Class information for:
Level 1: FOXC1//PETERS ANOMALY//AXENFELD RIEGER SYNDROME

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
14805 749 31.2 71%


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
196 3       GENETICS & HEREDITY//FRAGILE X SYNDROME//AMERICAN JOURNAL OF MEDICAL GENETICS 53756
395 2             GENETICS & HEREDITY//ANNALES DE GENETIQUE//HOLOPROSENCEPHALY 16816
14805 1                   FOXC1//PETERS ANOMALY//AXENFELD RIEGER SYNDROME 749

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 FOXC1 authKW 1395324 7% 66% 52
2 PETERS ANOMALY authKW 1359428 7% 68% 49
3 AXENFELD RIEGER SYNDROME authKW 1030959 4% 82% 31
4 PETERS PLUS SYNDROME authKW 700797 3% 90% 19
5 RIEGER SYNDROME authKW 561803 3% 66% 21
6 AXENFELD RIEGER ANOMALY authKW 492112 2% 93% 13
7 PITX2 authKW 400692 5% 24% 41
8 RING CHROMOSOME 6 authKW 330209 1% 90% 9
9 ANTERIOR SEGMENT DYSGENESIS authKW 318403 2% 46% 17
10 PEDIATRIC KERATOPLASTY authKW 249695 1% 88% 7

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 Ophthalmology 22714 47% 0% 350
2 Genetics & Heredity 3302 28% 0% 211
3 Developmental Biology 655 6% 0% 47
4 Pediatrics 342 8% 0% 62
5 Anatomy & Morphology 80 2% 0% 12
6 Biochemistry & Molecular Biology 75 13% 0% 97
7 Cell Biology 34 6% 0% 42
8 Dentistry, Oral Surgery & Medicine 12 2% 0% 12
9 Medical Ethics 11 0% 0% 2
10 Oncology 5 4% 0% 28

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 BEIJING DRUG TARGET DRUG SCREEN 81534 0% 100% 2
2 KELLOGG EYE 305 81534 0% 100% 2
3 OCULAR GENET 66575 1% 23% 7
4 MOL MED OPHTHALMOL 54354 0% 67% 2
5 458TH HOSP 40767 0% 100% 1
6 ANTERIOR SEGMENT CORNEAL SURG SERV 40767 0% 100% 1
7 BIOCHEM FOOD BIOL SCI 40767 0% 100% 1
8 CANC PREVENT THER Y GYNECOL ONCOL 40767 0% 100% 1
9 CLIN OPHTHALMOL SAVE SIGHT 40767 0% 100% 1
10 CNRSUNITE MIXTE RECH 6231 CRN2M 40767 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 OPHTHALMIC PAEDIATRICS AND GENETICS 10709 1% 3% 10
2 OPHTHALMIC GENETICS 8241 1% 2% 11
3 CORNEA 6705 4% 1% 30
4 JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS 6248 2% 1% 16
5 JOURNAL OF AAPOS 6114 2% 1% 18
6 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 5910 4% 1% 29
7 AMERICAN JOURNAL OF MEDICAL GENETICS 3616 4% 0% 28
8 KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE 2873 3% 0% 21
9 MOLECULAR VISION 2409 2% 0% 14
10 AMERICAN JOURNAL OF OPHTHALMOLOGY 1881 3% 0% 22

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 FOXC1 1395324 7% 66% 52 Search FOXC1 Search FOXC1
2 PETERS ANOMALY 1359428 7% 68% 49 Search PETERS+ANOMALY Search PETERS+ANOMALY
3 AXENFELD RIEGER SYNDROME 1030959 4% 82% 31 Search AXENFELD+RIEGER+SYNDROME Search AXENFELD+RIEGER+SYNDROME
4 PETERS PLUS SYNDROME 700797 3% 90% 19 Search PETERS+PLUS+SYNDROME Search PETERS+PLUS+SYNDROME
5 RIEGER SYNDROME 561803 3% 66% 21 Search RIEGER+SYNDROME Search RIEGER+SYNDROME
6 AXENFELD RIEGER ANOMALY 492112 2% 93% 13 Search AXENFELD+RIEGER+ANOMALY Search AXENFELD+RIEGER+ANOMALY
7 PITX2 400692 5% 24% 41 Search PITX2 Search PITX2
8 RING CHROMOSOME 6 330209 1% 90% 9 Search RING+CHROMOSOME+6 Search RING+CHROMOSOME+6
9 ANTERIOR SEGMENT DYSGENESIS 318403 2% 46% 17 Search ANTERIOR+SEGMENT+DYSGENESIS Search ANTERIOR+SEGMENT+DYSGENESIS
10 PEDIATRIC KERATOPLASTY 249695 1% 88% 7 Search PEDIATRIC+KERATOPLASTY Search PEDIATRIC+KERATOPLASTY

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 TUMER, Z , BACH-HOLM, D , (2009) AXENFELD-RIEGER SYNDROME AND SPECTRUM OF PITX2 AND FOXC1 MUTATIONS.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 17. ISSUE 12. P. 1527 -1539 48 77% 68
2 STRUNGARU, MH , DINU, I , WALTER, MA , (2007) GENOTYPE-PHENOTYPE CORRELATIONS IN AXENFELD-RIEGER MALFORMATION AND GLAUCOMA PATIENTS WITH FOXC1 AND PITX2 MUTATIONS.INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. VOL. 48. ISSUE 1. P. 228-237 46 85% 45
3 FOOTZ, T , IDREES, F , ACHARYA, M , KOZLOWSKI, K , WALTER, MA , (2009) ANALYSIS OF MUTATIONS OF THE PITX2 TRANSCRIPTION FACTOR FOUND IN PATIENTS WITH AXENFELD-RIEGER SYNDROME.INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. VOL. 50. ISSUE 6. P. 2599-2606 40 85% 16
4 TONOKI, H , HARADA, N , SHIMOKAWA, O , YOSOZUMI, A , MONZAKI, K , SATOH, K , KOSAKI, R , SATO, A , MATSUMOTO, N , IIZUKA, S , (2011) AXENFELD-RIEGER ANOMALY AND AXENFELD-RIEGER SYNDROME: CLINICAL, MOLECULAR-CYTOGENETIC, AND DNA ARRAY ANALYSES OF THREE PATIENTS WITH CHROMOSOMAL DEFECTS AT 6P25.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 155A. ISSUE 12. P. 2925 -2932 31 97% 5
5 BEBY, F , PORTES, VD , TILL, M , MOTTOLESE, C , DENIS, P , (2012) CHROMOSOME 6P25 DELETION SYNDROME: REPORT OF A CASE WITH OPTIC DISC COLOBOMA AND REVIEW OF PUBLISHED OPHTHALMIC FINDINGS.OPHTHALMIC GENETICS. VOL. 33. ISSUE 4. P. 240-248 34 87% 1
6 SEIFI, M , FOOTZ, T , TAYLOR, SAM , ELHADY, GM , ABDALLA, EM , WALTER, MA , (2016) NOVEL PITX2 GENE MUTATIONS IN PATIENTS WITH AXENFELD-RIEGER SYNDROME.ACTA OPHTHALMOLOGICA. VOL. 94. ISSUE 7. P. E571 -E579 41 65% 0
7 IDREES, F , VAIDEANU, D , FRASER, SG , SOWDEN, JC , KHAW, PT , (2006) A REVIEW OF ANTERIOR SEGMENT DYSGENESES.SURVEY OF OPHTHALMOLOGY. VOL. 51. ISSUE 3. P. 213 -231 53 56% 55
8 LINHARES, ND , SVARTMAN, M , RODRIGUES, TC , ROSENBERG, C , VALADARES, ER , (2015) SUBTELOMERIC 6P25 DELETION/DUPLICATION: REPORT OF A PATIENT WITH NEW CLINICAL FINDINGS AND GENOTYPE-PHENOTYPE CORRELATIONS.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 58. ISSUE 5. P. 310 -318 31 76% 3
9 REIS, LM , TYLER, RC , KLOSS, BAV , SCHILTER, KF , LEVIN, AV , LOWRY, RB , ZWIJNENBURG, PJG , STROH, E , BROECKEL, U , MURRAY, JC , ET AL (2012) PITX2 AND FOXC1 SPECTRUM OF MUTATIONS IN OCULAR SYNDROMES.EUROPEAN JOURNAL OF HUMAN GENETICS. VOL. 20. ISSUE 12. P. 1224-1233 31 78% 15
10 CHANG, TC , SUMMERS, CG , SCHIMMENTI, LA , GRAJEWSKI, AL , (2012) AXENFELD-RIEGER SYNDROME: NEW PERSPECTIVES.BRITISH JOURNAL OF OPHTHALMOLOGY. VOL. 96. ISSUE 3. P. 318-322 26 90% 17

Classes with closest relation at Level 1


Rank Class id link
1 13237 ANIRIDIA//PAX6//PAX6 GENE
2 16763 FOXA1//FORKHEAD//FOXJ2
3 9052 MYOCILIN//OPTINEURIN//MYOC
4 18084 IRIDOCORNEAL ENDOTHELIAL SYNDROME//SLC4A11//POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY
5 30234 MEGALOCORNEA//NEUHAUSER SYNDROME//ANTERIOR MEGALOPHTHALMOS
6 16562 ANOPHTHALMIA//NANOPHTHALMOS//MICROPHTHALMIA
7 27098 ACRO CARDIO FACIAL SYNDROME//CHROMOSOME 6Q DELETION//SIM1 GENE
8 36128 TORIELLO CAREY SYNDROME//RITSCHER SCHINZEL SYNDROME//3C SYNDROME
9 33440 TRISOMY 20P//TRISOMY 6P//NEURENSIN 2
10 33589 TRISOMY 16Q//TRISOMY 16P//DUPLICATION CHROMOSOME 16P

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