Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
20430 | 461 | 28.8 | 66% |
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 |