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Funded Projects​​​​​

​​​​​​​​
Supported Projects        

F30 - Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA)

Project Number Description
1F30HD086975-01A1 CZERMINSKI, JAN
UNIV OF MASSACHUSETTS MED SCH WORCESTER
MODELING DOWN SYNDROME NEURAL PHENOTYPES WITH CHROMOSOMAL SILENCING
5F30HD081853-03 MASI, SOPHIA
UNIVERSITY OF WASHINGTON
NOVEL DRIED BLOOD SPOT MASS SPECTROMETRY FUNCTIONAL ASSAYS FOR LYSOSOMAL ACID LIPASE AND N-ACETYLGALACTOSAMINE-SULFATE SULFATASES FOR USE IN NEWBORN SCREENING

F31 - Predoctoral Individual National Research Service Award

Project Number Description
1F31HD090937-01A1 TSANG, TAWNY
UNIVERSITY OF CALIFORNIA LOS ANGELES
IDENTIFYING RISK MARKERS FOR AUTISM SPECTRUM DISORDERS IN EARLY INFANCY: A MULTIMODAL APPROACH
5F31HD088043-02 ROUNDS, JOHN CHRISTOPHER
EMORY UNIVERSITY
DEFINING ROLES OF INTELLECTUAL DISABILITY PROTEIN DNAB2 IN NEURONAL TRANSLATION

F32 - Postdoctoral Individual National Research Service Award

Project Number Description
1F32HD090833-01 WARD, AMANDA JOY
MASSACHUSETTS INSTITUTE OF TECHNOLOGY
IDENTIFICATION AND FUNCTIONAL DISSECTION OF LONG NON-CODING RNAS IN GENOMIC IMPRINTING
3F32HD088016-01A1S1 KEIL, KIMBERLY PRESTON
UNIVERSITY OF CALIFORNIA AT DAVIS
PCBS AND HERITABLE MUTATIONS IN CALCIUM SIGNALING ACT VIA DNA METHYLATION TO DISRUPT DENDRITIC GROWTH ANDPLASTICITY
5F32HD085646-02 MOON, HYANG MI
STANFORD UNIVERSITY
EFFECTS OF MATERNAL IMMUNE ACTIVATION ON GABRB3-DEFICIENT NEOCORTICAL PROGENITORS
5F32HD088016-02 KEIL, KIMBERLY PRESTON
UNIVERSITY OF CALIFORNIA AT DAVIS
PCBS AND HERITABLE MUTATIONS IN CALCIUM SIGNALING ACT VIA DNA METHYLATION TO DISRUPT DENDRITIC GROWTH ANDPLASTICITY

K08 - Clinical Investigator Award

Project Number Description
5K08HD077040-05 ELMALLAH, MAI KAMAL
UNIV OF MASSACHUSETTS MED SCH WORCESTER
NOVEL APPROACHES FOR CORRECTING RESPIRATORY INSUFFICIENCY IN POMPE DISEASE
5K08HD086827-02 WEBB, BRYN D
ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
INTEGRATIVE APPROACH TO STUDY MITOCHONDRIAL AMINOACYL-TRNA SYNTHETASE DISORDERS

K23 - Mentored Patient-Oriented Research Devel Awd

Project Number Description
1K23HD088742-01A1 VORA, NEETA L
UNIV OF NORTH CAROLINA CHAPEL HILL
EARLY GENOMIC DIAGNOSIS
5K23HD079605-03 TARUI, TOMO
TUFTS MEDICAL CENTER
PRENATAL DIAGNOSIS OF BRAIN MALFORMATIONS: IMPROVING ASSESSMENT OF PROGNOSIS
5K23HD079836-03 SOORYA, LATHA V
RUSH UNIVERSITY MEDICAL CENTER
INTEGRATED TREATMENTS FOR CORE DEFICITS IN AUTISM SPECTRUM DISORDER
5K23HD087472-02 KERNS, CONNOR M
DREXEL UNIVERSITY
DEVELOPING MEASURES FOR COMMUNITY-BASED RESEARCH ON TRAUMA AND RELATED CONDITIONS IN ASD

K99 - Career Transition Award

Project Number Description
1K99HD092545-01 HUANG, WEI-HSIANG
STANFORD UNIVERSITY
THE NEURAL FUNCTIONS OF RAI1, THE CAUSAL GENE FOR SMITH-MAGENIS SYNDROME

P01 - Research Program Projects

Project Number Description
5P01HD083157-03 LAMANTIA, ANTHONY S.
GEORGE WASHINGTON UNIVERSITY
PATHOLOGY, DEVELOPMENTAL ORIGINS, AND PREVENTION OF PEDIATRIC DYSPHAGIA
5P01HD085928-02 BEARER, CYNTHIA FRANCES
UNIVERSITY OF MARYLAND BALTIMORE
EFFECTS OF PERINATAL HYPOXIA-ISCHEMIA ON THE DEVELOPING CEREBELLUM WITH AND WITHOUT PRIOR INFLAMMATION

R00 - Research Transition Award

Project Number Description
4R00HD082337-03 SCHAFFER, ASHLEIGH E
CASE WESTERN RESERVE UNIVERSITY
MOLECULAR MECHANISMS OF INTELLECTUAL DISABILITY
5R00HD073270-05 XU, LIBIN
UNIVERSITY OF WASHINGTON
7-DEHYDROCHOLESTEROL-DERIVED OXYSTEROLS IN SLOS: ROLE AND THERAPY
5R00HD076444-05 GOETZ, SARAH
DUKE UNIVERSITY
CHARACTERIZING THE ROLE OF TTBK PROTEINS IN CILIOGENESIS AND NEURAL FUNCTION
5R00HD080981-04 ORI-MCKENNEY, KASSANDRA MARIE
UNIVERSITY OF CALIFORNIA AT DAVIS
ROLE OF THE DOWN SYNDROME GENE, MINIBRAIN, IN NEURONAL DEVELOPMENT AND FUNCTION

R01 - Research Project

Project Number Description
1R01HD088007-01A1 GREGORY, SIMON G
DUKE UNIVERSITY
CHARACTERIZING THE (EPI)GENETICS OF OXYTOCIN RESPONSE IN CLINICAL AND ANIMAL MODELS
1R01HD088482-01A1 CUMMINGS, E. MARK
UNIVERSITY OF NOTRE DAME
FAMILIES OF YOUTH WITH DEVELOPMENTAL DISABILITIES: A THEORY-BASED INTERVENTION
1R01HD088832-01A1 JIN, LEE-WAY
UNIVERSITY OF CALIFORNIA AT DAVIS
MITOCHONDRIAL ROS AND MICROGLIA IN RETT SYNDROME
1R01HD089390-01A1 VERMA, RAGINI
UNIVERSITY OF PENNSYLVANIA
TEMPORAL CONNECTOMICS FOR INFANT BRAIN: NEURODEVELOPMENT MODULATED BY PATHOLOGY
1R01HD090138-01A1 JESTE, SHAFALI SPURLING
UNIVERSITY OF CALIFORNIA LOS ANGELES
MECHANISMS OF CHANGE WITH EARLY INTERVENTION IN TUBEROUS SCLEROSIS COMPLEX
1R01HD091325-01 DENG, WENBIN
UNIVERSITY OF CALIFORNIA AT DAVIS
DIFFERENTIATION AND INTEGRATION OF TRISOMY 21 IPSCS IN AN ANIMAL MODEL
1R01HD091972-01 PARKER, KAREN J.
STANFORD UNIVERSITY
INTRANASAL VASOPRESSIN TREATMENT IN CHILDREN WITH AUTISM
1R01HD092093-01 SAIJO, KAORU
UNIVERSITY OF CALIFORNIA BERKELEY
ESTROGEN RECEPTOR (ER)Β-MEDIATED REPRESSION OF PRENATAL INFLAMMATION IN FETAL MICROGLIA AND ITS IMPACT ON AUTISM
1R01HD092659-01 XU, LIBIN
UNIVERSITY OF WASHINGTON
OXYSTEROLS IN SLOS NEURODEVELOPMENT: PATHOLOGICAL ROLE AND THERAPY
1R01HD093012-01A1 BISHOP, SOMER L.
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
DEVELOPMENT OF A STANDARDIZED MEASURE OF SOCIAL-COMMUNICATION ABILITIES FOR CHILDREN WITH NEURODEVELOPMENTAL DISORDERS
1R01HD093572-01 BAILEY, DONALD B
RESEARCH TRIANGLE INSTITUTE
CHILD AND FAMILY CONSEQUENCES OF CONGENITAL ZIKA SYNDROME IN BRAZIL
2R01HD036071-19 HAGERMAN, RANDI J
UNIVERSITY OF CALIFORNIA AT DAVIS
GENOTYPE-PHENOTYPE RELATIONSHIPS IN FRAGILE X FAMILIES
2R01HD044763-11A1 SYMONS, FRANK J
UNIVERSITY OF MINNESOTA
SENSORY MECHANISMS AND SELF-INJURY
2R01HD045561-13A1 WALKLEY, STEVEN UPSHAW
ALBERT EINSTEIN COLLEGE OF MEDICINE, INC
ENDOSOMAL LYSOSOMAL FUNCTION IN NEURONAL STORAGE DISEASE
2R01HD060586-06A1 BURGHES, ARTHUR H. M.
OHIO STATE UNIVERSITY
BIOMARKERS AND ADDITIVE THERAPIES TO ENHANCE SYMPTOMATIC TREATMENT OF SPINAL MUSCULAR ATROPHY
2R01HD064743-06A1 CHANG, QIANG
UNIVERSITY OF WISCONSIN-MADISON
FUNCTION OF STIMULUS-INDUCED MECP2 PHOSPHORYLATION
3R01HD081336-03S1 HALL, SCOTT S
STANFORD UNIVERSITY
EFFECTS OF SOCIAL GAZE TRAINING ON BRAIN AND BEHAVIOR IN FRAGILE X SYNDROME
4R01HD070855-05 HERSHEY, TAMARA G
WASHINGTON UNIVERSITY
TRACKING NEURODEGENERATION IN EARLY WOLFRAM SYNDROME
5R01HD038384-17 REEVES, ROGER H
JOHNS HOPKINS UNIVERSITY
GENOMIC APPROACHES TO ANEUPLOIDY
5R01HD039961-14 ROBINS, DIANA L
DREXEL UNIVERSITY
EARLY DETECTION OF AUTISM SPECTRUM DISORDER
5R01HD040647-14 DARNELL, JENNIFER C
ROCKEFELLER UNIVERSITY
CELL-SPECIFIC RNA TARGETS OF THE FRAGILE X MENTAL RETARDATION PROTEIN FAMILY
5R01HD042182-13 LAMANTIA, ANTHONY S.
GEORGE WASHINGTON UNIVERSITY
REGULATION OF 22Q11 GENES IN EMBRYONIC AND ADULT FOREBRAIN
5R01HD042601-16 KATSANIS, NICHOLAS
DUKE UNIVERSITY
MOLECULAR GENETICS OF BBS
5R01HD052731-10 HUBER, KIMBERLY
UT SOUTHWESTERN MEDICAL CENTER
ROLE OF MEF2 AND NEURAL ACTIVITY IN CORTICAL SYNAPTIC WEAKENING AND ELIMINATION
5R01HD054453-09 PORTERA-CAILLIAU, CARLOS
UNIVERSITY OF CALIFORNIA LOS ANGELES
IMAGING DENDRITIC SPINE ABNORMALITIES AND CIRCUIT DEFECTS IN FRAGILE X MICE.
5R01HD064727-07 PORTER, NED ALLEN
VANDERBILT UNIVERSITY
SLOS AND NEURONAL OXIDATIVE STRESS
5R01HD064993-08 HEAD, ELIZABETH
UNIVERSITY OF KENTUCKY
AGING AND DEMENTIA IN DOWN SYNDROME: CONNECTIVITY, INFLAMMATION, AND CEREBROVASCULAR CONTRIBUTIONS
5R01HD069560-07 POWELL, CRAIG M
UT SOUTHWESTERN MEDICAL CENTER
NOVEL GENETIC MODELS OF AUTISM
5R01HD072418-05 CARMICHAEL, GORDON G
UNIVERSITY OF CONNECTICUT SCH OF MED/DNT
NUCLEAR-RETAINED LONG NONCODING RNAS
5R01HD073126-05 SYMONS, FRANK J
UNIVERSITY OF MINNESOTA
INTRATHECAL BACLOFEN AND PAIN OUTCOMES IN CEREBRAL PALSY
5R01HD073128-05 JUUL, SANDRA E
UNIVERSITY OF WASHINGTON
BIOMARKERS OF NEONATAL ENCEPHALOPATHY IN A NONHUMAN PRIMATE MODEL
5R01HD073254-05 KENET, TAL
MASSACHUSETTS GENERAL HOSPITAL
FUNCTIONAL CONNECTIVITY SUBSTRATES OF SOCIAL AND NON-SOCIAL DEFICITS IN ASD
5R01HD073255-05 IVERSON, JANA M
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
REACHING, POSTURE, OBJECT EXPLORATION, AND LANGUAGE IN HIGH- AND LOW-RISK INFANTS
5R01HD074346-05 ABBEDUTO, LEONARD J.
UNIVERSITY OF CALIFORNIA AT DAVIS
EXPRESSIVE LANGUAGE SAMPLING AS AN OUTCOME MEASURE
5R01HD074593-06 ZHANG, JIANGYANG
NEW YORK UNIVERSITY SCHOOL OF MEDICINE
IMAGING NEONATAL HYPOXIC ISCHEMIC INJURY
5R01HD075802-04 BEGGS, ALAN H.
BOSTON CHILDREN'S HOSPITAL
GENETIC SCREENING AND THERAPIES FOR NEMALINE MYOPATHIES
5R01HD075822-05 LOUVI, ANGELIKI
YALE UNIVERSITY
MOLECULAR MECHANISMS OF PRIMARY MICROCEPHALY
5R01HD076189-04 HESSL, DAVID R
UNIVERSITY OF CALIFORNIA AT DAVIS
A COGNITIVE TEST BATTERY FOR INTELLECTUAL DISABILITIES
5R01HD076258-04 GRANT, PATRICIA ELLEN
BOSTON CHILDREN'S HOSPITAL
PERINATAL BRAIN INJURY: POTENTIAL OF INNOVATIVE NIRS TO OPTIMIZE HYPOTHERMIA
5R01HD076653-05 HAGOPIAN, LOUIS P.
HUGO W. MOSER RES INST KENNEDY KRIEGER
DELINEATING SUBTYPES OF SELF-INJURIOUS BEHAVIOR MAINTAINED BY AUTOMATIC REINFORCE
5R01HD076903-05 BRADY, NANCY CAROLINE
UNIVERSITY OF KANSAS LAWRENCE
THE CCS: A TREATMENT OUTCOME MEASURE FOR INDIVIDUALS WITH SEVERE ID
5R01HD078410-04 WETHERBY, AMY M
FLORIDA STATE UNIVERSITY
SMART EARLY SCREENING FOR AUTISM AND COMMUNICATION DISORDERS IN PRIMARY CARE
5R01HD079113-04 FISHER, WAYNE W
UNIVERSITY OF NEBRASKA MEDICAL CENTER
STIMULUS CONTROL REFINEMENTS OF FCT INTERVENTIONS FOR DESTRUCTIVE BEHAVIOR IN ID
5R01HD079432-03 AZIZ-ZADEH, LISA SARAH
UNIVERSITY OF SOUTHERN CALIFORNIA
THE NEUROBIOLOGICAL BASIS OF HETEROGENEOUS SOCIAL AND MOTOR DEFICITS IN ASD
5R01HD079512-04 MAZEFSKY, CARLA A
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
CHANGE-SENSITIVE MEASUREMENT OF EMOTION DYSREGULATION IN ASD
5R01HD079533-03 WINDHAM, GAYLE
SEQUOIA FOUNDATION
ROLE OF PRE-NATAL VITAMIN D AND GENE INTERACTIONS IN AUTISM SPECTRUM DISORDERS; LEVERAGING AN EXISTING CASE-CONTROL STUDY
5R01HD079642-03 DONNELLY, JOSEPH E.
UNIVERSITY OF KANSAS MEDICAL CENTER
WEIGHT MANAGEMENT FOR ADOLESCENTS WITH IDD
5R01HD081037-03 MANDEL, GAIL
OREGON HEALTH & SCIENCE UNIVERSITY
THE MECHANISM OF RETT SYNDROME RESCUE BY ASTROCYTES
5R01HD081199-03 LORD, CATHERINE
WEILL MEDICAL COLL OF CORNELL UNIV
TRANSITIONING TO ADULTHOOD: A PROSPECTIVE LONGITUDINAL STUDY
5R01HD081206-03 DEVASKAR, SHERIN U
UNIVERSITY OF CALIFORNIA LOS ANGELES
PRENATAL ORIGINS OF NEUROMETABOLIC CONSEQUENCES
5R01HD081336-03 HALL, SCOTT S
STANFORD UNIVERSITY
EFFECTS OF SOCIAL GAZE TRAINING ON BRAIN AND BEHAVIOR IN FRAGILE X SYNDROME
5R01HD082110-03 MAILICK, MARSHA RUTH
UNIVERSITY OF WISCONSIN-MADISON
FMR1 PREMUTATION PHENOTYPES IN POPULATION-BASED & CLINICALLY-ASCERTAINED SAMPLES
5R01HD082127-03 BOYD, BRIAN ANTONIO
UNIV OF NORTH CAROLINA CHAPEL HILL
BEHAVIORAL INFLEXIBILITY IN IDD OUTCOME MEASUREMENT
5R01HD082148-03 ROTHWELL, ERIN
UNIVERSITY OF UTAH
THE EFFECT OF ELECTRONIC INFORMED CONSENT INFORMATION (EICI) ON RESIDUAL NEWBORN SPECIMEN RESEARCH
5R01HD082203-03 ALBERTS, JEFFREY R
INDIANA UNIVERSITY BLOOMINGTON
DEVELOPMENTAL LINKAGE OF METABOLIC HOMEOSTASIS AND SOCIALITY
5R01HD082373-03 YUAN, HONGJIE
EMORY UNIVERSITY
NMDAR MUTATIONS & NEURODEVELOPMENTAL DISORDER: FROM MECHANISM TO TARGETED THERAPY
5R01HD082814-03 MOLHOLM, SOPHIE
ALBERT EINSTEIN COLLEGE OF MEDICINE, INC
SENSORY INTEGRATION THERAPY IN AUTISM: MECHANISMS AND EFFECTIVENESS
5R01HD083214-03 FISHER, WAYNE W
UNIVERSITY OF NEBRASKA MEDICAL CENTER
PREVENTING RELAPSE OF DESTRUCTIVE BEHAVIOR USING BEHAVIORAL MOMENTUM THEORY
5R01HD083381-02 WILKINSON, KRISTA M
PENNSYLVANIA STATE UNIVERSITY-UNIV PARK
EYE TRACKING TECHNOLOGIES TO CHARACTERIZE AND OPTIMIZE VISUAL ATTENDING IN DOWN SYNDROME
5R01HD083680-03 HU, HUAIYU
UPSTATE MEDICAL UNIVERSITY
MECHANISMS OF COGNITIVE DEFICITS IN DYSTROGLYCANOPATHIES
5R01HD083828-02 ZUKIN, R. SUZANNE
ALBERT EINSTEIN COLLEGE OF MEDICINE, INC
EPIGENETIC REMODELING OF NMDA RECEPTORS
5R01HD083881-02 SUKHODOLSKY, DENIS G
YALE UNIVERSITY
NEURAL MECHANISMS OF CBT FOR ANXIETY IN CHILDREN WITH AUTISM SPECTRUM DISORDER
5R01HD084203-02 WALKER, CHERYL KATHERINE
UNIVERSITY OF CALIFORNIA AT DAVIS
MATERNAL OBESITY AND WEIGHT CHANGE IN NEUROBEHAVIORAL DEVELOPMENT
5R01HD084214-04 CHIN, FREDERICK T
STANFORD UNIVERSITY
CROSS-SPECIES MULTI-MODAL NEUROIMAGING TO INVESTIGATE GABA PHYSIOLOGY IN FRAGILE X SYNDROME
5R01HD084215-04 CHEN, LU
STANFORD UNIVERSITY
DEVELOPMENTAL PATHOPHYSIOLOGY OF SYNAPSES IN A MOUSE MODEL OF FRAGILE X SYNDROME
5R01HD084422-02 MOCHLY-ROSEN, DARIA
STANFORD UNIVERSITY
DEVELOPMENT OF A NOVEL TREATMENT FOR HYPERBILIRUBINEMIA-INDUCED KERNICTERUS
5R01HD084497-03 BAGNER, DANIEL MARC
FLORIDA INTERNATIONAL UNIVERSITY
INTERNET TREATMENT FOR BEHAVIOR PROBLEMS IN PRESCHOOLERS WITH DEVELOPMENTAL DELAY
5R01HD084500-03 PETERS, SARIKA U
VANDERBILT UNIVERSITY MEDICAL CENTER
MARKERS OF DISEASE PROGRESSION IN MECP2 DUPLICATION SYNDROME
5R01HD084563-02 WARREN, STEVEN F
UNIVERSITY OF KANSAS LAWRENCE
THE EFFECTS OF PARENTING ON THE DEVELOPMENT AND BEHAVIOR OF ADOLESCENTS WITH FXS
5R01HD086211-02 AILEY, SARAH HERRINK
RUSH UNIVERSITY MEDICAL CENTER
STEPS TO EFFECTIVE PROBLEM SOLVING
5R01HD086765-02 LARIN, KIRILL V
UNIVERSITY OF HOUSTON
OPTICAL COHERENCE TOMOGRAPHY TO STUDY EFFECT OF POLY - DRUG EXPOSURE ON FETAL BRAIN DEVELOPMENT
5R01HD086977-02 XIE, ZHONGCONG
MASSACHUSETTS GENERAL HOSPITAL
TAU/P-TAU AS BIOMARKERS OF ANESTHESIA- AND SURGERY-INDUCED COGNITIVE IMPAIRMENT IN YOUNG MICE
5R01HD087048-02 PARKER, KAREN J.
STANFORD UNIVERSITY
A MONKEY MODEL OF NATURALLY OCCURRING SOCIAL IMPAIRMENTS
5R01HD087302-02 KLORMAN, RAFAEL KLORMAN
UNIVERSITY OF ROCHESTER
EARLY INTENSIVE BEHAVIORAL INTERVENTION FOR AUTISM
5R01HD087915-02 CROEN, LISA A
KAISER FOUNDATION RESEARCH INSTITUTE
PRENATAL SSRI EXPOSURE, MATERNAL AND CHILD GENOTYPE, AND AUTISM SPECTRUM DISORDERS
5R01HD088409-02 EDGIN, JAMIE OGLINE
UNIVERSITY OF ARIZONA
MEMORY MEASURES FOR CLINICAL TRIALS IN DOWN SYNDROME AND FRAGILE X SYNDROME
5R01HD089491-02 LYNCH, GARY S
UNIVERSITY OF CALIFORNIA-IRVINE
LOSS AND RESCUE OF ENDOCANNABINOID-DEPENDENT LTP AND MEMORY IN FRAGILE-X MODEL MICE

R03 - Small Research Grants

Project Number Description
1R03HD090444-01 NAIR, NIKHIL UNNI
TUFTS UNIVERSITY MEDFORD
TOWARD ALTERED PROBIOTIC THERAPY FOR PHENYLKETONURIA
1R03HD091639-01 GARDINER, KATHELEEN
UNIVERSITY OF COLORADO DENVER
COGNITIVE DEFICITS IN DOWN SYNDROME: CONTRIBUTIONS FROM HSA21 ORTHOLOGS ON MOUSE CHROMOSOME 10
5R03HD083538-02 BHATTACHARYYA, ANITA
UNIVERSITY OF WISCONSIN-MADISON
DEFINING INTERNEURON DEFICITS IN DOWN SYNDROME BRAIN.
5R03HD083596-02 CHANNELL, MARIE MOORE
UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN
PARENT AND CHILD PREDICTORS OF MENTAL STATE LANGUAGE DEVELOPMENT IN DOWN SYNDROME
5R03HD083729-02 SHARP, WILLIAM
EMORY UNIVERSITY
THE AUTISM MEAL PLAN: A PARENT TRAINING CURRICULUM TO MANAGE EATING AVERSIONS AND LIMITED VARIETY AMONG CHILDREN WITH AUTISM
5R03HD086330-02 BEEBER, LINDA
UNIV OF NORTH CAROLINA CHAPEL HILL
ENHANCING COMMUNICATION BETWEEN CHILDREN IN EI AND THEIR DEPRESSED MOTHERS
5R03HD086523-02 CHANG, QIANG
UNIVERSITY OF WISCONSIN-MADISON
STEROL METABOLISM IN RETT SYNDROME
5R03HD088942-02 CHAPMAN, SUSAN CAROLINE
CLEMSON UNIVERSITY
CREATINE: A NOVEL MODULATOR OF GABA INHIBITORY SYNAPSES

R13 - Conferences

Project Number Description
1R13CA217038-01 SCHOYER, LISA
RASOPATHIES NETWORK USA
5TH INTERNATIONAL RASOPATHIES SYMPOSIUM
2R13HD062129-06 LONGO, NICOLA
UNIVERSITY OF UTAH
SOCIETY FOR INHERITED METABOLIC DISORDERS ANNUAL MEETING
5R13HD048170-13 KRANTZ, IAN D.
CHILDREN'S HOSP OF PHILADELPHIA
DAVID W. SMITH WORKSHOP ON MALFORMATIONS AND MORPHOGENESIS
5R13HD084155-02 ABBEDUTO, LEONARD J.
UNIVERSITY OF CALIFORNIA AT DAVIS
GATLINBURG CONFERENCE ON RESEARCH IN ID/DD

R15 - Academic Research Enhancement Awards (AREA)

Project Number Description
3R15HD076379-01A1S1 DERUISSEAU, LARA ROBERTS
LE MOYNE COLLEGE
INVESTIGATION INTO NEURAL AND MUSCULAR COMPONENTS OF BREATHING IN DOWN SYNDROME

R21 - Exploratory/Developmental Grants

Project Number Description
1R21HD079254-01A1 CHAM, RAKIE
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
ROLE OF ATTENTION IN BALANCE AND MOBILITY IN AUTISM SPECTRUM DISORDERS
1R21HD087795-01A1 JIANG, YONG-HUI
DUKE UNIVERSITY
A NOVEL PARADIGM TO DISSECT THE FUNCTION CONNECTIVITY IN SHANK3 AUTISM MODEL
1R21HD088833-01A1 HAYFLICK, SUSAN J
OREGON HEALTH & SCIENCE UNIVERSITY
COENZYME A REPLENISHMENT AS A THERAPEUTIC STRATEGY FOR INBORN ERRORS OF METABOLISM
1R21HD089731-01A1 STERNAD, DAGMAR
NORTHEASTERN UNIVERSITY
QUANTIFICATION OF PREDICTIVE MOTOR IMPAIRMENTS IN INDIVIDUALS WITH ASD
1R21HD091500-01 WALL, DENNIS PAUL
STANFORD UNIVERSITY
EVALUATION OF MACHINE LEARNING TO MOBILIZE DETECTION AND THERAPY OF DEVELOPMENTAL DELAY IN CHILDREN
1R21HD091547-01 WATSON, LINDA R
UNIV OF NORTH CAROLINA CHAPEL HILL
EVALUATION OF A NOVEL INTERVENTION FOR INFANTS AT RISK FOR NEURODEVELOPMENTAL DISORDERS
1R21HD093563-01 PHILLIPS, JOHN P
UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR
BUILDING RESEARCH CAPACITY IN CHILD NEUROLOGY: A US/SRI LANKA RESEARCH COLLABORATIVE
5R21HD078864-03 GERMAIN-LEE, EMILY L
UNIVERSITY OF CONNECTICUT SCH OF MED/DNT
THE ROLE OF G PROTEIN-COUPLED SIGNALING IN NEUROCOGNITIVE AND PSYCHOSOCIALABNORMALITIES
5R21HD082319-02 BHUTANI, VINOD K
STANFORD UNIVERSITY
BILIRUBIN BINDING CAPACITY TO ASSESS BILIRUBIN LOAD IN PRETERM INFANTS
5R21HD083916-02 SUZUKI, CAROLYN K
RBHS-NEW JERSEY MEDICAL SCHOOL
REGULATING MTDNA AND MTRNA DYNAMICS BY THE MITOCHONDRIAL AAA+ LON PROTEASE
5R21HD083944-02 D'SA, VIREN
MEMORIAL HOSPITAL OF RHODE ISLAND
LEAD EXPOSURE AND EARLY BRAIN DEVELOPMENT
5R21HD084204-02 KORNBLUM, HARLEY IAN
UNIVERSITY OF CALIFORNIA LOS ANGELES
STEM CELL- BASED STUDIES OF GENE-ENVIRONMENT INTERACTIONS IN PTEN- ASSOCIATED AUTISM
5R21HD084953-02 RAGOZZINO, MICHAEL E
UNIVERSITY OF ILLINOIS AT CHICAGO
STRIATAL GLUTAMATE SIGNALING AND COGNITION IN AUTISM MOUSE MODELS
5R21HD085061-02 BEARER, CYNTHIA FRANCES
UNIVERSITY OF MARYLAND BALTIMORE
THE ROLE OF LIPID RAFTS IN BILLIRUBIN NEUROTOXICITY
5R21HD086368-02 LOVETT-RACKE, AMY E
OHIO STATE UNIVERSITY
NEUROPROTECTIVE ROLE OF VITAMIN D DURING CHILDHOOD
5R21HD086491-02 CALL, NATHAN
EMORY UNIVERSITY
OBJECTIVE MEASUREMENT OF CHALLENGING BEHAVIORS IN INDIVIDUALS WITH ASD
5R21HD086620-03 GAMMILL, HILARY SEGLIN
UNIVERSITY OF WASHINGTON
ANEUPLOID FETAL MICROCHIMERISM: PERSISTENCE AND POTENTIAL FUNCTION
5R21HD086669-02 ASHWOOD, PAUL
UNIVERSITY OF CALIFORNIA AT DAVIS
IMMUNE REGULATION AND NEURODEVELOPMENTAL DISORDERS
5R21HD086769-02 GIULIVI, CECILIA
UNIVERSITY OF CALIFORNIA AT DAVIS
INFLUENCE OF PRENATAL FOLATE ON PLACENTAL MTDNA AND AUTISM RISK
5R21HD087645-02 KIM, SEOK-HYUNG
MEDICAL UNIVERSITY OF SOUTH CAROLINA
A MODEL OF ALPERS SYNDROME
5R21HD087818-02 LANGAN, THOMAS J
STATE UNIVERSITY OF NEW YORK AT BUFFALO
ENHANCEMENT NEWBORN SCREENING TO IMPROVE THE EFFICACY OF CORD BLOOD TRANSPLANT FOR KRABBE DISEASE
5R21HD087864-02 RYCKMAN, KELLI KAE
UNIVERSITY OF IOWA
NEWBORN METABOLIC SCREENING FOR PREDICTION OF CHILDHOOD RESPIRATORY PHENOTYPES
5R21HD087866-02 SNYDER, NATHANIEL W.
DREXEL UNIVERSITY
LIPIDOMICS OF MECONIUM IN NEURODEVELOPMENT
5R21HD089791-02 IDRO, RICHARD IWA
MAKERERE UNIVERSITY
BURDEN AND RISK OF NEUROLOGICAL AND COGNITIVE IMPAIRMENT IN PEDIATRIC SICKLE CELL ANEMIA IN UGANDA

R25 - Education Projects

Project Number Description
5R25HD078229-03 REGIER, DEBRA S
CHILDREN'S RESEARCH INSTITUTE
RARE DISEASE RESEARCH TRAINING PROGRAM

R37 - Method to Extend Research in Time (MERIT) Award

Project Number Description
4R37HD028607-26 SCHUCHMAN, EDWARD H.
ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
ACID SPHINGOMYELINASE AND NIEMANN-PICK DISEASE
5R37HD021341-33 HASSOLD, TERRY J
WASHINGTON STATE UNIVERSITY
A PROGRAM OF RESEARCH IN POPULATION CYTOGENETICS

R42 - * Small Business Technology Transfer (STTR) Grants - Phase II

Project Number Description
4R42HD089804-02 STACPOOLE, PETER WALLACE
MEDOSOME BIOTEC, LLC
PERSONALIZED DOSING OF DICHLOROACETATE FOR THE TREATMENT OF RARE AND COMMON DISEASES

R43 - Small Business Innovation Research Grants (SBIR) - Phase I

Project Number Description
1R43HD092128-01 BURCH, RONALD M
SPARK2FLAME, INC.
A DIAGNOSTIC FOR MATERNAL AUTOAB TO CASPR2 TO PREDICT INCREASED RISK OF AUTISM SPECTRUM DISORDER IN CHILDREN
1R43HD092155-01 LAN, TIAN
GLUCOSENTIENT, INC.
A RAPID AND PORTABLE TEST FOR HOME MONITORING OF PHENYLALANINE LEVELS BY PATIENTS WITH PHENYLKETONURIA USING A BLOOD GLUCOSE METER
1R43HD092205-01A1 JAIN, CHANDNI
ADVANCED REPRODUCTIVE TESTING, LLC
A PLATFORM FOR SAFE, NONINVASIVE PRENATAL GENETIC TESTING AT FIVE WEEKS OF PREGNANCY

R44 - Small Business Innovation Research Grants (SBIR) - Phase II

Project Number Description
1R44HD092154-01 PAMULA, VAMSEE K.
BAEBIES, INC.
COMPREHENSIVE, NEAR PATIENT ASSESSMENT OF SEVERE HYPOGLYCEMIA IN NEWBORNS USING LOW BLOOD VOLUME
4R44HD088211-02 NORTON, SCOTT MICHAEL
BAEBIES, INC.
POINT-OF-BIRTH NEWBORN SCREENING FOR MCAD/VLCAD AND GALACTOSEMIA TO ELIMINATE DEADLY DELAYS FOR TIME CRITICAL CONDITIONS
5R44HD087097-02 HENKENS, ROBERT W
ALDERON BIOSCIENCES, INC.
NEW TEST SYSTEM FOR BLOOD LEAD LEVELS IN CHILDREN

T32 - Institutional National Research Service Award

Project Number Description
2T32HD040127-16 PIVEN, JOSEPH
UNIV OF NORTH CAROLINA CHAPEL HILL
POSTDOCTORAL RESEARCH IN NEURODEVELOPMENTAL DISORDERS
3T32HD007489-22S1 MAILICK, MARSHA RUTH
UNIVERSITY OF WISCONSIN-MADISON
POST-DOCTORAL TRAINING IN INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH
5T32HD007009-42 SCHWARTZ, NANCY B
UNIVERSITY OF CHICAGO
GRADUATE TRAINING IN GROWTH AND DEVELOPMENT
5T32HD007149-40 NOONAN, JAMES P
YALE UNIVERSITY
GENETICS AND GENOMICS OF HUMAN DISEASE
5T32HD007489-23 MAILICK, MARSHA RUTH
UNIVERSITY OF WISCONSIN-MADISON
POST-DOCTORAL TRAINING IN INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH

U01 - Research Project (Cooperative Agreements)

Project Number Description
5U01HD079066-03 WOLFE, JOHN H
CHILDREN'S HOSP OF PHILADELPHIA
CHOROID PLEXUS-DIRECTED GENE THERAPY FOR ALPHA-MANNOSIDOSIS
5U01HL131003-02 KING, EILEEN
CINCINNATI CHILDRENS HOSP MED CTR
ADMINISTRATIVE COORDINATING CENTER: CARDIOVASCULAR DEVELOPMENT AND PEDIATRIC CARDIAC GENOMICS CONSORTIA
5U01NS096767-02 BERRY-KRAVIS, ELIZABETH MARA
RUSH UNIVERSITY MEDICAL CENTER
EFFECTS OF AFQ056 ON LANGUAGE LEARNING IN YOUNG CHILDREN WITH FRAGILE X SYNDROME (FXS)
7U01HD082806-03 VANDERVER, ADELINE LUCIE
CHILDREN'S HOSP OF PHILADELPHIA
REVERSE TRANSCRIPTASE INHIBITORS IN AICARDI GOUTIERES SYNDROME

U19 - Research Program (Cooperative Agreement)

Project Number Description
5U19MH108206-03 MCPARTLAND, JAMES CHARLES
YALE UNIVERSITY
THE AUTISM BIOMARKERS CONSORTIUM FOR CLINICAL TRIALS

U54 - Specialized Center (Cooperative Agreements)

Project Number Description
3U54HD083091-04S1 GURALNICK, MICHAEL J
UNIVERSITY OF WASHINGTON
INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
5U54AR068069-04 LEE, BRENDAN
BAYLOR COLLEGE OF MEDICINE
BRITTLE BONE DISORDERS CONSORTIUM OF THE RARE DISEASE CLINICAL RESEARCH NETWORK
5U54HD060848-11 EMERSON, CHARLES P.
UNIV OF MASSACHUSETTS MED SCH WORCESTER
BIOMARKERS FOR THERAPY OF FSHD (U54)
5U54HD061221-14 GROPMAN, ANDREA LYNNE
CHILDREN'S RESEARCH INSTITUTE
RARE DISEASES CLINICAL RESEARCH CONSORTIA (RDCRC) FOR THE RDCR NETWORK
5U54HD061939-09 RIZZO, WILLIAM B
UNIVERSITY OF NEBRASKA MEDICAL CENTER
STEROL AND ISOPRENOID DISEASES CONSORTIUM
5U54HD079124-05 PIVEN, JOSEPH
UNIV OF NORTH CAROLINA CHAPEL HILL
CLINICAL TRANSLATIONAL RESEARCH CENTER FOR NEURODEVELOPMENTAL DISORDERS
5U54HD079125-05 ABBEDUTO, LEONARD J.
UNIVERSITY OF CALIFORNIA AT DAVIS
MIND INSTITUTE INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
5U54HD082013-04 RICHTER, JOEL D
UNIV OF MASSACHUSETTS MED SCH WORCESTER
RESCUING THE FRAGILE X SYNDROME BY RESETTING TRANSLATIONAL HOMEOSTASIS
5U54HD083091-04 GURALNICK, MICHAEL J
UNIVERSITY OF WASHINGTON
INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
5U54HD083092-04 ZOGHBI, HUDA Y
BAYLOR COLLEGE OF MEDICINE
BAYLOR INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTERS
5U54HD083211-04 DYKENS, ELISABETH MAY
VANDERBILT UNIVERSITY MEDICAL CENTER
EUNICE KENNEDY SHRIVER INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER AT VANDERBILT UNIVERSITY
5U54HD086984-02 YUDKOFF, MARC
CHILDREN'S HOSP OF PHILADELPHIA
THE INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER AT CHOP/PENN
5U54HD087011-03 CONSTANTINO, JOHN N.
WASHINGTON UNIVERSITY
WASHINGTON UNIVERSITY INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
5U54HD087101-02 BOOKHEIMER, SUSAN Y
UNIVERSITY OF CALIFORNIA LOS ANGELES
UCLA CENTER FOR TRANSLATIONAL RESEARCH IN NEURODEVELOPMENT: UC-TRAN
5U54HD087351-03 OLSON, ERIC N
UT SOUTHWESTERN MEDICAL CENTER
MYOEDITING OF DUCHENNE MUSCULAR DYSTROPHY
5U54HD090256-02 MESSING, ALBEE
UNIVERSITY OF WISCONSIN-MADISON
WAISMAN INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
5U54HD090257-02 GALLO, VITTORIO
CHILDREN'S RESEARCH INSTITUTE
DISTRICT OF COLUMBIA INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER
5U54HD090260-02 WALKLEY, STEVEN UPSHAW
ALBERT EINSTEIN COLLEGE OF MEDICINE, INC
SUPPORT FOR THE ROSE F. KENNEDY IDDRC
5U54NS078059-07 HIRANO, MICHIO
COLUMBIA UNIVERSITY HEALTH SCIENCES
NAMDC: OVERALL RESEARCH PLAN
5U54NS092090-04 SAHIN, MUSTAFA
BOSTON CHILDREN'S HOSPITAL
DEVELOPMENTAL SYNAPTOPATHIES ASSOCIATED WITH TSC, PTEN AND SHANK3 MUTATIONS

UM1 - Research Project with Complex Structure Cooperative Agreement

Project Number Description
5UM1HL098123-09 GELB, BRUCE D
ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
GENETICS OF CONOTRUNCAL DEFECTS AND ASSOCIATED NEURODEVELOPMENTAL OUTCOMES
5UM1HL098147-09 NEWBURGER, JANE W.
BOSTON CHILDREN'S HOSPITAL
THE GENOMIC BASIS OF CONGENITAL HEART DISEASE AND NEURODEVELOPMENTAL OUTCOMES
5UM1HL098162-09 BRUECKNER, MARTINA
YALE UNIVERSITY
GENETICS AND GENOMICS OF CONGENITAL HEART DISEASE AND ASSOCIATED NEURODEVELOPMENTAL ABNORMALITIES
5UM1HL128711-03 TRISTANI-FIROUZI, MARTIN
UNIVERSITY OF UTAH
BRIDGING THE GAP BETWEEN GENOMICS AND CLINICAL OUTCOMES IN CHD
5UM1HL128761-03 SRIVASTAVA, DEEPAK
J. DAVID GLADSTONE INSTITUTES
GENETICS OF HYPOPLASTIC LEFT HEART SYNDROME
​​

Contact Information

Name: Dr Melissa Ann Parisi
Intellectual and Developmental Disabilities Branch
Phone: 301-496-1383
Email: parisima@mail.nih.gov

Staff Directory
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