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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:

Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequences
Miriam Elbracht, Deborah Mackay, Matthias Begemann, et al.
Human Reproduction Update (2020) Vol. 26, Iss. 2, pp. 197-213
Open Access | Times Cited: 64

Showing 26-50 of 64 citing articles:

Challenges in diagnosing hydatidiform moles: a review of promising molecular biomarkers
Yating Zhao, Bo Huang, Lin Zhou, et al.
Expert Review of Molecular Diagnostics (2022) Vol. 22, Iss. 8, pp. 783-796
Open Access | Times Cited: 10
Recent Advances in Noncoding RNAs

IntechOpen eBooks (2022)
Open Access | Times Cited: 9
A patient with multilocus imprinting disturbance involving hypomethylation at 11p15 and 14q32, and phenotypic features of Beckwith‐Wiedemann and Temple syndromes
Sarah E. Grosvenor, Justin H. Davies, Margaret Lever, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 6, pp. 1896-1903
Open Access | Times Cited: 8
Placental Mesenchymal Dysplasia and Beckwith–Wiedemann Syndrome
Hidenobu Soejima, Satoshi Hara, Takashi Ohba, et al.
Cancers (2022) Vol. 14, Iss. 22, pp. 5563-5563
Open Access | Times Cited: 8
Mosaic genome‐wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells
Gioia Mastromoro, Daniele Guadagnolo, Enrica Marchionni, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 4, pp. 1101-1106
Closed Access | Times Cited: 4
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
Impact of the Sire on Pregnancy Loss
Ky G Pohler, R.V. Oliveira Filho
Veterinary Clinics of North America Food Animal Practice (2023) Vol. 40, Iss. 1, pp. 121-129
Closed Access | Times Cited: 4
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
NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss
Е. А. Саженова, Nikitina Tv, S. A. Vasilyev, et al.
Journal of Assisted Reproduction and Genetics (2021) Vol. 38, Iss. 11, pp. 2893-2908
Open Access | Times Cited: 8
Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability
Marwan K. Tayeh, Janean DeVaul, Kristin LeSueur, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 7, pp. 2209-2216
Open Access | Times Cited: 6
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
Clinical spectrum and management of imprinting disorders
Miriam Elbracht, Gerhard Binder, Olaf Hiort, et al.
Medizinische Genetik (2020) Vol. 32, Iss. 4, pp. 321-334
Open Access | Times Cited: 8
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
Double sperm cloning (DSC) is a promising strategy in mammalian genetic engineering and stem cell research
Zhiping Zhang, Juntao Zhang, Shucheng Huang, et al.
Stem Cell Research & Therapy (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 6
A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 2
Kaori Hara‐Isono, Keiko Matsubara, Riku Hamada, et al.
Journal of Human Genetics (2021) Vol. 66, Iss. 11, pp. 1121-1126
Closed Access | Times Cited: 6
Lack of GNAS Remethylation During Oogenesis May Be a Cause of Sporadic Pseudohypoparathyroidism Type Ib
Angelo Milioto, Monica Reyes, Patrick Hanna, et al.
The Journal of Clinical Endocrinology & Metabolism (2021) Vol. 107, Iss. 4, pp. e1610-e1619
Open Access | Times Cited: 6
Basics and disturbances of genomic imprinting
Dirk Prawitt, Thomas Haaf
Medizinische Genetik (2020) Vol. 32, Iss. 4, pp. 297-304
Open Access | Times Cited: 6
Maternal effect genes as risk factors for congenital heart defects
Fadi I. Musfee, Omobola O. Oluwafemi, A. J. Agopian, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 2, pp. 100098-100098
Open Access | Times Cited: 4
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
Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia
Saori Aoki, Ken Higashimoto, Hidenori Hidaka, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
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
Molecular characterization of temple syndrome families with 14q32 epimutations
Johanna Brück, Matthias Begemann, Daniela Dey, et al.
European Journal of Medical Genetics (2020) Vol. 63, Iss. 12, pp. 104077-104077
Closed Access | Times Cited: 5
Improving the prenatal diagnosis of Beckwith–Wiedemann syndrome
Ignatia B. Van den Veyver
Prenatal Diagnosis (2021) Vol. 41, Iss. 7, pp. 795-797
Closed Access | Times Cited: 5
Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith–Wiedemann syndrome
Feifei Sun, Satoshi Hara, Chiyoko Tomita, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 10, pp. 3062-3067
Closed Access | Times Cited: 5
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Thomas Eggermann
Geburtshilfe und Frauenheilkunde (2021) Vol. 81, Iss. 07, pp. 780-788
Open Access | Times Cited: 5

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