Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
3685 | 1132 | 39.0 | 71% |
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 |
633 | 3 | TYROSINASE//MELANOGENESIS//PIGMENT CELL RESEARCH | 12915 |
3685 | 2 | HERMANSKY PUDLAK SYNDROME//CHEDIAK HIGASHI SYNDROME//DYSBINDIN | 1132 |
16260 | 1 | HERMANSKY PUDLAK SYNDROME//DYSBINDIN//DTNBP1 | 664 |
20278 | 1 | CHEDIAK HIGASHI SYNDROME//GRISCELLI SYNDROME//LYST | 468 |
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 | HERMANSKY PUDLAK SYNDROME | authKW | 1892876 | 8% | 77% | 91 |
2 | CHEDIAK HIGASHI SYNDROME | authKW | 1714574 | 7% | 76% | 84 |
3 | DYSBINDIN | authKW | 1683359 | 7% | 79% | 79 |
4 | DTNBP1 | authKW | 981224 | 4% | 74% | 49 |
5 | GRISCELLI SYNDROME | authKW | 587452 | 3% | 66% | 33 |
6 | SECT HUMAN BIOCHEM GENET | address | 467771 | 4% | 38% | 46 |
7 | BLOC 1 | authKW | 363422 | 1% | 84% | 16 |
8 | LYST | authKW | 328807 | 1% | 76% | 16 |
9 | DYSBINDIN 1 | authKW | 271977 | 1% | 92% | 11 |
10 | PLATELET DENSE GRANULE | authKW | 251054 | 1% | 85% | 11 |
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 | 2387 | 15% | 0% | 165 |
2 | Genetics & Heredity | 1648 | 17% | 0% | 191 |
3 | Cell Biology | 564 | 13% | 0% | 149 |
4 | Dermatology | 562 | 6% | 0% | 66 |
5 | Psychiatry | 419 | 8% | 0% | 90 |
6 | Pediatrics | 412 | 8% | 0% | 85 |
7 | Neurosciences | 334 | 12% | 0% | 140 |
8 | Pathology | 305 | 5% | 0% | 60 |
9 | Medicine, Research & Experimental | 133 | 5% | 0% | 59 |
10 | Ophthalmology | 122 | 3% | 0% | 39 |
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 | SECT HUMAN BIOCHEM GENET | 467771 | 4% | 38% | 46 |
2 | SOCIAL TRANSLAT NEUROSCI | 121376 | 1% | 75% | 6 |
3 | LEUVEN AUTISM CONSORTIUM LAU | 112386 | 0% | 83% | 5 |
4 | MED GENET BRANCH | 95081 | 4% | 7% | 48 |
5 | HERITABLE DISORDERS BRANCH | 70900 | 2% | 11% | 24 |
6 | HUMAN MED GENET PROGRAM | 55255 | 2% | 12% | 17 |
7 | CONSORTIUM NEUROPSYCHIAT PHEN | 53946 | 0% | 100% | 2 |
8 | INTERNAL MED ENDOCRINOL METAB HEMATOL | 53946 | 0% | 100% | 2 |
9 | STAGLIN IMHRO COGNIT NEUROSCI | 53946 | 0% | 100% | 2 |
10 | INTRAMURAL OFF RARE DIS | 39659 | 0% | 29% | 5 |
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 | TRAFFIC | 9460 | 2% | 1% | 26 |
2 | AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS | 2467 | 1% | 1% | 13 |
3 | MOLECULAR GENETICS AND METABOLISM | 1920 | 1% | 0% | 15 |
4 | PIGMENT CELL RESEARCH | 1593 | 1% | 1% | 8 |
5 | BLOOD | 1323 | 4% | 0% | 42 |
6 | MAMMALIAN GENOME | 1277 | 1% | 0% | 13 |
7 | PIGMENT CELL & MELANOMA RESEARCH | 1163 | 0% | 1% | 5 |
8 | MOLECULAR PSYCHIATRY | 944 | 1% | 0% | 9 |
9 | BEHAVIORAL AND BRAIN FUNCTIONS | 791 | 0% | 1% | 4 |
10 | INMUNOLOGIA | 756 | 0% | 1% | 2 |
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 | HERMANSKY PUDLAK SYNDROME | 1892876 | 8% | 77% | 91 | Search HERMANSKY+PUDLAK+SYNDROME | Search HERMANSKY+PUDLAK+SYNDROME |
2 | CHEDIAK HIGASHI SYNDROME | 1714574 | 7% | 76% | 84 | Search CHEDIAK+HIGASHI+SYNDROME | Search CHEDIAK+HIGASHI+SYNDROME |
3 | DYSBINDIN | 1683359 | 7% | 79% | 79 | Search DYSBINDIN | Search DYSBINDIN |
4 | DTNBP1 | 981224 | 4% | 74% | 49 | Search DTNBP1 | Search DTNBP1 |
5 | GRISCELLI SYNDROME | 587452 | 3% | 66% | 33 | Search GRISCELLI+SYNDROME | Search GRISCELLI+SYNDROME |
6 | BLOC 1 | 363422 | 1% | 84% | 16 | Search BLOC+1 | Search BLOC+1 |
7 | LYST | 328807 | 1% | 76% | 16 | Search LYST | Search LYST |
8 | DYSBINDIN 1 | 271977 | 1% | 92% | 11 | Search DYSBINDIN+1 | Search DYSBINDIN+1 |
9 | PLATELET DENSE GRANULE | 251054 | 1% | 85% | 11 | Search PLATELET+DENSE+GRANULE | Search PLATELET+DENSE+GRANULE |
10 | CHEDIAK HIGASHI | 245208 | 1% | 91% | 10 | Search CHEDIAK+HIGASHI | Search CHEDIAK+HIGASHI |
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 | WEI, AH , LI, W , (2013) HERMANSKYPUDLAK SYNDROME: PIGMENTARY AND NON-PIGMENTARY DEFECTS AND THEIR PATHOGENESIS.PIGMENT CELL & MELANOMA RESEARCH. VOL. 26. ISSUE 2. P. - | 104 | 59% | 31 |
2 | WEI, ML , (2006) HERMANSKY-PUDLAK SYNDROME: A DISEASE OF PROTEIN TRAFFICKING AND ORGANELLE FUNCTION.PIGMENT CELL RESEARCH. VOL. 19. ISSUE 1. P. 19-42 | 86 | 66% | 196 |
3 | KAPLAN, J , DE DOMENICO, I , WARD, DM , (2008) CHEDIAK-HIGASHI SYNDROME.CURRENT OPINION IN HEMATOLOGY. VOL. 15. ISSUE 1. P. 22-29 | 59 | 72% | 118 |
4 | GHIANI, CA , DELL'ANGELICA, EC , (2011) DYSBINDIN-CONTAINING COMPLEXES AND THEIR PROPOSED FUNCTIONS IN BRAIN: FROM ZERO TO (TOO) MANY IN A DECADE.ASN NEURO. VOL. 3. ISSUE 2. P. - | 60 | 65% | 21 |
5 | NAZARIAN, R , HUIZING, M , HELIP-WOOLEY, A , STARCEVIC, M , GAHL, WA , DELL'ANGELICA, EC , (2008) AN IMMUNOBLOTTING ASSAY TO FACILITATE THE MOLECULAR DIAGNOSIS OF HERMANSKY-PUDLAK SYNDROME.MOLECULAR GENETICS AND METABOLISM. VOL. 93. ISSUE 2. P. 134 -144 | 45 | 94% | 3 |
6 | MULLIN, AP , GOKHALE, A , LARIMORE, J , FAUNDEZ, V , (2011) CELL BIOLOGY OF THE BLOC-1 COMPLEX SUBUNIT DYSBINDIN, A SCHIZOPHRENIA SUSCEPTIBILITY GENE.MOLECULAR NEUROBIOLOGY. VOL. 44. ISSUE 1. P. 53-64 | 64 | 55% | 16 |
7 | SANCHEZ-GUIU, I , TORREGROSA, JM , VELASCO, F , ANTON, AI , LOZANO, ML , VICENTE, V , RIVERA, J , (2014) HERMANSKY-PUDLAK SYNDROME OVERVIEW OF CLINICAL AND MOLECULAR FEATURES AND CASE REPORT OF A NEW HPS-1 VARIANT.HAMOSTASEOLOGIE. VOL. 34. ISSUE 4. P. 301 -309 | 42 | 78% | 7 |
8 | EL-CHEMALY, S , YOUNG, LR , (2016) HERMANSKY-PUDLAK SYNDROME.CLINICS IN CHEST MEDICINE. VOL. 37. ISSUE 3. P. 505 -+ | 35 | 92% | 0 |
9 | PIERSON, DM , IONESCU, D , QING, GF , YONAN, AM , PARKINSON, K , COLBY, TC , LESLIE, K , (2006) PULMONARY FIBROSIS IN HERMANSKY-PUDLAK SYNDROME - A CASE REPORT AND REVIEW.RESPIRATION. VOL. 73. ISSUE 3. P. 382-395 | 53 | 73% | 26 |
10 | HUIZING, M , ANIKSTER, Y , GAHL, WA , (2001) HERMANSKY-PUDLAK SYNDROME AND CHEDIAK-HIGASHI SYNDROME: DISORDERS OF VESICLE FORMATION AND TRAFFICKING.THROMBOSIS AND HAEMOSTASIS. VOL. 86. ISSUE 1. P. 233 -245 | 68 | 62% | 61 |
Classes with closest relation at Level 2 |