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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:

Lessons learnt from prenatal exome sequencing
Natalie Chandler, Elizabeth Scotchman, Rhiannon Mellis, et al.
Prenatal Diagnosis (2022) Vol. 42, Iss. 7, pp. 831-844
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

‘Something that helped the whole picture’: Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service
Hannah McInnes‐Dean, Rhiannon Mellis, Morgan Daniel, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 4, pp. 465-479
Open Access | Times Cited: 14
Incremental yield of whole‐genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta‐analysis
Norman Shreeve, C. Sproule, Kwong Wai Choy, et al.
Ultrasound in Obstetrics and Gynecology (2023) Vol. 63, Iss. 1, pp. 15-23
Open Access | Times Cited: 21
Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals’ views and experiences
Michelle Peter, Rhiannon Mellis, Hannah McInnes‐Dean, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 6
Should we offer prenatal exome sequencing for intrauterine growth restriction or short long bones? A systematic review and meta-analysis
Fionnuala Mone, Rhiannon Mellis, Heinz Gabriel, et al.
American Journal of Obstetrics and Gynecology (2022) Vol. 228, Iss. 4, pp. 409-417.e4
Open Access | Times Cited: 25
Improving prenatal diagnosis through standards and aggregation
Michael H. Duyzend, Pilar Cacheiro, Julius O.B. Jacobsen, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 4, pp. 454-464
Open Access | Times Cited: 5
Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation
Alexandra Emms, James Castleman, Stephanie Allen, et al.
Genes (2022) Vol. 13, Iss. 9, pp. 1517-1517
Open Access | Times Cited: 20
Prenatal Genome-Wide Sequencing analysis (Exome or Genome) in detecting pathogenic Single Nucleotide Variants in fetal Central Nervous System Anomalies: systematic review and meta-analysis
Enrica Marchionni, Daniele Guadagnolo, Gioia Mastromoro, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 7, pp. 759-769
Closed Access | Times Cited: 4
Navigating the Challenges of Exome Sequencing in Structurally Normal Fetuses
Sylvie Langlois, Lyn S. Chitty
Prenatal Diagnosis (2025) Vol. 45, Iss. 3, pp. 273-275
Closed Access
Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort
Dana Brabbing‐Goldstein, Lily Bazak, Noa Ruhrman‐Shahar, et al.
Prenatal Diagnosis (2024)
Closed Access | Times Cited: 2
Prenatal detection of copy number variants
Mohamed Wafik, Alice Pendlebury-Watt, Kelly Price, et al.
Best Practice & Research Clinical Obstetrics & Gynaecology (2024) Vol. 97, pp. 102547-102547
Closed Access | Times Cited: 2
Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation
Rema Ramakrishnan, Corinne Mallinson, Steven Hardy, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies
Stephanie Allen, Natalie Chandler, Esther Kinning, et al.
Prenatal Diagnosis (2023) Vol. 44, Iss. 4, pp. 432-442
Closed Access | Times Cited: 5
When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta‐analysis
S. Sonner, Kelly Reilly, Adrian S. Woolf, et al.
Prenatal Diagnosis (2023) Vol. 44, Iss. 2, pp. 187-195
Open Access | Times Cited: 4
Current Status and Future of Genomics in Fetal and Maternal Medicine: A scientific review commissioned by European Board and College of Obstetrics and Gynaecology (EBCOG)
Megan B. O’Brien, Sarah Doyle, Fionnuala M. McAuliffe, et al.
European Journal of Obstetrics & Gynecology and Reproductive Biology (2024) Vol. 299, pp. 336-341
Closed Access | Times Cited: 1
The evolving genetic etiology of conotruncal anomalies
Adalina Sacco, Ronel Talker, Lyndall Sarkies, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 6-7, pp. 815-820
Open Access | Times Cited: 1
Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfalls
Lina Basel‐Vanagaite, Dana Brabbing‐Goldstein
Best Practice & Research Clinical Obstetrics & Gynaecology (2024) Vol. 97, pp. 102549-102549
Closed Access | Times Cited: 1
Prenatal testing technologies in Australia: Unintended clinical and emotional complexities in underprepared systems
Belinda Johnson, Pieta Shakes, Chris Maylea
Social Science & Medicine (2024) Vol. 361, pp. 117368-117368
Closed Access | Times Cited: 1
International Society for Prenatal Diagnosis 2022 debate 3—Fetal genome sequencing should be offered to all pregnant patients
Ignatia B. Van den Veyver, Yuval Yaron, Zandra C. Deans
Prenatal Diagnosis (2022) Vol. 43, Iss. 4, pp. 428-434
Open Access | Times Cited: 6
Enhancement of phenotyping for fetal investigation using next‐generation sequencing
Fionnuala Mone, Tessa Homfray, Karl Oliver Kagan, et al.
Ultrasound in Obstetrics and Gynecology (2023) Vol. 62, Iss. 4, pp. 459-461
Open Access | Times Cited: 3
Prenatal diagnosis of mucopolysaccharidosis type VII facilitating treatment in neonatal period
Natalie Chandler, Vijaya Ramachandran, Clare Beesley, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 12, pp. 1567-1569
Open Access | Times Cited: 2
Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis
Lyn S. Chitty, Ignatia B. Van den Veyver
Prenatal Diagnosis (2022) Vol. 42, Iss. 12, pp. 1479-1480
Closed Access | Times Cited: 4
Prenatal exomes and genomes – so much new and so much more to learn
Ignatia B. Van den Veyver
Prenatal Diagnosis (2022) Vol. 42, Iss. 6, pp. 659-661
Closed Access | Times Cited: 3
Likely pathogenic variant in the BICD2 gene in fetus presenting with non‐immune hydrops
Natalie Chandler, Poppy Brace, Rowenna Roberts, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 6, pp. 727-729
Open Access | Times Cited: 1
An incidental finding in prenatal exome sequencing—A case study and review of the clinical and ethical considerations
Ignatius Rudd, Gulvir Gill, Michael F. Buckley, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 12, pp. 2856-2859
Closed Access | Times Cited: 1
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