Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
35992 | 88 | 18.0 | 51% |
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 |
3549 | 2 | ARTHROGRYPOSIS//FREEMAN SHELDON SYNDROME//DISTAL ARTHROGRYPOSIS | 1350 |
35992 | 1 | HYDRANENCEPHALY//FOWLER SYNDROME//FLVCR2 | 88 |
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 | HYDRANENCEPHALY | authKW | 4055761 | 34% | 39% | 30 |
2 | FOWLER SYNDROME | authKW | 2125349 | 8% | 88% | 7 |
3 | FLVCR2 | authKW | 1110386 | 5% | 80% | 4 |
4 | HEMIHYDRANENCEPHALY | authKW | 780740 | 3% | 75% | 3 |
5 | PROLIFERATIVE VASCULOPATHY | authKW | 780740 | 3% | 75% | 3 |
6 | ANATOMOFOETOPATHOL | address | 693992 | 2% | 100% | 2 |
7 | HYDRANENCEPHALY HYDROCEPHALY | authKW | 693992 | 2% | 100% | 2 |
8 | ARTERIAL WEB | authKW | 346996 | 1% | 100% | 1 |
9 | BRAIN CONGENITAL ANOMALIES | authKW | 346996 | 1% | 100% | 1 |
10 | CAROTID ARTERY ANOMALY | authKW | 346996 | 1% | 100% | 1 |
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 | Pediatrics | 975 | 36% | 0% | 32 |
2 | Clinical Neurology | 455 | 32% | 0% | 28 |
3 | Obstetrics & Gynecology | 88 | 10% | 0% | 9 |
4 | Pathology | 80 | 9% | 0% | 8 |
5 | Radiology, Nuclear Medicine & Medical Imaging | 77 | 13% | 0% | 11 |
6 | Acoustics | 71 | 6% | 0% | 5 |
7 | Genetics & Heredity | 41 | 10% | 0% | 9 |
8 | Medicine, Legal | 36 | 2% | 0% | 2 |
9 | Otorhinolaryngology | 18 | 3% | 0% | 3 |
10 | Humanities, Multidisciplinary | 7 | 1% | 0% | 1 |
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 | ANATOMOFOETOPATHOL | 693992 | 2% | 100% | 2 |
2 | CHAIR CHILD NEUROSPYCHIAT | 346996 | 1% | 100% | 1 |
3 | CLIN ADM HEAD NEUROSURG | 346996 | 1% | 100% | 1 |
4 | FAMILY MED ETH | 346996 | 1% | 100% | 1 |
5 | PLACENTOL FOETOPATHOL | 346996 | 1% | 100% | 1 |
6 | RILEY HOSP CHILDREN MED | 173497 | 1% | 50% | 1 |
7 | UNIT PEDIAT PEDIAT EMERGENCY | 126177 | 2% | 18% | 2 |
8 | PRENATAL ULTRASOUND UNIT | 115664 | 1% | 33% | 1 |
9 | FETAL PATHOL | 92529 | 2% | 13% | 2 |
10 | FETAL MED INTE T GRP GIMEF | 69398 | 1% | 20% | 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 | JOURNAL OF CHILD NEUROLOGY | 4582 | 9% | 0% | 8 |
2 | ITALIAN JOURNAL OF PEDIATRICS | 2298 | 2% | 0% | 2 |
3 | PEDIATRIC NEUROSCIENCE | 1834 | 1% | 1% | 1 |
4 | PEDIATRIC PATHOLOGY | 1322 | 1% | 0% | 1 |
5 | BIRTH DEFECTS-ORIGINAL ARTICLE SERIES | 1278 | 1% | 0% | 1 |
6 | DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY | 1173 | 5% | 0% | 4 |
7 | NEUROPATHOLOGY | 967 | 2% | 0% | 2 |
8 | ANNALES DE PEDIATRIE | 955 | 2% | 0% | 2 |
9 | DEVELOPMENTAL NEUROREHABILITATION | 794 | 1% | 0% | 1 |
10 | PEDIATRIC NEUROLOGY | 735 | 3% | 0% | 3 |
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 | HYDRANENCEPHALY | 4055761 | 34% | 39% | 30 | Search HYDRANENCEPHALY | Search HYDRANENCEPHALY |
2 | FOWLER SYNDROME | 2125349 | 8% | 88% | 7 | Search FOWLER+SYNDROME | Search FOWLER+SYNDROME |
3 | FLVCR2 | 1110386 | 5% | 80% | 4 | Search FLVCR2 | Search FLVCR2 |
4 | HEMIHYDRANENCEPHALY | 780740 | 3% | 75% | 3 | Search HEMIHYDRANENCEPHALY | Search HEMIHYDRANENCEPHALY |
5 | PROLIFERATIVE VASCULOPATHY | 780740 | 3% | 75% | 3 | Search PROLIFERATIVE+VASCULOPATHY | Search PROLIFERATIVE+VASCULOPATHY |
6 | HYDRANENCEPHALY HYDROCEPHALY | 693992 | 2% | 100% | 2 | Search HYDRANENCEPHALY+HYDROCEPHALY | Search HYDRANENCEPHALY+HYDROCEPHALY |
7 | ARTERIAL WEB | 346996 | 1% | 100% | 1 | Search ARTERIAL+WEB | Search ARTERIAL+WEB |
8 | BRAIN CONGENITAL ANOMALIES | 346996 | 1% | 100% | 1 | Search BRAIN+CONGENITAL+ANOMALIES | Search BRAIN+CONGENITAL+ANOMALIES |
9 | CAROTID ARTERY ANOMALY | 346996 | 1% | 100% | 1 | Search CAROTID+ARTERY+ANOMALY | Search CAROTID+ARTERY+ANOMALY |
10 | CEREBRAL PROLIFERATIVE GLOMERULOID VASCULOPATHY | 346996 | 1% | 100% | 1 | Search CEREBRAL+PROLIFERATIVE+GLOMERULOID+VASCULOPATHY | Search CEREBRAL+PROLIFERATIVE+GLOMERULOID+VASCULOPATHY |
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 | PAVONE, P , PRATICO, AD , VITALITI, G , RUGGIERI, M , RIZZO, R , PARANO, E , PAVONE, L , PERO, G , FALSAPERLA, R , (2014) HYDRANENCEPHALY: CEREBRAL SPINAL FLUID INSTEAD OF CEREBRAL MANTLES.ITALIAN JOURNAL OF PEDIATRICS. VOL. 40. ISSUE . P. - | 26 | 63% | 1 |
2 | CECCHETTO, G , MILANESE, L , GIORDANO, R , VIERO, A , SUMA, V , MANARA, R , (2013) LOOKING AT THE MISSING BRAIN: HYDRANENCEPHALY CASE SERIES AND LITERATURE REVIEW.PEDIATRIC NEUROLOGY. VOL. 48. ISSUE 2. P. 152-158 | 20 | 69% | 13 |
3 | KVARNUNG, M , TAYLAN, F , NILSSON, D , ALBAGE, M , NORDENSKJOLD, M , ANDERLID, BM , NORDGREN, A , LUNDBERG, ES , (2016) MUTATIONS IN FLVCR2 ASSOCIATED WITH FOWLER SYNDROME AND SURVIVAL BEYOND INFANCY.CLINICAL GENETICS. VOL. 89. ISSUE 1. P. 99 -103 | 13 | 93% | 0 |
4 | SOSTER, EL , TUCKER, M , ESCOBAR, LF , VANCE, GH , (2015) HYDRANENCEPHALY IN A NEWBORN WITH A FLVCR2 MUTATION AND PRENATAL EXPOSURE TO COCAINE.BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY. VOL. 103. ISSUE 1. P. 45 -50 | 15 | 75% | 1 |
5 | WILLIAMS, D , PATEL, C , FALLET-BIANCO, C , KALYANASUNDARAM, K , YACOUBI, M , DECHELOTTE, P , SCOTT, R , BAZIN, A , BESSIERES, B , MARTON, T , ET AL (2010) FOWLER SYNDROME-A CLINICAL, RADIOLOGICAL, AND PATHOLOGICAL STUDY OF 14 CASES.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 152A. ISSUE 1. P. 153-160 | 10 | 100% | 4 |
6 | VERZELETTI, A , LEIDE, A , DE FERRARI, F , (2015) HYDRANENCEPHALY IN A CASE OF SUSPECTED INFANTICIDE.MEDICINE SCIENCE AND THE LAW. VOL. 55. ISSUE 2. P. 82 -85 | 9 | 90% | 0 |
7 | BALPANDE, DN , PATHAK, CS , AGRAWAL, A , SINGH, BR , (2009) HEMIHYDRANENCEPHALY; A CASE REPORT.IRANIAN JOURNAL OF PEDIATRICS. VOL. 19. ISSUE 2. P. 180-184 | 8 | 80% | 2 |
8 | COUNTER, SA , (2007) PRESERVATION OF BRAINSTEM NEUROPHYSIOLOGICAL FUNCTION IN HYDRANENCEPHALY.JOURNAL OF THE NEUROLOGICAL SCIENCES. VOL. 263. ISSUE 1-2. P. 198-207 | 9 | 69% | 3 |
9 | MEYER, E , RICKETTS, C , MORGAN, NV , MORRIS, MR , PASHA, S , TEE, LJ , RAHMAN, F , BAZIN, A , BESSIERES, B , DECHELOTTE, P , ET AL (2010) MUTATIONS IN FLVCR2 ARE ASSOCIATED WITH PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME (FOWLER SYNDROME).AMERICAN JOURNAL OF HUMAN GENETICS. VOL. 86. ISSUE 3. P. 471-478 | 12 | 43% | 16 |
10 | USTA, IM , ABUMUSA, AA , KHOURY, NG , NASSAR, AH , (2005) EARLY ULTRASONOGRAPHIC CHANGES IN FOWLER SYNDROME FEATURES AND REVIEW OF THE LITERATURE.PRENATAL DIAGNOSIS. VOL. 25. ISSUE 11. P. 1019-1023 | 6 | 86% | 5 |
Classes with closest relation at Level 1 |