Martin Erdel

3.2k total citations
72 papers, 2.3k citations indexed

About

Martin Erdel is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Martin Erdel has authored 72 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 26 papers in Genetics and 12 papers in Oncology. Recurrent topics in Martin Erdel's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (10 papers) and Chromosomal and Genetic Variations (10 papers). Martin Erdel is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (10 papers) and Chromosomal and Genetic Variations (10 papers). Martin Erdel collaborates with scholars based in Austria, Germany and United States. Martin Erdel's co-authors include Gerd Utermann, Yanhua Hu, Manuel Mayr, Qingbo Xu, Fergus Davison, Martina Witsch‐Baumgartner, Hartmut Glossmann, Barbara U. Fitzky, Young‐Ki Paik and Fabian F. Moebius and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Journal of Clinical Oncology.

In The Last Decade

Martin Erdel

70 papers receiving 2.2k citations

Peers

Countries citing papers authored by Martin Erdel

Since Specialization

Citations

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

Fields of papers citing papers by Martin Erdel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Erdel

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Erdel. A scholar is included among the top collaborators of Martin Erdel 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 Erdel. Martin Erdel 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	Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay 2014 ·American Journal of Medical Genetics Part A ·(unknown), Hans‐Christoph Duba, Martin Erdel, (unknown), Wolfgang Kranewitter, (unknown), (unknown), (unknown), (unknown), (unknown), Gerald Webersinke	7
2	Characterization of a newly identified ETV6-NTRK3 fusion transcript in acute myeloid leukemia 2011 ·Diagnostic Pathology ·(unknown), Wolfgang Kranewitter, Hans Bösmüller, (unknown), G. Tschurtschenthaler, Holger Rumpold, (unknown), Martin Erdel, Andreas Petzer, Gerald Webersinke	77
3	E2F3a Is Critically Involved in Epidermal Growth Factor Receptor–Directed Proliferation in Ovarian Cancer 2010 ·Cancer Research ·Daniel Reimer, Michael Hubalek, Svenja Riedle, Sergej Skvortsov, Martin Erdel, Nicole Concin, Heidi Fiegl, Elisabeth Müller‐Holzner, Christian Marth, Karl Illmensee, Peter Altevogt, Alain G. Zeimet	30
4	Clinical outcome of pretreated B-cell chronic lymphocytic leukemia following alemtuzumab therapy: a retrospective study on various cytogenetic risk categories 2010 ·Annals of Oncology ·Michael Fiegl, Martin Erdel, Ingeborg Tinhofer, Yvona Brychtová, (unknown), Michael Doubek, (unknown), Christa Fonatsch, Georg Hopfinger, (unknown), August Zabernigg, Florian Falkner, Günther Gastl, Jiřı́ Mayer, Richard Greil	22
5	Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite‐mediated haplotype analysis 2010 ·Clinical Genetics ·Vera Großmann, Martina Höckner, Houda Karmous‐Benailly, Desheng Liang, (unknown), Roberto Quadrelli, Benno Röthlisberger, Adam M. Huber, Lingqian Wu, (unknown), Christine Fauth, Martin Erdel, Johannes Zschocke, Gerd Utermann, Dieter Kotzot	24
6	Fludarabine/intermediate-dose cytarabine with or without allogeneic hematopoietic stem cell transplantation in poor-risk leukemia: a single center experience 2008 ·International Journal of Hematology ·Jutta Auberger, Johannes Clausen, Wolfgang Willenbacher, Martin Erdel, Eberhard Gunsilius, Andreas Petzer, Günther Gastl, David Nachbaur	0
7	Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia 2006 ·Clinical Genetics ·M. Leipoldt, Martin Erdel, (unknown), Marta Smyk, Milan Theurl, (unknown), J.R. Lupski, (unknown), (unknown), Paweł Stankiewicz, Gerd Scherer	82
8	Pre‐ and postnatal findings in trisomy 17 mosaicism 2006 ·American Journal of Medical Genetics Part A ·Barbara Utermann, Mariluce Riegel, Dru F. Leistritz, (unknown), Josef Wisser, Lorraine F. Meisner, Christine Fauth, Rosa Baldinger, Julie A. Johnson, Martin Erdel, (unknown), Richard M. Pauli, Alessandra Baumer, Albert Schinzel, Dieter Kotzot	17
9	Unfavourable prognosis of patients with trisomy 18q21 detected by fluorescence in situ hybridisation in t(11;18) negative, surgically resected, gastrointestinal B cell lymphomas 2004 ·Journal of Clinical Pathology ·Jens Krugmann, Alexandar Tzankov, S Dirnhofer, (unknown), Richard Greil, Reiner Siebert, Martin Erdel	14
10	Molecular genetics and structural genomics of the human protein kinase C gene module 2002 ·Genome biology ·Kurt Kofler, Martin Erdel, Gerd Utermann, Gottfried Baier	31
11	The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome 2002 ·European Journal of Human Genetics ·Hans‐Christoph Duba, Andreas Doll, (unknown), Martin Erdel, (unknown), I Hammerer, Gerd Utermann, Karl‐Heinz Grzeschik	19
12	LIM-domain protein cysteine- and glycine-rich protein 2 (CRP2) is a novel marker of hepatic stellate cells and binding partner of the protein inhibitor of activated STAT1 2001 ·Biochemical Journal ·Ralf Weiskirchen, Markus Moser, Sabine Weiskirchen, Martin Erdel, (unknown), Reinhard Buettner, Axel M. Gressner	54
13	Cloning, genomic sequence, and chromosome mapping of <i>Scyb11,</i> the murine homologue of SCYB11 (alias βR1/H174/SCYB9B/I-TAC/IP-9/CXCL11) 2000 ·Cytogenetic and Genome Research ·Markus R. Meyer, Martin Erdel, Hans‐Christoph Duba, Ernst R. Werner, Gabriele Werner‐Felmayer	15
14	Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome 1999 ·European Journal of Human Genetics ·Asli Silahtaroglu, Frans A. Hol, (unknown), Martin Erdel, Hans‐Christoph Duba, M.P.A. Geurds, Nine V.A.M. Knoers, Edwin C.M. Mariman, Zeynep Tümer, Gerd Utermann, Jutta Wirth, Merete Bugge, Niels Tommerup	16
15	Cytogenetic Characterization of 22 Human Renal Cell Tumors in Relation to a Histopathological Classification 1999 ·Cancer Genetics and Cytogenetics ·Irmgard Verdorfer, Alfred Hobisch, A Hittmair, Hans‐Christoph Duba, Georg Bartsch, Gerd Utermann, Martin Erdel	16
16	Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: A new strategy for remission assessment 1998 ·Genes Chromosomes and Cancer ·(unknown), (unknown), Wolfgang Hilbe, Oliver Bechter, Martin Erdel, Gerd Utermann, Hans‐Christoph Duba	43
17	Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations 1998 ·Cytogenetic and Genome Research ·Gerd Scherer, (unknown), Martin Erdel, Dieter Meschede, J. Horst, R Leśniewicz, Alina T. Midro	55
18	Assignment<footref rid="foot01"><sup>1</sup></footref> of CSRP1 encoding the LIM domain protein CRP1, to human chromosome 1q32 by fluorescence in situ hybridization 1998 ·Cytogenetic and Genome Research ·Martin Erdel, Ralf Weiskirchen	5
19	Genomic Organization and Chromosomal Localization of the HumanSGKProtein Kinase Gene 1998 ·Genomics ·(unknown), Martin Erdel, (unknown), Petra Barth, Gertraud Raber, (unknown), Gerd Utermann, Markus Paulmichl, Florian Lang	31
20	Cloning, Structural Analysis, and Chromosomal Localization of the HumanCSRP2Gene Encoding the LIM Domain Protein CRP2 1997 ·Genomics ·Ralf Weiskirchen, Martin Erdel, Gerd Utermann, Klaus Bister	33

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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