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, Shing Jen Tai, Roland W. Herzog, Linda B. Couto, Alan McClelland, Ciaran D. Scallan, Peter J. Larson and Erik D. Skarsgard 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

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. 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 →

Peers

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

#	Work	Indexed citations
1	Case report: Refractory Evans syndrome in two patients with spondyloenchondrodysplasia with immune dysregulation treated successfully with JAK1/JAK2 inhibition 2024 ·Frontiers in Immunology ·Yaël Gernez, (unknown), Alma‐Martina Cepika, (unknown), Elisabeth G. Hoyte, (unknown), Bertil Glader, (unknown), (unknown), (unknown), (unknown), Kenneth I. Weinberg, David B. Lewis, Rosa Bacchetta, Katja G. Weinacht	1
2	Activation of nemo-like kinase in diamond blackfan anemia suppresses early erythropoiesis by preventing mitochondrial biogenesis 2024 ·Journal of Biological Chemistry ·Mark C. Wilkes, (unknown), Y. Lucy Liu, (unknown), (unknown), (unknown), (unknown), Hye Na Kim, Bertil Glader, Paraic A. Kenny, Kathleen M. Sakamoto	1
3	The active component of ginseng, ginsenoside Rb1, improves erythropoiesis in models of Diamond–Blackfan anemia by targeting Nemo-like kinase 2021 ·Journal of Biological Chemistry ·Mark C. Wilkes, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Johan Flygare, Anupama Narla, Bertil Glader, Kathleen M. Sakamoto	10
4	Comorbidities and complications in adults with pyruvate kinase deficiency 2020 ·European Journal Of Haematology ·Audra Boscoe, (unknown), Elizabeth Hedgeman, Eduard J. van Beers, Hanny Al‐Samkari, Wilma Barcellini, Stefan Eber, Bertil Glader, Hassan M. Yaish, Satheesh Chonat, Mukta Sharma, Kevin H.M. Kuo, Ellis J. Neufeld, Heng Wang, Madeleine Verhovsek, Sujit Sheth, Rachael F. Grace	17
5	Transient Erythroblastopenia of Childhood 2019 ·PubMed ·Bertil Glader	0
6	Results Update from the DRIVE PK Study: Effects of AG-348, a Pyruvate Kinase Activator, in Patients with Pyruvate Kinase Deficiency 2017 ·Blood ·Rachael F. Grace, D. Mark Layton, Frédéric Galactéros, Christian Rosé, Wilma Barcellini, D. Holmes Morton, Eduard J. van Beers, Hassan M. Yaish, Yaddanapudi Ravindranath, Kevin H.M. Kuo, Sujit Sheth, Janet L. Kwiatkowski, Bruce A. Silver, Charles Kung, Marvin B. Cohen, Hua Yang, Penelope A. Kosinski, Lei Hua, Ann Barbier, Bertil Glader	2
7	TNF-mediated inflammation represses GATA1 and activates p38 MAP kinase in RPS19-deficient hematopoietic progenitors 2014 ·Blood ·Елена Бибикова, (unknown), Nadia Danilova, (unknown), Yoan Konto‐Ghiorghi, (unknown), Anupama Narla, Bertil Glader, Shuo Lin, Kathleen M. Sakamoto	55
8	Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond–Blackfan anemia 2013 ·Human Genetics ·Michael Landowski, Marie-Françoise O’Donohue, Christopher Buros, Roxanne Ghazvinian, Nathalie Montel-Lehry, Adrianna Vlachos, Colin A. Sieff, Peter E. Newburger, Edyta Niewiadomska, Michał Matysiak, Bertil Glader, Eva Atsidaftos, Jeffrey M. Lipton, Alan H. Beggs, Pierre‐Emmanuel Gleizes, Hanna T. Gazda	77
9	Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia 2010 ·The American Journal of Human Genetics ·Leana Doherty, Mee Rie Sheen, Adrianna Vlachos, Valérie Choesmel, Marie-Françoise O’Donohue, Catherine Clinton, Hal E. Schneider, Colin A. Sieff, Peter E. Newburger, Sarah E. Ball, Edyta Niewiadomska, Michał Matysiak, Bertil Glader, R.J. Arceci, Jason E. Farrar, Eva Atsidaftos, Jeffrey M. Lipton, Pierre‐Emmanuel Gleizes, Hanna T. Gazda	5
10	Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia 2010 ·The American Journal of Human Genetics ·Leana Doherty, Mee Rie Sheen, Adrianna Vlachos, Valérie Choesmel, Marie-Françoise O’Donohue, Catherine Clinton, Hal E. Schneider, Colin A. Sieff, Peter E. Newburger, Sarah E. Ball, Edyta Niewiadomska, Michał Matysiak, Bertil Glader, R.J. Arceci, Jason E. Farrar, Eva Atsidaftos, Jeffrey M. Lipton, Pierre‐Emmanuel Gleizes, Hanna T. Gazda	167
11	One year follow‐up of children and adolescents with chronic immune thrombocytopenic purpura (ITP) treated with rituximab 2008 ·Pediatric Blood & Cancer ·Brigitta U. Mueller, Carolyn M. Bennett, Henry A. Feldman, James B. Bussel, Thomas C. Abshire, Theodore B. Moore, (unknown), Mignon L. Loh, Zora R. Rogers, Bertil Glader, Maggie McCarthy, Donald H. Mahoney, Thomas A. Olson, Stephen A. Feig, Adonis Lorenzana, William C. Mentzer, George R. Buchanan, Ellis J. Neufeld	35
12	AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B breakdown → 2003 ·Blood ·Catherine S. Manno, (unknown), S Hutchison, Peter J. Larson, Roland W. Herzog, (unknown), Shing Jen Tai, Margaret V. Ragni, Alexis A. Thompson, Margareth C. Ozelo, Linda B. Couto, Debra G. B. Leonard, Freddie A. Johnson, Alan McClelland, Ciaran D. Scallan, Erik D. Skarsgard, Alan W. Flake, Mark A. Kay, Katherine A. High, Bertil Glader	578
13	Approach to the bleeding child 2002 ·Pediatric Clinics of North America ·Geoffrey Allen, Bertil Glader	9
14	Frequency of inhibitor development in haemophiliacs treated with low-purity factor VIII 1993 ·The Lancet ·Joseph E. Addiego, Carol K. Kasper, C F Abildgaard, M W Hilgartner, Jeanne M. Lusher, Bertil Glader, Louis M. Aledort	136
15	Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7. 1989 ·Journal of Clinical Investigation ·Kevin Shannon, Ali G. Turhan, (unknown), A. Bowcock, Paul Rogers, William L. Carroll, Morton J. Cowan, Bertil Glader, Connie J. Eaves, Allen Eaves	73
16	Reduced neutrophil counts in children with transient erythroblastopenia of childhood 1989 ·The Journal of Pediatrics ·Zora R. Rogers, (unknown), Michael D. Amylon, George R. Buchanan, Bertil Glader	14
17	Elevated red cell adenosine deaminase activity: a marker of disordered erythropoiesis in Diamond‐Blackfan anaemia and other haematologic diseases 1988 ·British Journal of Haematology ·Bertil Glader, Karen Backer	63
18	Benign course of extreme hyperbilirubinemia in sickle cell anemia: Analysis of six cases 1977 ·The Journal of Pediatrics ·George R. Buchanan, Bertil Glader	37
19	Evaluation of the hemolytic role of aspirin in glucose-6-phosphate dehydrogenase deficiency 1976 ·The Journal of Pediatrics ·Bertil Glader	24
20	Reticulo endothelial recognition and hemolysis of red blood cells with reduced surface charge 1970 ·Blood ·Ronald O. Gilcher, Bertil Glader, Marcel E. Conrad	3

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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