Bertil Glader

12.4k total citations · 2 hit papers
131 papers, 4.6k citations indexed

About

Bertil Glader is a scholar working on Physiology, Hematology and Molecular Biology. According to data from OpenAlex, Bertil Glader has authored 131 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Physiology, 48 papers in Hematology and 41 papers in Molecular Biology. Recurrent topics in Bertil Glader's work include Erythrocyte Function and Pathophysiology (50 papers), Neonatal Health and Biochemistry (29 papers) and RNA modifications and cancer (24 papers). Bertil Glader is often cited by papers focused on Erythrocyte Function and Pathophysiology (50 papers), Neonatal Health and Biochemistry (29 papers) and RNA modifications and cancer (24 papers). Bertil Glader collaborates with scholars based in United States, Italy and Canada. Bertil Glader's co-authors include Katherine A. High, Mark A. Kay, Alan W. Flake, Alan McClelland, Catherine S. Manno, Peter J. Larson, Margaret V. Ragni, Erik D. Skarsgard, Ciaran D. Scallan and Roland W. Herzog and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Bertil Glader

126 papers receiving 4.4k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector

2000 782 citations Mark A. Kay, Catherine S. Manno et al. Nature Genetics profile →
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B

2003 578 citations Catherine S. Manno, S Hutchison et al. Blood profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Bertil Glader	2.2k	1.6k	1.4k	710	694	131	4.6k
Melvin H. Freedman	1.6k 0.7×	1.6k 1.0×	1.8k 1.3×	1.5k 2.1×	1.2k 1.7×	140	6.0k
Hélène Cavé	2.2k 1.0×	1.2k 0.8×	2.4k 1.7×	718 1.0×	797 1.1×	154	6.3k
Dominique Vidaud	2.2k 1.0×	704 0.4×	496 0.4×	708 1.0×	466 0.7×	126	5.8k
Toshiro Nagasawa	1.2k 0.5×	350 0.2×	1.5k 1.1×	603 0.8×	581 0.8×	162	4.1k
D. W. van Bekkum	864 0.4×	483 0.3×	1.6k 1.2×	618 0.9×	632 0.9×	136	3.7k
Adalberto Benito	1.3k 0.6×	404 0.3×	738 0.5×	553 0.8×	471 0.7×	37	3.3k
Janette Lamb	838 0.4×	487 0.3×	475 0.3×	308 0.4×	659 0.9×	45	2.6k
Kenichi Koike	879 0.4×	346 0.2×	789 0.6×	400 0.6×	314 0.5×	158	2.5k
Shai Izraeli	2.6k 1.2×	583 0.4×	1.7k 1.2×	885 1.2×	421 0.6×	176	5.7k
Susan P. Perrine	1.5k 0.7×	173 0.1×	1.2k 0.8×	606 0.9×	1.8k 2.5×	88	3.5k

Countries citing papers authored by Bertil Glader

Since Specialization

Citations

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

Fields of papers citing papers by Bertil Glader

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bertil Glader

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

All Works

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20 of 20 papers shown

Gernez, Yaël, Alma‐Martina Cepika, Elisabeth G. Hoyte, et al.. (2024). Case report: Refractory Evans syndrome in two patients with spondyloenchondrodysplasia with immune dysregulation treated successfully with JAK1/JAK2 inhibition. Frontiers in Immunology. 14. 1328005–1328005. 1 indexed citations

Wilkes, Mark C., Y. Lucy Liu, Hye Na Kim, et al.. (2024). Activation of nemo-like kinase in diamond blackfan anemia suppresses early erythropoiesis by preventing mitochondrial biogenesis. Journal of Biological Chemistry. 300(8). 107542–107542. 1 indexed citations

Boscoe, Audra, Elizabeth Hedgeman, Eduard J. van Beers, et al.. (2020). Comorbidities and complications in adults with pyruvate kinase deficiency. European Journal Of Haematology. 106(4). 484–492. 17 indexed citations

Glader, Bertil. (2019). Transient Erythroblastopenia of Childhood. PubMed. 149(4). 69–128.

Grace, Rachael F., D. Mark Layton, Frédéric Galactéros, et al.. (2017). Results Update from the DRIVE PK Study: Effects of AG-348, a Pyruvate Kinase Activator, in Patients with Pyruvate Kinase Deficiency. Blood. 130. 2194–2194. 2 indexed citations

Бибикова, Елена, Nadia Danilova, Yoan Konto‐Ghiorghi, et al.. (2014). TNF-mediated inflammation represses GATA1 and activates p38 MAP kinase in RPS19-deficient hematopoietic progenitors. Blood. 124(25). 3791–3798. 55 indexed citations

Landowski, Michael, Marie-Françoise O’Donohue, Christopher Buros, et al.. (2013). Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond–Blackfan anemia. Human Genetics. 132(11). 1265–1274. 77 indexed citations

Gazda, Hanna T., Milena Preti, Mee Rie Sheen, et al.. (2012). Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia. Human Mutation. 33(7). 1037–1044. 109 indexed citations

Doherty, Leana, Mee Rie Sheen, Adrianna Vlachos, et al.. (2010). Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia. The American Journal of Human Genetics. 86(4). 655–656. 5 indexed citations

10.

Manno, Catherine S., S Hutchison, Peter J. Larson, et al.. (2003). AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B. Blood. 101(8). 2963–2972. 578 indexed citations breakdown →

11.

Gripp, Karen W., Donna M. McDonald‐McGinn, Noah Federman, et al.. (2001). Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia. American Journal of Medical Genetics. 101(3). 268–274. 24 indexed citations

12.

Kay, Mark A., Catherine S. Manno, Margaret V. Ragni, et al.. (2000). Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector. Nature Genetics. 24(3). 257–261. 782 indexed citations breakdown →

13.

Gamble, James G., Heather A. Vallier, Michael J. Rossi, & Bertil Glader. (1996). Loss of Elbow and Wrist Motion in Hemophilia. Clinical Orthopaedics and Related Research. 328(328). 94–101. 20 indexed citations

14.

Addiego, Joseph E., Carol K. Kasper, C F Abildgaard, et al.. (1993). Frequency of inhibitor development in haemophiliacs treated with low-purity factor VIII. The Lancet. 342(8869). 462–464. 136 indexed citations

15.

Hartman, Gary E., Sarah S. Donaldson, Arnold B. Gelb, et al.. (1993). Langerhans' cell histiocytosis presenting with the superior vena cava syndrome: A case report. Medical and Pediatric Oncology. 21(6). 456–459. 11 indexed citations

16.

Glader, Bertil, et al.. (1991). CRYPTOCOCCUS INFECTION IN A NINE-YEAR-OLD CHILD WITH HEMOPHILIA AND THE ACQUIRED IMMUNODEFICIENCY SYNDROME. The Pediatric Infectious Disease Journal. 10(1). 76–76. 9 indexed citations

17.

Shannon, Kevin, Ali G. Turhan, A. Bowcock, et al.. (1989). Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.. Journal of Clinical Investigation. 84(3). 984–989. 73 indexed citations

18.

Buchanan, George R. & Bertil Glader. (1977). Benign course of extreme hyperbilirubinemia in sickle cell anemia: Analysis of six cases. The Journal of Pediatrics. 91(1). 21–24. 37 indexed citations

19.

Glader, Bertil. (1976). Evaluation of the hemolytic role of aspirin in glucose-6-phosphate dehydrogenase deficiency. The Journal of Pediatrics. 89(6). 1027–1028. 24 indexed citations

20.

Gilcher, Ronald O., Bertil Glader, & Marcel E. Conrad. (1970). Reticulo endothelial recognition and hemolysis of red blood cells with reduced surface charge. Blood. 36(6). 840. 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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