Author

Shweta Belur

University of California, San Francisco

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aleksandar RajkoviciD· 1 shared Eleni A. GreenwoodiD· 1 shared Hakan ÇakmakiD· 1 shared Jia-Hua QuiD· 1 shared Marina SirotaiD· 1 shared Michael P. SnyderiD· 1 shared Mona Amin‐BeidokhtiiD· 1 shared Ruth Bunker LathiiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aleksandar RajkovicORCID

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Author profile →

1 paper

Recent·Most cited

Preconception Genetic Carrier Screening for Miscarriage Risk Assessment: A Bioinformatic Approach to Identifying Candidate Lethal Genes and Variants

Mona Amin‐Beidokhti, Jia-Hua Qu, Shweta Belur, Hakan Çakmak, Eleni A. Greenwood, Ruth Bunker Lathi, Marina Sirota, Michael P. Snyder, Svetlana A. Yatsenko, Aleksandar Rajkovic

The paper identifies 138 genes and variants associated with prenatal lethality across ethnic groups, suggesting preconception screening could identify couples at risk for miscarriage.

medRxiv · May 25, 2023 · PreprintGenetic & Genomic Medicine