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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:

Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network
Thomas Eggermann, Justin H. Davies, M. Tauber, et al.
Genes (2021) Vol. 12, Iss. 4, pp. 585-585
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

IGF2: Development, Genetic and Epigenetic Abnormalities
Céline Sélénou, Frédéric Brioude, Éloïse Giabicani, et al.
Cells (2022) Vol. 11, Iss. 12, pp. 1886-1886
Open Access | Times Cited: 64
Imprinting disorders
Thomas Eggermann, David Monk, Guiomar Pérez de Nanclares, et al.
Nature Reviews Disease Primers (2023) Vol. 9, Iss. 1
Closed Access | Times Cited: 33
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
First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders
Deborah Mackay, Jet Bliek, Masayo Kagami, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 26
Highlighting the trajectory from intrauterine growth restriction to future obesity
Katherina Vicky Gantenbein, Christina Kanaka‐Gantenbein
Frontiers in Endocrinology (2022) Vol. 13
Open Access | Times Cited: 24
The contribution of imprinted genes to neurodevelopmental and neuropsychiatric disorders
Anthony R Isles
Translational Psychiatry (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 23
The long non-coding RNA Meg3 mediates imprinted gene expression during stem cell differentiation
Sabina Farhadova, Amani Ghousein, François Charon, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 11, pp. 6183-6200
Open Access | Times Cited: 5
An integrated single-cell analysis of human adrenal cortex development
Ignacio del Valle, Matthew D. Young, Gerda Kildisiute, et al.
JCI Insight (2023) Vol. 8, Iss. 14
Open Access | Times Cited: 10
Association between imprinting disorders and assisted reproductive technologies
Masayo Kagami, Kaori Hara‐Isono, A. Sasaki, et al.
Epigenomics (2025), pp. 1-14
Open Access
Temple Syndrome: Clinical Findings, Body Composition and Cognition in 15 Patients
Alicia F. Juriaans, Gerthe F. Kerkhof, Eva F. Mahabier, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 21, pp. 6289-6289
Open Access | Times Cited: 16
DNA methylation analysis to differentiate reference, breed, and parent-of-origin effects in the bovine pangenome era
Callum MacPhillamy, Tong Chen, Stefan Hiendleder, et al.
GigaScience (2024) Vol. 13
Open Access | Times Cited: 3
Exploring chromatin structural roles of non-coding RNAs at imprinted domains
David Llères, Yui Imaizumi, Robert Feil
Biochemical Society Transactions (2021) Vol. 49, Iss. 4, pp. 1867-1879
Open Access | Times Cited: 16
Genomic Imprinting in the New Omics Era: A Model for Systems-Level Approaches
Jean-Noël Hubert, Julie Demars
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 11
The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype
Anthony Holland, Katie Manning, Joyce Whittington
EBioMedicine (2022) Vol. 78, pp. 103952-103952
Open Access | Times Cited: 8
ImprintedGrb10, encoding growth factor receptor bound protein 10, regulates fetal growth independently of the insulin-like growth factor type 1 receptor (Igf1r) and insulin receptor (Insr) genes
Kim Moorwood, Florentia M. Smith, Alastair S. Garfield, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Imprinted Grb10, encoding growth factor receptor bound protein 10, regulates fetal growth independently of the insulin-like growth factor type 1 receptor (Igf1r) and insulin receptor (Insr) genes
Kim Moorwood, Florentia M. Smith, Alastair S. Garfield, et al.
BMC Biology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
Molecular mechanisms of human overgrowth and use of omics in its diagnostics: chances and challenges
Dirk Prawitt, Thomas Eggermann
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 1
Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith–Wiedemann spectrum features
Siren Berland, Cecilie F. Rustad, Mariann H. L. Bentsen, et al.
Molecular Case Studies (2021) Vol. 7, Iss. 6, pp. a006113-a006113
Open Access | Times Cited: 6
Extra-uterine Growth Restriction in Preterm Infants
Akhil Maheshwari, Nitasha Bagga, Nalinikant Panigrahay
Newborn (2022) Vol. 1, Iss. 1, pp. 67-73
Open Access | Times Cited: 3
Imprinting as Basis for Complex Evolutionary Novelties in Eutherians
Maximillian Schuff, Amanda D. Strong, Lyvia Karoline Welborn, et al.
Biology (2024) Vol. 13, Iss. 9, pp. 682-682
Open Access
Prenatal diagnosis of a silver-russell syndrome caused by 11p15 duplication and pedigree analysis
Shurong Hong, Wei Hua, Xueyi Zhuang, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Genetics and Epigenetics of Precocious Puberty
Е. А. Саженова, S. A. Vasilyev, Л. В. Рычкова, et al.
Генетика (2023) Vol. 59, Iss. 12, pp. 1360-1371
Closed Access | Times Cited: 1
Genomic Imprinting: A Paradigm for Epigenetics of Human Diseases
Rosalind M. John, Louis Lefebvre, M. Azim Surani
Springer eBooks (2022), pp. 171-212
Closed Access | Times Cited: 2
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
Imprinting Disorders in Humans
Thomas Eggermann
Elsevier eBooks (2022), pp. 779-789
Closed Access | Times Cited: 1
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