Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
3382 | 1656 | 36.4 | 82% |
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 |
18053 | 1 | SECKEL SYNDROME//ASPM//MCPH1 | 569 |
26340 | 1 | COHEN SYNDROME//CHORIORETINAL DYSPLASIA//COH1 | 257 |
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 | 1175530 | 8% | 46% | 139 |
2 | SECKEL SYNDROME | authKW | 912097 | 4% | 85% | 58 |
3 | LIS1 | authKW | 729655 | 4% | 68% | 58 |
4 | COHEN SYNDROME | authKW | 707031 | 3% | 91% | 42 |
5 | MILLER DIEKER SYNDROME | authKW | 434954 | 2% | 69% | 34 |
6 | MICROCEPHALY | authKW | 331671 | 7% | 15% | 120 |
7 | DCX | authKW | 318082 | 2% | 51% | 34 |
8 | ASPM | authKW | 307705 | 1% | 76% | 22 |
9 | MCPH1 | authKW | 301137 | 1% | 78% | 21 |
10 | PRIMARY MICROCEPHALY | authKW | 289382 | 1% | 83% | 19 |
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 | 12837 | 37% | 0% | 610 |
2 | Pediatrics | 1422 | 11% | 0% | 181 |
3 | Clinical Neurology | 1272 | 13% | 0% | 221 |
4 | Neurosciences | 1105 | 17% | 0% | 283 |
5 | Cell Biology | 960 | 14% | 0% | 232 |
6 | Developmental Biology | 436 | 4% | 0% | 60 |
7 | Medical Ethics | 333 | 1% | 0% | 15 |
8 | Biochemistry & Molecular Biology | 276 | 15% | 0% | 250 |
9 | Neuroimaging | 83 | 1% | 0% | 17 |
10 | Pathology | 55 | 2% | 0% | 39 |
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 | HUMAN DNA DAMAGE PONSE DISORDERS GRP | 67873 | 1% | 41% | 9 |
2 | HARVARD MD PHD MSTP PROGRAM | 55313 | 0% | 100% | 3 |
3 | GENET DIS | 41875 | 1% | 11% | 21 |
4 | BETH ISRAEL DEACONESS MED GENETCHILDRENS | 36875 | 0% | 100% | 2 |
5 | GRP CYTOSKELETON CELL MOTIL | 36875 | 0% | 100% | 2 |
6 | POSTDOCTORAL ASSOCIATE PROGRAM | 36875 | 0% | 100% | 2 |
7 | MOL NEUROBIOL DEV | 33185 | 0% | 60% | 3 |
8 | DISABLED PERSONS | 24582 | 0% | 67% | 2 |
9 | DOUBLE STRAND BREAK REPAIR | 24582 | 0% | 67% | 2 |
10 | IMAGING SIGNALS MACHINE LEARNING GRP | 24582 | 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 | AMERICAN JOURNAL OF MEDICAL GENETICS | 16228 | 5% | 1% | 88 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 9600 | 3% | 1% | 55 |
3 | CLINICAL DYSMORPHOLOGY | 7258 | 1% | 2% | 21 |
4 | JOURNAL OF MEDICAL GENETICS | 6391 | 3% | 1% | 45 |
5 | CLINICAL GENETICS | 5739 | 2% | 1% | 40 |
6 | GENETIC COUNSELING | 4379 | 1% | 2% | 15 |
7 | HUMAN MOLECULAR GENETICS | 3763 | 3% | 0% | 45 |
8 | NEUROPEDIATRICS | 3601 | 1% | 1% | 20 |
9 | AMERICAN JOURNAL OF HUMAN GENETICS | 3432 | 2% | 0% | 39 |
10 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 1603 | 1% | 1% | 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 | 1175530 | 8% | 46% | 139 | Search LISSENCEPHALY | Search LISSENCEPHALY |
2 | SECKEL SYNDROME | 912097 | 4% | 85% | 58 | Search SECKEL+SYNDROME | Search SECKEL+SYNDROME |
3 | LIS1 | 729655 | 4% | 68% | 58 | Search LIS1 | Search LIS1 |
4 | COHEN SYNDROME | 707031 | 3% | 91% | 42 | Search COHEN+SYNDROME | Search COHEN+SYNDROME |
5 | MILLER DIEKER SYNDROME | 434954 | 2% | 69% | 34 | Search MILLER+DIEKER+SYNDROME | Search MILLER+DIEKER+SYNDROME |
6 | MICROCEPHALY | 331671 | 7% | 15% | 120 | Search MICROCEPHALY | Search MICROCEPHALY |
7 | DCX | 318082 | 2% | 51% | 34 | Search DCX | Search DCX |
8 | ASPM | 307705 | 1% | 76% | 22 | Search ASPM | Search ASPM |
9 | MCPH1 | 301137 | 1% | 78% | 21 | Search MCPH1 | Search MCPH1 |
10 | PRIMARY MICROCEPHALY | 289382 | 1% | 83% | 19 | Search PRIMARY+MICROCEPHALY | Search PRIMARY+MICROCEPHALY |
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 | 106 | 67% | 21 |
2 | MAHMOOD, S , AHMAD, W , HASSAN, MJ , (2011) AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY (MCPH): CLINICAL MANIFESTATIONS, GENETIC HETEROGENEITY AND MUTATION CONTINUUM.ORPHANET JOURNAL OF RARE DISEASES. VOL. 6. ISSUE . P. - | 78 | 76% | 72 |
3 | FAHEEM, M , NASEER, MI , RASOOL, M , CHAUDHARY, AG , KUMOSANI, TA , ILYAS, AM , PUSHPARAJ, PN , AHMED, F , ALGAHTANI, HA , AL-QAHTANI, MH , ET AL (2015) MOLECULAR GENETICS OF HUMAN PRIMARY MICROCEPHALY: AN OVERVIEW.BMC MEDICAL GENOMICS. VOL. 8. ISSUE . P. - | 56 | 66% | 21 |
4 | PULYERS, JN , JOURNIAC, N , ARAI, Y , NARDELLI, J , (2015) MCPH1: A WINDOW INTO BRAIN DEVELOPMENT AND EVOLUTION.FRONTIERS IN CELLULAR NEUROSCIENCE. VOL. 9. ISSUE . P. - | 81 | 58% | 0 |
5 | 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 |
6 | 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 |
7 | YIGIT, G , ROSIN, N , WOLLNIK, B , (2015) MOLECULAR BASIS OF AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY.MEDIZINISCHE GENETIK. VOL. 27. ISSUE 4. P. 345 -350 | 45 | 96% | 0 |
8 | LIU, XQ , ZHOU, ZW , WANG, ZQ , (2016) THE DNA DAMAGE RESPONSE MOLECULE MCPH1 IN BRAIN DEVELOPMENT AND BEYOND.ACTA BIOCHIMICA ET BIOPHYSICA SINICA. VOL. 48. ISSUE 7. P. 678 -685 | 44 | 88% | 1 |
9 | BARBELANNE, M , TSANG, WY , (2014) MOLECULAR AND CELLULAR BASIS OF AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY.BIOMED RESEARCH INTERNATIONAL. VOL. . ISSUE . P. - | 77 | 47% | 15 |
10 | 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 |
Classes with closest relation at Level 2 |