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:
The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome
Natali S. Sobel Naveh, Daniel Deegan, Jacklyn Huhn, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 11, pp. 6315-6330
Open Access | Times Cited: 15
Natali S. Sobel Naveh, Daniel Deegan, Jacklyn Huhn, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 11, pp. 6315-6330
Open Access | Times Cited: 15
Showing 15 citing articles:
Widespread allele-specific topological domains in the human genome are not confined to imprinted gene clusters
Stephen Richer, Yuan Tian, Stefan Schoenfelder, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 19
Stephen Richer, Yuan Tian, Stefan Schoenfelder, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 19
Tissue-specific Grb10/Ddc insulator drives allelic architecture for cardiac development
Aimee M. Juan, Yee Hoon Foong, Joanne L. Thorvaldsen, et al.
Molecular Cell (2022) Vol. 82, Iss. 19, pp. 3613-3631.e7
Open Access | Times Cited: 21
Aimee M. Juan, Yee Hoon Foong, Joanne L. Thorvaldsen, et al.
Molecular Cell (2022) Vol. 82, Iss. 19, pp. 3613-3631.e7
Open Access | Times Cited: 21
TRF2 cooperates with CTCF for controlling the oncomiR-193b-3p in colorectal cancer
Roberto Dinami, Eleonora Petti, Manuela Porru, et al.
Cancer Letters (2022) Vol. 533, pp. 215607-215607
Open Access | Times Cited: 14
Roberto Dinami, Eleonora Petti, Manuela Porru, et al.
Cancer Letters (2022) Vol. 533, pp. 215607-215607
Open Access | Times Cited: 14
Differential 3D genome architecture and imprinted gene expression: cause or consequence?
Benoît Moindrot, Yui Imaizumi, Robert Feil
Biochemical Society Transactions (2024) Vol. 52, Iss. 3, pp. 973-986
Open Access | Times Cited: 2
Benoît Moindrot, Yui Imaizumi, Robert Feil
Biochemical Society Transactions (2024) Vol. 52, Iss. 3, pp. 973-986
Open Access | Times Cited: 2
Genomic Imprinting in the New Omics Era: A Model for Systems-Level Approaches
Jean-Noël Hubert, Julie Demars
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 11
Jean-Noël Hubert, Julie Demars
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 11
Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
Yahan Li, Jordana S. Lopes, Pilar Coy, et al.
Epigenetics (2022) Vol. 17, Iss. 11, pp. 1477-1496
Open Access | Times Cited: 11
Yahan Li, Jordana S. Lopes, Pilar Coy, et al.
Epigenetics (2022) Vol. 17, Iss. 11, pp. 1477-1496
Open Access | Times Cited: 11
Exploring chromatin structural roles of non-coding RNAs at imprinted domains
David Llères, Yui Imaizumi, Robert Feil
Biochemical Society Transactions (2021) Vol. 49, Iss. 4, pp. 1867-1879
Open Access | Times Cited: 15
David Llères, Yui Imaizumi, Robert Feil
Biochemical Society Transactions (2021) Vol. 49, Iss. 4, pp. 1867-1879
Open Access | Times Cited: 15
Allele-specific aberration of imprinted domain chromosome architecture associates with large offspring syndrome
Yahan Li, Frimpong Boadu, Max Highsmith, et al.
iScience (2022) Vol. 25, Iss. 5, pp. 104269-104269
Open Access | Times Cited: 9
Yahan Li, Frimpong Boadu, Max Highsmith, et al.
iScience (2022) Vol. 25, Iss. 5, pp. 104269-104269
Open Access | Times Cited: 9
The structure of the TH/INS locus and the parental allele expressed are not conserved between mammals
Trent Newman, Teruhito Ishihara, Geoff Shaw, et al.
Heredity (2024) Vol. 133, Iss. 1, pp. 21-32
Open Access | Times Cited: 1
Trent Newman, Teruhito Ishihara, Geoff Shaw, et al.
Heredity (2024) Vol. 133, Iss. 1, pp. 21-32
Open Access | Times Cited: 1
Identification and characterization of an enhancer element regulating expression of Cdkn1c (p57 gene)
Daisuke Koga, Shogo Nakayama, Tsunaki Higa, et al.
Genes to Cells (2024) Vol. 29, Iss. 12, pp. 1264-1274
Open Access | Times Cited: 1
Daisuke Koga, Shogo Nakayama, Tsunaki Higa, et al.
Genes to Cells (2024) Vol. 29, Iss. 12, pp. 1264-1274
Open Access | Times Cited: 1
Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
Yahan Li, Jordana S. Lopes, Pilar Coy, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 4
Yahan Li, Jordana S. Lopes, Pilar Coy, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 4
The counterpart congenital overgrowth syndromes Beckwith-Wiedemann Syndrome in human and large offspring syndrome in bovine involve alterations in DNA methylation, transcription, and chromatin configuration
Yahan Li, Ping Xiao, Frimpong Boadu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Yahan Li, Ping Xiao, Frimpong Boadu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Widespread allele-specific topological domains in the human genome are not confined to imprinted gene clusters
Stephen Richer, Tian Yuan, Stefan Schoenfelder, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Stephen Richer, Tian Yuan, Stefan Schoenfelder, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
Beckwith-Wiedemann syndrome with long QT caused by a deletion involving KCNQ1 but not KCNQ1OT1:TSS-DMR
Tatsuki Urakawa, Junichi Ozawa, Masato Tanaka, et al.
European Journal of Medical Genetics (2022) Vol. 66, Iss. 1, pp. 104671-104671
Closed Access
Tatsuki Urakawa, Junichi Ozawa, Masato Tanaka, et al.
European Journal of Medical Genetics (2022) Vol. 66, Iss. 1, pp. 104671-104671
Closed Access
