Faculty

Institution

Unit

Venue

Carolyn Mervis

PhD

University of Louisville

Affiliations

Arts & Sciences, College of

Psychological and Brain Sciences

Carolyn Mervis is currently serving as an Arts & Sciences, College Of PhD at University of Louisville.

Honors

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Experiences

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Education

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Carolyn Mervis

University of Louisville

PhD

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genetics child development pediatrics language development williams syndrome human genetics cognitive science child language linguistics developmental psychology medical genetics neurodevelopmental disorders cognitive development genetic disorders developmental psychopathology genomics developmental neurobiology intellectual disability early childhood development young children duplication syndrome cognition child psychology genome biology language comprehension cognitive psychology cytogenetics applied developmental psychology early childhood developmental disorders chromosome biology adolescent psychology heredity developmental science reading research developmental disabilities down syndrome intellectual abilities psychological science child neurology developmental cognitive neuroscience object categorization genetic basis neural science adaptive behavior language education vision research behavioral characteristics early lexical development adult input inversion polymorphism language learning classification method psychodynamic cognitive linguistics brain function psychiatric genetics disease gene identification chromosomal rearrangements internal structure novel name-nameless category mental retardation williams syndrome region basic object categories genetic contributions vocabulary abilities environmental psychology social categorization human cognition metacognition order theory genetic analysis developmental anomalies working memory white matter developmental genetics

Notable Scholarly Works

Notable Federal Grants

Collaborators

Altered Pubertal Timing in 7Q11.23 Copy Number Variations and Associated Genetic Mechanisms. iScience (2024)

Shau-Ming WeiMichael D GregoryTiffany NashAndrea de Abreu E GouvêaCarolyn B MervisKatherine M ColeMadeline H GarveyJ Shane KippenhanDaniel P EisenbergBhaskar KolachanaPeter J SchmidtKaren F Berman

copy number variationsclimate changegeneticspubertal timing

Concurrent Predictors of Mathematics Achievement for 9-Year-Old Children With Williams Syndrome. Scientific Reports (2024)

Vitor N. GuimaraesCarolyn B. Mervis

concurrent predictorsmathematicschild development

Contrasting Neurofunctional Correlates of Face- and Visuospatial-Processing in Children and Adolescents With Williams Syndrome: Convergent Results From Four Fmri Paradigms. Scientific Reports (2024)

Madeline H. GarveyTiffany NashJ. Shane KippenhanPhilip KohnCarolyn B. MervisDaniel P. EisenbergJean YeMichael D. GregoryKaren F. Berman

cognitive neuroscienceneuroimagingfmri paradigmsgeneticswilliams syndromepediatricsneuroscience

Identifying Individuals at Risk for Surgical Supravalvar Aortic Stenosis by Polygenic Risk Score With Graded Phenotyping. medRxiv (2024)

D. LiuC.B. MervisM.D. LevinE. BiaminoM.F. BedeschiM.C. DigilioG.M. SqueoR. VillaS. OsgoodJ.A. FreemanN. RajaG. MerlaA.E. RobertsC.A. MorrisL.R. OsborneB.A. Kozel

public healthmedicinepatient safetydisease susceptibilitygenetic predispositiondisease risk assessmentgeneticsprognostic evaluationgraded phenotypingpolygenic risk scorepolygenic riskcardiovascular surgerysystemic riskgenetic epidemiologycardiovascular disease

Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams–Beuren Syndrome. Journal of the American Heart Association (2024)

Delong LiuCharles J. BillingtonNeelam RajaZoe C. WongMark D. LevinWulfgang ReschCamille AlbaDaniel N. HupaloElisa BiaminoMaria Francesca BedeschiMaria Cristina DigilioGabriella Maria SqueoRoberta VillaPheobe C. R. ParrishRussell H. KnutsenSharon OsgoodJoy A. FreemanClifton L. DalgardGiuseppe MerlaBarbara R. PoberCarolyn B. MervisAmy E. RobertsColleen A. MorrisLucy R. OsborneBeth A. Kozel

emergency medicineclinical evidencevascular diseasevascular adaptationhematologythrombosisvascular biologycardiologycerebrovascular diseaseimmune pathwayswilliams-beuren syndromemammalian biologyhepatologydevelopmental biologystrokeimmunologycardiovascular researchvascular outcomesrespiratory medicinevalve diseasecardiovascular disease

P212: Modifiers of Arterial Stenosis in Williams Syndrome: Using Genomics to Discover Drivers of Vessel-Specific Outcomes. Genetics in Medicine Open (2024)

Ashley GolbusDelong LiuMark LevinNeelam RajaElisa BiaminoMaria BedeschiMaria DigilioGabriella SqueoRoberta VillaJoy Lynne FreemanSharon OsgoodGiuseppe MerlaBarbara PoberCarolyn MervisAmy RobertsColleen MorrisLucy OsborneBeth Kozel

genomic medicineangiologyapplied geneticswilliams syndromehuman geneticsgenome biologymedicinehematologyvessel-specific outcomesvascular biologymedical geneticshealth sciencescardiologycerebrovascular diseasefunctional genomicsgenomicsarterial stenosisvascular surgerycardiovascular researchgeneticsexperimental medicine

Syntaxin1A Overexpression and Pain Insensitivity in Individuals With 7Q11.23 Duplication Syndrome. JCI Insight (2024)

Michael J. IadarolaMatthew R. SapioAmelia J. LoydpiersonCarolyn B. MervisJill C. FehrenbacherMichael R. VaskoDragan MaricDaniel P. EisenbergTiffany A. NashJ. Shane KippenhanMadeline H. GarveyAndrew J. MannesMichael D. GregoryKaren F. Berman

genetic disordersneurogeneticsgeneticspain insensitivityneurodevelopmental disordersduplication syndromedevelopmental biologyhuman geneticsneuroscience

313. Alterations in Cerebral Blood Flow in Williams Syndrome. Biological Psychiatry (2023)

Olivia R. KlineTiffany A. NashMichael D. GregoryJ. Shane KippenhanDanya A. AdamsAnne K. IlsleyCourtney J. PfisterMadeline R. HamborgPhilip D. KohnDaniel P. EisenbergCarolyn B. MervisKaren F. Berman

biological psychiatryneurologygeneticspsychiatrycerebral blood flowwilliams syndromehuman genetics

344. Developmental Trajectories of Neural Activation During Face Processing in Williams Syndrome. Biological Psychiatry (2023)

Danya A. AdamsTiffany A. NashJ. Shane KippenhanOlivia R. KlineAnne K. IlsleyCourtney J. PfisterMadeline R. HamborgMichael D. GregoryPhilip D. KohnDaniel EisenbergCarolyn B. MervisKaren F. Berman

biological psychiatrygeneticsdevelopmental trajectoriesface processingpsychiatrydevelopmental neurobiologywilliams syndromeneuroscienceneural activation

Dna Methylation Profiles in Individuals With Rare, Atypical 7Q11.23 Cnvs Correlate With Gtf2I and Gtf2Ird1 Copy Number. npj Genomic Medicine (2023)

Emma StrongCarolyn B. MervisElaine TamColleen A. MorrisBonita P. Klein-TasmanShelley L. VellemanLucy R. Osborne

genomicsgeneticsgenetic variationdna methylation profilesmolecular biologyhuman genetics

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Carolyn Mervis

PhD

University of Louisville

Affiliations

Arts & Sciences, College of

Psychological and Brain Sciences

Carolyn Mervis is currently serving as an Arts & Sciences, College Of PhD at University of Louisville.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Carolyn Mervis

University of Louisville

PhD

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Altered Pubertal Timing in 7Q11.23 Copy Number Variations and Associated Genetic Mechanisms. iScience (2024)

Shau-Ming WeiMichael D GregoryTiffany NashAndrea de Abreu E GouvêaCarolyn B MervisKatherine M ColeMadeline H GarveyJ Shane KippenhanDaniel P EisenbergBhaskar KolachanaPeter J SchmidtKaren F Berman

copy number variationsclimate changegeneticspubertal timing

Concurrent Predictors of Mathematics Achievement for 9-Year-Old Children With Williams Syndrome. Scientific Reports (2024)

Vitor N. GuimaraesCarolyn B. Mervis

concurrent predictorsmathematicschild development

Madeline H. GarveyTiffany NashJ. Shane KippenhanPhilip KohnCarolyn B. MervisDaniel P. EisenbergJean YeMichael D. GregoryKaren F. Berman

cognitive neuroscienceneuroimagingfmri paradigmsgeneticswilliams syndromepediatricsneuroscience

Identifying Individuals at Risk for Surgical Supravalvar Aortic Stenosis by Polygenic Risk Score With Graded Phenotyping. medRxiv (2024)

D. LiuC.B. MervisM.D. LevinE. BiaminoM.F. BedeschiM.C. DigilioG.M. SqueoR. VillaS. OsgoodJ.A. FreemanN. RajaG. MerlaA.E. RobertsC.A. MorrisL.R. OsborneB.A. Kozel

Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams–Beuren Syndrome. Journal of the American Heart Association (2024)

P212: Modifiers of Arterial Stenosis in Williams Syndrome: Using Genomics to Discover Drivers of Vessel-Specific Outcomes. Genetics in Medicine Open (2024)

Syntaxin1A Overexpression and Pain Insensitivity in Individuals With 7Q11.23 Duplication Syndrome. JCI Insight (2024)

genetic disordersneurogeneticsgeneticspain insensitivityneurodevelopmental disordersduplication syndromedevelopmental biologyhuman geneticsneuroscience

313. Alterations in Cerebral Blood Flow in Williams Syndrome. Biological Psychiatry (2023)

Olivia R. KlineTiffany A. NashMichael D. GregoryJ. Shane KippenhanDanya A. AdamsAnne K. IlsleyCourtney J. PfisterMadeline R. HamborgPhilip D. KohnDaniel P. EisenbergCarolyn B. MervisKaren F. Berman

biological psychiatryneurologygeneticspsychiatrycerebral blood flowwilliams syndromehuman genetics

344. Developmental Trajectories of Neural Activation During Face Processing in Williams Syndrome. Biological Psychiatry (2023)

Danya A. AdamsTiffany A. NashJ. Shane KippenhanOlivia R. KlineAnne K. IlsleyCourtney J. PfisterMadeline R. HamborgMichael D. GregoryPhilip D. KohnDaniel EisenbergCarolyn B. MervisKaren F. Berman

biological psychiatrygeneticsdevelopmental trajectoriesface processingpsychiatrydevelopmental neurobiologywilliams syndromeneuroscienceneural activation

Dna Methylation Profiles in Individuals With Rare, Atypical 7Q11.23 Cnvs Correlate With Gtf2I and Gtf2Ird1 Copy Number. npj Genomic Medicine (2023)

Emma StrongCarolyn B. MervisElaine TamColleen A. MorrisBonita P. Klein-TasmanShelley L. VellemanLucy R. Osborne

genomicsgeneticsgenetic variationdna methylation profilesmolecular biologyhuman genetics

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2
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18
10 / page

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