Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
16099 | 673 | 46.9 | 89% |
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 |
100 | 3 | NEUROSCIENCES//METABOTROPIC GLUTAMATE RECEPTOR//HIPPOCAMPUS | 73970 |
891 | 2 | POSTSYNAPTIC DENSITY//LONG TERM POTENTIATION//SYNAPTIC PLASTICITY | 11396 |
16099 | 1 | SHANK3//HOMER//HOMER PROTEINS | 673 |
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 | SHANK3 | authKW | 2369403 | 9% | 83% | 63 |
2 | HOMER | authKW | 1212520 | 12% | 32% | 84 |
3 | HOMER PROTEINS | authKW | 833681 | 3% | 88% | 21 |
4 | PHELAN MCDERMID SYNDROME | authKW | 791912 | 4% | 73% | 24 |
5 | 22Q13 DELETION SYNDROME | authKW | 683227 | 2% | 94% | 16 |
6 | SHANK | authKW | 658688 | 4% | 52% | 28 |
7 | HOMER1 | authKW | 606302 | 3% | 64% | 21 |
8 | HOMER 1A | authKW | 571654 | 3% | 60% | 21 |
9 | 22Q13 DELETION | authKW | 523093 | 2% | 82% | 14 |
10 | 22Q133 DELETION SYNDROME | authKW | 502566 | 2% | 92% | 12 |
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 | Neurosciences | 5068 | 50% | 0% | 339 |
2 | Genetics & Heredity | 1319 | 19% | 0% | 130 |
3 | Biochemistry & Molecular Biology | 308 | 21% | 0% | 144 |
4 | Psychiatry | 192 | 7% | 0% | 48 |
5 | Cell Biology | 186 | 10% | 0% | 70 |
6 | Clinical Neurology | 54 | 5% | 0% | 37 |
7 | Behavioral Sciences | 34 | 2% | 0% | 14 |
8 | Pharmacology & Pharmacy | 33 | 7% | 0% | 46 |
9 | Developmental Biology | 20 | 1% | 0% | 10 |
10 | Biophysics | 14 | 3% | 0% | 19 |
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 | WG MOL ANAL SYN TOPATHIES | 216040 | 1% | 48% | 10 |
2 | MOL PSYCHIAT PSYCHOPHARMACOTHER Y | 145185 | 1% | 80% | 4 |
3 | MOL PSYCHIAT PSYCHOPHARMACOTHER EUT | 131239 | 1% | 32% | 9 |
4 | SEAVER AUTISM TREATMENT | 103677 | 2% | 14% | 16 |
5 | BEHAV NEURAL GENET | 102083 | 0% | 75% | 3 |
6 | EXPERTISE CHILD DEV CARE | 90741 | 0% | 100% | 2 |
7 | MOL PSYCHIAT PSYCHOPHARMACOTHER YSECT PSY | 90741 | 0% | 100% | 2 |
8 | OFF BIOINFORMAT EPIDEMIOL | 90741 | 0% | 100% | 2 |
9 | AG MOL NEUROBIOL | 74095 | 1% | 23% | 7 |
10 | I U | 60493 | 0% | 67% | 2 |
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 AUTISM | 14063 | 1% | 3% | 9 |
2 | JOURNAL OF NEUROSCIENCE | 2919 | 7% | 0% | 47 |
3 | JOURNAL OF NEURODEVELOPMENTAL DISORDERS | 1553 | 0% | 1% | 3 |
4 | JOURNAL OF MEDICAL GENETICS | 1516 | 2% | 0% | 14 |
5 | CLINICAL DYSMORPHOLOGY | 1454 | 1% | 1% | 6 |
6 | MOLECULAR BRAIN | 1380 | 1% | 1% | 4 |
7 | DEVELOPMENTAL NEUROBIOLOGY | 1182 | 1% | 1% | 5 |
8 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 934 | 2% | 0% | 11 |
9 | NEURON | 919 | 2% | 0% | 13 |
10 | MOLECULAR AND CELLULAR NEUROSCIENCE | 785 | 1% | 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 | SHANK3 | 2369403 | 9% | 83% | 63 | Search SHANK3 | Search SHANK3 |
2 | HOMER | 1212520 | 12% | 32% | 84 | Search HOMER | Search HOMER |
3 | HOMER PROTEINS | 833681 | 3% | 88% | 21 | Search HOMER+PROTEINS | Search HOMER+PROTEINS |
4 | PHELAN MCDERMID SYNDROME | 791912 | 4% | 73% | 24 | Search PHELAN+MCDERMID+SYNDROME | Search PHELAN+MCDERMID+SYNDROME |
5 | 22Q13 DELETION SYNDROME | 683227 | 2% | 94% | 16 | Search 22Q13+DELETION+SYNDROME | Search 22Q13+DELETION+SYNDROME |
6 | SHANK | 658688 | 4% | 52% | 28 | Search SHANK | Search SHANK |
7 | HOMER1 | 606302 | 3% | 64% | 21 | Search HOMER1 | Search HOMER1 |
8 | HOMER 1A | 571654 | 3% | 60% | 21 | Search HOMER+1A | Search HOMER+1A |
9 | 22Q13 DELETION | 523093 | 2% | 82% | 14 | Search 22Q13+DELETION | Search 22Q13+DELETION |
10 | 22Q133 DELETION SYNDROME | 502566 | 2% | 92% | 12 | Search 22Q133+DELETION+SYNDROME | Search 22Q133+DELETION+SYNDROME |
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 | SALA, C , VICIDOMINI, C , BIGI, I , MOSSA, A , VERPELLI, C , (2015) SHANK SYNAPTIC SCAFFOLD PROTEINS: KEYS TO UNDERSTANDING THE PATHOGENESIS OF AUTISM AND OTHER SYNAPTIC DISORDERS.JOURNAL OF NEUROCHEMISTRY. VOL. 135. ISSUE 5. P. 849 -858 | 58 | 74% | 7 |
2 | HARONY-NICOLAS, H , DE RUBEIS, S , KOLEVZON, A , BUXBAUM, JD , (2015) PHELAN MCDERMID SYNDROME: FROM GENETIC DISCOVERIES TO ANIMAL MODELS AND TREATMENT.JOURNAL OF CHILD NEUROLOGY. VOL. 30. ISSUE 14. P. 1861 -1870 | 66 | 69% | 3 |
3 | SHIRAISHI-YAMAGUCHI, Y , FURUICHI, T , (2007) THE HOMER FAMILY PROTEINS.GENOME BIOLOGY. VOL. 8. ISSUE 2. P. - | 54 | 79% | 108 |
4 | KOLEVZON, A , ANGARITA, B , BUSH, L , WANG, AT , FRANK, Y , YANG, A , RAPAPORT, R , SALAND, J , SRIVASTAVA, S , FARRELL, C , ET AL (2014) PHELAN-MCDERMID SYNDROME: A REVIEW OF THE LITERATURE AND PRACTICE PARAMETERS FOR MEDICAL ASSESSMENT AND MONITORING.JOURNAL OF NEURODEVELOPMENTAL DISORDERS. VOL. 6. ISSUE . P. - | 47 | 82% | 6 |
5 | GUILMATRE, A , HUGUET, G , DELORME, R , BOURGERON, T , (2014) THE EMERGING ROLE OF SHANK GENES IN NEUROPSYCHIATRIC DISORDERS.DEVELOPMENTAL NEUROBIOLOGY. VOL. 74. ISSUE 2. P. 113-122 | 39 | 71% | 50 |
6 | JARAMILLO, TC , SPEED, HE , XUAN, Z , REIMERS, JM , ESCAMILLA, CO , WEAVER, TP , LIU, SA , FILONOVA, I , POWELL, CM , (2017) NOVEL SHANK3 MUTANT EXHIBITS BEHAVIORS WITH FACE VALIDITY FOR AUTISM AND ALTERED STRIATAL AND HIPPOCAMPAL FUNCTION.AUTISM RESEARCH. VOL. 10. ISSUE 1. P. 42 -65 | 35 | 64% | 1 |
7 | JIANG, YH , EHLERS, MD , (2013) MODELING AUTISM BY SHANK GENE MUTATIONS IN MICE.NEURON. VOL. 78. ISSUE 1. P. 8-27 | 58 | 46% | 93 |
8 | LUO, P , LI, X , FEI, Z , POON, WS , (2012) SCAFFOLD PROTEIN HOMER 1: IMPLICATIONS FOR NEUROLOGICAL DISEASES.NEUROCHEMISTRY INTERNATIONAL. VOL. 61. ISSUE 5. P. 731-738 | 54 | 68% | 17 |
9 | COSTALES, JL , KOLEVZON, A , (2015) PHELAN-MCDERMID SYNDROME AND SHANK3: IMPLICATIONS FOR TREATMENT.NEUROTHERAPEUTICS. VOL. 12. ISSUE 3. P. 620 -630 | 58 | 60% | 2 |
10 | FOA, L , GASPERINI, R , (2009) DEVELOPMENTAL ROLES FOR HOMER: MORE THAN JUST A PRETTY SCAFFOLD.JOURNAL OF NEUROCHEMISTRY. VOL. 108. ISSUE 1. P. 1 -10 | 52 | 70% | 19 |
Classes with closest relation at Level 1 |