Kerry K. Brown
Tissue Gene (United States)(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Congenital heart defects research, Hearing, Cochlea, Tinnitus, Genetics, Congenital Heart Disease Studies
Most-Cited Works
- → De novo mutations in histone-modifying genes in congenital heart disease(2013)953 cited
- → American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants(2011)952 cited
- → ACMG clinical laboratory standards for next-generation sequencing(2013)914 cited
- → Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project(2008)150 cited
- → Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)(2009)83 cited
- → HOXA2Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss(2013)51 cited
- → NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness(2009)46 cited
- → Molecular Diagnosis of Hearing Loss(2012)28 cited
- → X-Linked Deafness-2 (DFNX2) Phenotype Associated With a Paracentric Inversion Upstream of POU3F4(2014)22 cited
- → Loss of LDAH associated with prostate cancer and hearing loss(2018)18 cited