C. Esteves

Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing

V. Jobanputra, C. Morton, M. Talkowski, 2015, Prenatal diagnosis.

Sequencing and curation strategies for identifying candidate glioblastoma treatments

Ajay K. Royyuru, Vladimir Vacic, Laxmi Parida, 2019, BMC Medical Genomics.

Using FISH to increase the yield and accuracy of karyotypes from spontaneous abortion specimens

V. Jobanputra, D. Warburton, J. Kline, 2011, Prenatal diagnosis.

Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency

V. Jobanputra, A. Abhyankar, M. Lamendola-Essel, 2017, Clinical case reports.

Sequencing and curation strategies for identifying candidate glioblastoma treatments

Ewa A. Bergmann, Vanessa V. Michelini, V. Jobanputra, 2019, BMC Medical Genomics.