User profiles for Doga Gulhan
Doğa GülhanFaculty Member, Harvard Medical School Verified email at hms.harvard.edu Cited by 2954 |
Detecting the mutational signature of homologous recombination deficiency in clinical samples
Mutations in BRCA1 and/or BRCA2 (BRCA1/2) are the most common indication of deficiency
in the homologous recombination (HR) DNA repair pathway. However, recent genome-…
in the homologous recombination (HR) DNA repair pathway. However, recent genome-…
Computational analysis of cancer genome sequencing data
Distilling biologically meaningful information from cancer genome sequencing data requires
comprehensive identification of somatic alterations using rigorous computational methods. …
comprehensive identification of somatic alterations using rigorous computational methods. …
[HTML][HTML] Immunogenomic profiling determines responses to combined PARP and PD-1 inhibition in ovarian cancer
Combined PARP and immune checkpoint inhibition has yielded encouraging results in
ovarian cancer, but predictive biomarkers are lacking. We performed immunogenomic profiling …
ovarian cancer, but predictive biomarkers are lacking. We performed immunogenomic profiling …
Erratum to: A hybrid strong/weak coupling approach to jet quenching
We propose and explore a new hybrid approach to jet quenching in a strongly coupled
medium. The basis of this phenomenological approach is to treat physics processes at different …
medium. The basis of this phenomenological approach is to treat physics processes at different …
[HTML][HTML] The origins and genetic interactions of KRAS mutations are allele- and tissue-specific
Mutational activation of KRAS promotes the initiation and progression of cancers, especially
in the colorectum, pancreas, lung, and blood plasma, with varying prevalence of specific …
in the colorectum, pancreas, lung, and blood plasma, with varying prevalence of specific …
[HTML][HTML] ERα-associated translocations underlie oncogene amplifications in breast cancer
Focal copy-number amplification is an oncogenic event. Although recent studies have revealed
the complex structure 1 , 2 – 3 and the evolutionary trajectories 4 of oncogene amplicons…
the complex structure 1 , 2 – 3 and the evolutionary trajectories 4 of oncogene amplicons…
Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements
Accurate somatic mutation detection from single-cell DNA sequencing is challenging due to
amplification-related artifacts. To reduce this artifact burden, an improved amplification …
amplification-related artifacts. To reduce this artifact burden, an improved amplification …
[HTML][HTML] Phase II study of avelumab in patients with mismatch repair deficient and mismatch repair proficient recurrent/persistent endometrial cancer
…, W Luo, JF Liu, DC Gulhan… - Journal of Clinical …, 2019 - ncbi.nlm.nih.gov
PURPOSE Despite the tissue-agnostic approval of pembrolizumab in mismatch repair deficient
(MMRD) solid tumors, important unanswered questions remain about the role of immune …
(MMRD) solid tumors, important unanswered questions remain about the role of immune …
[HTML][HTML] Angular structure of jet quenching within a hybrid strong/weak coupling model
Within the context of a hybrid strong/weak coupling model of jet quenching, we study the
modification of the angular distribution of the energy within jets in heavy ion collisions, as …
modification of the angular distribution of the energy within jets in heavy ion collisions, as …
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing
We characterize the landscape of somatic mutations—mutations occurring after fertilization—in
the human brain using ultra-deep (~250×) whole-genome sequencing of prefrontal …
the human brain using ultra-deep (~250×) whole-genome sequencing of prefrontal …