Faculty

Institution

Unit

Venue

James S. Sutcliffe, PhD

Associate Professor

Vanderbilt University

Affiliations

School of Medicine

Molecular Physiology & Biophysics

James S. Sutcliffe, Phd is currently serving as a Molecular Physiology & Biophysics Associate Professor at Vanderbilt University.

Honors

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Experiences

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Education

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James S. Sutcliffe, PhD

Vanderbilt University

Associate Professor

You can click a keyword to filter the displayed items

genetics autism human genetics genomics neuroscience medical genetics psychiatric genetics molecular biology neurogenetics population genetics molecular genetics neurology genetic disorders molecular psychiatry autism spectrum disorder neurodevelopmental disorders gene expression neuropharmacology genome biology neuropsychopharmacology biological psychiatry genome-wide association studies developmental genetics cytogenetics translational psychiatry linkage analysis child psychiatry autism spectrum disorders prader-willi syndrome behavioral disorders molecular neurobiology brain function molecular imprinting linkage disequilibrium neurotransmission genetic predisposition neuropsychiatry angelman syndrome febrile seizures autism families serotonin transporter maternal serotonin levels molecular neurodegeneration developmental psychology psychiatric research disease gene identification somatic variant chromosome biology variant interpretation clinical psychiatry neuroinformatics adolescent psychology genome structure developmental disorders neurodiversity syndromic autism genetic analysis genotype-phenotype association knockout mice genome analysis genetic linkage common genetic variants snrpn gene risk genes social science research developmental cognitive neuroscience affective neuroscience mammalian biology bayesian analysis family studies splicing variant mutagenesis length variation cgg repeat coincident breakpoint cluster region chromatin genes psychiatry epigenetics genetic basis statistical genetics

Notable Scholarly Works

Notable Federal Grants

Collaborators

Long Covid-19 and Peripheral Serotonin: A Commentary and Reconsideration. Journal of Inflammation Research (2024)

George AndersonEdwin CookRandy BlakelyJames SutcliffeJeremy Veenstra-VanderWeele

neurologymedicinelong covidpharmacologyneuroinflammationcovid-19chronic inflammationclinical researchinflammatory diseasesinflammatory markersperipheral serotonininflammation

Maternal Serotonin Levels and Neurodevelopmental Severity in Autistic Children: A Partial Replication and Extension. JAACAP Open (2024)

Amandeep JutlaLauren C. ShuffreyStephen J. GuterGeorge M. AndersonKally C. O'ReillyAlicia K. MontgomeryJames S. SutcliffeEdwin H. CookJeremy Veenstra-VanderWeele

neurodevelopmental severitypsychologyneurodevelopmental disordersmaternal serotonin levelsautistic children

Relationship Between Maternal Serotonin Levels and Autism-Associated Genetic Variants. Journal of Clinical Investigation (2024)

Amandeep JutlaLauren C. ShuffreyStephen J. GuterKally C. O’ReillyGeorge M. AndersonJames S. SutcliffeEdwin H. CookJeremy Veenstra-VanderWeele

neurologyautism-associated genetic variantsgeneticspsychiatryclinical researchpsychiatric geneticsclinical investigationmedical geneticsmaternal serotonin levelsautism

Examining the Latent Structure and Correlates of Sensory Reactivity in Autism: A Multi-Site Integrative Data Analysis by the Autism Sensory Research Consortium. Molecular Autism (2023)

Zachary J. WilliamsRoseann SchaafKarla K. AusderauGrace T. BaranekD. Jonah BarrettCarissa J. CascioRachel L. DumontEkomobong E. EyohMichelle D. FaillaJacob I. FeldmanJennifer H. Foss-FeigHeather L. GreenShulamite A. GreenJason L. HeElizabeth A. Kaplan-KahnBahar Keçeli-KaysılıKeren MacLennanZoe MaillouxElysa J. MarcoLisa E. MashElizabeth P. McKernanSophie MolholmStewart H. MostofskyNicolaas A. J. PutsCaroline E. RobertsonNatalie RussoNicole SheaJohn SiderisJames S. SutcliffeTeresa TavassoliMark T. WallaceEricka L. WodkaTiffany G. Woynaroski

latent structuresensory reactivityneuroscienceautism

A Phenome‐Wide Association Study of Polygenic Scores for Attention Deficit Hyperactivity Disorder Across Two Genetic Ancestries in Electronic Health Record Data. American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2022)

Maria NiarchouJulia M. SealockPeter StraubSandra Sanchez‐RoigeJames S. SutcliffeLea K. Davis

genomicsgeneticsgenetic ancestriespolygenic scoresmedical geneticsgenome-wide association studies

Calculating Genetic Risk for Dysfunction in Pleiotropic Biological Processes Using Whole Exome Sequencing Data. Journal of Neurodevelopmental Disorders (2022)

Olivia J. VeatchDiego R. MazzottiRobert T. SchultzTed AbelJacob J. MichaelsonEdward S. BrodkinBirkan TuncSusan G. AssoulineThomas Nickl-JockschatBeth A. MalowJames S. SutcliffeAllan I. Pack

genomicsgeneticspleiotropic biological processesdevelopmental neurobiologydevelopmental biologyneurosciencegenetic riskbioinformatics

Characterizing Sleep Disorders in an Autism-Specific Collection of Electronic Health Records. Sleep Medicine (2022)

E.V. SingerM. NiarchouA. Maxwell-HornD. HucksR. JohnstonJ.S. SutcliffeL.K. DavisB.A. Malow

pediatricsautism-specific collectionsleep medicine

Rare Coding Variation Provides Insight Into the Genetic Architecture and Phenotypic Context of Autism. Nature Genetics (2022)

Jack M. FuF. Kyle SatterstromMinshi PengHarrison BrandRyan L. CollinsShan DongBrie WamsleyLambertus KleiLily WangStephanie P. HaoChristine R. StevensCaroline CusickMehrtash BabadiEric BanksBrett CollinsSheila DodgeStacey B. GabrielLaura GauthierSamuel K. LeeLindsay LiangAlicia LjungdahlBehrang MahjaniLaura SloofmanAndrey N. SmirnovMafalda BarbosaCatalina BetancurAlfredo BruscoBrian H. Y. ChungEdwin H. CookMichael L. CuccaroEnrico DomeniciGiovanni Battista FerreroJ. Jay GargusGail E. HermanIrva Hertz-PicciottoPatricia MacielDara S. ManoachMaria Rita Passos-BuenoAntonio M. PersicoAlessandra RenieriJames S. SutcliffeFlora TassoneElisabetta TrabettiGabriele CamposSimona CardaropoliDiana CarliMarcus C. Y. ChanChiara FalleriniElisa GiorgioAna Cristina GirardiEmily Hansen-KissSo Lun LeeCarla LintasYunin LudenaRachel NguyenLisa PavinatoMargaret Pericak-VanceIsaac N. PessahRebecca J. SchmidtMoyra SmithClaudia I. S. CostaSlavica TrajkovaJaqueline Y. T. WangMullin H. C. YuBranko AleksicMykyta ArtomovElisa BenettiMonica Biscaldi-SchaferAnders D. BørglumAngel CarracedoAndreas G. ChiocchettiHilary CoonRyan N. DoanMontserrat Fernández-PrietoChristine M. FreitagSherif GergesStephen GuterDavid M. HougaardChristina M. HultmanSuma JacobMiia KaartinenAlexander KolevzonItaru KushimaTerho LehtimäkiCaterina Lo RizzoNell MaltmanMarianna ManaraGal MeiriIdan MenasheJudith MillerNancy MinshewMatthew MosconiNorio OzakiAarno PalotieMara ParelladaKaija PuuraAbraham ReichenbergSven SandinStephen W. SchererSabine Schlitt

genomicsgeneticsphenotypic contextpsychiatric geneticshuman geneticsgenetic architectureautism

Statistical and Functional Convergence of Common and Rare Genetic Influences on Autism at Chromosome 16p. Nature Genetics (2022)

Daniel J. WeinerEmi LingSerkan ErdinDerek J. C. TaiRachita YadavJakob GroveJack M. FuAjay NadigCaitlin E. CareyNikolas BayaJonas Bybjerg-GrauholmPreben B. MortensenThomas WergeDitte DemontisOle MorsMerete NordentoftThomas D. AlsMarie Baekvad-HansenAnders RosengrenAlexandra HavdahlAnne HedemandAarno PalotieAravinda ChakravartiDan ArkingArvis SulovariAnna StarnawskaBhooma ThiruvahindrapuramChristiaan de LeeuwCaitlin CareyChristine Ladd-AcostaCelia van der MerweBernie DevlinEdwin H. CookEvan EichlerElisabeth CorfieldGwen DielemanGerard SchellenbergHakon HakonarsonHilary CoonIsabel DziobekJacob VorstmanJessica GiraultJames S. SutcliffeJinjie DuanJohn NurnbergerJoachim HallmayerJoseph BuxbaumJoseph PivenLauren WeissLea DavisMagdalena JaneckaManuel MattheisenMatthew W. StateMichael GillMark DalyMohammed UddinOle AndreassenPeter SzatmariPhil Hyoun LeeRichard AnneyStephan RipkeKyle SatterstromSusan SantangeloSusan KuoLudger Tebartz van ElstThomas RollandThomas BougeronTinca PoldermanTychele TurnerJack UnderwoodVeera ManikandanVamsee PillalamarriVarun WarrierAlexandra PhilipsenAndreas ReifAnke HinneyBru CormandClaiton H. D. BauDiego Luiz RovarisEdmund Sonuga-BarkeElizabeth CorfieldEugenio Horacio GrevetGiovanni SalumHenrik LarssonJan BuitelaarJan HaavikJames McGoughJonna KuntsiJosephine EliaKlaus-Peter LeschMarieke KleinMark BellgroveMartin TesliPatrick W. L. LeungPedro M. PanSoren DalsgaardSandra LooSarah MedlandStephen V. FaraoneTed Reichborn-Kjennerud

geneticsfunctional convergencestatistical geneticshuman geneticsautism

Analyses of Gwas and Sub-Threshold Loci Lead to the Discovery of Dendrite Development and Morphology Dysfunction Underlying Schizophrenia Genetic Risk. Research Square (Research Square) (2021)

Rui ChenQuan WangChongchong XuQiang WeiHai YangJames SutcliffeYi JiangYing JiFeixiong ChengEdwin CookXue ZhongNancy CoxZhexing WenBingshan Li

genomicsschizophreniaschizophrenia genetic riskgeneticsmorphology dysfunctionstatisticsdendrite developmentpsychiatric genetics

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James S. Sutcliffe, PhD

Associate Professor

Vanderbilt University

Affiliations

School of Medicine

Molecular Physiology & Biophysics

James S. Sutcliffe, Phd is currently serving as a Molecular Physiology & Biophysics Associate Professor at Vanderbilt University.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

James S. Sutcliffe, PhD

Vanderbilt University

Associate Professor

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Long Covid-19 and Peripheral Serotonin: A Commentary and Reconsideration. Journal of Inflammation Research (2024)

George AndersonEdwin CookRandy BlakelyJames SutcliffeJeremy Veenstra-VanderWeele

neurologymedicinelong covidpharmacologyneuroinflammationcovid-19chronic inflammationclinical researchinflammatory diseasesinflammatory markersperipheral serotonininflammation

Maternal Serotonin Levels and Neurodevelopmental Severity in Autistic Children: A Partial Replication and Extension. JAACAP Open (2024)

Amandeep JutlaLauren C. ShuffreyStephen J. GuterGeorge M. AndersonKally C. O'ReillyAlicia K. MontgomeryJames S. SutcliffeEdwin H. CookJeremy Veenstra-VanderWeele

neurodevelopmental severitypsychologyneurodevelopmental disordersmaternal serotonin levelsautistic children

Relationship Between Maternal Serotonin Levels and Autism-Associated Genetic Variants. Journal of Clinical Investigation (2024)

Amandeep JutlaLauren C. ShuffreyStephen J. GuterKally C. O’ReillyGeorge M. AndersonJames S. SutcliffeEdwin H. CookJeremy Veenstra-VanderWeele

neurologyautism-associated genetic variantsgeneticspsychiatryclinical researchpsychiatric geneticsclinical investigationmedical geneticsmaternal serotonin levelsautism

Examining the Latent Structure and Correlates of Sensory Reactivity in Autism: A Multi-Site Integrative Data Analysis by the Autism Sensory Research Consortium. Molecular Autism (2023)

latent structuresensory reactivityneuroscienceautism

Maria NiarchouJulia M. SealockPeter StraubSandra Sanchez‐RoigeJames S. SutcliffeLea K. Davis

genomicsgeneticsgenetic ancestriespolygenic scoresmedical geneticsgenome-wide association studies

Calculating Genetic Risk for Dysfunction in Pleiotropic Biological Processes Using Whole Exome Sequencing Data. Journal of Neurodevelopmental Disorders (2022)

Olivia J. VeatchDiego R. MazzottiRobert T. SchultzTed AbelJacob J. MichaelsonEdward S. BrodkinBirkan TuncSusan G. AssoulineThomas Nickl-JockschatBeth A. MalowJames S. SutcliffeAllan I. Pack

genomicsgeneticspleiotropic biological processesdevelopmental neurobiologydevelopmental biologyneurosciencegenetic riskbioinformatics

Characterizing Sleep Disorders in an Autism-Specific Collection of Electronic Health Records. Sleep Medicine (2022)

E.V. SingerM. NiarchouA. Maxwell-HornD. HucksR. JohnstonJ.S. SutcliffeL.K. DavisB.A. Malow

pediatricsautism-specific collectionsleep medicine

Rare Coding Variation Provides Insight Into the Genetic Architecture and Phenotypic Context of Autism. Nature Genetics (2022)

genomicsgeneticsphenotypic contextpsychiatric geneticshuman geneticsgenetic architectureautism

Statistical and Functional Convergence of Common and Rare Genetic Influences on Autism at Chromosome 16p. Nature Genetics (2022)

geneticsfunctional convergencestatistical geneticshuman geneticsautism

Analyses of Gwas and Sub-Threshold Loci Lead to the Discovery of Dendrite Development and Morphology Dysfunction Underlying Schizophrenia Genetic Risk. Research Square (Research Square) (2021)

Rui ChenQuan WangChongchong XuQiang WeiHai YangJames SutcliffeYi JiangYing JiFeixiong ChengEdwin CookXue ZhongNancy CoxZhexing WenBingshan Li

genomicsschizophreniaschizophrenia genetic riskgeneticsmorphology dysfunctionstatisticsdendrite developmentpsychiatric genetics

1
2
3
4
5
14
10 / page

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