Class information for:
Level 1: NALCN//ABNORMAL RESPIRATORY RHYTHM//ADDIC MENTAL HLTH

Basic class information

Class id #P Avg. number of
references
Database coverage
of references
37662 51 37.2 91%



Bar chart of Publication_year

Last years might be incomplete

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



Rank Class id link
1 4233 C ELEGANS//CAENORHABDITIS ELEGANS//LULU ANTHONY WANG NEURAL CIRCUITS BEHAV
2 35565 MKIAA//ATAD3//ATAD3A
3 18617 PKAN//NBIA//HALLERVORDEN SPATZ SYNDROME
4 3493 ANESTHETIC MECHANISMS//HALOTHANE//GENERAL ANESTHETICS
5 12679 ARTHROGRYPOSIS//FREEMAN SHELDON SYNDROME//AMYOPLASIA
6 36366 BLOOMINGTON DROSOPHILA STOCK//BEIJING SPREADING WING//EDGP
7 33416 SODIUM ACTIVATED POTASSIUM CHANNELS//NA ACTIVATED K CHANNELS//CHANNEL PROTEIN INTERACTIONS
8 32712 BRAIN INFORMAT PROC COGNIT NEURODYNAM//AVERAGE NUMBER DENSITY//COGNIT NEURODYNAM
9 13375 MEMBRANE TRANSPORT//TRK1//ENA1
10 3448 PIGMENT DISPERSING FACTOR//TIMELESS//CIRCADIAN CLOCK

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