Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
12679 | 888 | 20.8 | 57% |
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 |
3549 | 2 | ARTHROGRYPOSIS//FREEMAN SHELDON SYNDROME//DISTAL ARTHROGRYPOSIS | 1350 |
12679 | 1 | ARTHROGRYPOSIS//FREEMAN SHELDON SYNDROME//AMYOPLASIA | 888 |
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 | ARTHROGRYPOSIS | authKW | 1386918 | 12% | 39% | 103 |
2 | FREEMAN SHELDON SYNDROME | authKW | 741053 | 3% | 86% | 25 |
3 | AMYOPLASIA | authKW | 673688 | 3% | 85% | 23 |
4 | NEU LAXOVA SYNDROME | authKW | 659295 | 2% | 91% | 21 |
5 | DISTAL ARTHROGRYPOSIS | authKW | 657494 | 3% | 68% | 28 |
6 | ARTHROGRYPOSIS MULTIPLEX CONGENITA | authKW | 653760 | 4% | 51% | 37 |
7 | RESTRICTIVE DERMOPATHY | authKW | 606315 | 3% | 77% | 23 |
8 | MULTIPLE PTERYGIUM SYNDROME | authKW | 591094 | 2% | 90% | 19 |
9 | FETAL AKINESIA DEFORMATION SEQUENCE | authKW | 451689 | 2% | 77% | 17 |
10 | MARDEN WALKER SYNDROME | authKW | 429810 | 2% | 83% | 15 |
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 | 7236 | 38% | 0% | 335 |
2 | Pediatrics | 3115 | 21% | 0% | 186 |
3 | Orthopedics | 3038 | 16% | 0% | 143 |
4 | Obstetrics & Gynecology | 1119 | 11% | 0% | 101 |
5 | Medical Ethics | 342 | 1% | 0% | 11 |
6 | Surgery | 276 | 11% | 0% | 102 |
7 | Clinical Neurology | 235 | 9% | 0% | 76 |
8 | Pathology | 204 | 5% | 0% | 44 |
9 | Anesthesiology | 182 | 3% | 0% | 27 |
10 | Acoustics | 103 | 2% | 0% | 21 |
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 PRECURSORY EMBRYON SCI TECH | 68770 | 0% | 100% | 2 |
2 | WELLCHILD PAEDIAT | 61891 | 0% | 60% | 3 |
3 | AHMANSON PEDIATSTEVEN SPIELBERG PED | 34385 | 0% | 100% | 1 |
4 | ALL INDIA | 34385 | 0% | 100% | 1 |
5 | CARDIOGENET MYOGENET MOL CELLULAIRE | 34385 | 0% | 100% | 1 |
6 | CHIEF NEUROMUSCULAR CLIN | 34385 | 0% | 100% | 1 |
7 | CHU PARIS SUD BICETRE | 34385 | 0% | 100% | 1 |
8 | CHU PARIS SUD BICETRE ASSISTANCE PUBL | 34385 | 0% | 100% | 1 |
9 | COCUK GENET UNITESI | 34385 | 0% | 100% | 1 |
10 | DR ENRIQUE CORONA RIVERA HUMAN GENET MO | 34385 | 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 | AMERICAN JOURNAL OF MEDICAL GENETICS | 55702 | 13% | 1% | 119 |
2 | CLINICAL DYSMORPHOLOGY | 16283 | 3% | 2% | 23 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 12574 | 5% | 1% | 46 |
4 | JOURNAL OF PEDIATRIC ORTHOPAEDICS | 8722 | 4% | 1% | 36 |
5 | CLINICAL GENETICS | 5646 | 3% | 1% | 29 |
6 | PRENATAL DIAGNOSIS | 5500 | 3% | 1% | 30 |
7 | GENETIC COUNSELING | 4400 | 1% | 1% | 11 |
8 | JOURNAL OF MEDICAL GENETICS | 3390 | 3% | 0% | 24 |
9 | NEUROPEDIATRICS | 2420 | 1% | 1% | 12 |
10 | JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B | 2237 | 1% | 1% | 11 |
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 | ARTHROGRYPOSIS | 1386918 | 12% | 39% | 103 | Search ARTHROGRYPOSIS | Search ARTHROGRYPOSIS |
2 | FREEMAN SHELDON SYNDROME | 741053 | 3% | 86% | 25 | Search FREEMAN+SHELDON+SYNDROME | Search FREEMAN+SHELDON+SYNDROME |
3 | AMYOPLASIA | 673688 | 3% | 85% | 23 | Search AMYOPLASIA | Search AMYOPLASIA |
4 | NEU LAXOVA SYNDROME | 659295 | 2% | 91% | 21 | Search NEU+LAXOVA+SYNDROME | Search NEU+LAXOVA+SYNDROME |
5 | DISTAL ARTHROGRYPOSIS | 657494 | 3% | 68% | 28 | Search DISTAL+ARTHROGRYPOSIS | Search DISTAL+ARTHROGRYPOSIS |
6 | ARTHROGRYPOSIS MULTIPLEX CONGENITA | 653760 | 4% | 51% | 37 | Search ARTHROGRYPOSIS+MULTIPLEX+CONGENITA | Search ARTHROGRYPOSIS+MULTIPLEX+CONGENITA |
7 | RESTRICTIVE DERMOPATHY | 606315 | 3% | 77% | 23 | Search RESTRICTIVE+DERMOPATHY | Search RESTRICTIVE+DERMOPATHY |
8 | MULTIPLE PTERYGIUM SYNDROME | 591094 | 2% | 90% | 19 | Search MULTIPLE+PTERYGIUM+SYNDROME | Search MULTIPLE+PTERYGIUM+SYNDROME |
9 | FETAL AKINESIA DEFORMATION SEQUENCE | 451689 | 2% | 77% | 17 | Search FETAL+AKINESIA+DEFORMATION+SEQUENCE | Search FETAL+AKINESIA+DEFORMATION+SEQUENCE |
10 | MARDEN WALKER SYNDROME | 429810 | 2% | 83% | 15 | Search MARDEN+WALKER+SYNDROME | Search MARDEN+WALKER+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 | HALL, JG , (2009) PENA-SHOKEIR PHENOTYPE (FETAL AKINESIA DEFORMATION SEQUENCE) REVISITED.BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY. VOL. 85. ISSUE 8. P. 677 -694 | 75 | 73% | 23 |
2 | KOWALCZYK, B , FELUS, J , (2016) ARTHROGRYPOSIS: AN UPDATE ON CLINICAL ASPECTS, ETIOLOGY, AND TREATMENT STRATEGIES.ARCHIVES OF MEDICAL SCIENCE. VOL. 12. ISSUE 1. P. 10 -24 | 56 | 61% | 1 |
3 | CHEN, CP , (2012) PRENATAL DIAGNOSIS AND GENETIC ANALYSIS OF FETAL AKINESIA DEFORMATION SEQUENCE AND MULTIPLE PTERYGIUM SYNDROME ASSOCIATED WITH NEUROMUSCULAR JUNCTION DISORDERS: A REVIEW.TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. VOL. 51. ISSUE 1. P. 12 -17 | 48 | 79% | 10 |
4 | OBERLECHNER, E , SEIDEL, H , SCHRAMM, T , REHDER, H , GULLOTTA, F , STECHELE, F , HOGEL, B , ROTHEMUND, E , FICHTEL, G , (1994) FETAL AKINESIA-HYPOKINESIA SEQUENCE (PENA-SHOKEIR PHENOTYPE).GEBURTSHILFE UND FRAUENHEILKUNDE. VOL. 54. ISSUE 5. P. 276-285 | 56 | 78% | 6 |
5 | HALL, JG , ALDINGER, KA , TANAKA, KI , (2014) AMYOPLASIA REVISITED.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 3. P. 700 -730 | 46 | 44% | 8 |
6 | KIMBER, E , TAJSHARGHI, H , KROKSMARK, AK , OLDFORS, A , TULINIUS, M , (2012) DISTAL ARTHROGRYPOSIS: CLINICAL AND GENETIC FINDINGS.ACTA PAEDIATRICA. VOL. 101. ISSUE 8. P. 877 -887 | 25 | 83% | 8 |
7 | HALL, JG , (2014) AMYOPLASIA INVOLVING ONLY THE UPPER LIMBS OR ONLY INVOLVING THE LOWER LIMBS WITH REVIEW OF THE RELEVANT DIFFERENTIAL DIAGNOSES.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 4. P. 859 -873 | 36 | 55% | 0 |
8 | HOELLEN, F , SCHROER, A , KELLING, K , KRAPP, M , AXT-FLIEDNER, R , GEMBRUCH, U , WEICHERT, J , (2011) ARTHROGRYPOSIS MULTIPLEX CONGENITA AND PENA-SHOKEIR PHENOTYPE: CHALLENGE OF PRENATAL DIAGNOSIS - REPORT OF 21 CASES, ANTENATAL FINDINGS AND REVIEW.FETAL DIAGNOSIS AND THERAPY. VOL. 30. ISSUE 4. P. 289-298 | 22 | 92% | 3 |
9 | LI, XF , JIANG, M , HAN, WT , ZHAO, N , LIU, W , SUI, Y , LU, YP , LI, JX , (2013) A NOVEL TNNI2 MUTATION CAUSES FREEMAN-SHELDON SYNDROME IN A CHINESE FAMILY WITH AN AFFECTED ADULT WITH ONLY FACIAL CONTRACTURES.GENE. VOL. 527. ISSUE 2. P. 630-635 | 19 | 100% | 3 |
10 | MANNING, MA , CUNNIFF, CM , COLBY, CE , EL-SAYED, YY , HOYME, HE , (2004) NEU-LAXOVA SYNDROME: DETAILED PRENATAL DIAGNOSTIC AND POST-MORTEM FINDINGS AND LITERATURE REVIEW.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 125A. ISSUE 3. P. 240-249 | 23 | 100% | 19 |
Classes with closest relation at Level 1 |