Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
2927 | 2251 | 36.4 | 72% |
Classes in level above (level 3) |
Classes in level below (level 1) |
ID, lev. below | Publications | Label for level below |
---|---|---|
12579 | 833 | HERMANSKY PUDLAK SYNDROME//CHEDIAK HIGASHI SYNDROME//LYST |
12964 | 805 | ALBINISM//OCULOCUTANEOUS ALBINISM//OCULAR ALBINISM |
15963 | 613 | MYOSIN VA//RAB27A//GRISCELLI SYNDROME |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | HERMANSKY PUDLAK SYNDROME | Author keyword | 137 | 80% | 4% | 86 |
2 | CHEDIAK HIGASHI SYNDROME | Author keyword | 106 | 73% | 4% | 81 |
3 | GRISCELLI SYNDROME | Author keyword | 96 | 88% | 2% | 45 |
4 | OCULOCUTANEOUS ALBINISM | Author keyword | 70 | 69% | 3% | 60 |
5 | RAB27A | Author keyword | 69 | 71% | 2% | 56 |
6 | ALBINISM | Author keyword | 69 | 37% | 7% | 149 |
7 | MYOSIN VA | Author keyword | 67 | 76% | 2% | 47 |
8 | MELANOPHILIN | Author keyword | 61 | 95% | 1% | 20 |
9 | SECT HUMAN BIOCHEM GENET | Address | 31 | 44% | 2% | 53 |
10 | LYST | Author keyword | 23 | 79% | 1% | 15 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | HERMANSKY PUDLAK SYNDROME | 137 | 80% | 4% | 86 | Search HERMANSKY+PUDLAK+SYNDROME | Search HERMANSKY+PUDLAK+SYNDROME |
2 | CHEDIAK HIGASHI SYNDROME | 106 | 73% | 4% | 81 | Search CHEDIAK+HIGASHI+SYNDROME | Search CHEDIAK+HIGASHI+SYNDROME |
3 | GRISCELLI SYNDROME | 96 | 88% | 2% | 45 | Search GRISCELLI+SYNDROME | Search GRISCELLI+SYNDROME |
4 | OCULOCUTANEOUS ALBINISM | 70 | 69% | 3% | 60 | Search OCULOCUTANEOUS+ALBINISM | Search OCULOCUTANEOUS+ALBINISM |
5 | RAB27A | 69 | 71% | 2% | 56 | Search RAB27A | Search RAB27A |
6 | ALBINISM | 69 | 37% | 7% | 149 | Search ALBINISM | Search ALBINISM |
7 | MYOSIN VA | 67 | 76% | 2% | 47 | Search MYOSIN+VA | Search MYOSIN+VA |
8 | MELANOPHILIN | 61 | 95% | 1% | 20 | Search MELANOPHILIN | Search MELANOPHILIN |
9 | LYST | 23 | 79% | 1% | 15 | Search LYST | Search LYST |
10 | MYOSIN V | 21 | 40% | 2% | 42 | Search MYOSIN+V | Search MYOSIN+V |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | MELANOSOME TRANSPORT | 119 | 72% | 4% | 94 |
2 | HERMANSKY PUDLAK SYNDROME | 80 | 36% | 8% | 182 |
3 | PALE EAR EP | 74 | 84% | 2% | 41 |
4 | GRISCELLI SYNDROME | 68 | 56% | 4% | 83 |
5 | OCULOCUTANEOUS ALBINISM | 61 | 40% | 5% | 119 |
6 | MYOSIN VA | 60 | 49% | 4% | 89 |
7 | PARTIAL ALBINISM | 59 | 70% | 2% | 49 |
8 | STORAGE POOL DEFICIENCY | 54 | 46% | 4% | 87 |
9 | LYSOSOME RELATED ORGANELLES | 52 | 45% | 4% | 87 |
10 | BETA 3A SUBUNIT | 52 | 68% | 2% | 45 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Increasing the complexity: new genes and new types of albinism | 2014 | 12 | 57 | 82% |
Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function | 2006 | 185 | 131 | 71% |
Walking to work: roles for class V myosins as cargo transporters | 2012 | 60 | 143 | 44% |
Versatile role of Rab27 in membrane trafficking: Focus on the Rab27 effector families | 2005 | 140 | 62 | 79% |
Griscelli syndrome: a model system to study vesicular trafficking | 2009 | 51 | 107 | 79% |
Oculocutaneous albinism | 2007 | 78 | 38 | 76% |
Histological review of skin cancers in African Albinos: a 10-year retrospective review | 2014 | 6 | 12 | 58% |
Disorders of lysosome-related organelle biogenesis: Clinical and molecular genetics | 2008 | 110 | 120 | 54% |
Rab27 Effectors, Pleiotropic Regulators in Secretory Pathways | 2013 | 17 | 149 | 64% |
Molecular determinants of platelet delta storage pool deficiencies: an update | 2013 | 16 | 36 | 64% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | SECT HUMAN BIOCHEM GENET | 31 | 44% | 2.4% | 53 |
2 | FUKUDA INITIAT UNIT | 18 | 43% | 1.4% | 32 |
3 | MEMBRANE TRAFFICKING MECHANISMS | 9 | 83% | 0.2% | 5 |
4 | BEIJING TONGREN AFFILIATED HOSP | 6 | 80% | 0.2% | 4 |
5 | LEUVEN AUTISM CONSORTIUM LAU | 6 | 80% | 0.2% | 4 |
6 | MEMBRANE TRAFFICKING MECH | 5 | 29% | 0.6% | 14 |
7 | LIFE SCIAOBA KU | 5 | 32% | 0.5% | 12 |
8 | NETRA NIRAMAY NIKETAN | 3 | 100% | 0.1% | 3 |
9 | HUMAN MED GENET PROGRAM | 3 | 14% | 0.9% | 20 |
10 | UNITE RECH DEV NORMAL PATHOL SYST IMMUNITAIRE | 3 | 35% | 0.3% | 6 |
Related classes at same level (level 2) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000032965 | VITILIGO//TYROSINASE//MELANOGENESIS |
2 | 0.0000021492 | CLATHRIN//COPII//TRAFFIC |
3 | 0.0000014808 | EXOCYTOSIS//SYNAPTIC VESICLE//SNARE |
4 | 0.0000014415 | KINESIN//DYNEIN//AXONEME |
5 | 0.0000013700 | HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS//JUVENILE IDIOPATHIC ARTHRITIS//ADULT ONSET STILLS DISEASE |
6 | 0.0000010693 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//PAR 4 |
7 | 0.0000008924 | WISKOTT ALDRICH SYNDROME//GELSOLIN//COFILIN |
8 | 0.0000007012 | SMITH LEMLI OPITZ SYNDROME//INCONTINENTIA PIGMENTI//CHONDRODYSPLASIA PUNCTATA |
9 | 0.0000006573 | SMOOTH PURSUIT//SACCADES//SACCADE |
10 | 0.0000006454 | CLOPIDOGREL//PRASUGREL//ASPIRIN RESISTANCE |