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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:

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

Showing 1-25 of 31 citing articles:

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
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: 26
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
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
Two novel mutations in PADI6 and TLE6 genes cause female infertility due to arrest in embryonic development
Juan Liu, Zongjian Tan, Jun He, et al.
Journal of Assisted Reproduction and Genetics (2021) Vol. 38, Iss. 6, pp. 1551-1559
Open Access | Times Cited: 26
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 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
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
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
Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1B
Zahra Anvar, Imen Chakchouk, Momal Sharif, et al.
Reproductive Sciences (2023) Vol. 30, Iss. 9, pp. 2780-2793
Open Access | Times Cited: 4
Genetic variants underlying developmental arrests in human preimplantation embryos
Saffet Öztürk
Molecular Human Reproduction (2023) Vol. 29, Iss. 8
Open Access | Times Cited: 4
Whole genome sequencing identifies a missense polymorphism in PADI6 associated with testicular/ovotesticular XX disorder of sex development in dogs
Joanna Nowacka‐Woszuk, Monika Stachowiak, Izabela Szczerbal, et al.
Genomics (2022) Vol. 114, Iss. 4, pp. 110389-110389
Open Access | Times Cited: 7
The genetics of recurrent hydatidiform moles in Mexico: further evidence of a strong founder effect for one mutation in NLRP7 and its widespread
Mónica Aguinaga‐Ríos, Maryam Rezaei, Irma E. Monroy, et al.
Journal of Assisted Reproduction and Genetics (2021) Vol. 38, Iss. 7, pp. 1879-1886
Open Access | Times Cited: 7
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
The Landscape of Point Mutations in Human Protein Coding Genes Leading to Pregnancy Loss
Evgeniia M. Maksiutenko, Yury A. Barbitoff, Yulia A. Nasykhova, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 24, pp. 17572-17572
Open Access | Times Cited: 2
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
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
Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases
Zaletaev Dv, М. В. Немцова, V. V. Strelnikov
Molecular Biology (2022) Vol. 56, Iss. 1, pp. 1-28
Closed Access | Times Cited: 3
Maternal loss-of-function of Nlrp2 results in failure of epigenetic reprogramming in mouse oocytes
Zahra Anvar, Michael D. Jochum, Imen Chakchouk, et al.
Research Square (Research Square) (2024)
Open Access
Structural Insight into the Function of Human Peptidyl Arginine Deiminase 6
Jack Williams, S. Mouilleron, Rolando Hernandez Trapero, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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