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:

Psychiatric and Cognitive Aspects of Phenylketonuria: The Limitations of Diet and Promise of New Treatments
Killian Ashe, Wendy Kelso, Sarah Farrand, et al.
Frontiers in Psychiatry (2019) Vol. 10
Open Access | Times Cited: 117

Showing 1-25 of 117 citing articles:

A comprehensive review on the applications of nano-biosensor-based approaches for non-communicable and communicable disease detection
Rout George Kerry, Kingsley Eghonghon Ukhurebor, Swati Kumari, et al.
Biomaterials Science (2021) Vol. 9, Iss. 10, pp. 3576-3602
Closed Access | Times Cited: 68
Phenylketonuria and the brain
Valentina Rovelli, Nicola Longo
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 1, pp. 107583-107583
Closed Access | Times Cited: 29
Functional contribution of the intestinal microbiome in autism spectrum disorder, attention deficit hyperactivity disorder, and Rett syndrome: a systematic review of pediatric and adult studies
Valentina Caputi, Lee Hill, Melanie Figueiredo, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 12
Breaking genetic shackles: The advance of base editing in genetic disorder treatment
Fang Xu, Caiyan Zheng, Weihui Xu, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 8
Mandatory newborn screening in the United States: History, current status, and existential challenges
Shawn E. McCandless, Erica J. Wright
Birth Defects Research (2020) Vol. 112, Iss. 4, pp. 350-366
Closed Access | Times Cited: 57
Identification of key metabolites during cisplatin-induced acute kidney injury using an HPLC-TOF/MS-based non-targeted urine and kidney metabolomics approach in rats
Xiaoyu Qu, Huan Gao, Jingmeng Sun, et al.
Toxicology (2020) Vol. 431, pp. 152366-152366
Closed Access | Times Cited: 51
Major Depressive Disorder: Existing Hypotheses about Pathophysiological Mechanisms and New Genetic Findings
Muhammad Kamran, Farhana Bibi, Asim ur Rehman, et al.
Genes (2022) Vol. 13, Iss. 4, pp. 646-646
Open Access | Times Cited: 36
Efficient in vivo prime editing corrects the most frequent phenylketonuria variant, associated with high unmet medical need
Dominique L. Brooks, Madelynn N. Whittaker, Ping Qü, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 12, pp. 2003-2014
Open Access | Times Cited: 18
The Utility of Amino Acid Metabolites in the Diagnosis of Major Depressive Disorder and Correlations with Depression Severity
Cyrus S. H. Ho, Gabrielle Wann Nii Tay, Hai Ning Wee, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 3, pp. 2231-2231
Open Access | Times Cited: 16
Two years of pegvaliase in Germany: Experiences and best practice recommendations
Johannes Krämer, Christoph Baerwald, Christian Heimbold, et al.
Molecular Genetics and Metabolism (2023) Vol. 139, Iss. 1, pp. 107564-107564
Open Access | Times Cited: 16
ADHD symptoms in neurometabolic diseases: Underlying mechanisms and clinical implications
Selina Cannon Homaei, Helene Barone, Rune Kleppe, et al.
Neuroscience & Biobehavioral Reviews (2021) Vol. 132, pp. 838-856
Open Access | Times Cited: 37
Behavioral and Psychiatric Disorders in Syndromic Autism
Ann Genovese, Merlin G. Butler
Brain Sciences (2024) Vol. 14, Iss. 4, pp. 343-343
Open Access | Times Cited: 4
Systematic literature review of the somatic comorbidities experienced by adults with phenylketonuria
Kaleigh Bulloch Whitehall, Sarah Rose, Gillian E. Clague, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 4
Evaluation of primary health care nurses’ knowledge and neonatal screening performance for phenylketonuria in Alexandria
Esraa Ismail, Wafaa Elarousy, Shaymaa Saeed Mohamed Badawe, et al.
BMC Nursing (2025) Vol. 24, Iss. 1
Open Access
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature
Guido Leone, Concetta Meli, Raffaele Falsaperla, et al.
Nutrients (2025) Vol. 17, Iss. 4, pp. 678-678
Open Access
Our lives with PKU: German patient voices - “Nothing about us without us”
Karin Lange, Jens Böhmer, Yvonne Deich, et al.
Molecular Genetics and Metabolism Reports (2025) Vol. 43, pp. 101201-101201
Closed Access
Diagnosing late-onset PKU in the shadow of refractory seizures
Ameer Awashra, Haroun Neiroukh, Aya Milhem, et al.
Radiology Case Reports (2025) Vol. 20, Iss. 5, pp. 2368-2372
Closed Access
Metabolism navigates neural cell fate in development, aging and neurodegeneration
Larissa Traxler, Jessica Lagerwall, Sophie Eichhorner, et al.
Disease Models & Mechanisms (2021) Vol. 14, Iss. 8
Open Access | Times Cited: 30
Nutrition, Microbiota and Role of Gut-Brain Axis in Subjects with Phenylketonuria (PKU): A Review
Elvira Verduci, Maria Teresa Carbone, Elisa Borghi, et al.
Nutrients (2020) Vol. 12, Iss. 11, pp. 3319-3319
Open Access | Times Cited: 27
Do early‐treated adults with phenylketonuria sense high phenylalanine levels?
Laura Hauri, Raphaela Muri, Regula Everts, et al.
JIMD Reports (2024) Vol. 65, Iss. 5, pp. 354-358
Open Access | Times Cited: 3
The effect of improved dietary control on cognitive and psychiatric functioning in adults with phenylketonuria: the ReDAPT study
Nicholas M. Burgess, Wendy Kelso, Charles B. Malpas, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 22
Characterisation and differential diagnosis of neurological complications in adults with phenylketonuria: literature review and expert opinion
Martin Merkel, Daniela Berg, Norbert Brüggemann, et al.
Journal of Neurology (2023) Vol. 270, Iss. 8, pp. 3675-3687
Open Access | Times Cited: 8
Evaluating change in diet with pegvaliase treatment in adults with phenylketonuria: Analysis of phase 3 clinical trial data
Fran Rohr, Barbara K. Burton, Anne Dee, et al.
Molecular Genetics and Metabolism (2023) Vol. 141, Iss. 3, pp. 108122-108122
Open Access | Times Cited: 8
Peripheral blood and urine metabolites and biological functions in post-stroke depression
Haiyan Liu, Juncai Pu, Qinxiang Zhou, et al.
Metabolic Brain Disease (2022) Vol. 37, Iss. 5, pp. 1557-1568
Closed Access | Times Cited: 13
Pegvaliase therapy for phenylketonuria: Real-world case series and clinical insights
Iris Scala, Lucia Brodosi, Daniela Gueraldi, et al.
Molecular Genetics and Metabolism (2024) Vol. 142, Iss. 1, pp. 108151-108151
Open Access | Times Cited: 2
Page 1 - Next Page

Scroll to top