Class information for:
Level 1: CHARCOT MARIE TOOTH DISEASE//PMP22//CHARCOT MARIE TOOTH

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
1350 2608 36.0 77%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
736 11912 CHARCOT MARIE TOOTH DISEASE//MYELIN//OLIGODENDROCYTE

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 CHARCOT MARIE TOOTH DISEASE Author keyword 523 72% 16% 415
2 PMP22 Author keyword 198 83% 4% 112
3 CHARCOT MARIE TOOTH Author keyword 126 66% 5% 118
4 CMT1A Author keyword 125 86% 2% 63
5 HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES Author keyword 124 90% 2% 54
6 MYELIN PROTEIN ZERO Author keyword 92 82% 2% 54
7 HNPP Author keyword 91 85% 2% 47
8 HEREDITARY MOTOR AND SENSORY NEUROPATHY Author keyword 85 69% 3% 73
9 MPZ Author keyword 76 86% 1% 38
10 HEREDITARY NEUROPATHY Author keyword 73 66% 3% 68

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 CHARCOT MARIE TOOTH DISEASE 523 72% 16% 415 Search CHARCOT+MARIE+TOOTH+DISEASE Search CHARCOT+MARIE+TOOTH+DISEASE
2 PMP22 198 83% 4% 112 Search PMP22 Search PMP22
3 CHARCOT MARIE TOOTH 126 66% 5% 118 Search CHARCOT+MARIE+TOOTH Search CHARCOT+MARIE+TOOTH
4 CMT1A 125 86% 2% 63 Search CMT1A Search CMT1A
5 HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES 124 90% 2% 54 Search HEREDITARY+NEUROPATHY+WITH+LIABILITY+TO+PRESSURE+PALSIES Search HEREDITARY+NEUROPATHY+WITH+LIABILITY+TO+PRESSURE+PALSIES
6 MYELIN PROTEIN ZERO 92 82% 2% 54 Search MYELIN+PROTEIN+ZERO Search MYELIN+PROTEIN+ZERO
7 HNPP 91 85% 2% 47 Search HNPP Search HNPP
8 HEREDITARY MOTOR AND SENSORY NEUROPATHY 85 69% 3% 73 Search HEREDITARY+MOTOR+AND+SENSORY+NEUROPATHY Search HEREDITARY+MOTOR+AND+SENSORY+NEUROPATHY
9 MPZ 76 86% 1% 38 Search MPZ Search MPZ
10 HEREDITARY NEUROPATHY 73 66% 3% 68 Search HEREDITARY+NEUROPATHY Search HEREDITARY+NEUROPATHY

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 HEREDITARY MOTOR 541 68% 18% 477
2 PRESSURE PALSIES 390 83% 9% 223
3 HEREDITARY NEUROPATHY 303 77% 8% 208
4 MARIE TOOTH DISEASE 286 37% 24% 629
5 PMP22 GENE 279 87% 5% 138
6 TOMACULOUS NEUROPATHY 272 98% 2% 65
7 TREMBLER J MOUSE 239 88% 4% 114
8 DISEASE TYPE 1A 184 83% 4% 105
9 DEJERINE SOTTAS 165 91% 3% 69
10 NEUROPATHY TYPE I 159 81% 4% 95

Journals


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 JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM 8 12% 3% 66

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success 2014 16 85 81%
Diagnosis, natural history, and management of Charcot-Marie-Tooth disease 2009 132 103 83%
Hereditary motor and sensory neuropathies: Understanding molecular pathogenesis could lead to future treatment strategies 2015 3 104 58%
Clinical implications of genetic advances in Charcot-Marie-Tooth disease 2013 41 23 61%
Charcot-Marie-Tooth Disease Type 2A From Typical to Rare Phenotypic and Genotypic Features 2014 9 27 81%
The PMP22 Gene and Its Related Diseases 2013 26 205 78%
Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies 1999 146 112 95%
Update on Charcot-Marie-Tooth Disease 2011 55 48 77%
Diagnosis and new treatments in genetic neuropathies 2009 71 91 66%
Charcot-marie-tooth disease: A clinico-genetic confrontation 2008 69 156 73%

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 UNITE NEUROGENET MOL 24 91% 0.4% 10
2 PERIPHERAL NEUROPATHY GRP 18 45% 1.2% 30
3 UNIT CLIN CENT PERIPHERAL DEGENERAT NEUROPATHIE 8 75% 0.2% 6
4 MRC NEUROMUSCULAR DIS 7 17% 1.5% 38
5 SECT DEV NEUROBIOL 7 27% 0.8% 22
6 SECT NEUROL NEUROL REHABIL 6 80% 0.2% 4
7 MOL NEUROGEN GRP 6 53% 0.3% 8
8 BORN BUNGE FDN 6 13% 1.6% 42
9 C BESTA NEUROL 6 39% 0.5% 12
10 AZIENDA OU POLICLIN CATANZARO 6 100% 0.2% 4

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000116311 SCHWANN CELL//CHRONIC NERVE COMPRESSION INJURY//HUMANANAT EMBRYOL
2 0.0000111806 GIANT AXONAL NEUROPATHY//GIGAXONIN//GAN MUTATIONS
3 0.0000093203 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
4 0.0000071476 MYELIN ASSOCIATED GLYCOPROTEIN//L MAG//CEREBELLAR SOLUBLE LECTIN
5 0.0000059322 PELIZAEUS MERZBACHER DISEASE//PROTEOLIPID PROTEIN//PL NEUROBIOL GRP
6 0.0000054083 AUDITORY NEUROPATHY//AUDITORY NEUROPATHY SPECTRUM DISORDER//OTOF
7 0.0000052390 MULTIFOCAL MOTOR NEUROPATHY//CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY//CIDP
8 0.0000048684 MARINESCO SJOGREN SYNDROME//MICRO SYNDROME//WARBURG MICRO SYNDROME
9 0.0000046332 GAS7//GAS1//GROWTH ARREST SPECIFIC 1
10 0.0000039797 FAMILIAL DYSAUTONOMIA//RILEY DAY SYNDROME//CONGENITAL INSENSITIVITY TO PAIN WITH ANHIDROSIS