Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
11696 | 961 | 31.6 | 68% |
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 |
196 | 3 | GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS | 53756 |
3243 | 2 | PSEUDOHYPOPARATHYROIDISM//FAHRS DISEASE//MENINGIOANGIOMATOSIS | 1993 |
11696 | 1 | PSEUDOHYPOPARATHYROIDISM//ALBRIGHT HEREDITARY OSTEODYSTROPHY//ALBRIGHTS HEREDITARY OSTEODYSTROPHY | 961 |
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 | PSEUDOHYPOPARATHYROIDISM | authKW | 3172457 | 13% | 79% | 126 |
2 | ALBRIGHT HEREDITARY OSTEODYSTROPHY | authKW | 1037473 | 4% | 82% | 40 |
3 | ALBRIGHTS HEREDITARY OSTEODYSTROPHY | authKW | 684757 | 3% | 86% | 25 |
4 | OSTEOMA CUTIS | authKW | 671196 | 3% | 81% | 26 |
5 | GNAS | authKW | 671144 | 5% | 41% | 52 |
6 | PSEUDOPSEUDOHYPOPARATHYROIDISM | authKW | 569553 | 2% | 81% | 22 |
7 | PROGRESSIVE OSSEOUS HETEROPLASIA | authKW | 387321 | 2% | 76% | 16 |
8 | GNAS1 | authKW | 369988 | 2% | 61% | 19 |
9 | ACRODYSOSTOSIS | authKW | 311368 | 1% | 70% | 14 |
10 | PSEUDOHYPOPARATHYROIDISM TYPE IA | authKW | 222411 | 1% | 100% | 7 |
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 | 7184 | 34% | 0% | 323 |
2 | Dermatology | 1699 | 11% | 0% | 101 |
3 | Pediatrics | 1527 | 14% | 0% | 139 |
4 | Genetics & Heredity | 752 | 13% | 0% | 123 |
5 | Medicine, General & Internal | 223 | 9% | 0% | 83 |
6 | Medicine, Research & Experimental | 74 | 4% | 0% | 43 |
7 | Orthopedics | 50 | 3% | 0% | 25 |
8 | Biochemistry & Molecular Biology | 18 | 9% | 0% | 84 |
9 | Medical Laboratory Technology | 7 | 1% | 0% | 7 |
10 | Cell Biology | 6 | 4% | 0% | 34 |
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 | METAB DIS BRANCH | 188036 | 5% | 13% | 44 |
2 | REFERENCE RARE DISORDERS CALCIUM PHOSPHORUS | 142976 | 1% | 75% | 6 |
3 | REFERENCE MALAD RA METAB CALCIUM PHOSPHO | 141529 | 1% | 64% | 7 |
4 | ALBRIGHT CLIN | 132386 | 1% | 83% | 5 |
5 | MOL EPI GENET | 91573 | 1% | 41% | 7 |
6 | INSERM U1169 | 79428 | 1% | 50% | 5 |
7 | BIOARABA HLTH | 72206 | 1% | 45% | 5 |
8 | BICETRE PARIS SUD HOSP | 63546 | 0% | 100% | 2 |
9 | FDN IST RICOVERO CURAENDOCRINOL DIABETOL UNI | 63546 | 0% | 100% | 2 |
10 | MED SERV MINERAL METAB SECT | 63546 | 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 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 12316 | 10% | 0% | 96 |
2 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 3898 | 2% | 1% | 21 |
3 | JOURNAL OF BONE AND MINERAL RESEARCH | 2077 | 2% | 0% | 21 |
4 | ANNALES D ENDOCRINOLOGIE | 1533 | 1% | 0% | 10 |
5 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | 1016 | 1% | 0% | 13 |
6 | CLINICAL ENDOCRINOLOGY | 808 | 1% | 0% | 14 |
7 | CALCIFIED TISSUE INTERNATIONAL | 778 | 1% | 0% | 11 |
8 | ENDOCRINE JOURNAL | 692 | 1% | 0% | 8 |
9 | HAUTARZT | 647 | 1% | 0% | 10 |
10 | HORMONE RESEARCH IN PAEDIATRICS | 609 | 0% | 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 | PSEUDOHYPOPARATHYROIDISM | 3172457 | 13% | 79% | 126 | Search PSEUDOHYPOPARATHYROIDISM | Search PSEUDOHYPOPARATHYROIDISM |
2 | ALBRIGHT HEREDITARY OSTEODYSTROPHY | 1037473 | 4% | 82% | 40 | Search ALBRIGHT+HEREDITARY+OSTEODYSTROPHY | Search ALBRIGHT+HEREDITARY+OSTEODYSTROPHY |
3 | ALBRIGHTS HEREDITARY OSTEODYSTROPHY | 684757 | 3% | 86% | 25 | Search ALBRIGHTS+HEREDITARY+OSTEODYSTROPHY | Search ALBRIGHTS+HEREDITARY+OSTEODYSTROPHY |
4 | OSTEOMA CUTIS | 671196 | 3% | 81% | 26 | Search OSTEOMA+CUTIS | Search OSTEOMA+CUTIS |
5 | GNAS | 671144 | 5% | 41% | 52 | Search GNAS | Search GNAS |
6 | PSEUDOPSEUDOHYPOPARATHYROIDISM | 569553 | 2% | 81% | 22 | Search PSEUDOPSEUDOHYPOPARATHYROIDISM | Search PSEUDOPSEUDOHYPOPARATHYROIDISM |
7 | PROGRESSIVE OSSEOUS HETEROPLASIA | 387321 | 2% | 76% | 16 | Search PROGRESSIVE+OSSEOUS+HETEROPLASIA | Search PROGRESSIVE+OSSEOUS+HETEROPLASIA |
8 | GNAS1 | 369988 | 2% | 61% | 19 | Search GNAS1 | Search GNAS1 |
9 | ACRODYSOSTOSIS | 311368 | 1% | 70% | 14 | Search ACRODYSOSTOSIS | Search ACRODYSOSTOSIS |
10 | PSEUDOHYPOPARATHYROIDISM TYPE IA | 222411 | 1% | 100% | 7 | Search PSEUDOHYPOPARATHYROIDISM+TYPE+IA | Search PSEUDOHYPOPARATHYROIDISM+TYPE+IA |
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 | MANTOVANI, G , SPADA, A , ELLI, FM , (2016) PSEUDOHYPOPARATHYROIDISM AND G(S)ALPHA-CAMP-LINKED DISORDERS: CURRENT VIEW AND OPEN ISSUES.NATURE REVIEWS ENDOCRINOLOGY. VOL. 12. ISSUE 6. P. 347 -356 | 102 | 85% | 1 |
2 | MANTOVANI, G , (2011) PSEUDOHYPOPARATHYROIDISM: DIAGNOSIS AND TREATMENT.JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. VOL. 96. ISSUE 10. P. 3020 -3030 | 90 | 91% | 54 |
3 | TURAN, S , BASTEPE, M , (2013) THE GNAS COMPLEX LOCUS AND HUMAN DISEASES ASSOCIATED WITH LOSS-OF-FUNCTION MUTATIONS OR EPIMUTATIONS WITHIN THIS IMPRINTED GENE.HORMONE RESEARCH IN PAEDIATRICS. VOL. 80. ISSUE 4. P. 229-241 | 92 | 90% | 9 |
4 | PLAGGE, A , KELSEY, G , GERMAIN-LEE, EL , (2008) PHYSIOLOGICAL FUNCTIONS OF THE IMPRINTED GNAS LOCUS AND ITS PROTEIN VARIANTS G ALPHA(S) AND XL ALPHA(S) IN HUMAN AND MOUSE.JOURNAL OF ENDOCRINOLOGY. VOL. 196. ISSUE 2. P. 193-214 | 119 | 76% | 39 |
5 | MANTOVANI, G , ELLI, FM , SPADA, A , (2012) GNAS EPIGENETIC DEFECTS AND PSEUDOHYPOPARATHYROIDISM: TIME FOR A NEW CLASSIFICATION?.HORMONE AND METABOLIC RESEARCH. VOL. 44. ISSUE 10. P. 716 -723 | 81 | 90% | 19 |
6 | BASTEPE, M , (2012) RELATIVE FUNCTIONS OF GAS AND ITS EXTRA-LARGE VARIANT XL ALPHA S IN THE ENDOCRINE SYSTEM.HORMONE AND METABOLIC RESEARCH. VOL. 44. ISSUE 10. P. 732-740 | 90 | 82% | 9 |
7 | TURAN, S , BASTEPE, M , (2015) GNAS SPECTRUM OF DISORDERS.CURRENT OSTEOPOROSIS REPORTS. VOL. 13. ISSUE 3. P. 146 -158 | 85 | 73% | 6 |
8 | THIELE, S , MANTOVANI, G , BARLIER, A , BOLDRIN, V , BORDOGNA, P , DE SANCTIS, L , ELLI, FM , FRESON, K , GARIN, I , GRYBEK, V , ET AL (2016) FROM PSEUDOHYPOPARATHYROIDISM TO INACTIVATING PTH/PTHRP SIGNALLING DISORDER (IPPSD), A NOVEL CLASSIFICATION PROPOSED BY THE EUROPHP NETWORK.EUROPEAN JOURNAL OF ENDOCRINOLOGY. VOL. 175. ISSUE 6. P. P1 -P17 | 81 | 81% | 0 |
9 | LEMOS, MC , THAKKER, RV , (2015) GNAS MUTATIONS IN PSEUDOHYPOPARATHYROIDISM TYPE 1A AND RELATED DISORDERS.HUMAN MUTATION. VOL. 36. ISSUE 1. P. 11 -19 | 62 | 90% | 6 |
10 | CHEESEMAN, MT , VOWELL, K , HOUGH, TA , JONES, L , PATHAK, P , TYRER, HE , KELLY, M , COX, R , WARREN, MV , PETERS, J , (2012) A MOUSE MODEL FOR OSSEOUS HETEROPLASIA.PLOS ONE. VOL. 7. ISSUE 12. P. - | 57 | 100% | 2 |
Classes with closest relation at Level 1 |