Search Results - "Green, Claire"
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Relative Alignment between the Magnetic Field and Molecular Gas Structure in the Vela C Giant Molecular Cloud Using Low- and High-density Tracers
Published in The Astrophysical journal (20-06-2019)“…We compare the magnetic field orientation for the young giant molecular cloud Vela C inferred from 500 m polarization maps made with the BLASTPol balloon-borne…”
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2
The prognostic significance of IDH2 mutations in AML depends on the location of the mutation
Published in Blood (14-07-2011)“…We have investigated the prognostic significance of isocitrate dehydrogenase 2 (IDH2) mutations in 1473 younger adult acute myeloid leukemia patients treated…”
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3
Prognostic Significance of CEBPA Mutations in a Large Cohort of Younger Adult Patients With Acute Myeloid Leukemia: Impact of Double CEBPA Mutations and the Interaction With FLT3 and NPM1 Mutations
Published in Journal of clinical oncology (01-06-2010)“…To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein alpha (CEBPA) gene in acute myeloid leukemia (AML) and to examine…”
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4
Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2
Published in Nature genetics (01-12-2011)“…Adrienne Flanagan and colleagues report the identification of somatic mosaic mutations in the IDH1 and IDH2 genes in tumors from individuals with Ollier…”
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5
Interventions Targeting Depression and Posttraumatic Stress Disorder in United States Black Women Experiencing Intimate Partner Violence: A Systematic Review
Published in Trauma, Violence, & Abuse (01-07-2024)“…There is a dearth of evidence indicating the effectiveness of psychological interventions targeting depression and/or posttraumatic stress disorder (PTSD) for…”
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Book Review Journal Article -
6
The Pathway Coexpression Network: Revealing pathway relationships
Published in PLoS computational biology (01-03-2018)“…A goal of genomics is to understand the relationships between biological processes. Pathways contribute to functional interplay within biological processes…”
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The prognostic significance of IDH1 mutations in younger adult patients with acute myeloid leukemia is dependent on FLT3/ITD status
Published in Blood (14-10-2010)“…Mutations in the isocitrate dehydrogenase gene (IDH1) were recently described in patients with acute myeloid leukemia (AML). To investigate their prognostic…”
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Journal Article -
8
Integrated methylome and phenome study of the circulating proteome reveals markers pertinent to brain health
Published in Nature communications (09-08-2022)“…Characterising associations between the methylome, proteome and phenome may provide insight into biological pathways governing brain health. Here, we report an…”
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Mutation of the Wilms’ Tumor 1 Gene Is a Poor Prognostic Factor Associated With Chemotherapy Resistance in Normal Karyotype Acute Myeloid Leukemia: The United Kingdom Medical Research Council Adult Leukaemia Working Party
Published in Journal of clinical oncology (20-11-2008)“…To determine the clinical relevance of Wilms' tumor 1 (WT1) gene mutations in acute myeloid leukemia (AML) with normal karyotype (NK). Exons 7 and 9 of WT1…”
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Journal Article Conference Proceeding -
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Social network analysis and whole genome sequencing in a cohort study to investigate TB transmission in an educational setting
Published in BMC infectious diseases (13-02-2019)“…TB outbreaks in educational institutions can result in significant transmission and pose a considerable threat to TB control. Investigation using traditional…”
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Structural brain correlates of childhood trauma with replication across two large, independent community-based samples
Published in European psychiatry (26-01-2023)“…Childhood trauma and adversity are common across societies and have strong associations with physical and psychiatric morbidity throughout the life-course. One…”
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Epigenome-wide association study of global cortical volumes in generation Scotland: Scottish family health study
Published in Epigenetics (03-10-2022)“…A complex interplay of genetic and environmental risk factors influence global brain structural alterations associated with brain health and disease…”
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13
GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations
Published in British journal of haematology (01-06-2013)“…Summary GATA2 mutations have recently been reported in acute myeloid leukaemia (AML) patients with CEBPA‐double mutations. To explore their impact on this…”
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14
Hair glucocorticoids are associated with childhood adversity, depressive symptoms and reduced global and lobar grey matter in Generation Scotland
Published in Translational psychiatry (12-10-2021)“…Hypothalamic–pituitary–adrenal (HPA) axis dysregulation has been commonly reported in major depressive disorder (MDD), but with considerable heterogeneity of…”
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15
A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis
Published in Acta neuropathologica communications (16-03-2017)“…Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease that lacks a predictive and broadly applicable biomarker. Continued focus on…”
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16
It’s All Over: Romantic Relationships, Endurance and Loyalty in the Songs of Northern Irish Politically-Motivated Prisoners
Published in Estudios irlandeses (01-03-2019)“…This article examines the issue of romantic relationships in the cultural production of politically-motivated prisoners during the recent Northern Irish…”
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A Tapestried Review of the Fully-virtual, Non-traditional (Un)conference "MAKING shiFt HAPPEN: Female Academics Creating Personal and Professional Alchemy in the Academy," Co-convened by Alison Black and Rachael Dwyer
Published in Art/Research International (30-08-2019)“…These storied and aesthetic offerings are presented as an alchemic tapestry of experiences and responses to the conference MAKING shiFt HAPPEN. This innovative…”
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New approach is needed to address K-12 equity gaps
Published in Indianapolis Business Journal (13-08-2021)Get full text
Journal Article Trade Publication Article -
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Restoring optimism begins with building trust
Published in Indianapolis Business Journal (23-08-2019)Get full text
Journal Article Trade Publication Article -
20
De novo SETD5 loss‐of‐function variant as a cause for intellectual disability in a 10‐year old boy with an aberrant blind ending bronchus
Published in American journal of medical genetics. Part A (01-12-2017)“…Although rare, 3p microdeletion cases have been well described in the clinical literature. The clinical phenotype includes; intellectual disability (ID),…”
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