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9,482 authors found
quering by "Fragile X Syndrome"
.
Showing
the first 25
sort by ONE Index.
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936
One Index
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Goodhill, Geoffrey PhD 0000-0001-9789-9355 |
580 docs (1976 - 2024)
Representation Learning , Backpropagation Learning , Deep Learning , Boltzmann machine , Representation (politics) |
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924
One Index
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Jaenisch, Rudolf PhD 0000-0002-2540-7099 |
785 docs (1966 - 2024)
Reprogramming , DNA Methylation , Cellular Reprogramming , Multiplex Genome Editing , Epigenetic Remodeling |
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915
One Index
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Piven, Joseph PhD 0000-0003-0255-9003 |
368 docs (1990 - 2024)
Autism , Brain Development , Fragile X Syndrome , Heritability of autism , Autism Spectrum Disorders |
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914
One Index
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Ben-Shlomo, Yoav PhD 0000-0001-6648-3007 |
1390 docs (1981 - 2024)
Genome-wide association study , Parkinson's Disease , Genetic association , Life course approach , Diagnostic Criteria |
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908
One Index
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Collingridge, Graham PhD 0000-0002-9572-5359 |
443 docs (1978 - 2024)
Glutamate Receptors , NMDA Receptors , Long-term depression , Synaptic Plasticity , Kainate receptor |
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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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904
One Index
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Järvelä, Irma PhD 0000-0002-1770-6187 |
294 docs (1989 - 2024)
Autism , Lactase , Neuronal Ceroid Lipofuscinoses , Batten disease , Neuronal ceroid lipofuscinosis |
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902
One Index
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Dahl, Niklas PhD 0000-0002-8122-0800 |
432 docs (1987 - 2024)
Breast Cancer , cancer susceptibility , Diamond–Blackfan anemia , Cancer Risk , BRCA1 |
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902
One Index
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Jin, Peng PhD 0000-0001-6137-6659 |
322 docs (1999 - 2024)
Fragile X Syndrome , mRNA modification , 5-Hydroxymethylcytosine , FMR1 , Gene Expression Regulation |
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901
One Index
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Clayton-Smith, Jill PhD 0000-0002-9602-2321 |
371 docs (1988 - 2024)
Haploinsufficiency , Angelman Syndrome , Maternal Epilepsy , Antiepileptic Drugs , Microcephaly |
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897
One Index
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Hoeft, Fumiko PhD 0000-0003-3932-9201 |
176 docs (2006 - 2024)
Neurological Basis of Reading , Reading Acquisition , Reading Comprehension , Dyslexia , Language Development |
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896
One Index
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De Vries, Jantina PhD 0000-0001-7192-2633 |
178 docs (2003 - 2024)
Research Participation , Research ethics , Philosophy of medicine , Bioethics , Data sharing |
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896
One Index
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Reiss, Allan PhD 0000-0002-1979-4942 |
633 docs (1948 - 2024)
Fragile X Syndrome , Autism , Brain Development , Williams Syndrome , Neuroimaging Data Analysis |
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896
One Index
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de Vries, Bert PhD 0000-0002-0000-2917 |
254 docs (1992 - 2024)
Haploinsufficiency , Microcephaly , Comparative genomic hybridization , Autism , Phenotype Analysis |
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895
One Index
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Elvassore, Nicola PhD 0000-0002-7029-6287 |
234 docs (1997 - 2024)
Microfluidic Devices , Reprogramming , Cardiac Tissue Engineering , Extracellular Matrix , Decellularization |
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894
One Index
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Segal, Menahem PhD 0000-0001-7592-0408 |
361 docs (1972 - 2024)
Locus coeruleus , Hippocampus , Synaptic Plasticity , Dendritic Spines , Dendritic filopodia |
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894
One Index
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Raymond, Frances Lucy PhD 0000-0003-2652-3355 |
180 docs (2003 - 2024)
Brain Development , Exome , Exome Sequencing , Photoreceptor Degeneration , Proband |
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894
One Index
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Wang, Daifeng PhD 0000-0001-9190-3704 |
122 docs (2006 - 2024)
Gene regulatory network , Cell type , Genomic Data Integration , Cell Heterogeneity , Gene Set Enrichment Analysis |
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891
One Index
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Welt, Corrine PhD 0000-0002-8219-5504 |
141 docs (1997 - 2024)
Polycystic Ovary Syndrome , Hyperandrogenism , Genome-wide association study , Gonadotropin , Follistatin |
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887
One Index
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Sherman, Stephanie PhD 0000-0002-1094-0798 |
289 docs (1982 - 2023)
Fragile X Syndrome , FMR1 , Trisomy , Nondisjunction , Trisomy Detection |
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887
One Index
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John M. Olichney PhD |
232 docs (1993 - 2024)
Neuroimaging , Neuroimaging Data Analysis , Apolipoprotein E , Genome-wide association study , Alzheimer's Disease |
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887
One Index
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Clarke, Angus PhD 0000-0002-1200-9286 |
394 docs (1975 - 2024)
Genetic Testing , Hypohidrotic ectodermal dysplasia , Rett syndrome , Medical genetics , genomic medicine |
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886
One Index
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De Rubeis, Silvia PhD 0000-0001-9383-6883 |
97 docs (2007 - 2024)
Autism , Neurodevelopmental disorder , Brain Development , Fragile X Syndrome , Haploinsufficiency |
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886
One Index
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Kolevzon, Alexander PhD 0000-0001-8129-2671 |
187 docs (1995 - 2024)
Autism , Neurodevelopmental disorder , Brain Development , Haploinsufficiency , ADHD |
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884
One Index
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Douzgou, Sofia PhD 0000-0001-8890-7544 |
146 docs (2004 - 2024)
Haploinsufficiency , Exome , Macrocephaly , Proband , Loss function |
