Michael J. Higgins

5.5k total citations
104 papers, 4.2k citations indexed

About

Michael J. Higgins is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Michael J. Higgins has authored 104 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 45 papers in Genetics and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Michael J. Higgins's work include Epigenetics and DNA Methylation (33 papers), Genetic Syndromes and Imprinting (28 papers) and Prenatal Screening and Diagnostics (17 papers). Michael J. Higgins is often cited by papers focused on Epigenetics and DNA Methylation (33 papers), Genetic Syndromes and Imprinting (28 papers) and Prenatal Screening and Diagnostics (17 papers). Michael J. Higgins collaborates with scholars based in United States, Canada and United Kingdom. Michael J. Higgins's co-authors include Paul D. Soloway, Enrique C. G. Ventureyra, Bradley N. White, Wolf Reik, Torbjoern G. Nygaard, Evangelos Pavlou, Timothy Lynch, Kirk C. Wilhelmsen, Christine B. Ambrosone and Jong-Yeon Shin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Michael J. Higgins

103 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael J. Higgins United States 31 3.1k 1.9k 995 585 315 104 4.2k
Jo Peters United Kingdom 31 2.6k 0.9× 2.0k 1.1× 537 0.5× 323 0.6× 110 0.3× 66 3.8k
Rolph Pfundt Netherlands 42 2.6k 0.8× 2.9k 1.5× 586 0.6× 436 0.7× 89 0.3× 136 5.2k
Arif B. Ekici Germany 42 2.6k 0.8× 1.6k 0.8× 299 0.3× 569 1.0× 169 0.5× 195 5.1k
Elizabeth Baker Australia 44 3.4k 1.1× 2.9k 1.5× 366 0.4× 318 0.5× 123 0.4× 116 6.7k
Catherine M. Suter Australia 36 3.7k 1.2× 708 0.4× 778 0.8× 1.5k 2.6× 131 0.4× 74 5.3k
Trilochan Sahoo United States 36 1.9k 0.6× 2.8k 1.5× 1.1k 1.1× 241 0.4× 302 1.0× 67 4.1k
Alexander G. Bassuk United States 37 2.4k 0.8× 1.0k 0.5× 408 0.4× 246 0.4× 313 1.0× 153 4.4k
Reinhard Stöger United Kingdom 25 2.3k 0.7× 1.6k 0.8× 806 0.8× 260 0.4× 62 0.2× 46 3.1k
Heidemarie Neitzel Germany 30 2.5k 0.8× 1.5k 0.8× 302 0.3× 448 0.8× 76 0.2× 95 4.0k
Erik G. Puffenberger United States 38 2.8k 0.9× 2.9k 1.5× 413 0.4× 452 0.8× 158 0.5× 74 6.7k

Countries citing papers authored by Michael J. Higgins

Since Specialization
Citations

This map shows the geographic impact of Michael J. Higgins'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 Michael J. Higgins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael J. Higgins more than expected).

Fields of papers citing papers by Michael J. Higgins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael J. Higgins. 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 Michael J. Higgins. The network helps show where Michael J. Higgins may publish in the future.

Co-authorship network of co-authors of Michael J. Higgins

This figure shows the co-authorship network connecting the top 25 collaborators of Michael J. Higgins. A scholar is included among the top collaborators of Michael J. Higgins 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 Michael J. Higgins. Michael J. Higgins is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ambrosone, Christine B., Song Yao, Mark D. Long, et al.. (2025). Associations of DNA methylation in breast tumour subtypes with parity and breastfeeding in a cohort of 1459 Black women: implications for public health. PubMed. 4(1). e000675–e000675. 1 indexed citations
2.
Chen, Jianhong, Mark D. Long, Sung Jun, et al.. (2023). An epigenome-wide analysis of socioeconomic position and tumor DNA methylation in breast cancer patients. Clinical Epigenetics. 15(1). 68–68. 6 indexed citations
3.
Chen, Jianhong, Michael J. Higgins, Qiang Hu, et al.. (2023). DNA methylation differences in noncoding regions in ER negative breast tumors between Black and White women. Frontiers in Oncology. 13. 1167815–1167815. 1 indexed citations
4.
Gong, Zhihong, Jianhong Chen, Jie Wang, et al.. (2021). Differential methylation and expression patterns of microRNAs in relation to breast cancer subtypes among American women of African and European ancestry. PLoS ONE. 16(3). e0249229–e0249229. 10 indexed citations
6.
Pugacheva, Elena M., Carter J. Barger, Spencer R. Rosario, et al.. (2019). BORIS Expression in Ovarian Cancer Precursor Cells Alters the CTCF Cistrome and Enhances Invasiveness through GALNT14. Molecular Cancer Research. 17(10). 2051–2062. 22 indexed citations
7.
Cheng, Ting‐Yuan David, Song Yao, Angela R. Omilian, et al.. (2019). FOXA1 Protein Expression in ER+ and ER− Breast Cancer in Relation to Parity and Breastfeeding in Black and White Women. Cancer Epidemiology Biomarkers & Prevention. 29(2). 379–385. 8 indexed citations
8.
Wilson, Kayla E., et al.. (2017). Blocked transcription through KvDMR1 results in absence of methylation and gene silencing resembling Beckwith-Wiedemann syndrome. Development. 144(10). 1820–1830. 30 indexed citations
9.
Roberts, Michelle, Chi‐Chen Hong, Stephen B. Edge, et al.. (2013). Case-only analyses of the associations between polymorphisms in the metastasis-modifying genes BRMS1 and SIPA1 and breast tumor characteristics, lymph node metastasis, and survival. Breast Cancer Research and Treatment. 139(3). 873–885. 9 indexed citations
10.
Smith, Adam C., Masako Suzuki, Reid F. Thompson, et al.. (2011). Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression. Genomics. 99(1). 25–35. 11 indexed citations
11.
McDevitt, Jane, Ryan Tierney, Jamie L. Mansell, et al.. (2011). Neuronal structural protein polymorphism and concussion in college athletes. Brain Injury. 25(11). 1108–1113. 12 indexed citations
12.
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
13.
Higgins, Michael J.. (2006). Dental Anesthesiology - An Access to Care Issue. PubMed. 99(2). 56–63. 2 indexed citations
14.
Ji, Yonggang, Nancy A. Rebert, John M. Joslin, et al.. (2000). Structure of the Highly Conserved HERC2 Gene and of Multiple Partially Duplicated Paralogs in Human. Genome Research. 10(3). 319–329. 47 indexed citations
15.
Cooper, Paul R., Norma J. Nowak, Michael J. Higgins, Deanna M. Church, & T.B. Shows. (1998). Transcript Mapping of the Human Chromosome 11q12–q13.1 Gene-Rich Region Identifies Several Newly Described Conserved Genes. Genomics. 49(3). 419–429. 14 indexed citations
16.
Ventureyra, Enrique C. G. & Michael J. Higgins. (1994). Traumatic intracranial aneurysms in childhood and adolescence. Child s Nervous System. 10(6). 361–379. 105 indexed citations
17.
Qin, Shizhen, Cary Isaacs, S Nagafuchi, et al.. (1993). A Chromosome 11 YAC Library. Genomics. 16(3). 580–585. 29 indexed citations
18.
Bhargava, Ravi, et al.. (1992). Prenatal demonstration of a cervical myelocystocele. Prenatal Diagnosis. 12(8). 653–659. 20 indexed citations
19.
Higgins, Michael J.. (1990). Martires y virgenes: la religión popular en México y en Nicaragua. Hispana. 1(37). 85–106. 1 indexed citations
20.
Higgins, Michael J., Chantal Turmel, Jaan Noolandi, & M. Lalande. (1989). Detection of Saccharomyces cerevisiae chromosome size markers directly on Southern blots of pulsed-field gels with a single DNA hybridization probe. Nucleic Acids Research. 17(23). 10136–10136. 3 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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