Jacek Majewski

32.3k total citations
216 papers, 9.6k citations indexed

About

Jacek Majewski is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Jacek Majewski has authored 216 papers receiving a total of 9.6k indexed citations (citations by other indexed papers that have themselves been cited), including 145 papers in Molecular Biology, 73 papers in Genetics and 22 papers in Clinical Biochemistry. Recurrent topics in Jacek Majewski's work include RNA modifications and cancer (39 papers), RNA Research and Splicing (29 papers) and Genomics and Rare Diseases (26 papers). Jacek Majewski is often cited by papers focused on RNA modifications and cancer (39 papers), RNA Research and Splicing (29 papers) and Genomics and Rare Diseases (26 papers). Jacek Majewski collaborates with scholars based in Canada, United States and United Kingdom. Jacek Majewski's co-authors include Jürg Ott, Jeremy Schwartzentruber, Frederick M. Cohan, Kym M. Boycott, Somayyeh Fahiminiya, Jasmin Coulombe‐Huntington, Nada Jabado, Tomi Pastinen, Emilie Lalonde and Dennis E. Bulman and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Jacek Majewski

210 papers receiving 9.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacek Majewski Canada 56 6.1k 2.9k 1.1k 958 689 216 9.6k
Melanie Bahlo Australia 47 3.3k 0.5× 2.1k 0.7× 434 0.4× 1.5k 1.6× 428 0.6× 203 9.3k
P. Naresh Kumar United States 5 3.7k 0.6× 2.5k 0.9× 741 0.7× 415 0.4× 462 0.7× 7 6.5k
Lap‐Chee Tsui Canada 57 5.8k 0.9× 2.8k 1.0× 368 0.3× 616 0.6× 619 0.9× 145 12.6k
David R. Beier United States 58 7.1k 1.2× 3.4k 1.1× 664 0.6× 2.1k 2.2× 1.4k 2.0× 175 13.7k
Thomas B. Shows United States 54 6.9k 1.1× 2.3k 0.8× 937 0.9× 1.5k 1.5× 1.1k 1.7× 175 10.9k
David F. Callen Australia 52 5.1k 0.8× 3.2k 1.1× 1.3k 1.2× 629 0.7× 1.4k 2.0× 265 9.6k
Isabelle Callebaut France 59 7.9k 1.3× 1.7k 0.6× 726 0.7× 2.5k 2.6× 1.3k 2.0× 239 12.9k
Roger L. Eddy United States 53 5.7k 0.9× 1.5k 0.5× 850 0.8× 1.6k 1.7× 1.0k 1.5× 129 9.9k
Mitinori Saitou Japan 67 15.0k 2.4× 4.1k 1.4× 1.1k 1.1× 841 0.9× 861 1.2× 158 19.0k
Nikolaus Blin Germany 40 4.4k 0.7× 1.2k 0.4× 762 0.7× 958 1.0× 863 1.3× 203 7.7k

Countries citing papers authored by Jacek Majewski

Since Specialization
Citations

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

Fields of papers citing papers by Jacek Majewski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jacek Majewski. 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 Jacek Majewski. The network helps show where Jacek Majewski may publish in the future.

Co-authorship network of co-authors of Jacek Majewski

This figure shows the co-authorship network connecting the top 25 collaborators of Jacek Majewski. A scholar is included among the top collaborators of Jacek Majewski 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 Jacek Majewski. Jacek Majewski 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.
2.
Lee, Jimmy, Emma Carlson, Evelyn E. Schwager, et al.. (2024). Etiology of craniofacial and cardiac malformations in a mouse model of SF3B4 -related syndromes. Proceedings of the National Academy of Sciences. 121(39). e2405523121–e2405523121. 5 indexed citations
3.
Rezaei, Maryam, Mónica Aguinaga‐Ríos, Jianhua Qian, et al.. (2021). Novel pathogenic variants in NLRP7 , NLRP5 , and PADI6 in patients with recurrent hydatidiform moles and reproductive failure. Clinical Genetics. 99(6). 823–828. 25 indexed citations
4.
Weinberg, Daniel N., Xiao Chen, Douglas Barrows, et al.. (2021). Two competing mechanisms of DNMT3A recruitment regulate the dynamics of de novo DNA methylation at PRC1-targeted CpG islands. Nature Genetics. 53(6). 794–800. 66 indexed citations
5.
Rajagopalan, Kartik N., Xiao Chen, Daniel N. Weinberg, et al.. (2021). Depletion of H3K36me2 recapitulates epigenomic and phenotypic changes induced by the H3.3K36M oncohistone mutation. Proceedings of the National Academy of Sciences. 118(9). 34 indexed citations
6.
Wojcik, John, Dylan M. Marchione, Simone Sidoli, et al.. (2019). Epigenomic Reordering Induced by Polycomb Loss Drives Oncogenesis but Leads to Therapeutic Vulnerabilities in Malignant Peripheral Nerve Sheath Tumors. Cancer Research. 79(13). 3205–3219. 38 indexed citations
7.
Keser, Vafa, Ayesha Khan, Sorath Noorani Siddiqui, et al.. (2017). The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families. Investigative Ophthalmology & Visual Science. 58(2). 1028–1028. 16 indexed citations
8.
Hartley, Taila, Eric Bareke, Kym M. Boycott, et al.. (2017). Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1. Journal of Human Genetics. 62(6). 661–663. 11 indexed citations
9.
Frosk, Patrick, Heleen H. Arts, Julien Philippe, et al.. (2017). A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis. Journal of Medical Genetics. 54(7). 490–501. 35 indexed citations
10.
Tétreault, Martine, Luan T. Tran, Myriam Srour, et al.. (2017). Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy. Annals of Neurology. 82.
11.
Lacaria, Melanie, Myriam Srour, Jacques L. Michaud, et al.. (2017). Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet. American Journal of Medical Genetics Part A. 173(6). 1611–1619. 15 indexed citations
12.
Janer, Alexandre, Julien Prudent, Vincent Paupe, et al.. (2016). SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome. 5. 14 indexed citations
13.
Richer, Julie, Hussein Daoud, Pavel Geier, et al.. (2015). Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE. American Journal of Medical Genetics Part A. 167(7). 1654–1658. 12 indexed citations
14.
Joseph, Jeffrey T., A. Micheil Innes, Amanda Smith, et al.. (2014). Neuropathologic Features of Pontocerebellar Hypoplasia Type 6. Journal of Neuropathology & Experimental Neurology. 73(11). 1009–1025. 21 indexed citations
15.
Fahiminiya, Somayyeh, Jacek Majewski, John S. Mort, et al.. (2013). Mutations in WNT1 are a cause of osteogenesis imperfecta. Journal of Medical Genetics. 50(5). 345–348. 162 indexed citations
16.
Gupta, Indra R., Cindy Baldwin, Kevin Ha, et al.. (2013). ARHGDIA : a novel gene implicated in nephrotic syndrome. Journal of Medical Genetics. 50(5). 330–338. 66 indexed citations
17.
Caignard, Grégory, Michael Leney-Greene, Anne Dumaine, et al.. (2013). Genome-Wide Mouse Mutagenesis Reveals CD45-Mediated T Cell Function as Critical in Protective Immunity to HSV-1. PLoS Pathogens. 9(9). e1003637–e1003637. 21 indexed citations
18.
Rauch, Frank, Pierre Moffatt, Moira Cheung, et al.. (2012). Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.−14C>T mutation in all patients. Journal of Medical Genetics. 50(1). 21–24. 86 indexed citations
19.
Coulombe‐Huntington, Jasmin & Jacek Majewski. (2006). Characterization of intron loss events in mammals. Genome Research. 17(1). 23–32. 119 indexed citations
20.
Weleber, Richard G., Jacek Majewski, David Schultz, et al.. (2003). Age-related Macular Degeneration: A Genome-wide Scan in Extended Families. Investigative Ophthalmology & Visual Science. 44(13). 1503–1503. 2 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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