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:

Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders
Wenman Wu, Xuanyou Zhou, Zhengwen Jiang, et al.
Human Genomics (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 11

Showing 11 citing articles:

Fetal gene therapy
Simon N. Waddington, William H. Peranteau, Ahad A. Rahim, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 47, Iss. 1, pp. 192-210
Open Access | Times Cited: 14
First‐trimester noninvasive prenatal diagnosis of seven facioscapulohumeral muscular dystrophy type 1 families using SNP‐based amplicon sequencing: An earlier, rapid and safer way
Xinyu Fu, Zhenhua Zhao, Lingrong Kong, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 6
Closed Access | Times Cited: 2
Variable fragment length allele-specific polymerase chain reaction (VFLASP), a method for simple and reliable genotyping
Tamás Tóth, Ákos Csaba, Attila Bokor, et al.
Molecular and Cellular Probes (2023) Vol. 69, pp. 101910-101910
Open Access | Times Cited: 5
Developing and Validating Noninvasive Prenatal Testing for de novo Autosomal Dominant Monogenic Diseases in Vietnam
Thi Yen Nhi Nguyen, Y‐Thanh Lu, Anh Duy Nguyen, et al.
Personalized Medicine (2023) Vol. 20, Iss. 5, pp. 425-433
Closed Access | Times Cited: 4
Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles
Bo Gao, Yi Jiang, Mingyu Han, et al.
Journal of Molecular Diagnostics (2024) Vol. 26, Iss. 7, pp. 638-651
Open Access | Times Cited: 1
Non-invasive prenatal detection of dominant single-gene disorders in fetal structural abnormalities: a clinical feasibility study
Lei Wang, Xiaoli Wu, Mou Jing, et al.
Archives of Gynecology and Obstetrics (2024) Vol. 310, Iss. 6, pp. 2943-2955
Closed Access | Times Cited: 1
Population monitoring of trisomy 21: problems and approaches
Karl Sperling, Hagen Scherb, Heidemarie Neitzel
Molecular Cytogenetics (2023) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Report on the diagnosis and treatment of hemophilia in China (Version 2024)
Feng Xue, Jing Dai, Lixia Chen, et al.
LabMed discovery. (2024) Vol. 1, Iss. 1, pp. 100007-100007
Open Access
Fetal Origin Circulating Cell-Free Nucleic Acids in Maternal Circulation and Their Clinical Importance
Riyaz Ahmad Rather
(2024), pp. 17-35
Closed Access
Sequencing: A Promising Path in the Detection of Fetal Health
Indu Sharma, Neha Negi, Subhas Chandra Saha
(2024), pp. 273-288
Closed Access
SERPINB7 mutation causes Nagashima‐type palmoplantar keratosis and its spatiotemporal expression in zebrafish
Chen Lyu, Fan Zhang, Tingting Liu, et al.
Experimental Dermatology (2023) Vol. 32, Iss. 6, pp. 766-776
Open Access | Times Cited: 1
Page 1

Scroll to top