Class information for:
Level 1: APLASIA CUTIS CONGENITA//ADAMS OLIVER SYNDROME//CUTIS MARMORATA TELANGIECTATICA CONGENITA

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
19553 500 19.1 61%


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
14 4 ORTHOPEDICS//DENTISTRY, ORAL SURGERY & MEDICINE//SPORT SCIENCES 808941
474 3       CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS 23888
1564 2             DISTRACTION OSTEOGENESIS//HEMIFACIAL MICROSOMIA//PIERRE ROBIN SEQUENCE 7357
19553 1                   APLASIA CUTIS CONGENITA//ADAMS OLIVER SYNDROME//CUTIS MARMORATA TELANGIECTATICA CONGENITA 500

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 APLASIA CUTIS CONGENITA authKW 3585698 16% 73% 80
2 ADAMS OLIVER SYNDROME authKW 3070322 11% 93% 54
3 CUTIS MARMORATA TELANGIECTATICA CONGENITA authKW 791453 4% 72% 18
4 SETLEIS SYNDROME authKW 615784 2% 92% 11
5 CUTIS APLASIA authKW 579018 3% 59% 16
6 CUTIS MARMORATA authKW 569974 3% 67% 14
7 APLASIA CUTIS CONGENITAL authKW 517289 2% 71% 12
8 SCALP DEFECT authKW 508120 4% 40% 21
9 CUTIS MARMORATA TELANGIECTATICA authKW 494662 2% 90% 9
10 MACROCEPHALY CUTIS MARMORATA TELANGIECTATICA CONGENITA authKW 305348 1% 100% 5

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 Dermatology 6530 28% 0% 138
2 Pediatrics 3877 31% 0% 153
3 Genetics & Heredity 1920 26% 0% 132
4 Surgery 515 19% 0% 94
5 Medical Ethics 180 1% 0% 6
6 Clinical Neurology 159 9% 0% 46
7 Obstetrics & Gynecology 42 4% 0% 18
8 Ophthalmology 26 3% 0% 13
9 Neuroimaging 2 0% 0% 2
10 Medicine, General & Internal 1 2% 0% 12

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 CCDHB 61070 0% 100% 1
2 CENT UNIV PLASENCIA 61070 0% 100% 1
3 CLIN CIRUGIA PEDIAT 61070 0% 100% 1
4 CLIN DIPARTIMENTO OSTETRICO GINECOL PEDIAT 61070 0% 100% 1
5 EQUIPE GENET ANOMALIES DEV GAD 61070 0% 100% 1
6 FEINBERG MED DERMATOL 61070 0% 100% 1
7 HOSP EPILEPSY GENET PROGRAM 61070 0% 100% 1
8 HOSP MESELIK 61070 0% 100% 1
9 IHSAN DOGRAMACI CHILDREN HOSP CLIN GENET 61070 0% 100% 1
10 INHERITED DIS MED 61070 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 PEDIATRIC DERMATOLOGY 25157 8% 1% 39
2 CLINICAL DYSMORPHOLOGY 19753 4% 2% 19
3 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 8882 6% 1% 29
4 PEDIATRIKA 6784 0% 11% 1
5 AMERICAN JOURNAL OF MEDICAL GENETICS 6254 6% 0% 30
6 GENETIC COUNSELING 2324 1% 1% 6
7 JOURNAL OF CRANIOFACIAL SURGERY 2105 3% 0% 16
8 INTERNATIONAL JOURNAL OF DERMATOLOGY 1399 3% 0% 13
9 ARCHIVES OF DERMATOLOGY 975 2% 0% 10
10 JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY 961 3% 0% 14

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 APLASIA CUTIS CONGENITA 3585698 16% 73% 80 Search APLASIA+CUTIS+CONGENITA Search APLASIA+CUTIS+CONGENITA
2 ADAMS OLIVER SYNDROME 3070322 11% 93% 54 Search ADAMS+OLIVER+SYNDROME Search ADAMS+OLIVER+SYNDROME
3 CUTIS MARMORATA TELANGIECTATICA CONGENITA 791453 4% 72% 18 Search CUTIS+MARMORATA+TELANGIECTATICA+CONGENITA Search CUTIS+MARMORATA+TELANGIECTATICA+CONGENITA
4 SETLEIS SYNDROME 615784 2% 92% 11 Search SETLEIS+SYNDROME Search SETLEIS+SYNDROME
5 CUTIS APLASIA 579018 3% 59% 16 Search CUTIS+APLASIA Search CUTIS+APLASIA
6 CUTIS MARMORATA 569974 3% 67% 14 Search CUTIS+MARMORATA Search CUTIS+MARMORATA
7 APLASIA CUTIS CONGENITAL 517289 2% 71% 12 Search APLASIA+CUTIS+CONGENITAL Search APLASIA+CUTIS+CONGENITAL
8 SCALP DEFECT 508120 4% 40% 21 Search SCALP+DEFECT Search SCALP+DEFECT
9 CUTIS MARMORATA TELANGIECTATICA 494662 2% 90% 9 Search CUTIS+MARMORATA+TELANGIECTATICA Search CUTIS+MARMORATA+TELANGIECTATICA
10 MACROCEPHALY CUTIS MARMORATA TELANGIECTATICA CONGENITA 305348 1% 100% 5 Search MACROCEPHALY+CUTIS+MARMORATA+TELANGIECTATICA+CONGENITA Search MACROCEPHALY+CUTIS+MARMORATA+TELANGIECTATICA+CONGENITA

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 WINSTON, KR , KETCH, LL , (2016) APLASIA CUTIS CONGENITA OF THE SCALP, COMPOSITE TYPE: THE CRITICALITY AND INSEPARABILITY OF NEUROSURGICAL AND PLASTIC SURGICAL MANAGEMENT.PEDIATRIC NEUROSURGERY. VOL. 51. ISSUE 3. P. 111 -120 51 91% 0
2 SNAPE, KMG , RUDDY, D , ZENKER, M , WUYTS, W , WHITEFORD, M , JOHNSON, D , LAM, W , TREMBATH, RC , (2009) THE SPECTRA OF CLINICAL PHENOTYPES IN APLASIA CUTIS CONGENITA AND TERMINAL TRANSVERSE LIMB DEFECTS.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 149A. ISSUE 8. P. 1860-1881 50 91% 33
3 UDAYAKUMARAN, S , MATHEW, J , PANIKAR, D , (2013) DILEMMAS AND CHALLENGES IN THE MANAGEMENT OF A NEONATE WITH ADAMS-OLIVER SYNDROME WITH INFECTED GIANT APLASIA CUTIS LESION AND EXSANGUINATION: A CASE-BASED UPDATE.CHILDS NERVOUS SYSTEM. VOL. 29. ISSUE 4. P. 535-541 30 97% 3
4 STEINBACHER, J , RATH, T , TZOU, CHJ , (2016) APLASIA CUTIS CONGENITA.HANDCHIRURGIE MIKROCHIRURGIE PLASTISCHE CHIRURGIE. VOL. 48. ISSUE 4. P. 239 -243 29 94% 0
5 TEMTAMY, SA , AGLAN, MS , ASHOUR, AM , ZAKI, MS , (2007) ADAMS-OLIVER SYNDROME: FURTHER EVIDENCE OF AN AUTOSOMAL RECESSIVE VARIANT.CLINICAL DYSMORPHOLOGY. VOL. 16. ISSUE 3. P. 141-149 30 94% 13
6 WEAVER, DD , NORBY, AR , ROSENFELD, JA , PROUD, VK , SPANGLER, BE , MING, JE , CHISHOLM, E , ZACKAI, EH , LEE, BH , EDELMANN, L , ET AL (2015) CHROMOSOME 1P36.22P36.21 DUPLICATIONS/TRIPLICATION CAUSES SETLEIS SYNDROME (FOCAL FACIAL DERMAL DYSPLASIA TYPE III).AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 167. ISSUE 5. P. 1061 -1070 25 81% 1
7 DE OLIVEIRA, RS , JUCA, CEB , LINS-NETO, AL , REGO, MADC , FARINA, J , MACHADO, HR , (2006) APLASIA CUTIS CONGENITA OF THE SCALP: IS THERE A BETTER TREATMENT STRATEGY?.CHILDS NERVOUS SYSTEM. VOL. 22. ISSUE 9. P. 1072 -1079 25 96% 24
8 BELKHOU, A , FRANCOIS, C , BENNIS, Y , DUQUENNOY-MARTINOT, V , GUERRESCHI, P , (2016) APLASIA CUTIS CONGENITA: UPDATE AND MANAGEMENT.ANNALES DE CHIRURGIE PLASTIQUE ESTHETIQUE. VOL. 61. ISSUE 5. P. 450 -461 23 85% 0
9 WRIGHT, DR , FRIEDEN, IJ , ORLOW, SJ , SHIN, HT , CHAMLIN, S , SCHAFFER, JV , PALLER, AS , (2009) THE MISNOMER "MACROCEPHALY-CUTIS MARMORATA TELANGIECTATICA CONGENITA SYNDROME" REPORT OF 12 NEW CASES AND SUPPORT FOR REVISING THE NAME TO MACROCEPHALY-CAPILLARY MALFORMATIONS.ARCHIVES OF DERMATOLOGY. VOL. 145. ISSUE 3. P. 287-293 26 81% 32
10 MESSERER, M , DIABIRA, S , BELLIARD, H , HAMLAT, A , (2010) ADAMS-OLIVER SYNDROME: A CASE WITH MINIMAL EXPRESSION.ARCHIVES DE PEDIATRIE. VOL. 17. ISSUE 10. P. 1460-1464 23 96% 1

Classes with closest relation at Level 1


Rank Class id link
1 32361 PARIETAL FORAMINA//FORAMINA PARIETALIA PERMAGNA//POTOCKI SHAFFER SYNDROME
2 19108 KLIPPEL TRENAUNAY SYNDROME//KLIPPEL TRENAUNAY WEBER SYNDROME//PARKES WEBER SYNDROME
3 14681 PROTEUS SYNDROME//MACRODACTYLY//ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS
4 22311 TWIN SPOTTING//PHACOMATOSIS PIGMENTOVASCULARIS//MONGOLIAN SPOT
5 17315 AMNIOTIC BAND SYNDROME//LIMB BODY WALL COMPLEX//AMNIOTIC BANDS
6 18443 ECTOPIC MENINGIOMA//INTRAOSSEOUS MENINGIOMA//SPHENO ORBITAL MENINGIOMA
7 26340 COHEN SYNDROME//CHORIORETINAL DYSPLASIA//COH1
8 16693 POLAND SYNDROME//MOEBIUS SYNDROME//MOBIUS SYNDROME
9 19877 ANGIOKERATOMA//ECCRINE ANGIOMATOUS HAMARTOMA//HOBNAIL HEMANGIOMA
10 22503 AICARDI SYNDROME//FOCAL DERMAL HYPOPLASIA//GOLTZ SYNDROME

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