Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
16260 | 664 | 44.0 | 80% |
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 |
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 | 3227141 | 14% | 77% | 91 |
2 | DYSBINDIN | authKW | 2869934 | 12% | 79% | 79 |
3 | DTNBP1 | authKW | 1672878 | 7% | 74% | 49 |
4 | SECT HUMAN BIOCHEM GENET | address | 664853 | 6% | 34% | 42 |
5 | BLOC 1 | authKW | 619592 | 2% | 84% | 16 |
6 | DYSBINDIN 1 | authKW | 463687 | 2% | 92% | 11 |
7 | PLATELET DENSE GRANULE | authKW | 428017 | 2% | 85% | 11 |
8 | LYSOSOME RELATED ORGANELLES | authKW | 287111 | 2% | 39% | 16 |
9 | HERMANSKY PUDLAK | authKW | 281661 | 1% | 88% | 7 |
10 | DYSBINDIN GENE | authKW | 275914 | 1% | 100% | 6 |
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 | Genetics & Heredity | 1362 | 20% | 0% | 131 |
2 | Hematology | 857 | 12% | 0% | 77 |
3 | Psychiatry | 727 | 13% | 0% | 85 |
4 | Neurosciences | 487 | 18% | 0% | 118 |
5 | Cell Biology | 415 | 14% | 0% | 96 |
6 | Dermatology | 394 | 6% | 0% | 42 |
7 | Biochemistry & Molecular Biology | 132 | 16% | 0% | 106 |
8 | Ophthalmology | 118 | 4% | 0% | 28 |
9 | Respiratory System | 89 | 4% | 0% | 24 |
10 | Pediatrics | 37 | 4% | 0% | 24 |
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 | 664853 | 6% | 34% | 42 |
2 | SOCIAL TRANSLAT NEUROSCI | 206933 | 1% | 75% | 6 |
3 | MED GENET BRANCH | 130130 | 6% | 7% | 43 |
4 | HERITABLE DISORDERS BRANCH | 101591 | 3% | 10% | 22 |
5 | CONSORTIUM NEUROPSYCHIAT PHEN | 91971 | 0% | 100% | 2 |
6 | INTERNAL MED ENDOCRINOL METAB HEMATOL | 91971 | 0% | 100% | 2 |
7 | STAGLIN IMHRO COGNIT NEUROSCI | 91971 | 0% | 100% | 2 |
8 | HUMAN MED GENET PROGRAM | 83463 | 2% | 11% | 16 |
9 | OPHTHALM GENET CLIN SERV BRANCH | 57475 | 1% | 25% | 5 |
10 | OFF RARE DIS | 49649 | 1% | 12% | 9 |
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 | AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS | 4223 | 2% | 1% | 13 |
2 | TRAFFIC | 2881 | 2% | 1% | 11 |
3 | PIGMENT CELL RESEARCH | 2086 | 1% | 1% | 7 |
4 | PIGMENT CELL & MELANOMA RESEARCH | 1989 | 1% | 1% | 5 |
5 | MOLECULAR GENETICS AND METABOLISM | 1766 | 2% | 0% | 11 |
6 | MOLECULAR PSYCHIATRY | 1622 | 1% | 0% | 9 |
7 | BEHAVIORAL AND BRAIN FUNCTIONS | 1355 | 1% | 1% | 4 |
8 | BLOOD | 1086 | 4% | 0% | 29 |
9 | OPHTHALMIC PAEDIATRICS AND GENETICS | 1083 | 0% | 1% | 3 |
10 | HAMOSTASEOLOGIE | 950 | 0% | 1% | 3 |
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 | 3227141 | 14% | 77% | 91 | Search HERMANSKY+PUDLAK+SYNDROME | Search HERMANSKY+PUDLAK+SYNDROME |
2 | DYSBINDIN | 2869934 | 12% | 79% | 79 | Search DYSBINDIN | Search DYSBINDIN |
3 | DTNBP1 | 1672878 | 7% | 74% | 49 | Search DTNBP1 | Search DTNBP1 |
4 | BLOC 1 | 619592 | 2% | 84% | 16 | Search BLOC+1 | Search BLOC+1 |
5 | DYSBINDIN 1 | 463687 | 2% | 92% | 11 | Search DYSBINDIN+1 | Search DYSBINDIN+1 |
6 | PLATELET DENSE GRANULE | 428017 | 2% | 85% | 11 | Search PLATELET+DENSE+GRANULE | Search PLATELET+DENSE+GRANULE |
7 | LYSOSOME RELATED ORGANELLES | 287111 | 2% | 39% | 16 | Search LYSOSOME+RELATED+ORGANELLES | Search LYSOSOME+RELATED+ORGANELLES |
8 | HERMANSKY PUDLAK | 281661 | 1% | 88% | 7 | Search HERMANSKY+PUDLAK | Search HERMANSKY+PUDLAK |
9 | DYSBINDIN GENE | 275914 | 1% | 100% | 6 | Search DYSBINDIN+GENE | Search DYSBINDIN+GENE |
10 | HPS1 | 275914 | 1% | 100% | 6 | Search HPS1 | Search HPS1 |
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. - | 99 | 57% | 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 | 82 | 63% | 196 |
3 | 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 |
4 | 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 |
5 | EL-CHEMALY, S , YOUNG, LR , (2016) HERMANSKY-PUDLAK SYNDROME.CLINICS IN CHEST MEDICINE. VOL. 37. ISSUE 3. P. 505 -+ | 35 | 92% | 0 |
6 | 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 | 43 | 90% | 3 |
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 | 41 | 76% | 7 |
8 | 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 | 52 | 71% | 26 |
9 | CARMONA-RIVERA, C , GOLAS, G , HESS, RA , CARDILLO, ND , MARTIN, EH , O'BRIEN, K , TSILOU, E , GOCHUICO, BR , WHITE, JG , HUIZING, M , ET AL (2011) CLINICAL, MOLECULAR, AND CELLULAR FEATURES OF NON-PUERTO RICAN HERMANSKY-PUDLAK SYNDROME PATIENTS OF HISPANIC DESCENT.JOURNAL OF INVESTIGATIVE DERMATOLOGY. VOL. 131. ISSUE 12. P. 2394-2400 | 33 | 97% | 7 |
10 | WEI, AH , HE, X , LI, W , (2013) HYPOPIGMENTATION IN HERMANSKYPUDLAK SYNDROME.JOURNAL OF DERMATOLOGY. VOL. 40. ISSUE 5. P. 325-329 | 42 | 67% | 2 |
Classes with closest relation at Level 1 |