Class information for:
Level 1: MOWAT WILSON SYNDROME//ATBF1//ZFHX1B

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
25417 282 35.2 90%


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
27 3       DEVELOPMENTAL BIOLOGY//DEVELOPMENT//AGR2 109777
2641 2             EPITHELIAL MESENCHYMAL TRANSITION//EMT//SNAIL 3501
25417 1                   MOWAT WILSON SYNDROME//ATBF1//ZFHX1B 282

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 MOWAT WILSON SYNDROME authKW 3490634 12% 92% 35
2 ATBF1 authKW 1307105 5% 93% 13
3 ZFHX1B authKW 1205206 6% 70% 16
4 DELTA EF1 authKW 1158996 6% 63% 17
5 ZEB2 GENE authKW 974530 3% 100% 9
6 SIP1 authKW 615978 6% 36% 16
7 MOWAT WILSON authKW 556872 2% 86% 6
8 ZFHX1 authKW 433124 1% 100% 4
9 AREB6 authKW 346498 1% 80% 4
10 AT MOTIF BINDING FACTOR 1 ATBF1 authKW 324843 1% 100% 3

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 1656 32% 0% 91
2 Developmental Biology 1030 12% 0% 35
3 Cell Biology 354 20% 0% 55
4 Biochemistry & Molecular Biology 259 28% 0% 79
5 Pediatrics 61 6% 0% 17
6 Anatomy & Morphology 38 2% 0% 5
7 Biophysics 32 5% 0% 14
8 Oncology 18 6% 0% 18
9 Pathology 16 3% 0% 8
10 Cell & Tissue Engineering 13 1% 0% 2

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 MOL BIOL CELGEN 316382 5% 19% 15
2 NIIGATA ROSAI HOSP 247496 1% 57% 4
3 BIOL BIOPHYS SCI DENT 108281 0% 100% 1
4 BRAIN KOREA PROJECT 21 ORAL BIOL DENT 108281 0% 100% 1
5 CELL GROWTH DIFFERENTIAT DEV V1B07 108281 0% 100% 1
6 CHEM BIOCHEM PHYS HEMATOL 108281 0% 100% 1
7 CLIN PLA AFFILIATED 108281 0% 100% 1
8 GRP MED XENOMCEGENPRB2 108281 0% 100% 1
9 GULHANE MIL MED GATA 108281 0% 100% 1
10 INSERM EQUIPE 11 U955 108281 0% 100% 1

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 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 6766 7% 0% 19
2 CLINICAL DYSMORPHOLOGY 3487 2% 1% 6
3 EUROPEAN JOURNAL OF MEDICAL GENETICS 1517 1% 0% 4
4 MECHANISMS OF DEVELOPMENT 1242 2% 0% 6
5 JOURNAL OF MEDICAL GENETICS 907 2% 0% 7
6 MOLECULAR CYTOGENETICS 889 1% 0% 2
7 HUMAN MOLECULAR GENETICS 699 3% 0% 8
8 MOLECULAR AND CELLULAR BIOLOGY 574 4% 0% 11
9 GENE EXPRESSION PATTERNS 431 1% 0% 2
10 PAEDIATRIA CROATICA 383 0% 0% 1

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 MOWAT WILSON SYNDROME 3490634 12% 92% 35 Search MOWAT+WILSON+SYNDROME Search MOWAT+WILSON+SYNDROME
2 ATBF1 1307105 5% 93% 13 Search ATBF1 Search ATBF1
3 ZFHX1B 1205206 6% 70% 16 Search ZFHX1B Search ZFHX1B
4 DELTA EF1 1158996 6% 63% 17 Search DELTA+EF1 Search DELTA+EF1
5 ZEB2 GENE 974530 3% 100% 9 Search ZEB2+GENE Search ZEB2+GENE
6 SIP1 615978 6% 36% 16 Search SIP1 Search SIP1
7 MOWAT WILSON 556872 2% 86% 6 Search MOWAT+WILSON Search MOWAT+WILSON
8 ZFHX1 433124 1% 100% 4 Search ZFHX1 Search ZFHX1
9 AREB6 346498 1% 80% 4 Search AREB6 Search AREB6
10 AT MOTIF BINDING FACTOR 1 ATBF1 324843 1% 100% 3 Search AT+MOTIF+BINDING+FACTOR+1+ATBF1 Search AT+MOTIF+BINDING+FACTOR+1+ATBF1

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 WENGER, TL , HARR, M , RICCIARDI, S , BHOJ, E , SANTANI, A , ADAM, MP , BARNETT, SS , GANETZKY, R , MCDONALD-MCGINN, DM , BATTAGLIA, D , ET AL (2014) CHARGE-LIKE PRESENTATION, CRANIOSYNOSTOSIS AND MILD MOWAT-WILSON SYNDROME DIAGNOSED BY RECOGNITION OF THE DISTINCTIVE FACIAL GESTALT IN A COHORT OF 28 NEW CASES.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 164. ISSUE 10. P. 2557 -2566 40 91% 6
2 COYLE, D , PURI, P , (2015) HIRSCHSPRUNG'S DISEASE IN CHILDREN WITH MOWAT-WILSON SYNDROME.PEDIATRIC SURGERY INTERNATIONAL. VOL. 31. ISSUE 8. P. 711 -717 34 87% 1
3 GARAVELLI, L , MAINARDI, PC , (2007) MOWAT-WILSON SYNDROME.ORPHANET JOURNAL OF RARE DISEASES. VOL. 2. ISSUE . P. - 31 82% 53
4 GARAVELLI, L , ZOLLINO, M , MAINARDI, PC , GURRIERI, F , RIVIERI, F , SOLI, F , VERRI, R , ALBERTINI, E , FAVARON, E , ZIGNANI, M , ET AL (2009) MOWAT-WILSON SYNDROME: FACIAL PHENOTYPE CHANGING WITH AGE: STUDY OF 19 ITALIAN PATIENTS AND REVIEW OF THE LITERATURE.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 149A. ISSUE 3. P. 417-426 25 96% 39
5 MOAL, FDL , WILSON, M , MOWAT, D , COLLOT, N , NIEL, F , GOOSSENS, M , (2007) ZFHX1B MUTATIONS IN PATIENTS WITH MOWAT-WILSON SYNDROME.HUMAN MUTATION. VOL. 28. ISSUE 4. P. 313 -321 30 88% 4
6 HEGARTY, SV , SULLIVAN, AM , O'KEEFFE, GW , (2015) ZEB2: A MULTIFUNCTIONAL REGULATOR OF NERVOUS SYSTEM DEVELOPMENT.PROGRESS IN NEUROBIOLOGY. VOL. 132. ISSUE . P. 81 -95 55 35% 3
7 HIGASHI, Y , WAKAMATSU, N , (2003) FUNCTION OF ZFHX1 FAMILY AND MOLECULAR GENETIC ANALYSIS OF ITS DEFICIENCY.SEIKAGAKU. VOL. 75. ISSUE 1. P. 27-36 30 79% 0
8 BURANIQI, E , MOODLEY, M , (2015) ZEB2 GENE MUTATION AND DUPLICATION OF 22Q11.23 IN MOWAT-WILSON SYNDROME.JOURNAL OF CHILD NEUROLOGY. VOL. 30. ISSUE 1. P. 32 -36 19 86% 2
9 TANTELES, GA , CHRISTOPHIDOU-ANASTASIADOU, V , (2014) OCULAR PHENOTYPE OF MOWAT-WILSON SYNDROME IN THE FIRST REPORTED CYPRIOT PATIENTS: AN UNDER-RECOGNIZED ASSOCIATION.CLINICAL DYSMORPHOLOGY. VOL. 23. ISSUE 1. P. 20-23 17 100% 2
10 KILIC, E , CETINKAYA, A , UTINE, GE , BODUROGLU, K , (2016) A DIAGNOSIS TO CONSIDER IN INTELLECTUAL DISABILITY: MOWAT-WILSON SYNDROME.JOURNAL OF CHILD NEUROLOGY. VOL. 31. ISSUE 7. P. 913 -917 13 100% 1

Classes with closest relation at Level 1


Rank Class id link
1 29445 ZNF217//CTBP//CTBP1
2 11097 ENTERIC NERVOUS SYSTEM//HIRSCHSPRUNGS DISEASE//HIRSCHSPRUNG DISEASE
3 1411 EPITHELIAL MESENCHYMAL TRANSITION//EMT//SNAIL
4 5796 HIRSCHSPRUNGS DISEASE//INTESTINAL NEURONAL DYSPLASIA//HIRSCHSPRUNG DISEASE
5 18084 IRIDOCORNEAL ENDOTHELIAL SYNDROME//SLC4A11//POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY
6 10986 TINMAN//MYOBLAST FUSION//DORSAL VESSEL
7 6924 SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5
8 20601 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT//CHROMOTHRIPSIS
9 14961 HEPATOID ADENOCARCINOMA//HEPATOID CARCINOMA//YOLK SAC TUMOR
10 9279 C MYB//B MYB//MYB

Go to start page