Publications
34
Citations
388
Est. group size
—
Recurring co-author estimate
Active years
18
Publishing since 2009
Laura Rust's work centers on prenatal genetic diagnosis and genetic counseling, including case reports of rare fetal conditions detected through ultrasound and genome sequencing, as well as broader public health topics like infectious disease surveillance and reproductive healthcare access. The publications suggest a clinical and applied focus, often involving case studies and short reports relevant to genetic counselors and clinicians working in prenatal and pediatric care settings.
Publication output has grown over the last decade, increasing from just a few papers per year in 2017-2021 to a peak of 8 in 2025, with a five-year average of 4.0 publications per year.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- P784: Prenatal diagnosis of Rubinstein-Taybi syndrome in a fetus with posterior encephalocele
Genetics in Medicine Open · 2026
- <i>Notes from the Field:</i> Severe Health Outcomes Linked to Consumption of Mushroom-Based Psychoactive Microdosing Products — Arizona, June–October 2024
MMWR Morbidity and Mortality Weekly Report · 2025
- Special considerations in assisted reproductive technology for patients with pulmonary disease
Fertility and Sterility · 2025
- Decreasing the Use of Albuterol Nebulizer Solution in the Management of Asthma Exacerbations in the Emergency Department
Pediatric Quality and Safety · 2025
- P852: Prenatal whole genome sequencing to diagnosis rare presentations of hydrops fetalis
Genetics in Medicine Open · 2025
- Large Clusters of Invasive <i>emm</i>49 Group A <i>Streptococcus</i> Identified Within Arizona Health Care Facilities Through Statewide Genomic Surveillance System, 2019–2021
The Journal of Infectious Diseases · 2024
- Prenatal Ultrasonographic Features Associated With <i>ARSL</i> and X‐Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series
Prenatal Diagnosis · 2024
- P665: Genome sequencing defines the breakpoints of a TP53 promoter region deletion required for the purpose of preimplantation genetic testing
Genetics in Medicine Open · 2024
- P086: Mosaic Li-Fraumeni syndrome identified in patient with a previously presumed germline variant following preimplantation genetic testing: A case report
Genetics in Medicine Open · 2023
- P608: Specialization in prenatal genetic counseling: Defining the role of fetal therapy genetic counselors
Genetics in Medicine Open · 2023
- Nu Niet Zwanger in bijna twee derde van alle gemeenten in Nederland
TSG - Tijdschrift voor gezondheidswetenschappen · 2023
- eP459: Rare clinical gene variant of SOX9: Acampomelic campomelic dysplasia
Genetics in Medicine · 2022
- eP460: Diagnostic dilemma in a case of suspected fetal skeletal dysplasia
Genetics in Medicine · 2022
- Notes at your fingertips: Open note considerations regarding pediatric and adolescent care
Current problems in pediatric and adolescent health care · 2021
- Reproductive and contraceptive healthcare for vulnerable people in the Netherlands: Pregnant not now!
European Journal of Public Health · 2019
- Genetics in Medicine Open×5
- PEDIATRICS×4
- Pediatric Quality and Safety×2
- Genetics in Medicine×2
- International Journal of Antimicrobial Agents×1
- Christopher Winslow
Medicine · The Ohio State University
- Daniel T. Cater
Medicine · Indiana University
- Christine Motzkus
Medicine · Indiana University
- Daniel Eiferman
Medicine · The Ohio State University
- Elizabeth Rozycki
Medicine · The Ohio State 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.
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