Standout Papers
- Motor Neuron Degeneration in Mice that Express a Human Cu,Zn Superoxide Dismutase Mutation (1994)
- Pathological TDP‐43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations (2007)
- The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis (2001)
- Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity (1991)
Immediate Impact
19 by Nobel laureates 59 from Science/Nature 142 standout
Citing Papers
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
Discoveries in structure and physiology of mechanically activated ion channels
2020 StandoutNatureNobel
Works of Teepu Siddique being referenced
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4
2009
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene
2006
Author Peers
| Author | Last Decade | Papers | Cites | |||
|---|---|---|---|---|---|---|
| Teepu Siddique | 9278 | 5180 | 4572 | 163 | 13.2k | |
| Vincent Meininger | 10063 | 5660 | 3678 | 211 | 13.8k | |
| Wim Robberecht | 8152 | 4371 | 3805 | 128 | 11.2k | |
| P. Nigel Leigh | 9478 | 4311 | 3104 | 164 | 12.6k | |
| Ammar Al‐Chalabi | 14418 | 8052 | 5416 | 266 | 17.7k | |
| Linda K. Kwong | 9926 | 4064 | 5879 | 87 | 14.1k | |
| Mark E. Gurney | 5882 | 3132 | 3821 | 89 | 10.9k | |
| Ian R. Mackenzie | 13447 | 5307 | 7309 | 203 | 19.1k | |
| Manuela Neumann | 15219 | 5592 | 7865 | 127 | 20.1k | |
| Kevin Talbot | 6693 | 4903 | 5178 | 239 | 12.1k | |
| Leo McCluskey | 7902 | 3240 | 3362 | 90 | 10.8k |
All Works
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