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Profil bibliographique

Cathy L. Budman

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

20Publications signalées
2967Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Obsessive-Compulsive Spectrum DisordersPersonality Disorders and PsychopathologyGambling Behavior and TreatmentsAutism Spectrum Disorder ResearchWilliams Syndrome Research

Les publications récentes

Accès ouvert 2025 article OpenAlex

Sex Differences in Natural History and Health Outcomes Among Individuals With Tic Disorders

Marisela Dy-Hollins, Lori B. Chibnik, Natasha Tracy, Lisa Osiecki et autres

OBJECTIVES: To analyze sex differences in outcomes in Tourette syndrome (TS) and Persistent Motor or Vocal tic disorders (PMVT) in the Tourette Association of America International Consortium for Genetics (TAAICG) dataset. METHODS: The relationship between sex and clinical measures was explored in …

us, nl, ca (code pays fourni par la source)

11 citations Neurology
Accès ouvert 2020 preprint OpenAlex

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

Fotis Tsetsos, Dongmei Yu, Jae Hoon Sul, Alden Y. Huang et autres

Abstract Tourette Syndrome (TS) is a neuropsychiatric disorder of complex genetic architecture involving multiple interacting genes. Here, we sought to elucidate the pathways that underlie the neurobiology of the disorder through genome-wide analysis. We analyzed genome-wide genotypic data of 3581 individuals with …

gr, us, de, ca, gb, at, hu, fr, pl, it, nl, ru (code pays fourni par la source)

7 citations medRxiv
Accès ouvert 2019 article OpenAlex

Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies

Dongmei Yu, Jae Hoon Sul, Fotis Tsetsos, Muhammad Sulaman Nawaz et autres

OBJECTIVE: Tourette's syndrome is polygenic and highly heritable. Genome-wide association study (GWAS) approaches are useful for interrogating the genetic architecture and determinants of Tourette's syndrome and other tic disorders. The authors conducted a GWAS meta-analysis and probed aggregated Tourette's syndrome polygenic risk …

us (code pays fourni par la source)

451 citations American Journal of Psychiatry
Accès ouvert 2017 article OpenAlex

Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome

Matthew E. Hirschtritt, Sabrina M. Darrow, Cornelia Illmann, Lisa Osiecki et autres

BACKGROUND: The unique phenotypic and genetic aspects of obsessive-compulsive (OCD) and attention-deficit/hyperactivity disorder (ADHD) among individuals with Tourette syndrome (TS) are not well characterized. Here, we examine symptom patterns and heritability of OCD and ADHD in TS families. METHOD: OCD and ADHD …

us, ca, nl (code pays fourni par la source)

49 citations Psychological Medicine
Accès ouvert 2016 article OpenAlex

Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome

Sabrina M. Darrow, Matthew E. Hirschtritt, Lea K. Davis, Cornelia Illmann et autres

OBJECTIVE: Phenotypic heterogeneity in Tourette syndrome is partly due to complex genetic relationships among Tourette syndrome, obsessive-compulsive disorder (OCD), and attention deficit hyperactivity disorder (ADHD). Identifying symptom-based endophenotypes across diagnoses may aid gene-finding efforts. METHOD: Assessments for Tourette syndrome, OCD, and ADHD …

ca, us (code pays fourni par la source)

57 citations American Journal of Psychiatry
Accès ouvert 2016 article OpenAlex

Social disinhibition is a heritable subphenotype of tics in Tourette syndrome

Matthew E. Hirschtritt, Sabrina M. Darrow, Cornelia Illmann, Lisa Osiecki et autres

OBJECTIVE: To identify heritable symptom-based subtypes of Tourette syndrome (TS). METHODS: Forty-nine motor and phonic tics were examined in 3,494 individuals (1,191 TS probands and 2,303 first-degree relatives). Item-level exploratory factor and latent class analyses (LCA) were used to identify tic-based subtypes. …

us (code pays fourni par la source)

35 citations Neurology
Accès ouvert 2014 article OpenAlex

Genetic association signal near NTN 4 in T ourette syndrome

Peristera Paschou, Dongmei Yu, Gloria F. Gerber, Patrick Evans et autres

Tourette syndrome (TS) is a neurodevelopmental disorder with a complex genetic etiology. Through an international collaboration, we genotyped 42 single nucleotide polymorphisms (p < 10(-3) ) from the recent TS genomewide association study (GWAS) in 609 independent cases and 610 ancestry-matched controls. …

gr, us, de, at, hu, it, fr, nl, ca, pl, tw (code pays fourni par la source)

68 citations Annals of Neurology

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