User profiles for Doga Gulhan

Doğa Gülhan

Faculty Member, Harvard Medical School
Verified email at hms.harvard.edu
Cited by 2954

Detecting the mutational signature of homologous recombination deficiency in clinical samples

DC Gulhan, JJK Lee, GEM Melloni, I Cortes-Ciriano… - Nature …, 2019 - nature.com
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-…

Computational analysis of cancer genome sequencing data

I Cortés-Ciriano, DC Gulhan, JJK Lee… - Nature Reviews …, 2022 - nature.com
Distilling biologically meaningful information from cancer genome sequencing data requires
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

A Färkkilä, DC Gulhan, J Casado, CA Jacobson… - Nature …, 2020 - nature.com
Combined PARP and immune checkpoint inhibition has yielded encouraging results in
ovarian cancer, but predictive biomarkers are lacking. We performed immunogenomic profiling …

Erratum to: A hybrid strong/weak coupling approach to jet quenching

J Casalderrey-Solana, DC Gulhan, JG Milhano… - Journal of High Energy …, 2015 - Springer
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 …

[HTML][HTML] The origins and genetic interactions of KRAS mutations are allele- and tissue-specific

JH Cook, GEM Melloni, DC Gulhan, PJ Park… - Nature …, 2021 - nature.com
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 …

[HTML][HTML] ERα-associated translocations underlie oncogene amplifications in breast cancer

…, TC Cheong, J Espejo Valle-Inclan, C Chu, DC Gulhan… - Nature, 2023 - nature.com
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…

Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements

…, Z Zhou, CL Bohrson, Y Zhao, H Jin, D Gulhan… - Nature …, 2022 - nature.com
Accurate somatic mutation detection from single-cell DNA sequencing is challenging due to
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 …

[HTML][HTML] Angular structure of jet quenching within a hybrid strong/weak coupling model

J Casalderrey-Solana, DC Gulhan, JG Milhano… - Journal of High Energy …, 2017 - Springer
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 …

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

…, SN Kim, A Nadig, LJ Luquette, DC Gulhan… - Nature …, 2021 - nature.com
We characterize the landscape of somatic mutations—mutations occurring after fertilization—in
the human brain using ultra-deep (~250×) whole-genome sequencing of prefrontal …