Scientific Areas of Integrated Review Groups (IRGs)

For a listing of the Scientific Review Administrator and membership roster for each study section, click on the study section roster under the study section name within the IRG shown below or go to the study section index (study sections listed alphabetically) and click on the specified roster next to the name of the study section.

Last updated on 26th October, 2004

 

Referral & Review

 

Brain Disorders and Clinical Neuroscience IRG [BDCN]           



 

The Brain Disorders and Clinical Neuroscience [BDCN] IRG reviews grant applications that have neural disorders and/or injury of the nervous system as their main focus. Investigations appropriate for review in the BDCN IRG may include those using animal models of neural injury or disease, investigations based on the study of specific patient populations, or investigations focused on the development of rehabilitative and therapeutic strategies. Specific areas of interest include the investigation of traumatic brain or spinal cord injury, the consequences of episodes of ischemia or hypoxia, the study of mental disorders, neurodegenerative diseases, and other neuropathies. These specific areas of interest may be studied from the perspective of neuroanatomical or neurophysiological alterations, changes in neurotransmitter or neurotrophin function or metabolism, the genetic, cellular, or molecular basis of alterations induced by disease or injury, the influence or involvement of the immune or vascular systems in a neural disease process or response, and the neurological basis of addictive, cognitive, behavioral, and emotional disorders.

In addition to this IRG, the Molecular, Cellular, and Developmental Neuroscience [MDCN] and Integrative, Functional, and Cognitive Neuroscience [IFCN] IRGs within CSR focus on the review of neuroscience-related applications, and the Biobehavioral and Behavioral Processes [BBBP] IRG also has some shared interests with the BDCN IRG. Please see the descriptions and shared interest statements of these IRGs for a complete description of their review venues.

The following Study Sections are included within the BDCN IRG:

Clinical Neuroscience and Disease Study Section [CND]Formerly BDCN1

Clinical Neuroplasticity and Neurotransmitters Study Section [CNNT] Formerly BDCN-2

Cell Death and Injury in Neurodegeneration Study Section [CDIN] Formerly BDCN-3

Clinical Neuroimmunology and Brain Tumors Study Section [CNBT] Formerly BDCN-4

Developmental Brain Disorders Study Section [DBD] Formerly BDCN-5

Neural Basis of Psychopathology, Addictions and Sleep Disorders Study Section [NPAS] Formerly BDCN-6

Anterior Eye Disease Study Section [AED] Formerly VISA

BDCN Small Business [SBIR/STTR] Activities Special Emphasis Panels [BDCN Small Business SEPs]
Brain Disorders and Related Neurosciences Fellowship Study Section [F01]




Clinical Neuroscience and Disease Study Section [CND]

 

[CND Roster]

 

Formerly BDCN-1

The Clinical Neuroscience and Disease [CND] Study Section addresses anatomical, cellular and functional basis of neural disease and injury across the life span. Emphasis is on the neural substrate, functional consequences [cognitive, sensory/motor, behavioral, pathophysiological], rehabilitation, and the development of therapeutic strategies. Relevant disorders include stroke/ischemia, neurodegenerative diseases, epilepsy, spinal cord injury, traumatic brain injury, dystonia/ataxia, and neuropathies. This Study Section considers patient-oriented research and animal models.

Specific areas covered by CND:

·         Anatomical, neuropathological, neuroimaging, electrophysiological, functional mapping, and autopsy studies to monitor the onset, progression and treatment of brain and spinal cord disease and injury; therapeutic approaches and clinical studies; cerebral blood flow and metabolism in the context of clinical neuroimaging

·         Functional and anatomical changes in sensory and motor systems associated with the initiation, progression, and treatment of neural disorders and injury

·         Changes in learning, memory, language, attention, behavior, and other functional domains that are consequences of disease and injury; strategies for therapeutic intervention

·         Cellular, anatomical, and systems-based studies of changes in the neural substrate and function of brain and spinal cord in response to disease and injury

·         Recovery of function/rehabilitation; beneficial and compensatory changes in the neural substrate in response to clinical interventions; neurological and functional evaluation of neural prostheses, electrical/magnetic stimulation, behavioral and pharmacological interventions, and physical therapy

·         Evaluation of pharmacological, transplantational, surgical, electrophysiological, physical or behavioral interventions to reduce loss, enhance function, and facilitate recovery

 

CND has the following shared interests within the BDCN IRG:

 

·         Brain imaging studies that focus on specific neurotransmitter systems and receptors should be reviewed in CNNT, while more general brain imaging studies of neuropathological pathways and brain dysfunction should be reviewed in CND.

·         CDIN reviews studies of the molecular and cellular basis of neural disorders. CND reviews studies that focus on the neuroanatomical substrate and functional consequences. CDIN may be more appropriate for studies of gene, cell and tissue transplantation, especially if the focus is on molecular and cellular mechanisms.

·         CNBT reviews applications focused on immune, inflammatory and vascular mechanisms, while CND reviews the anatomical and functional basis of neural disorders and injury, including functional imaging studies.
 

·         DBD reviews studies of neurodevelopmental disorders, especially when the focus is on unique aspects of the developing nervous system. Neuroanatomical and functional disease processes that are in common between children and adults may be reviewed in CND.

·         While CND may review applications on dementias, NPAS has particular expertise to review studies of addictive, behavioral, cognitive and emotional disorders, in addition to the dementias.

 

CND has the following shared interests outside the BDCN IRG:

·         With the Genes, Genomes and Genetics [GGG] IRG: The GGG IRG has shared interests with CND with respect to an interest in diseases of the nervous system.  However, when the focus is primarily on molecular genetic approaches, large-scale gene/genomic/genetic studies, gene discovery using complex or novel technologies, the application may be reviewed in the GGG IRG.  Applications that focus primarily on the anatomical, functional and pathologic basis of the neural disorder or injury may be reviewed in CND.

 

·         With the Biology of  Development and Aging [BDA] IRG: Studies with a focus on multiple system manifestations of age-related neurological diseases such as Alzheimer’s disease may be reviewed within the BDA IRG, while functional and neuroanatomical changes associated with these diseases could be reviewed in CND.

·         With the Health of the Population [HOP] IRG: Studies dealing with descriptive and analytical epidemiologic aspects of various neurologic disorders including Alzheimer’s disease, Parkinson’s disease, stroke and epilepsy may be reviewed with the HOP IRG, while studies on the neural basis of these disorders could be reviewed within CND.

·         With the Biobehavioral and Behavioral Processes [BBBP] IRG: Studies that focus primarily on behavior and behavioral approaches may be reviewed in the BBBP IRG. Applications that focus mainly on the anatomical and functional basis of the neural disorder or injury could be reviewed in CND. 

·         With the Cardiovascular Sciences [CVS] IRG: Studies dealing with cerebral circulation and hemodynamics may be assigned to the CVS IRG, while those focusing on cerebral blood flow and metabolism in the context of neuroimaging for analysis of brain and spinal cord disease or injury or the functional consequences of ischemia, hypoxia, stroke on brain or spinal cord function could be assigned to CND.

·         With the Musculoskeletal, Oral and Skin Sciences [MOSS] IRG: CND has shared interests within the MOSS IRG with respect to research on recovery and rehabilitation. While MOSS has broad expertise in physical therapy, physiology, and non-neuronal systems, CND has particular expertise in the neural basis of rehabilitation and recovery as well as disease that effect motor control (e.g. Parkinson’s disease, Huntington disease, essential tremor).

 

·         With the Surgical Sciences, Biomedical Imaging and Bioengineering [SBIB] IRG:  Both CND and the SBIB IRG review applications dealing with functional brain imaging; however, CND may review those applications using imaging as a tool to study neurological disorders or injury or their treatment. SBIB may review applications concerning the development and evaluation of imaging procedures.  SBIB is appropriate for studies with focus on the development of imaging technology. However, where the proposed research is more oriented toward the application of imaging techniques for studying neurological disorders or injury or their treatment, CND may be a better review locus.

·         With the Molecular, Cellular, Developmental Neuroscience [MDCN] IRG:  Both MDCN and CND share a common interest in neurologic diseases.  However, MDCN focuses largely on basic cellular and molecular processes whereas, CND reviews applications related to the cellular, anatomical and functional aspects these diseases. 

·         With the Integrative, Functional and Cognitive Neuroscience [IFCN] IRG: Both IFCN and CND share common interests in disorders of learning and memory and diseases that involve motor systems.  However, when the focus is to elucidate specific normal memory processes or the neural substrates of motor function, then applications may be assigned to IFCN.  Applications that focus largely on neurologic disorders and their treatment may be reviewed within CND. 

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Clinical Neuroplasticity and Neurotransmitters Study Section [CNNT]

Formerly BDCN-2

[CNNT Roster]


The Clinical Neuroplasticity and Neurotransmitters [CNNT] Study Section addresses the area of neural disease and injury across the life span that focuses on neurotransmitter or neurotrophic function including associated receptors. This includes studies of plasticity, regeneration, and therapeutic strategies. Relevant disorders include stroke/ischemia, neurodegenerative diseases, epilepsy, spinal cord injury, traumatic brain injury, dystonia/ataxia, and neuropathies. Studies primarily involve animal models although patient-oriented research may be reviewed.

Specific areas covered by CNNT:

·         Neurotransmitter synthesis, regulation, release, degradation, and inactivation; abnormalities of receptor number, distribution and function; abnormalities of synaptic physiology; functional imaging of particular neurotransmitter pathways; role of growth factors, neurotrophins, and neurohormones

·         Pharmacological studies; diagnostics and therapeutic strategies involving receptor agonists and antagonists; pharmacological effects on synaptic physiology and second messenger pathways; neurotrophins and neurohormones

·         Mechanisms of degeneration, plasticity and recovery; neuropathological and compensatory changes in neurotransmitter function; role of trophic factors; therapeutic interventions

·         Therapeutic approaches involving neurotransmitter function;pre-clinical and clinical studies of drugs, gene therapy, cell and tissue transplantation, including stem cells, and delivery across the blood-brain barrier.

 

CNNT has the following shared interests within the BDCN IRG:

 

·         CND reviews applications on the anatomical and functional basis of neural disease and injury, while CNNT reviews applications on neurotransmitter and receptor function. Imaging studies other than those related to neurotransmitter function could be reviewed in CND.

·         CDIN reviews applications on the molecular and cellular basis of neural disorders, including apoptosis, oxidative or general metabolic mechanisms, protein and macromolecular metabolism other than neurotransmitter-, neurotrophin- or neurohormone-related proteins.

·         CNBT reviews studies of neural disorders that focus on immune, inflammatory and vascular mechanisms.
 

·         DBD reviews studies of neurodevelopmental disorders, especially when the focus is on unique aspects of the developing nervous system. Neurotransmitter and receptor disease processes that are in common between children and adults may be reviewed in CNNT.

·         NPAS has particular expertise to review studies of addictive, behavioral, cognitive and emotional disorders.

 

CNNT has the following shared interests outside the BDCN IRG:

 

·         With the Genes, Genomes and Genetics [GGG] IRG: The GGG IRG has shared interests with CNNT with respect to an interest in diseases of the nervous system.  However, when the focus is primarily on molecular genetic approaches, large-scale gene/genomic/genetic studies, gene discovery using complex or novel technologies, the application could be reviewed in the GGG IRG.  Applications that focus primarily on trophic, neurotransmitter and receptor function in the neural disorder or injury could be reviewed in CNNT.

·         With the Health of the Population [HOP] IRG: Studies dealing with descriptive and analytical epidemiologic aspects of various neurologic disorders including Alzheimer’s disease, Parkinson’s disease, stroke and epilepsy may be reviewed within the HOP IRG, while applications that focus primarily on trophic, neurotransmitter and receptor function in the neural disorder or injury could be reviewed in CNNT.

·         With the Biobehavioral and Behavioral Processes [BBBP] IRG: Studies where the primary focus is on behavior and behavioral approaches may be reviewed in BBBP IRG. Applications that focus mainly on neurotransmitter and receptor function in the neural disorder or injury may be reviewed in CNNT.

·         With the Immunology [IMM] IRG: Studies focusing on organ-specific aspects of the physiology and pathology of transplantation could be reviewed within the IMM IRG, while studies dealing with transplantation of tissue into the brain as a therapeutic tool could be reviewed within CNNT.

·         With the Hematology [HEME] IRG: Studies that focus on hematopoiesis, blood cells and related diseases could be assigned to the HEME IRG.  Applications that focus on the use of hematopoietic stem cells as therapeutic intervention following brain and spinal cord injury could be referred to CNNT.

·         With the Endocrinology, Metabolism, Nutrition and Reproductive Sciences [EMNR] IRG: Studies that focus on the neuroendrocrine control of reproduction, gonadotropin releasing hormones, pituitary hypothalamic connections and pituitary gonadal interactions could be assigned to the EMNR IRG, while those applications focusing on the effects of neurodegenerative disease and brain injury on neuroendrocrine function could be reviewed within CNNT.

 

·         With the Musculoskeletal, Oral and Skin Sciences [MOSS] IRG: CNNT has shared interests with the MOSS IRG with respect to research on recovery and rehabilitation following injury to the CNS.  While MOSS has broad expertise in physical therapy, physiology, and non-neuronal systems, CNNT has particular expertise in the neural basis of rehabilitation and recovery particularly following spinal cord injury.

·         With the Renal and Urological Sciences [RUS] IRG: Studies focusing on central nervous systems regulation of urological function could be assigned to the RUS IRG, while applications dealing with bladder problems secondary to spinal cord injury may be assigned to CNNT.

·          With the Surgical Sciences, Biomedical Imaging and Bioengineering [SBIB] IRG:  The SBIB IRG may review studies with focus on the development of imaging technology. However, where the proposed research is more oriented toward the application of imaging techniques for studying neurological disorders or injury or their treatment, CNNT may be more appropriate.  Both CNNT and the SBIB IRG may review applications dealing with functional brain imaging; however, CNNT may be more appropriate to review those applications using imaging as a tool to study neurological disorders or injury or their treatment. SBIB may be more appropriate to review applications concerning the development and evaluation of imaging procedures.

·         With the Molecular, Cellular and Developmental Neuroscience [MDCN] IRG: The MDCN IRG reviews applications on the basic mechanisms of neurotransmitter and receptor function, and review applications more focused on fundamental cellular and molecular mechanisms. Studies of the fundamental role of neurotransmitters and related molecules in development and plasticity could be reviewed in the MDCN IRG, while applications focusing on trophic, neurotransmitter and receptor function in the neural disorder or injury could be reviewed in CNNT.  In addition, studies using stem cells where the primary goal is to advance understanding of neural induction, specification, or differentiation are appropriate for the MDCN IRG.  Studies focused primarily on restorative/therapeutic outcome may be appropriate for review within CNNT.

·         With the Integrative, Functional and Cognitive Neuroscience [IFCN] IRG: In general, BDCN study sections review applications relating to abnormal and pathological states, while the IFCN IRG reviews normal aspects of brain function.  For example, while IFCN and CNNT share common interests in disorders of learning and memory and diseases that involve motor systems, if the focus is to elucidate specific normal memory processes or the neural substrates of motor function, then applications may be assigned to IFCN.  Applications that focus primarily on trophic, neurotransmitter and receptor function in the neural disorder or injury may be reviewed in CNNT.


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Cell Death and Injury in Neurodegeneration Study Section [CDIN]

Formerly BDCN-3

[CDIN Roster]

The Cell Death and Injury in Neurodegeneration [CDIN] Study Section addresses the genetic, molecular, and cellular basis of neural disorders and injury across the life span. This includes studies of neuronal cell death and protein and macromolecular function in neurodegenerative disease. Relevant disorders include stroke/ischemia, neurodegenerative diseases, spinal cord injury, traumatic brain injury, dystonia/ataxia, and neuropathies. This Study Section can review studies of in vitro systems, animal models, and to a lesser extent patient-oriented research.

Specific areas covered by CDIN:

·         Pathology and clinical interventions; molecular, cellular, and neurochemical changes in human brain and spinal cord associated with neurodegeneration in disease or injury; analysis of autopsy material; therapeutic approaches and clinical trials to prevent or treat neuropathological damage, including gene therapy and tissue and cell transplantation

·         Tissue culture and animal models of neurodegeneration or trauma; generation of relevant transgenic models; models to evaluate treatments to limit or prevent cell injury and death

·         Metabolic abnormalities in degeneration and injury; neuron viability; oxidative and free radical metabolism; mitochondrial function; glial metabolism; secondary inflammation; interaction of genetics, environment, drugs, metabolites, and age on cell dysfunction and neuropathology.

·         Abnormal protein and macromolecular metabolism and function; synthesis, assembly, processing, trafficking, structure/function, regulation, and degradation of proteins and other macromolecules implicated in neurodegenerative diseases and injury.

·         Mechanisms of cell degeneration; neurotoxicity and mechanisms of cell death in neurodegenerative diseases; role of intracellular Ca++, glutamate excitotoxicity, metals, oxidative stress and free radicals, amyloid and paired helical filaments.

·         Genetic basis of neurological disorders; identification and expression of genes associated with neurological disorders, genomic screening, and linkage analysis

 

CDIN has the following shared interests within the BDCN IRG:

 

·         CND reviews the anatomical and functional basis of neural disease and injury, while CDIN reviews studies at the cellular and molecular level. CDIN may be more appropriate for studies of gene, cell and tissue transplantation, especially if the focus is on molecular and cellular mechanisms.

·         CNNT reviews applications that focus primarily on the neurotransmitter abnormalities, while CDIN may be more appropriate for other aspects of neurochemistry and cell physiology.

·         CNBT reviews studies of neural disorders and injury that focus on immune, inflammatory and vascular mechanisms, although CDIN could be more appropriate for studies where inflammation is secondary to some other pathophysiological process.

·         DBD reviews studies of neurodevelopmental disorders, especially when the focus is on unique aspects of the developing nervous system. Molecular and cellular processes that are in common between children and adults may be reviewed in CDIN.

·         NPAS has particular expertise to review studies of addictive, behavioral, cognitive and emotional disorders.

 

CDIN has the following shared interests outside the BDCN IRG:

 

·         With the Cell Biology [CB] IRG: Studies focusing on basic cell processes or an emerging cell biologic approach may be assigned to the CB IRG, while studies on the cellular mechanism of neurodegenerative diseases may be assigned to CDIN.

·         With the Genes, Genomes and Genetics [GGG] IRG: The GGG IRG has shared interests with CDIN with respect to an interest in diseases of the nervous system.  However, when the focus is primarily on molecular genetic approaches, large-scale gene/genomic/genetic studies, gene discovery using complex or novel technologies, the application could be assigned to the GGG IRG.  CDIN may be more appropriate for studies where the primary focus is on cellular and molecular pathophysiology within the nervous system.  In addition, studies of genomic screening and linkage analysis could be reviewed in the GGG IRG.  However, if the primary focus is on neurological mechanisms and outcomes, then CDIN may be more appropriate.

·         With the Biology of Development and Aging [BDA] IRG: Studies with a focus on multiple system manifestations of age-related neurological diseases such as Alzheimer’s disease could be reviewed within the BDA IRG, while cellular and molecular changes associated with these diseases could be reviewed in CDIN.

·         With the Bioengineering Sciences and Technologies [BST] IRG: Applications with a focus on the design, development, and introduction of technology for gene and drug delivery in the nervous system could be assigned to the BST IRG, while applications focused on the mechanisms and functional implications associated with gene delivery into the central nervous system may be assigned to CDIN.

·         With the Health of the Population [HOP] IRG: Studies dealing with descriptive and analytical epidemiologic aspects of various neurologic disorders including Alzheimer’s disease, Parkinson’s disease, stroke and epilepsy may be reviewed within the HOP IRG, while applications that focus primarily on the cellular and molecular aspects of these disease may be reviewed in CDIN.

 

·         With the Biobehavioral and Behavioral Processes [BBBP] IRG: Studies where the primary focus is on behavior and behavioral approaches could be reviewed in BBBP IRG. Applications that focus mainly on the genetic, molecular, or cellular functional basis of the neural disorder or injury could be reviewed in CDIN.

·         With the Cardiovascular Sciences [CVS] IRG: Studies dealing with cerebral circulation and hemodynamics may be assigned to the CVS IRG, while those focusing on cerebral blood flow and the cellular and molecular consequences of ischemia, hypoxia, stroke on brain or spinal cord function could be assigned to CDIN.

·         With the Molecular, Cellular and Developmental Neuroscience [MDCN] IRG