Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
6251 | 1508 | 35.9 | 74% |
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 |
6251 | 1 | BATTEN DISEASE//NEURONAL CEROID LIPOFUSCINOSIS//NEURONAL CEROID LIPOFUSCINOSES | 1508 |
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 | BATTEN DISEASE | authKW | 4621029 | 16% | 93% | 245 |
2 | NEURONAL CEROID LIPOFUSCINOSIS | authKW | 4219391 | 16% | 89% | 235 |
3 | NEURONAL CEROID LIPOFUSCINOSES | authKW | 1388897 | 5% | 91% | 75 |
4 | CLN3 | authKW | 1347742 | 6% | 79% | 84 |
5 | NCL | authKW | 810689 | 4% | 65% | 62 |
6 | INFANTILE NEURONAL CEROID LIPOFUSCINOSIS | authKW | 650157 | 2% | 94% | 34 |
7 | CEROID LIPOFUSCINOSIS | authKW | 635190 | 3% | 78% | 40 |
8 | JUVENILE NEURONAL CEROID LIPOFUSCINOSIS | authKW | 628275 | 2% | 97% | 32 |
9 | PEDIAT STORAGE DISORDERS | address | 493631 | 2% | 76% | 32 |
10 | CLN6 | authKW | 465686 | 2% | 100% | 23 |
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 | 6037 | 27% | 0% | 406 |
2 | Clinical Neurology | 4928 | 26% | 0% | 387 |
3 | Neurosciences | 2015 | 23% | 0% | 346 |
4 | Pathology | 1179 | 8% | 0% | 128 |
5 | Medicine, Research & Experimental | 1016 | 11% | 0% | 161 |
6 | Pediatrics | 868 | 9% | 0% | 138 |
7 | Biochemistry & Molecular Biology | 550 | 20% | 0% | 297 |
8 | Endocrinology & Metabolism | 488 | 8% | 0% | 122 |
9 | Ophthalmology | 282 | 4% | 0% | 65 |
10 | Veterinary Sciences | 203 | 5% | 0% | 78 |
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 | PEDIAT STORAGE DISORDERS | 493631 | 2% | 76% | 32 |
2 | PATHOL NEUROBIOL | 206118 | 2% | 36% | 28 |
3 | KINGS HLTH PARTNERS NEURODEGENERAT | 138828 | 1% | 57% | 12 |
4 | MOL NEUROGENET DIAGNOST | 121483 | 0% | 100% | 6 |
5 | AGING DEV BIOL | 108212 | 2% | 14% | 37 |
6 | SECT DEV GENET | 88034 | 1% | 23% | 19 |
7 | CELLULAR BASIS BEHAV PSYCHIAT | 80989 | 0% | 100% | 4 |
8 | MASON EYE | 73387 | 2% | 13% | 27 |
9 | MRC NEURODEGENERAT PSYCHIAT | 64790 | 0% | 80% | 4 |
10 | NEUROL VISUAL SCI NEUROL | 64790 | 0% | 80% | 4 |
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 | MOLECULAR GENETICS AND METABOLISM | 26516 | 4% | 2% | 64 |
2 | ADVANCES IN GENETICS INCORPORATING MOLECULAR GENETIC MEDICINE | 19812 | 1% | 8% | 12 |
3 | NEUROPEDIATRICS | 16719 | 3% | 2% | 41 |
4 | JOURNAL OF INHERITED METABOLIC DISEASE | 12031 | 3% | 1% | 52 |
5 | AMERICAN JOURNAL OF MEDICAL GENETICS | 10621 | 5% | 1% | 68 |
6 | BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 8472 | 2% | 1% | 37 |
7 | NEUROBIOLOGY OF DISEASE | 5271 | 2% | 1% | 31 |
8 | HUMAN MOLECULAR GENETICS | 4918 | 3% | 1% | 49 |
9 | JOURNAL OF CHILD NEUROLOGY | 3967 | 2% | 1% | 31 |
10 | BRAIN PATHOLOGY | 3014 | 1% | 1% | 15 |
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 | BATTEN DISEASE | 4621029 | 16% | 93% | 245 | Search BATTEN+DISEASE | Search BATTEN+DISEASE |
2 | NEURONAL CEROID LIPOFUSCINOSIS | 4219391 | 16% | 89% | 235 | Search NEURONAL+CEROID+LIPOFUSCINOSIS | Search NEURONAL+CEROID+LIPOFUSCINOSIS |
3 | NEURONAL CEROID LIPOFUSCINOSES | 1388897 | 5% | 91% | 75 | Search NEURONAL+CEROID+LIPOFUSCINOSES | Search NEURONAL+CEROID+LIPOFUSCINOSES |
4 | CLN3 | 1347742 | 6% | 79% | 84 | Search CLN3 | Search CLN3 |
5 | NCL | 810689 | 4% | 65% | 62 | Search NCL | Search NCL |
6 | INFANTILE NEURONAL CEROID LIPOFUSCINOSIS | 650157 | 2% | 94% | 34 | Search INFANTILE+NEURONAL+CEROID+LIPOFUSCINOSIS | Search INFANTILE+NEURONAL+CEROID+LIPOFUSCINOSIS |
7 | CEROID LIPOFUSCINOSIS | 635190 | 3% | 78% | 40 | Search CEROID+LIPOFUSCINOSIS | Search CEROID+LIPOFUSCINOSIS |
8 | JUVENILE NEURONAL CEROID LIPOFUSCINOSIS | 628275 | 2% | 97% | 32 | Search JUVENILE+NEURONAL+CEROID+LIPOFUSCINOSIS | Search JUVENILE+NEURONAL+CEROID+LIPOFUSCINOSIS |
9 | CLN6 | 465686 | 2% | 100% | 23 | Search CLN6 | Search CLN6 |
10 | JNCL | 446281 | 2% | 96% | 23 | Search JNCL | Search JNCL |
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 | BOND, M , HOLTHAUS, SMK , TAMMEN, I , TEAR, G , RUSSELL, C , (2013) USE OF MODEL ORGANISMS FOR THE STUDY OF NEURONAL CEROID LIPOFUSCINOSIS.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1832. ISSUE 11. P. 1842-1865 | 225 | 79% | 20 |
2 | JALANKO, A , BRAULKE, T , (2009) NEURONAL CEROID LIPOFUSCINOSES.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH. VOL. 1793. ISSUE 4. P. 697 -709 | 188 | 85% | 144 |
3 | KOUSI, M , LEHESJOKI, AE , MOLE, SE , (2012) UPDATE OF THE MUTATION SPECTRUM AND CLINICAL CORRELATIONS OF OVER 360 MUTATIONS IN EIGHT GENES THAT UNDERLIE THE NEURONAL CEROID LIPOFUSCINOSES.HUMAN MUTATION. VOL. 33. ISSUE 1. P. 42-63 | 153 | 94% | 89 |
4 | KOLLMANN, K , UUSI-RAUVA, K , SCIFO, E , TYYNELA, J , JALANKO, A , BRAULKE, T , (2013) CELL BIOLOGY AND FUNCTION OF NEURONAL CEROID LIPOFUSCINOSIS-RELATED PROTEINS.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1832. ISSUE 11. P. 1866 -1881 | 198 | 62% | 37 |
5 | SHACKA, JJ , (2012) MOUSE MODELS OF NEURONAL CEROID LIPOFUSCINOSES: USEFUL PRE-CLINICAL TOOLS TO DELINEATE DISEASE PATHOPHYSIOLOGY AND VALIDATE THERAPEUTICS.BRAIN RESEARCH BULLETIN. VOL. 88. ISSUE 1. P. 43-57 | 145 | 87% | 22 |
6 | MOLE, SE , WILLIAMS, RE , GOEBEL, HH , (2005) CORRELATIONS BETWEEN GENOTYPE, ULTRASTRUCTURAL MORPHOLOGY AND CLINICAL PHENOTYPE IN THE NEURONAL CEROID LIPOFUSCINOSES.NEUROGENETICS. VOL. 6. ISSUE 3. P. 107 -126 | 132 | 94% | 141 |
7 | PALMER, DN , BARRY, LA , TYYNELA, J , COOPER, JD , (2013) NCL DISEASE MECHANISMS.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1832. ISSUE 11. P. 1882-1893 | 126 | 86% | 19 |
8 | CARCEL-TRULLOLS, J , KOVACS, AD , PEARCE, DA , (2015) CELL BIOLOGY OF THE NCL PROTEINS: WHAT THEY DO AND DON'T DO.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1852. ISSUE 10. P. 2242 -2255 | 137 | 57% | 13 |
9 | GETTY, AL , PEARCE, DA , (2011) INTERACTIONS OF THE PROTEINS OF NEURONAL CEROID LIPOFUSCINOSIS: CLUES TO FUNCTION.CELLULAR AND MOLECULAR LIFE SCIENCES. VOL. 68. ISSUE 3. P. 453 -474 | 141 | 68% | 24 |
10 | KYTTALA, A , LAHTINEN, U , BRAULKE, T , HOFMANN, SL , (2006) FUNCTIONAL BIOLOGY OF THE NEURONAL CEROID LIPOFUSCINOSES (NCL) PROTEINS.BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. VOL. 1762. ISSUE 10. P. 920 -933 | 143 | 74% | 43 |
Classes with closest relation at Level 1 |