Class information for: |
Basic class information |
Class id | #P | Avg. number of references |
Database coverage of references |
---|---|---|---|
37662 | 51 | 37.2 | 91% |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
14 | 4 | ORTHOPEDICS//DENTISTRY, ORAL SURGERY & MEDICINE//SPORT SCIENCES | 808941 |
474 | 3 | CLEFT PALATE-CRANIOFACIAL JOURNAL//CLEFT PALATE//CRANIOSYNOSTOSIS | 23888 |
3549 | 2 | ARTHROGRYPOSIS//FREEMAN SHELDON SYNDROME//DISTAL ARTHROGRYPOSIS | 1350 |
37662 | 1 | NALCN//ABNORMAL RESPIRATORY RHYTHM//ADDIC MENTAL HLTH | 51 |
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 | NALCN | authKW | 4276706 | 20% | 71% | 10 |
2 | ABNORMAL RESPIRATORY RHYTHM | authKW | 598740 | 2% | 100% | 1 |
3 | ADDIC MENTAL HLTH | address | 598740 | 2% | 100% | 1 |
4 | AREA RIC GENET MALATTIE RARE | address | 598740 | 2% | 100% | 1 |
5 | CENTRAL HYPERTONIA | authKW | 598740 | 2% | 100% | 1 |
6 | GENOM PLATFORM IMAGINE | address | 598740 | 2% | 100% | 1 |
7 | KAUSA DNA RE | address | 598740 | 2% | 100% | 1 |
8 | MOL PATHOPHYSIOL BASES COGNIT DISORDERSINS | address | 598740 | 2% | 100% | 1 |
9 | NALCN GENE | authKW | 598740 | 2% | 100% | 1 |
10 | NECKER ENFANTS MALAD HOSPINSERMUMR 1163 | address | 598740 | 2% | 100% | 1 |
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 | 321 | 33% | 0% | 17 |
2 | Cell Biology | 97 | 24% | 0% | 12 |
3 | Neurosciences | 87 | 25% | 0% | 13 |
4 | Biochemistry & Molecular Biology | 62 | 31% | 0% | 16 |
5 | Biology | 17 | 6% | 0% | 3 |
6 | Clinical Neurology | 11 | 8% | 0% | 4 |
7 | Reproductive Biology | 3 | 2% | 0% | 1 |
8 | Developmental Biology | 3 | 2% | 0% | 1 |
9 | Evolutionary Biology | 3 | 2% | 0% | 1 |
10 | Behavioral Sciences | 2 | 2% | 0% | 1 |
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 | ADDIC MENTAL HLTH | 598740 | 2% | 100% | 1 |
2 | AREA RIC GENET MALATTIE RARE | 598740 | 2% | 100% | 1 |
3 | GENOM PLATFORM IMAGINE | 598740 | 2% | 100% | 1 |
4 | KAUSA DNA RE | 598740 | 2% | 100% | 1 |
5 | MOL PATHOPHYSIOL BASES COGNIT DISORDERSINS | 598740 | 2% | 100% | 1 |
6 | NECKER ENFANTS MALAD HOSPINSERMUMR 1163 | 598740 | 2% | 100% | 1 |
7 | NORWEGIAN NEWBORN SCREENING PROGRAM | 598740 | 2% | 100% | 1 |
8 | PHAMACOGENOM | 299369 | 2% | 50% | 1 |
9 | PEDIAT NEUROL UNIT PEDIAT | 199579 | 2% | 33% | 1 |
10 | ZUSSMAN CHILD DEV | 199579 | 2% | 33% | 1 |
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 | CHANNELS | 4575 | 4% | 0% | 2 |
2 | AMERICAN JOURNAL OF HUMAN GENETICS | 2685 | 12% | 0% | 6 |
3 | ISLETS | 2063 | 2% | 0% | 1 |
4 | ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY | 1942 | 2% | 0% | 1 |
5 | EMBO REPORTS | 1105 | 4% | 0% | 2 |
6 | FRONTIERS IN MOLECULAR NEUROSCIENCE | 1027 | 2% | 0% | 1 |
7 | NEURON | 658 | 6% | 0% | 3 |
8 | CURRENT BIOLOGY | 605 | 6% | 0% | 3 |
9 | GENES BRAIN AND BEHAVIOR | 555 | 2% | 0% | 1 |
10 | PHARMACOGENETICS AND GENOMICS | 526 | 2% | 0% | 1 |
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 | NALCN | 4276706 | 20% | 71% | 10 | Search NALCN | Search NALCN |
2 | ABNORMAL RESPIRATORY RHYTHM | 598740 | 2% | 100% | 1 | Search ABNORMAL+RESPIRATORY+RHYTHM | Search ABNORMAL+RESPIRATORY+RHYTHM |
3 | CENTRAL HYPERTONIA | 598740 | 2% | 100% | 1 | Search CENTRAL+HYPERTONIA | Search CENTRAL+HYPERTONIA |
4 | NALCN GENE | 598740 | 2% | 100% | 1 | Search NALCN+GENE | Search NALCN+GENE |
5 | SOCIAL SPACE INDEX | 598740 | 2% | 100% | 1 | Search SOCIAL+SPACE+INDEX | Search SOCIAL+SPACE+INDEX |
6 | SODIUM LEAK CONDUCTANCE CHANNEL | 598740 | 2% | 100% | 1 | Search SODIUM+LEAK+CONDUCTANCE+CHANNEL | Search SODIUM+LEAK+CONDUCTANCE+CHANNEL |
7 | SODIUM LEAK CURRENT CHANNEL | 598740 | 2% | 100% | 1 | Search SODIUM+LEAK+CURRENT+CHANNEL | Search SODIUM+LEAK+CURRENT+CHANNEL |
8 | UNC 79 | 598740 | 2% | 100% | 1 | Search UNC+79 | Search UNC+79 |
9 | UNC 80 | 598740 | 2% | 100% | 1 | Search UNC+80 | Search UNC+80 |
10 | UNC80 | 598740 | 2% | 100% | 1 | Search UNC80 | Search UNC80 |
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 | LOZIC, B , JOHANSSON, S , KOJUNDZIC, SL , MARKIC, J , KNAPPSKOG, PM , HAHN, AF , BOMAN, H , (2016) NOVEL NALCN VARIANT: ALTERED RESPIRATORY AND CIRCADIAN RHYTHM, ANESTHETIC SENSITIVITY.ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. VOL. 3. ISSUE 11. P. 876 -883 | 15 | 71% | 0 |
2 | STRAY-PEDERSEN, A , COBBEN, JM , PRESCOTT, TE , LEES, S , CANG, CL , ARANDA, K , AHMED, S , ALDERS, M , GERSTNER, T , ASLAKSEN, K , ET AL (2016) BIALLELIC MUTATIONS IN UNC80 CAUSE PERSISTENT HYPOTONIA, ENCEPHALOPATHY, GROWTH RETARDATION, AND SEVERE INTELLECTUAL DISABILITY.AMERICAN JOURNAL OF HUMAN GENETICS. VOL. 98. ISSUE 1. P. 202 -209 | 13 | 52% | 6 |
3 | PEREZ, Y , KADIR, R , VOLODARSKY, M , NOYMAN, I , FLUSSER, H , SHORER, Z , GRADSTEIN, L , BIRNBAUM, RY , BIRK, OS , (2016) UNC80 MUTATION CAUSES A SYNDROME OF HYPOTONIA, SEVERE INTELLECTUAL DISABILITY, DYSKINESIA AND DYSMORPHISM, SIMILAR TO THAT CAUSED BY MUTATIONS IN ITS INTERACTING CATION CHANNEL NALCN.JOURNAL OF MEDICAL GENETICS. VOL. 53. ISSUE 6. P. 397 -402 | 12 | 71% | 1 |
4 | GAL, M , MAGEN, D , ZAHRAN, Y , RAVID, S , ERAN, A , KHAYAT, M , GAFNI, C , LEVANON, EY , MANDEL, H , (2016) A NOVEL HOMOZYGOUS SPLICE SITE MUTATION IN NALCN IDENTIFIED IN SIBLINGS WITH CACHEXIA, STRABISMUS, SEVERE INTELLECTUAL DISABILITY, EPILEPSY AND ABNORMAL RESPIRATORY RHYTHM.EUROPEAN JOURNAL OF MEDICAL GENETICS. VOL. 59. ISSUE 4. P. 204 -209 | 11 | 58% | 5 |
5 | VALKANAS, E , SCHAFFER, K , DUNHAM, C , MADURO, V , DU SOUICH, C , RUPPS, R , ADAMS, DR , BARADARAN-HERAVI, A , FLYNN, E , MALICDAN, MC , ET AL (2016) PHENOTYPIC EVOLUTION OF UNC80 LOSS OF FUNCTION.AMERICAN JOURNAL OF MEDICAL GENETICS PART A. VOL. 170. ISSUE 12. P. 3106 -3114 | 14 | 54% | 0 |
6 | CHONG, JX , MCMILLIN, MJ , SHIVELY, KM , BECK, AE , MARVIN, CT , ARMENTEROS, JR , BUCKINGHAM, KJ , NKINSI, NT , BOYLE, EA , BERRY, MN , ET AL (2015) DE NOVO MUTATIONS IN NALCN CAUSE A SYNDROME CHARACTERIZED BY CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY.AMERICAN JOURNAL OF HUMAN GENETICS. VOL. 96. ISSUE 3. P. 462 -473 | 16 | 36% | 20 |
7 | AOYAGI, K , ROSSIGNOL, E , HAMDAN, FF , MULCAHY, B , XIE, L , NAGAMATSU, S , ROULEAU, GA , ZHEN, M , MICHAUD, JL , (2015) A GAIN-OF-FUNCTION MUTATION IN NALCN IN A CHILD WITH INTELLECTUAL DISABILITY, ATAXIA, AND ARTHROGRYPOSIS.HUMAN MUTATION. VOL. 36. ISSUE 8. P. 753 -757 | 10 | 56% | 10 |
8 | BEND, EG , SI, Y , STEVENSON, DA , BAYRAK-TOYDEMIR, P , NEWCOMB, TM , JORGENSEN, EM , SWOBODA, KJ , (2016) NALCN CHANNELOPATHIES: DISTINGUISHING GAIN-OF-FUNCTION AND LOSS-OF-FUNCTION MUTATIONS.NEUROLOGY. VOL. 87. ISSUE 11. P. 1131 -1139 | 11 | 52% | 1 |
9 | SHAMSELDIN, HE , FAQEIH, E , ALASMARI, A , ZAKI, MS , GLEESON, JG , ALKURAYA, FS , (2016) MUTATIONS IN UNC80, ENCODING PART OF THE UNC79-UNC80-NALCN CHANNEL COMPLEX, CAUSE AUTOSOMAL-RECESSIVE SEVERE INFANTILE ENCEPHALOPATHY.AMERICAN JOURNAL OF HUMAN GENETICS. VOL. 98. ISSUE 1. P. 210 -215 | 10 | 45% | 4 |
10 | COCHET-BISSUEL, M , LORY, P , MONTEIL, A , (2014) THE SODIUM LEAK CHANNEL, NALCN, IN HEALTH AND DISEASE.FRONTIERS IN CELLULAR NEUROSCIENCE. VOL. 8. ISSUE . P. - | 28 | 19% | 12 |
Classes with closest relation at Level 1 |