Paul S. Wang

Adelaide, SA, Australia

Last Updated: 09/26/2026

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Found 19 publications

Mitochondrial DNA mutations are associated with impaired oxidative phosphorylation and enhanced imatinib response in chronic myeloid leukemia.

Mitochondrial DNA mutations are associated with impaired oxidative phosphorylation and enhanced imatinib response in chronic myeloid leukemia.

Journal: HemaSphere

Published: March 18, 2026

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.

Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.

Journal: Nature medicine

Published: July 10, 2023

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.

Journal: Blood advances

Published: February 23, 2023

Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention.

Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention.

Journal: Haematologica

Published: October 06, 2022

TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype.

TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype.

Journal: Blood

Published: September 06, 2022

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.

Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.

Journal: Nature medicine

Published: December 29, 2021

RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia.

RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia.

Journal: The Journal of molecular diagnostics : JMD

Published: December 05, 2021

Childhood acute myeloid leukemia shows a high level of germline predisposition.

Childhood acute myeloid leukemia shows a high level of germline predisposition.

Journal: Blood

Published: May 28, 2021

Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia.

Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia.

Journal: BMC medical genomics

Published: December 24, 2020

Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas.

Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas.

Journal: Journal of the Endocrine Society

Published: February 18, 2020

Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome.

Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome.

Journal: American journal of medical genetics. Part A

Published: December 20, 2019

Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia.

Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia.

Journal: Leukemia

Published: November 04, 2019

Showing 1-12 of 19

Last Updated: 09/26/2026