K. Walker

发表

Trans-ancestry mutational landscape of hepatocellular carcinoma genomes

Hiromi Nakamura, Hidenori Ojima, Yasushi Totoki, 2014, Nature Genetics.

The relationship of JAK2V617F and acquired UPD at chromosome 9p in polycythemia vera

R. Gibbs, D. Muzny, D. Wheeler, 2014, Leukemia.

The third international hackathon for applying insights into large-scale genomic composition to use cases in a wide range of organisms

Sree Rohit Raj Kolora, Rupesh K. Kesharwani, David C. Molik, 2022, F1000Research.

Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytes

R. Gibbs, D. Muzny, D. Wheeler, 2014, Leukemia.

Characterizing reduced coverage regions through comparison of exome and genome sequencing data across ten centers

Mahdi Sarmady, Rashesh V. Sanghvi, Christian J. Buhay, 2017, Genetics in Medicine.

Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol).

Carolyn R Rohrer Vitek, Tammy M. McAllister, R. Gibbs, 2019, International journal of epidemiology.

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Karynne E. Patterson, E. Venner, D. Kalra, 2022, medRxiv.

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2

C. Shaw, J. Lupski, R. Gibbs, 2019, Cell.

Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death

J. Lupski, R. Gibbs, D. Muzny, 2015, Molecular genetics & genomic medicine.

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates

Mark J. P. Chaisson, Arun K. Subramaniyan, Justin N. Vaughn, 2021, F1000Research.

An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates.

Eric T. Dawson, Daniel L. Cameron, Zev N. Kronenberg, 2021, F1000Research.

Frequency of genomic incidental findings among 21,915 eMERGE network participants

Magalie S Leduc, Marc S. Williams, N. Lennon, 2020, Genetics in Medicine.

Ampullary Cancers Harbor ELF3 Tumor Suppressor Gene Mutations and Exhibit Frequent WNT Dysregulation.

R. Gibbs, D. Muzny, H. Dinh, 2016, Cell reports.

Human genome meeting 2016

Kumar Kshitij Patel, A. Pang, W. Chung, 2016, Human Genomics.

Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.

Joseph A. Sutton, Krishna R. Kalari, Sebastian M. Armasu, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Population-based studies reveal differences in the allelic frequencies of two functionally significant human interleukin-4 receptor polymorphisms in several ethnic groups

M. Caggana, K. Walker, A. Walsh, 1999, Genetics in Medicine.

Whole genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

N. Lennon, R. Gibbs, D. Nickerson, 2021, medRxiv.

Human genome meeting 2016

A. Pang, W. Chung, J. Lupski, 2016, Human Genomics.

Human genome meeting 2016

Kumar Kshitij Patel, Jose Maria Gonzalez-Izarzugaza, A. Pang, 2016, Human Genomics.

Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

N. Lennon, R. Gibbs, D. Nickerson, 2022, Genome Medicine.