Michael Kneba

323 papers receiving 35.5k citations

Michael Kneba's Hit Papers

Patterns of somatic structural variation in human cancer genomes 2020 · 550 citations
5500+4+9Years since publication50010001.5k2.0k

Peers

Michael Kneba
Comparison fields: 5 of 178
  • Genetics 13.1k
  • Pathology and Forensic Medicine 13.5k
  • Hematology 6.5k
  • Cancer Research 5.1k
  • Oncology 8.2k
Replace Brunangelo Falini with:
Brunangelo Falini Italy
Wolfgang Hiddemann Germany
Robin Foà Italy
Thomas J. Kipps United States
Bruce D. Cheson United States
Emili Montserrat Spain
German Ott Germany
Stephan Stilgenbauer Germany
John G. Gribben United Kingdom
Armando López‐Guillermo Spain
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Citations per field
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Citations per year

Countries citing papers authored by Michael Kneba

Since Specialization
Citations

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

Fields of papers citing papers by Michael Kneba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Michael Kneba, 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 Michael Kneba Line = papers co-authored together Michael Kneba links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 336 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: Report of the BIOMED-2 Concerted Action BMH4-CT98-3936
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20032613
2
The repertoire of mutational signatures in human cancer
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20202339
3
Pan-cancer analysis of whole genomes
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20202109
4
Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): a randomised, phase 2/3 trial
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20191869
5
Addition of rituximab to fludarabine and cyclophosphamide in patients with chronic lymphocytic leukaemia: a randomised, open-label, phase 3 trial
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20101557
6
Obinutuzumab plus Chlorambucil in Patients with CLL and Coexisting Conditions
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20141221
7
Mutations driving CLL and their evolution in progression and relapse
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2015844
8
Targeted Therapy With the T-Cell–Engaging Antibody Blinatumomab of Chemotherapy-Refractory Minimal Residual Disease in B-Lineage Acute Lymphoblastic Leukemia Patients Results in High Response Rate and Prolonged Leukemia-Free Survival
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2011780
9
Long-term remissions after FCR chemoimmunotherapy in previously untreated patients with CLL: updated results of the CLL8 trial
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2015709
10
ESPEN Guidelines on Enteral Nutrition: Non-surgical oncology
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2006708
11
The evolutionary history of 2,658 cancers
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2020705
12
Patterns of somatic structural variation in human cancer genomes
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2020550
13
First-line chemoimmunotherapy with bendamustine and rituximab versus fludarabine, cyclophosphamide, and rituximab in patients with advanced chronic lymphocytic leukaemia (CLL10): an international, open-label, randomised, phase 3, non-inferiority trial
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2016497
14
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
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2020476
15
Reduced-intensity chemotherapy and PET-guided radiotherapy in patients with advanced stage Hodgkin's lymphoma (HD15 trial): a randomised, open-label, phase 3 non-inferiority trial
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2012466
16 2005453
17
Gene mutations and treatment outcome in chronic lymphocytic leukemia: results from the CLL8 trial
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2014436
18
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
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2020419
19
Adult patients with acute lymphoblastic leukemia and molecular failure display a poor prognosis and are candidates for stem cell transplantation and targeted therapies
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2012416
20
Long-term follow-up of hematologic relapse-free survival in a phase 2 study of blinatumomab in patients with MRD in B-lineage ALL
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2012406

About Michael Kneba

Michael Kneba is a scholar working on Genetics, Pathology and Forensic Medicine, Hematology, Immunology and Oncology, having authored 336 papers that have together received 36.4k indexed citations. Recurring topics across this work include Chronic Lymphocytic Leukemia Research (176 papers), Lymphoma Diagnosis and Treatment (159 papers), Chronic Myeloid Leukemia Treatments (60 papers), Immunodeficiency and Autoimmune Disorders (53 papers), Acute Lymphoblastic Leukemia research (51 papers), Viral-associated cancers and disorders (31 papers), Monoclonal and Polyclonal Antibodies Research (26 papers) and Cancer Genomics and Diagnostics (24 papers). The work is most often cited by research in Genetics (13.1k citations), Pathology and Forensic Medicine (13.5k citations), Hematology (6.5k citations), Cancer Research (5.1k citations) and Oncology (8.2k citations). Michael Kneba has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Matthias Ritgen, Monika Brüggemann, Thorsten Raff, Michael J. Hallek, Christiane Pott, Stephan Stilgenbauer, Sebastian Böttcher, Hartmut Doehner, Nicola Gökbuget and Peter Dreger. Their work appears in journals such as Blood, Leukemia, Nature Communications, Haematologica and Journal of Clinical Oncology.

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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