Martin Granzow

5.8k total citations · 1 hit paper
42 papers, 3.7k citations indexed

About

Martin Granzow is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Martin Granzow has authored 42 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Genetics and 8 papers in Hematology. Recurrent topics in Martin Granzow's work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Multiple Myeloma Research and Treatments (6 papers). Martin Granzow is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Multiple Myeloma Research and Treatments (6 papers). Martin Granzow collaborates with scholars based in Germany, United States and Poland. Martin Granzow's co-authors include Thomas Ragg, Wolfram Menzel, Odilo Mueller, Susanne Stocker, Marcus Gassmann, Ruediger Salowsky, Andreas Schröeder, Michael J. Leiber, Anna Jauch and Roland Eils and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Blood.

In The Last Decade

Martin Granzow

42 papers receiving 3.6k 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.

The RIN: an RNA integrity number for assigning integrity values to RNA measurements

2006 1.9k citations Andreas Schröeder, Odilo Mueller et al. BMC Molecular Biology profile →

Peers

Martin Granzow

ONCOL

GENET

HEMAT

Gang Wu United States

Shu‐Wha Lin Taiwan

Weijun Luo United States

Renée X. de Menezes Netherlands

Claudio Santoro Italy

Jan Willem Voncken Netherlands

T Sekiya Japan

Jennifer M. Lee United States

Francesco Ferrari Italy

Debashis Sahoo United States

Gang Wu United States

Martin Granzow

3.0k ×1.4

520 ×0.7

483 ×0.7

ONCOL

552 ×1.1

GENET

408 ×1.1

HEMAT

Citations per year, relative to Martin Granzow Martin Granzow (= 1×) peers Gang Wu

Countries citing papers authored by Martin Granzow

Since Specialization

Citations

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

Fields of papers citing papers by Martin Granzow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Granzow

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Granzow. A scholar is included among the top collaborators of Martin Granzow 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 Martin Granzow. Martin Granzow 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

Granzow, Martin, et al.. (2022). Analysis of the complete lambda light chain germline usage in patients with AL amyloidosis and dominant heart or kidney involvement. PLoS ONE. 17(2). e0264407–e0264407. 13 indexed citations

Martínez, Cristina, Felix Lasitschka, Martin Granzow, et al.. (2020). Comparative expression profiling in the intestine of patients with Giardia ‐induced postinfectious functional gastrointestinal disorders. Neurogastroenterology & Motility. 32(9). e13868–e13868. 6 indexed citations

Ott, Tim, Lilian Kaufmann, Martin Granzow, et al.. (2019). The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1. Frontiers in Physiology. 10. 134–134. 14 indexed citations

Evers, Christina, Christian Staufner, Martin Granzow, et al.. (2017). Impact of clinical exomes in neurodevelopmental and neurometabolic disorders. Molecular Genetics and Metabolism. 121(4). 297–307. 34 indexed citations

Hoffmann, Sandra, Stefanie Schmitteckert, Alexandra Rolletschek, et al.. (2017). Comparative expression analysis of Shox2-deficient embryonic stem cell-derived sinoatrial node-like cells. Stem Cell Research. 21. 51–57. 8 indexed citations

Bochtler, Tilmann, Ute Hegenbart, Christina Kunz, et al.. (2016). Prognostic impact of cytogenetic aberrations in AL amyloidosis patients after high-dose melphalan: a long-term follow-up study. Blood. 128(4). 594–602. 53 indexed citations

Schneider, Marc A., Martin Granzow, Arne Warth, et al.. (2015). Glycodelin: A New Biomarker with Immunomodulatory Functions in Non–Small Cell Lung Cancer. Clinical Cancer Research. 21(15). 3529–3540. 45 indexed citations

Evers, Christina, Nagarajan Paramasivam, Katrin Hinderhofer, et al.. (2015). SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract. European Journal of Human Genetics. 23(12). 1627–1633. 15 indexed citations

Granzow, Martin, Nagarajan Paramasivam, Katrin Hinderhofer, et al.. (2015). Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline. Molecular and Cellular Probes. 29(5). 323–329. 20 indexed citations

10.

Kahn, Nicolas, Martin Granzow, Michael Meister, et al.. (2015). Transcriptome analysis in endobronchial epithelial lining fluid compared to bronchoalveolar lavage in idiopathic pulmonary fibrosis. Pneumologie. 69(7). 1 indexed citations

11.

Dikow, Nicola, Stephanie Karch, Martin Granzow, et al.. (2014). 3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behavior. American Journal of Medical Genetics Part A. 164(12). 3061–3068. 29 indexed citations

12.

Bochtler, Tilmann, Ute Hegenbart, Christina Kunz, et al.. (2014). Gain of chromosome 1q21 is an independent adverse prognostic factor in light chain amyloidosis patients treated with melphalan/dexamethasone. Amyloid. 21(1). 9–17. 67 indexed citations

13.

Gottschling, Sandra, Martin Granzow, Ruprecht Kuner, et al.. (2013). Mesenchymal stem cells in non-small cell lung cancer—Different from others? Insights from comparative molecular and functional analyses. Lung Cancer. 80(1). 19–29. 41 indexed citations

14.

Reinmuth, Niels, Anna Jauch, Elizabeth C. Xu, et al.. (2008). Correlation of EGFR mutations with chromosomal alterations and expression of EGFR, ErbB3 and VEGF in tumor samples of lung adenocarcinoma patients. Lung Cancer. 62(2). 193–201. 42 indexed citations

15.

Schröeder, Andreas, Odilo Mueller, Susanne Stocker, et al.. (2006). The RIN: an RNA integrity number for assigning integrity values to RNA measurements. BMC Molecular Biology. 7(1). 3–3. 1949 indexed citations breakdown →

16.

Schmidt‐Kittler, Oleg, Thomas Ragg, Martin Granzow, et al.. (2003). From latent disseminated cells to overt metastasis: Genetic analysis of systemic breast cancer progression. Proceedings of the National Academy of Sciences. 100(13). 7737–7742. 493 indexed citations

17.

Joos, Stefan, Martin Granzow, Reiner Siebert, et al.. (2002). Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2. International Journal of Cancer. 103(4). 489–495. 115 indexed citations

18.

Popp, Susanne, Martin Granzow, Brigitte Schoell, et al.. (2001). Comparative genomic hybridization in childhood acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 124(2). 89–97. 14 indexed citations

19.

Granzow, Martin, Susanne Popp, Monika Keller, et al.. (2000). Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals. Human Genetics. 107(1). 51–57. 19 indexed citations

20.

Cremer, Christoph, Martin Granzow, A. Jauch, et al.. (1996). Nuclear architecture and the induction of chromosomal aberrations. Mutation Research/Reviews in Genetic Toxicology. 366(2). 97–116. 100 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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