Class information for:
Level 1: SECKEL SYNDROME//ASPM//MCPH1

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
18053 569 34.2 81%


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
0 4 BIOCHEMISTRY & MOLECULAR BIOLOGY//CELL BIOLOGY//ONCOLOGY 4064930
365 3       MICROTUBULES//MITOSIS//KINETOCHORE 34118
3382 2             LISSENCEPHALY//SECKEL SYNDROME//LIS1 1656
18053 1                   SECKEL SYNDROME//ASPM//MCPH1 569

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 SECKEL SYNDROME authKW 2654761 10% 85% 58
2 ASPM authKW 895619 4% 76% 22
3 MCPH1 authKW 876499 4% 78% 21
4 PRIMARY MICROCEPHALY authKW 842281 3% 83% 19
5 MICROCEPHALIN authKW 551967 2% 86% 12
6 MOPD II authKW 541108 2% 92% 11
7 MCPH authKW 533475 2% 76% 13
8 PRIMORDIAL DWARFISM authKW 503087 3% 63% 15
9 WDR62 authKW 447195 2% 83% 10
10 FILIPPI SYNDROME authKW 429310 1% 100% 8

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 8844 51% 0% 293
2 Pediatrics 655 12% 0% 71
3 Medical Ethics 449 2% 0% 10
4 Cell Biology 313 14% 0% 78
5 Clinical Neurology 138 8% 0% 47
6 Biochemistry & Molecular Biology 63 13% 0% 76
7 Developmental Biology 42 2% 0% 12
8 Evolutionary Biology 24 2% 0% 10
9 Medicine, Research & Experimental 21 4% 0% 20
10 Dentistry, Oral Surgery & Medicine 17 2% 0% 11

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 HUMAN DNA DAMAGE PONSE DISORDERS GRP 197570 2% 41% 9
2 DOUBLE STRAND BREAK REPAIR 71550 0% 67% 2
3 HARVARD MD PHD MSTP PROGRAM 71550 0% 67% 2
4 7020 53664 0% 100% 1
5 ANAT CELL HUMAN BIOL GRP 53664 0% 100% 1
6 BIOCHEM NCBES 53664 0% 100% 1
7 BIOMED BIOTECHNOL MED 53664 0% 100% 1
8 CAGUG 53664 0% 100% 1
9 CERVEAU MOELLE RECHCNRSUMR9225UMR 9 53664 0% 100% 1
10 CHROMOSOME BIOL GRPCLIN SCI 53664 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 11373 6% 1% 35
2 AMERICAN JOURNAL OF MEDICAL GENETICS 9784 7% 0% 40
3 CLINICAL DYSMORPHOLOGY 9414 2% 1% 14
4 GENETIC COUNSELING 5683 2% 1% 10
5 JOURNAL OF MEDICAL GENETICS 3324 3% 0% 19
6 AMERICAN JOURNAL OF HUMAN GENETICS 3207 4% 0% 22
7 CLINICAL GENETICS 1500 2% 0% 12
8 HUMAN MOLECULAR GENETICS 1216 3% 0% 15
9 ORPHANET JOURNAL OF RARE DISEASES 1199 1% 0% 5
10 NATURE GENETICS 1069 2% 0% 10

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 SECKEL SYNDROME 2654761 10% 85% 58 Search SECKEL+SYNDROME Search SECKEL+SYNDROME
2 ASPM 895619 4% 76% 22 Search ASPM Search ASPM
3 MCPH1 876499 4% 78% 21 Search MCPH1 Search MCPH1
4 PRIMARY MICROCEPHALY 842281 3% 83% 19 Search PRIMARY+MICROCEPHALY Search PRIMARY+MICROCEPHALY
5 MICROCEPHALIN 551967 2% 86% 12 Search MICROCEPHALIN Search MICROCEPHALIN
6 MOPD II 541108 2% 92% 11 Search MOPD+II Search MOPD+II
7 MCPH 533475 2% 76% 13 Search MCPH Search MCPH
8 PRIMORDIAL DWARFISM 503087 3% 63% 15 Search PRIMORDIAL+DWARFISM Search PRIMORDIAL+DWARFISM
9 WDR62 447195 2% 83% 10 Search WDR62 Search WDR62
10 FILIPPI SYNDROME 429310 1% 100% 8 Search FILIPPI+SYNDROME Search FILIPPI+SYNDROME

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 MAHMOOD, S , AHMAD, W , HASSAN, MJ , (2011) AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY (MCPH): CLINICAL MANIFESTATIONS, GENETIC HETEROGENEITY AND MUTATION CONTINUUM.ORPHANET JOURNAL OF RARE DISEASES. VOL. 6. ISSUE . P. - 76 74% 72
2 FAHEEM, M , NASEER, MI , RASOOL, M , CHAUDHARY, AG , KUMOSANI, TA , ILYAS, AM , PUSHPARAJ, PN , AHMED, F , ALGAHTANI, HA , AL-QAHTANI, MH , ET AL (2015) MOLECULAR GENETICS OF HUMAN PRIMARY MICROCEPHALY: AN OVERVIEW.BMC MEDICAL GENOMICS. VOL. 8. ISSUE . P. - 56 66% 21
3 PULYERS, JN , JOURNIAC, N , ARAI, Y , NARDELLI, J , (2015) MCPH1: A WINDOW INTO BRAIN DEVELOPMENT AND EVOLUTION.FRONTIERS IN CELLULAR NEUROSCIENCE. VOL. 9. ISSUE . P. - 81 58% 0
4 YIGIT, G , ROSIN, N , WOLLNIK, B , (2015) MOLECULAR BASIS OF AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY.MEDIZINISCHE GENETIK. VOL. 27. ISSUE 4. P. 345 -350 45 96% 0
5 LIU, XQ , ZHOU, ZW , WANG, ZQ , (2016) THE DNA DAMAGE RESPONSE MOLECULE MCPH1 IN BRAIN DEVELOPMENT AND BEYOND.ACTA BIOCHIMICA ET BIOPHYSICA SINICA. VOL. 48. ISSUE 7. P. 678 -685 44 88% 1
6 BARBELANNE, M , TSANG, WY , (2014) MOLECULAR AND CELLULAR BASIS OF AUTOSOMAL RECESSIVE PRIMARY MICROCEPHALY.BIOMED RESEARCH INTERNATIONAL. VOL. . ISSUE . P. - 77 47% 15
7 VENKATESH, T , SURESH, PS , (2014) EMERGING ROLES OF MCPH1: EXPEDITION FROM PRIMARY MICROCEPHALY TO CANCER.EUROPEAN JOURNAL OF CELL BIOLOGY. VOL. 93. ISSUE 3. P. 98-105 52 68% 8
8 KHETARPAL, P , DAS, S , PANIGRAHI, I , MUNSHI, A , (2016) PRIMORDIAL DWARFISM: OVERVIEW OF CLINICAL AND GENETIC ASPECTS.MOLECULAR GENETICS AND GENOMICS. VOL. 291. ISSUE 1. P. 1 -15 58 60% 0
9 KAINDL, AM , PASSEMARD, S , KUMAR, P , KRAEMER, N , ISSA, L , ZWIRNER, A , GERARD, B , VERLOES, A , MANI, S , GRESSENS, P , (2010) MANY ROADS LEAD TO PRIMARY AUTOSOMAL RECESSIVE MICROCEPHALY.PROGRESS IN NEUROBIOLOGY. VOL. 90. ISSUE 3. P. 363 -383 56 52% 72
10 SAADI, A , VERNY, F , SIQUIER-PERNET, K , BOLE-FEYSOT, C , NITSCHKE, P , MUNNICH, A , ABADA-DENDIB, M , CHAOUCH, M , ABRAMOWICZ, M , COLLEAUX, L , (2016) REFINING THE PHENOTYPE ASSOCIATED WITH CASC5 MUTATION.NEUROGENETICS. VOL. 17. ISSUE 1. P. 71 -78 29 85% 3

Classes with closest relation at Level 1


Rank Class id link
1 26340 COHEN SYNDROME//CHORIORETINAL DYSPLASIA//COH1
2 3081 CENTROSOME//CENTRIOLE//GAMMA TUBULIN
3 34066 MULIBREY NANISM//3 M SYNDROME//TRIM37
4 13532 LISSENCEPHALY//LIS1//MILLER DIEKER SYNDROME
5 16424 ZIKA VIRUS//ZIKA//MICROCEPHALY
6 36907 PACHYDERMODACTYLY//ATROPHIA MACULOSA VARIOLIFORMIS CUTIS//DIGITAL FIBROMATOSIS
7 35936 DYGGVE MELCHIOR CLAUSEN SYNDROME//DYMECLIN//AXIAL OSTEOMALACIA
8 33700 SCHIMKE IMMUNO OSSEOUS DYSPLASIA//SMARCAL1//SIOD
9 2421 NINA IRELAND DEV NEUROBIOL//MEDIAL GANGLIONIC EMINENCE//CORTICOGENESIS
10 24536 RUBINSTEIN TAYBI SYNDROME//FLOATING HARBOR SYNDROME//CORNEAL KELOID

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