Class information for:
Level 2: ARRAY CGH//GENETICS & HEREDITY//HOLOPROSENCEPHALY

Basic class information

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
16 4 DENTISTRY, ORAL SURGERY & MEDICINE//ORTHOPEDICS//DENT 796976
201 3       CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS 52632
387 2             ARRAY CGH//GENETICS & HEREDITY//HOLOPROSENCEPHALY 17402
5245 1                   CHORIONIC VILLUS SAMPLING//CONFINED PLACENTAL MOSAICISM//AMNIOCENTESIS 1682
5433 1                   COPY NUMBER VARIATION//DNA COPY NUMBER//PENNCNV 1655
8049 1                   SUBTELOMERIC REARRANGEMENTS//ARRAY CGH//MBD5 1321
12021 1                   HOLOPROSENCEPHALY//TGIF//OTOCEPHALY 965
12351 1                   MEIOTIC SEGREGATION//SPERM ANEUPLOIDY//INTERCHROMOSOMAL EFFECT 943
14032 1                   RECURRENT MISCARRIAGE//PRODUCTS OF CONCEPTION//SPONTANEOUS ABORTION 827
14571 1                   TRISOMY 9//TETRASOMY 9P//TRISOMY 9P 790
16067 1                   NONDISJUNCTION//DOUBLE ANEUPLOIDY//DOWN SYNDROME 701
16770 1                   MONOSOMY 21//RING CHROMOSOME 21//RING CHROMOSOME 20 661
17075 1                   SPECTRAL SIMILARITY MAPPING//CYTOCHEM CYTOMETRY//M FISH 646
18658 1                   CAT EYE SYNDROME//SMALL SUPERNUMERARY MARKER CHROMOSOME//SUPERNUMERARY MARKER CHROMOSOME 565
18675 1                   CRI DU CHAT SYNDROME//CRI DU CHAT//5P DELETION 564
18901 1                   WOLF HIRSCHHORN SYNDROME//4P DELETION//LETM1 554
19087 1                   COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT//CHROMOTHRIPSIS 544
19155 1                   18Q SYNDROME//PITT HOPKINS SYNDROME//CHROMOSOME 18 541
21615 1                   CORNELIA DE LANGE SYNDROME//BRACHMANN DE LANGE SYNDROME//NIPBL 436
22343 1                   QF PCR//UNCULTURED AMNIOCYTES//RAPID ANEUPLOIDY DETECTION 408
23912 1                   BLEPHAROPHIMOSIS//BPES//BLEPHAROPHIMOSIS PTOSIS EPICANTHUS INVERSUS SYNDROME 353
24305 1                   PALLISTER KILLIAN SYNDROME//FRYNS SYNDROME//TETRASOMY 12P 339
24379 1                   TRISOMY 16Q//13Q SYNDROME//13Q DELETION 337
24575 1                   ACRO CARDIO FACIAL SYNDROME//CHROMOSOME 6Q DELETION//SIM1 GENE 330
24879 1                   CHROMOSOME 2//2Q DELETION//PARTIAL TRISOMY 2Q 321
24985 1                   TRISOMY 1Q//PARTIAL TRISOMY 1Q//ZNF238 318
25098 1                   JUMPING TRANSLOCATION//SODIUM GLYCIDIDAZOLE//TELOMERE PNA FISH 314
25172 1                   SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME 312
25592 1                   JACOBSEN SYNDROME//11Q SYNDROME//C SYNDROME 300
26143 1                   TRICHORHINOPHALANGEAL SYNDROME//TRPS1//LANGER GIEDION SYNDROME 283
28901 1                   TRISOMY 10Q//MONOSOMY 10Q//10P DUPLICATION 215
30823 1                   MICROCLONING//MICRODISSECTION AND MICROCLONING//CHROMOSOME SPECIFIC LIBRARY 177

Terms with highest relevance score



rank Category termType chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 ARRAY CGH authKW 372868 3% 42% 487
2 GENETICS & HEREDITY WoSSC 366365 60% 2% 10364
3 HOLOPROSENCEPHALY authKW 327830 2% 62% 291
4 AMERICAN JOURNAL OF MEDICAL GENETICS PART A journal 318309 6% 17% 1029
5 PRENATAL DIAGNOSIS journal 300592 6% 17% 972
6 ANNALES DE GENETIQUE journal 293227 2% 38% 431
7 AMERICAN JOURNAL OF MEDICAL GENETICS journal 292253 7% 14% 1190
8 WOLF HIRSCHHORN SYNDROME authKW 221969 1% 93% 132
9 MOSAICISM authKW 206479 2% 31% 371
10 CORNELIA DE LANGE SYNDROME authKW 192249 1% 78% 136

Web of Science journal categories



chi_square_rank Category chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 Genetics & Heredity 366365 60% 2% 10364
2 Obstetrics & Gynecology 46996 16% 1% 2822
3 Medical Ethics 11590 2% 2% 281
4 Reproductive Biology 6387 4% 1% 708
5 Pediatrics 3601 6% 0% 1031
6 Biotechnology & Applied Microbiology 2599 7% 0% 1155
7 Mathematical & Computational Biology 1673 2% 0% 370
8 Andrology 1012 1% 1% 91
9 Developmental Biology 703 2% 0% 287
10 Cell Biology 641 5% 0% 920

Address terms



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 CYTOGENET 151678 3% 17% 506
2 MED GENET 121781 9% 4% 1651
3 CLIN COMMUNITY HLTH NURSING 66593 1% 34% 110
4 CLIN GENET 65596 4% 6% 624
5 HUMAN GENET 63084 7% 3% 1272
6 MOL HUMAN GENET 32523 2% 6% 314
7 SIGNATURE GENOM S 30919 0% 46% 37
8 GENET 28083 7% 1% 1151
9 WESSEX REG GENET 26101 0% 19% 77
10 UNITAT BIOL CELLULAR 22466 0% 34% 37

Journals



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass
1 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 318309 6% 17% 1029
2 PRENATAL DIAGNOSIS 300592 6% 17% 972
3 ANNALES DE GENETIQUE 293227 2% 38% 431
4 AMERICAN JOURNAL OF MEDICAL GENETICS 292253 7% 14% 1190
5 GENETIC COUNSELING 144043 2% 29% 278
6 JOURNAL OF MEDICAL GENETICS 133144 4% 11% 658
7 EUROPEAN JOURNAL OF MEDICAL GENETICS 130356 2% 24% 297
8 MOLECULAR CYTOGENETICS 128665 1% 37% 191
9 CLINICAL GENETICS 121318 3% 11% 593
10 HUMAN GENETICS 85772 4% 8% 619

Author Key Words



chi_square_rank term chi_square shrOfCwithTerm shrOfTermInClass termInClass LCSH search Wikipedia search
1 ARRAY CGH 372868 3% 42% 487 Search ARRAY+CGH Search ARRAY+CGH
2 HOLOPROSENCEPHALY 327830 2% 62% 291 Search HOLOPROSENCEPHALY Search HOLOPROSENCEPHALY
3 WOLF HIRSCHHORN SYNDROME 221969 1% 93% 132 Search WOLF+HIRSCHHORN+SYNDROME Search WOLF+HIRSCHHORN+SYNDROME
4 MOSAICISM 206479 2% 31% 371 Search MOSAICISM Search MOSAICISM
5 CORNELIA DE LANGE SYNDROME 192249 1% 78% 136 Search CORNELIA+DE+LANGE+SYNDROME Search CORNELIA+DE+LANGE+SYNDROME
6 PRENATAL DIAGNOSIS 191397 5% 13% 848 Search PRENATAL+DIAGNOSIS Search PRENATAL+DIAGNOSIS
7 CHORIONIC VILLUS SAMPLING 179679 1% 53% 186 Search CHORIONIC+VILLUS+SAMPLING Search CHORIONIC+VILLUS+SAMPLING
8 AMNIOCENTESIS 156649 2% 33% 262 Search AMNIOCENTESIS Search AMNIOCENTESIS
9 MENTAL RETARDATION 134440 3% 15% 507 Search MENTAL+RETARDATION Search MENTAL+RETARDATION
10 COPY NUMBER VARIATION 125431 2% 25% 278 Search COPY+NUMBER+VARIATION Search COPY+NUMBER+VARIATION

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.

Classes with closest relation at Level 2



rank cluster_id2 link
1 3276 VELOCARDIOFACIAL SYNDROME//DIGEORGE SYNDROME//22Q112 DELETION SYNDROME
2 2979 PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A
3 1414 TURNER SYNDROME//KLINEFELTER SYNDROME//PREMATURE OVARIAN FAILURE
4 3686 KABUKI SYNDROME//CHARGE SYNDROME//CHOANAL ATRESIA
5 2203 GENOMICS//MEIOTIC DRIVE//MAMMALIAN GENOME
6 2518 CELL FREE DNA//CELL FREE FETAL DNA//NON INVASIVE PRENATAL DIAGNOSIS
7 2580 GENOMIC IMPRINTING//IMPRINTING//SILVER RUSSELL SYNDROME
8 755 B CHROMOSOMES//CHROMOSOMA//MEIOSIS
9 1341 NUCHAL TRANSLUCENCY//PAPP A//SPINA BIFIDA
10 2623 DOWN SYNDROME//DYRK1A//TS65DN

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