Class information for:
Level 1: PSEUDOHYPOPARATHYROIDISM//ALBRIGHT HEREDITARY OSTEODYSTROPHY//ALBRIGHTS HEREDITARY OSTEODYSTROPHY

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
11553 907 31.0 65%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
2321 4046 VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//PSEUDOHYPOPARATHYROIDISM

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 PSEUDOHYPOPARATHYROIDISM Author keyword 167 76% 13% 116
2 ALBRIGHT HEREDITARY OSTEODYSTROPHY Author keyword 57 79% 4% 37
3 ALBRIGHTS HEREDITARY OSTEODYSTROPHY Author keyword 47 86% 3% 24
4 OSTEOMA CUTIS Author keyword 44 85% 3% 23
5 PSEUDOPSEUDOHYPOPARATHYROIDISM Author keyword 23 76% 2% 16
6 PROGRESSIVE OSSEOUS HETEROPLASIA Author keyword 21 75% 2% 15
7 GNAS Author keyword 20 39% 4% 40
8 ACRODYSOSTOSIS Author keyword 17 75% 1% 12
9 PSEUDOHYPOPARATHYROIDISM TYPE IA Author keyword 14 100% 1% 7
10 CUTANEOUS OSSIFICATION Author keyword 13 80% 1% 8

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 PSEUDOHYPOPARATHYROIDISM 167 76% 13% 116 Search PSEUDOHYPOPARATHYROIDISM Search PSEUDOHYPOPARATHYROIDISM
2 ALBRIGHT HEREDITARY OSTEODYSTROPHY 57 79% 4% 37 Search ALBRIGHT+HEREDITARY+OSTEODYSTROPHY Search ALBRIGHT+HEREDITARY+OSTEODYSTROPHY
3 ALBRIGHTS HEREDITARY OSTEODYSTROPHY 47 86% 3% 24 Search ALBRIGHTS+HEREDITARY+OSTEODYSTROPHY Search ALBRIGHTS+HEREDITARY+OSTEODYSTROPHY
4 OSTEOMA CUTIS 44 85% 3% 23 Search OSTEOMA+CUTIS Search OSTEOMA+CUTIS
5 PSEUDOPSEUDOHYPOPARATHYROIDISM 23 76% 2% 16 Search PSEUDOPSEUDOHYPOPARATHYROIDISM Search PSEUDOPSEUDOHYPOPARATHYROIDISM
6 PROGRESSIVE OSSEOUS HETEROPLASIA 21 75% 2% 15 Search PROGRESSIVE+OSSEOUS+HETEROPLASIA Search PROGRESSIVE+OSSEOUS+HETEROPLASIA
7 GNAS 20 39% 4% 40 Search GNAS Search GNAS
8 ACRODYSOSTOSIS 17 75% 1% 12 Search ACRODYSOSTOSIS Search ACRODYSOSTOSIS
9 PSEUDOHYPOPARATHYROIDISM TYPE IA 14 100% 1% 7 Search PSEUDOHYPOPARATHYROIDISM+TYPE+IA Search PSEUDOHYPOPARATHYROIDISM+TYPE+IA
10 CUTANEOUS OSSIFICATION 13 80% 1% 8 Search CUTANEOUS+OSSIFICATION Search CUTANEOUS+OSSIFICATION

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 ALBRIGHT HEREDITARY OSTEODYSTROPHY 149 64% 16% 145
2 GS ALPHA GENE 110 74% 9% 82
3 IMPRINTING CONTROL ELEMENT 102 85% 6% 53
4 ALBRIGHTS HEREDITARY OSTEODYSTROPHY 63 77% 5% 43
5 CYCLASE COUPLING PROTEIN 58 92% 3% 23
6 PSEUDOHYPOPARATHYROIDISM 54 55% 7% 67
7 PSEUDOHYPOPARATHYROIDISM TYPE IB 53 58% 7% 61
8 EPIGENETIC DEFECTS 53 85% 3% 28
9 HUMAN GNAS1 GENE 50 86% 3% 25
10 PSEUDOHYPOPARATHYROIDISM TYPE IA 47 88% 2% 22

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Possibilities and challenges of China's forestry biomass resource utilization 2015 2 2 50%
Pseudohypoparathyroidism: Diagnosis and Treatment 2011 40 99 90%
GNAS-Related Loss-of-Function Disorders and the Role of Imprinting 2013 7 59 85%
Physiological functions of the imprinted Gnas locus and its protein variants G alpha(s) and XL alpha(s) in human and mouse 2008 38 157 75%
An update on the clinical and molecular characteristics of pseudohypoparathyroidism 2012 15 44 93%
The GNAS Complex Locus and Human Diseases Associated with Loss-of-Function Mutations or Epimutations within This Imprinted Gene 2013 5 102 90%
GNAS Epigenetic Defects and Pseudohypoparathyroidism: Time for a New Classification? 2012 13 90 89%
GNAS locus and pseudohypoparathyroidism 2005 89 52 90%
Endocrine manifestations of stimulatory G protein alpha-subunit mutations and the role of genomic imprinting 2001 236 349 35%
Relative Functions of Gas and its Extra-large Variant XL alpha s in the Endocrine System 2012 8 110 82%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 REFERENCE RARE DISORDERS CALCIUM PHOSPHORUS 12 86% 0.7% 6
2 ALBRIGHT CLIN 9 83% 0.6% 5
3 REFERENCE MALAD RA METAB CALCIUM PHOSPHO 8 70% 0.8% 7
4 METAB DIS BRANCH 6 13% 4.6% 42
5 MOL EPI GENET 3 45% 0.6% 5
6 BIOARABA HLTH 2 67% 0.2% 2
7 FDN RICOVERO CURA CARATTERE SCI POLICLIN S 2 67% 0.2% 2
8 SIGNAL TRANSDUCT SECT 2 31% 0.6% 5
9 ILYSSA MOL CELLULAR ENDOCRINOL 2 23% 0.8% 7
10 BICETRE PARIS SUD HOSP 1 100% 0.2% 2

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000160621 HDR SYNDROME//KENNY CAFFEY SYNDROME//HYPOPARATHYROIDISM
2 0.0000114256 GPRC5A//GNAS1//CELLULAR SIGNALINGCANC
3 0.0000089680 FAHRS DISEASE//BASAL GANGLIA CALCIFICATION//FAHRS SYNDROME
4 0.0000072232 PTH ASSAYS//WHOLE PTH//INTACT PTH
5 0.0000064987 GENOMIC IMPRINTING//H19//BECKWITH WIEDEMANN SYNDROME
6 0.0000060682 SATB1//2Q DELETION//SATB2
7 0.0000059952 FIBROUS DYSPLASIA//MCCUNE ALBRIGHT SYNDROME//CEMENTO OSSIFYING FIBROMA
8 0.0000057971 BIOCHEM MEMBRANE RECEPTORS GRP//MEMBRANE RECEPTORS//TRIMERIC G PROTEINS
9 0.0000049992 BAROREFLEX FAILURE//NEUROVASCULAR COMPRESSION//CAROTID SINUS DENERVATION
10 0.0000049477 ARHI//NEURONATIN//APLASIA RAS HOMOLOG MEMBER I