Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
25706 | 274 | 20.1 | 71% |
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 |
25706 | 1 | PALLISTER KILLIAN SYNDROME//TETRASOMY 12P//ISOCHROMOSOME 12P | 274 |
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 | PALLISTER KILLIAN SYNDROME | authKW | 6712771 | 23% | 94% | 64 |
2 | TETRASOMY 12P | authKW | 2340295 | 8% | 100% | 21 |
3 | ISOCHROMOSOME 12P | authKW | 1123689 | 8% | 46% | 22 |
4 | TRISOMY 12P | authKW | 1037270 | 4% | 85% | 11 |
5 | MOSAIC TETRASOMY 12P | authKW | 780098 | 3% | 100% | 7 |
6 | PALLISTER KILLIAN | authKW | 780098 | 3% | 100% | 7 |
7 | PALLISTER KILLIAN SYNDROME PKS | authKW | 557213 | 2% | 100% | 5 |
8 | 12P TETRASOMY | authKW | 445770 | 1% | 100% | 4 |
9 | TRISOMY 12P SYNDROME | authKW | 356615 | 1% | 80% | 4 |
10 | 12Q DUPLICATION | authKW | 222885 | 1% | 100% | 2 |
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 | 9728 | 77% | 0% | 211 |
2 | Obstetrics & Gynecology | 654 | 15% | 0% | 42 |
3 | Pediatrics | 157 | 9% | 0% | 25 |
4 | Medical Ethics | 35 | 1% | 0% | 2 |
5 | Clinical Neurology | 22 | 5% | 0% | 15 |
6 | Medical Laboratory Technology | 2 | 1% | 0% | 2 |
7 | Education, Special | 2 | 0% | 0% | 1 |
8 | Dermatology | 1 | 1% | 0% | 3 |
9 | Ophthalmology | 1 | 1% | 0% | 3 |
10 | Otorhinolaryngology | 1 | 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 | ABT SOZIALPADIAT ENTWICKLUNGSNEUROL | 111443 | 0% | 100% | 1 |
2 | AMB GENET CLIN | 111443 | 0% | 100% | 1 |
3 | ARC 1007 | 111443 | 0% | 100% | 1 |
4 | ARC 1007C | 111443 | 0% | 100% | 1 |
5 | CHILD ADOLOSCENCE NEUROPSYCHIAT UNIT | 111443 | 0% | 100% | 1 |
6 | CITOGENHCFMUSPLIM 03 | 111443 | 0% | 100% | 1 |
7 | COMPREHENS GENET SERV | 111443 | 0% | 100% | 1 |
8 | CONSULTAT NEUROPEDIAT | 111443 | 0% | 100% | 1 |
9 | CORNELIA DE LANGE SYNDROME RELATED DIAG | 111443 | 0% | 100% | 1 |
10 | COUNSULTING KLIN | 111443 | 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 | 27936 | 14% | 1% | 38 |
2 | EUROPEAN JOURNAL OF MEDICAL GENETICS | 19200 | 5% | 1% | 14 |
3 | AMERICAN JOURNAL OF MEDICAL GENETICS | 15613 | 13% | 0% | 35 |
4 | CLINICAL GENETICS | 12613 | 9% | 0% | 24 |
5 | ANNALES DE GENETIQUE | 11765 | 4% | 1% | 11 |
6 | PRENATAL DIAGNOSIS | 10546 | 8% | 0% | 23 |
7 | CLINICAL DYSMORPHOLOGY | 4888 | 3% | 1% | 7 |
8 | JAPANESE JOURNAL OF HUMAN GENETICS | 3468 | 1% | 1% | 4 |
9 | JOURNAL OF MEDICAL GENETICS | 3243 | 5% | 0% | 13 |
10 | MOLECULAR CYTOGENETICS | 2062 | 1% | 1% | 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 | PALLISTER KILLIAN SYNDROME | 6712771 | 23% | 94% | 64 | Search PALLISTER+KILLIAN+SYNDROME | Search PALLISTER+KILLIAN+SYNDROME |
2 | TETRASOMY 12P | 2340295 | 8% | 100% | 21 | Search TETRASOMY+12P | Search TETRASOMY+12P |
3 | ISOCHROMOSOME 12P | 1123689 | 8% | 46% | 22 | Search ISOCHROMOSOME+12P | Search ISOCHROMOSOME+12P |
4 | TRISOMY 12P | 1037270 | 4% | 85% | 11 | Search TRISOMY+12P | Search TRISOMY+12P |
5 | MOSAIC TETRASOMY 12P | 780098 | 3% | 100% | 7 | Search MOSAIC+TETRASOMY+12P | Search MOSAIC+TETRASOMY+12P |
6 | PALLISTER KILLIAN | 780098 | 3% | 100% | 7 | Search PALLISTER+KILLIAN | Search PALLISTER+KILLIAN |
7 | PALLISTER KILLIAN SYNDROME PKS | 557213 | 2% | 100% | 5 | Search PALLISTER+KILLIAN+SYNDROME+PKS | Search PALLISTER+KILLIAN+SYNDROME+PKS |
8 | 12P TETRASOMY | 445770 | 1% | 100% | 4 | Search 12P+TETRASOMY | Search 12P+TETRASOMY |
9 | TRISOMY 12P SYNDROME | 356615 | 1% | 80% | 4 | Search TRISOMY+12P+SYNDROME | Search TRISOMY+12P+SYNDROME |
10 | 12Q DUPLICATION | 222885 | 1% | 100% | 2 | Search 12Q+DUPLICATION | Search 12Q+DUPLICATION |
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 | BLYTH, M , MALONEY, V , BEAL, S , COLLINSON, M , HUANG, SW , CROLLA, J , TEMPLE, IK , BARALLE, D , (2015) PALLISTER-KILLIAN SYNDROME: A STUDY OF 22 BRITISH PATIENTS.JOURNAL OF MEDICAL GENETICS. VOL. 52. ISSUE 7. P. 454 -464 | 30 | 100% | 3 |
2 | DORAY, B , GIRARD-LEMAIRE, F , GASSER, B , BALDAUF, JJ , DE GEETER, B , SPIZZO, M , ZEIDAN, C , FLORI, E , (2002) PALLISTER-KILLIAN SYNDROME: DIFFICULTIES OF PRENATAL DIAGNOSIS.PRENATAL DIAGNOSIS. VOL. 22. ISSUE 6. P. 470 -477 | 39 | 85% | 36 |
3 | LIU, YH , XIE, RG , ZHANG, XY , WEI, SD , HE, Y , XU, WF , LIN, YY , XIONG, F , (2012) A NEW PARTIAL TRISOMY 12P WITH ARTERY CATHETER VAGUS, CONGENITAL CATARACTS, EXTERNAL AUDITORY CANAL, AND NO TURBINATE.GENE. VOL. 509. ISSUE 1. P. 164 -167 | 25 | 100% | 1 |
4 | CHIESA, J , HOFFET, M , ROUSSEAU, O , BOURGEOIS, JM , SARDA, P , MARES, P , BUREAU, JP , (1998) PALLISTER-KILLIAN SYNDROME [I(12P)]: FIRST PRE-NATAL DIAGNOSIS USING CORDOCENTESIS IN THE SECOND TRIMESTER CONFIRMED BY IN SITU HYBRIDIZATION.CLINICAL GENETICS. VOL. 54. ISSUE 4. P. 294-302 | 39 | 93% | 15 |
5 | SUKAROVA-ANGELOVSKA, E , KOCOVA, M , ILIEVA, G , ANGELKOVA, N , KOCHOVA, E , (2016) RARE CASE OF KILLIAN-PALLISTER SYNDROME ASSOCIATED WITH IDIOPATHIC SHORT STATURE DETECTED WITH FLUORESCENT IN SITU HYBRIDIZATION ON BUCCAL SMEAR.MOLECULAR CYTOGENETICS. VOL. 9. ISSUE . P. - | 22 | 96% | 0 |
6 | DE LAGUNA, LTB , DEL CAMPO-CASANELLES, M , SANTANA-RODRIGUEZ, A , SANTANA-ARTILES, A , SEBASTIAN-GARCIA, I , CABRERA-LOPEZ, JC , (2014) THREE CASES OF PALLISTER-KILLIAN SYNDROME.REVISTA DE NEUROLOGIA. VOL. 58. ISSUE 2. P. 63-68 | 22 | 96% | 0 |
7 | BIELANSKA, MM , KHALIFA, MM , DUNCAN, AMV , (1996) BRIEF CLINICAL REPORT - PALLISTER-KILLIAN SYNDROME: A MILD CASE DIAGNOSED BY FLUORESCENCE IN SITU HYBRIDIZATION. REVIEW OF THE LITERATURE AND EXPANSION OF THE PHENOTYPE.AMERICAN JOURNAL OF MEDICAL GENETICS. VOL. 65. ISSUE 2. P. 104-108 | 32 | 97% | 31 |
8 | MOWERYRUSHTON, PA , STADLER, MP , KOCHMAR, SJ , MCPHERSON, E , SURTI, U , HOGGE, WA , (1997) THE USE OF INTERPHASE FISH FOR PRENATAL DIAGNOSIS OF PALLISTER-KILLIAN SYNDROME.PRENATAL DIAGNOSIS. VOL. 17. ISSUE 3. P. 255-265 | 39 | 74% | 16 |
9 | CHEN, CP , TSAI, FJ , CHERN, SR , LEE, CC , TOWN, DD , WANG, W , (2007) CYTOGENETIC VARIABILITY IN THE PROPORTION OF ABNORMAL CELLS BETWEEN THE VARIOUS TISSUES IN PRENATALLY DETECTED MOSAIC TETRASOMY 12P.PRENATAL DIAGNOSIS. VOL. 27. ISSUE 12. P. 1170-1173 | 19 | 100% | 2 |
10 | BAGLAJ, M , KING, J , CARACHI, R , (2008) PALLISTER-KILLIAN SYNDROME: A REPORT OF 2 CASES AND REVIEW OF ITS SURGICAL ASPECTS.JOURNAL OF PEDIATRIC SURGERY. VOL. 43. ISSUE 6. P. 1218-1221 | 18 | 100% | 9 |
Classes with closest relation at Level 1 |