Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
455 | 25359 | 35.1 | 69% |
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 |
1216 | 2 | PU1//ETS 1//GATA 1 | 9149 |
1642 | 2 | SICKLE CELL DISEASE//SICKLE CELL ANEMIA//ACUTE CHEST SYNDROME | 6938 |
1768 | 2 | HEMOGLOBIN//ALPHA THALASSEMIA//HEMOGLOBINOPATHIES | 6399 |
2870 | 2 | G6PD DEFICIENCY//GLUCOSE 6 PHOSPHATE DEHYDROGENASE//GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY | 2873 |
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 | 1934830 | 8% | 85% | 1902 |
2 | SICKLE CELL DISEASE | authKW | 1386407 | 7% | 64% | 1802 |
3 | SICKLE CELL ANEMIA | authKW | 442683 | 2% | 65% | 563 |
4 | HEMOGLOBINOPATHIES | authKW | 290857 | 2% | 61% | 398 |
5 | HEMATOLOGY | WoSSC | 277030 | 32% | 3% | 8126 |
6 | ALPHA THALASSEMIA | authKW | 253492 | 1% | 81% | 259 |
7 | BETA THALASSEMIA | authKW | 185284 | 1% | 43% | 360 |
8 | SICKLE CELL | authKW | 181721 | 1% | 57% | 267 |
9 | ACUTE CHEST SYNDROME | authKW | 154991 | 1% | 92% | 140 |
10 | G6PD DEFICIENCY | authKW | 152190 | 1% | 73% | 174 |
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 | 277030 | 32% | 3% | 8126 |
2 | Biochemistry & Molecular Biology | 21514 | 27% | 0% | 6883 |
3 | Cell Biology | 12001 | 13% | 0% | 3268 |
4 | Genetics & Heredity | 7548 | 9% | 0% | 2157 |
5 | Pediatrics | 6307 | 6% | 0% | 1623 |
6 | Oncology | 2666 | 7% | 0% | 1891 |
7 | Medicine, General & Internal | 2572 | 6% | 0% | 1613 |
8 | Medical Laboratory Technology | 2558 | 2% | 1% | 487 |
9 | Medicine, Research & Experimental | 2391 | 5% | 0% | 1220 |
10 | Immunology | 1924 | 6% | 0% | 1542 |
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 | 60075 | 0% | 88% | 57 |
2 | SICKLE CELL UNIT | 58791 | 0% | 69% | 71 |
3 | SICKLE CELL | 50999 | 0% | 72% | 59 |
4 | COMPREHENS SICKLE CELL | 45915 | 0% | 66% | 58 |
5 | GUANGZHOU WOMEN CHILDREN MED | 43941 | 0% | 76% | 48 |
6 | THALASSEMIA | 42075 | 0% | 33% | 107 |
7 | PRENATAL DIAGNOST | 36969 | 0% | 44% | 70 |
8 | SICKLE CELL DIS | 35684 | 0% | 37% | 80 |
9 | HEMATOL | 35495 | 5% | 3% | 1237 |
10 | EXCELLENCE SICKLE CELL DIS | 26917 | 0% | 80% | 28 |
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 | 1934830 | 8% | 85% | 1902 |
2 | AMERICAN JOURNAL OF HEMATOLOGY | 84744 | 3% | 11% | 650 |
3 | BLOOD | 59576 | 5% | 4% | 1322 |
4 | BLOOD CELLS MOLECULES AND DISEASES | 45770 | 1% | 15% | 261 |
5 | BRITISH JOURNAL OF HAEMATOLOGY | 42752 | 3% | 5% | 700 |
6 | ACTA HAEMATOLOGICA | 22471 | 1% | 7% | 256 |
7 | PEDIATRIC BLOOD & CANCER | 12165 | 1% | 5% | 217 |
8 | JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 11036 | 1% | 5% | 185 |
9 | INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 10867 | 0% | 10% | 90 |
10 | MOLECULAR AND CELLULAR BIOLOGY | 10628 | 2% | 2% | 459 |
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 | SICKLE CELL DISEASE | 1386407 | 7% | 64% | 1802 | Search SICKLE+CELL+DISEASE | Search SICKLE+CELL+DISEASE |
2 | SICKLE CELL ANEMIA | 442683 | 2% | 65% | 563 | Search SICKLE+CELL+ANEMIA | Search SICKLE+CELL+ANEMIA |
3 | HEMOGLOBINOPATHIES | 290857 | 2% | 61% | 398 | Search HEMOGLOBINOPATHIES | Search HEMOGLOBINOPATHIES |
4 | ALPHA THALASSEMIA | 253492 | 1% | 81% | 259 | Search ALPHA+THALASSEMIA | Search ALPHA+THALASSEMIA |
5 | BETA THALASSEMIA | 185284 | 1% | 43% | 360 | Search BETA+THALASSEMIA | Search BETA+THALASSEMIA |
6 | SICKLE CELL | 181721 | 1% | 57% | 267 | Search SICKLE+CELL | Search SICKLE+CELL |
7 | ACUTE CHEST SYNDROME | 154991 | 1% | 92% | 140 | Search ACUTE+CHEST+SYNDROME | Search ACUTE+CHEST+SYNDROME |
8 | G6PD DEFICIENCY | 152190 | 1% | 73% | 174 | Search G6PD+DEFICIENCY | Search G6PD+DEFICIENCY |
9 | FETAL HEMOGLOBIN | 150565 | 1% | 67% | 186 | Search FETAL+HEMOGLOBIN | Search FETAL+HEMOGLOBIN |
10 | THALASSEMIA | 134787 | 2% | 26% | 431 | Search THALASSEMIA | Search THALASSEMIA |
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 | 346 | 99% | 0 |
2 | (1995) IHIC VARIANTS LIST.HEMOGLOBIN. VOL. 19. ISSUE 1-2. P. 39-124 | 305 | 100% | 0 |
3 | KATSUMURA, KR , DEVILBISS, AW , POPE, NJ , JOHNSON, KD , BRESNICK, EH , (2013) TRANSCRIPTIONAL MECHANISMS UNDERLYING HEMOGLOBIN SYNTHESIS.COLD SPRING HARBOR PERSPECTIVES IN MEDICINE. VOL. 3. ISSUE 9. P. - | 188 | 85% | 8 |
4 | CARVER, MFH , KUTLAR, A , (1994) INTERNATIONAL HEMOGLOBIN INFORMATION-CENTER VARIANT LIST.HEMOGLOBIN. VOL. 18. ISSUE 2. P. R5-& | 284 | 100% | 0 |
5 | BALLAS, SK , KESEN, MR , GOLDBERG, MF , LUTTY, GA , DAMPIER, C , OSUNKWO, I , WANG, WC , HOPPE, C , HAGAR, W , DARBARI, DS , ET AL (2012) BEYOND THE DEFINITIONS OF THE PHENOTYPIC COMPLICATIONS OF SICKLE CELL DISEASE: AN UPDATE ON MANAGEMENT.SCIENTIFIC WORLD JOURNAL. VOL. . ISSUE . P. - | 266 | 55% | 19 |
6 | ALAPAN, Y , FRAIWAN, A , KUCUKAL, E , HASAN, MN , UNG, R , KIM, M , ODAME, I , LITTLE, JA , GURKAN, UA , (2016) EMERGING POINT-OF-CARE TECHNOLOGIES FOR SICKLE CELL DISEASE SCREENING AND MONITORING.EXPERT REVIEW OF MEDICAL DEVICES. VOL. 13. ISSUE 12. P. 1073 -1093 | 169 | 82% | 0 |
7 | 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-& | 270 | 100% | 0 |
8 | ROTHENBERG, EV , (2014) TRANSCRIPTIONAL CONTROL OF EARLY T AND B CELL DEVELOPMENTAL CHOICES.ANNUAL REVIEW OF IMMUNOLOGY, VOL 32. VOL. 32. ISSUE . P. 283-321 | 164 | 62% | 36 |
9 | PULIDO-SALGADO, M , VIDAL-TABOADA, JM , SAURA, J , (2015) C/EBP BETA AND C/EBP DELTA TRANSCRIPTION FACTORS: BASIC BIOLOGY AND ROLES IN THE CNS.PROGRESS IN NEUROBIOLOGY. VOL. 132. ISSUE . P. 1 -33 | 224 | 52% | 4 |
10 | 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-& | 254 | 100% | 0 |
Classes with closest relation at Level 3 |