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

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
1380 2690 34.9 77%


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
351 3       GAP JUNCTION//CONNEXIN//OLIGODENDROCYTE 35607
1735 2             SPINAL MUSCULAR ATROPHY//CHARCOT MARIE TOOTH DISEASE//NEUROFILAMENT 6545
1380 1                   CHARCOT MARIE TOOTH DISEASE//PMP22//CHARCOT MARIE TOOTH 2690

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 CHARCOT MARIE TOOTH DISEASE authKW 3789206 17% 73% 459
2 PMP22 authKW 1083082 4% 82% 116
3 CHARCOT MARIE TOOTH authKW 1054470 5% 68% 137
4 HEREDITARY MOTOR AND SENSORY NEUROPATHY authKW 932215 4% 76% 108
5 HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES authKW 709186 3% 92% 68
6 HEREDITARY NEUROPATHY authKW 665785 3% 67% 88
7 CMT1A authKW 639344 2% 87% 65
8 MYELIN PROTEIN ZERO authKW 490442 2% 79% 55
9 HNPP authKW 450837 2% 83% 48
10 CMT authKW 415798 3% 44% 83

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 Clinical Neurology 36842 51% 0% 1364
2 Neurosciences 13843 42% 0% 1134
3 Genetics & Heredity 4953 19% 0% 505
4 Pathology 364 4% 0% 107
5 Pediatrics 206 4% 0% 109
6 Psychiatry 167 4% 0% 107
7 Rehabilitation 112 2% 0% 47
8 Orthopedics 56 2% 0% 51
9 Surgery 39 4% 0% 121
10 Sport Sciences 36 1% 0% 37

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 UNITE NEUROGENET MOL 103176 0% 91% 10
2 PERIPHERAL NEUROPATHY GRP 90765 1% 33% 24
3 BORN BUNGE FDN 69459 2% 14% 44
4 SECT DEV NEUROBIOL 66958 1% 27% 22
5 REFERENCE NEUROPATHIES PERIPHER RA 64546 1% 36% 16
6 C BESTA NEUROL 61798 1% 34% 16
7 UNIT CLIN CENT PERIPHERAL DEGENERAT NEUROPATHIE 61789 0% 78% 7
8 MRC NEUROMUSCULAR DIS 61280 1% 14% 40
9 SERV CLIN NEUROPHYSIOL 54798 1% 30% 16
10 CLIN CENT PERIPHERAL DEGENERAT NEUROPATHIES UNI 47278 0% 42% 10

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 THE PERIPHERAL NERVOUS SYSTEM 118744 3% 13% 80
2 NEUROMUSCULAR DISORDERS 61507 4% 5% 113
3 NEUROGENETICS 29991 1% 7% 40
4 MUSCLE & NERVE 20358 4% 2% 113
5 NEUROLOGY 10795 5% 1% 143
6 JOURNAL OF THE NEUROLOGICAL SCIENCES 6912 3% 1% 79
7 BRAIN 6386 2% 1% 60
8 NEUROMOLECULAR MEDICINE 5845 1% 3% 17
9 ANNALS OF NEUROLOGY 5696 2% 1% 63
10 JOURNAL OF NEUROLOGY 5573 2% 1% 55

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 CHARCOT MARIE TOOTH DISEASE 3789206 17% 73% 459 Search CHARCOT+MARIE+TOOTH+DISEASE Search CHARCOT+MARIE+TOOTH+DISEASE
2 PMP22 1083082 4% 82% 116 Search PMP22 Search PMP22
3 CHARCOT MARIE TOOTH 1054470 5% 68% 137 Search CHARCOT+MARIE+TOOTH Search CHARCOT+MARIE+TOOTH
4 HEREDITARY MOTOR AND SENSORY NEUROPATHY 932215 4% 76% 108 Search HEREDITARY+MOTOR+AND+SENSORY+NEUROPATHY Search HEREDITARY+MOTOR+AND+SENSORY+NEUROPATHY
5 HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES 709186 3% 92% 68 Search HEREDITARY+NEUROPATHY+WITH+LIABILITY+TO+PRESSURE+PALSIES Search HEREDITARY+NEUROPATHY+WITH+LIABILITY+TO+PRESSURE+PALSIES
6 HEREDITARY NEUROPATHY 665785 3% 67% 88 Search HEREDITARY+NEUROPATHY Search HEREDITARY+NEUROPATHY
7 CMT1A 639344 2% 87% 65 Search CMT1A Search CMT1A
8 MYELIN PROTEIN ZERO 490442 2% 79% 55 Search MYELIN+PROTEIN+ZERO Search MYELIN+PROTEIN+ZERO
9 HNPP 450837 2% 83% 48 Search HNPP Search HNPP
10 CMT 415798 3% 44% 83 Search CMT Search CMT

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 LI, J , PARKER, B , MARTYN, C , NATARAJAN, C , GUO, JS , (2013) THE PMP22 GENE AND ITS RELATED DISEASES.MOLECULAR NEUROBIOLOGY. VOL. 47. ISSUE 2. P. 673-698 159 78% 44
2 VAN PAASSEN, BW , VAN DER KOOI, AJ , VAN SPAENDONCK-ZWARTS, KY , VERHAMME, C , BAAS, F , DE VISSER, M , (2014) PMP22 RELATED NEUROPATHIES: CHARCOT-MARIE-TOOTH DISEASE TYPE 1A AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES.ORPHANET JOURNAL OF RARE DISEASES. VOL. 9. ISSUE . P. - 125 79% 14
3 SANMANEECHAI, O , FEELY, S , SCHERER, SS , HERRMANN, DN , BURNS, J , MUNTONI, F , LI, J , SISKIND, CE , DAY, JW , LAURA, M , ET AL (2015) GENOTYPE-PHENOTYPE CHARACTERISTICS AND BASELINE NATURAL HISTORY OF HERITABLE NEUROPATHIES CAUSED BY MUTATIONS IN THE MPZ GENE.BRAIN. VOL. 138. ISSUE . P. - 97 94% 3
4 BERGER, P , YOUNG, P , SUTER, U , (2002) MOLECULAR CELL BIOLOGY OF CHARCOT-MARIE-TOOTH DISEASE.NEUROGENETICS. VOL. 4. ISSUE 1. P. 1-15 149 80% 74
5 PAREYSON, D , MARCHESI, C , (2009) DIAGNOSIS, NATURAL HISTORY, AND MANAGEMENT OF CHARCOT-MARIE-TOOTH DISEASE.LANCET NEUROLOGY. VOL. 8. ISSUE 7. P. 654-667 89 86% 171
6 FLEDRICH, R , STASSART, RM , SEREDA, MW , (2012) MURINE THERAPEUTIC MODELS FOR CHARCOT-MARIE-TOOTH (CMT) DISEASE.BRITISH MEDICAL BULLETIN. VOL. 102. ISSUE 1. P. 89-113 114 77% 22
7 YOUNG, P , SUTER, U , (2003) THE CAUSES OF CHARCOT-MARIE-TOOTH DISEASE.CELLULAR AND MOLECULAR LIFE SCIENCES. VOL. 60. ISSUE 12. P. 2547-2560 149 78% 31
8 KLEOPA, KA , SCHERER, SS , (2002) INHERITED NEUROPATHIES.NEUROLOGIC CLINICS. VOL. 20. ISSUE 3. P. 679 -+ 133 90% 13
9 YIU, EM , RYAN, MM , (2012) DEMYELINATING PRENATAL AND INFANTILE DEVELOPMENTAL NEUROPATHIES.JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. VOL. 17. ISSUE 1. P. 32-52 126 70% 3
10 HOULDEN, H , REILLY, MM , (2006) MOLECULAR GENETICS OF AUTOSOMAL-DOMINANT DEMYELINATING CHARCOT-MARIE-TOOTH DISEASE.NEUROMOLECULAR MEDICINE. VOL. 8. ISSUE 1-2. P. 43 -62 111 87% 36

Classes with closest relation at Level 1


Rank Class id link
1 32627 IGHMBP2//SMARD1//SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS
2 8120 SCHWANN CELL//MYELINATION//SCHWANN CELL PRECURSORS
3 34608 GIANT AXONAL NEUROPATHY//GIGAXONIN//GAN MUTATIONS
4 24588 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
5 36499 RIGID SPINE SYNDROME//RIGID SPINE//1ST AFFILIATED HOSP NEUROL
6 30096 MARINESCO SJOGREN SYNDROME//SIL1//WARBURG MICRO SYNDROME
7 24707 AUDITORY NEUROPATHY//AUDITORY NEUROPATHY SPECTRUM DISORDER//AUDITORY DYS SYNCHRONY
8 19643 NEURALGIC AMYOTROPHY//PARSONAGE TURNER SYNDROME//DIABETIC AMYOTROPHY
9 35295 ANAESTHESIA OBSTETRIC ARTERIOVENOUS MALFORMATION//CIRCUMFERENTIAL BODY LIFT//COMBINED SPINALEPIDURAL
10 3457 PELIZAEUS MERZBACHER DISEASE//PROTEOLIPID PROTEIN//MYELIN BASIC PROTEIN

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