Class information for:
Level 1: HOLOPROSENCEPHALY//OTOCEPHALY//HPE

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
11024 948 30.0 62%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
409 16055 WOLF HIRSCHHORN SYNDROME//HOLOPROSENCEPHALY//ANNALES DE GENETIQUE

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 HOLOPROSENCEPHALY Author keyword 199 55% 26% 247
2 OTOCEPHALY Author keyword 41 87% 2% 20
3 HPE Author keyword 29 73% 2% 22
4 CYCLOPIA Author keyword 26 48% 4% 39
5 AGNATHIA Author keyword 23 76% 2% 16
6 APROSENCEPHALY Author keyword 21 85% 1% 11
7 TGIF Author keyword 20 53% 3% 27
8 PREMAXILLARY AGENESIS Author keyword 14 100% 1% 7
9 ZIC2 Author keyword 11 41% 2% 21
10 ETHMOCEPHALY Author keyword 11 100% 1% 6

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 HOLOPROSENCEPHALY 199 55% 26% 247 Search HOLOPROSENCEPHALY Search HOLOPROSENCEPHALY
2 OTOCEPHALY 41 87% 2% 20 Search OTOCEPHALY Search OTOCEPHALY
3 HPE 29 73% 2% 22 Search HPE Search HPE
4 CYCLOPIA 26 48% 4% 39 Search CYCLOPIA Search CYCLOPIA
5 AGNATHIA 23 76% 2% 16 Search AGNATHIA Search AGNATHIA
6 APROSENCEPHALY 21 85% 1% 11 Search APROSENCEPHALY Search APROSENCEPHALY
7 TGIF 20 53% 3% 27 Search TGIF Search TGIF
8 PREMAXILLARY AGENESIS 14 100% 1% 7 Search PREMAXILLARY+AGENESIS Search PREMAXILLARY+AGENESIS
9 ZIC2 11 41% 2% 21 Search ZIC2 Search ZIC2
10 ETHMOCEPHALY 11 100% 1% 6 Search ETHMOCEPHALY Search ETHMOCEPHALY

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 CYCLOPIA 89 78% 6% 58
2 SONIC HEDGEHOG GENE 50 55% 7% 62
3 ZIC2 23 60% 3% 25
4 ALOBAR 18 89% 1% 8
5 ANENCEPHALIC HUMAN SPECIMENS 18 89% 1% 8
6 SMAD TRANSCRIPTIONAL COREPRESSOR 17 47% 3% 27
7 AGNATHIA 16 65% 2% 15
8 MIDDLE INTERHEMISPHERIC VARIANT 14 65% 1% 13
9 4 BRAZILIAN PATIENTS 14 100% 1% 7
10 7Q TERMINAL DELETION 14 100% 1% 7

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
Holoprosencephaly 2007 118 88 55%
Holoprosencephaly: Clinical, anatomic, and molecular dimensions 2006 88 108 52%
Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans 2015 2 139 40%
Role of TG-interacting factor (Tgif) in lipid metabolism 2015 1 54 52%
The Molecular Genetics of Holoprosencephaly 2010 42 104 40%
Holoprosencephaly: A guide to diagnosis and clinical management 2011 4 37 92%
Evaluation and management of children with holoprosencephaly 2004 40 49 82%
Holoprosencephaly: recommendations for diagnosis and management 2010 10 40 90%
Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literature 2012 4 34 71%
Solitary median maxillary central incisor (SMMCI) syndrome 2006 17 48 75%

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 MED GENET BRANCH 7 10% 6.5% 62
2 GENET DEV UMR6061 2 67% 0.2% 2
3 BRANCH GENET DEV PATHOL 1 100% 0.2% 2
4 GENET PATHOL LIEES DEV BRANCH 1 100% 0.2% 2
5 HOLOPROSENCEPHALY GRP 1 100% 0.2% 2
6 PEDIAT NEUROL NEUROPHYSIOL 1 40% 0.2% 2
7 UMR 6061 CNRS 1 40% 0.2% 2
8 ARC SPECIAL MOL GENET DEV MOL GENET 1 50% 0.1% 1
9 BIRTH DEFECTS SURVEILLANCE EPIDEMIOL BRANCH 1 50% 0.1% 1
10 CELLULES SOUCHES CERVEAU 1 50% 0.1% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000128539 PITT HOPKINS SYNDROME//18Q DELETION SYNDROME//18Q SYNDROME
2 0.0000120945 FETAL FACE//FETAL PALATE//HDLIVE
3 0.0000112942 SHUNT TREATMENT//CHONDROID TISSUE//SELLA TURCICA
4 0.0000106867 RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15
5 0.0000101041 SEPTO OPTIC DYSPLASIA//SEPTUM PELLUCIDUM//OPTIC NERVE HYPOPLASIA
6 0.0000098879 HYDRANENCEPHALY//FOWLER SYNDROME//FLVCR2
7 0.0000092366 CHARGE SYNDROME//CHOANAL ATRESIA//CHARGE ASSOCIATION
8 0.0000083771 FRONTONASAL DYSPLASIA//PROBOSCIS LATERALIS//CRANIOFRONTONASAL DYSPLASIA
9 0.0000083011 GAS7//GAS1//GROWTH ARREST SPECIFIC 1
10 0.0000073641 VAN DER WOUDE SYNDROME//SYNGNATHIA//LIP PITS