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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:

Next Generation Sequencing and the Future of Genetic Diagnosis
Katja Lohmann, Christine Klein
Neurotherapeutics (2014) Vol. 11, Iss. 4, pp. 699-707
Open Access | Times Cited: 154

Showing 1-25 of 154 citing articles:

MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search
Noa Rappaport, Michal Twik, Inbar Plaschkes, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D877-D887
Open Access | Times Cited: 534
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 3, pp. 466-483
Open Access | Times Cited: 208
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease
Hernán Gonorazky, Sergey Naumenko, Arun Ramani, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 5, pp. 1007-1007
Open Access | Times Cited: 193
Laboratory diagnosis of thalassemia
Valentina Brancaleoni, Elena Di Pierro, Irene Motta, et al.
International Journal of Laboratory Hematology (2016) Vol. 38, Iss. S1, pp. 32-40
Open Access | Times Cited: 186
A Comprehensive Review of Performance of Next-Generation Sequencing Platforms
Muhammad Tariq Pervez, Mirza Jawad ul Hasnain, Syed Hassan Abbas, et al.
BioMed Research International (2022) Vol. 2022, pp. 1-12
Open Access | Times Cited: 117
Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development
Carin Yates, Kristin G. Monaghan, Deborah Copenheaver, et al.
Genetics in Medicine (2017) Vol. 19, Iss. 10, pp. 1171-1178
Open Access | Times Cited: 141
Gut Microbiota Dysbiosis as Risk and Premorbid Factors of IBD and IBS Along the Childhood–Adulthood Transition
Lorenza Putignani, Federica Del Chierico, Pamela Vernocchi, et al.
Inflammatory Bowel Diseases (2015) Vol. 22, Iss. 2, pp. 487-504
Open Access | Times Cited: 133
Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes
Paul J. Dunn, Cassie L. Albury, Neven Maksemous, et al.
Frontiers in Genetics (2018) Vol. 9
Open Access | Times Cited: 130
Genetics of Parkinson disease
Aloysius Domingo, Christine Klein
Handbook of clinical neurology (2018), pp. 211-227
Closed Access | Times Cited: 129
Precision and Personalized Medicine: How Genomic Approach Improves the Management of Cardiovascular and Neurodegenerative Disease
Oriana Strianese, Francesca Rizzo, Michele Ciccarelli, et al.
Genes (2020) Vol. 11, Iss. 7, pp. 747-747
Open Access | Times Cited: 125
Genomic newborn screening: public health policy considerations and recommendations
Jan M. Friedman, Martina C. Cornel, Aaron J. Goldenberg, et al.
BMC Medical Genomics (2017) Vol. 10, Iss. 1
Open Access | Times Cited: 116
Update on the Genetics of Dystonia
Katja Lohmann, Christine Klein
Current Neurology and Neuroscience Reports (2017) Vol. 17, Iss. 3
Closed Access | Times Cited: 110
Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons
Gaël Nicolas, David Wallon, Camille Charbonnier, et al.
European Journal of Human Genetics (2015) Vol. 24, Iss. 5, pp. 710-716
Open Access | Times Cited: 92
Nucleic-Acid-Based Molecular Fungal Diagnostics: A Way to a Better Future
Rajendra Gudisa, Ritika Harchand, Shivaprakash M. Rudramurthy
Diagnostics (2024) Vol. 14, Iss. 5, pp. 520-520
Open Access | Times Cited: 11
Unsolved challenges of clinical whole-exome sequencing: a systematic literature review of end-users’ views
Gabrielle Bertier, Martin Hétu, Yann Joly
BMC Medical Genomics (2016) Vol. 9, Iss. 1
Open Access | Times Cited: 79
The expanding phenotypic spectra of kidney diseases: insights from genetic studies
Marijn Stokman, Kirsten Y. Renkema, Rachel H. Giles, et al.
Nature Reviews Nephrology (2016) Vol. 12, Iss. 8, pp. 472-483
Closed Access | Times Cited: 74
Clinical presentation and diagnosis of mucopolysaccharidoses
Molly Stapleton, Nivethitha Arunkumar, Francyne Kubaski, et al.
Molecular Genetics and Metabolism (2018) Vol. 125, Iss. 1-2, pp. 4-17
Closed Access | Times Cited: 73
Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing
Yimin Wang, Xiaonan Du, Bin Rao, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 66
Mucopolysaccharidosis type VI (MPS VI) and molecular analysis: Review and classification of published variants in theARSBgene
Rosella Tomanin, Litsa Karageorgos, Alessandra Zanetti, et al.
Human Mutation (2018) Vol. 39, Iss. 12, pp. 1788-1802
Open Access | Times Cited: 63
Pharmacogenetics: An Important Part of Drug Development with A Focus on Its Application
J T Oates, Daisy D. Colon Lopez
International Journal of Biomedical Investigation (2018) Vol. 1, Iss. 2, pp. 1-16
Open Access | Times Cited: 60
Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes
Francesca Magrinelli, Bettina Balint, Kailash P. Bhatia
Movement Disorders Clinical Practice (2021) Vol. 8, Iss. 3, pp. 299-310
Open Access | Times Cited: 52
Digital detection of biomarkers assisted by nanoparticles: application to diagnostics
Marina Cretich, George G. Daaboul, Laura Solá, et al.
Trends in biotechnology (2015) Vol. 33, Iss. 6, pp. 343-351
Closed Access | Times Cited: 60
Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis
Laila C. Schenkel, Jennifer Kerkhof, Alan Stuart, et al.
Journal of Molecular Diagnostics (2016) Vol. 18, Iss. 5, pp. 657-667
Open Access | Times Cited: 55
Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans
Katja Lohmann, Ikuo Masuho, Dipak N. Patil, et al.
Human Molecular Genetics (2017), pp. ddx018-ddx018
Open Access | Times Cited: 55
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome
Giovanni Ponti, Ester Castellsagué, Cristel Ruini, et al.
Clinical Genetics (2014) Vol. 87, Iss. 6, pp. 507-516
Closed Access | Times Cited: 53
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