Mental Retardation & Developmental Disabilities (MRDD) Branch Supported Projects for 2007
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F31 - Predoctoral Individual National Research Service Award |
Project Number |
Description |
1F31HD056566-01 |
PEDERSEN Y ARBONA, ANITA L
ARIZONA STATE UNIVERSITY-TEMPE CAMPUS
A LONGITUDINAL STUDY: ADAPTATION IN FAMILIES OF CHILDREN WITH DEVELOPMENTAL DELAY
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F32 - Postdoctoral Individual National Research Service Award |
Project Number |
Description |
1F32HD055143-01 |
SWANBERG, SUSAN E
UNIVERSITY OF CALIFORNIA DAVIS
HINDBRAIN DYSGENESIS IN RETT SYNDROME AND OTHER AUTISM-SPECTRUM DISORDERS
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1F32HD055745-01 |
MALONEY, MICHAEL T
STANFORD UNIVERSITY
RETROGRADE TRANSPORT AT THE CROSSROADS OF COGNITIVE DELCINE AND NEURODEGENERATION
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5F32HD049248-02 |
DINDOT, SCOTT V
BAYLOR COLLEGE OF MEDICINE
ANALYSIS OF GENOMIC IMPRINTING AT THE UBE3A LOCUS.
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5F32HD049997-04 |
GUAN, WEI
WESTERN INSTITUTE FOR BIOMEDICAL RES
MIGRATION OF CAJAL-RETZIUS CELLS
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5F32HD054159-02 |
GIN, PETER K
UNIVERSITY OF CALIFORNIA LOS ANGELES
LAMINOPATHY TREATMENT WITH FARNESYLTRANSFERASE INHIBITOR
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K02 - Research Scientist Development Award - Research |
Project Number |
Description |
5K02HD042269-05 |
MALKOVA, LUDISE
GEORGETOWN UNIVERSITY
NEURAL SUBSTRATES OF SOCIOEMOTIONAL DEVELOPMENT
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5K02HD047201-02 |
SYMONS, FRANK J
UNIVERSITY OF MINNESOTA TWIN CITIES
SELF-INJURY: PAIN AND STRESS MECHANISMS
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K08 - Clinical Investigator Award |
Project Number |
Description |
1K08HD055488-01 |
DEARDORFF, MATTHEW A
CHILDREN'S HOSPITAL OF PHILADELPHIA
THE COHESIN COMPLEX AND CORNELIA DE LANGE SYNDROME
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1K08HD057555-01A1 |
LIPSHUTZ, GERALD S
UNIVERSITY OF CALIFORNIA LOS ANGELES
THE IMMUNE RESPONSE TO VIRAL VECTOR AND TRANSGENES IN THE FETUS
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5K08HD043112-06 |
LEVY, BRYNN
COLUMBIA UNIVERSITY HEALTH SCIENCES
CHROMOSOME ANALYSIS OF SINGLE CELLS
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5K08HD044716-05 |
BELL, MICHAEL J
CHILDREN'S RESEARCH INSTITUTE
EFFECTS OF INFLAMMATION ON DEVELOPING GLIA
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7K08HD044716-06 |
BELL, MICHAEL J
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
EFFECTS OF INFLAMMATION ON DEVELOPING GLIA
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K23 - Mentored Patient-Oriented Research Devel Awd |
Project Number |
Description |
5K23HD043179-05 |
KEREN, RON
CHILDREN'S HOSPITAL OF PHILADELPHIA
PREDICITING SEVERE NEONATAL HYPERBILIRUBINEMIA
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5K23HD044789-05 |
WANG, TAO
JOHNS HOPKINS UNIVERSITY
ID OF GENES RESPONSIBLE FOR X-LINKED MENTAL RETARDATION
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5K23HD046541-04 |
ARNOLD, GEORGIANNE L
UNIVERSITY OF ROCHESTER
ATTENTIONAL DYSFUNCTION IN CHILDREN WITH PHENYLKETONURIA
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5K23HD047713-04 |
SICES, LAURA
CASE WESTERN RESERVE UNIVERSITY
IDENTIFICATION AND MANAGEMENT OF DEVELOPMENTAL DELAYS
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5K23HD048502-03 |
RAUEN, KATHERINE ANNA
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
ELUCIDATION OF THE GENETIC ETIOLOGY OF COSTELLO SYNDROME
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7K23HD047713-05 |
SICES, LAURA
BOSTON MEDICAL CENTER
IDENTIFICATION AND MANAGEMENT OF DEVELOPMENTAL DELAYS
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K24 - Midcareer Investigator Awd in Patient-Oriented Res |
Project Number |
Description |
5K24HD046712-03 |
GLASS, IAN A
UNIVERSITY OF WASHINGTON
GENETIC ANALYSES OF CEREBELLAR MALFORMATIONS
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K99 - Career Transition Award |
Project Number |
Description |
1K99HD055333-01 |
KALANTRY, SUNDEEP
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
EPIGENETIC MECHANISMS OF X-CHROMOSOME INACTIVATION
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P01 - Research Program Projects |
Project Number |
Description |
2P01HD018955-21A2 |
SAUNDERS, RICHARD R
UNIVERSITY OF KANSAS LAWRENCE
COMMUNICATION OF PEOPLE WITH MENTAL RETARDATION
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2P01HD025995-17 |
MCILVANE, WILLIAM J
UNIV OF MASSACHUSETTS MED SCH WORCESTER
STIMULUS CONTROL IN MENTAL RETARDATION
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5P01HD003008-39 |
VOLKMAR, FRED R
YALE UNIVERSITY
AUSTISM AND RELATED DISORDERS: DEVELOPMENT AND OUTCOME
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5P01HD009402-30 |
SCHWARTZ, NANCY B
UNIVERSITY OF CHICAGO
BIOLOGICAL BASIS OF MENTAL RETARDATION
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5P01HD016596-23 |
ZIELKE, H. RONALD
UNIVERSITY OF MARYLAND BALTIMORE
METABOLIC & DEVELOPMENTAL ASPECTS OF MENTAL RETARDATION
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5P01HD024448-20 |
NAIDU, SAKKUBAI R
HUGO W. MOSER RES INST KENNEDY KRIEGER
PATHOGENESIS OF RETT SYNDROME
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5P01HD029587-14 |
LIPTON, STUART A
BURNHAM INSTITUTE FOR MEDICAL RESEARCH
CELLULAR/MOLECULAR PATHOPHYSIOLOGY OF MENTAL RETARDATION
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5P01HD032062-13 |
DIMAURO, SALVATORE
COLUMBIA UNIVERSITY HEALTH SCIENCES
MITOCHONDRIAL ENCEPHALOMYOPATHIES AND MENTAL RETARDATION
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5P01HD032652-12 |
WHITLEY, CHESTER B
UNIVERSITY OF MINNESOTA TWIN CITIES
GENE THERAPY FOR METABOLIC DISORDERS
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5P01HD033113-12 |
BELLUGI, URSULA
SALK INSTITUTE FOR BIOLOGICAL STUDIES
WILLIAMS SYNDROME: BRIDGING COGNITION, BRAIN AND GENES
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5P01HD035897-21 |
SILVERMAN, WAYNE P
HUGO W. MOSER RES INST KENNEDY KRIEGER
CHANGES IN FUNCTIONING AMONG MENTALLY RETARDED ADULTS
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5P01HD035946-08 |
FLETCHER, JACK M
UNIVERSITY OF HOUSTON
SPINA BIFIDA: COGNITIVE AND NEUROBIOLOGICAL VARIABILITY
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5P01HD039833-05 |
PEREZ-POLO, J. REGINO
UNIVERSITY OF TEXAS MEDICAL BR GALVESTON
BRAIN CELL DEATH MECHANISMS AFTER PERINATAL ISCHEMIA
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5P01HD046666-04 |
DUBE, WILLIAM V
UNIV OF MASSACHUSETTS MED SCH WORCESTER
BEHAVIORAL ALLOCATION AND CHOICE PROCESSES IN MR
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5P01HD047281-03 |
GARDNER, JUDITH M
INSTITUTE FOR BASIC RES IN DEV DISABIL
AROUSAL AND ATTENTION REGULATION IN HIGH RISK CHILDREN
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P30 - Center Core Grants |
Project Number |
Description |
3P30HD015052-27S1 |
LEVITT, PAT R
VANDERBILT UNIVERSITY
JOHN F. KENNEDY CENTER FOR MENTAL RETARDATION
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3P30HD038985-05S1 |
PERCY, ALAN K
UNIVERSITY OF ALABAMA AT BIRMINGHAM
UAB MENTAL RETARDATION RESEARCH CENTER (MRRC)
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5P30HD002274-40 |
GURALNICK, M J
UNIVERSITY OF WASHINGTON
RESEARCH IN MENTAL RETARDATION AND CHILD DEVELOPMENT
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5P30HD002528-41 |
WARREN, STEVEN F
UNIVERSITY OF KANSAS LAWRENCE
KANSAS MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER (MRDDRC)
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5P30HD003110-40 |
PIVEN, JOSEPH
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
UNC MRDD RESEARCH CENTER
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5P30HD003352-41 |
SELTZER, MARSHA MAILICK
UNIVERSITY OF WISCONSIN MADISON
WISCONSIN CENTER ON MENTAL RETARDATION: CORE SUPPORT
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5P30HD004024-39 |
PFENNINGER, KARL H
UNIVERSITY OF COLORADO DENVER
MRDD RESEARCH CENTER
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5P30HD004147-35 |
MCILVANE, WILLIAM J
UNIV OF MASSACHUSETTS MED SCH WORCESTER
INTERDISCIPLINARY RESEARCH IN MENTAL RETARDATION
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5P30HD004612-37 |
DE VELLIS, JEAN
UNIVERSITY OF CALIFORNIA LOS ANGELES
MENTAL RETARDATION RESEARCH CENTER
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5P30HD015052-27 |
LEVITT, PAT R
VANDERBILT UNIVERSITY
JOHN F. KENNEDY CENTER FOR MENTAL RETARDATION
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5P30HD018655-26 |
GREENBERG, MICHAEL E
CHILDREN'S HOSPITAL BOSTON
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH CENTERS 2006
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5P30HD024061-20 |
CATALDO, MICHAEL F
HUGO W. MOSER RES INST KENNEDY KRIEGER
MRDD RESEARCH CENTER
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5P30HD024064-19 |
ZOGHBI, HUDA Y
BAYLOR COLLEGE OF MEDICINE
BAYLOR MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIE*
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5P30HD026979-18 |
YUDKOFF, MARC
CHILDREN'S HOSPITAL OF PHILADELPHIA
MENTAL RETARDATION AND DEVELOPMENT DISABILITIES RESEARCH
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5P30HD040677-07 |
GALLO, VITTORIO
CHILDREN'S RESEARCH INSTITUTE
MRDDRC AT CHILDREN'S NATIONAL MEDICAL CENTER
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5P30HD054275-02 |
SCHWARTZ, NANCY B
UNIVERSITY OF CHICAGO
J.P.KENNEDY MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES CENTER
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P50 - Specialized Center |
Project Number |
Description |
1P50HD055748-01 |
MINSHEW, NANCY J
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
BIOLOGICAL AND INFORMATION PROCESSING MECHANISMS UNDERLYING AUTISM
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1P50HD055751-01 |
COOK, EDWIN H
UNIVERSITY OF ILLINOIS AT CHICAGO
ACE: TRANSLATIONAL STUDIES OF INSISTENCE ON SAMENESS IN AUTISM
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1P50HD055782-01 |
KING, BRYAN H
UNIVERSITY OF WASHINGTON
UW AUTISM CENTER OF EXCELLENCE
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1P50HD055784-01 |
SIGMAN, MARIAN D
UNIVERSITY OF CALIFORNIA LOS ANGELES
DETERMINANTS OF SOCIAL, COMMUNICATIVE, AND OTHER CORE DEFICITS IN AUTISM
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1P50MH081755-01 |
COURCHESNE, ERIC
UNIVERSITY OF CALIFORNIA SAN DIEGO
BIOMARKERS OF AUTISM AT 12 MONTHS: FROM BRAIN OVERGROWTH TO GENES
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5P50HG003374-04 |
BURKE, WYLIE G
UNIVERSITY OF WASHINGTON
GENOMIC HEALTH CARE AND THE MEDICALLY UNDERSERVED
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R01 - Research Project |
Project Number |
Description |
1R01HD050557-01A2 |
LOBATO, DEBRA J
RHODE ISLAND HOSPITAL (PROVIDENCE, RI)
LATINO SIBLINGS AND MR/DD
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1R01HD052074-01A2 |
FATEMI, S. HOSSEIN
UNIVERSITY OF MINNESOTA TWIN CITIES
GABAERGIC DYSFUNCTION IN AUTISM
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1R01HD052664-01A1 |
OLNEY, JOHN W
WASHINGTON UNIVERSITY
ANESTHESIA-INDUCED DEVELOPMENTAL NEUROAPOPTOSIS IN NON-HUMAN PRIMATES
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1R01HD052680-01A1 |
WANG, TAO
JOHNS HOPKINS UNIVERSITY
X CHROMOSOME CDNA MICROARRAY SCREENING AND FUNCTIONAL STUDY OF NOVEL XLMR GENES
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1R01HD052682-01A1 |
FULLER, DAVID
UNIVERSITY OF FLORIDA
CONTROL OF BREATHING & GLYCOGEN STORAGE DISEASE
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1R01HD052820-01A2 |
JUUL, SANDRA E
UNIVERSITY OF WASHINGTON
OPTIMIZING NEUROPROTECTION FOLLOWING PERINATAL ASPHYXIA
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1R01HD053053-01A1 |
HAMBIDGE, K MICHAEL
UNIVERSITY OF COLORADO DENVER
ZN & MATERNAL-INFANT BRAIN FUNCTION IN S. ETHIOPIA: RANDOMIZED CONTROLLED TRIALS
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1R01HD053594-01A1 |
TAIT, ALAN R
UNIVERSITY OF MICHIGAN AT ANN ARBOR
STRATEGIES TO OPTIMIZE COMMUNICATION OF INFORMED CONSENT FOR PEDIATRIC RESEARCH
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1R01HD054413-01A1 |
LORSON, CHRISTIAN L.
UNIVERSITY OF MISSOURI-COLUMBIA
STIMULATING SMN2 EXON 7 INCLUSION WITH SHORT RNAS
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1R01HD054453-01 |
PORTERA-CAILLIAU, CARLOS
UNIVERSITY OF CALIFORNIA LOS ANGELES
IMAGING THE ORIGIN OF DENDRITIC SPINE ABNORMALITIES IN FRAGILE X MICE
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1R01HD054599-01 |
SWOBODA, KATHRYN J
UNIVERSITY OF UTAH
THERAPEUTIC OPPORTUNITIES IN SPINAL MUSCULAR ATROPHY
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1R01HD054744-01 |
LAI, KENT
UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
INNOVATIVE THERAPIES AND CLINICAL STUDIES FOR CLASSIC GALACTOSEMIA
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1R01HD054905-01 |
BROWN, STEPHEN A
UNIVERSITY OF VERMONT & ST AGRIC COLLEGE
PRENATAL DIAGNOSIS THROUGH SELECTIVE DNA AMPLIFICATION
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1R01HD054979-01A2 |
IVERSON, JANA M
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
EARLY IDENTIFICATION OF AUTISM: A PROSPECTIVE STUDY
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1R01HD055461-01 |
SANDS, MARK S
WASHINGTON UNIVERSITY
NOVEL THERAPIES FOR GLOBOID-CELL LEUKODYSTROPHY
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1R01HD055741-01 |
PIVEN, JOSEPH
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
A LONGITUDINAL MRI STUDY OF INFANTS AT RISK FOR AUTISM
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1R01HD055835-01 |
BASSELL, GARY J
EMORY UNIVERSITY
SPINAL MUSCULAR ATROPHY: SMNS ROLE IN MRNA LOCALIZATION AND LOCAL TRANSLATION
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1R01HD056031-01 |
RIVERA, SUSAN M
UNIVERSITY OF CALIFORNIA DAVIS
VISUAL PROCESSING AND LATER COGNITIVE EFFECTS IN INFANTS WITH FRAGILE X SYNDROME
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1R01HD056369-01 |
SCACHERI, PETER C
CASE WESTERN RESERVE UNIVERSITY
GENOMIC STUDIES OF CHD7 IN CHARGE SYNDROME
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1R01HD056452-01 |
CARREL, LAURA
PENNSYLVANIA STATE UNIV HERSHEY MED CTR
COMPARATIVE GENOMIC AND FUNCTIONAL ANALYSIS OF INACTIVE X EXPRESSION
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1R01MH081757-01 |
ROGERS, SALLY J
UNIVERSITY OF CALIFORNIA DAVIS
A MULTI-SITE RANDOMIZED STUDY OF INTENSIVE TREATMENT FOR TODDLERS WITH AUTISM
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2R01AG016381-06A2 |
DALTON, ARTHUR J
INSTITUTE FOR BASIC RES IN DEV DISABIL
VITAMIN E TRIAL IN PERSONS WITH DOWN SYNDROME
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2R01HD020521-21A1 |
WARREN, STEPHEN T
EMORY UNIVERSITY
MOLECULAR CLONING OF THE FRAGILE X SITE
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2R01HD023333-15A2 |
WIGHTMAN, FREDERIC L
UNIVERSITY OF LOUISVILLE
LISTENING SKILLS IN CHILDREN WITH AND WITHOUT COCHLEAR IMPLANTS
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2R01HD026456-16A2 |
BORKOWSKI, JOHN G
UNIVERSITY OF NOTRE DAME
PRECURSORS OF RETARDATION IN CHILDREN WITH TEEN MOTHERS
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2R01HD028607-16A1 |
SCHUCHMAN, EDWARD H
MOUNT SINAI SCHOOL OF MEDICINE OF NYU
ACID SPHINGOMYELINASE & NIEMANN-PICK DISEASE
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2R01HD036071-09A1 |
HAGERMAN, RANDI J
UNIVERSITY OF CALIFORNIA DAVIS
GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE X FAMILIES
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2R01HD037872-06A1 |
RESNICK, JAMES L
UNIVERSITY OF FLORIDA
GENETIC COMPLEMENTATION OF A MOUSE MODEL FOR PWS
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2R01HD038819-06A2 |
ROBERTS, JOANNE E
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
PRAGMATIC SKILLS OF YOUNG MALES AND FEMALES WITH FRAGILE X SYNDROME
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2R01HD039276-06 |
RAYMOND, GERALD V
HUGO W. MOSER RES INST KENNEDY KRIEGER
A PHASE III TRIAL OF LORENZO'S OIL IN ADRENOMYELONEUROPATHY
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2R01HD040182-07A2 |
VALLEE, RICHARD
COLUMBIA UNIVERSITY HEALTH SCIENCES
MECHANISM OF ACTION OF THE LISSENCEPHALY GENE LIS-1
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2R01HD040661-05A1 |
HAGERMAN, PAUL J
UNIVERSITY OF CALIFORNIA DAVIS
EXPRESSION OF THE FRAGILE X GENE
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2R01HD041590-06A1 |
SVAREN, JOHN P
UNIVERSITY OF WISCONSIN MADISON
GENETIC CONTROL OF MYELINATION BY EGR2 AND NAB PROTEINS
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3R01HD017332-18S1 |
SCHWARTZ, NANCY B
UNIVERSITY OF CHICAGO
PROTEOGLYCAN SYNTHESIS IN MUTANT MOUSE SYSTEMS
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3R01HD029402-15S1 |
WACKER, DAVID P
UNIVERSITY OF IOWA
MAINTENANCE EFFECTS OF FUNCTIONAL COMMUNICATION TRAINING
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3R01HD038384-06A1S1 |
REEVES, ROGER H
JOHNS HOPKINS UNIVERSITY
GENOMIC APPROACHES TO ANEUPLOIDY
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3R01HD040661-05A1S1 |
HAGERMAN, PAUL J
UNIVERSITY OF CALIFORNIA DAVIS
EXPRESSION OF THE FRAGILE X GENE
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3R01HD054453-01S1 |
PORTERA-CAILLIAU, CARLOS
UNIVERSITY OF CALIFORNIA LOS ANGELES
IMAGING THE ORIGIN OF DENDRITIC SPINE ABNORMALITIES IN FRAGILE X MICE
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5R01HD021341-23 |
HASSOLD, TERRY J
WASHINGTON STATE UNIVERSITY
A PROGRAM OF RESEARCH IN POPULATION CYTOGENETICS
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5R01HD024356-17 |
ABBEDUTO, LEONARD J
UNIVERSITY OF WISCONSIN MADISON
LANGUAGE DEVELOPMENT IN FRAGILE X SYNDROME
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5R01HD029402-15 |
WACKER, DAVID P
UNIVERSITY OF IOWA
MAINTENANCE EFFECTS OF FUNCTIONAL COMMUNICATION TRAINING
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5R01HD029909-12 |
SHERMAN, STEPHANIE L.
EMORY UNIVERSITY
GENETICS EPIDEMIOLOGY OF THE FMR1 GENE
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5R01HD033470-14 |
TAGER-FLUSBERG, HELEN B.
BOSTON UNIVERSITY MEDICAL CAMPUS
SOCIAL COGNITION IN WILLIAMS SYNDROME
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5R01HD033531-12 |
DAVIDSON, BEVERLY L
UNIVERSITY OF IOWA
AAV CORRECTION OF CNS DEFICITS IN AN MPS MODEL OF LSD
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5R01HD035496-10 |
CAI, ZHENGWEI
UNIVERSITY OF MISSISSIPPI MEDICAL CENTER
PERINATAL HYPOXIA-ISCHEMIA, GLUTAMATE RECEPTORS, AND NOS
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5R01HD035617-08 |
NELSON, DAVID LOREN
BAYLOR COLLEGE OF MEDICINE
MOLECULAR ANALYSIS OF XQ28-LINKED INCONTINENTIA PIGMENTI
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5R01HD035684-11 |
DYKENS, ELISABETH M
VANDERBILT UNIVERSITY
PRADER-WILLI SYNDROME: CORRELATES OF COMPULSIVITY
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5R01HD037283-09 |
BEAUDET, ARTHUR L.
BAYLOR COLLEGE OF MEDICINE
GENETICS OF PRADER-WILLI/ANGELMAN SYNDROME
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5R01HD037874-08 |
SCHANEN, N. CAROLYN
ALFRED I. DU PONT HOSP FOR CHILDREN
INVESTIGATION OF MECP2 FUNCTION IN RETT SYNDROME
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5R01HD038038-08 |
NELSON, DAVID LOREN
BAYLOR COLLEGE OF MEDICINE
FRAGILE X RELATED GENES MENTAL RETARDIATION/DEVELOPMENT
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5R01HD038384-07 |
REEVES, ROGER H
JOHNS HOPKINS UNIVERSITY
GENOMIC APPROACHES TO ANEUPLOIDY
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5R01HD038466-07 |
BUSCIGLIO, JORGE A
UNIVERSITY OF CALIFORNIA IRVINE
MITOCHONDRIAL DYSFUNCTION IN DOWN'S SYNDROME
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5R01HD038979-08 |
SHERMAN, STEPHANIE L.
EMORY UNIVERSITY
TRISOMY 21: RISK FACTORS FOR CHROMOSOME NON-DISJUNCTION
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5R01HD039110-07 |
BLACK, STEPHEN M
MEDICAL COLLEGE OF GEORGIA (MCG)
ROLE OF NEURONAL NOS IN NEUROTOXICITY
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5R01HD039331-07 |
SRIVASTAVA, ANAND K
GREENWOOD GENETIC CENTER
CLONING GENES THAT CAUSE MENTAL RETARDATION
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5R01HD039708-06 |
PROHASKA, JOSEPH R
UNIVERSITY OF MINNESOTA DULUTH
NUTRITIONAL COPPER STATUS AND THE NERVOUS SYSTEM
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5R01HD040647-06 |
DARNELL, JENNIFER C
ROCKEFELLER UNIVERSITY
IDENTIFICATION AND VALIDATION OF FMRP TARGET RNAS
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5R01HD041671-05 |
LUCYSHYN, JOSEPH M
UNIVERSITY OF BRITISH COLUMBIA
TRANSFORMING COERCIVE PROCESSES IN FAMILY ROUTINES
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5R01HD042053-04 |
BIANCHI, DIANA W
TUFTS MEDICAL CENTER
FETO-MATERNAL DNA/RNA TRAFFICKING:BIOLOGY & APPLICATIONS
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5R01HD042182-05 |
LAMANTIA, ANTHONY S
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
REGULATION OF 22Q11 GENES IN EMBRYONIC & ADULT FOREBRAIN
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5R01HD042541-05 |
CONSTANTINO, JOHN N
WASHINGTON UNIVERSITY
AUTISTIC TRAITS: LIFE COURSE AND GENETIC STRUCTURE
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5R01HD042601-05 |
KATSANIS, NICHOLAS
JOHNS HOPKINS UNIVERSITY
MOLECULAR GENETICS OF BARDET-BIEDL SYNDROME
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5R01HD042807-04 |
MCILVANE, WILLIAM J
UNIV OF MASSACHUSETTS MED SCH WORCESTER
BEHAVIORAL STUDIES OF MENTAL RETARDATION AND DEPRESSION
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5R01HD043100-05 |
LEONARD, HELEN M
UNIVERSITY OF WESTERN AUSTRALIA
RETT SYNDROME: DETERMINANTS OF OUTCOME AND BURDEN
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5R01HD043120-05 |
ZHANG, JOHN H.
LOMA LINDA UNIVERSITY
OXYGEN THERAPY IN NEONATAL HYPOXIA-ISCHEMIA
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5R01HD043292-05 |
STONE, WENDY L.
VANDERBILT UNIVERSITY
EARLY SOCIAL ORIENTING IN SIBLINGS OF CHILDREN WITH ASD
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5R01HD043569-06 |
EICHLER, EVAN E.
UNIVERSITY OF WASHINGTON
SEGMENTAL ANEUSOMY BETWEEN BLOCKS OF DUPLICATED DNA
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5R01HD043960-04 |
WEGIEL, JERZY
INSTITUTE FOR BASIC RES IN DEV DISABIL
THE ROLE OF MNBK IN DS BRAIN DEVELOPMENT AND AGING
|
5R01HD044011-04 |
HU, HUAIYU
UPSTATE MEDICAL UNIVERSITY
MOLECULAR STUDIES OF BRAIN MALFORMATIONS
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5R01HD044111-04 |
CRAIG, WENDY Y
FOUNDATION FOR BLOOD RESEARCH
ARE IQS LOW IN OFFSPRING OF EUTHYROID WOMEN WITH LOW T4
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5R01HD044721-05 |
BRITT, WILLIAM J
UNIVERSITY OF ALABAMA AT BIRMINGHAM
CNS MALDEVELOPMENT AND PERINANTAL INFECTION
|
5R01HD044731-03 |
WILLIAMS, DEAN C
UNIVERSITY OF KANSAS LAWRENCE
LABORATORY MODELS OF MALADAPTIVE ESCAPE BEHAVIORS
|
5R01HD044752-05 |
GAO, FEN-BIAO
J. DAVID GLADSTONE INSTITUTES
CONTROL OF DENDRITIC DEVELOPMENT BY FMR1
|
5R01HD044763-04 |
SYMONS, FRANK J
UNIVERSITY OF MINNESOTA TWIN CITIES
BIOBEHAVIORAL ANALYSIS OF SELF-INJURY & PAIN
|
5R01HD044901-05 |
WHITE, DESIREE A
WASHINGTON UNIVERSITY
PREFRONTALLY-MEDIATED MEMORY IN PHENYLKETONURIA
|
5R01HD044935-05 |
ROBERTS, JOANNE E.
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
SPEECH OF YOUNG MALES WITH FRAGILE X SYNDROME
|
5R01HD045224-05 |
MACLEAN, KENNETH N
UNIVERSITY OF COLORADO DENVER
GENETICS, NEUROBIOLOGY, AND COGNITION IN DOWN SYNDROME
|
5R01HD045225-05 |
KORENBERG, JULIE R
CEDARS-SINAI MEDICAL CENTER
DOWN SYNDROME: BRIDGING GENES AND NEURAL PATHWAYS
|
5R01HD045561-04 |
WALKLEY, STEVEN U
YESHIVA UNIVERSITY
ENDOSOMAL-LYSOSOMAL FUNCTION IN NEURONAL STORAGE DISEASE
|
5R01HD045745-04 |
KAISER, ANN
VANDERBILT UNIVERSITY
SOCIAL COMMUNICATIVE EFFECTS OF LANGUAGE INTERVENTION
|
5R01HD045907-04 |
CODY, JANNINE D
UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT
IDENTIFICATION OF DOSAGE SENSITIVE GENES ON 18Q
|
5R01HD046034-04 |
ROY, ANANDA L
TUFTS UNIVERSITY BOSTON
MOLECULAR ANALYSIS OF WILLIAMS SYNDROME
|
5R01HD046368-11 |
BASSELL, GARY J
EMORY UNIVERSITY
BETA-ACTING MRNA LOCALIZATION IN NEURONS
|
5R01HD046500-02 |
FELDMAN, HEIDI M
STANFORD UNIVERSITY
FMRI AND DTI IN CHILDREN WITH PVH/PVL
|
5R01HD046565-03 |
SPELTZ, MATTHEW L
CHILDREN'S HOSPITAL AND REG MEDICAL CTR
NEURODEVELOPMENT AMONG INFANTS WITH DEFORMATIONAL PLAGIOCEPHALY
|
5R01HD046609-03 |
LANDRY, SUSAN
UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
LONGITUDINAL EFFECTS OF SPINA BIFIDA ON LEARNING
|
5R01HD046623-03 |
BISCHOFF, FARIDEH Z
BAYLOR COLLEGE OF MEDICINE
MOLECULAR NATURE OF FETAL DNA IN MATERNAL PLASMA
|
5R01HD046667-03 |
VASSILEV, PETER M
BRIGHAM AND WOMEN'S HOSPITAL
ELUCIDATION AND RESCUE OF PHENOTYPIC ALTERATIONS IN MLIV
|
5R01HD046722-03 |
KURTZ, PATRICIA F
HUGO W. MOSER RES INST KENNEDY KRIEGER
RISK FACTORS FOR PERSISTENT SELF INJURY
|
5R01HD046918-05 |
NEWELL, KARL M
PENNSYLVANIA STATE UNIVERSITY-UNIV PARK
NOVEL ANTIPSYCHOTICS AND STEREOTYPED MOVEMENT DISORDER
|
5R01HD046943-05 |
BEAR, MARK F
MASSACHUSETTS INSTITUTE OF TECHNOLOGY
MECHANISMS AND FUNCTIONS OF FMRP IN NEURONAL DEVELOPMENT
|
5R01HD047029-05 |
MACLEAN, KENNETH N
UNIVERSITY OF COLORADO DENVER
ATTENTIONAL DYSFUNCTION IN FRAGILE X SYNDROME
|
5R01HD047567-02 |
ULRICH, BEVERLY D
UNIVERSITY OF MICHIGAN AT ANN ARBOR
SENSORIMOTOR DEVELOPMENT: INFANTS BORN WITH SPINA BIFIDA
|
5R01HD047656-03 |
WENGER, GALEN R
UNIVERSITY OF ARKANSAS MED SCIS LTL ROCK
AGE AND COGNITION IN A MOUSE MODEL OF DOWN SYNDROME
|
5R01HD048489-03 |
AKBARIAN, SCHAHRAM
UNIV OF MASSACHUSETTS MED SCH WORCESTER
CHROMATIN ALTERATIONS IN RETT SYNDROME
|
5R01HD048528-02 |
SAUNDERS, KATHRYN J
UNIVERSITY OF KANSAS LAWRENCE
RECOMBINATIVE GENERALIZATION OF WITHIN-SYLLABLE UNITS IN MR
|
5R01HD048629-03 |
HOLMBECK, GRAYSON NEIL
LOYOLA UNIVERSITY OF CHICAGO
PSYCHOSOCIAL ADJUSTMENT IN ADOLESCENTS WITH SPINA BIFIDA
|
5R01HD048799-03 |
LASALLE, JANINE M
UNIVERSITY OF CALIFORNIA DAVIS
EPIGENETIC ETIOLOGIES OF AUTISM-SPECTRUM DISORDERS
|
5R01HD048947-02 |
SANDMAN, CURT A.
UNIVERSITY OF CALIFORNIA IRVINE
EMERGENCE OF SIB IN DEVELOPMENTALLY DELAYED INDIVIDUALS
|
5R01HD049686-02 |
KUPPERMANN, MIRIAM
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
EXPANDED PRENATAL TESTING OPTIONS AND INFORMED CHOICE
|
5R01HD049753-02 |
DELEON, ISER
HUGO W. MOSER RES INST KENNEDY KRIEGER
BEHAVIORAL ECONOMICS IN MRDD AND BEHAVIOR DISORDERS
|
5R01HD049792-02 |
FITCH, ROSLYN H
UNIVERSITY OF CONNECTICUT STORRS
EARLY H-1 BRAIN INJURY AND BEHAVIORAL OUTCOME IN RATS
|
5R01HD050832-02 |
HAYFLICK, SUSAN J
OREGON HEALTH & SCIENCE UNIVERSITY
THE MOLECULAR BASIS OF INFANTILE NEUROAXONAL DYSTROPHY
|
5R01HD051873-02 |
JAMES, SANDRA JILL
ARKANSAS CHILDREN'S HOSPITAL RES INST
METABOLIC BIOMARKERS OF AUTISM: PREDICTIVE POTENTIAL AND GENETIC SUSCEPTIBILITY
|
5R01HD052083-02 |
FALLON, JUSTIN R
BROWN UNIVERSITY
EXPERIENCE-DEPENDENT REGULATION OF THE FRAGILE X GENE
|
5R01HD053036-02 |
SHACKLETON, CEDRIC H
CHILDREN'S HOSPITAL & RES CTR AT OAKLAND
PATHOGENESIS/TREATMENT-INHERITED CHOLESTEROL DEFICIENCY
|
5R01MH076435-03 |
BRZUSTOWICZ, LINDA M
RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK
IDENTIFICATION AND FUNCTIONAL ASSESSMENT OF AUTISM SUSCEPTIBILITY GENES
|
5R01MH076624-03 |
MILLONIG, JAMES H
UNIV OF MED/DENT NJ-R W JOHNSON MED SCH
IDENTIFICATION AND FUNCTIONAL ASSESSMENT OF AUTISM SUSCEPTIBILITY GENES
|
|
R03 - Small Research Grants |
Project Number |
Description |
1R03HD052768-01A1 |
PASTORE, LISA M
UNIVERSITY OF VIRGINIA CHARLOTTESVILLE
FRAGILE X PREMUTATIONS AMONG WOMEN DIAGNOSED WITH DIMINISHED OVARIAN RESERVE
|
1R03HD054559-01 |
LUTZ, CAROL S
UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL
MECHANISMS OF MECP2 GENE EXPRESSION REGULATION
|
1R03HD054586-01A1 |
TURKSTRA, LYN S
UNIVERSITY OF WISCONSIN MADISON
SOCIAL COGNITION IN FEMALE ADOLESCENTS WITH FRAGILE X SYNDROME
|
1R03HD054925-01A1 |
DOBRUNZ, LYNN E
UNIVERSITY OF ALABAMA AT BIRMINGHAM
DEVELOPMENTAL CHANGES IN EXCITATORY SYNAPSES IN HIPPOCAMPUS
|
1R03HD055365-01 |
FARBER, NURI B
WASHINGTON UNIVERSITY
GLUCOCORTICOIDS AND APOPTOSIS OF CEREBELLAR NEURAL PROGENITOR CELLS
|
5R03HD047711-02 |
MCINTYRE, LAURA LEE
SYRACUSE UNIVERSITY
PARENT TRAINING, DUAL DIAGNOSIS, AND CHILDREN WITH MR
|
5R03HD049517-02 |
PRICE, WAYNE A
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
WHITE MATTER DAMAGE IN THE DEVELOPING MOUSE BRAIN
|
5R03HD049532-02 |
DAVIES, PATRICIA L
COLORADO STATE UNIVERSITY-FORT COLLINS
SENSORY GATING MEDIATED BY ATTENTION
|
5R03HD050372-02 |
KAGERER, FLORIAN A
UNIVERSITY OF MARYLAND COLLEGE PK CAMPUS
DEVELOPMENT OF SENSORIMOTOR INTEGRATION IN CHILDREN
|
5R03HD051656-02 |
LIU, YIJUN
UNIVERSITY OF FLORIDA
DIFFUSION TENSOR IMAGING IN AUTISM
|
5R03HD051816-03 |
CONROY, MAUREEN
VIRGINIA COMMONWEALTH UNIVERSITY
FUNCTIONS OF PROSOCIAL BEHAVIORS IN CHILDREN WITH AUTISM
|
5R03HD051829-02 |
LAUTERBORN, JULIE C
UNIVERSITY OF CALIFORNIA IRVINE
ALTERED HYPOTHALAMIC-PITUITARY-ADRENAL FUNCTION IN THE FRAGILE X MOUSE
|
5R03HD051943-02 |
PLESA-SKWERER, DANIELA
BOSTON UNIVERSITY MEDICAL CAMPUS
DEVELOPMENT OF SOCIAL-EMOTIONAL FUNCTIONING IN CHILDREN WITH WILLIAMS SYNDROME
|
5R03HD052770-02 |
PRICE, THOMAS M
DUKE UNIVERSITY
MODULATION OF MITOCHONDRIAL CALCIUM BY A NOVEL PROGESTERONE RECEPTOR
|
|
R13 - Conferences |
Project Number |
Description |
1R13HD055810-01 |
GARDINER, KATHELEEN
UNIVERSITY OF DENVER
THE BIOLOGY OF CHROMOSOME 21 GENES: TOWARDS GENE-PHENOTYPE CORRELATIONS IN DOWN
|
1R13HD055817-01 |
RAUEN, KATHERINE ANNA
UNIVERSITY OF CALIFORNIA SAN FRANCISCO
1ST COSTELLO SYNDROME SYMPOSIUM
|
1R13MH072277-01A2 |
CHASE, MICHAEL H
WEBSCIENCES INTERNATIONAL
TRAINING WORKSHOPS IN BASIC SLEEP RESEARCH
|
1R13MH079632-01 |
SPRUSTON, NELSON P.
GORDON RESEARCH CONFERENCES
2006 DENDRITES: MOLECULES, STRUCTURE AND FUNCTION (GORDON RESEARCH CONFERENCE)
|
1R13NS057996-01 |
WILSON, ROBERT B
FRIEDREICH'S ATAXIA RESEARCH ALLIANCE
3RD INTERNATIONAL FRIEDREICH'S ATAXIA SCIENTIFIC CONFERENCE
|
1R13NS059295-01 |
PEARCE, DAVID A
UNIVERSITY OF ROCHESTER
11TH INTERNATIONAL CONGRESS ON NEURONAL CEROID LIPOFUSCINOSIS
|
1R13NS060363-01 |
GIBSON, K MICHAEL
CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS
MEDICAL MANAGEMENT OF PEDIATRIC NEUROTRANSMITTER DISORDERS- A MULTIDISCIPLINARY
|
2R13MH070772-04 |
ROGERS, SALLY J
UNIVERSITY OF CALIFORNIA DAVIS
INTERNATIONAL MEETING FOR AUTISM RESEARCH (IMFAR)
|
5R13AA016249-02 |
CRABBE, JOHN C.
OREGON HEALTH & SCIENCE UNIVERSITY
IBANGS ANNUAL MEETING SUPPORT
|
5R13HD038335-09 |
SELTZER, MARSHA MAILICK
UNIVERSITY OF WISCONSIN MADISON
THE GATLINBURG CONFERENCE ON RESEARCH IN ID/DD
|
5R13HD044529-05 |
WATSON, MICHAEL
AMERICAN COLLEGE OF MEDICAL GENETICS
CONFERENCE--GENETIC DISEASE RESEARCH NEED /OPPORTUNITY
|
5R13HD048170-04 |
GOLDEN, JEFFREY A
CHILDREN'S HOSPITAL OF PHILADELPHIA
DAVID W SMITH WORKSHOP ON MALFORMATIONS/MORPHOGENESIS
|
5R13HD054328-02 |
VOCKLEY, GERARD
CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS
SOCIETY FOR INHERITED METABOLIC DISORDERS ANNUAL MEETING
|
5R13MH062008-08 |
FOX, PETER T
UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT
INTERNAT'L CONF. ON FUNCTIONAL MAPPING OF THE HUMANBRAIN
|
5R13MH063153-07 |
GREENOUGH, WILLIAM T
UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN
FRAGILE X SYNDROME: BANBURY CONFERENCES
|
7R13HD055810-02 |
GARDINER, KATHELEEN
UNIVERSITY OF COLORADO DENVER
THE BIOLOGY OF CHROMOSOME 21 GENES: TOWARDS GENE-PHENOTYPE CORRELATIONS IN DOWN
|
|
R15 - Academic Research Enhancement Awards (AREA) |
Project Number |
Description |
3R15HD041444-02S1 |
DAVIS, TAMARA L
BRYN MAWR COLLEGE
DEVELOPMENTAL ANALYSIS OF IMPRINTING MARK MODIFICATIONS
|
|
R21 - Exploratory/Developmental Grants |
Project Number |
Description |
1R21AA016747-01 |
VYTHILINGUM, BAVANISHA
STELLENBOSCH UNIVERSITY TYGERBERG CAMPUS
FETAL ALCOHOL SPECTRUM DISORDERS IN THE PHASE 1 COHORT OF THE SAFE PASSAGE STUDY
|
1R21HD050538-01A2 |
LECHNER, MARK S
DREXEL UNIVERSITY
A ROLE FOR THE CDLS GENE NIPBL IN HP1 GENE SILENCING
|
1R21HD051805-01A1 |
VAN DEN VEYVER, IGNATIA B
BAYLOR COLLEGE OF MEDICINE
NEW STRATEGIES TO IDENTIFY THE GENE MUTATED IN AICARDI SYNDROME.
|
1R21HD052592-01A1 |
WARSCHAUSKY, SETH A
UNIVERSITY OF MICHIGAN AT ANN ARBOR
ADAPTED NEUROPSYCHOLOGICAL ASSESSMENT IN CHILDREN WITH CEREBRAL PALSY
|
1R21HD052947-01A1 |
MCILVANE, WILLIAM J
UNIV OF MASSACHUSETTS MED SCH WORCESTER
OPTIMIZING DISCRETE-TRIAL PROCEDURES FOR ASD CHILDREN
|
1R21HD053057-01A1 |
NAIR, MKC
INTERNTL CLINICAL EPIDEMIOLOGY NETWORK
NEURO-DEVELOPMENTAL DISABILITIES AMONG CHILDREN IN INDIA: AN INCLEN STUDY
|
1R21HD053556-01A1 |
DELEON, ISER
HUGO W. MOSER RES INST KENNEDY KRIEGER
TRANSLATIONAL RESEARCH ON NCR INTERVENTIONS FOR BEHAVIOR DISORDERS
|
1R21HD055189-01 |
HORNER-JOHNSON, WILLI E
OREGON HEALTH & SCIENCE UNIVERSITY
EFFICACY OF A HEALTH INTERVENTION FOR PEOPLE WITH INTELLECTUAL DISABILITIES
|
1R21HD055414-01 |
RONCA, APRIL ELIZABETH
WAKE FOREST UNIVERSITY HEALTH SCIENCES
METHODS FOR IN VIVO BEHAVIORAL OBSERVATION OF THE MOUSE FETUS
|
1R21HD056130-01 |
ROSSOLL, WILFRIED
EMORY UNIVERSITY
SPINAL MUSCULAR ATROPHY: A NOVEL ROLE OF SMN IN AXONAL RIBONUCLEOPROTEIN COMPLEXE
|
1R21HD056195-01 |
ANDREADIS, ATHENA
UNIV OF MASSACHUSETTS MED SCH WORCESTER
TAU MISSPLICING CAUSED BY RNA PROCESSING PROTEINS LOCATED ON CHROMOSOME 21
|
1R21HD058311-01A1 |
DIDONATO, CHRISTINE
CHILDREN'S MEMORIAL HOSPITAL (CHICAGO)
CREATION OF HYPOMORPHIC PANEL OF SMN MICE THAT MIMIC HUMAN SMN2 SPLICING
|
5R21HD048881-02 |
JINNAH, HYDER A
JOHNS HOPKINS UNIVERSITY
LESCH-NYHAN DISEASE: DISSECTING THE FUNCTIONS OF HGPRT
|
5R21HD048989-02 |
BANDINI, LINDA G.
UNIV OF MASSACHUSETTS MED SCH WORCESTER
DIET, ACTIVITY AND OBESITY IN CHILDREN WITH AUTISM
|
5R21HD050817-02 |
YAMAGUCHI, YU
BURNHAM INSTITUTE FOR MEDICAL RESEARCH
NEURONAL HEPARAN SULFATE DEFICIENCY AND AUTISM
|
5R21HD052126-02 |
OZERDEM, UGUR
LA JOLLA INST FOR MOLECULAR MEDICINE
TARGETING VASCULOGENESIS AND INTERSTITIAL HYPERTENSION IN NEUROFIBROMATOSIS TYPE1
|
5R21HD053037-03 |
PINKERT, CARL A
AUBURN UNIVERSITY AT AUBURN
MOUSE MODELING OF LEIGH DISEASE AND COMPLEX I ASSEMBLY
|
7R21HD052126-03 |
OZERDEM, UGUR
LA JOLLA BIOENGINEERING INSTITUTE
TARGETING VASCULOGENESIS AND INTERSTITIAL HYPERTENSION IN NEUROFIBROMATOSIS TYPE1
|
|
R24 - Resource-Related Research Projects |
Project Number |
Description |
5R24HD047142-05 |
PULLIUM, JENNIFER K.
MOUNT SINAI SCHOOL OF MEDICINE OF NYU
HOMOLOGOUS PREPUBERTAL CANINE GONAD TRANSPLANTATION
|
|
R37 - Method to Extend Research in Time (MERIT) Award |
Project Number |
Description |
5R37HD029957-15 |
MERVIS, CAROLYN B.
UNIVERSITY OF LOUISVILLE
EARLY DEVELOPMENT WITH WILLIAMS OR DOWN SYNDROME
|
|
R42 - * Small Business Technology Transfer (STTR) Grants - Phase II |
Project Number |
Description |
2R42HD049230-02 |
HOSONO, SEIYU
JS GENETICS, LLC
NEWBORN SCREENING FOR SEX CHROMOSOME DISORDERS
|
2R42HD055021-02A2 |
FLEMING, RICHARD K
PRAXIS, INC.
EDUCATING PARENTS: BEHAVIORAL INTERVENTION IN AUTISM
|
4R42HD054077-02 |
DUBE, WILLIAM V
PRAXIS, INC.
PRAXIS BEHAVIORAL OBSERVATION SOFTWARE
|
5R42HD043640-03 |
SERNA, RICHARD W
PRAXIS, INC.
BEHAVIORAL TECHNOLOGY FOR TEACHING SYMBOLIC RELATIONS
|
5R42HD048137-03 |
JACOBSON, ALLAN S
PTC THERAPEUTICS, INC.
MECHANISM OF NONSENSE MUTATION SUPPRESSION THERAPY
|
|
R43 - Small Business Innovation Research Grants (SBIR) - Phase I |
Project Number |
Description |
1R43HD054958-01A1 |
RABINOWITZ, MATTHEW
GENE SECURITY NETWORK
PHASE I APPLICATION: CLEANING OF SINGLE CELL DNA MEASUREMENTS IN-SILICO
|
1R43HD054992-01 |
PARKER, B EUGENE
BARRON ASSOCIATES, INC.
EARLY IDENTIFICATION OF DEVELOPMENTAL DISORDERS IN INFANTS
|
1R43HD056578-01 |
STRICKLAND, DOROTHY CAY
VIRTUAL REALITY AIDS, INC.
SOCIAL SKILLS INTERVENTION FOR ADOLESCENTS WITH HIGH FUNCTIONING AUTISM/ASPERGER
|
1R43HD057713-01 |
PAMULA, VAMSEE K
ADVANCED LIQUID LOGIC
LAB-ON-A-CHIP FOR MULTIPLEXED NEWBORN SCREENING OF LYSOSOMAL STORAGE DISORDERS
|
|
R44 - Small Business Innovation Research Grants (SBIR) - Phase II |
Project Number |
Description |
2R44HD037789-04 |
CRAINE, BRIAN L
WESTERN RESEARCH COMPANY, INC.
QUALITY CONTROL TOOL FOR NEWBORN SCREENING BLOOD SAMPLES
|
2R44HD048138-02A2 |
CARR, KENNETH L
MERIDIAN MEDICAL SYSTEMS, LLC
BRAIN TEMPERATURE MONITORING IN NEONATES (PHASE II)
|
2R44HD051132-02A2 |
SCHROEDER, JAMES E
APPLIED HUMAN FACTORS, INC.
CYBERCOACH: KEEPING PEOPLE WITH MEMORY DISABILITIES EMPLOYED AND INDEPENDENT
|
2R44HD052303-02 |
ZHANG, YUN
ARMAGEN TECHNOLOGIES, INC.
RECOMBINANT ENZYME FUSION PROTEIN FOR LYSOSOMAL STORAGE DISORDERS
|
2R44HD052340-02 |
OBERLEITNER, RONALD
EMERGE MEDICAL TECHNOLOGIES, LLC
NOVEL DATA CAPTURE AND ASSESSMENT TECHNOLOGY FOR BEHAVIOR DISORDERS
|
2R44HD054460-02A1 |
VAN BUSKIRK, ROBERT G.
CELL PRESERVATION SERVICES, INC.
IMPROVED PRESERVATION OF SUSPENDED CELLS
|
4R44HD053215-02 |
DOBROWOLSKI, STEVEN F
IDAHO TECHNOLOGY
NEWBORN SCREENING FOR PKU AND BH4 RESPONSIVENESS
|
4R44HD054028-02 |
LANCASTER, PAULA E
EDGE ENTERPRISES, INC.
CD VOCABULARY INSTRUCTION FOR STUDENTS WITH DISABILITIES
|
5R44HD047050-03 |
JONES, LAURA M
IRIS MEDIA, INC.
PARENT EDUCATION FOR PARENTS WITH COGNITIVE LIMITATIONS
|
5R44HD048144-03 |
KLEDARAS, JOANNE B
PRAXIS, INC.
MONETARY EQUIVALENCE: RELATIONAL INSTRUCTIONAL TRACK
|
|
T15 - Continuing Education Training Program |
Project Number |
Description |
5T15HD007306-22 |
NAGGERT, JUERGEN K.
JACKSON LABORATORY
COURSE IN MEDICAL AND EXPERIMENTAL MAMMALIAN GENETICS
|
|
T32 - Institutional National Research Service Award |
Project Number |
Description |
5T32HD007032-29 |
DE VELLIS, JEAN
UNIVERSITY OF CALIFORNIA LOS ANGELES
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES
|
5T32HD007105-30 |
DESNICK, ROBERT J
MOUNT SINAI SCHOOL OF MEDICINE OF NYU
MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES
|
5T32HD007149-30 |
LIFTON, RICHARD P
YALE UNIVERSITY
GENETICS AND GENOMICS OF HUMAN DISEASE
|
5T32HD007184-27 |
BORKOWSKI, JOHN G
UNIVERSITY OF NOTRE DAME
RESEARCH TRAINING IN MENTAL RETARDATION
|
5T32HD007226-29 |
WALDEN, TEDRA A
VANDERBILT UNIVERSITY
BEHAVIORAL RESEARCH TRAINING IN DEVELOPMENTAL DISABILITY
|
5T32HD007473-13 |
QUITTNER, ALEXANDRA L
UNIVERSITY OF MIAMI CORAL GABLES
TRAINING-MENTAL RETARDATION/DEVELOPMENTAL DISABILITIES
|
5T32HD007489-13 |
ABBEDUTO, LEONARD J
UNIVERSITY OF WISCONSIN MADISON
POSTDOCTORAL TRAINING IN MENTAL RETARDATION RESEARCH
|
5T32HD040127-07 |
PIVEN, JOSEPH
UNIVERSITY OF NORTH CAROLINA CHAPEL HILL
POSTDOCTORAL RESEARCH IN NEURODEVELOPMENTAL DISORDERS
|
5T32HD046388-02 |
GALLO, VITTORIO
CHILDREN'S RESEARCH INSTITUTE
POSTDOCTORAL TRAINING IN DEVELOPMENTAL DISABILITIES RESEARCH
|
|
U01 - Research Project (Cooperative Agreements) |
Project Number |
Description |
1U01MH078270-01A1 |
CARPENTER, RANDALL L
SEASIDE THERAPEUTICS, LLC
DEVELOPMENT OF MGLUR5 ANTAGONISTS TO TREAT FRAGILE X SYNDROME AND AUTISM
|
5U01HD045023-06 |
DUKES, KIMBERLY A.
DM-STAT, INC.
CPEA DATA COORDINATING CENTER
|
|
U13 - Conference (Cooperative Agreement) |
Project Number |
Description |
1U13NS059269-01 |
MOLDIN, STEVEN OWEN
UNIVERSITY OF SOUTHERN CALIFORNIA
SHARED NEUROBIOLOGY OF AUTISM AND RELATED DISORDERS
|
5U13HD054282-02 |
HATZ, JODY L
NATIONAL CONFERENCE/STATE LEGISLATURES
IMPROVING CHILD HEALTH: THE ROLE OF POLICYMAKERS IN PREVENTION AND TREATMENT OF B
|
|
U19 - Research Program (Cooperative Agreement) |
Project Number |
Description |
5U19HD035466-10 |
RODIER, PATRICIA M
UNIVERSITY OF ROCHESTER
GENOTYPE AND PHENOTYPE OF BRAINSTEM INJURY IN AUTISM
|
|
U54 - Specialized Center (Cooperative Agreements) |
Project Number |
Description |
3U54HD053177-01A1S2 |
HOFFMAN, ERIC P
CHILDREN'S RESEARCH INSTITUTE
WELLSTONE MUSCULAR DYSTROPHY CENTER: CHILDREN'S NAT'L MED CTR
|
3U54HD053177-02S1 |
HOFFMAN, ERIC P
CHILDREN'S RESEARCH INSTITUTE
WELLSTONE MUSCULAR DYSTROPHY CENTER: CHILDREN'S NAT'L MED CTR
|
5U54HD047175-05 |
CHAMBERLAIN, JEFFREY S
UNIVERSITY OF WASHINGTON
MUSCULAR DYSTROPHY COOPERATIVE RESEARCH CENTER
|
5U54HD053177-03 |
HOFFMAN, ERIC P
CHILDREN'S RESEARCH INSTITUTE
WELLSTONE MUSCULAR DYSTROPHY CENTER: CHILDREN'S NAT'L MED CTR
|
5U54MH066397-05 |
RODIER, PATRICIA M
UNIVERSITY OF ROCHESTER
GENOTYPE AND PHENOTYPE OF RESPONSE TO TREATMENTS OF AUTISM
|
5U54MH066398-05 |
TAGER-FLUSBERG, HELEN B.
BOSTON UNIVERSITY MEDICAL CAMPUS
SOCIAL AND AFFECTIVE PROCESSES IN AUTISM
|
5U54MH066399-05 |
AYLWARD, ELIZABETH H
UNIVERSITY OF WASHINGTON
UW AUTISM RESEARCH CENTER OF EXCELLENCE
|
5U54MH066417-05 |
LANDA, REBECCA
HUGO W. MOSER RES INST KENNEDY KRIEGER
NEUROBIOLOGIC ORIGINS AND INNOVATIVE TREATMENT OF AUTISM
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5U54MH066673-05 |
HOLLANDER, ERIC
MOUNT SINAI SCHOOL OF MEDICINE OF NYU
GREATER NEW YORK AUTISM RESEARCH CENTER OF EXCELLENCE
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5U54MH068172-05 |
SIGMAN, MARIAN D
UNIVERSITY OF CALIFORNIA LOS ANGELES
SOCIAL & LANGUAGE DEFICITS IN AUTISM-BIOLOGY & TREAMENT
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5U54RR019453-05 |
BATSHAW, MARK L
CHILDREN'S RESEARCH INSTITUTE
RARE DISEASES CRC- UREA CYCLE DISORDERS
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5U54RR019478-05 |
BEAUDET, ARTHUR L.
BAYLOR COLLEGE OF MEDICINE
RARE DISEASE CRC FOR NEW THERAPIES AND NEW DIAGNOSTICS
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