Marissa S. Ellingson

CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum

R. Pfundt, O. Pietiläinen, A. Palotie, 2019, Genetics in Medicine.

Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapy

Ann M. Moyer, Steven N. Hart, Krishna R. Kalari, 2015, Breast Cancer Research and Treatment.

Determining the frequency of pathogenic germline variants from exome sequencing in patients with castrate-resistant prostate cancer

Krishna R. Kalari, Kimberly A. Schahl, K. Kalari, 2016, BMJ Open.

Creating Technical Documentation for Digital Natives

Marissa S. Ellingson, 2014 .

Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol.

Christopher G Chute, Eric D Wieben, Jyotishman Pathak, 2014, Mayo Clinic proceedings.

A prospective genome-wide study of prostate cancer metastases reveals association of wnt pathway activation and increased cell cycle proliferation with primary resistance to abiraterone acetate–prednisone

Krishna R. Kalari, Liang Wang, K. Kalari, 2018, Annals of oncology : official journal of the European Society for Medical Oncology.

WDR37 syndrome: identification of a distinct new cluster of disease-associated variants and functional analyses of mutant proteins

E. Sorokina, D. Babovic‐Vuksanovic, Marissa S. Ellingson, 2021, Human Genetics.

CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity

Magalie S Leduc, D. Goldstein, E. van Binsbergen, 2021, Epilepsia.

Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart review

N. Lindor, I. Winship, Marissa S. Ellingson, 2014, Genetics in Medicine.

Impact of integrated translational research on clinical exome sequencing

Michael T. Zimmermann, Gavin R. Oliver, Tammy M. McAllister, 2020, Genetics in Medicine.

RNA‐Seq detects a SAMD12‐EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas

Gavin R. Oliver, E. Thorland, P. Blackburn, 2019, Molecular genetics & genomic medicine.