Class information for:
Level 2: PSEUDOHYPOPARATHYROIDISM//FAHRS DISEASE//MENINGIOANGIOMATOSIS

Basic class information

Class id #P Avg. number of
references
Database coverage
of references
3243 1993 28.0 65%



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
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



Rank Class id link
1 2439 GENOMIC IMPRINTING//BECKWITH WIEDEMANN SYNDROME//SILVER RUSSELL SYNDROME
2 3109 VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//22Q112 DELETION SYNDROME
3 433 HYPERPARATHYROIDISM//PRIMARY HYPERPARATHYROIDISM//SECONDARY HYPERPARATHYROIDISM
4 1079 BETA3 ADRENOCEPTOR//ADENYLYL CYCLASE//G PROTEIN
5 2373 ADRENAL INSUFFICIENCY//AIRE//APECED
6 2111 KLOTHO//FIBROBLAST GROWTH FACTOR 23//HYPOPHOSPHATEMIA
7 1536 OSTEOID OSTEOMA//FIBROUS DYSPLASIA//ANEURYSMAL BONE CYST
8 2103 THYROIDECTOMY//THYROID SURGERY//THYROGLOSSAL DUCT CYST
9 2080 VASCULAR CALCIFICATION//CALCIPHYLAXIS//FETUIN A
10 2900 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A

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