METABOLISM. VOL. 101. ISSUE 2-3. P. 99-109 | 147 | 94% | 45 |
4 | KUMER, SC , VRANA, KE , (1996) INTRICATE REGULATION OF TYROSINE HYDROXYLASE ACTIVITY AND GENE EXPRESSION.JOURNAL OF NEUROCHEMISTRY. VOL. 67. ISSUE 2. P. 443 -462 | 157 | 86% | 514 |
5 | MITCHELL, JJ , TRAKADIS, YJ , SCRIVER, CR , (2011) PHENYLALANINE HYDROXYLASE DEFICIENCY.GENETICS IN MEDICINE. VOL. 13. ISSUE 8. P. 697 -707 | 104 | 95% | 41 |
6 | KAPPOCK, TJ , CARADONNA, JP , (1996) PTERIN-DEPENDENT AMINO ACID HYDROXYLASES.CHEMICAL REVIEWS. VOL. 96. ISSUE 7. P. 2659 -2756 | 247 | 50% | 229 |
7 | FITZPATRICK, PF , (1999) TETRAHYDROPTERIN-DEPENDENT AMINO ACID HYDROXYLASES.ANNUAL REVIEW OF BIOCHEMISTRY. VOL. 68. ISSUE . P. 355 -381 | 112 | 90% | 282 |
8 | SINGH, RH , CUNNINGHAM, AC , MOFIDI, S , DOUGLAS, TD , FRAZIER, DM , HOOK, DG , JEFFERS, L , MCCUNE, H , MOSELEY, KD , OGATA, B , ET AL (2016) UPDATED, WEB-BASED NUTRITION MANAGEMENT GUIDELINE FOR PKU: AN EVIDENCE AND CONSENSUS BASED APPROACH.MOLECULAR GENETICS AND METABOLISM. VOL. 118. ISSUE 2. P. 72 -83 | 94 | 95% | 0 |
9 | DICKSON, PW , VON NAGY-FELSOBUKI, EI , GRAHAM, ME , BOBROVSKAYA, L , DUNKLEY, PR , (2004) TYROSINE HYDROXYLASE PHOSPHORYLATION: REGULATION AND CONSEQUENCES.JOURNAL OF NEUROCHEMISTRY. VOL. 91. ISSUE 5. P. 1025-1043 | 95 | 88% | 249 |
10 | BLAU, N , VAN SPRONSEN, FJ , LEVY, HL , (2010) PHENYLKETONURIA.LANCET. VOL. 376. ISSUE 9750. P. 1417 -1427 | 74 | 90% | 158 |
Classes with closest relation at Level 2 |