Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
1768 | 6399 | 23.9 | 58% |
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 |
5340 | 1 | HEMOGLOBIN//HEMOGLOBIN VARIANTS//HEMOGLOBIN HB VARIANT | 1637 |
24056 | 1 | CONGENITAL DYSERYTHROPOIETIC ANEMIA//CONGENITAL DYSERYTHROPOIETIC ANAEMIA//HEMPAS | 325 |
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 | 6463250 | 27% | 78% | 1745 |
2 | ALPHA THALASSEMIA | authKW | 759238 | 4% | 71% | 225 |
3 | HEMOGLOBINOPATHIES | authKW | 496529 | 4% | 40% | 261 |
4 | BETA THALASSEMIA | authKW | 448544 | 4% | 33% | 281 |
5 | ALPHA THALASSEMIA ALPHA THAL | authKW | 359141 | 1% | 94% | 80 |
6 | HB H DISEASE | authKW | 313802 | 1% | 90% | 73 |
7 | THALASSEMIA | authKW | 306896 | 5% | 20% | 326 |
8 | BETA THALASSEMIA BETA THAL | authKW | 303739 | 1% | 81% | 79 |
9 | HEMOGLOBIN VARIANTS | authKW | 245872 | 1% | 67% | 77 |
10 | HEMATOLOGY | WoSSC | 230881 | 58% | 1% | 3680 |
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 | 230881 | 58% | 1% | 3680 |
2 | Biochemistry & Molecular Biology | 10450 | 36% | 0% | 2273 |
3 | Medical Laboratory Technology | 5233 | 5% | 0% | 318 |
4 | Genetics & Heredity | 3941 | 12% | 0% | 738 |
5 | Medicine, General & Internal | 715 | 7% | 0% | 421 |
6 | Pediatrics | 424 | 4% | 0% | 246 |
7 | Medicine, Research & Experimental | 361 | 4% | 0% | 257 |
8 | Obstetrics & Gynecology | 355 | 3% | 0% | 197 |
9 | Pathology | 267 | 3% | 0% | 163 |
10 | Biology | 220 | 2% | 0% | 153 |
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 | 230117 | 1% | 86% | 56 |
2 | GUANGZHOU WOMEN CHILDREN MED | 167228 | 1% | 75% | 47 |
3 | PRENATAL DIAGNOST | 134592 | 1% | 42% | 67 |
4 | ASSOCIATED MED SCI | 92331 | 2% | 15% | 130 |
5 | THALASSEMIA | 84397 | 1% | 23% | 76 |
6 | HAEMOGLOBINOPATHY REFERENCE | 82951 | 0% | 87% | 20 |
7 | MED DIAGNOST S | 79547 | 1% | 32% | 52 |
8 | PROV HEMOGLOBINOPATHY DNA DIAGNOST | 57578 | 0% | 93% | 13 |
9 | INSERM U468 | 52164 | 0% | 58% | 19 |
10 | U468 | 47215 | 0% | 32% | 31 |
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 | 6463250 | 27% | 78% | 1745 |
2 | AMERICAN JOURNAL OF HEMATOLOGY | 60483 | 4% | 5% | 275 |
3 | BRITISH JOURNAL OF HAEMATOLOGY | 36146 | 5% | 2% | 321 |
4 | ACTA HAEMATOLOGICA | 30143 | 2% | 4% | 148 |
5 | INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 26341 | 1% | 8% | 70 |
6 | BLOOD CELLS MOLECULES AND DISEASES | 19746 | 1% | 5% | 86 |
7 | HUMAN GENETICS | 12375 | 2% | 2% | 145 |
8 | EUROPEAN JOURNAL OF HAEMATOLOGY | 9765 | 1% | 2% | 89 |
9 | BIRTH DEFECTS-ORIGINAL ARTICLE SERIES | 9269 | 0% | 8% | 23 |
10 | BLOOD | 7585 | 4% | 1% | 239 |
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 | 759238 | 4% | 71% | 225 | Search ALPHA+THALASSEMIA | Search ALPHA+THALASSEMIA |
2 | HEMOGLOBINOPATHIES | 496529 | 4% | 40% | 261 | Search HEMOGLOBINOPATHIES | Search HEMOGLOBINOPATHIES |
3 | BETA THALASSEMIA | 448544 | 4% | 33% | 281 | Search BETA+THALASSEMIA | Search BETA+THALASSEMIA |
4 | ALPHA THALASSEMIA ALPHA THAL | 359141 | 1% | 94% | 80 | Search ALPHA+THALASSEMIA+ALPHA+THAL | Search ALPHA+THALASSEMIA+ALPHA+THAL |
5 | HB H DISEASE | 313802 | 1% | 90% | 73 | Search HB+H+DISEASE | Search HB+H+DISEASE |
6 | THALASSEMIA | 306896 | 5% | 20% | 326 | Search THALASSEMIA | Search THALASSEMIA |
7 | BETA THALASSEMIA BETA THAL | 303739 | 1% | 81% | 79 | Search BETA+THALASSEMIA+BETA+THAL | Search BETA+THALASSEMIA+BETA+THAL |
8 | HEMOGLOBIN VARIANTS | 245872 | 1% | 67% | 77 | Search HEMOGLOBIN+VARIANTS | Search HEMOGLOBIN+VARIANTS |
9 | ALPHA THALASSAEMIA | 229102 | 1% | 69% | 70 | Search ALPHA+THALASSAEMIA | Search ALPHA+THALASSAEMIA |
10 | THALASSEMIA THAL | 197119 | 1% | 92% | 45 | Search THALASSEMIA+THAL | Search THALASSEMIA+THAL |
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 | (1997) VARIANTS OF THE ALPHA CHAIN.HEMOGLOBIN. VOL. 21. ISSUE 6. P. 507 -602 | 345 | 99% | 0 |
2 | (1995) IHIC VARIANTS LIST.HEMOGLOBIN. VOL. 19. ISSUE 1-2. P. 39-124 | 304 | 99% | 0 |
3 | CARVER, MFH , KUTLAR, A , (1994) INTERNATIONAL HEMOGLOBIN INFORMATION-CENTER VARIANT LIST.HEMOGLOBIN. VOL. 18. ISSUE 2. P. R5-& | 283 | 100% | 0 |
4 | CARVER, MFH , HUISMAN, THJ , (1993) POLICIES OF THE INTERNATIONAL HEMOGLOBIN INFORMATION-CENTER LABORATORY OF PROTEIN CHEMISTRY DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR-BIOLOGY MEDICAL-COLLEGE-OF-GEORGIA AUGUSTA, GA 30912-2100, USA.HEMOGLOBIN. VOL. 17. ISSUE 2. P. R5-& | 269 | 100% | 0 |
5 | CARVER, MFH , HUISMAN, THJ , (1992) POLICIES OF THE INTERNATIONAL HEMOGLOBIN INFORMATION-CENTER LABORATORY OF PROTEIN CHEMISTRY DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR-BIOLOGY MEDICAL-COLLEGE-OF-GEORGIA AUGUSTA, GA 30912-2100, USA.HEMOGLOBIN. VOL. 16. ISSUE 3. P. R5-& | 253 | 100% | 0 |
6 | 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 |
7 | 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 | 93 | 96% | 0 |
8 | HARTEVELD, CL , HIGGS, DR , (2010) ALPHA-THALASSAEMIA.ORPHANET JOURNAL OF RARE DISEASES. VOL. 5. ISSUE . P. - | 89 | 82% | 120 |
9 | 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 |
10 | BAYSAL, E , CARVER, MFH , (1995) THE BETA-THALASSEMIA AND DELTA-THALASSEMIA REPOSITORY - 8TH EDITION.HEMOGLOBIN. VOL. 19. ISSUE 3-4. P. 213-236 | 127 | 100% | 83 |
Classes with closest relation at Level 2 |