Publications
1,077
Citations
55,428
Est. group size
~8
Recurring co-author estimate
Active years
55
Publishing since 1972
Ronald J. Wapner's research focuses on prenatal diagnosis and maternal-fetal medicine, including genetic testing methods like amniocentesis and genomic sequencing to detect fetal chromosomal and structural abnormalities. His work also examines pregnancy complications such as preterm birth, preeclampsia, and fetal growth issues, often linking genetic and biomarker data to clinical outcomes for babies and mothers. This work is aimed at improving how doctors screen for and counsel patients about genetic and developmental conditions during pregnancy.
Publication output peaked around 2020 and has gradually declined since, though the researcher remains active with a steady stream of recent publications.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Pathways to enhancing prenatal diagnosis of skeletal dysplasias
Pregnancy · 2026
- Omega-3 supplementation in addition to prenatal vitamins during pregnancy is associated with lower rates of preterm birth and small for gestational age
Frontiers in Nutrition · 2026
- Precision Diagnosis in <i>APOL1</i> Kidney Disease With the p.N264K M1 Protective Variant
JAMA Network Open · 2026
- Sex-differentiated placental methylation and gene expression regulation has implications for neonatal traits and adult diseases
Nature Communications · 2025
- CIROZ is dispensable in ancestral vertebrates but essential for left-right patterning in humans
The American Journal of Human Genetics · 2025
- Amniocentesis in Pregnancies at or Beyond 24 Weeks: An International Multicenter Study
Obstetrical & Gynecological Survey · 2025
- Maternal parity modifies the association of birthweight polygenic score with fetal growth
Scientific Reports · 2025
- Childhood outcomes of fetal genomic copy-number variants: The prenatal microarray cohort study
Genetics in Medicine Open · 2025
- The Perspectives and Experiences of Prospective Parents Declining Diagnostic Prenatal Genome Sequencing in Continuing Pregnancies With Fetal Structural Anomalies
Prenatal Diagnosis · 2025
- Early pregnancy placental biomarkers as predictors of preeclampsia with severe features
Pregnancy · 2025
- Development of a Clinically Applicable High-Resolution Assay for Sperm Mosaicism
Journal of Molecular Diagnostics · 2025
- Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell‐Silver Syndrome in Infancy
Prenatal Diagnosis · 2025
- Differential Predictability of Preterm Birth Types: Strong Signals for Indicated Cases versus Limited Success in Spontaneous Preterm Birth
medRxiv · 2025
- P635: Validating fetal RNA sequencing to improve classification of splicing variants in prenatal diagnosis*
Genetics in Medicine Open · 2025
- Prenatal Diagnostic Testing for Adult‐Onset Neurodegenerative Disease
Prenatal Diagnosis · 2025
- American Journal of Obstetrics and Gynecology×87
- UNC Libraries×64
- American Journal of Perinatology×47
- Obstetrics and Gynecology×44
- Prenatal Diagnosis×25
- Pamela Foy
Medicine · The Ohio State University
- Anthony Shanks
Medicine · Indiana University
- Brittany Smart
Medicine · Indiana University
- Uma M. Reddy
Medicine · The Ohio State University
- Zachary S. Bowman
Medicine · Indiana University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
Claim or correct this profile