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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:

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: 24

Showing 24 citing articles:

Long read sequencing on its way to the routine diagnostics of genetic diseases
Giulia Olivucci, Emanuela Iovino, Giovanni Innella, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 19
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
Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes
Cate Paschal, Miranda Galey, Anita Beck, et al.
Journal of Molecular Diagnostics (2025)
Open Access | Times Cited: 1
Human Reproduction and Disturbed Genomic Imprinting
Thomas Eggermann
Genes (2024) Vol. 15, Iss. 2, pp. 163-163
Open Access | Times Cited: 4
Congenital Imprinting Diseases: Aetiology, Pre- and Perinatal Manifestations, Diagnosis and Care of Affected Families and Pregnancies
Thomas Eggermann, Karl Oliver Kagan, Andreas Dufke
Geburtshilfe und Frauenheilkunde (2025)
Open Access
Maternal uniparental disomy of chromosome 7: how chromosome 7-encoded imprinted genes contribute to the Silver–Russell phenotype
Matthias Begemann, Anna Lengyel, Éva Pinti, et al.
Clinical Epigenetics (2025) Vol. 17, Iss. 1
Open Access
Comprehensive study on central precocious puberty: molecular and clinical analyses in 90 patients
Hiromune Narusawa, Tomoe Ogawa, Hideaki Yagasaki, et al.
The Journal of Clinical Endocrinology & Metabolism (2024)
Open Access | Times Cited: 3
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
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
Maternal uniparental disomy for chromosome 6 in 2 prenatal cases with IUGR: case report and literature review
Yan Jiang, Yang Xue Xiao, Jiao Jiao Xiong, et al.
Molecular Cytogenetics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 1
Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes
Cate Paschal, Miranda Galey, Anita Beck, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer
Francesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Cancers (2023) Vol. 15, Iss. 7, pp. 1944-1944
Open Access | Times Cited: 3
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
First‐time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Elia Schlaich, Wouter Hubens, Thomas Eggermann
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 12
Open Access | Times Cited: 2
Bovine Serum Albumin Molecularly Imprinted Electrochemical Sensors Modified by Carboxylated Multi-Walled Carbon Nanotubes/CaAlg Hydrogels
Letian Cheng, Zhilong Guo, Yuansheng Lin, et al.
Gels (2023) Vol. 9, Iss. 8, pp. 673-673
Open Access | Times Cited: 2
Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening
Jéssica Mallmann Erbes Schaefer Martins, Barbara Leitao Braga, Klevia Sampaio, et al.
Archives of Endocrinology and Metabolism (2024) Vol. 68
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
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
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
Prognostic importance of direct assignment of parent-of-origin via long-read genome and epigenome sequencing in retinoblastoma
Andrew W. Stacey, Kazuo Nakamichi, Jennifer Huey, et al.
JCI Insight (2024)
Open Access
A Long-term Follow-up of a Late Diagnosed Patient with Temple Syndrome – a Case Report
Nikolinka Yordanova, Violeta Iotova, D. J. G. Mackay, et al.
Journal of Clinical Research in Pediatric Endocrinology (2023)
Open Access | Times Cited: 1
Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders
Hwa Young Kim, Choong Ho Shin, Chang Ho Shin, et al.
PLoS ONE (2023) Vol. 18, Iss. 8, pp. e0290450-e0290450
Open Access | Times Cited: 1
Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?
África Manero-Azua, Arrate Pereda, Isabel Llano‐Rivas, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 1
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