Class information for:
Level 1: CONGENITAL CENTRAL HYPOVENTILATION SYNDROME//PHOX2B//PHOX2B GENE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
14699 686 36.6 75%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
306 17788 SUDDEN INFANT DEATH SYNDROME//CAROTID BODY//CONTROL OF BREATHING

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 CONGENITAL CENTRAL HYPOVENTILATION SYNDROME Author keyword 125 78% 12% 82
2 PHOX2B Author keyword 72 60% 11% 78
3 PHOX2B GENE Author keyword 58 92% 3% 23
4 ONDINES CURSE Author keyword 52 75% 6% 38
5 PHOX2A Author keyword 33 74% 4% 25
6 HADDAD SYNDROME Author keyword 20 100% 1% 9
7 SYMPATHOADRENAL CELL LINEAGE Author keyword 18 83% 1% 10
8 CCHS Author keyword 18 59% 3% 20
9 AUTON MED PEDIAT Address 11 69% 1% 9
10 DISEASE CONGENITAL CENTRAL HYPOVENTILATION SYNDROME Author keyword 9 83% 1% 5

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 CONGENITAL CENTRAL HYPOVENTILATION SYNDROME 125 78% 12% 82 Search CONGENITAL+CENTRAL+HYPOVENTILATION+SYNDROME Search CONGENITAL+CENTRAL+HYPOVENTILATION+SYNDROME
2 PHOX2B 72 60% 11% 78 Search PHOX2B Search PHOX2B
3 PHOX2B GENE 58 92% 3% 23 Search PHOX2B+GENE Search PHOX2B+GENE
4 ONDINES CURSE 52 75% 6% 38 Search ONDINES+CURSE Search ONDINES+CURSE
5 PHOX2A 33 74% 4% 25 Search PHOX2A Search PHOX2A
6 HADDAD SYNDROME 20 100% 1% 9 Search HADDAD+SYNDROME Search HADDAD+SYNDROME
7 SYMPATHOADRENAL CELL LINEAGE 18 83% 1% 10 Search SYMPATHOADRENAL+CELL+LINEAGE Search SYMPATHOADRENAL+CELL+LINEAGE
8 CCHS 18 59% 3% 20 Search CCHS Search CCHS
9 DISEASE CONGENITAL CENTRAL HYPOVENTILATION SYNDROME 9 83% 1% 5 Search DISEASE++CONGENITAL+CENTRAL+HYPOVENTILATION+SYNDROME Search DISEASE++CONGENITAL+CENTRAL+HYPOVENTILATION+SYNDROME
10 CONGENITAL HYPOVENTILATION SYNDROME 8 100% 1% 5 Search CONGENITAL+HYPOVENTILATION+SYNDROME Search CONGENITAL+HYPOVENTILATION+SYNDROME

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 ONSET CENTRAL HYPOVENTILATION 103 97% 4% 30
2 POLYALANINE EXPANSIONS 64 86% 5% 32
3 ONDINES CURSE 63 70% 8% 53
4 HOMEOBOX GENE PHOX2B 40 48% 9% 61
5 PHOX2B 30 48% 7% 46
6 NEUROTRANSMITTER BIOSYNTHETIC GENES 29 72% 3% 23
7 VENTILATION ONDINES CURSE 27 92% 2% 11
8 PHOX2B MUTATIONS 26 80% 2% 16
9 CENTRAL HYPOVENTILATION SYNDROME 26 26% 12% 84
10 PHOX2B GENE 15 82% 1% 9

Journals

Reviews


Title Publ. year Cit. Active
references		 % act. ref.
to same field
Segregation of neuronal and neuroendocrine differentiation in the sympathoadrenal lineage 2015 1 93 30%
Congenital Central Hypoventilation Syndrome From Past to Future: Model for Translational and Transitional Autonomic Medicine 2009 24 86 87%
Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation: review and update 2014 2 26 88%
Resolved and open issues in chromaffin cell development 2013 6 21 71%
Peripheral chemoreceptors in congenital central hypoventilation syndrome 2013 5 48 73%
The sympathoadrenal cell lineage: Specification, diversification, and new perspectives 2006 76 69 55%
Congenital Central Hypoventilation Syndrome in Children 2011 11 53 87%
Central hypoventilation with PHOX2B expansion mutation presenting in adulthood 2007 15 8 100%
The development of the chromaffin cell lineage from the neural crest 2009 22 56 57%
Phox2 genes - from patterning to connectivity 2002 136 52 52%

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 AUTON MED PEDIAT 11 69% 1.3% 9
2 NEUROL PHYSIOL DEV 6 44% 1.6% 11
3 PROGRAM NEUROSCI DEGENERAT DIS 4 75% 0.4% 3
4 RG DEV NEUROBIOL 4 75% 0.4% 3
5 RUSH CHILDRENS HOSP 3 28% 1.3% 9
6 UNITE RECH AD TAT PHYSIOL COMPORTEMENTALES 2 32% 0.9% 6
7 UMR 8542 2 14% 2.2% 15
8 INSERMU393 2 67% 0.3% 2
9 MEDINSERMU781 2 67% 0.3% 2
10 GRP DEV NEUROBIOL 2 25% 1.0% 7

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000104343 PHENYLETHANOLAMINE N METHYLTRANSFERASE//PSYCHIAT MOL DEV NEUROBIOL//TYROSINE HYDROXYLASE GENE
2 0.0000099889 NEURAL CREST//PIGMENT PATTERN//FOXD3
3 0.0000098862 DIAPHRAGM PACING//CROSSED PHRENIC PHENOMENON//LONG TERM FACILITATION
4 0.0000094616 CILIARY NEUROTROPHIC FACTOR//CNTF//CNTFR ALPHA
5 0.0000080385 HIRSCHSPRUNG DISEASE//INTESTINAL NEURONAL DYSPLASIA//AGANGLIONOSIS
6 0.0000073876 PRE BOTZINGER COMPLEX//RETROTRAPEZOID NUCLEUS//RESPIRATORY RHYTHM GENERATION
7 0.0000062965 MECHANICAL INSUFFLATION EXSUFFLATION//PEAK COUGH FLOW//EXSUFFLATION
8 0.0000061426 OCULOPHARYNGEAL MUSCULAR DYSTROPHY//PABPN1//OPMD
9 0.0000057555 SERINE THREONINE KINASE RECEPTORS//SERUM FREE MOUSE EMBRYO CELL//SERUM FREE MOUSE EMBRYO CELLS
10 0.0000053646 ALMITRINE//ALMITRINE BISMESYLATE//DRUG INDUCED LIPIDOSIS