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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

The Role of Genome Sequencing in Neonatal Intensive Care Units
Stephen F. Kingsmore, F. Sessions Cole
Annual Review of Genomics and Human Genetics (2022) Vol. 23, Iss. 1, pp. 427-448
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases
Stephen F. Kingsmore, Laurie D. Smith, Chris M. Kunard, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 9, pp. 1605-1619
Open Access | Times Cited: 110
Rapid genomic sequencing for genetic disease diagnosis and therapy in intensive care units: a review
Stephen F. Kingsmore, Russell Nofsinger, Kasia Ellsworth
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 22
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
Alissa M. D’Gama, Sarah Mulhern, Beth Rosen Sheidley, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 9, pp. 812-825
Open Access | Times Cited: 41
Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencing
Jeong‐Min Kim, Hye-Won Cho, Dong Mun Shin, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access | Times Cited: 1
Rapid Whole-Genome Sequencing and Clinical Management in the PICU: A Multicenter Cohort, 2016–2023*
Katherine M. Rodriguez, Jordan Vaught, Lisa Salz, et al.
Pediatric Critical Care Medicine (2024) Vol. 25, Iss. 8, pp. 699-709
Open Access | Times Cited: 7
Dispatches from Biotech beginning BeginNGS: Rapid newborn genome sequencing to end the diagnostic and therapeutic odyssey
Stephen F. Kingsmore
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 2, pp. 243-256
Open Access | Times Cited: 27
Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting
Lauren Thompson, Austin Larson, Lisa Salz, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access | Times Cited: 5
How Neonatologists Use Genetic Information
Katharine Press Callahan, Rebecca Mueller, Steven Joffe, et al.
The Journal of Pediatrics (2025), pp. 114508-114508
Closed Access
SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns
Tara Wenger, Abbey Scott, Lukas Kruidenier, et al.
The American Journal of Human Genetics (2025)
Open Access
Rapid Whole-Genome Sequencing in Critically Ill Infants and Children with Suspected, Undiagnosed Genetic Diseases: Evolution to a First-Tier Clinical Laboratory Test in the Era of Precision Medicine
Rina Kansal
Children (2025) Vol. 12, Iss. 4, pp. 429-429
Open Access
Genetics
Aditi Shah Parikh
Elsevier eBooks (2025), pp. 105-122.e1
Closed Access
Precision medicine in the pediatric and neonatal intensive care units through genomics
Phan Q. Duy, Benjamin Dylik, Engin Deniz
Current Opinion in Pediatrics (2025)
Closed Access
Evidence from 2100 index cases supports genome sequencing as a first-tier genetic test
Fen Guo, Ruby Liu, Yinghong Pan, et al.
Genetics in Medicine (2023) Vol. 26, Iss. 1, pp. 100995-100995
Open Access | Times Cited: 10
Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit
Amy A. Lemke, Michelle L. Thompson, Emily C. Gimpel, et al.
Journal of Personalized Medicine (2023) Vol. 13, Iss. 7, pp. 1026-1026
Open Access | Times Cited: 7
Errors in genome sequencing result disclosures: A randomized controlled trial comparing neonatology non-genetics healthcare professionals and genetic counselors
Tanner Coleman, Jada Pugh, Whitley V. Kelley, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 9, pp. 101198-101198
Closed Access | Times Cited: 2
Assessing Diversity in Newborn Genomic Sequencing Research Recruitment: Race/Ethnicity and Primary Spoken Language Variation in Eligibility, Enrollment, and Reasons for Declining
Julie A. Cakici, David Dimmock, Sara Caylor, et al.
Clinical Therapeutics (2023) Vol. 45, Iss. 8, pp. 736-744
Open Access | Times Cited: 6
Genomic medicine in neonatal care: progress and challenges
Alissa M. D’Gama, Pankaj B. Agrawal
European Journal of Human Genetics (2023) Vol. 31, Iss. 12, pp. 1357-1363
Closed Access | Times Cited: 6
Role of genomic medicine and implementing equitable access for critically ill infants in neonatal intensive care units
Alissa M. D’Gama, Pankaj B. Agrawal
Journal of Perinatology (2023) Vol. 43, Iss. 7, pp. 963-967
Open Access | Times Cited: 5
A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates
Ahmad Abou Tayoun, Alawi Alsheikh‐Ali
Nature Medicine (2023) Vol. 29, Iss. 12, pp. 2979-2980
Closed Access | Times Cited: 4
Implementation of rapid genomic sequencing in safety-net neonatal intensive care units: protocol for the VIrtual GenOme CenteR (VIGOR) proof-of-concept study
Alissa M. D’Gama, Sonia Hills, Jessica Douglas, et al.
BMJ Open (2024) Vol. 14, Iss. 2, pp. e080529-e080529
Open Access | Times Cited: 1
Diagnostic Utility of Whole Genome Sequencing After Negative Karyotyping/Chromosomal Microarray in Infants Born With Multiple Congenital Anomalies
Misun Yang, Jee Ah Kim, Heui Seung Jo, et al.
Journal of Korean Medical Science (2024) Vol. 39, Iss. 36
Open Access | Times Cited: 1
Inborn Errors of Immunity in Early Childhood: Essential Insights for the Neonatologist
Johannes Dirks, Matthias Wölfl, Christian P. Speer, et al.
Neonatology (2024) Vol. 121, Iss. 5, pp. 646-655
Closed Access | Times Cited: 1
Implementation of multi-omics in diagnosis of pediatric rare diseases
Sara Ali, Qifei Li, Pankaj B. Agrawal
Pediatric Research (2024)
Open Access | Times Cited: 1
Going Back in Time: Prenatal Presentations of Postnatal Genetic Diagnoses Made in a Neonatal Intensive Care Unit
Michael H. Duyzend, Malika Sud, Alissa M. D’Gama, et al.
Prenatal Diagnosis (2024)
Closed Access | Times Cited: 1
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial
Stephen F. Kingsmore, Meredith S. Wright, L. Olsen, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 12, pp. 2643-2667
Closed Access | Times Cited: 1
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