Author

Lucinda L. Antonacci-Fulton

Washington University in St. Louis

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

Biology Disciplines

Click to filter author papers

Genomics· 4

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 4 Approach:statistical model· 4 Assay:whole-genome sequencing· 4 Research Focus:variant calling· 3 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Research Focus:eQTL / molecular QTL mapping· 1

Frequent Co-Authors

Ann M. Mc CartneyiD· 4 shared David PorubskỳiD· 4 shared Jana EbleriD· 4 shared Katherine M. MunsoniD· 4 shared Mobin AsriiD· 4 shared Pi-Chuan ChangiD· 4 shared Silvia BuonaiutoiD· 4 shared Adam FrankishiD· 3 shared

Activity by Year

2023-2026 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

4 shared papersGenomics

Ann M. Mc CartneyORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

A global view of human centromere variation and evolution

Shenghan Gao, Keisuke K. Oshima, Shu-Cheng Chuang, Mark G. Loftus, Tamara Potapova, Annalaura Montanari, David Gordon, Zikun Yang, Hufsah Ashraf, Peter A. Audano, Marcelo Ayllon, Andrey G Azov, Parithi Balachandran, Anna Okula Basile, Christine R. Beck, , Pi-Chuan Chang

The paper assembles and characterizes 2,110 human centromeres, revealing novel haplotypes, mobile element insertions, and mutation rate variation across chromosomes.

Nature · Jul 29, 2026Peer-reviewedGenomics

HPRC2: A human pangenome reference with near-complete coverage of common genetic variation

Julian Lucas, Prajna Hebbar, Wen‐Wei Liao, Juan F Macias-Velasco, Adam M. Novak, Mobin Asri, Jennifer Balacco, Andrew P. Blair, Jana Ebler, Joshua M.V. Gardner, Margarita Geleta, Cristian Groza, Andrea Guarracino, Peter Heringer, Glenn Hickey, , Jane E. Loveland

460 haplotypes from 230 genomes, selected to maximize common-variant coverage, capture 99.43% of All of Us common small variants and halve structurally unreliable regions and base errors versus HPRC1.

bioRxiv · Jul 22, 2026 · PreprintGenomics✦ In-depth digest

Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversion.

David Porubskỳ, DongAhn Yoo, Nidhi Koundinya, Erika L. Souche, Philip C. Dishuck, Nicolas Dierckxsens, William T. Harvey, Katherine M. Munson, Kendra Hoekzema, Daniel D. Chan, Tiffany Y. Leung, Marta S. Santos, Senne Meynants, Ann Swillen, Jeroen Breckpot, , Todd L. Hillaker

The paper analyzes chromosome 22q11.2 haplotypes to show how structural variations in specific regions correlate with microdeletion and inversion risks across populations.

Nature Communications · Apr 18, 2026Peer-reviewedGenomics

Recombination between heterologous human acrocentric chromosomes

Andrea Guarracino, Silvia Buonaiuto, Leonardo Gomes de Lima, Tamara Potapova, Arang Rhie, Sergey Koren, BORIS Y. RUBINSTEIN, Christian Fischer, Haley Abel, Lucinda L. Antonacci-Fulton, Mobin Asri, Gunjan Baid, Carl A. Baker, Anastasiya Belyaeva, Konstantinos Billis, , Ashley D. Sanders

The paper shows recombination between heterologous human acrocentric chromosomes using pangenome data, revealing pseudo-homologous regions linked to Robertsonian translocations.

Nature · May 10, 2023Peer-reviewedGenomics