Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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 1-25 of 64 citing articles:

Mammalian oocytes store proteins for the early embryo on cytoplasmic lattices
Ida Jentoft, Felix J.B. Bäuerlein, Luisa M. Welp, et al.
Cell (2023) Vol. 186, Iss. 24, pp. 5308-5327.e25
Open Access | Times Cited: 62
The subcortical maternal complex: emerging roles and novel perspectives
Daniela Bebbere, David F. Albertini, Giovanni Coticchio, et al.
Molecular Human Reproduction (2021) Vol. 27, Iss. 7
Open Access | Times Cited: 58
Epigenetics of pregnancy: looking beyond the DNA code
Daniela Zuccarello, Ugo Sorrentino, Valeria Brasson, et al.
Journal of Assisted Reproduction and Genetics (2022) Vol. 39, Iss. 4, pp. 801-816
Open Access | Times Cited: 45
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
Genetic mechanisms of fertilization failure and early embryonic arrest: a comprehensive review
Yiqiu Wei, Jingxuan Wang, Rui Qu, et al.
Human Reproduction Update (2023) Vol. 30, Iss. 1, pp. 48-80
Closed Access | Times Cited: 28
The genetics of female and male infertility
Frank Tüttelmann, Margot J. Wyrwoll, Johanna Steingröver, et al.
Deutsches Ärzteblatt international (2025)
Closed Access | Times Cited: 1
Maternal effect genes: Update and review of evidence for a link with birth defects
Laura E. Mitchell
Human Genetics and Genomics Advances (2021) Vol. 3, Iss. 1, pp. 100067-100067
Open Access | Times Cited: 43
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
Maria Vittoria Cubellis, Laura Pignata, Ankit Verma, et al.
Clinical Epigenetics (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 50
DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting
Zahra Anvar, Imen Chakchouk, Hannah Demond, et al.
Genes (2021) Vol. 12, Iss. 8, pp. 1214-1214
Open Access | Times Cited: 38
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: 24
Gene mutations impede oocyte maturation, fertilization, and early embryonic development
Cai‐feng Fei, Liquan Zhou
BioEssays (2022) Vol. 44, Iss. 10
Closed Access | Times Cited: 23
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
Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice
Thomas Eggermann, Eamonn R. Maher, Christian P. Kratz, et al.
Cancers (2022) Vol. 14, Iss. 13, pp. 3083-3083
Open Access | Times Cited: 20
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
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
Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same family
Thomas Eggermann, Gundula Kadgien, Matthias Begemann, et al.
European Journal of Human Genetics (2020) Vol. 29, Iss. 4, pp. 575-580
Open Access | Times Cited: 31
Relevance of sperm imprinted gene methylation on assisted reproductive technique outcomes and pregnancy loss: a systematic review
Rossella Cannarella, Andrea Crafa, Rosita A. Condorelli, et al.
Systems Biology in Reproductive Medicine (2021) Vol. 67, Iss. 4, pp. 251-259
Closed Access | Times Cited: 27
The Role of Long Non-coding RNAs in Human Imprinting Disorders: Prospective Therapeutic Targets
Tingxuan Wang, Jian Jian Li, Liuyi Yang, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 22
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances
Laura Pignata, Francesco Cecere, Ankit Verma, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 14
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith–Wiedemann progeny
Pierpaola Tannorella, Luciano Calzari, Cecilia Daolio, et al.
Clinical Epigenetics (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 13
Loss of function variant in CIP2A associated with female infertility with early embryonic arrest and fragmentation
Zhenxing Liu, Qingsong Xi, Meiqi Hou, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2024) Vol. 1870, Iss. 6, pp. 167228-167228
Closed Access | Times Cited: 2
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
Long Non-Coding RNAs: Biogenesis, Mechanism of Action and Role in Different Biological and Pathological Processes
Ishteyaq Majeed Shah, Mashooq Ahmad Dar, Kaiser Ahmad Bhat, et al.
IntechOpen eBooks (2022)
Open Access | Times Cited: 11
Page 1 - Next Page

Scroll to top