Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
14232 | 783 | 35.6 | 81% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
6 | 4 | GASTROENTEROLOGY & HEPATOLOGY//ONCOLOGY//SURGERY | 1371034 |
139 | 3 | THYROID//THYROID CANCER//GRAVES DISEASE | 64904 |
224 | 2 | GRAVES DISEASE//THYROID//CONGENITAL HYPOTHYROIDISM | 20534 |
14232 | 1 | THYROID DYSGENESIS//THYROID HEMIAGENESIS//BENIGN HEREDITARY CHOREA | 783 |
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 | THYROID DYSGENESIS | authKW | 959883 | 5% | 62% | 40 |
2 | THYROID HEMIAGENESIS | authKW | 917040 | 3% | 87% | 27 |
3 | BENIGN HEREDITARY CHOREA | authKW | 748723 | 3% | 80% | 24 |
4 | CONGENITAL HYPOTHYROIDISM | authKW | 607947 | 12% | 16% | 96 |
5 | DUOX | authKW | 483937 | 3% | 56% | 22 |
6 | DUOX2 | authKW | 383953 | 2% | 62% | 16 |
7 | DUAL OXIDASE | authKW | 254762 | 2% | 47% | 14 |
8 | THYROID DEVELOPMENT | authKW | 243721 | 1% | 63% | 10 |
9 | TITF 1 | authKW | 243721 | 1% | 63% | 10 |
10 | BRAIN THYROID LUNG SYNDROME | authKW | 233979 | 1% | 100% | 6 |
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 | Endocrinology & Metabolism | 10450 | 44% | 0% | 348 |
2 | Pediatrics | 427 | 9% | 0% | 70 |
3 | Developmental Biology | 251 | 4% | 0% | 31 |
4 | Biochemistry & Molecular Biology | 200 | 17% | 0% | 136 |
5 | Cell Biology | 162 | 9% | 0% | 73 |
6 | Genetics & Heredity | 106 | 6% | 0% | 49 |
7 | Clinical Neurology | 96 | 6% | 0% | 50 |
8 | Anatomy & Morphology | 62 | 1% | 0% | 11 |
9 | Medical Laboratory Technology | 22 | 1% | 0% | 9 |
10 | Respiratory System | 19 | 2% | 0% | 15 |
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 | ECCELLENZA AMBISEN | 126337 | 1% | 36% | 9 |
2 | ENDOCRINOL GENET METAB PEDIAT | 116990 | 0% | 100% | 3 |
3 | NEONATAL SCREENING CARE | 103988 | 1% | 67% | 4 |
4 | U486 | 100270 | 1% | 43% | 6 |
5 | INTERDISCIPLINARY MOL HUMAN BIOL | 87741 | 0% | 75% | 3 |
6 | CURSO POS BIOTECNOL SAUDE MED INVEST | 77993 | 0% | 100% | 2 |
7 | FRE CNRS 2939 | 77993 | 0% | 100% | 2 |
8 | MASS SCREENING METAB DIS | 77993 | 0% | 100% | 2 |
9 | MOL TIROIDE LIM25 | 77993 | 0% | 100% | 2 |
10 | ST ANTONIE HOSP | 77993 | 0% | 100% | 2 |
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 | THYROID | 26480 | 6% | 1% | 50 |
2 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 6908 | 8% | 0% | 65 |
3 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 6803 | 3% | 1% | 25 |
4 | JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY | 4796 | 1% | 2% | 6 |
5 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | 2832 | 2% | 0% | 19 |
6 | MOLECULAR AND CELLULAR ENDOCRINOLOGY | 1959 | 3% | 0% | 21 |
7 | HORMONE RESEARCH IN PAEDIATRICS | 1692 | 1% | 1% | 6 |
8 | CLINICAL ENDOCRINOLOGY | 1148 | 2% | 0% | 15 |
9 | HORMONE RESEARCH | 1105 | 1% | 0% | 10 |
10 | MOVEMENT DISORDERS | 842 | 2% | 0% | 12 |
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 | THYROID DYSGENESIS | 959883 | 5% | 62% | 40 | Search THYROID+DYSGENESIS | Search THYROID+DYSGENESIS |
2 | THYROID HEMIAGENESIS | 917040 | 3% | 87% | 27 | Search THYROID+HEMIAGENESIS | Search THYROID+HEMIAGENESIS |
3 | BENIGN HEREDITARY CHOREA | 748723 | 3% | 80% | 24 | Search BENIGN+HEREDITARY+CHOREA | Search BENIGN+HEREDITARY+CHOREA |
4 | CONGENITAL HYPOTHYROIDISM | 607947 | 12% | 16% | 96 | Search CONGENITAL+HYPOTHYROIDISM | Search CONGENITAL+HYPOTHYROIDISM |
5 | DUOX | 483937 | 3% | 56% | 22 | Search DUOX | Search DUOX |
6 | DUOX2 | 383953 | 2% | 62% | 16 | Search DUOX2 | Search DUOX2 |
7 | DUAL OXIDASE | 254762 | 2% | 47% | 14 | Search DUAL+OXIDASE | Search DUAL+OXIDASE |
8 | THYROID DEVELOPMENT | 243721 | 1% | 63% | 10 | Search THYROID+DEVELOPMENT | Search THYROID+DEVELOPMENT |
9 | TITF 1 | 243721 | 1% | 63% | 10 | Search TITF+1 | Search TITF+1 |
10 | BRAIN THYROID LUNG SYNDROME | 233979 | 1% | 100% | 6 | Search BRAIN+THYROID+LUNG+SYNDROME | Search BRAIN+THYROID+LUNG+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 | NETTORE, IC , CACACE, V , DE FUSCO, C , COLAO, A , MACCHIA, PE , (2013) THE MOLECULAR CAUSES OF THYROID DYSGENESIS: A SYSTEMATIC REVIEW.JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION. VOL. 36. ISSUE 8. P. 654-664 | 94 | 83% | 12 |
2 | DE DEKEN, X , CORVILAIN, B , DUMONT, JE , MIOT, F , (2014) ROLES OF DUOX-MEDIATED HYDROGEN PEROXIDE IN METABOLISM, HOST DEFENSE, AND SIGNALING.ANTIOXIDANTS & REDOX SIGNALING. VOL. 20. ISSUE 17. P. 2776 -2793 | 92 | 49% | 15 |
3 | SZINNAI, G , (2014) GENETICS OF NORMAL AND ABNORMAL THYROID DEVELOPMENT IN HUMANS.BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 28. ISSUE 2. P. 133-150 | 69 | 56% | 16 |
4 | DE SANCTIS, V , SOLIMAN, AT , DI MAIO, S , ELSEDFY, H , SOLIMAN, NA , ELALAILY, R , (2016) THYROID HEMIAGENESIS FROM CHILDHOOD TO ADULTHOOD: REVIEW OF LITERATURE AND PERSONAL EXPERIENCE.PEDIATRIC ENDOCRINOLOGY REVIEWS PER. VOL. 13. ISSUE 3. P. 612 -619 | 40 | 77% | 1 |
5 | STOUPA, A , KARIYAWASAM, D , CARRE, A , POLAK, M , (2016) UPDATE OF THYROID DEVELOPMENTAL GENES.ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA. VOL. 45. ISSUE 2. P. 243 -+ | 39 | 78% | 1 |
6 | CASSIO, A , NICOLETTI, A , RIZZELLO, A , ZAZZETTA, E , BAL, M , BALDAZZI, L , (2013) CURRENT LOSS-OF-FUNCTION MUTATIONS IN THE THYROTROPIN RECEPTOR GENE: WHEN TO INVESTIGATE, CLINICAL EFFECTS, AND TREATMENT.JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY. VOL. 5. ISSUE . P. 29 -39 | 42 | 75% | 10 |
7 | FERNANDEZ, LP , LOPEZ-MARQUEZ, A , SANTISTEBAN, P , (2015) THYROID TRANSCRIPTION FACTORS IN DEVELOPMENT, DIFFERENTIATION AND DISEASE.NATURE REVIEWS ENDOCRINOLOGY. VOL. 11. ISSUE 1. P. 29 -42 | 67 | 38% | 14 |
8 | MEDEIROS-NETO, G , NOGUEIRA, CR , CHAGAS, AJ , DIAS, VMA , VIANA, MF , KOPP, P , PERONE, D , (2016) ANALYSIS OF THE PAX8 GENE IN 32 CHILDREN WITH THYROID DYSGENESIS AND FUNCTIONAL CHARACTERIZATION OF A PROMOTER VARIANT.JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM. VOL. 29. ISSUE 2. P. 193 -201 | 37 | 80% | 0 |
9 | VENEZIANO, L , PARKINSON, MH , MANTUANO, E , FRONTALI, M , BHATIA, KP , GIUNTI, P , (2014) A NOVEL DE NOVO MUTATION OF THE TITF1/NKX2-1 GENE CAUSING ATAXIA, BENIGN HEREDITARY CHOREA, HYPOTHYROIDISM AND A PITUITARY MASS IN A UK FAMILY AND REVIEW OF THE LITERATURE.CEREBELLUM. VOL. 13. ISSUE 5. P. 588 -595 | 38 | 78% | 4 |
10 | RAMOS, HE , CARRE, A , CHEVRIER, L , SZINNAI, G , TRON, E , CERQUEIRA, TLO , LEGER, J , CABROL, S , PUEL, O , QUEINNEC, C , ET AL (2014) EXTREME PHENOTYPIC VARIABILITY OF THYROID DYSGENESIS IN SIX NEW CASES OF CONGENITAL HYPOTHYROIDISM DUE TO PAX8 GENE LOSS-OF-FUNCTION MUTATIONS.EUROPEAN JOURNAL OF ENDOCRINOLOGY. VOL. 171. ISSUE 4. P. 499 -507 | 30 | 94% | 9 |
Classes with closest relation at Level 1 |