Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
3243 | 1993 | 28.0 | 65% |
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 |
17964 | 1 | FAHRS DISEASE//FAHRS SYNDROME//SLC20A2 | 573 |
23941 | 1 | HDR SYNDROME//HYPOPARATHYROIDISM//KENNY CAFFEY SYNDROME | 329 |
33060 | 1 | MENINGIOANGIOMATOSIS//CALCIFYING PSEUDONEOPLASM//CAPNON | 130 |
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 | 1755925 | 7% | 85% | 135 |
2 | FAHRS DISEASE | authKW | 1002921 | 4% | 92% | 71 |
3 | MENINGIOANGIOMATOSIS | authKW | 722614 | 3% | 94% | 50 |
4 | ALBRIGHT HEREDITARY OSTEODYSTROPHY | authKW | 500215 | 2% | 82% | 40 |
5 | HYPOPARATHYROIDISM | authKW | 494301 | 7% | 24% | 133 |
6 | HDR SYNDROME | authKW | 405510 | 2% | 88% | 30 |
7 | ALBRIGHTS HEREDITARY OSTEODYSTROPHY | authKW | 330156 | 1% | 86% | 25 |
8 | FAHRS SYNDROME | authKW | 328458 | 1% | 79% | 27 |
9 | OSTEOMA CUTIS | authKW | 323616 | 1% | 81% | 26 |
10 | GNAS | authKW | 323564 | 3% | 41% | 52 |
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 | 7068 | 24% | 0% | 470 |
2 | Clinical Neurology | 2829 | 18% | 0% | 349 |
3 | Pediatrics | 1839 | 11% | 0% | 225 |
4 | Genetics & Heredity | 939 | 10% | 0% | 205 |
5 | Dermatology | 773 | 5% | 0% | 104 |
6 | Medicine, General & Internal | 627 | 10% | 0% | 194 |
7 | Neuroimaging | 451 | 2% | 0% | 40 |
8 | Pathology | 320 | 4% | 0% | 85 |
9 | Neurosciences | 287 | 10% | 0% | 190 |
10 | Radiology, Nuclear Medicine & Medical Imaging | 259 | 6% | 0% | 113 |
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 | KEIZO ASAMI | 122548 | 1% | 67% | 12 |
2 | METAB DIS BRANCH | 90623 | 2% | 13% | 44 |
3 | REFERENCE MALAD RA METAB CALCIUM PHOSPHO | 89127 | 0% | 73% | 8 |
4 | REFERENCE RARE DISORDERS CALCIUM PHOSPHORUS | 68935 | 0% | 75% | 6 |
5 | ALBRIGHT CLIN | 63830 | 0% | 83% | 5 |
6 | MOL EPI GENET | 44148 | 0% | 41% | 7 |
7 | INSERM U1169 | 38294 | 0% | 50% | 5 |
8 | BIOARABA HLTH | 34812 | 0% | 45% | 5 |
9 | BICETRE PARIS SUD HOSP | 30639 | 0% | 100% | 2 |
10 | FDN IST RICOVERO CURAENDOCRINOL DIABETOL UNI | 30639 | 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 | 11311 | 7% | 1% | 133 |
2 | JOURNAL OF BONE AND MINERAL RESEARCH | 3813 | 2% | 1% | 41 |
3 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 2860 | 1% | 1% | 26 |
4 | ANNALES D ENDOCRINOLOGIE | 1440 | 1% | 1% | 14 |
5 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | 1270 | 1% | 0% | 21 |
6 | ANALES ESPANOLES DE PEDIATRIA | 1198 | 0% | 4% | 2 |
7 | ENDOCRINE PRACTICE | 1112 | 0% | 1% | 9 |
8 | ENDOCRINE JOURNAL | 1017 | 1% | 0% | 14 |
9 | CLINICAL ENDOCRINOLOGY | 952 | 1% | 0% | 22 |
10 | JAPANESE JOURNAL OF MEDICINE | 876 | 0% | 1% | 6 |
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 | 1755925 | 7% | 85% | 135 | Search PSEUDOHYPOPARATHYROIDISM | Search PSEUDOHYPOPARATHYROIDISM |
2 | FAHRS DISEASE | 1002921 | 4% | 92% | 71 | Search FAHRS+DISEASE | Search FAHRS+DISEASE |
3 | MENINGIOANGIOMATOSIS | 722614 | 3% | 94% | 50 | Search MENINGIOANGIOMATOSIS | Search MENINGIOANGIOMATOSIS |
4 | ALBRIGHT HEREDITARY OSTEODYSTROPHY | 500215 | 2% | 82% | 40 | Search ALBRIGHT+HEREDITARY+OSTEODYSTROPHY | Search ALBRIGHT+HEREDITARY+OSTEODYSTROPHY |
5 | HYPOPARATHYROIDISM | 494301 | 7% | 24% | 133 | Search HYPOPARATHYROIDISM | Search HYPOPARATHYROIDISM |
6 | HDR SYNDROME | 405510 | 2% | 88% | 30 | Search HDR+SYNDROME | Search HDR+SYNDROME |
7 | ALBRIGHTS HEREDITARY OSTEODYSTROPHY | 330156 | 1% | 86% | 25 | Search ALBRIGHTS+HEREDITARY+OSTEODYSTROPHY | Search ALBRIGHTS+HEREDITARY+OSTEODYSTROPHY |
8 | FAHRS SYNDROME | 328458 | 1% | 79% | 27 | Search FAHRS+SYNDROME | Search FAHRS+SYNDROME |
9 | OSTEOMA CUTIS | 323616 | 1% | 81% | 26 | Search OSTEOMA+CUTIS | Search OSTEOMA+CUTIS |
10 | GNAS | 323564 | 3% | 41% | 52 | Search GNAS | Search GNAS |
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 | 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 | 82 | 82% | 0 |
8 | TURAN, S , BASTEPE, M , (2015) GNAS SPECTRUM OF DISORDERS.CURRENT OSTEOPOROSIS REPORTS. VOL. 13. ISSUE 3. P. 146 -158 | 85 | 73% | 6 |
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 2 |