Kodi Taraszka

发表

Ensemble neural network model for detecting thyroid eye disease using external photographs

E. Eskin, N. Lapierre, D. Rootman, 2022, British Journal of Ophthalmology.

Ancestry-driven recalibration of tumor mutational burden and disparate clinical outcomes in response to immune checkpoint inhibitors.

N. Schultz, M. Berger, L. Macconaill, 2022, Cancer cell.

Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations

E. Eskin, N. Zaitlen, Kodi Taraszka, 2022, PLoS genetics.

Germline determinants of the prostate tumor genome

Natalie S. Fox, Kathleen E. Houlahan, Takafumi N. Yamaguchi, 2022, bioRxiv.

Constructing germline research cohorts from the discarded reads of clinical tumor sequences

A. Gusev, N. Zaitlen, S. Groha, 2021, Genome Medicine.

Technology dictates algorithms: recent developments in read alignment

C. Alkan, O. Mutlu, M. Alser, 2020, Genome Biology.

Leveraging pleiotropy in genome-wide association studies in multiple traits with per trait interpretations

E. Eskin, N. Zaitlen, K. Taraszka, 2020, bioRxiv.

Identifying causal variants by fine mapping across multiple studies

E. Eskin, F. Hormozdiari, N. Lapierre, 2020, bioRxiv.

Constructing germline research cohorts from the discarded reads of clinical tumor sequences

N. Zaitlen, S. Groha, A. Gusev, 2021, Genome Medicine.

MSGene: Derivation and validation of a multistate model for lifetime risk of coronary artery disease using genetic risk and the electronic health record

P. Ellinor, S. Khurshid, A. Fahed, 2023, medRxiv.

A comprehensive analysis of clinical and polygenic germline influences on somatic mutational burden.

E. Ziv, S. Groha, Robert W. Tell, 2024, American journal of human genetics.

Supplementary Note: Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations

E. Eskin, N. Zaitlen, Kodi Taraszka, 2022 .