Jacek Majewski

32.3k citations

216 papers · 9.6k indexed · h-index 56

Genetics top 0.5%
- Genomics and Rare Diseases 26
Molecular Biology top 0.5%
- RNA modifications and cancer 39
- RNA Research and Splicing 29
- RNA and protein synthesis mechanisms 24
- Mitochondrial Function and Pathology 22
- Epigenetics and DNA Methylation 16
- Genomics and Chromatin Dynamics 14
Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders 22
Cancer Research top 1%
Genetics top 2%
- Genomics and Rare Diseases 26

Co-authors: Jürg Ott Jeremy Schwartzentruber Frederick M. Cohan Kym M. Boycott Somayyeh Fahiminiya Jasmin Coulombe‐Huntington Nada Jabado Tomi Pastinen
Cited by: Genetics Molecular Biology Clinical Biochemistry
Journals: The American Journal of Human Genetics (18 papers)Journal of Medical Genetics (15 papers)Clinical Genetics (11 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Jacek Majewski

210 papers receiving 9.4k citations

Peers

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

The 25 scholars most cited alongside Jacek Majewski, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jacek Majewski Line = papers co-authored together Jacek Majewski links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disorders Molecular Genetics and Metabolism ·Anthony Cheung,Erminia Di Pietro,Qiu‐Li Wang,Eric Bareke,Fabian Schoch,Ratna Dua Puri,S. Sirri Kiliç,Rebecca Ganetzky,Amy B. Goldstein,Adeline Vanderver,Shruthi Mohan,Jacek Majewski,Heinrich Segmüller,Nancy Braverman	2025	0
2	A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage Molecular Genetics & Genomic Medicine ·장현규,Sebastián Pacheco-Acosta,Eric Bareke,Sanaa Choufani,Sujatha Jagadeesh,Rosanna Weksberg,Jacek Majewski,Rima Slim	2024	1
3	Systematic perturbations of SETD2, NSD1, NSD2, NSD3, and ASH1L reveal their distinct contributions to H3K36 methylation Genome biology ·Zhenxing Huang,Sylvia Octa Putri,Cynthia Horth,Bo Hu,Eric Bareke,Saeed Isah,Cornelia Paula Dorothea Brussaard,Benjamin A. García,Chao Lü,Jacek Majewski	2024	6
4	H2A.Z histone variants facilitate HDACi-dependent removal of H3.3K27M mutant protein in pediatric high-grade glioma cells Cell Reports ·Katarzyna B. Leszczyńska,Nabila Ihza Nur Muttaqi,Young Owan Choi,G. A. Dolgopolov,Saeed Isah,Cynthia Horth,Kamil Wojnicki,Bartłomiej Gielniewski,N.E. Rosilawati,Beata Kaza,Javad Nazarian,S Nandasena,Joanna Trubicka,Wiesława Grajkowska,Benjamin A. Garcia,Jacek Majewski,Bożena Kamińska,Jakub Mieczkowski	2024	5
5	Etiology of craniofacial and cardiac malformations in a mouse model of SF3B4 -related syndromes Proceedings of the National Academy of Sciences ·Nicolas Lavielle,Shokoufeh Borzabadi,Jimmy Lee,Emma Carlson,Данило Калюжний,Evelyn E. Schwager,A British Merchant,Jennifer L. Fish,Jacek Majewski,Loydie A. Jerome‐Majewska	2024	5
6	Novel pathogenic variants in NLRP7 , NLRP5 , and PADI6 in patients with recurrent hydatidiform moles and reproductive failure Clinical Genetics ·Maryam Rezaei,Sebastián Pacheco-Acosta,Yifan Zhou,克幹籾倉,Mónica Aguinaga‐Ríos,Jianhua Qian,Rashmi Bagga,Majid Fardaei,G. F. Karabadzak,Sujatha Jagadeesh,Jacek Majewski,Rima Slim	2021	25
7	Depletion of H3K36me2 recapitulates epigenomic and phenotypic changes induced by the H3.3K36M oncohistone mutation Proceedings of the National Academy of Sciences ·Kartik N. Rajagopalan,Xiao Chen,Daniel N. Weinberg,Haifeng Chen,Jacek Majewski,C. David Allis,Chao Lü	2021	34
8	Two competing mechanisms of DNMT3A recruitment regulate the dynamics of de novo DNA methylation at PRC1-targeted CpG islands Nature Genetics ·Daniel N. Weinberg,孔晓燕 KONG Xiaoyan,Xiao Chen,Douglas Barrows,Cynthia Horth,Matthew R. Marunde,Irina K Popova,沈漪,Michael‐Christopher Keogh,Chao Lü,Jacek Majewski,C. David Allis	2021	66
9	Epigenomic Reordering Induced by Polycomb Loss Drives Oncogenesis but Leads to Therapeutic Vulnerabilities in Malignant Peripheral Nerve Sheath Tumors Cancer Research ·John Wojcik,Dylan M. Marchione,Simone Sidoli,Anissa Djedid,Borges da Silva,Jacek Majewski,Benjamin A. García	2019	38
10	ZBTB7B (ThPOK) Is Required for Pathogenesis of Cerebral Malaria and Protection against Pulmonary Tuberculosis Infection and Immunity ·James Kennedy,С М Грігор’єв,Angelia V. Bassenden,Silvia M. Vidal,Albert M. Berghuis,Ichiro Taniuchi,Jacek Majewski,Mark Lathrop,Marcel A. Behr,David Langlais,Philippe Gros	2019	4
11	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 ·Melanie Lacaria,Myriam Srour,Jacques L. Michaud,Asif Doja,Elka Miller,Jeremy Schwartzentruber,Shehzad Nadeem,Jacek Majewski,Kym M. Boycott	2017	15
12	A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis Journal of Medical Genetics ·Patrick Frosk,Heleen H. Arts,Julien Philippe,SALLY NDILA MASAKU,均笹井,M Al-Mosawi Reham,Louise R. Simard,Jacek Majewski,Somayyeh Fahiminiya,上野高義,Yangfan P. Liu,(unknown),Robert A. Hegele,Nicholas Katsanis,E M Nyenze,Marc R. Del Bigio,Erica E. Davis	2017	35
13	Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy Annals of Neurology ·恵末永,Y Liu,Martine Tétreault,Luan T. Tran,金颖王,Myriam Srour,JamjanMeeboon,Catherine Brunel‐Guitton,Jacek Majewski,Long Long,Jean-Marie Sédès,Michael J. Gambello,Cas Simons,Adeline Vanderver,Geneviève Bernard	2017	0
14	Molecular analyses reveal close similarities between small cell carcinoma of the ovary, hypercalcemic type and atypical teratoid/rhabdoid tumor Oncotarget ·Somayyeh Fahiminiya,Leora Witkowski,Javad Nadaf,Jian Carrot‐Zhang,Catherine Goudie,Martin Hasselblatt,Pascal D. Johann,Marcel Kool,Ryan S. Lee,Tenzin Gayden,Charles W.M. Roberts,Jaclyn A. Biegel,Nada Jabado,Jacek Majewski,William D. Foulkes	2015	32
15	Mutations in WNT1 are a cause of osteogenesis imperfecta Journal of Medical Genetics ·Somayyeh Fahiminiya,Jacek Majewski,John S. Mort,Pierre Moffatt,Francis H. Glorieux,Frank Rauch	2013	162
16	ARHGDIA : a novel gene implicated in nephrotic syndrome Journal of Medical Genetics ·Indra R. Gupta,Cindy Baldwin,F. S. Oliver,Kevin Ha,Jasminka Petek Krapljan,Somayyeh Fahiminiya,Martin Bitzan,Chantal Bernard,Mohammad R. Akbari,Steven A. Narod,David S. Rosenblatt,Jacek Majewski,Tomoko Takano	2013	66
17	Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation Journal of Allergy and Clinical Immunology ·Despina Moshous,Emmanuel Martin,Wassila Carpentier,Apiradee Lim,Isabelle Callebaut,Danielle Canioni,Fabian Hauck,Jacek Majewski,Jeremy Schwartzentruber,Patrick Nitschké,Nicolas Sirvent,Pierre Frange,Capucine Pïcard,Stéphane Blanche,Patrick Revy,Alain Fischer,Sylvain Latour,Nada Jabado,Jean‐Pierre de Villartay	2013	103
18	Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.−14C>T mutation in all patients Journal of Medical Genetics ·Frank Rauch,Pierre Moffatt,Moira Cheung,Peter J. Roughley,Liljana Lalic,Allan M. Lund,Norman Ramírez,Somayyeh Fahiminiya,Jacek Majewski,Francis H. Glorieux	2012	86
19	Variants Of Anterior Segment Dysgenesis In A Large Family With A Novel COL4A1 Mutation Investigative Ophthalmology & Visual Science ·Eyvind Rødahl,Per M. Knappskog,Jacek Majewski,Wenche Telstad,Jostein Kråkenes,Helge Boman	2011	1
20	Age-related Macular Degeneration: A Genome-wide Scan in Extended Families Investigative Ophthalmology & Visual Science ·Richard G. Weleber,Jacek Majewski,David Schultz,Mitchell Schain,Tara C. Matise,J. Ott,T.S. Acott,Martin Klein	2003	2

About Jacek Majewski

Jacek Majewski is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology, having authored 216 papers that have together received 9.6k indexed citations. Recurring topics across this work include RNA modifications and cancer (39 papers), RNA Research and Splicing (29 papers), Genomics and Rare Diseases (26 papers), RNA and protein synthesis mechanisms (24 papers), Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (22 papers), Epigenetics and DNA Methylation (16 papers) and Genomics and Chromatin Dynamics (14 papers). The work is most often cited by research in Genetics (2.9k citations), Molecular Biology (6.1k citations) and Clinical Biochemistry (546 citations). Jacek Majewski has collaborated with scholars based in Canada, United States and United Kingdom. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics, Human Mutation and Human Molecular Genetics.

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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