Jessica Van Ziffle, PhD
Associate Clinical Professor; Technical Director, Clinical Cancer Genomics Laboratory and Genomic Medicine Laboratory
Pathology
Division
Genetics and Genomics Services; Molecular Pathology
Specialty Areas
Laboratory Genetics and Genomics
UCSF
Pathology, Box 1389
2340 Sutter Street, Room N144
San Francisco, CA 94143
United States
Hospital Affiliations
UCSF Mount Zion
Other UCSF Organizational Association(s)
Clinical Cancer Genomics Laboratory
Genomic Medicine Laboratory
Institute for Human Genetics
Selected Publications
- Lee TD, Aisner DL, David MP, Eno CC, Gagan J, Gocke CD, Guseva NV, Haley L, Jajosky AN, Jones D, Mansukhani MM, Mroz P, Murray SS, Newsom KJ, Paulson V, Roy S, Rushton C, Segal JP, Senaratne TN, Siddon AJ, Starostik P, Van Ziffle JAG, Wu D, Xian RR, Yohe S, Kim AS. Current clinical practices and challenges in molecular testing: a GOAL Consortium Hematopathology Working Group report. Blood Adv.2023 Aug 22;7(16):4599-4607. doi: 10.1182/bloodadvances.2023010149. PubMed PMID: 37236162; PubMed Central PMCID: PMC10425685.
- Saglam A, Singh K, Kumar J, Gollapudi S, Mukherjee S, Singh A, Butzmann A, Kaplan L, Andreadis C, Ai WZ, Fakhri B, Rajkovic A, Wen KW, Onodera C, Van Ziffle J, Devine PW, Ohgami RS. Copy Number Loss at Chromosome 14q11.2 Correlates With the Proportion of T Cells in Biopsies and Helps Identify T-Cell Neoplasms. Arch Pathol Lab Med. 2023 Aug 1;147(8):940-948. doi: 10.5858/arpa.2022-0193-OA. PubMed PMID: 36445717.
- Williams EA, Ravindranathan A, Gupta R, Stevers NO, Suwala AK, Hong C, Kim S, Yuan JB, Wu J, Barreto J, Lucas CG, Chan E, Pekmezci M, LeBoit PE, Mully T, Perry A, Bollen A, Van Ziffle J, Devine WP, Reddy AT, Gupta N, Basnet K, Macaulay R, Malafronte P, Lee H, Yong WH, Williams KJ, Juratli TA, Mata DA, Huang RSP, Hiemenz MC, Pavlick DC, Frampton GM, Janovitz T, Ross JS, Chang SM, Berger MS, Jacques L, Song JS, Costello JF, Solomon DA. Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs. Neuro Oncol. 2023 Jul 12;. doi: 10.1093/neuonc/noad121. [Epub ahead of print] PubMed PMID: 37436963.
- Apsel Winger B, Devine WP, Hsiao EC, Zapala M, Van Ziffle J, Gupta N, Frieden IJ, Shimano KA. EML4::ALK fusions in complex lymphatic malformations. Pediatr Blood Cancer. 2023 Jun 28;:e30516. doi: 10.1002/pbc.30516. [Epub ahead of print] PubMed PMID: 37377128.
- Sparks TN, Lianoglou BR, Adami RR, Pluym ID, Holliman K, Duffy J, Downum SL, Patel S, Faubel A, Boe NM, Field NT, Murphy A, Laurent LC, Jolley J, Uy C, Slavotinek AM, Devine P, Hodoglugil U, Van Ziffle J, Sanders SJ, MacKenzie TC, Norton ME. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis. N Engl J Med. 2020 Oct 29;383(18):1746-1756. doi: 10.1056/NEJMoa2023643. Epub 2020 Oct 7. PubMed PMID: 33027564; PubMed Central PMCID: PMC7650529.
Link to complete list of publications in PubMed:
https://www.ncbi.nlm.nih.gov/myncbi/jessica.van%20ziffle.1/bibliography/public/