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6,417 authors found
quering by "Hereditary Spastic Paraplegia"
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the first 25
sort by ONE Index.
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970
One Index
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Rubinsztein, David PhD 0000-0001-5002-5263 |
460 docs (1990 - 2024)
Autophagy , Mitophagy , Autophagosome , Cellular Self-Digestion , Huntingtin Protein |
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939
One Index
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Bonifacino, Juan S. PhD 0000-0002-5673-6370 |
370 docs (1978 - 2024)
Organelle , Transport protein , Retromer , Clathrin adaptor proteins , Protein Sorting Signals |
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928
One Index
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Gleeson, Jo PhD 0000-0002-0889-9220 |
277 docs (1982 - 2024)
Microcephaly , Doublecortin , Joubert syndrome , Brain Development , Ciliopathy |
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925
One Index
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Kruer, Michael PhD 0000-0002-1373-7891 |
173 docs (2004 - 2024)
Microcephaly , Cerebral Palsy , Neurodegeneration , Movement disorders , Neurodevelopmental disorder |
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922
One Index
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Chelban, Viorica PhD 0000-0002-5817-6290 |
63 docs (2016 - 2024)
Hereditary Spastic Paraplegia , Parkinsonism , Genome-wide association study , Synucleinopathies , Compound heterozygosity |
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922
One Index
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Habibzadeh, Parham PhD 0000-0002-2086-0425 |
86 docs (2013 - 2024)
2019-20 coronavirus outbreak , Acid-Base Balance , Pandemic , Hereditary Spastic Paraplegia , Acetazolamide |
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913
One Index
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Rouleau, Guy PhD 0000-0001-8403-1418 |
1152 docs (1981 - 2024)
Genome-wide association study , Genetic association , Neurodegeneration , Hereditary Spastic Paraplegia , Genetic linkage |
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909
One Index
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Yu, Hao PhD 0000-0002-9778-8855 |
239 docs (1997 - 2024)
Plant Development , Fertilization Mechanisms , Agamous , Adolescent Idiopathic Scoliosis , MMP3 |
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909
One Index
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Blackstone, Craig PhD 0000-0003-1261-9655 |
161 docs (1988 - 2024)
Hereditary Spastic Paraplegia , Glutamate Receptors , Organelle , Mitochondrial Fission , Paraplegia |
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905
One Index
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Gao, Fen-Biao PhD 0000-0001-8873-5404 |
160 docs (1993 - 2024)
C9orf72 , Neurodegeneration , ESCRT , Haploinsufficiency , Motor Neuron |
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905
One Index
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Houlden, Henry PhD 0000-0002-2866-7777 |
1458 docs (1950 - 2024)
Genome-wide association study , Ataxia , Neurodegeneration , Genetic association , Cerebellar ataxia |
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904
One Index
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Huang, Yining PhD 0000-0002-1657-4151 |
249 docs (1998 - 2024)
Stroke (engine) , Infarction Treatment , Intracranial Hypotension , Intracranial Pressure , Clinical endpoint |
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904
One Index
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Kaiyrzhanov, Rauan PhD 0000-0003-1640-4010 |
69 docs (2017 - 2024)
Microcephaly , Parkinsonism , LRRK2 , Neuroimaging , Thyroid-Associated Ophthalmopathy |
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898
One Index
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Bonnenmann, Carsten PhD |
21 docs (2019 - 2024)
Loss function , Neurodevelopmental disorder , Proband , Microcephaly , Clinical Genomics |
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898
One Index
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Sue, Carolyn PhD 0000-0003-1255-3617 |
347 docs (1985 - 2024)
Mitochondrial Dysfunction , Mitochondrial disease , Mitochondrial Function , Mitochondria , Hereditary Spastic Paraplegia |
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898
One Index
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Brice, Alexis PhD 0000-0002-0941-3990 |
1353 docs (1973 - 2024)
Neurodegeneration , Parkinsonism , LRRK2 , Ataxia , Parkinson's Disease |
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897
One Index
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Durr, Alexandra PhD 0000-0002-8921-7104 |
766 docs (1970 - 2024)
Ataxia , Cerebellar ataxia , Hereditary Spastic Paraplegia , Gene Expression Dysregulation , Machado–Joseph disease |
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894
One Index
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Hubbard, Tim @timjph PhD 0000-0002-1767-9318 |
354 docs (1969 - 2024)
Ensembl , genome annotation , Sequence (biology) , Proteins , Pseudogene |
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892
One Index
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Nilsson, Christer PhD 0000-0003-1186-8115 |
396 docs (1970 - 2023)
Habitat Fragmentation , Vegetation Dynamics , Hydrological Impacts , Restoration ecology , Ecosystem Resilience |
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892
One Index
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Zuchner, Stephan PhD 0000-0002-8498-5235 |
367 docs (1986 - 2024)
Charcot-Marie-Tooth Disease , Neurofilament Mutations , Exome , Hereditary Spastic Paraplegia , Axonal Degeneration |
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892
One Index
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Ganley, Ian PhD 0000-0003-1481-9407 |
112 docs (2001 - 2024)
Autophagy , Mitophagy , PINK1 , LRRK2 , Autophagosome |
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890
One Index
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Depienne, Christel PhD 0000-0002-7212-9554 |
277 docs (2000 - 2024)
Hereditary Spastic Paraplegia , Epilepsy , Dravet syndrome , Haploinsufficiency , Exome |
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889
One Index
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Halai, Dina PhD |
48 docs (2010 - 2024)
Genomic Analysis , Table (database) , Genome-wide association study , Brachyury , Chordoma |
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888
One Index
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Odhams, Christopher PhD 0000-0003-2396-6150 |
43 docs (2016 - 2024)
Genome-wide association study , Genetic association , Haploinsufficiency , Candidate gene , Exome |
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888
One Index
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Synofzik, Matthis PhD 0000-0002-2280-7273 |
610 docs (2004 - 2024)
Ataxia , Neurodegeneration , C9orf72 , Cerebellar ataxia , Frontotemporal lobar degeneration |
