A TMPRSS2‐ERG gene signature predicts prognosis of patients with prostate adenocarcinoma
Zhou, Emily, Zhang, Baoyi, Zhu, Kenneth, Schaafsma, Evelien, Kumar, Runjun D., Cheng, Chao
Published in Clinical and translational medicine (01.12.2020)
Published in Clinical and translational medicine (01.12.2020)
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Journal Article
A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testing
Kumar, Runjun D., Burrage, Lindsay C., Bartos, Jan, Ali, Saima, Schmitt, Eric, Nagamani, Sandesh C.S., LeMons, Cynthia
Published in Molecular genetics and metabolism reports (01.03.2021)
Published in Molecular genetics and metabolism reports (01.03.2021)
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Journal Article
DGIdb: mining the druggable genome
Griffith, Malachi, Griffith, Obi L, Coffman, Adam C, Weible, James V, McMichael, Josh F, Spies, Nicholas C, Koval, James, Das, Indraniel, Callaway, Matthew B, Eldred, James M, Miller, Christopher A, Subramanian, Janakiraman, Govindan, Ramaswamy, Kumar, Runjun D, Bose, Ron, Ding, Li, Walker, Jason R, Larson, David E, Dooling, David J, Smith, Scott M, Ley, Timothy J, Mardis, Elaine R, Wilson, Richard K
Published in Nature methods (01.12.2013)
Published in Nature methods (01.12.2013)
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Journal Article
Clinical genome sequencing: Three years’ experience at a tertiary children’s hospital
Kumar, Runjun D., Saba, Lisa F., Streff, Haley, Shaw, Chad A., Mizerik, Elizabeth, Snyder, Matthew T., Lopez-Terrada, Dolores, Scull, Jennifer
Published in Genetics in medicine (01.10.2023)
Published in Genetics in medicine (01.10.2023)
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Journal Article
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis
Kumar, Runjun D., Meng, Linyan, Liu, Pengfei, Miyake, Christina Y., Worley, Kim C., Bi, Weimin, Lalani, Seema R.
Published in American journal of medical genetics. Part A (01.11.2022)
Published in American journal of medical genetics. Part A (01.11.2022)
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Journal Article
Brain abscesses, neutropenia, and B-ALL: Multiple testing modalities required to confirm PDCD10 and ETV6 dual diagnoses
Kumar, Runjun D., Vossaert, Liesbeth, Bi, Weimin, Owen, Nichole, Rau, Rachel E., Helber, Hannah L., Sasa, Ghadir, Reuther, Jacquelyn, Roy, Angshumoy, Fisher, Kevin E.
Published in Cancer genetics (01.11.2024)
Published in Cancer genetics (01.11.2024)
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Journal Article
Facial Nerve Palsy in a Child With Fever of Unknown Origin
Mutucumarana, Charmaine P, Kumar, Runjun D, Foradori, Dana M, Ramgopal, Veena, Demmler, Gail J
Published in Clinical pediatrics (01.05.2020)
Published in Clinical pediatrics (01.05.2020)
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Journal Article
Response of a Metastatic Breast Carcinoma With a Previously Uncharacterized ERBB2 G776V Mutation to Human Epidermal Growth Factor Receptor 2-Targeted Therapy
Chudnovsky, Yakov, Kumar, Runjun D, Schrock, Alexa B, Connelly, Caitlin, Gowen, Kyle, Frampton, Garrett M, Erlich, Rachel L, Stephens, Philip J, Miller, Vincent A, Ross, Jeffrey S, Ali, Siraj M, Bose, Ron
Published in JCO precision oncology (01.11.2017)
Published in JCO precision oncology (01.11.2017)
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