Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Expanded carrier screening: What conditions should we screen for?
Judith D. Goldberg, Summer Pierson, Katherine Johansen Taber
Prenatal Diagnosis (2023) Vol. 43, Iss. 4, pp. 496-505
Open Access | Times Cited: 21

Showing 21 citing articles:

Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies
Jinglan Zhang, Yanting Wu, Songchang Chen, et al.
Nature Medicine (2024) Vol. 30, Iss. 2, pp. 470-479
Closed Access | Times Cited: 21
Beyond severity: utility as a criterion for setting the scope of RGCS
Lisa Dive, Anne‐Marie Laberge, Lucinda Freeman, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 4
Tailoring Monogenic Disease Carrier Screening Panels for Chinese Populations: The Importance of Considering Regional Differences
Wei Hou, Xiaolin Fu, Xiaoxiao Xie, et al.
European Journal of Medical Genetics (2025), pp. 105002-105002
Open Access
Towards a patient-centred classification of genetic disease severity
Mojca Čižek Sajko, Lovro Vidmar, Bernarda Prosenc, et al.
European Journal of Human Genetics (2025)
Closed Access
Perspective Chapter: Next-Generation Sequencing and Variant Cataloging for Screening and Diagnosis of Sphingolipidoses and Mucopolysaccharidoses
Irina Vlasova-St. Louis, Uri Barak, Svetlana F. Khaiboullina
IntechOpen eBooks (2025)
Closed Access
Expanded Carrier Screening for Prevention of Genetic Recessive Diseases
Maurizio Poli, Lucrezia Pilenzi, Roberta Giansante, et al.
Elsevier eBooks (2025)
Closed Access
Medicare‐funded reproductive genetic carrier screening in Australia has arrived: are we ready?
Alice Rogers, Lara Fitzgerald, Jan Liebelt, et al.
The Medical Journal of Australia (2024) Vol. 220, Iss. 8, pp. 394-397
Open Access | Times Cited: 3
Considering screening for hereditary cancer syndromes at the time of obstetrical prenatal carrier screening
Luiza Perez, Shayan Dioun, Michelle Primiano, et al.
Cancer (2024) Vol. 130, Iss. 24, pp. 4213-4220
Closed Access | Times Cited: 3
Implementing preconception expanded carrier screening in a universal health care system: A model-based cost-effectiveness analysis
Andrea Busnelli, Oriana Ciani, Silvia Caroselli, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 11, pp. 100943-100943
Closed Access | Times Cited: 9
Rare-ID: The First Neonate Diagnostic Approach Using Genome Sequencing for Complex Pediatric Cases in a Greek Cohort
Yannis L. Loukas, Katherine K. Anagnostopoulou, Georgia Thodi, et al.
(2024)
Open Access | Times Cited: 1
Reproductive genetic carrier screening in pregnancy: improving health outcomes and expanding access
Jenny Y. Mei, Lawrence D. Platt
Journal of Perinatal Medicine (2024) Vol. 52, Iss. 7, pp. 688-695
Closed Access | Times Cited: 1
Leveraging diverse genomic data to guide equitable carrier screening: Insights from gnomAD v.4.1.0
Matthew J Schmitz, Aryan Bashar, Vishal Soman, et al.
The American Journal of Human Genetics (2024)
Closed Access | Times Cited: 1
Cellular and molecular mechanisms of aspartoacylase and its role in Canavan disease
Martin Grønbæk-Thygesen, Rasmus Hartmann‐Petersen
Cell & Bioscience (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population
Teresa Campbell, Jesse Slone, Hallie Metzger, et al.
Genetics in Medicine Open (2023) Vol. 2, pp. 100841-100841
Open Access | Times Cited: 2
Preconception carrier screening and preimplantation genetic testing in the infertility management
Silvia Caroselli, Maurizio Poli, Valentina Gatta, et al.
Andrology (2024)
Open Access
A capillary electrophoresis-based assay for carrier screening of the hotspot mutations in the CYP21A2 gene
Juan Tan, Shuping Jin, Linxiang Huang, et al.
Heliyon (2024) Vol. 10, Iss. 19, pp. e38222-e38222
Open Access
Prevalence of thalassaemia among childbearing-age Li and Han populations in Hainan Province
Fangchao Tao, Yanquan Lai, Jiaqi Chen, et al.
Hematology (2024) Vol. 29, Iss. 1
Open Access
A brief clinical genetics review: stepwise diagnostic processes of a monogenic disorder—hypertriglyceridemia
Masako Ueda
Translational Pediatrics (2024) Vol. 13, Iss. 10, pp. 1828-1848
Open Access
Estimating at-risk couple rates across 1000 exome sequencing data cohort for 176 genes and its importance relevance for health policies
Nikolaos M. Marinakis, Faidon‐Nikolaos Tilemis, Danai Veltra, et al.
European Journal of Human Genetics (2024)
Closed Access
The Diagnostic Performance of Noninvasive Prenatal Testing for Single-Gene Disorders: A Systematic Review and Meta-Analysis
Yangyi Liu, Yanting Yang, Jincheng Zhang, et al.
(2024)
Closed Access
Highlights of the 26th ISPD annual conference, hosted in a vibrant Canadian city along with the Montreal grand prix 2022
Nanette Okun, R. Douglas Wilson
Prenatal Diagnosis (2023) Vol. 43, Iss. 4, pp. 409-410
Closed Access
Evaluation of carrier frequency of pathogenic variants in genes associated with the development of autosomal and X-linked recessive diseases
Е. А. Сотникова, А. В. Киселева, Marija Zaicenoka, et al.
Russian Journal of Preventive Medicine (2023) Vol. 26, Iss. 12, pp. 73-73
Closed Access
Page 1

Scroll to top