Aaron Bogutz

1.3k total citations
18 papers, 681 citations indexed

About

Aaron Bogutz is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Aaron Bogutz has authored 18 papers receiving a total of 681 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Aaron Bogutz's work include Epigenetics and DNA Methylation (15 papers), Genetic Syndromes and Imprinting (10 papers) and Prenatal Screening and Diagnostics (8 papers). Aaron Bogutz is often cited by papers focused on Epigenetics and DNA Methylation (15 papers), Genetic Syndromes and Imprinting (10 papers) and Prenatal Screening and Diagnostics (8 papers). Aaron Bogutz collaborates with scholars based in Canada, Japan and United States. Aaron Bogutz's co-authors include Louis Lefebvre, Matthew C. Lorincz, Julie Brind’Amour, Kenjiro Shirane, Mohammad M. Karimi, Hiroyuki Sasaki, Sheng Liu, Yoichi Shinkai, Hisato Kobayashi and Michelle King and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Genes & Development.

In The Last Decade

Aaron Bogutz

18 papers receiving 676 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Aaron Bogutz Canada	14	566	223	180	85	56	18	681
Ching-Yeu Liang Switzerland	8	463 0.8×	146 0.7×	123 0.7×	39 0.5×	85 1.5×	12	643
Liina Nagirnaja United States	15	384 0.7×	359 1.6×	157 0.9×	60 0.7×	91 1.6×	29	861
Manuel Viotti United States	16	720 1.3×	323 1.4×	609 3.4×	45 0.5×	31 0.6×	41	1.3k
Vincent Gâtinois France	11	269 0.5×	279 1.3×	206 1.1×	94 1.1×	6 0.1×	28	600
Noémie Ranisavljevic France	9	341 0.6×	139 0.6×	83 0.5×	57 0.7×	58 1.0×	35	571
Jing Fu China	17	505 0.9×	286 1.3×	419 2.3×	39 0.5×	43 0.8×	43	1.1k
Qianhua Xu China	11	738 1.3×	194 0.9×	161 0.9×	58 0.7×	21 0.4×	27	877
V. Cacheux France	8	165 0.3×	129 0.6×	156 0.9×	43 0.5×	11 0.2×	10	453
Paolo Guanciali‐Franchi Italy	10	222 0.4×	144 0.6×	154 0.9×	37 0.4×	18 0.3×	24	443
Muhammad B. Ekram United States	10	354 0.6×	219 1.0×	83 0.5×	26 0.3×	7 0.1×	15	484

Countries citing papers authored by Aaron Bogutz

Since Specialization

Citations

This map shows the geographic impact of Aaron Bogutz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Aaron Bogutz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aaron Bogutz more than expected).

Fields of papers citing papers by Aaron Bogutz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aaron Bogutz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Aaron Bogutz. The network helps show where Aaron Bogutz may publish in the future.

Co-authorship network of co-authors of Aaron Bogutz

This figure shows the co-authorship network connecting the top 25 collaborators of Aaron Bogutz. A scholar is included among the top collaborators of Aaron Bogutz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aaron Bogutz. Aaron Bogutz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Ito, Takamasa, Yuri Murakami, Aaron Bogutz, et al.. (2022). DNMT1 regulates the timing of DNA methylation by DNMT3 in an enzymatic activity-dependent manner in mouse embryonic stem cells. PLoS ONE. 17(1). e0262277–e0262277. 8 indexed citations

Mochizuki, Kentaro, Jafar Sharif, Kenjiro Shirane, et al.. (2021). Repression of germline genes by PRC1.6 and SETDB1 in the early embryo precedes DNA methylation-mediated silencing. Nature Communications. 12(1). 7020–7020. 39 indexed citations

Haage, Amanda, Wenjun Deng, Katharine Goodwin, et al.. (2020). Precise coordination of cell-ECM adhesion is essential for efficient melanoblast migration during development. Development. 147(14). 13 indexed citations

Yeung, Wan Kin Au, Hisato Kobayashi, Ryutaro Hirasawa, et al.. (2020). Maternal DNMT3A-dependent de novo methylation of the paternal genome inhibits gene expression in the early embryo. Nature Communications. 11(1). 5417–5417. 22 indexed citations

Bogutz, Aaron, Julie Brind’Amour, Hisato Kobayashi, et al.. (2019). Evolution of imprinting via lineage-specific insertion of retroviral promoters. Nature Communications. 10(1). 5674–5674. 37 indexed citations

Bogutz, Aaron, et al.. (2018). Transcription factor ASCL2 is required for development of the glycogen trophoblast cell lineage. PLoS Genetics. 14(8). e1007587–e1007587. 21 indexed citations

Brind’Amour, Julie, Hisato Kobayashi, Kenjiro Shirane, et al.. (2018). LTR retrotransposons transcribed in oocytes drive species-specific and heritable changes in DNA methylation. Nature Communications. 9(1). 3331–3331. 56 indexed citations

Haage, Amanda, Katharine Goodwin, Aaron Bogutz, et al.. (2018). Talin Autoinhibition Regulates Cell-ECM Adhesion Dynamics and Wound Healing In Vivo. Cell Reports. 25(9). 2401–2416.e5. 34 indexed citations

Thompson, I. Richard, et al.. (2018). Development and application of an integrated allele-specific pipeline for methylomic and epigenomic analysis (MEA). BMC Genomics. 19(1). 463–463. 10 indexed citations

10.

Branco, Miguel R., Michelle King, Vicente Pérez-García, et al.. (2016). Maternal DNA Methylation Regulates Early Trophoblast Development. Developmental Cell. 36(2). 152–163. 92 indexed citations

11.

Yang, Christine, et al.. (2015). Impact of flanking chromosomal sequences on localization and silencing by the human non-coding RNA XIST. Genome biology. 16(1). 208–208. 37 indexed citations

12.

Liu, Sheng, Julie Brind’Amour, Mohammad M. Karimi, et al.. (2014). Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells. Genes & Development. 28(18). 2041–2055. 206 indexed citations

13.

Brind’Amour, Julie, Sheng Liu, Mohammad M. Karimi, Aaron Bogutz, & Matthew C. Lorincz. (2013). Genome-wide mapping of chromatin marks from 1,000 cells to study epigenetic reprogramming in primordial germ cells. Epigenetics & Chromatin. 6(S1). 1 indexed citations

14.

Bogutz, Aaron, et al.. (2011). Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction. Developmental Biology. 351(2). 277–286. 49 indexed citations

15.

MacIsaac, Julia L., Aaron Bogutz, A. Sorana Morrissy, & Louis Lefebvre. (2011). Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2. Nucleic Acids Research. 40(4). 1523–1535. 20 indexed citations

16.

Jones, Meaghan J., Aaron Bogutz, & Louis Lefebvre. (2011). An Extended Domain of Kcnq1ot1 Silencing Revealed by an Imprinted Fluorescent Reporter. Molecular and Cellular Biology. 31(14). 2827–2837. 13 indexed citations

17.

Bogutz, Aaron, et al.. (2010). Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome. BMC Developmental Biology. 10(1). 50–50. 10 indexed citations

18.

Lefebvre, Louis, Lynn Mar, Aaron Bogutz, et al.. (2009). The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith–Wiedemann region. Human Molecular Genetics. 18(22). 4255–4267. 13 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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