Class information for:
Level 2: AMYOTROPHIC LATERAL SCLEROSIS//SPINAL MUSCULAR ATROPHY//MOTOR NEURON DISEASE

Basic class information

ID Publications Average number
of references
Avg. shr. active
ref. in WoS
799 11424 42.8 81%



Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 3)



ID, lev.
above
Publications Label for level above
60 87899 ALZHEIMERS DISEASE//DEMENTIA//AMYOTROPHIC LATERAL SCLEROSIS

Classes in level below (level 1)



ID, lev. below Publications Label for level below
372 3500 AMYOTROPHIC LATERAL SCLEROSIS//SOD1//ALS
3494 1893 AMYOTROPHIC LATERAL SCLEROSIS//AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION//MOTOR NEURON DISEASE
4185 1755 SPINAL MUSCULAR ATROPHY//SURVIVAL MOTOR NEURON//SMN2
5539 1544 TDP 43//C9ORF72//TARDBP
8283 1199 PRIMARY LATERAL SCLEROSIS//BUNINA BODY//MOTOR NEURON DISEASE
20224 408 SPINAL AND BULBAR MUSCULAR ATROPHY//KENNEDYS DISEASE//KENNEDY DISEASE
21632 354 HIRAYAMA DISEASE//BROWN VIALETTO VAN LAERE SYNDROME//MONOMELIC AMYOTROPHY
22677 317 SANATORIUM CHIBA//ALS TREATMENT//BRAIN CORTEX SYNAPTOSOMES
25160 241 RILUZOLE//2 CYCLOPROPYLIMINO 3 METHYL 1 3 THIAZOLINE HYDROCHLORIDE//ANTIGLUTAMATE
26260 213 WOBBLER MOUSE//T 588//WOBBLER MICE

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 AMYOTROPHIC LATERAL SCLEROSIS Author keyword 2783 60% 27% 3058
2 SPINAL MUSCULAR ATROPHY Author keyword 678 69% 5% 578
3 MOTOR NEURON DISEASE Author keyword 654 58% 7% 763
4 ALS Author keyword 637 52% 8% 868
5 TDP 43 Author keyword 392 68% 3% 340
6 AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION Journal 288 79% 2% 187
7 SOD1 Author keyword 254 59% 3% 286
8 C9ORF72 Author keyword 253 82% 1% 147
9 SURVIVAL MOTOR NEURON Author keyword 232 96% 1% 72
10 SMN1 Author keyword 215 94% 1% 77

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 AMYOTROPHIC LATERAL SCLEROSIS 2783 60% 27% 3058 Search AMYOTROPHIC+LATERAL+SCLEROSIS Search AMYOTROPHIC+LATERAL+SCLEROSIS
2 SPINAL MUSCULAR ATROPHY 678 69% 5% 578 Search SPINAL+MUSCULAR+ATROPHY Search SPINAL+MUSCULAR+ATROPHY
3 MOTOR NEURON DISEASE 654 58% 7% 763 Search MOTOR+NEURON+DISEASE Search MOTOR+NEURON+DISEASE
4 ALS 637 52% 8% 868 Search ALS Search ALS
5 TDP 43 392 68% 3% 340 Search TDP+43 Search TDP+43
6 SOD1 254 59% 3% 286 Search SOD1 Search SOD1
7 C9ORF72 253 82% 1% 147 Search C9ORF72 Search C9ORF72
8 SURVIVAL MOTOR NEURON 232 96% 1% 72 Search SURVIVAL+MOTOR+NEURON Search SURVIVAL+MOTOR+NEURON
9 SMN1 215 94% 1% 77 Search SMN1 Search SMN1
10 SMN2 200 95% 1% 69 Search SMN2 Search SMN2

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 ALS 2090 68% 16% 1849
2 MOTOR NEURON DISEASE 1473 56% 16% 1813
3 AMYOTROPHIC LATERAL SCLEROSIS 1324 29% 33% 3824
4 FAMILIAL ALS 779 89% 3% 356
5 FRONTOTEMPORAL LOBAR DEGENERATION 569 46% 8% 913
6 MOTOR NEURON GENE 500 91% 2% 209
7 MOTOR NEURON DEGENERATION 477 62% 4% 491
8 CU ZN SUPEROXIDE DISMUTASE 446 44% 7% 775
9 MUTANT SOD1 409 85% 2% 219
10 ALS PATIENTS 348 80% 2% 215

Journals



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 AMYOTROPHIC LATERAL SCLEROSIS 757 75% 5% 546
2 AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION 288 79% 2% 187
3 AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS 60 69% 0% 51

Reviews



Title Publ. year Cit. Active references % act. ref.
to same field
State of play in amyotrophic lateral sclerosis genetics 2014 102 89 74%
The changing scene of amyotrophic lateral sclerosis 2013 155 228 72%
Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis 2013 121 241 73%
C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis 2015 4 116 91%
Unraveling the mechanisms involved in motor neuron degeneration in ALS 2004 771 146 66%
ALS: A disease of motor neurons and their nonneuronal neighbors 2006 642 245 73%
Sporadic and hereditary amyotrophic lateral sclerosis (ALS) 2015 4 59 83%
Controversies and priorities in amyotrophic lateral sclerosis 2013 80 107 90%
From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS 2001 786 125 75%
Neuroprotective agents target molecular mechanisms of disease in ALS 2015 4 92 72%

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 ELEANOR LOU GEHRIG MDA ALS 155 95% 0.5% 53
2 ALS 53 43% 0.8% 94
3 ALS CLIN 49 66% 0.4% 45
4 SHEFFIELD TRANSLAT NEUROSCI SITRAN 44 67% 0.3% 39
5 SLA 31 47% 0.4% 48
6 NEUROL CLIN TRIALS UNIT 28 60% 0.3% 31
7 P TON MND CARE 27 92% 0.1% 11
8 RITA LEVI MONTALCINI NEUROSCI 25 62% 0.2% 26
9 TRAFFORD BIOMED 23 74% 0.1% 17
10 FDN SERENA ONLUS 20 66% 0.2% 19

Related classes at same level (level 2)



Rank Relatedness score Related classes
1 0.0000038894 FRONTOTEMPORAL DEMENTIA//PROGRANULIN//PRIMARY PROGRESSIVE APHASIA
2 0.0000024852 BMAA//ALS PDC//BETA N METHYLAMINO L ALANINE
3 0.0000015618 NON INVASIVE VENTILATION//POST POLIO SYNDROME//NONINVASIVE MECHANICAL VENTILATION
4 0.0000011738 2 5 HEXANEDIONE//NEUROFILAMENT//NEUROFILAMENTS
5 0.0000009427 HUNTINGTONS DISEASE//HUNTINGTIN//HUNTINGTON DISEASE
6 0.0000008487 SOMATOSENSORY EVOKED POTENTIALS//MOTOR UNIT NUMBER ESTIMATION//SOMATOSENSORY EVOKED POTENTIAL
7 0.0000007705 HEREDITARY SPASTIC PARAPLEGIA//FRIEDREICHS ATAXIA//FRIEDREICH ATAXIA
8 0.0000007292 EXTRACELLULAR SUPEROXIDE DISMUTASE//SUPEROXIDE DISMUTASE//MANGANESE SUPEROXIDE DISMUTASE
9 0.0000005987 RKIP//RAF KINASE INHIBITOR PROTEIN//HIPPOCAMPAL CHOLINERGIC NEUROSTIMULATING PEPTIDE
10 0.0000005649 TRANSHYDROGENASE//WLDS//NAD KINASE