Class information for:
Level 1: MAY HEGGLIN ANOMALY//INHERITED THROMBOCYTOPENIA//EPSTEIN SYNDROME

Basic class information
Class id #P Avg. number of
references		 Database coverage
of references
15313 719 33.0 75%


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
8 4 CARDIAC & CARDIOVASCULAR SYSTEM//PERIPHERAL VASCULAR DISEASES//CARDIOL 1276458
131 3       HEMATOLOGY//HAEMOPHILIA//TRANSFUSION 66936
697 2             MEAN PLATELET VOLUME//PLATELETS//HEMATOLOGY 13039
15313 1                   MAY HEGGLIN ANOMALY//INHERITED THROMBOCYTOPENIA//EPSTEIN SYNDROME 719

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 MAY HEGGLIN ANOMALY authKW 1369024 5% 92% 35
2 INHERITED THROMBOCYTOPENIA authKW 1092022 4% 86% 30
3 EPSTEIN SYNDROME authKW 934293 3% 100% 22
4 MYH9 RELATED DISEASE authKW 851286 3% 95% 21
5 MACROTHROMBOCYTOPENIA authKW 770762 5% 55% 33
6 FECHTNER SYNDROME authKW 721954 2% 100% 17
7 GRAY PLATELET SYNDROME authKW 585751 3% 69% 20
8 MYH9 GENE authKW 584432 2% 81% 17
9 TAR SYNDROME authKW 530843 2% 83% 15
10 MYH9 DISORDERS authKW 509614 2% 100% 12

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 Hematology 26263 58% 0% 416
2 Peripheral Vascular Diseases 1251 13% 0% 92
3 Pediatrics 446 9% 0% 68
4 Genetics & Heredity 339 10% 0% 74
5 Medical Laboratory Technology 133 3% 0% 18
6 Medicine, Research & Experimental 70 5% 0% 35
7 Medicine, General & Internal 70 6% 0% 45
8 Pathology 69 3% 0% 25
9 Obstetrics & Gynecology 68 4% 0% 27
10 Cell Biology 40 6% 0% 43

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 ADV DIAG 219141 2% 30% 17
2 PLATELET PATHOL UNIT 218404 1% 86% 6
3 ADULT HAEMOPHILIA 212339 1% 100% 5
4 AZIENDA SANTOBONO PAUSILIPON 191102 1% 75% 6
5 ADV DIAGNAKA KU 169871 1% 100% 4
6 IRCCS POLICLIN SAN MATTEO FDN 156330 3% 20% 18
7 IMPERIAL HLTH SCI 96512 1% 45% 5
8 PLATEFORME TECHNOL INNOVAT BIOMED 96512 1% 45% 5
9 FRENCH REFERENCE INHERITED PLATELET DISORDERS 95551 0% 75% 3
10 HLTH BIO OURCE RARE DIS 95551 0% 75% 3

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 PLATELETS 34167 5% 2% 37
2 SEMINARS IN THROMBOSIS AND HEMOSTASIS 12575 4% 1% 28
3 JOURNAL OF THROMBOSIS AND HAEMOSTASIS 10406 4% 1% 31
4 HAMOSTASEOLOGIE 7927 1% 2% 9
5 INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY 6902 2% 1% 12
6 BLOOD 4701 9% 0% 62
7 BRITISH JOURNAL OF HAEMATOLOGY 3190 4% 0% 32
8 HAEMATOLOGICA 2611 2% 0% 15
9 THROMBOSIS AND HAEMOSTASIS 2422 3% 0% 24
10 JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY 2275 2% 0% 14

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 MAY HEGGLIN ANOMALY 1369024 5% 92% 35 Search MAY+HEGGLIN+ANOMALY Search MAY+HEGGLIN+ANOMALY
2 INHERITED THROMBOCYTOPENIA 1092022 4% 86% 30 Search INHERITED+THROMBOCYTOPENIA Search INHERITED+THROMBOCYTOPENIA
3 EPSTEIN SYNDROME 934293 3% 100% 22 Search EPSTEIN+SYNDROME Search EPSTEIN+SYNDROME
4 MYH9 RELATED DISEASE 851286 3% 95% 21 Search MYH9+RELATED+DISEASE Search MYH9+RELATED+DISEASE
5 MACROTHROMBOCYTOPENIA 770762 5% 55% 33 Search MACROTHROMBOCYTOPENIA Search MACROTHROMBOCYTOPENIA
6 FECHTNER SYNDROME 721954 2% 100% 17 Search FECHTNER+SYNDROME Search FECHTNER+SYNDROME
7 GRAY PLATELET SYNDROME 585751 3% 69% 20 Search GRAY+PLATELET+SYNDROME Search GRAY+PLATELET+SYNDROME
8 MYH9 GENE 584432 2% 81% 17 Search MYH9+GENE Search MYH9+GENE
9 TAR SYNDROME 530843 2% 83% 15 Search TAR+SYNDROME Search TAR+SYNDROME
10 MYH9 DISORDERS 509614 2% 100% 12 Search MYH9+DISORDERS Search MYH9+DISORDERS

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 BALDUINI, CL , PECCI, A , SAVOIA, A , (2011) RECENT ADVANCES IN THE UNDERSTANDING AND MANAGEMENT OF MYH9-RELATED INHERITED THROMBOCYTOPENIAS.BRITISH JOURNAL OF HAEMATOLOGY. VOL. 154. ISSUE 2. P. 161 -174 52 79% 64
2 GRESELE, P , BURY, L , FALCINELLI, E , (2016) INHERITED PLATELET FUNCTION DISORDERS: ALGORITHMS FOR PHENOTYPIC AND GENETIC INVESTIGATION.SEMINARS IN THROMBOSIS AND HEMOSTASIS. VOL. 42. ISSUE 3. P. 292 -305 49 60% 3
3 ALTHAUS, K , GREINACHER, A , (2009) MYH9-RELATED PLATELET DISORDERS.SEMINARS IN THROMBOSIS AND HEMOSTASIS. VOL. 35. ISSUE 2. P. 189-203 47 66% 83
4 BALDUINI, CL , PECCI, A , NORIS, P , (2012) INHERITED THROMBOCYTOPENIAS THE EVOLVING SPECTRUM.HAMOSTASEOLOGIE. VOL. 32. ISSUE 4. P. 259 -+ 43 64% 16
5 PECCI, A , (2016) DIAGNOSIS AND TREATMENT OF INHERITED THROMBOCYTOPENIAS.CLINICAL GENETICS. VOL. 89. ISSUE 2. P. 141 -153 39 53% 4
6 SAVOIA, A , (2016) MOLECULAR BASIS OF INHERITED THROMBOCYTOPENIAS.CLINICAL GENETICS. VOL. 89. ISSUE 2. P. 154 -162 42 46% 4
7 KUNISHIMA, S , SAITO, H , (2010) ADVANCES IN THE UNDERSTANDING OF MYH9 DISORDERS.CURRENT OPINION IN HEMATOLOGY. VOL. 17. ISSUE 5. P. 405-410 33 72% 38
8 ISRAELS, SJ , KAHR, WHA , BLANCHETTE, VS , LUBAN, NLC , RIVARD, GE , RAND, ML , (2011) PLATELET DISORDERS IN CHILDREN: A DIAGNOSTIC APPROACH.PEDIATRIC BLOOD & CANCER. VOL. 56. ISSUE 6. P. 975 -983 39 60% 21
9 GRESELE, P , (2015) DIAGNOSIS OF INHERITED PLATELET FUNCTION DISORDERS: GUIDANCE FROM THE SSC OF THE ISTH.JOURNAL OF THROMBOSIS AND HAEMOSTASIS. VOL. 13. ISSUE 2. P. 314 -322 27 61% 22
10 SAVOIA, A , DE ROCCO, D , PANZA, E , BOZZI, V , SCANDELLARI, R , LOFFREDO, G , MUMFORD, A , HELLER, PG , NORIS, P , DE GROOT, MR , ET AL (2010) HEAVY CHAIN MYOSIN 9-RELATED DISEASE (MYH9-RD): NEUTROPHIL INCLUSIONS OF MYOSIN-9 AS A PATHOGNOMONIC SIGN OF THE DISORDER.THROMBOSIS AND HAEMOSTASIS. VOL. 103. ISSUE 4. P. 826 -832 25 89% 25

Classes with closest relation at Level 1


Rank Class id link
1 16281 BERNARD SOULIER SYNDROME//GPIB IX V COMPLEX//BERNARD SOULIER
2 16260 HERMANSKY PUDLAK SYNDROME//DYSBINDIN//DTNBP1
3 17085 OPEN CANALICULAR SYSTEM//FIBRINOGEN GOLD//2E4 KAPTIN
4 17686 BLEBBISTATIN//NONMUSCLE MYOSIN//NON MUSCLE MYOSIN
5 25553 JACOBSEN SYNDROME//11Q SYNDROME//11Q TERMINAL DELETION DISORDER
6 5175 GLANZMANN THROMBASTHENIA//GLANZMANNS THROMBASTHENIA//THROMBASTHENIA
7 1537 THROMBOPOIETIN//MEGAKARYOCYTES//C MPL
8 37094 STICKY PLATELET SYNDROME//PLATELET HYPERAGGREGABILITY//PEAR1
9 22060 DESMOPRESSIN//DDAVP//PHARMACOLOGY DESMOPRESSIN
10 30554 GFI1B//GFI1//ZELLBIOL TUMORFOR

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