Class information for:
Level 2: TURNER SYNDROME//SRY//TURNERS SYNDROME

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
955 10314 34.1 69%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 3)


ID, lev.
above		 Publications Label for level above
96 73697 DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME

Classes in level below (level 1)


ID, lev. below Publications Label for level below
4491 1702 TURNER SYNDROME//TURNERS SYNDROME//ULLRICH TURNER SYNDROME
4910 1634 SRY//XX SEX REVERSAL//TESTIS DETERMINATION
6653 1386 MIXED GONADAL DYSGENESIS//GONADOBLASTOMA//RING Y CHROMOSOME
7696 1259 AZFC//DAZ//AZF
8255 1202 CAMPOMELIC DYSPLASIA//SOX4//SOX9
10536 989 PREMATURE OVARIAN FAILURE//PRIMARY OVARIAN INSUFFICIENCY//AUTOIMMUNE OOPHORITIS
11629 901 KLINEFELTER SYNDROME//KLINEFELTERS SYNDROME//47 XXY
19615 432 MALE ENHANCED ANTIGEN//SDM ANTIGEN//CNRS EMBRYOL
21781 348 LERI WEILL DYSCHONDROSTEOSIS//SHOX//MADELUNGS DEFORMITY
24115 270 47 XYY MALES//TAURODONTISM//MANDIBULAR PROGNATHISM
27265 191 MAMMALIAN MOL GENET GRP//ADRENAL X ZONE MORPHOLOGY//DDD MOUSE

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 TURNER SYNDROME Author keyword 704 70% 6% 590
2 SRY Author keyword 248 62% 2% 253
3 TURNERS SYNDROME Author keyword 228 67% 2% 206
4 KLINEFELTER SYNDROME Author keyword 198 59% 2% 224
5 PREMATURE OVARIAN FAILURE Author keyword 137 42% 2% 252
6 AZFC Author keyword 112 97% 0% 32
7 SHOX Author keyword 108 83% 1% 60
8 LERI WEILL DYSCHONDROSTEOSIS Author keyword 107 97% 0% 31
9 SOX9 Author keyword 106 38% 2% 223
10 Y CHROMOSOME Author keyword 99 23% 4% 379

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 TURNER SYNDROME 704 70% 6% 590 Search TURNER+SYNDROME Search TURNER+SYNDROME
2 SRY 248 62% 2% 253 Search SRY Search SRY
3 TURNERS SYNDROME 228 67% 2% 206 Search TURNERS+SYNDROME Search TURNERS+SYNDROME
4 KLINEFELTER SYNDROME 198 59% 2% 224 Search KLINEFELTER+SYNDROME Search KLINEFELTER+SYNDROME
5 PREMATURE OVARIAN FAILURE 137 42% 2% 252 Search PREMATURE+OVARIAN+FAILURE Search PREMATURE+OVARIAN+FAILURE
6 AZFC 112 97% 0% 32 Search AZFC Search AZFC
7 SHOX 108 83% 1% 60 Search SHOX Search SHOX
8 LERI WEILL DYSCHONDROSTEOSIS 107 97% 0% 31 Search LERI+WEILL+DYSCHONDROSTEOSIS Search LERI+WEILL+DYSCHONDROSTEOSIS
9 SOX9 106 38% 2% 223 Search SOX9 Search SOX9
10 Y CHROMOSOME 99 23% 4% 379 Search Y+CHROMOSOME Search Y+CHROMOSOME

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 SRY 359 58% 4% 415
2 CAMPOMELIC DYSPLASIA 357 60% 4% 386
3 SRY RELATED GENE 309 59% 3% 346
4 SEX DETERMINING REGION 230 54% 3% 293
5 AUTOSOMAL SEX REVERSAL 222 57% 3% 261
6 TESTIS DETERMINING GENE 215 83% 1% 120
7 DETERMINING REGION 176 47% 3% 281
8 SEVERE OLIGOZOOSPERMIA 174 80% 1% 108
9 HUMAN Y CHROMOSOME 172 39% 3% 347
10 47 XXY 168 91% 1% 70

Journals


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 SEXUAL DEVELOPMENT 24 27% 1% 79

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
From CNS stem cells to neurons and glia: Sox for everyone 2015 5 87 45%
Clinical practice guideline - Care of girls and women with Turner syndrome: A guideline of the Turner Syndrome Study Group 2007 261 149 89%
EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013 2014 14 83 98%
Klinefelter Syndrome-A Clinical Update 2013 45 114 75%
Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators 2000 444 87 79%
From head to toes: the multiple facets of Sox proteins 1999 533 112 79%
Pairing SOX off with partners in the regulation of embryonic development 2000 373 30 83%
The Sox Family of Transcription Factors: Versatile Regulators of Stem and Progenitor Cell Fate 2013 111 139 25%
Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors 2007 183 174 71%
Turner's syndrome 2004 239 87 95%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 INTRAMURAL PROGRAM REPROD ADULT ENDOCRINOL 21 73% 0.2% 16
2 SECT MOL GENET INFERTIL 15 82% 0.1% 9
3 INTEGRATED CANC THER Y UROL 15 77% 0.1% 10
4 CELL DEV GENET 12 38% 0.3% 26
5 GAMETE IMMUNO BIOL 12 86% 0.1% 6
6 INTEGRAT REPROD MED GRP 12 86% 0.1% 6
7 MAMMALIAN MOL GENET GRP 10 58% 0.1% 11
8 UNIDAD INVEST MED BIOL DESARROLLO 8 70% 0.1% 7
9 CELL MOL GENET SECT 8 75% 0.1% 6
10 AARHUS SYGEHUS NBG 8 56% 0.1% 10

Related classes at same level (level 2)


Rank Relatedness score Related classes
1 0.0000025534 XIST//X CHROMOSOME INACTIVATION//TSIX
2 0.0000015282 KABUKI SYNDROME//KABUKI MAKE UP SYNDROME//TRICHORHINOPHALANGEAL SYNDROME
3 0.0000012675 WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE
4 0.0000010804 DIOECIOUS PLANT//PLANT DEV GENET//SILENE LATIFOLIA
5 0.0000009337 HYPOSPADIAS//BLADDER EXSTROPHY//ANORECTAL MALFORMATION
6 0.0000008312 RETT SYNDROME//MECP2//MECP2 GENE
7 0.0000007100 SMITH LEMLI OPITZ SYNDROME//INCONTINENTIA PIGMENTI//CHONDRODYSPLASIA PUNCTATA
8 0.0000007004 TESTIS//SERTOLI CELLS//SPERMATOGENESIS
9 0.0000006284 FRAGILE X SYNDROME//FRAGILE X//FMR1
10 0.0000006219 RBM5//MEIOTIC DRIVE//HUMAN CHROMOSOME 3