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Claire C. Homan · SciRah

Researcher profile · Semantic Scholar

Claire C. Homan

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Claire C. Homan — researcher profile on SciRah

h-index: 16
Works: 30
Citations: 989

Most-cited papers

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.
Anna L. Brown, P. Arts, C. Carmichael, M. Babic +55 more
2020Blood Advances138 citations Open access
Semantic Scholar
Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth.
Claire C. Homan, Raman Kumar, L. Nguyen, E. Haan +7 more
2014American Journal of Human Genetics138 citations Open access
Semantic Scholar
The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth.
L. Jolly, Claire C. Homan, Reuben K. Jacob, S. Barry +1 more
2013Human Molecular Genetics132 citations
Semantic Scholar
Zinc and Zinc Transporters in Macrophages and Their Roles in Efferocytosis in COPD
R. Hamon, Claire C. Homan, H. Tran, Violet Mukaro +9 more
2014PLoS ONE80 citations Open access
Semantic Scholar
Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice
Daniel T. Pederick, Claire C. Homan, E. Jaehne, Sandra G. Piltz +6 more
2016Scientific Reports68 citations Open access
Semantic Scholar
Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26
Claire C. Homan, H. Scott, Anna L. Brown
2023Blood55 citations Open access
Semantic Scholar
GATA2 deficiency syndrome: A decade of discovery
Claire C. Homan, P. Venugopal, P. Arts, N. Shahrin +9 more
2021Human Mutation53 citations Open access
Semantic Scholar
PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy.
Claire C. Homan, S. Pederson, Thu-Hien To, Chuan Tan +6 more
2018Neurobiology of Disease53 citations Open access
Semantic Scholar
Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies
C. Saygin, G. Roloff, C. Hahn, R. Chhetri +16 more
2022Blood Advances43 citations Open access
Semantic Scholar
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
Claire C. Homan, Sarah L. King-Smith, D. Lawrence, P. Arts +39 more
2021Haematologica40 citations Open access
Semantic Scholar
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
Claire C. Homan, M. Drazer, Kai Yu, D. Lawrence +61 more
2023Blood Advances36 citations Open access
Semantic Scholar
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα)
Duyen H. Pham, Chuan Tan, Claire C. Homan, Kristy L. Kolc +6 more
2017Human Molecular Genetics31 citations Open access
Semantic Scholar
Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery
Raman Kumar, A. Gardner, Claire C. Homan, Evelyn Douglas +27 more
2018Human Mutation25 citations Open access
Semantic Scholar
Disrupted Excitatory Synaptic Contacts and Altered Neuronal Network Activity Underpins the Neurological Phenotype in PCDH19-Clustering Epilepsy (PCDH19-CE)
S. Mincheva-Tasheva, A. N. Nieto Guil, Claire C. Homan, J. Gécz +1 more
2021Molecular Neurobiology24 citations
Semantic Scholar
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations
M. Drazer, Claire C. Homan, Kai Yu, Marcela Cavalcante de Andrade Silva +19 more
2022Blood Advances21 citations Open access
Semantic Scholar
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females
Matilda R. Jackson, Karagh E. Loring, Claire C. Homan, M. Thai +7 more
2019Life Science Alliance20 citations Open access
Semantic Scholar
Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Jiarna R. Zerella, Claire C. Homan, P. Arts, Xuzhu Lin +49 more
2024Blood14 citations Open access
Semantic Scholar
Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41
Anna L. Brown, Claire C. Homan, M. Drazer, Kai Yu +60 more
2022Blood6 citations
Semantic Scholar
Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy
Jiarna R. Zerella, Claire C. Homan, P. Arts, Anna L. Brown +2 more
2023Frontiers in Oncology4 citations Open access
Semantic Scholar
Robust imaging and gene delivery to study human lymphoblastoid cell lines
L. Jolly, Ying Sun, R. Carroll, Claire C. Homan +1 more
2018Journal of Human Genetics4 citations
Semantic Scholar
An Integrative Genomic Approach to Examine Mutations and Biological Pathways Associated with Hematological Malignancy Development in DDX41 Mutated Families
P. Venugopal, J. Cheah, L. Eshraghi, N. Shahrin +9 more
2019Blood2 citations Open access
Semantic Scholar
Another Fanconi anemia gene joins the club
Claire C. Homan, Hamish S. Scott, P. Venugopal
2025Journal of Clinical Investigation1 citations Open access
Semantic Scholar
Targeting RUNX1 Germline Variants: Agents Under Investigation
Saman Ghalamkari, Christopher N. Hahn, Amelia Lau, Hamish S. Scott +2 more
2025Current Hematologic Malignancy Reports1 citations
Semantic Scholar
ERG Is a New Predisposition Gene for Bone Marrow Failure and Hematological Malignancy
Hamish S. Scott, Jiarna R. Zerella, Claire C. Homan, P. Arts +35 more
2023Blood1 citations Open access
Semantic Scholar
Protocadherin Mutations in Neurodevelopmental Disorders
Duyen H. Pham, Chuan Tan, Claire C. Homan, L. Jolly +1 more
20161 citations
Semantic Scholar
ANKRD26-related thrombocytopenia: Hematologic malignancy characteristics, clinical outcomes, and precursor states
Lauren G. Banaszak, Bianca Barredo, M. Wlodarski, Sara Lewis +40 more
2025Blood0 citations
Semantic Scholar
Cover, Volume 42, Issue 11
Claire C. Homan, P. Venugopal, P. Arts, N. Shahrin +9 more
2021Human Mutation0 citations Open access
Semantic Scholar
Clonal hematopoiesis in individuals with ANKRD26 or ETV6 germline mutations
M. Drazer, Claire C. Homan, Kai Yu, M. C. de Andrade Silva +18 more
2021bioRxiv0 citations Open access
Semantic Scholar
DEVELOPMENT OF A DATA PORTAL FOR AGGREGATION AND ANALYSIS OF GENOMICS DATA IN FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO MYELOID MALIGNANCY – THE RUNX1.DB
Claire C. Homan, M. Armstrong, J. Dobbins, D. Lawrence +7 more
2019Experimental Hematology0 citations Open access
Semantic Scholar
AN INTEGRATIVE GENOMIC APPROACH TO EXAMINE MUTATIONS AND BIOLOGICAL PATHWAYS ASSOCIATED WITH HAEMATOLOGICAL MALIGNANCY DEVELOPMENT IN DDX41 MUTATED FAMILIES
J. Cheah, Anna L. Brown, L. Eshraghi, Jing-Hua Feng +8 more
2019Experimental Hematology0 citations Open access
Semantic Scholar

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