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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:

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

Showing 1-25 of 28 citing articles:

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
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos
Carlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Genes & Development (2024) Vol. 38, Iss. 3-4, pp. 131-150
Open Access | Times Cited: 8
Syndromic forms of congenital hyperinsulinism
Martin Zenker, Klaus Mohnike, Katja Palm
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 13
PADI6: What we know about the elusive fifth member of the peptidyl arginine deiminase family
Jack Williams, Louise J. Walport
Philosophical Transactions of the Royal Society B Biological Sciences (2023) Vol. 378, Iss. 1890
Open Access | Times Cited: 12
Role of the PADI family in inflammatory autoimmune diseases and cancers: A systematic review
Changhui Zhu, Chunyan Liu, Zhengbin Chai
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 11
Human Reproduction and Disturbed Genomic Imprinting
Thomas Eggermann
Genes (2024) Vol. 15, Iss. 2, pp. 163-163
Open Access | Times Cited: 4
New insights into oocyte cytoplasmic lattice-associated proteins
Carlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Trends in Genetics (2024) Vol. 40, Iss. 10, pp. 880-890
Closed Access | Times Cited: 4
Two Novel Protein‐Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal Complex
Zeynep Yalcin, Zheng Gao, Ibrahim M. Abdelrazek, et al.
Clinical Genetics (2025)
Open Access
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
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Larissa Bilo, Eguzkine Ochoa, Sunwoo Lee, et al.
Clinical Epigenetics (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Identification of differentially methylated regions in rare diseases from a single-patient perspective
Robin Grolaux, Alexis Hardy, Catharina Olsen, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 8
Prenatal testing for Imprinting Disorders: A clinical perspective
Andreas Dufke, Thomas Eggermann, Karl Oliver Kagan, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 8, pp. 983-992
Open Access | Times Cited: 4
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
Laura Pignata, Francesco Cecere, Fabio Acquaviva, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 4
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
A case of an Angelman-syndrome caused by an intragenic duplication of UBE3A uncovered by adaptive nanopore sequencing
Laura Holthöfer, Stefan Diederich, Verena Haug, et al.
Clinical Epigenetics (2024) Vol. 16, Iss. 1
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
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
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum
Francesco Fioravanti Passaretti, Laura Pignata, Giuseppina Vitiello, et al.
Genes (2022) Vol. 13, Iss. 10, pp. 1875-1875
Open Access | Times Cited: 4
Increased copy number of imprinted genes in the chromosomal region 20q11-q13.32 is associated with resistance to antitumor agents in cancer cell lines
Julia Krushkal, Suleyman Vural, Travis L. Jensen, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 3
Clinical Significance of Monogenic Mutations in the Euploid Embryo Genome Associated with Miscarriage
Е. V. Kudryavtseva, О. П. Ковтун, В. В. Ковалев
Annals of the Russian academy of medical sciences (2024) Vol. 79, Iss. 2, pp. 123-130
Closed Access
Structural insight into the function of human peptidyl arginine deiminase 6
Jack Williams, S. Mouilleron, Rolando Hernandez Trapero, et al.
Computational and Structural Biotechnology Journal (2024) Vol. 23, pp. 3258-3269
Open Access
A clinical case of multilocus imprinting disturbances: the first description in the Russian Federation
E. G. Panchenko, O. V. Vasyukova, П. Л. Окороков, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2024) Vol. 69, Iss. 4, pp. 90-96
Open Access
Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
Tatsuki Urakawa, Hidenobu Soejima, Kaori Yamoto, et al.
Clinical Epigenetics (2024) Vol. 16, Iss. 1
Open Access
A novel homozygous mutation in the NLRP2 gene causes early embryonic arrest
Menghan Chai, Xingxing Wen, Dandan Yang, et al.
Journal of Assisted Reproduction and Genetics (2024) Vol. 41, Iss. 12, pp. 3347-3355
Closed Access
Temple Syndrome: Comprehensive Clinical Study in Genetically Confirmed 60 Japanese Patients
Tomoe Ogawa, Hiromune Narusawa, Keisuke Nagasaki, et al.
The Journal of Clinical Endocrinology & Metabolism (2024)
Open Access
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