Kristen Suhrie
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
29
Citations
431
Est. group size
~1
Recurring co-author estimate
Active years
13
Publishing since 2014
Kristen Suhrie studies genetic and metabolic disorders in newborns, focusing on how genomic testing—such as rapid whole-genome sequencing—can help diagnose sick infants in neonatal intensive care units (NICUs). The work spans specific conditions like urea cycle disorders, Kabuki syndrome, Down syndrome, and esophageal/lung malformations, as well as how genetic medicine services are delivered across hospitals. The research aims to improve diagnosis, care, and outcomes for critically ill newborns with suspected genetic diseases.
Publication activity grew over the decade, peaking around 2022-2023 and continuing at a steady pace into recent years.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- A multicenter descriptive study of neonatal-onset urea cycle disorder patients hospitalized in level IV NICUs
Journal of Perinatology · 2026
- P179: A multicenter descriptive study of 176 neonatal-onset urea cycle disorder patients hospitalized in Level IV neonatal intensive care units
Genetics in Medicine Open · 2025
- A Practical Guide to Whole Genome Sequencing in the NICU
NeoReviews · 2024
- Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder
JAMA · 2023
- Provision and availability of genomic medicine services in Level IV neonatal intensive care units
Genetics in Medicine · 2023
- Esophageal Atresia With or Without Tracheoesophageal Fistula: Comorbidities, Genetic Evaluations, and Neonatal Outcomes
Cureus · 2023
- Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome‐wide sequencing
American Journal of Medical Genetics Part A · 2023
- P210: Esophageal atresia with or without tracheoesophageal fistula: Genetic evaluation and clinical outcomes
Genetics in Medicine Open · 2023
- P378: Inter-center variation in the availability and provision of genetic medicine services in Level IV NICUs*
Genetics in Medicine Open · 2023
- Detection and impact of genetic disease in a level IV neonatal intensive care unit
Journal of Perinatology · 2022
- Hypothermia and Metabolic Acidosis in a Term Infant
NeoReviews · 2022
- Novel Variant Findings and Challenges Associated With the Clinical Integration of Genomic Testing
JAMA Pediatrics · 2021
- Clinical RNA sequencing confirms compound heterozygous intronic variants in <i>RYR1</i> in a patient with congenital myopathy, respiratory failure, neonatal brain hemorrhage, and d‐transposition of the great arteries
Molecular Genetics & Genomic Medicine · 2021
- Neonatal complications of Down syndrome and factors necessitating intensive care
American Journal of Medical Genetics Part A · 2020
- Early behavioral and developmental interventions in ADNP‐syndrome: A case report of SWI/SNF‐related neurodevelopmental syndrome
Molecular Genetics & Genomic Medicine · 2020
- Genetics in Medicine Open×5
- The Journal of Pediatrics×3
- Journal of Perinatology×3
- American Journal of Medical Genetics Part A×2
- Genetics in Medicine×2
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 11, 2026.
Claim or correct this profile