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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 influence of social determinants of health on the genetic diagnostic odyssey: who remains undiagnosed, why, and to what effect?
Yarden S. Fraiman, Monica H. Wojcik
Pediatric Research (2020) Vol. 89, Iss. 2, pp. 295-300
Open Access | Times Cited: 75

Showing 1-25 of 75 citing articles:

Confronting Racism in All Forms of Pain Research: Reframing Study Designs
Janelle E. Letzen, Vani A. Mathur, Mary R. Janevic, et al.
Journal of Pain (2022) Vol. 23, Iss. 6, pp. 893-912
Open Access | Times Cited: 79
Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors
Lacey Smith, Jennifer Malinowski, Sophia Ceulemans, et al.
Journal of Genetic Counseling (2022) Vol. 32, Iss. 2, pp. 266-280
Open Access | Times Cited: 70
Psychosocial Considerations for the Child with Rare Disease: A Review with Recommendations and Calls to Action
Leslee Throckmorton Belzer, S. Margaret Wright, Emily Goodwin, et al.
Children (2022) Vol. 9, Iss. 7, pp. 933-933
Open Access | Times Cited: 37
Rare diseases, common barriers: disparities in pediatric clinical genetics outcomes
Monica H. Wojcik, Mairead Bresnahan, Maya C. del Rosario, et al.
Pediatric Research (2022) Vol. 93, Iss. 1, pp. 110-117
Open Access | Times Cited: 33
Burden of Mendelian disorders in a large Middle Eastern biobank
Waleed Aamer, Aljazi Al-Maraghi, Najeeb Syed, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 8
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders
Kristen Wigby, Deanna Brockman, Gregory Costain, et al.
npj Genomic Medicine (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 7
Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populations
Ana S.A. Cohen, Courtney Berrios, Tricia Zion, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 5, pp. 825-832
Closed Access | Times Cited: 7
Advancing diagnosis and research for rare genetic diseases in Indigenous peoples
Gareth Baynam, Daria Julkowska, Sarah Bowdin, et al.
Nature Genetics (2024)
Open Access | Times Cited: 6
Navigating the U.S. health insurance landscape for children with rare diseases: a qualitative study of parents’ experiences
Tai L. S. Pasquini, Sarah L. Goff, Jennifer M. Whitehill
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 34
Delayed diagnosis and racial bias in children with genetic conditions
Jacklyn Omorodion, Leah Dowsett, Robin D. Clark, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 4, pp. 1118-1123
Open Access | Times Cited: 23
Committing to genomic answers for all kids: Evaluating inequity in genomic research enrollment
Natalie Kane, Ana S.A. Cohen, Courtney Berrios, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 9, pp. 100895-100895
Open Access | Times Cited: 15
Advancing Understanding of Inequities in Rare Disease Genomics
Jillian Serrano, Melanie O’Leary, Grace E. VanNoy, et al.
Clinical Therapeutics (2023) Vol. 45, Iss. 8, pp. 745-753
Open Access | Times Cited: 15
Validation of the Observer-Reported Communication Ability (ORCA) Measure for Individuals With Angelman Syndrome
Christina K. Zigler, Li Lin, Molly McFatrich, et al.
American Journal on Intellectual and Developmental Disabilities (2023) Vol. 128, Iss. 3, pp. 204-218
Closed Access | Times Cited: 11
Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone
Rhett G. Marchant, Samantha J. Bryen, Melanie Bahlo, et al.
Annals of Clinical and Translational Neurology (2024) Vol. 11, Iss. 5, pp. 1250-1266
Open Access | Times Cited: 4
The impact of social-environmental factors on IQ in syndromic intellectual developmental disabilities
Walker S. McKinney, Desireé N Williford, Leonard Abbeduto, et al.
Journal of Clinical and Translational Science (2024) Vol. 8, Iss. 1
Open Access | Times Cited: 4
Breaking barriers: fostering equitable access to pediatric genomics through innovative care models and technologies
Sabrina Malone Jenkins, Rachel Palmquist, Brian J. Shayota, et al.
Pediatric Research (2025)
Closed Access
Self‐Reported Access to Specialized Genetics Providers Among Families of Young Children With Birth Defects in Texas
Dayana Betancourt, Charles Shumate, Caitlyn Yantz, et al.
American Journal of Medical Genetics Part A (2025)
Open 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
Sex‐Specific Association Between Polymorphisms in Estrogen Receptor Alpha Gene (ESR1) and Depression: A Genome‐Wide Association Study of All of Us and UK Biobank Data
Yue Hu, Menglu Che, Heping Zhang
Genetic Epidemiology (2025) Vol. 49, Iss. 3
Closed Access
Next-generation nephrology: part 2—mainstreaming genomics in nephrology, a global perspective
Asheeta Gupta, Kushani Jayasinghe, Amar J. Majmundar, et al.
Pediatric Nephrology (2025)
Open Access
Nursing’s Role in Advancing Care for Rare Genetic Diseases
Andrew Dwyer, Suja Somanadhan
Nursing Clinics of North America (2025)
Closed Access
COVID-19 Pandemic-related differences in the prevalence of genetic conditions and healthcare utilization and access for children with genetic conditions the United States.
Abhinav Thakral, Divya Moorthy, Tanya Tandon, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Antiracism in the Field of Neonatology: A Foundation and Concrete Approaches
Diana Montoya‐Williams, Yarden S. Fraiman, Michelle-Marie Peña, et al.
NeoReviews (2021) Vol. 23, Iss. 1, pp. e1-e12
Open Access | Times Cited: 26
Results From the WAGR Syndrome Patient Registry: Characterization of WAGR Spectrum and Recommendations for Care Management
Kelly A. Duffy, Kelly L. Trout, Jennifer M. Gunckle, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 25
Toward representative genomic research: the children’s rare disease cohorts experience
Zoë J. Frazier, Eurnestine Brown, Shira Rockowitz, et al.
Therapeutic Advances in Rare Disease (2023) Vol. 4
Open Access | Times Cited: 9
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