Class information for:
Level 1: PROXIMAL SYMPHALANGISM//SYMPHALANGISM//NOG

Basic class information

Class id #P Avg. number of
references
Database coverage
of references
20430 461 28.8 66%



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
0 4 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
27 3       DEVELOPMENTAL BIOLOGY//DEVELOPMENT//AGR2 109777
1072 2             TGF BETA//SMAD//ENDOGLIN 9938
20430 1                   PROXIMAL SYMPHALANGISM//SYMPHALANGISM//NOG 461

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 PROXIMAL SYMPHALANGISM authKW 799564 3% 93% 13
2 SYMPHALANGISM authKW 678248 3% 64% 16
3 NOG authKW 647953 3% 65% 15
4 BRACHYDACTYLY TYPE C authKW 596126 2% 100% 9
5 GDF 5 authKW 588744 4% 44% 20
6 FACIOAUDIOSYMPHALANGISM SYNDROME authKW 529890 2% 100% 8
7 GDF5 authKW 508662 5% 32% 24
8 NOG GENE authKW 471011 2% 89% 8
9 ACROMESOMELIC DYSPLASIA authKW 447090 2% 75% 9
10 GROWTH DIFFERENTIATION FACTOR 5 authKW 420772 4% 35% 18

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 4819 43% 0% 196
2 Orthopedics 378 8% 0% 38
3 Developmental Biology 246 5% 0% 23
4 Dentistry, Oral Surgery & Medicine 194 6% 0% 26
5 Anatomy & Morphology 144 3% 0% 12
6 Pediatrics 92 6% 0% 27
7 Medical Ethics 85 1% 0% 4
8 Otorhinolaryngology 84 3% 0% 15
9 Rheumatology 74 3% 0% 12
10 Endocrinology & Metabolism 66 6% 0% 27

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 LEHRSTUHL PHYSIOL CHEM 2 151386 2% 29% 8
2 GRP DEV DIS 113539 1% 29% 6
3 BERLIN BRANDENBURG REGENERAT THER IES BSRT 82215 1% 21% 6
4 BOVERI BIOSCI PHYSIOL CHEM 2 66236 0% 100% 1
5 CLIN DEVSHINJYUKU KU 66236 0% 100% 1
6 DENT MED ORAL REHABIL BIOMAT SKELETAL 66236 0% 100% 1
7 E ONTARIO REG GENET PROGRAMME 66236 0% 100% 1
8 GENET NEPHROL HYPERTENS VASC INJURY 66236 0% 100% 1
9 GENKARTIERUNGSZENTRUM 66236 0% 100% 1
10 HEADQUARTER HEIDELBERG 66236 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 12095 9% 0% 40
2 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 7156 5% 0% 25
3 JOURNAL DE GENETIQUE HUMAINE 5690 1% 2% 4
4 GROWTH FACTORS 4074 2% 1% 7
5 EUROPEAN JOURNAL OF MEDICAL GENETICS 3716 2% 1% 8
6 CLINICAL GENETICS 2910 3% 0% 15
7 CLINICAL DYSMORPHOLOGY 2900 2% 1% 7
8 JOURNAL OF MEDICAL GENETICS 1917 3% 0% 13
9 PEDIATRIC RADIOLOGY 1407 3% 0% 12
10 GENETIC COUNSELING 1118 1% 0% 4

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 PROXIMAL SYMPHALANGISM 799564 3% 93% 13 Search PROXIMAL+SYMPHALANGISM Search PROXIMAL+SYMPHALANGISM
2 SYMPHALANGISM 678248 3% 64% 16 Search SYMPHALANGISM Search SYMPHALANGISM
3 NOG 647953 3% 65% 15 Search NOG Search NOG
4 BRACHYDACTYLY TYPE C 596126 2% 100% 9 Search BRACHYDACTYLY+TYPE+C Search BRACHYDACTYLY+TYPE+C
5 GDF 5 588744 4% 44% 20 Search GDF+5 Search GDF+5
6 FACIOAUDIOSYMPHALANGISM SYNDROME 529890 2% 100% 8 Search FACIOAUDIOSYMPHALANGISM+SYNDROME Search FACIOAUDIOSYMPHALANGISM+SYNDROME
7 GDF5 508662 5% 32% 24 Search GDF5 Search GDF5
8 NOG GENE 471011 2% 89% 8 Search NOG+GENE Search NOG+GENE
9 ACROMESOMELIC DYSPLASIA 447090 2% 75% 9 Search ACROMESOMELIC+DYSPLASIA Search ACROMESOMELIC+DYSPLASIA
10 GROWTH DIFFERENTIATION FACTOR 5 420772 4% 35% 18 Search GROWTH+DIFFERENTIATION+FACTOR+5 Search GROWTH+DIFFERENTIATION+FACTOR+5

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 JIN, L , LI, XD , (2013) GROWTH DIFFERENTIATION FACTOR 5 REGULATION IN BONE REGENERATION.CURRENT PHARMACEUTICAL DESIGN. VOL. 19. ISSUE 19. P. 3364-3373 58 51% 4
2 COLEMAN, CM , SCHEREMETA, BH , BOYCE, AT , MAUCK, RL , TUAN, RS , (2011) DELAYED FRACTURE HEALING IN GROWTH DIFFERENTIATION FACTOR 5-DEFICIENT MICE: A PILOT STUDY.CLINICAL ORTHOPAEDICS AND RELATED RESEARCH. VOL. 469. ISSUE 10. P. 2915-2924 36 77% 3
3 VAN DEN ENDE, JJ , BORRA, V , VAN HUL, W , (2013) NEGATIVE MUTATION SCREENING OF THE NOG, BMPR1B, GDF5, AND FGF9 GENES INDICATES FURTHER GENETIC HETEROGENEITY OF THE FACIOAUDIOSYMPHALANGISM SYNDROME.CLINICAL DYSMORPHOLOGY. VOL. 22. ISSUE 1. P. 1-6 27 93% 2
4 POTTI, TA , PETTY, EM , LESPERANCE, MM , (2011) A COMPREHENSIVE REVIEW OF REPORTED HERITABLE NOGGIN-ASSOCIATED SYNDROMES AND PROPOSED CLINICAL UTILITY OF ONE BROADLY INCLUSIVE DIAGNOSTIC TERM: NOG-RELATED-SYMPHALANGISM SPECTRUM DISORDER (NOG-SSD).HUMAN MUTATION. VOL. 32. ISSUE 8. P. 877 -886 38 63% 24
5 ISHINO, T , TAKENO, S , HIRAKAWA, K , (2015) NOVEL NOG MUTATION IN JAPANESE PATIENTS WITH STAPES ANKYLOSIS WITH BROAD THUMBS AND TOES.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 58. ISSUE 9. P. 427 -432 22 92% 1
6 BYRNES, AM , RACACHO, L , NIKKEL, SM , XIAO, FX , MACDONALD, H , UNDERHILL, TM , BULMAN, DE , (2010) MUTATIONS IN GDF5 PRESENTING AS SEMIDOMINANT BRACHYDACTYLY A1.HUMAN MUTATION. VOL. 31. ISSUE 10. P. 1155-1162 31 69% 14
7 AL-QATTAN, MM , AL-MOTAIRI, MI , AL BALWI, MA , (2015) TWO NOVEL HOMOZYGOUS MISSENSE MUTATIONS IN THE GDF5 GENE CAUSE BRACHYDACTYLY TYPE C.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 167. ISSUE 7. P. 1621 -1626 20 91% 4
8 THOMEER, HGXM , ADMIRAAL, RJC , HOEFSLOOT, L , KUNST, HPM , CREMERS, CWRJ , (2011) PROXIMAL SYMPHALANGISM, HYPEROPIA, CONDUCTIVE HEARING IMPAIRMENT, AND THE NOG GENE: 2 NEW MUTATIONS.OTOLOGY & NEUROTOLOGY. VOL. 32. ISSUE 4. P. 632 -638 24 86% 6
9 RACACHO, L , BYRNES, AM , MACDONALD, H , DRANSE, HJ , NIKKEL, SM , ALLANSON, J , ROSSER, E , UNDERHILL, TM , BULMAN, DE , (2015) TWO NOVEL DISEASE-CAUSING VARIANTS IN BMPR1B ARE ASSOCIATED WITH BRACHYDACTYLY TYPE A1.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 23. ISSUE 12. P. 1640 -1645 28 62% 3
10 USAMI, S , ABE, S , NISHIO, S , SAKURAI, Y , KOJIMA, H , TONO, T , SUZUKI, N , (2012) MUTATIONS IN THE NOG GENE ARE COMMONLY FOUND IN CONGENITAL STAPES ANKYLOSIS WITH SYMPHALANGISM, BUT NOT IN OTOSCLEROSIS.CLINICAL GENETICS. VOL. 82. ISSUE 6. P. 514 -520 19 95% 8

Classes with closest relation at Level 1



Rank Class id link
1 29076 MIIP//BETAGLYCAN//T BETA RIII
2 8983 SOX9//CHONDROCYTE DIFFERENTIATION//IHH
3 27105 LARSEN SYNDROME//CONGENITAL DISLOCATION OF THE KNEE//DESBUQUOIS DYSPLASIA
4 22902 SHOX//LERI WEILL DYSCHONDROSTEOSIS//SHOX GENE
5 1542 BONE MORPHOGENETIC PROTEIN//RHBMP 2//BONE INDUCTION
6 11314 HAND OSTEOARTHRITIS//EROSIVE OSTEOARTHRITIS//HAND OA
7 12726 BONE MORPHOGENETIC PROTEIN 9//BMP9//BONE MORPHOGENETIC PROTEIN
8 20102 TARSAL COALITION//CALCANEONAVICULAR COALITION//TALOCALCANEAL COALITION
9 3672 LIMB DEVELOPMENT//APICAL ECTODERMAL RIDGE//LIMB
10 17760 WNT5A//ROR2//ROBINOW SYNDROME

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