Jessica Van Ziffle

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 16 papers. Top paper: “Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs”.

Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs

Neuro-Oncology(2023)10.1093/neuonc/noad121

N/A

1.0DataRank · unranked

31 citations

Ajay Ravindranathan, Rohit Gupta, Nicholas Stevers, Abigail K. Suwala, Chibo Hong +36 more

Gliomas arising in the setting of Li-Fraumeni syndrome stratify into two molecular subgroups with divergent clinicopathologic features

Acta Neuropathologica(2020)10.1007/s00401-020-02144-8

N/A

0.581DataRank · unranked

47 citations

Stephanie Hilz, Rohit Gupta, Cathryn R. Cadwell, Biswarathan Ramani, Jeffrey W. Hofmann +33 more

Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

npj Genomic Medicine(2023)10.1038/s41525-023-00353-0

N/A

0.568DataRank · unranked

43 citations

Shannon Rego, Nuriye Sahin‐Hodoglugil, Mark Kvale, Billie R. Lianoglou, Tiffany Yip +33 more

Loss of p16 expression is a sensitive marker of CDKN2A homozygous deletion in malignant meningiomas

Acta Neuropathologica(2023)10.1007/s00401-023-02544-6

N/A

0.483DataRank · unranked

24 citations

Rufei Lu, Kanish Mirchia, Jessica Van Ziffle, Patrick Devine, Julieann Lee +6 more

Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis

American Journal of Obstetrics and Gynecology(2021)10.1016/j.ajog.2021.07.014

N/A

0DataRank · unranked

37 citations

Jessica Van Ziffle, Billie R. Lianoglou, Uğur Hodoğlugil, W. Patrick Devine, Teresa N. Sparks +1 more

Preference for secondary findings in prenatal and pediatric exome sequencing

Prenatal Diagnosis(2021)10.1002/pd.5973

N/A

0DataRank · unranked

17 citations

Teresa N. Sparks, Billie R. Lianoglou, Flavia Chen, Sarah L. Downum, Sachi Patel +7 more

Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-Ganglioglioma

Journal of Neuropathology & Experimental Neurology(2022)10.1093/jnen/nlac044

N/A

0DataRank · unranked

8 citations

Christian J. Davidson, Mouied Alashari, Angelica R. Putnam, Nicholas Whipple, Carol S. Bruggers +22 more

The utility of pathologic examination and comprehensive phenotyping for accurate diagnosis with perinatal exome sequencing

Prenatal Diagnosis(2022)10.1002/pd.6197

N/A

0DataRank · unranked

4 citations

Mary E. Norton, Billie R. Lianoglou, Angie C. Jelin, Uğur Hodoğlugil, Jessica Van Ziffle +3 more

Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry

medRxiv(2023)10.1101/2023.05.19.23290066

N/A

0DataRank · unranked

0 citations

Nuriye Sahin‐Hodoglugil, Uğur Hodoğlugil, Mark Kvale, Pierre‐Marie Martin, Jessica Van Ziffle +8 more

Genetic ancestry and diagnostic yield of exome sequencing in a diverse population

npj Genomic Medicine(2024)10.1038/s41525-023-00385-6

N/A

0DataRank · unranked

19 citations

Nuriye Sahin‐Hodoglugil, Uğur Hodoğlugil, Mark Kvale, Pierre‐Marie Martin, Jessica Van Ziffle +8 more

The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101820

N/A

0DataRank · unranked

2 citations

Vimla S. Aggarwal, A. Bale, Daniel B. Bellissimo, Jessica K. Booker, Yang Cao +30 more

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.011

N/A

0DataRank · unranked

112 citations

Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner +25 more

Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions

Prenatal Diagnosis(2025)10.1002/pd.70016

N/A

0DataRank · unranked

0 citations

Daniella Rogerson, Patrick Devine, Jessica Van Ziffle, Teresa N. Sparks, Susan A. Vargo

Pediatric bithalamic gliomas have a distinct epigenetic signature and frequent EGFR exon 20 insertions resulting in potential sensitivity to targeted kinase inhibition

Acta Neuropathologica(2020)10.1007/s00401-020-02155-5

N/A

0DataRank · unranked

96 citations

Julieann C. Lee, Ajay Ravindranathan, Javier Villanueva-Meyer, Quynh T. Tran, Sariah J. Allen +37 more

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

Genetics in Medicine(2020)10.1038/s41436-020-01020-w

N/A

0DataRank · unranked

47 citations

Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker +53 more

A missense variant, p.(Ile269Asn), in MC4R as a secondary finding in a child with BCL11A-related intellectual disability

European Journal of Medical Genetics(2020)10.1016/j.ejmg.2020.103969

N/A

0DataRank · unranked

5 citations

Jessica Van Ziffle, Uğur Hodoğlugil, Anne Slavotinek, Daniah Beleford