Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
13532 | 830 | 42.7 | 87% |
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 |
365 | 3 | MICROTUBULES//MITOSIS//KINETOCHORE | 34118 |
3382 | 2 | LISSENCEPHALY//SECKEL SYNDROME//LIS1 | 1656 |
13532 | 1 | LISSENCEPHALY//LIS1//MILLER DIEKER SYNDROME | 830 |
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 | LISSENCEPHALY | authKW | 2147526 | 16% | 44% | 133 |
2 | LIS1 | authKW | 1455908 | 7% | 68% | 58 |
3 | MILLER DIEKER SYNDROME | authKW | 867879 | 4% | 69% | 34 |
4 | DCX | authKW | 634699 | 4% | 51% | 34 |
5 | PAFAH1B1 | authKW | 414476 | 2% | 87% | 13 |
6 | TUBA1A | authKW | 370945 | 1% | 92% | 11 |
7 | NUDC | authKW | 343347 | 2% | 67% | 14 |
8 | DOUBLECORTIN | authKW | 290010 | 7% | 14% | 57 |
9 | HNUDC | authKW | 257517 | 1% | 100% | 7 |
10 | NEURONAL MIGRATION | authKW | 253811 | 9% | 10% | 72 |
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 | 2167 | 22% | 0% | 183 |
2 | Neurosciences | 1889 | 29% | 0% | 241 |
3 | Clinical Neurology | 1190 | 18% | 0% | 146 |
4 | Cell Biology | 915 | 18% | 0% | 153 |
5 | Developmental Biology | 505 | 5% | 0% | 44 |
6 | Pediatrics | 370 | 8% | 0% | 68 |
7 | Biochemistry & Molecular Biology | 295 | 20% | 0% | 162 |
8 | Pathology | 74 | 3% | 0% | 28 |
9 | Neuroimaging | 47 | 1% | 0% | 9 |
10 | Biophysics | 8 | 2% | 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 | GENET DIS | 83589 | 3% | 11% | 21 |
2 | BETH ISRAEL DEACONESS MED GENETCHILDRENS | 73576 | 0% | 100% | 2 |
3 | GRP CYTOSKELETON CELL MOTIL | 73576 | 0% | 100% | 2 |
4 | POSTDOCTORAL ASSOCIATE PROGRAM | 73576 | 0% | 100% | 2 |
5 | MOL NEUROBIOL DEV | 66216 | 0% | 60% | 3 |
6 | IMAGING SIGNALS MACHINE LEARNING GRP | 49050 | 0% | 67% | 2 |
7 | SERV BIOL MOL GENET | 49050 | 0% | 67% | 2 |
8 | AICHI HUMAN SERV PATHOL | 36788 | 0% | 100% | 1 |
9 | BETH ISRAEL DEACONESS MED HOWARD HUGHES MED I | 36788 | 0% | 100% | 1 |
10 | BIOBANCO RED REG MURCIA BIOBANC MUR NODO ARRIXACA | 36788 | 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 | HUMAN MOLECULAR GENETICS | 3134 | 3% | 0% | 29 |
2 | NEURON | 1957 | 3% | 0% | 21 |
3 | NEUROGENETICS | 1513 | 1% | 1% | 5 |
4 | NEUROPEDIATRICS | 1453 | 1% | 0% | 9 |
5 | JOURNAL OF MEDICAL GENETICS | 1224 | 2% | 0% | 14 |
6 | JOURNAL OF NEUROSCIENCE | 1211 | 4% | 0% | 34 |
7 | BRAIN & DEVELOPMENT | 1209 | 1% | 0% | 11 |
8 | DEVELOPMENTAL NEUROSCIENCE | 1147 | 1% | 0% | 7 |
9 | AMERICAN JOURNAL OF MEDICAL GENETICS | 1050 | 2% | 0% | 16 |
10 | PEDIATRIC NEUROLOGY | 853 | 1% | 0% | 10 |
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 | LISSENCEPHALY | 2147526 | 16% | 44% | 133 | Search LISSENCEPHALY | Search LISSENCEPHALY |
2 | LIS1 | 1455908 | 7% | 68% | 58 | Search LIS1 | Search LIS1 |
3 | MILLER DIEKER SYNDROME | 867879 | 4% | 69% | 34 | Search MILLER+DIEKER+SYNDROME | Search MILLER+DIEKER+SYNDROME |
4 | DCX | 634699 | 4% | 51% | 34 | Search DCX | Search DCX |
5 | PAFAH1B1 | 414476 | 2% | 87% | 13 | Search PAFAH1B1 | Search PAFAH1B1 |
6 | TUBA1A | 370945 | 1% | 92% | 11 | Search TUBA1A | Search TUBA1A |
7 | NUDC | 343347 | 2% | 67% | 14 | Search NUDC | Search NUDC |
8 | DOUBLECORTIN | 290010 | 7% | 14% | 57 | Search DOUBLECORTIN | Search DOUBLECORTIN |
9 | HNUDC | 257517 | 1% | 100% | 7 | Search HNUDC | Search HNUDC |
10 | NEURONAL MIGRATION | 253811 | 9% | 10% | 72 | Search NEURONAL+MIGRATION | Search NEURONAL+MIGRATION |
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 | FRIOCOURT, G , MARCORELLES, P , SAUGIER-VEBER, P , QUILLE, ML , MARRET, S , LAQUERRIERE, A , (2011) ROLE OF CYTOSKELETAL ABNORMALITIES IN THE NEUROPATHOLOGY AND PATHOPHYSIOLOGY OF TYPE I LISSENCEPHALY.ACTA NEUROPATHOLOGICA. VOL. 121. ISSUE 2. P. 149 -170 | 104 | 65% | 21 |
2 | FRY, AE , CUSHION, TD , PILZ, DT , (2014) THE GENETICS OF LISSENCEPHALY.AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. VOL. 166. ISSUE 2. P. 198 -210 | 65 | 66% | 13 |
3 | WYNSHAW-BORIS, A , PRAMPARO, T , YOUN, YH , HIROTSUNE, S , (2010) LISSENCEPHALY: MECHANISTIC INSIGHTS FROM ANIMAL MODELS AND POTENTIAL THERAPEUTIC STRATEGIES.SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY. VOL. 21. ISSUE 8. P. 823 -830 | 52 | 85% | 40 |
4 | REINER, O , COQUELLE, FM , (2005) MISSENSE MUTATIONS RESULTING IN TYPE 1 LISSENCEPHALY.CELLULAR AND MOLECULAR LIFE SCIENCES. VOL. 62. ISSUE 4. P. 425-434 | 74 | 64% | 7 |
5 | BAHI-BUISSON, N , SOUVILLE, I , FOURNIOL, FJ , TOUSSAINT, A , MOORES, CA , HOUDUSSE, A , LEMAITRE, JY , POIRIER, K , KHALAF-NAZZAL, R , HULLY, M , ET AL (2013) NEW INSIGHTS INTO GENOTYPE-PHENOTYPE CORRELATIONS FOR THE DOUBLECORTIN-RELATED LISSENCEPHALY SPECTRUM.BRAIN. VOL. 136. ISSUE . P. 223-244 | 46 | 71% | 18 |
6 | KERJAN, G , GLEESON, JG , (2007) GENETIC MECHANISMS UNDERLYING ABNORMAL NEURONAL MIGRATION IN CLASSICAL LISSENCEPHALY.TRENDS IN GENETICS. VOL. 23. ISSUE 12. P. 623-630 | 47 | 78% | 57 |
7 | CARDOSO, C , LEVENTER, RJ , DOWLING, JJ , WARD, HL , CHUNG, J , PETRAS, KS , ROSEBERRY, JA , WEISS, AM , DAS, S , MARTIN, CL , ET AL (2002) CLINICAL AND MOLECULAR BASIS OF CLASSICAL LISSENCEPHALY: MUTATIONS IN THE LIS1 GENE (PAFAH1B1).HUMAN MUTATION. VOL. 19. ISSUE 1. P. 4 -15 | 45 | 94% | 49 |
8 | YAP, CC , DIGILIO, L , MCMAHON, L , ROSZKOWSKA, M , BOTT, CJ , KRUCZEK, K , WINCKLER, B , (2016) DIFFERENT DOUBLECORTIN (DCX) PATIENT ALLELES SHOW DISTINCT PHENOTYPES IN CULTURED NEURONS EVIDENCE FOR DIVERGENT LOSS-OF-FUNCTION AND "OFF-PATHWAY" CELLULAR MECHANISMS.JOURNAL OF BIOLOGICAL CHEMISTRY. VOL. 291. ISSUE 52. P. 26613 -26626 | 34 | 92% | 0 |
9 | ROMANIELLO, R , ARRIGONI, F , BASSI, MT , BORGATTI, R , (2015) MUTATIONS IN ALPHA- AND BETA-TUBULIN ENCODING GENES: IMPLICATIONS IN BRAIN MALFORMATIONS.BRAIN & DEVELOPMENT. VOL. 37. ISSUE 3. P. 273 -280 | 30 | 81% | 14 |
10 | SAILLOUR, Y , CARION, N , QUELIN, C , LEGER, PL , BODDAERT, N , ELIE, C , TOUTAIN, A , BAHI-BUISSON, N , BELDJORD, C , CHELLY, J , ET AL (2009) LIS1-RELATED ISOLATED LISSENCEPHALY SPECTRUM OF MUTATIONS AND RELATIONSHIPS WITH MALFORMATION SEVERITY.ARCHIVES OF NEUROLOGY. VOL. 66. ISSUE 8. P. 1007-1015 | 35 | 88% | 18 |
Classes with closest relation at Level 1 |