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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:

Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study
Ahmed Alhendi, Derek Lim, Shane McKee, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 6, pp. 613-622
Open Access | Times Cited: 15

Showing 15 citing articles:

Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
Thomas Eggermann, Elzem Yapici, Jet Bliek, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 28
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Deborah Mackay, Gabriella Gazdagh, David Monk, et al.
Clinical Epigenetics (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Approach to the Patient With Short Stature: Genetic Testing
Reena Perchard, Philip Murray, Peter Clayton
The Journal of Clinical Endocrinology & Metabolism (2022) Vol. 108, Iss. 4, pp. 1007-1017
Closed Access | Times Cited: 10
Effect of Obstructive Sleep Apnea during Pregnancy on Fetal Development: Gene Expression Profile of Cord Blood
Laura Cànaves-Gómez, Aarne Fleischer, Josep Muncunill-Farreny, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 10, pp. 5537-5537
Open Access | Times Cited: 1
Approach to the Patient With Suspected Silver-Russell Syndrome
Uttara Kurup, David Lim, Helena Palau, et al.
The Journal of Clinical Endocrinology & Metabolism (2024) Vol. 109, Iss. 10, pp. e1889-e1901
Open Access | Times Cited: 1
Prenatal testing for imprinting disorders: A laboratory perspective
Jasmin Beygo, Silvia Russo, Pierpaola Tannorella, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 8, pp. 973-982
Open Access | Times Cited: 3
Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives
Danielle Christine Maria van der Kaay, Anne Rochtus, Gerhard Binder, et al.
Endocrine Connections (2022) Vol. 11, Iss. 11
Open Access | Times Cited: 5
Ongoing Challenges in the Diagnosis of 11p15.5-Associated Imprinting Disorders
Deborah Mackay, I. Karen Temple
Molecular Diagnosis & Therapy (2022) Vol. 26, Iss. 3, pp. 263-272
Open Access | Times Cited: 4
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes
Naomi Baba, Anna Lengyel, Éva Pinti, et al.
Molecular Cytogenetics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Stx4 is required to regulate cardiomyocyte Ca2+ handling during vertebrate cardiac development
Eliyahu Perl, Padmapriyadarshini Ravisankar, Manu Beerens, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 3, pp. 100115-100115
Open Access | Times Cited: 3
A long way to syndromic short stature
Federica Gaudioso, Camilla Meossi, Lidia Pezzani, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2024) Vol. 50, Iss. 1
Open Access
Rare Causes and Differential Diagnosis in Patients With Silver‐Russell Syndrome
Barbara Leitao Braga, Renata C. Scalco, Thaís Kataoka Homma, et al.
Clinical Genetics (2024)
Closed Access
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study
Luise Kessler, Jeremias Krause, Florian Kraft, et al.
Clinical Genetics (2024)
Open Access
A case of mosaic deletion of paternally‐inherited PLAGL1 and two cases of upd(6)mat add to evidence for PLAGL1 under‐expression as a cause of growth restriction
Ahmed Alhendi, Gabriella Gazdagh, Derek Lim, et al.
American Journal of Medical Genetics Part A (2023) Vol. 194, Iss. 2, pp. 383-388
Closed Access | Times Cited: 1
Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome
Petra Loid, Marita Lipsanen‐Nyman, Sirpa Ala‐Mello, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 2
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