J. Saldivar

Robert Brian Jenkins, Marc Ladanyi, Philip T Cagle, 2013, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

G. Giaccone, M. Ladanyi, M. Beasley, 2013, The Journal of molecular diagnostics : JMD.

Prostatic adenocarcinoma with novel NTRK3 gene fusion: a case report.

Shu Yang, Xiuping Yu, J. Saldivar, 2019, American journal of clinical and experimental urology.

Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma.

G. Hannum, C. Deciu, M. Ehrich, 2015, Clinical chemistry.

Non-Invasive Prenatal Chromosomal Aneuploidy Testing - Clinical Experience: 100,000 Clinical Samples

Amin R. Mazloom, Paul Oeth, Cosmin Deciu, 2014, PloS one.

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acids

S S Sommer, S. Sommer, Jinong Feng, 2008, Oncogene.

Familial deletion within NLGN4 associated with autism and Tourette syndrome

S. Sommer, J. Picker, J. Saldivar, 2008, European Journal of Human Genetics.

EGFR-Mutated Lung Cancer With T 790 M-Acquired Resistance in the Brain and Histologic Transformation in the Lung

A. Marchevsky, M. Fishbein, K. Reckamp, 2013 .

Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking‐associated signature

Kathleen A Hill, Kai Li, S. Sommer, 2007, Human mutation.

Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma

Amin R. Mazloom, W. Meschino, J. Canick, 2013, Prenatal diagnosis.

Clinical Impact of Pharmacogenetic-Guided Treatment for Patients Exhibiting Neuropsychiatric Disorders: A Randomized Controlled Trial.

S. Vaishnavi, J. Gariépy, J. Saldivar, 2017, The primary care companion for CNS disorders.

Initial assessment of the benefits of implementing pharmacogenetics into the medical management of patients in a long-term care facility

J. Saldivar, D. Taylor, E. Sugarman, 2016, Pharmacogenomics and personalized medicine.

Validation of an exome and transcriptome based diagnostic platform enabling clinical cancer therapy selection and emerging composite biomarkers for immunotherapy.

M. Clark, M. Morra, P. Tandon, 2020 .

Noninvasive prenatal testing for microdeletion syndromes and expanded trisomies: proceed with caution.

D. H. Farkas, A. Bombard, J. Saldivar, 2014, Obstetrics and gynecology.

Analytic validation of NeXT Dx™, a comprehensive genomic profiling assay

J. Lyle, M. Morra, L. Goodman, 2023, Oncotarget.

Hereditary leukemia due to rare RUNX1c splice variant (L472X) presents with eczematous phenotype.

J. Weitzel, R. Bhatia, P. Parker, 2012, International journal of clinical medicine.

EGF Receptor Testing for Non‐Small Cell Lung Carcinomas

S. Sommer, J. Saldivar, Zhenbin Chen, 2006, Current protocols in human genetics.