Class information for:
Level 1: POLG//MNGIE//DEOXYRIBONUCLEOSIDE KINASE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
8495 1180 32.7 84%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1233 8561 DEOXYCYTIDINE KINASE//PURINE NUCLEOSIDE PHOSPHORYLASE//NUCLEOSIDE TRANSPORT

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 POLG Author keyword 63 67% 5% 57
2 MNGIE Author keyword 59 81% 3% 35
3 DEOXYRIBONUCLEOSIDE KINASE Author keyword 53 95% 2% 18
4 ALPERS SYNDROME Author keyword 40 79% 2% 26
5 MITOCHONDRIAL DNA DEPLETION SYNDROME Author keyword 36 83% 2% 20
6 MITOCHONDRIAL DNA DEPLETION Author keyword 31 66% 2% 29
7 ALPERS HUTTENLOCHER SYNDROME Author keyword 31 92% 1% 12
8 MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY Author keyword 30 84% 1% 16
9 MPV17 Author keyword 26 87% 1% 13
10 DGUOK Author keyword 23 100% 1% 10

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 POLG 63 67% 5% 57 Search POLG Search POLG
2 MNGIE 59 81% 3% 35 Search MNGIE Search MNGIE
3 DEOXYRIBONUCLEOSIDE KINASE 53 95% 2% 18 Search DEOXYRIBONUCLEOSIDE+KINASE Search DEOXYRIBONUCLEOSIDE+KINASE
4 ALPERS SYNDROME 40 79% 2% 26 Search ALPERS+SYNDROME Search ALPERS+SYNDROME
5 MITOCHONDRIAL DNA DEPLETION SYNDROME 36 83% 2% 20 Search MITOCHONDRIAL+DNA+DEPLETION+SYNDROME Search MITOCHONDRIAL+DNA+DEPLETION+SYNDROME
6 MITOCHONDRIAL DNA DEPLETION 31 66% 2% 29 Search MITOCHONDRIAL+DNA+DEPLETION Search MITOCHONDRIAL+DNA+DEPLETION
7 ALPERS HUTTENLOCHER SYNDROME 31 92% 1% 12 Search ALPERS+HUTTENLOCHER+SYNDROME Search ALPERS+HUTTENLOCHER+SYNDROME
8 MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY 30 84% 1% 16 Search MITOCHONDRIAL+NEUROGASTROINTESTINAL+ENCEPHALOMYOPATHY Search MITOCHONDRIAL+NEUROGASTROINTESTINAL+ENCEPHALOMYOPATHY
9 MPV17 26 87% 1% 13 Search MPV17 Search MPV17
10 DGUOK 23 100% 1% 10 Search DGUOK Search DGUOK

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 ALPERS SYNDROME 102 76% 6% 71
2 POLG MUTATIONS 100 74% 6% 73
3 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA 67 29% 17% 197
4 W748S MUTATION 48 91% 2% 20
5 DEOXYGUANOSINE KINASE 45 66% 4% 42
6 POLG 44 76% 3% 31
7 MITOCHONDRIAL DNA DEPLETION 43 44% 6% 74
8 MTDNA DEPLETION 42 46% 6% 68
9 TK2 DEFICIENCY 41 100% 1% 15
10 DEOXYRIBONUCLEOSIDE KINASES 38 55% 4% 48

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Defects in mitochondrial DNA replication and human disease 2012 59 102 90%
Inherited mitochondrial diseases of DNA replication 2008 125 79 85%
Mitochondrial DNA Depletion Syndromes: Review and Updates of Genetic Basis, Manifestations, and Therapeutic Options 2013 23 122 84%
Mitochondrial DNA depletion syndromes - Many genes, common mechanisms 2010 62 80 91%
The role of the Mpv17 protein mutations of which cause mitochondrial DNA depletion syndrome (MDDS): lessons from homologs in different species 2015 1 60 53%
The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders 2010 32 59 83%
Polymerase Gamma 1 Mutations Clinical Correlations 2010 32 68 82%
Syndromes associated with mitochondrial DNA depletion 2014 4 67 75%
Alpers-Huttenlocher Syndrome 2013 8 64 81%
Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1) 2009 24 51 100%

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 SECT VET MED BIOCHEM 19 70% 1.4% 16
2 VET MED CHEM 10 26% 3.0% 35
3 EXPT TECHNOL MED 8 70% 0.6% 7
4 PATOL MITOCONDRIAL 4 75% 0.3% 3
5 UNIT MOL NEUROGENET 4 17% 1.9% 22
6 PIERFRANCO LUISA MARIANI STUDY CHILDRENS MI 3 29% 0.8% 10
7 PROGRAMME MOL NEUROL 3 50% 0.3% 4
8 HUMAN GENET JOINT PHD PROGRAM 3 60% 0.3% 3
9 MITOCHONDRIAL SCI MED 3 32% 0.6% 7
10 MITOCHONDRIAL METAB DIS 2 23% 0.8% 9

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000216697 CLOFARABINE//CANC THER EUT IMMUNOL//NELARABINE
2 0.0000153581 MITOCHONDRIAL NUCLEOIDS//TFAM//MITOCHONDRIAL NUCLEOID
3 0.0000146017 MELAS//MITOCHONDRIAL ENCEPHALOMYOPATHY//KEARNS SAYRE SYNDROME
4 0.0000126334 THYMIDINE KINASE 1//SERUM THYMIDINE KINASE 1//DNA SYNTHESIZING ENZYMES
5 0.0000110660 GEMCITABINE//TROXACITABINE//DEOXYCYTIDINE KINASE
6 0.0000102845 SUCCINYL COA SYNTHETASE//OFF VP//CANADA GRP PROT STRUCT FUNCT
7 0.0000099127 MITOCHONDRIAL TOXICITY//DISTAL SENSORY POLYNEUROPATHY//ANTIRETROVIRAL TOXIC NEUROPATHY
8 0.0000094353 DAP3//ICT1//MITOCHONDRIAL RIBOSOMAL PROTEINS
9 0.0000063994 4977 BP DELETION//MTDNA MUTATOR MICE//COMMON DELETION
10 0.0000062458 DNTP IMBALANCE//BLC 2//MICROBIAL TEST SYSTEMS