Class information for:
Level 2: ARTHROGRYPOSIS//FREEMAN SHELDON SYNDROME//DISTAL ARTHROGRYPOSIS

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
3549 1350 21.6 53%


Bar chart of Publication_year

Last years might be incomplete

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
33304 1                   COMPUTER ASSISTED DIAGNOSIS COMPUTER AIDED//CONGENITAL MALFORMATION SYNDROMES//DYSMORPHOLOGY DATABASE 126
34428 1                   GRADE OF MEMBERSHIP//GRADE OF MEMBERSHIP ANALYSIS//DEMOG STUDIES 111
35992 1                   HYDRANENCEPHALY//FOWLER SYNDROME//FLVCR2 88
36093 1                   CHRONIC NK CELL LEUKEMIA//FAMILY NODECODES//IDENTITY STATES 86
37662 1                   NALCN//ABNORMAL RESPIRATORY RHYTHM//ADDIC MENTAL HLTH 51

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 966132 8% 40% 106
2 FREEMAN SHELDON SYNDROME authKW 487431 2% 86% 25
3 DISTAL ARTHROGRYPOSIS authKW 463910 2% 71% 29
4 AMYOPLASIA authKW 443121 2% 85% 23
5 NEU LAXOVA SYNDROME authKW 433655 2% 91% 21
6 ARTHROGRYPOSIS MULTIPLEX CONGENITA authKW 430004 3% 51% 37
7 RESTRICTIVE DERMOPATHY authKW 398805 2% 77% 23
8 MULTIPLE PTERYGIUM SYNDROME authKW 388796 1% 90% 19
9 FETAL AKINESIA DEFORMATION SEQUENCE authKW 371121 1% 86% 19
10 MARDEN WALKER SYNDROME authKW 282709 1% 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 7563 32% 0% 426
2 Pediatrics 3372 18% 0% 241
3 Orthopedics 1906 11% 0% 143
4 Obstetrics & Gynecology 919 9% 0% 116
5 Clinical Neurology 338 8% 0% 113
6 Medical Ethics 261 1% 0% 12
7 Pathology 221 4% 0% 58
8 Surgery 169 8% 0% 111
9 Medical Informatics 159 1% 0% 20
10 Anesthesiology 113 2% 0% 28

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 ANATOMOFOETOPATHOL 45234 0% 100% 2
2 GENET PRECURSORY EMBRYON SCI TECH 45234 0% 100% 2
3 WELLCHILD PAEDIAT 40708 0% 60% 3
4 DEMOG STUDIES 33057 1% 9% 16
5 ADDIC MENTAL HLTH 22617 0% 100% 1
6 AHMANSON PEDIATSTEVEN SPIELBERG PED 22617 0% 100% 1
7 ALL INDIA 22617 0% 100% 1
8 AREA RIC GENET MALATTIE RARE 22617 0% 100% 1
9 BENFEY DURHAM 22617 0% 100% 1
10 CARDIOGENET MYOGENET MOL CELLULAIRE 22617 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 48496 10% 2% 137
2 CLINICAL DYSMORPHOLOGY 11647 2% 2% 24
3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 10954 4% 1% 53
4 JOURNAL OF PEDIATRIC ORTHOPAEDICS 5712 3% 1% 36
5 CLINICAL GENETICS 4505 2% 1% 32
6 JOURNAL OF MEDICAL GENETICS 3956 2% 1% 32
7 PRENATAL DIAGNOSIS 3844 2% 1% 31
8 GENETIC COUNSELING 2887 1% 1% 11
9 INFORMATION SCIENCES-APPLICATIONS 2441 0% 5% 2
10 AMERICAN JOURNAL OF HUMAN GENETICS 2164 2% 0% 28

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 966132 8% 40% 106 Search ARTHROGRYPOSIS Search ARTHROGRYPOSIS
2 FREEMAN SHELDON SYNDROME 487431 2% 86% 25 Search FREEMAN+SHELDON+SYNDROME Search FREEMAN+SHELDON+SYNDROME
3 DISTAL ARTHROGRYPOSIS 463910 2% 71% 29 Search DISTAL+ARTHROGRYPOSIS Search DISTAL+ARTHROGRYPOSIS
4 AMYOPLASIA 443121 2% 85% 23 Search AMYOPLASIA Search AMYOPLASIA
5 NEU LAXOVA SYNDROME 433655 2% 91% 21 Search NEU+LAXOVA+SYNDROME Search NEU+LAXOVA+SYNDROME
6 ARTHROGRYPOSIS MULTIPLEX CONGENITA 430004 3% 51% 37 Search ARTHROGRYPOSIS+MULTIPLEX+CONGENITA Search ARTHROGRYPOSIS+MULTIPLEX+CONGENITA
7 RESTRICTIVE DERMOPATHY 398805 2% 77% 23 Search RESTRICTIVE+DERMOPATHY Search RESTRICTIVE+DERMOPATHY
8 MULTIPLE PTERYGIUM SYNDROME 388796 1% 90% 19 Search MULTIPLE+PTERYGIUM+SYNDROME Search MULTIPLE+PTERYGIUM+SYNDROME
9 FETAL AKINESIA DEFORMATION SEQUENCE 371121 1% 86% 19 Search FETAL+AKINESIA+DEFORMATION+SEQUENCE Search FETAL+AKINESIA+DEFORMATION+SEQUENCE
10 MARDEN WALKER SYNDROME 282709 1% 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 78 76% 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 57 79% 6
5 CHONG, JX , MCMILLIN, MJ , SHIVELY, KM , BECK, AE , MARVIN, CT , ARMENTEROS, JR , BUCKINGHAM, KJ , NKINSI, NT , BOYLE, EA , BERRY, MN , ET AL (2015) DE NOVO MUTATIONS IN NALCN CAUSE A SYNDROME CHARACTERIZED BY CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY.AMERICAN JOURNAL OF HUMAN GENETICS. VOL. 96. ISSUE 3. P. 462 -473 27 60% 20
6 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
7 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
8 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
9 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
10 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

Classes with closest relation at Level 2


Rank Class id link
1 3382 LISSENCEPHALY//SECKEL SYNDROME//LIS1
2 2244 CLUBFOOT//HIGH TIBIAL OSTEOTOMY//JOURNAL OF PEDIATRIC ORTHOPAEDICS
3 1564 DISTRACTION OSTEOGENESIS//HEMIFACIAL MICROSOMIA//PIERRE ROBIN SEQUENCE
4 2658 ACHONDROPLASIA//SKELETAL DYSPLASIA//HYPOCHONDROPLASIA
5 1857 TITIN//INCLUSION BODY MYOSITIS//NEMALINE MYOPATHY
6 2940 CHYLOTHORAX//CHYLOUS ASCITES//THORACIC DUCT
7 2436 LAMIN//LAMINOPATHY//NUCLEAR ENVELOPE
8 1735 SPINAL MUSCULAR ATROPHY//CHARCOT MARIE TOOTH DISEASE//NEUROFILAMENT
9 1063 NUCHAL TRANSLUCENCY//PRENATAL DIAGNOSIS//PRENATAL SCREENING
10 2848 CHARGE SYNDROME//CHOANAL ATRESIA//AICARDI SYNDROME

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