Author

Fang Qian

University of IowaORCID 0000-0002-2861-6099Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Assay:DNA methylation· 2 Research Focus:gene regulatory network inference· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aline Lourenço PetriniD· 3 shared Azeez ButaliiD· 3 shared Jeffrey C. MurrayiD· 3 shared Ligiane Alves Machado‐PaulaiD· 3 shared Lina M. Moreno UribeiD· 3 shared Christina Spencer· 2 shared Waheed A. AwotoyeiD· 2 shared Amanda Seaberg· 1 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 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

3 shared papersGenetic & Genomic Medicine

Aline Lourenço PetrinORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 22, 2026

Laterality, Symmetry and Completeness Patterns of Nonsyndromic Orofacial Clefts in a Multiethnic Cohort

Christina Spencer, Ligiane Alves Machado‐Paula, Fang Qian…·Aline Lourenço Petrin

The paper analyzes the laterality, symmetry, and completeness of nonsyndromic orofacial clefts in a multiethnic cohort, finding sex, race, and ethnicity influence these traits but not completeness.

DOI 10.64898/2025.12.29.25343144

humanstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicineHuman Molecular GeneticsPeer-reviewedJan 1, 2026

Genetic and Epigenetic Contributors to Cleft Laterality: Evidence from Monozygotic Mirror Twins and Replication Cohorts

Aline Lourenço Petrin, Waheed A. Awotoye, Christina Spencer…·Lina M. Moreno‐Uribe

This study identifies genetic and epigenetic factors contributing to cleft laterality using monozygotic twins and replication cohorts, finding methylation differences in ARID5B, ZFP57, and HOOK2 associated with cleft side and severity.

DOI 10.1093/hmg/ddag088

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicineThe Cleft Palate-Craniofacial JournalPeer-reviewedAug 7, 2024

DNA methylation effects on Van der Woude Syndrome phenotypic variability

Amanda Seaberg, Waheed A. Awotoye, Fang Qian…·Aline Lourenço Petrin

The paper investigates DNA methylation differences in IRF6 and TP63 regulatory regions in Van der Woude Syndrome patients and finds hypermethylation in IRF6 promoters correlates with more severe phenotypes.

6 citations

humanDNA methylation

𝕏 PostBluesky