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:

Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative
Christoffer Nellåker, Fowzan S. Alkuraya, Gareth Baynam, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 15

Showing 15 citing articles:

The case for open science: rare diseases
Yaffa Rubinstein, Peter N. Robinson, William A. Gahl, et al.
JAMIA Open (2020) Vol. 3, Iss. 3, pp. 472-486
Open Access | Times Cited: 45

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16

Democratising or disrupting diagnosis? Ethical issues raised by the use of AI tools for rare disease diagnosis
Nina Hallowell, Shirlene Badger, Francis McKay, et al.
SSM - Qualitative Research in Health (2023) Vol. 3, pp. 100240-100240
Open Access | Times Cited: 14

The ethical and legal landscape of brain data governance
Paschal Ochang, Bernd Carsten Stahl, Damian Eke
PLoS ONE (2022) Vol. 17, Iss. 12, pp. e0273473-e0273473
Open Access | Times Cited: 14

Optimizing Genetic Diagnosis of Neurodevelopmental Disorders in the Clinical Setting
David Michelson, Robin D. Clark
Clinics in Laboratory Medicine (2020) Vol. 40, Iss. 3, pp. 231-256
Closed Access | Times Cited: 16

Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome
Alexander J.M. Dingemans, Diante E. Stremmelaar, Roos van der Donk, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 9, pp. 1418-1423
Open Access | Times Cited: 13

Towards standardization guidelines for in silico approaches in personalized medicine
Søren Brunak, Catherine Bjerre Collin, Katharina Ó Cathaoir, et al.
Berichte aus der medizinischen Informatik und Bioinformatik/Journal of integrative bioinformatics (2020) Vol. 17, Iss. 2-3
Open Access | Times Cited: 14

Computational facial analysis for rare Mendelian disorders
Tzung‐Chien Hsieh, Peter Krawitz
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2023) Vol. 193, Iss. 3
Open Access | Times Cited: 4

A Scoping Review on Analysis of the Barriers and Support Factors of Open Data
Norbert Lichtenauer, Lukas Schmidbauer, Sebastian Wilhelm, et al.
Information (2023) Vol. 15, Iss. 1, pp. 5-5
Open Access | Times Cited: 2

Digital/computational phenotyping: What are the differences in the science and the ethics?
Federica Lucivero, Nina Hallowell
Big Data & Society (2021) Vol. 8, Iss. 2
Open Access | Times Cited: 5

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Research Square (Research Square) (2024)
Open Access

Digitizing the Pharma Neurons – A Technological Operation in Progress!
Payal Bhardwaj, Raj Kumar Yadav, Sojan Kurian
Reviews on Recent Clinical Trials (2020) Vol. 15, Iss. 3, pp. 178-187
Closed Access

Is Sharing Datasets the Answer to the New Challenges of Reproductive Biology Research?
Andrea Sixto-Costoya, Rut Lucas-Domínguez, Rafaél Aleixandre-Benavent, et al.
Reproductive Sciences (2021) Vol. 28, Iss. 4, pp. 1023-1025
Open Access

Informationstechnik (IT) und Seltene Erkrankungen

Elsevier eBooks (2021), pp. 93-114
Closed Access

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