Class information for:
Level 1: GLUCOSE 6 PHOSPHATASE//SECT CELLULAR DIFFERENTIAT//GLYCOGEN STORAGE DISEASE

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
7488 1362 29.6 65%


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
584 3       POMPE DISEASE//PIN1//CYCLOPHILIN 15652
1662 2             POMPE DISEASE//GLYCOGEN STORAGE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II 6857
7488 1                   GLUCOSE 6 PHOSPHATASE//SECT CELLULAR DIFFERENTIAT//GLYCOGEN STORAGE DISEASE 1362

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 GLUCOSE 6 PHOSPHATASE authKW 1588135 12% 43% 163
2 SECT CELLULAR DIFFERENTIAT address 895010 3% 87% 46
3 GLYCOGEN STORAGE DISEASE authKW 839732 7% 39% 96
4 GLYCOGEN STORAGE DISEASE TYPE III authKW 762827 3% 97% 35
5 GLYCOGEN STORAGE DISEASE TYPE IA authKW 620420 2% 86% 32
6 GLYCOGEN STORAGE DISEASE TYPE I authKW 483136 2% 86% 25
7 GLUCOSE 6 PHOSPHATE TRANSPORTER authKW 389870 1% 87% 20
8 GLYCOGEN DEBRANCHING ENZYME authKW 368697 2% 66% 25
9 GLYCOGEN STORAGE DISEASE TYPE IB authKW 363165 1% 90% 18
10 GLYCOGEN STORAGE DISEASE TYPE 1 authKW 337584 1% 94% 16

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 Endocrinology & Metabolism 3359 20% 0% 271
2 Pediatrics 3021 17% 0% 230
3 Genetics & Heredity 2916 20% 0% 274
4 Medicine, Research & Experimental 1995 15% 0% 206
5 Biochemistry & Molecular Biology 1142 27% 0% 368
6 Biophysics 455 8% 0% 104
7 Nutrition & Dietetics 261 4% 0% 58
8 Gastroenterology & Hepatology 246 5% 0% 66
9 Medical Laboratory Technology 124 2% 0% 25
10 Transplantation 71 2% 0% 26

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 SECT CELLULAR DIFFERENTIAT 895010 3% 87% 46
2 GLYCOGEN STORAGE DIS PROGRAM 290525 1% 72% 18
3 U855 264335 2% 47% 25
4 HERITABLE DISORDERS BRANCH 180503 3% 19% 42
5 NINEWELLS HOSP MED OBSTET GYNAECOL 130427 1% 73% 8
6 MED LYON EST LAENNEC 67254 0% 100% 3
7 REFERENCE MALAD HEREDITAI METAB HEPAT 57639 0% 43% 6
8 NUTR ENDOCRINOL METAB 56040 0% 50% 5
9 U449 49877 1% 14% 16
10 BIOCHEMGRP RECH TRANSPORT MEMBRANAIRE 44836 0% 100% 2

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 65484 8% 3% 115
2 EUROPEAN JOURNAL OF PEDIATRICS 12690 5% 1% 65
3 MOLECULAR GENETICS AND METABOLISM 4451 2% 1% 25
4 JOURNAL OF PEDIATRICS 1451 2% 0% 30
5 GENETICS IN MEDICINE 1373 1% 1% 10
6 JOURNAL OF BIOLOGICAL CHEMISTRY 1125 7% 0% 92
7 DIABETES 1037 2% 0% 24
8 JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION 995 1% 0% 18
9 JOURNAL OF HUMAN GENETICS 954 1% 0% 10
10 PEDIATRIC RESEARCH 949 1% 0% 20

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 GLUCOSE 6 PHOSPHATASE 1588135 12% 43% 163 Search GLUCOSE+6+PHOSPHATASE Search GLUCOSE+6+PHOSPHATASE
2 GLYCOGEN STORAGE DISEASE 839732 7% 39% 96 Search GLYCOGEN+STORAGE+DISEASE Search GLYCOGEN+STORAGE+DISEASE
3 GLYCOGEN STORAGE DISEASE TYPE III 762827 3% 97% 35 Search GLYCOGEN+STORAGE+DISEASE+TYPE+III Search GLYCOGEN+STORAGE+DISEASE+TYPE+III
4 GLYCOGEN STORAGE DISEASE TYPE IA 620420 2% 86% 32 Search GLYCOGEN+STORAGE+DISEASE+TYPE+IA Search GLYCOGEN+STORAGE+DISEASE+TYPE+IA
5 GLYCOGEN STORAGE DISEASE TYPE I 483136 2% 86% 25 Search GLYCOGEN+STORAGE+DISEASE+TYPE+I Search GLYCOGEN+STORAGE+DISEASE+TYPE+I
6 GLUCOSE 6 PHOSPHATE TRANSPORTER 389870 1% 87% 20 Search GLUCOSE+6+PHOSPHATE+TRANSPORTER Search GLUCOSE+6+PHOSPHATE+TRANSPORTER
7 GLYCOGEN DEBRANCHING ENZYME 368697 2% 66% 25 Search GLYCOGEN+DEBRANCHING+ENZYME Search GLYCOGEN+DEBRANCHING+ENZYME
8 GLYCOGEN STORAGE DISEASE TYPE IB 363165 1% 90% 18 Search GLYCOGEN+STORAGE+DISEASE+TYPE+IB Search GLYCOGEN+STORAGE+DISEASE+TYPE+IB
9 GLYCOGEN STORAGE DISEASE TYPE 1 337584 1% 94% 16 Search GLYCOGEN+STORAGE+DISEASE+TYPE+1 Search GLYCOGEN+STORAGE+DISEASE+TYPE+1
10 GLYCOGEN STORAGE DISEASE TYPE 1A 270614 1% 93% 13 Search GLYCOGEN+STORAGE+DISEASE+TYPE+1A Search GLYCOGEN+STORAGE+DISEASE+TYPE+1A

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 VAN SCHAFTINGEN, E , GERIN, I , (2002) THE GLUCOSE-6-PHOSPHATASE SYSTEM.BIOCHEMICAL JOURNAL. VOL. 362. ISSUE . P. 513 -532 159 74% 187
2 CHOU, JY , JUN, HS , MANSFIELD, BC , (2010) GLYCOGEN STORAGE DISEASE TYPE I AND G6PASE-BETA DEFICIENCY: ETIOLOGY AND THERAPY.NATURE REVIEWS ENDOCRINOLOGY. VOL. 6. ISSUE 12. P. 676-688 100 88% 27
3 FROISSART, R , PIRAUD, M , BOUDJEMLINE, AM , VIANEY-SABAN, C , PETIT, F , HUBERT-BURON, A , EBERSCHWEILER, PT , GAJDOS, V , LABRUNE, P , (2011) GLUCOSE-6-PHOSPHATASE DEFICIENCY.ORPHANET JOURNAL OF RARE DISEASES. VOL. 6. ISSUE . P. - 93 87% 32
4 CHOU, JY , MANSFIELD, BC , (2008) MUTATIONS IN THE GLUCOSE-6-PHOSPHATASE-ALPHA (G6PC) GENE THAT CAUSE TYPE IA GLYCOGEN STORAGE DISEASE.HUMAN MUTATION. VOL. 29. ISSUE 7. P. 921 -930 82 92% 38
5 WOLFSDORF, JI , HOLM, IA , WEINSTEIN, DA , (1999) GLYCOGEN STORAGE DISEASES - PHENOTYPIC, GENETIC, AND BIOCHEMICAL CHARACTERISTICS, AND THERAPY.ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA. VOL. 28. ISSUE 4. P. 801-+ 111 81% 30
6 KISHNANI, PS , AUSTIN, SL , ARN, P , BALI, DS , MED, AB , CASE, LE , CHUNG, WK , DESAI, DM , EL-GHARBAWY, A , HALLER, R , ET AL (2010) GLYCOGEN STORAGE DISEASE TYPE III DIAGNOSIS AND MANAGEMENT GUIDELINES.GENETICS IN MEDICINE. VOL. 12. ISSUE 7. P. 446 -463 65 80% 48
7 VAN DE WERVE, G , LANGE, A , NEWGARD, C , MECHIN, MC , LI, YZ , BERTELOOT, A , (2000) NEW LESSONS IN THE REGULATION OF GLUCOSE METABOLISM TAUGHT BY THE GLUCOSE 6-PHOSPHATASE SYSTEM.EUROPEAN JOURNAL OF BIOCHEMISTRY. VOL. 267. ISSUE 6. P. 1533 -1549 114 63% 76
8 KOEBERL, DD , KISHNANI, PS , BALI, D , CHEN, YT , (2009) EMERGING THERAPIES FOR GLYCOGEN STORAGE DISEASE TYPE I.TRENDS IN ENDOCRINOLOGY AND METABOLISM. VOL. 20. ISSUE 5. P. 252 -258 53 90% 13
9 CHOU, JY , JUN, HS , MANSFIELD, BC , (2013) THE SLC37 FAMILY OF PHOSPHATE-LINKED SUGAR PHOSPHATE ANTIPORTERS.MOLECULAR ASPECTS OF MEDICINE. VOL. 34. ISSUE 2-3. P. 601-611 53 83% 3
10 RAKE, JP , VISSER, G , LABRUNE, P , LEONARD, JV , ULLRICH, K , SMIT, GPA , (2002) GLYCOGEN STORAGE DISEASE TYPE I: DIAGNOSIS, MANAGEMENT, CLINICAL COURSE AND OUTCOME. RESULTS OF THE EUROPEAN STUDY ON GLYCOGEN STORAGE DISEASE TYPE I (ESGSD I).EUROPEAN JOURNAL OF PEDIATRICS. VOL. 161. ISSUE . P. S20-S34 55 90% 118

Classes with closest relation at Level 1


Rank Class id link
1 21200 PHOSPHORYLASE KINASE//PHOSPHORYLASE KINASE DEFICIENCY//GLYCOGEN STORAGE DISEASE TYPE IX
2 20822 MCARDLES DISEASE//MYOPHOSPHORYLASE//GLYCOGENOSIS TYPE V
3 31620 FANCONI BICKEL SYNDROME//GLYCOGEN STORAGE DISEASE TYPE XI//FANCONI BICKEL
4 7510 GLUCONEOGENESIS//GLYCOGENOLYSIS//ENDOGENOUS GLUCOSE PRODUCTION
5 16803 LAFORA DISEASE//POLYGLUCOSAN BODIES//LAFORIN
6 10597 POMPE DISEASE//GLYCOGEN STORAGE DISEASE TYPE II//ACID ALPHA GLUCOSIDASE
7 34724 POLYUNSATURATED FREE FATTY ACID//2 2 DISULFONIC ACID//4 4 DINITROSTILBENE
8 30179 OBSTET GYNECOL ANAT//MODIFIED WACHSTEIN AND MEISEL METHOD//N ACETYLHOMOTAURINATE
9 9288 SEVERE CONGENITAL NEUTROPENIA//CYCLIC NEUTROPENIA//CONGENITAL NEUTROPENIA
10 10494 GLUCOKINASE//GLUCOKINASE ACTIVATOR//GLUCOKINASE REGULATORY PROTEIN

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