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Annals of Medicine|April 25, 2007
Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia?Jung Jin Kim, Brian H Shirts, Madhulika Dayal, et al.Journal of the National Comprehensive Cancer Network : JNCCN|September 4, 2020
Complexities of Next-Generation Sequencing in Solid Tumors: Case StudiesAlexandra O Sokolova, Brian H Shirts, Eric Q Konnick, et al.JAMA Oncology|June 28, 2019
Comparison of CDH1 Penetrance Estimates in Clinically Ascertained Families vs Families Ascertained for Multiple Gastric CancersMaegan E Roberts, John Michael O Ranola, Megan L Marshall, et al.Genome Medicine|April 18, 2023
Diagnostic yield of genetic screening in a diverse, community-ascertained cohortNandana D Rao, Jailanie Kaganovsky, Emily A Malouf, et al.Cancer Causes & Control : CCC|February 16, 2021
The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancerSukh Makhnoon, Deborah J Bowen, Brian H Shirts, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Refining the structure and content of clinical genomic reportsMichael O Dorschner, Laura M Amendola, Brian H Shirts, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 3, 2006
Aggressive prenatal care results in successful fetal outcomes in CF womenEdith Y Cheng, Chris H Goss, Edward F McKone, et al.Journal of Genetic Counseling|December 6, 2015
Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch SyndromeCarlos J Gallego, Matthew L Perez, Amber Burt, et al.Schizophrenia Research|February 9, 2010
Grey matter changes associated with host genetic variation and exposure to Herpes Simplex Virus 1 (HSV1) in first episode schizophreniaKonasale M Prasad, Mikhil N Bamne, Brian H Shirts, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2014
Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposisBrian H Shirts, Stephen J Salipante, Silvia Casadei, et al.Pageof 15