Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
95 | 4437 | 25.2 | 64% |
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 |
455 | 3 | HEMOGLOBIN//SICKLE CELL DISEASE//SICKLE CELL ANEMIA | 25359 |
1768 | 2 | HEMOGLOBIN//ALPHA THALASSEMIA//HEMOGLOBINOPATHIES | 6399 |
95 | 1 | HEMOGLOBIN//ALPHA THALASSEMIA//BETA THALASSEMIA | 4437 |
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 | HEMOGLOBIN | journal | 2596142 | 21% | 41% | 921 |
2 | ALPHA THALASSEMIA | authKW | 990679 | 5% | 67% | 214 |
3 | BETA THALASSEMIA | authKW | 597439 | 6% | 32% | 270 |
4 | ALPHA THALASSEMIA ALPHA THAL | authKW | 443220 | 2% | 87% | 74 |
5 | HB H DISEASE | authKW | 440310 | 2% | 89% | 72 |
6 | BETA THALASSEMIA BETA THAL | authKW | 438119 | 2% | 81% | 79 |
7 | HEMOGLOBINOPATHIES | authKW | 375517 | 4% | 29% | 189 |
8 | THALASSEMIA | authKW | 375015 | 7% | 18% | 300 |
9 | ALPHA THALASSAEMIA | authKW | 330470 | 2% | 69% | 70 |
10 | THALASSEMIA THAL | authKW | 213548 | 1% | 80% | 39 |
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 | 140149 | 54% | 1% | 2390 |
2 | Genetics & Heredity | 5304 | 15% | 0% | 685 |
3 | Biochemistry & Molecular Biology | 4356 | 29% | 0% | 1277 |
4 | Medical Laboratory Technology | 3174 | 5% | 0% | 207 |
5 | Medicine, General & Internal | 701 | 7% | 0% | 331 |
6 | Obstetrics & Gynecology | 558 | 4% | 0% | 186 |
7 | Biology | 349 | 3% | 0% | 143 |
8 | Medicine, Research & Experimental | 316 | 4% | 0% | 193 |
9 | Pediatrics | 311 | 4% | 0% | 174 |
10 | Anthropology | 309 | 2% | 0% | 67 |
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 | HEMOGLOBINOPATHIES | 214314 | 1% | 69% | 45 |
2 | GUANGZHOU WOMEN CHILDREN MED | 201898 | 1% | 68% | 43 |
3 | PRENATAL DIAGNOST | 171667 | 1% | 40% | 63 |
4 | ASSOCIATED MED SCI | 129200 | 3% | 15% | 128 |
5 | MED DIAGNOST S | 110394 | 1% | 31% | 51 |
6 | THALASSEMIA | 100370 | 2% | 21% | 69 |
7 | HAEMOGLOBINOPATHY REFERENCE | 76569 | 0% | 70% | 16 |
8 | DEV MED DIAGNOST S | 60014 | 1% | 36% | 24 |
9 | PROV HEMOGLOBINOPATHY DNA DIAGNOST | 59459 | 0% | 79% | 11 |
10 | THALASSAEMIA | 51201 | 0% | 34% | 22 |
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 | HEMOGLOBIN | 2596142 | 21% | 41% | 921 |
2 | AMERICAN JOURNAL OF HEMATOLOGY | 48980 | 5% | 3% | 206 |
3 | BRITISH JOURNAL OF HAEMATOLOGY | 31172 | 6% | 2% | 248 |
4 | INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 27938 | 1% | 7% | 60 |
5 | ACTA HAEMATOLOGICA | 24030 | 2% | 3% | 110 |
6 | BLOOD CELLS MOLECULES AND DISEASES | 19990 | 2% | 4% | 72 |
7 | HUMAN GENETICS | 14872 | 3% | 2% | 132 |
8 | BIRTH DEFECTS-ORIGINAL ARTICLE SERIES | 12247 | 0% | 8% | 22 |
9 | PRENATAL DIAGNOSIS | 8557 | 2% | 2% | 84 |
10 | EUROPEAN JOURNAL OF HAEMATOLOGY | 8481 | 2% | 2% | 69 |
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 | ALPHA THALASSEMIA | 990679 | 5% | 67% | 214 | Search ALPHA+THALASSEMIA | Search ALPHA+THALASSEMIA |
2 | BETA THALASSEMIA | 597439 | 6% | 32% | 270 | Search BETA+THALASSEMIA | Search BETA+THALASSEMIA |
3 | ALPHA THALASSEMIA ALPHA THAL | 443220 | 2% | 87% | 74 | Search ALPHA+THALASSEMIA+ALPHA+THAL | Search ALPHA+THALASSEMIA+ALPHA+THAL |
4 | HB H DISEASE | 440310 | 2% | 89% | 72 | Search HB+H+DISEASE | Search HB+H+DISEASE |
5 | BETA THALASSEMIA BETA THAL | 438119 | 2% | 81% | 79 | Search BETA+THALASSEMIA+BETA+THAL | Search BETA+THALASSEMIA+BETA+THAL |
6 | HEMOGLOBINOPATHIES | 375517 | 4% | 29% | 189 | Search HEMOGLOBINOPATHIES | Search HEMOGLOBINOPATHIES |
7 | THALASSEMIA | 375015 | 7% | 18% | 300 | Search THALASSEMIA | Search THALASSEMIA |
8 | ALPHA THALASSAEMIA | 330470 | 2% | 69% | 70 | Search ALPHA+THALASSAEMIA | Search ALPHA+THALASSAEMIA |
9 | THALASSEMIA THAL | 213548 | 1% | 80% | 39 | Search THALASSEMIA+THAL | Search THALASSEMIA+THAL |
10 | BETA GLOBIN GENE | 213221 | 1% | 50% | 62 | Search BETA+GLOBIN+GENE | Search BETA+GLOBIN+GENE |
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 | COLAH, R , GORAKSHAKAR, A , NADKARNI, A , (2010) GLOBAL BURDEN, DISTRIBUTION AND PREVENTION OF BETA-THALASSEMIAS AND HEMOGLOBIN E DISORDERS.EXPERT REVIEW OF HEMATOLOGY. VOL. 3. ISSUE 1. P. 103-117 | 96 | 99% | 30 |
2 | FLINT, J , HARDING, RM , BOYCE, AJ , CLEGG, JB , (1998) THE POPULATION GENETICS OF THE HAEMOGLOBINOPATHIES.BAILLIERES CLINICAL HAEMATOLOGY. VOL. 11. ISSUE 1. P. 1 -51 | 130 | 86% | 151 |
3 | FARASHI, S , NAJMABADI, H , (2015) DIAGNOSTIC PITFALLS OF LESS WELL RECOGNIZED HBH DISEASE.BLOOD CELLS MOLECULES AND DISEASES. VOL. 55. ISSUE 4. P. 387 -395 | 91 | 94% | 0 |
4 | HARTEVELD, CL , HIGGS, DR , (2010) ALPHA-THALASSAEMIA.ORPHANET JOURNAL OF RARE DISEASES. VOL. 5. ISSUE . P. - | 87 | 80% | 120 |
5 | BAYSAL, E , CARVER, MFH , (1995) THE BETA-THALASSEMIA AND DELTA-THALASSEMIA REPOSITORY - 8TH EDITION.HEMOGLOBIN. VOL. 19. ISSUE 3-4. P. 213-236 | 126 | 99% | 83 |
6 | HENDERSON, S , TIMBS, A , MCCARTHY, J , GALLIENNE, A , VAN MOURIK, M , MASTERS, G , MAY, A , KHALIL, MSM , SCHUH, A , OLD, J , (2009) INCIDENCE OF HAEMOGLOBINOPATHIES IN VARIOUS POPULATIONS - THE IMPACT OF IMMIGRATION.CLINICAL BIOCHEMISTRY. VOL. 42. ISSUE 18. P. 1745 -1756 | 74 | 100% | 22 |
7 | THEIN, SL , (2013) THE MOLECULAR BASIS OF BETA-THALASSEMIA.COLD SPRING HARBOR PERSPECTIVES IN MEDICINE. VOL. 3. ISSUE 5. P. - | 72 | 82% | 28 |
8 | THEIN, SL , (1998) BETA-THALASSAEMIA.BAILLIERES CLINICAL HAEMATOLOGY. VOL. 11. ISSUE 1. P. 91 -126 | 112 | 85% | 37 |
9 | FLINT, J , HARDING, RM , BOYCE, AJ , CLEGG, JB , (1993) THE POPULATION-GENETICS OF THE HEMOGLOBINOPATHIES.BAILLIERES CLINICAL HAEMATOLOGY. VOL. 6. ISSUE 1. P. 215-262 | 117 | 87% | 100 |
10 | GIAMBONA, A , PASSARELLO, C , RENDA, D , MAGGIO, A , (2009) THE SIGNIFICANCE OF THE HEMOGLOBIN A(2) VALUE IN SCREENING FOR HEMOGLOBINOPATHIES.CLINICAL BIOCHEMISTRY. VOL. 42. ISSUE 18. P. 1786 -1796 | 85 | 72% | 18 |
Classes with closest relation at Level 1 |