Class information for:
Level 1: NEWBORN SCREENING//MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY//UNIT MOL MED

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
2388 2263 29.5 73%


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
389 3       PEROXISOME//CARNITINE//JOURNAL OF INHERITED METABOLIC DISEASE 30841
2144 2             JOURNAL OF INHERITED METABOLIC DISEASE//NEWBORN SCREENING//METHYLMALONIC ACIDEMIA 5035
2388 1                   NEWBORN SCREENING//MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY//UNIT MOL MED 2263

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 NEWBORN SCREENING authKW 1092800 13% 27% 305
2 MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY authKW 498904 2% 86% 43
3 UNIT MOL MED address 435627 4% 38% 86
4 MCAD DEFICIENCY authKW 434918 2% 92% 35
5 INBORN ERRORS OF METABOLISM authKW 345210 5% 23% 112
6 JOURNAL OF INHERITED METABOLIC DISEASE journal 294232 14% 7% 314
7 FATTY ACID OXIDATION DISORDERS authKW 253326 1% 72% 26
8 SHORT CHAIN ACYL COA DEHYDROGENASE DEFICIENCY authKW 230064 1% 95% 18
9 ETHYLMALONIC ENCEPHALOPATHY authKW 216612 1% 94% 17
10 MULTIPLE ACYL COA DEHYDROGENASE DEFICIENCY authKW 211752 1% 83% 19

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 Genetics & Heredity 13127 32% 0% 726
2 Pediatrics 11314 25% 0% 561
3 Medicine, Research & Experimental 9715 25% 0% 565
4 Endocrinology & Metabolism 6719 22% 0% 491
5 Medical Laboratory Technology 4183 7% 0% 166
6 Medical Ethics 1002 1% 0% 30
7 Ethics 349 1% 0% 32
8 Clinical Neurology 291 6% 0% 147
9 Social Sciences, Biomedical 102 1% 0% 24
10 Biochemistry & Molecular Biology 101 10% 0% 237

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 UNIT MOL MED 435627 4% 38% 86
2 UNITE ETUD MALAD METAB 69383 0% 86% 6
3 GENET METAB DIS 55667 3% 7% 59
4 KIMBERLY H COURTWRIGHT JOSEPH W SUMMERS ME 47961 0% 44% 8
5 GENET SERV BRANCH 41310 0% 44% 7
6 NEWBORN SCREENING PROGRAM 40869 0% 30% 10
7 INVEST BIOQUIM CLIN PATOL MOL 40475 0% 100% 3
8 PUBL HLTH NEWBORN SCREENING STATE BAVARIA 40475 0% 100% 3
9 NEW ENGLAND NEWBORN SCREENING PROGRAM 37343 1% 23% 12
10 GENET METAB DISEMMA CHILDRENS HOSP 35975 0% 67% 4

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 INHERITED METABOLIC DISEASE 294232 14% 7% 314
2 MOLECULAR GENETICS AND METABOLISM 77564 6% 4% 134
3 GENETICS IN MEDICINE 25243 2% 3% 55
4 PEDIATRIC RESEARCH 7782 3% 1% 73
5 PUBLIC HEALTH GENOMICS 5811 1% 4% 12
6 EUROPEAN JOURNAL OF PEDIATRICS 5615 2% 1% 56
7 JOURNAL OF PEDIATRICS 4809 3% 1% 70
8 PEDIATRICS 4313 3% 0% 79
9 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3865 0% 3% 11
10 CLINICA CHIMICA ACTA 3359 2% 0% 53

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 NEWBORN SCREENING 1092800 13% 27% 305 Search NEWBORN+SCREENING Search NEWBORN+SCREENING
2 MEDIUM CHAIN ACYL COA DEHYDROGENASE DEFICIENCY 498904 2% 86% 43 Search MEDIUM+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY Search MEDIUM+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY
3 MCAD DEFICIENCY 434918 2% 92% 35 Search MCAD+DEFICIENCY Search MCAD+DEFICIENCY
4 INBORN ERRORS OF METABOLISM 345210 5% 23% 112 Search INBORN+ERRORS+OF+METABOLISM Search INBORN+ERRORS+OF+METABOLISM
5 FATTY ACID OXIDATION DISORDERS 253326 1% 72% 26 Search FATTY+ACID+OXIDATION+DISORDERS Search FATTY+ACID+OXIDATION+DISORDERS
6 SHORT CHAIN ACYL COA DEHYDROGENASE DEFICIENCY 230064 1% 95% 18 Search SHORT+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY Search SHORT+CHAIN+ACYL+COA+DEHYDROGENASE+DEFICIENCY
7 ETHYLMALONIC ENCEPHALOPATHY 216612 1% 94% 17 Search ETHYLMALONIC+ENCEPHALOPATHY Search ETHYLMALONIC+ENCEPHALOPATHY
8 MULTIPLE ACYL COA DEHYDROGENASE DEFICIENCY 211752 1% 83% 19 Search MULTIPLE+ACYL+COA+DEHYDROGENASE+DEFICIENCY Search MULTIPLE+ACYL+COA+DEHYDROGENASE+DEFICIENCY
9 VLCAD DEFICIENCY 202373 1% 100% 15 Search VLCAD+DEFICIENCY Search VLCAD+DEFICIENCY
10 ACYLCARNITINES 191551 3% 21% 67 Search ACYLCARNITINES Search ACYLCARNITINES

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 WAJNER, M , AMARAL, AU , (2016) MITOCHONDRIAL DYSFUNCTION IN FATTY ACID OXIDATION DISORDERS: INSIGHTS FROM HUMAN AND ANIMAL STUDIES.BIOSCIENCE REPORTS. VOL. 36. ISSUE . P. - 88 75% 1
2 GREGERSEN, N , ANDRESEN, BS , CORYDON, M , CORYDON, TJ , OLSEN, RKJ , BOLUND, L , BROSS, P , (2001) MUTATION ANALYSIS IN MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS: EXEMPLIFIED BY ACYL-COA DEHYDROGENASE DEFICIENCIES, WITH SPECIAL FOCUS ON GENOTYPE-PHENOTYPE RELATIONSHIP.HUMAN MUTATION. VOL. 18. ISSUE 3. P. 169 -189 99 77% 103
3 HOUTEN, SM , VIOLANTE, S , VENTURA, FV , WANDERS, RJA , (2016) THE BIOCHEMISTRY AND PHYSIOLOGY OF MITOCHONDRIAL FATTY ACID BETA-OXIDATION AND ITS GENETIC DISORDERS.ANNUAL REVIEW OF PHYSIOLOGY, VOL 78. VOL. 78. ISSUE . P. 23 -44 72 54% 5
4 NICHOLLS, SG , WILSON, BJ , ETCHEGARY, H , BREHAUT, JC , POTTER, BK , HAYEEMS, R , CHAKRABORTY, P , MILBURN, J , PULLMAN, D , TURNER, L , ET AL (2014) BENEFITS AND BURDENS OF NEWBORN SCREENING: PUBLIC UNDERSTANDING AND DECISION-MAKING.PERSONALIZED MEDICINE. VOL. 11. ISSUE 6. P. 593 -607 71 72% 1
5 GREGERSEN, N , ANDRESEN, BS , PEDERSEN, CB , OLSEN, RKJ , CORYDON, TJ , BROSS, P , (2008) MITOCHONDRIAL FATTY ACID OXIDATION DEFECTS-REMAINING CHALLENGES.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 31. ISSUE 5. P. 643-657 59 87% 58
6 MAK, CM , LEE, HCH , CHAN, AYW , LAM, CW , (2013) INBORN ERRORS OF METABOLISM AND EXPANDED NEWBORN SCREENING: REVIEW AND UPDATE.CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES. VOL. 50. ISSUE 6. P. 142-162 97 45% 15
7 WANDERS, RJA , VREKEN, P , DEN BOER, MEJ , WIJBURG, FA , VAN GENNIP, AH , IJLST, L , (1999) DISORDERS OF MITOCHONDRIAL FATTY ACYL-COA BETA-OXIDATION.JOURNAL OF INHERITED METABOLIC DISEASE. VOL. 22. ISSUE 4. P. 442 -487 95 61% 136
8 ANDRESEN, BS , LUND, AM , HOUGAARD, DM , CHRISTENSEN, E , GAHRN, B , CHRISTENSEN, M , BROSS, P , VESTED, A , SIMONSEN, H , SKOGSTRAND, K , ET AL (2012) MCAD DEFICIENCY IN DENMARK.MOLECULAR GENETICS AND METABOLISM. VOL. 106. ISSUE 2. P. 175-188 47 94% 11
9 BENNETT, MJ , RINALDO, P , STRAUSS, AW , (2000) INBORN ERRORS OF MITOCHONDRIAL FATTY ACID OXIDATION.CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES. VOL. 37. ISSUE 1. P. 1 -44 91 64% 60
10 SIM, KG , HAMMOND, J , WILCKEN, B , (2002) STRATEGIES FOR THE DIAGNOSIS OF MITOCHONDRIAL FATTY ACID BETA-OXIDATION DISORDERS.CLINICA CHIMICA ACTA. VOL. 323. ISSUE 1-2. P. 37-58 82 63% 52

Classes with closest relation at Level 1


Rank Class id link
1 17561 ELECTRON TRANSFERRING FLAVOPROTEIN//ISOVALERIC ACIDEMIA//ACYL COA DEHYDROGENASE
2 17020 GLUTARIC ACIDURIA TYPE I//GLUTARIC ACIDURIA TYPE 1//L 2 HYDROXYGLUTARIC ACIDURIA
3 14230 BETA KETOTHIOLASE DEFICIENCY//MITOCHONDRIAL ACETOACETYL COA THIOLASE//THIOLASE
4 8921 CARNITINE PALMITOYLTRANSFERASE//CARNITINE PALMITOYLTRANSFERASE I//CARNITINE PALMITOYLTRANSFERASE DEFICIENCY
5 36999 MED HUMANITIES SOCIAL SCI//ANXIETY ABOUT BABYS DIABETES RISK//CLIN RIGHT ISAR
6 30827 DODECANEDIOIC ACID//DIETHYL SEBACATE//AZELAIC ACID
7 20380 TERT BUTYLDIMETHYLSILYLATION//PROTEINOUS AMINO ACIDS//STAR SYMBOL PLOT
8 9072 METHYLMALONIC ACIDEMIA//PROPIONIC ACIDEMIA//METHYLMALONIC ACIDURIA
9 973 CARNITINE//L CARNITINE//CARNITINE DEFICIENCY
10 24942 3 HYDROXY 3 METHYLGLUTARIC ACIDURIA//3 METHYLGLUTACONIC ACIDURIA//3 METHYLGLUTARIC ACID

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