Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
32581 | 137 | 14.9 | 45% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
14 | 4 | ORTHOPEDICS//DENTISTRY, ORAL SURGERY & MEDICINE//SPORT SCIENCES | 808941 |
474 | 3 | CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS | 23888 |
1564 | 2 | DISTRACTION OSTEOGENESIS//HEMIFACIAL MICROSOMIA//PIERRE ROBIN SEQUENCE | 7357 |
32581 | 1 | CEREBRO COSTO MANDIBULAR SYNDROME//MALPUECH SYNDROME//MICHELS SYNDROME | 137 |
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 | CEREBRO COSTO MANDIBULAR SYNDROME | authKW | 4011970 | 13% | 100% | 18 |
2 | MALPUECH SYNDROME | authKW | 2451760 | 8% | 100% | 11 |
3 | MICHELS SYNDROME | authKW | 1337323 | 4% | 100% | 6 |
4 | JUBERG HAYWARD SYNDROME | authKW | 891549 | 3% | 100% | 4 |
5 | CARNEVALE SYNDROME | authKW | 668662 | 2% | 100% | 3 |
6 | RIB DEFECTS | authKW | 501495 | 2% | 75% | 3 |
7 | AMINOPTERIN LIKE SYNDROME | authKW | 445774 | 1% | 100% | 2 |
8 | CCM SYNDROME | authKW | 445774 | 1% | 100% | 2 |
9 | CRANE HEISE SYNDROME | authKW | 445774 | 1% | 100% | 2 |
10 | OROCRANIODIGITAL SYNDROME | authKW | 445774 | 1% | 100% | 2 |
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 | 2903 | 60% | 0% | 82 |
2 | Pediatrics | 300 | 17% | 0% | 23 |
3 | Anthropology | 235 | 7% | 0% | 9 |
4 | Dermatology | 51 | 5% | 0% | 7 |
5 | Biology | 34 | 5% | 0% | 7 |
6 | Obstetrics & Gynecology | 28 | 5% | 0% | 7 |
7 | Radiology, Nuclear Medicine & Medical Imaging | 26 | 7% | 0% | 9 |
8 | Medical Laboratory Technology | 7 | 1% | 0% | 2 |
9 | Orthopedics | 4 | 2% | 0% | 3 |
10 | Medicine, General & Internal | 4 | 4% | 0% | 6 |
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 | DENIS DIDEROT MED U676 | 222887 | 1% | 100% | 1 |
2 | E676 | 222887 | 1% | 100% | 1 |
3 | FETAL WELF | 222887 | 1% | 100% | 1 |
4 | MED MED INTERNA SERV | 222887 | 1% | 100% | 1 |
5 | N E THAMES REG GENET | 222887 | 1% | 100% | 1 |
6 | PAEDIAT DENTO IAL SURG | 222887 | 1% | 100% | 1 |
7 | PEDIAT OPHTHALMOL STRABISMUS SEVICES | 222887 | 1% | 100% | 1 |
8 | SALUD CARLOS IIIECEMC CIAC | 222887 | 1% | 100% | 1 |
9 | SORBONNE PARIS CITE IMAGINEINSERMU1163DEP | 222887 | 1% | 100% | 1 |
10 | UNIDAD PREVENC MINUSVALIAS | 222887 | 1% | 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 | CLINICAL DYSMORPHOLOGY | 12789 | 6% | 1% | 8 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 6531 | 9% | 0% | 13 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS | 6523 | 12% | 0% | 16 |
4 | HUMAN HEREDITY | 3891 | 4% | 0% | 6 |
5 | HUMAN BIOLOGY | 2957 | 4% | 0% | 5 |
6 | JAPANESE JOURNAL OF HUMAN GENETICS | 1734 | 1% | 0% | 2 |
7 | REVISTA BRASILEIRA DE GENETICA | 1123 | 1% | 0% | 2 |
8 | PEDIATRIC DERMATOLOGY | 961 | 3% | 0% | 4 |
9 | CONGENITAL ANOMALIES | 935 | 1% | 0% | 1 |
10 | BRAZILIAN JOURNAL OF GENETICS | 931 | 1% | 0% | 1 |
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 | CEREBRO COSTO MANDIBULAR SYNDROME | 4011970 | 13% | 100% | 18 | Search CEREBRO+COSTO+MANDIBULAR+SYNDROME | Search CEREBRO+COSTO+MANDIBULAR+SYNDROME |
2 | MALPUECH SYNDROME | 2451760 | 8% | 100% | 11 | Search MALPUECH+SYNDROME | Search MALPUECH+SYNDROME |
3 | MICHELS SYNDROME | 1337323 | 4% | 100% | 6 | Search MICHELS+SYNDROME | Search MICHELS+SYNDROME |
4 | JUBERG HAYWARD SYNDROME | 891549 | 3% | 100% | 4 | Search JUBERG+HAYWARD+SYNDROME | Search JUBERG+HAYWARD+SYNDROME |
5 | CARNEVALE SYNDROME | 668662 | 2% | 100% | 3 | Search CARNEVALE+SYNDROME | Search CARNEVALE+SYNDROME |
6 | RIB DEFECTS | 501495 | 2% | 75% | 3 | Search RIB+DEFECTS | Search RIB+DEFECTS |
7 | AMINOPTERIN LIKE SYNDROME | 445774 | 1% | 100% | 2 | Search AMINOPTERIN+LIKE+SYNDROME | Search AMINOPTERIN+LIKE+SYNDROME |
8 | CCM SYNDROME | 445774 | 1% | 100% | 2 | Search CCM+SYNDROME | Search CCM+SYNDROME |
9 | CRANE HEISE SYNDROME | 445774 | 1% | 100% | 2 | Search CRANE+HEISE+SYNDROME | Search CRANE+HEISE+SYNDROME |
10 | OROCRANIODIGITAL SYNDROME | 445774 | 1% | 100% | 2 | Search OROCRANIODIGITAL+SYNDROME | Search OROCRANIODIGITAL+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 | TOOLEY, M , LYNCH, D , BERNIER, F , PARBOOSINGH, J , BHOJ, E , ZACKAI, E , CALDER, A , ITASAKI, N , WAKELING, E , SCOTT, R , ET AL (2016) CEREBRO-COSTO-MANDIBULAR SYNDROME: CLINICAL, RADIOLOGICAL, AND GENETIC FINDINGS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 170. ISSUE 5. P. 1115 -1126 | 18 | 75% | 0 |
2 | JAMES, PA , AFTIMOS, S , (2003) FAMILIAL CEREBRO-COSTO-MANDIBULAR SYNDROME: A CASE WITH UNUSUAL PRENATAL FINDINGS AND REVIEW.CLINICAL DYSMORPHOLOGY. VOL. 12. ISSUE 1. P. 63-68 | 14 | 100% | 8 |
3 | MATIC, A , VELISAVLJEV-FILIPOVIC, G , LOVRENSKI, J , GAJDOBRANSKI, D , (2016) A CASE OF SEVERE TYPE OF CEREBRO-COSTO-MANDIBULAR SYNDROME.SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO. VOL. 144. ISSUE 7-8. P. 431 -435 | 13 | 72% | 0 |
4 | AL KAISSI, A , KLAUSHOFER, K , SAFI, H , BEN CHEHIDA, F , BEN GHACHEM, M , CHAABOUNNI, M , HENNEKAM, RCM , (2007) ASYMMETRICAL SKULL, PTOSIS, HYPERTELORISM, HIGH NASAL BRIDGE, CLEFTING, UMBILICAL ANOMALIES, AND SKELETAL ANOMALIES IN SIBS: IS CARNEVALE SYNDROME A SEPARATE ENTITY?.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 143A. ISSUE 4. P. 349 -354 | 11 | 100% | 9 |
5 | ZEEVAERT, R , FOULQUIER, F , DIMITROV, B , REYNDERS, E , VAN DAMME-LOMBAERTS, R , SIMEONOV, E , ANNAERT, W , MATTHIJS, G , JAEKEN, J , (2009) CEREBROCOSTOMANDIBULAR-LIKE SYNDROME AND A MUTATION IN THE CONSERVED OLIGOMERIC GOLGI COMPLEX, SUBUNIT 1.HUMAN MOLECULAR GENETICS. VOL. 18. ISSUE 3. P. 517-524 | 17 | 55% | 15 |
6 | MEGIER, P , AYEVA-DERMAN, M , ESPERANDIEU, O , AUBRY, MC , COULY, G , DESROCHES, A , (1998) PRENATAL ULTRASONOGRAPHIC DIAGNOSIS OF THE CEREBRO-COSTO-MANDIBULAR SYNDROME: CASE REPORT AND REVIEW OF THE LITERATURE.PRENATAL DIAGNOSIS. VOL. 18. ISSUE 12. P. 1294-1299 | 13 | 100% | 10 |
7 | NAGASAWA, H , YAMAMOTO, Y , KOHNO, Y , (2010) CEREBRO-COSTO-MANDIBULAR SYNDROME: PROGNOSIS AND PROPOSAL FOR CLASSIFICATION.CONGENITAL ANOMALIES. VOL. 50. ISSUE 3. P. 171 -174 | 10 | 83% | 6 |
8 | VAN DEN ENDE, JJ , SCHRANDER-STUMPEL, C , RUPPRECHT, E , MEINECKE, P , MAROTEAUX, P , DE DIE-SMULDERS, C , HAMEL, BCJ , (1998) THE CEREBRO-COSTO-MANDIBULAR SYNDROME: SEVEN PATIENTS AND REVIEW OF THE LITERATURE.CLINICAL DYSMORPHOLOGY. VOL. 7. ISSUE 2. P. 87-95 | 12 | 92% | 18 |
9 | KRAOUA, L , CAPRI, Y , PERRIN, L , BENMANSOUR, A , VERLOES, A , (2012) PSEUDOAMINOPTERIN SYNDROME.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 158A. ISSUE 9. P. 2233-2238 | 14 | 54% | 0 |
10 | COUVREUR-LIONNAIS, S , ROUSSEAU, T , LAURENT, N , THAUVIN-ROBINET, C , SENET-LACOMBE, E , DELEZOIDE, AL , MUGNERET, F , DURAND, C , FAIVRE, L , SAGOT, P , (2005) PRENATAL DIAGNOSIS OF JUBERG-HAYWARD SYNDROME.PRENATAL DIAGNOSIS. VOL. 25. ISSUE 2. P. 172-175 | 9 | 90% | 1 |
Classes with closest relation at Level 1 |