Class information for:
Level 1: PELGER HUET ANOMALY//PELGER HUET//INTERSTITIAL 1Q DELETION

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
29431 152 20.5 64%


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 PELGER HUET ANOMALY Author keyword 7 50% 7% 10
2 PELGER HUET Author keyword 6 80% 3% 4
3 INTERSTITIAL 1Q DELETION Author keyword 6 100% 3% 4
4 ZNF238 Author keyword 5 63% 3% 5
5 PSEUDO PELGER HUET Author keyword 4 75% 2% 3
6 CHROMOSOME 1Q DELETION Author keyword 3 100% 2% 3
7 FAM36A Author keyword 2 67% 1% 2
8 1Q43 44 DELETION Author keyword 1 100% 1% 2
9 1Q44 DELETION Author keyword 1 100% 1% 2
10 CEP170 Author keyword 1 100% 1% 2

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 PELGER HUET ANOMALY 7 50% 7% 10 Search PELGER+HUET+ANOMALY Search PELGER+HUET+ANOMALY
2 PELGER HUET 6 80% 3% 4 Search PELGER+HUET Search PELGER+HUET
3 INTERSTITIAL 1Q DELETION 6 100% 3% 4 Search INTERSTITIAL+1Q+DELETION Search INTERSTITIAL+1Q+DELETION
4 ZNF238 5 63% 3% 5 Search ZNF238 Search ZNF238
5 PSEUDO PELGER HUET 4 75% 2% 3 Search PSEUDO+PELGER+HUET Search PSEUDO+PELGER+HUET
6 CHROMOSOME 1Q DELETION 3 100% 2% 3 Search CHROMOSOME+1Q+DELETION Search CHROMOSOME+1Q+DELETION
7 FAM36A 2 67% 1% 2 Search FAM36A Search FAM36A
8 1Q43 44 DELETION 1 100% 1% 2 Search 1Q43+44+DELETION Search 1Q43+44+DELETION
9 1Q44 DELETION 1 100% 1% 2 Search 1Q44+DELETION Search 1Q44+DELETION
10 CEP170 1 100% 1% 2 Search CEP170 Search CEP170

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 1QTER DELETION 18 89% 5% 8
2 PROXIMAL DELETION 17 100% 5% 8
3 1Q DELETION 14 100% 5% 7
4 DEL1Q21 Q25 8 100% 3% 5
5 DEL1Q23 Q25 6 100% 3% 4
6 CORPUS CALLOSUM ABNORMALITIES 4 75% 2% 3
7 REGION 1Q44 4 75% 2% 3
8 DISTAL LONG ARM 2 19% 8% 12
9 MB DELETION 2 33% 4% 6
10 HOMOZYGOUS FORM 2 67% 1% 2

Journals

Reviews


Title Publ. year Cit. Active
references		 % act. ref.
to same field
PRENATAL DIAGNOSIS AND MOLECULAR CHARACTERIZATION OF AN INTERSTITIAL 1q24.3-31.3 DELETION: CASE REPORT AND REVIEW 2011 5 22 95%
Historical perspective and clinical implications of the Pelger-Huet cell 2009 16 24 38%
Acquired Pelger-Huet: What does it really mean? 2010 6 19 53%
Phenotypes of AKT3 Deletion: A Case Report and Literature Review 2015 0 17 53%
INTERSTITIAL DELETION OF CHROMOSOME 1 DEL (1) (Q32 Q42) - CASE-REPORT AND REVIEW OF THE LITERATURE 1992 2 5 60%

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 CLIN IMMUNOL CANC 1 50% 0.7% 1
2 POLO UNICO OSPED SANTA MARIA MISERICORDIA 1 50% 0.7% 1
3 SERV GENET BIOL MOL 1 50% 0.7% 1
4 UNIT INFANT NEUROPSYCHIAT 1 50% 0.7% 1
5 POLE ENFANTS 0 33% 0.7% 1
6 SECT PAUL BROCA 0 33% 0.7% 1
7 CIBER ENFERMEDADES RARAS CIBERER U724 0 25% 0.7% 1
8 DEV PAEDIAT UNIT 0 25% 0.7% 1
9 MED PREMATURE NEONATAL INFANTS 0 25% 0.7% 1
10 POLE 0 25% 0.7% 1

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000170589 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
2 0.0000131874 IQI JIC MOUSE//BIOINMUNOL MOL//6 METHYL PREDNISOLONE
3 0.0000122037 RING CHROMOSOME 21//MONOSOMY 21//RING CHROMOSOME 15
4 0.0000115040 NUCLEAR LAMINA//EMERIN//NUCLEAR ENVELOPE
5 0.0000102103 CRI DU CHAT SYNDROME//CRI DU CHAT//3P DELETION SYNDROME
6 0.0000093602 TRISOMY 10Q//MONOSOMY 10Q//10P TRISOMY
7 0.0000092660 TRISOMY 9P//TETRASOMY 9P//PARTIAL TRISOMY 7P
8 0.0000068585 VAN DER WOUDE SYNDROME//SYNGNATHIA//LIP PITS
9 0.0000065403 CHROMOSOME 6Q DELETION//SIM1 GENE//6Q DELETION
10 0.0000062772 MARINESCO SJOGREN SYNDROME//MICRO SYNDROME//WARBURG MICRO SYNDROME