Author

Christina G. Tise

Stanford Maternal and Child Health Research InstituteORCID 0000-0002-6227-7895Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David K. StevensoniD· 2 shared Gary Michael ShawiD· 2 shared Jonathan Adam BernsteiniD· 2 shared Marina SirotaiD· 2 shared Michael P. SnyderiD· 2 shared Mona Amin‐BeidokhtiiD· 2 shared Ruth Bunker LathiiD· 2 shared Svetlana A. YatsenkoiD· 2 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

David K. StevensonORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedMar 3, 2026

The Human Intolerome: a curated database to prioritize genomic variants in stillbirth, pregnancy loss, and neonatal death

Svetlana A. Yatsenko, Amrita Nagasuri, Vishal Soman…·Aleksandar Rajkovic

The paper introduces the Intolerome Database, a curated resource of genes essential for human viability, to help prioritize genomic variants in cases of stillbirth, pregnancy loss, and neonatal death.

1 citation

humanwhole-exome sequencing

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Genetic & Genomic MedicinemedRxivPreprintOct 1, 2025

Genetic Variants in Recurrent Euploid Pregnancy Loss

Mona Amin‐Beidokhti, Michelle M. Halstead, Marta Rodríguez-Escribà…·Aleksandar Rajkovic

The paper identifies genetic variants in 30 families with unexplained euploid pregnancy loss, finding monogenic causes in 25% of cases and expanding understanding of early human lethality.

2 citations

humanwhole-genome sequencing

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