Introduction
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...
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2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...
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3CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...
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4CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...
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5CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference0 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference1 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference2 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference3 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference4 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference5 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference6 The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field’s most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference7 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference8. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference9 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference0. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference1 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference2. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference3 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference4. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference5 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference6. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference7 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference8. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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2CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference9 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference0. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference1 A second motivation is the recognition that “SST interneuron” is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference2. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference3 Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer’s disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference4. These associations have motivated therapeutic strategies targeting SST circuits, from i...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference5 Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer’s disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference6. These associations have motivated therapeutic strategies targeting SST circuits, from i...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference7 Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer’s disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions 1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference8. These associations have motivated therapeutic strategies targeting SST circuits, from i...
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1CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference9 Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer’s disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions 3CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference0. These associations have motivated therapeutic strategies targeting SST circuits, from i...
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3CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference1 Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer’s disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions 3CitationSomatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...content/01_introduction.md:line 3Open reference2. These associations have motivated therapeutic strategies targeting SST circuits, from i...
References
- [Rudy2011] “Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...”
- [Wilson2012] “Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...”
- [Pi2013] “Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...”
- [Adesnik2012] “Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...”
- [LovettBarron2014] “Somatostatin-expressing (SST) interneurons constitute approximately 30% of the GABAergic neuron population in the mammalian cortex [Rudy2011] and have become one of the most intensively studied cell classes in systems neuroscience. Over the past two decades, optogenetic tools, single-cell transcriptomics, and multimodal profiling have generated an enormous body of data on SST neurons — their molecular identities, de...”
- [Nigro2018] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Wu2023] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Beierlein2003] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Wang2004] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Shapiro2025] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Dipoppa2018] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Nienborg2013] “The premise of this review is that the SST interneuron literature suffers from a specific structural problem: the field's most-cited functional claims are not its best-supported ones. Anatomical and electrophysiological characterizations — the distinction between Martinotti and non-Martinotti subtypes, the identification of facilitating excitatory inputs, the mapping of dendritic-targeting axons — rest on convergent...”
- [Tasic2018] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [Gouwens2020] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [Agmon2024] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [MullerKomorowska2020] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [Veres2023] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [Rachel2025] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [Fisher2024] “A second motivation is the recognition that "SST interneuron" is not a natural kind. What was once treated as a unitary cell class has fractured into at least ten transcriptomically distinct supertypes, with finer subdivisions proliferating as profiling technologies improve [Tasic2018, Gouwens2020, Agmon2024]. These molecular subtypes differ in morphology, intrinsic physiology, connectivity, laminar distribution, an...”
- [Duncan2025] “Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer's disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions [Duncan2025, Hughes2024, Singer2026]. These associations have motivated therapeutic strategies targeting SST circuits, from i...”
- [Hughes2024] “Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer's disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions [Duncan2025, Hughes2024, Singer2026]. These associations have motivated therapeutic strategies targeting SST circuits, from i...”
- [Singer2026] “Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer's disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions [Duncan2025, Hughes2024, Singer2026]. These associations have motivated therapeutic strategies targeting SST circuits, from i...”
- [Casalia2021] “Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer's disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions [Duncan2025, Hughes2024, Singer2026]. These associations have motivated therapeutic strategies targeting SST circuits, from i...”
- [Drexel2022] “Third, the translational stakes are high and rising. SST interneuron dysfunction has been implicated in schizophrenia, epilepsy, Alzheimer's disease, and autism spectrum disorder, with postmortem studies consistently reporting reduced SST expression across multiple neuropsychiatric conditions [Duncan2025, Hughes2024, Singer2026]. These associations have motivated therapeutic strategies targeting SST circuits, from i...”
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