Class information for:
Level 1: MELAS//MITOCHONDRIAL ENCEPHALOMYOPATHY//KEARNS SAYRE SYNDROME

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
82 4404 34.0 80%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
201 20439 MELAS//MITOCHONDRIAL DNA//LEBERS HEREDITARY OPTIC NEUROPATHY

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 MELAS Author keyword 405 78% 6% 268
2 MITOCHONDRIAL ENCEPHALOMYOPATHY Author keyword 189 79% 3% 122
3 KEARNS SAYRE SYNDROME Author keyword 177 79% 3% 112
4 MITOCHONDRIAL MYOPATHY Author keyword 149 54% 4% 190
5 PEARSON SYNDROME Author keyword 126 95% 1% 41
6 MITOCHONDRIAL DISEASE Author keyword 125 41% 5% 235
7 LEIGH SYNDROME Author keyword 119 60% 3% 131
8 MERRF Author keyword 106 81% 1% 64
9 MELAS SYNDROME Author keyword 101 81% 1% 62
10 MITOCHONDRIAL ENCEPHALOMYOPATHIES Author keyword 74 79% 1% 48

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 MELAS 405 78% 6% 268 Search MELAS Search MELAS
2 MITOCHONDRIAL ENCEPHALOMYOPATHY 189 79% 3% 122 Search MITOCHONDRIAL+ENCEPHALOMYOPATHY Search MITOCHONDRIAL+ENCEPHALOMYOPATHY
3 KEARNS SAYRE SYNDROME 177 79% 3% 112 Search KEARNS+SAYRE+SYNDROME Search KEARNS+SAYRE+SYNDROME
4 MITOCHONDRIAL MYOPATHY 149 54% 4% 190 Search MITOCHONDRIAL+MYOPATHY Search MITOCHONDRIAL+MYOPATHY
5 PEARSON SYNDROME 126 95% 1% 41 Search PEARSON+SYNDROME Search PEARSON+SYNDROME
6 MITOCHONDRIAL DISEASE 125 41% 5% 235 Search MITOCHONDRIAL+DISEASE Search MITOCHONDRIAL+DISEASE
7 LEIGH SYNDROME 119 60% 3% 131 Search LEIGH+SYNDROME Search LEIGH+SYNDROME
8 MERRF 106 81% 1% 64 Search MERRF Search MERRF
9 MELAS SYNDROME 101 81% 1% 62 Search MELAS+SYNDROME Search MELAS+SYNDROME
10 MITOCHONDRIAL ENCEPHALOMYOPATHIES 74 79% 1% 48 Search MITOCHONDRIAL+ENCEPHALOMYOPATHIES Search MITOCHONDRIAL+ENCEPHALOMYOPATHIES

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 STROKE LIKE EPISODES 726 79% 11% 468
2 KEARNS SAYRE SYNDROME 714 70% 13% 593
3 MELAS 416 70% 8% 349
4 RAGGED RED FIBERS 410 79% 6% 264
5 ENCEPHALOMYOPATHIES 380 83% 5% 213
6 TRANSFER RNALEUUUR GENE 336 78% 5% 221
7 ENCEPHALOMYOPATHY 293 68% 6% 258
8 LACTIC ACIDOSIS 269 30% 17% 760
9 MTDNA MUTATION 230 76% 4% 159
10 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA 178 44% 7% 304

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 MITOCHONDRION 11 11% 2% 101

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Mitochondrial diseases in man and mouse 1999 1822 84 36%
Mitochondrial DNA mutations in human disease 2005 539 158 42%
Mechanisms of disease: Mitochondrial respiratory-chain diseases 2003 704 70 36%
Human mitochondrial DNA: roles of inherited and somatic mutations 2012 112 126 29%
Systematic review of cardiac electrical disease in Kearns-Sayre syndrome and mitochondrial cytopathy 2015 1 37 59%
Mitochondrial DNA mutations and pathogenesis 1997 273 162 77%
Mitochondrial DNA and disease 2012 71 98 40%
Mitochondrial DNA mutations and human disease 2010 102 238 49%
Concise Reviews: Assisted Reproductive Technologies to Prevent Transmission of Mitochondrial DNA Disease 2015 1 44 48%
Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks 2015 1 71 46%

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 MITOCHONDRIAL GRP 42 31% 2.6% 114
2 H HOUSTON MERRITT CLIN MUSCULAR DYSTROPHY 16 48% 0.6% 25
3 WELLCOME TRUST MITOCHONDRIAL 9 26% 0.7% 31
4 NEUROL NEUROBIOL PSYCHIAT 7 16% 1.0% 42
5 NIJMEGEN MITOCHONDRIAL DISORDERS 7 16% 0.9% 40
6 ST VINCENTS MELBOURNE NEUROMUSCULAR DIAGNOST 6 80% 0.1% 4
7 UNIT GENET EPIDEMIOL MOL 6 80% 0.1% 4
8 UNIT MOL NEUROGENET 6 20% 0.6% 27
9 MENTAL RETARDAT BIRTH DEFECT 6 14% 0.9% 39
10 NEUROPEDIAT MUSCLE DISORDERS UNIT 6 100% 0.1% 4

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000146017 POLG//MNGIE//DEOXYRIBONUCLEOSIDE KINASE
2 0.0000128142 4977 BP DELETION//MTDNA MUTATOR MICE//COMMON DELETION
3 0.0000128138 LEBERS HEREDITARY OPTIC NEUROPATHY//LHON//LEBER HEREDITARY OPTIC NEUROPATHY
4 0.0000103124 PONTOSUBICULAR NECROSIS//INFANTILE BILATERAL STRIATAL NECROSIS//BRAINSTEM NECROSIS
5 0.0000094205 D310//MITOCHONDRIAL MICROSATELLITE INSTABILITY//MITOCHONDRIAL HAPLOGROUPS
6 0.0000092867 DAP3//ICT1//MITOCHONDRIAL RIBOSOMAL PROTEINS
7 0.0000091251 DOUBLY UNIPARENTAL INHERITANCE//PATERNAL LEAKAGE//MITOCHONDRIAL POLARITY
8 0.0000088657 YIDC//OXA1//COX17
9 0.0000081155 COMPLEX I//NADH UBIQUINONE OXIDOREDUCTASE//NADH UBIQUINONE OXIDOREDUCTASE
10 0.0000075033 BLUE NATIVE ELECTROPHORESIS//TMEM70//BCS1L