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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:

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

Showing 1-25 of 50 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
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
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
Genetics of Oocyte Maturation Defects and Early Embryo Development Arrest
О. А. Соловова, В. Б. Черных
Genes (2022) Vol. 13, Iss. 11, pp. 1920-1920
Open Access | Times Cited: 28
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: 5
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
A Maternal Loss‐of‐Function Variant in KHDC3L Gene Causes a Range of Adverse Pregnancy Outcomes: A Case Report
Zahra Anvar, Farnoosh Jafarpour, Bahia Namavar Jahromi, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 1
Open Access
Subcortical Maternal Complex in Female Infertility: A Transition from Animal Models to Human Studies
Sibte Hassan, Nomia Ashraf, Khola Hanif, et al.
Molecular Biology Reports (2025) Vol. 52, Iss. 1
Closed Access
Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure
Maryam Rezaei, Beena Suresh, Eric Bereke, et al.
Clinical Genetics (2021) Vol. 99, Iss. 6, pp. 823-828
Closed Access | Times Cited: 27
Investigation of Multilocus Imprinting Disturbance (MLID) in 101 Beckwith-Wiedemann Spectrum patients
Alejandro Parra, Mario Cazalla, Carlos Rodríguez‐Antolín, et al.
Research Square (Research Square) (2025)
Closed Access
Novel biallelic mutations in PADI6 in patients with early embryonic arrest
Jie Dong, Jing Fu, Zheng Yan, et al.
Journal of Human Genetics (2022) Vol. 67, Iss. 5, pp. 285-293
Closed Access | Times Cited: 15
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
A novel homozygous mutation in the PADI6 gene causes early embryo arrest
Xiaoxia Wang, Huimin Zhu, Yi He, et al.
Reproductive Health (2022) Vol. 19, Iss. 1
Open Access | Times Cited: 13
NLRP7 Promotes Choriocarcinoma Growth and Progression through the Establishment of an Immunosuppressive Microenvironment
Déborah Reynaud, Roland Abi Nahed, Nicolas Lemaître, et al.
Cancers (2021) Vol. 13, Iss. 12, pp. 2999-2999
Open Access | Times Cited: 17
ImprintSeq, a novel tool to interrogate DNA methylation at human imprinted regions and diagnose multilocus imprinting disturbance
Eguzkine Ochoa, Sunwoo Lee, Benoît Lan-Leung, et al.
Genetics in Medicine (2021) Vol. 24, Iss. 2, pp. 463-474
Closed Access | Times Cited: 17
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance
Masayo Kagami, Kaori Hara‐Isono, Keiko Matsubara, et al.
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 16
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
Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study
Ahmed Alhendi, Derek Lim, Shane McKee, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 6, pp. 613-622
Open Access | Times Cited: 15
Maternal exome analysis for the diagnosis of oocyte maturation defects and early embryonic developmental arrest
Antonio Capalbo, Silvia Buonaiuto, Matteo Figliuzzi, et al.
Reproductive BioMedicine Online (2022) Vol. 45, Iss. 3, pp. 508-518
Open Access | Times Cited: 10
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
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