Volker Endris

997 total citations
6 papers, 467 citations indexed

About

Volker Endris is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Volker Endris has authored 6 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Pulmonary and Respiratory Medicine, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Volker Endris's work include Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (1 paper) and Advanced Breast Cancer Therapies (1 paper). Volker Endris is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (1 paper) and Advanced Breast Cancer Therapies (1 paper). Volker Endris collaborates with scholars based in Germany, United States and Canada. Volker Endris's co-authors include Michael Bonin, Ute Moog, Gudrun Rappold, Péter Szatmári, Rolf Sprengel, Christian R. Marshall, Jennifer Howe, Dalila Pinto, Angelika Rieß and Wendy Roberts and has published in prestigious journals such as Science, Nature Genetics and Journal of Hepatology.

In The Last Decade

Volker Endris

6 papers receiving 455 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Volker Endris Germany	3	320	243	229	87	49	6	467
Zhong Xuan United States	7	330 1.0×	239 1.0×	278 1.2×	110 1.3×	51 1.0×	9	489
Hannah M. Grayton United Kingdom	7	276 0.9×	238 1.0×	158 0.7×	91 1.0×	29 0.6×	7	470
Mei Yuan China	6	201 0.6×	191 0.8×	223 1.0×	153 1.8×	46 0.9×	16	458
Yingratana McLennan United States	11	401 1.3×	269 1.1×	273 1.2×	48 0.6×	31 0.6×	21	490
Christelle M. Durand France	5	197 0.6×	167 0.7×	150 0.7×	100 1.1×	49 1.0×	6	349
Hsiu‐Chun Chuang Taiwan	8	137 0.4×	159 0.7×	135 0.6×	96 1.1×	31 0.6×	10	359
Kristen C. Hoffbuhr United States	9	311 1.0×	600 2.5×	217 0.9×	54 0.6×	22 0.4×	10	824
Christine Ochoa Escamilla United States	6	176 0.6×	168 0.7×	131 0.6×	49 0.6×	30 0.6×	6	305
Inge Heulens Belgium	8	383 1.2×	241 1.0×	298 1.3×	76 0.9×	27 0.6×	9	448
Hélène Cheval France	7	492 1.5×	428 1.8×	284 1.2×	79 0.9×	27 0.6×	9	673

Countries citing papers authored by Volker Endris

Since Specialization

Citations

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

Fields of papers citing papers by Volker Endris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Volker Endris

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Schneider, F, Volker Endris, Martina Kirchner, et al.. (2022). BAP1 and PTEN mutations shape the immunological landscape of clear cell renal cell carcinoma and reveal the intertumoral heterogeneity of T cell suppression: a proof-of-concept study. Cancer Immunology Immunotherapy. 72(6). 1603–1618. 10 indexed citations

2.

Sinn, Hans‐Peter, Andreas Schneeweiß, Volker Endris, et al.. (2017). Intrinsic subtypes and risk scores in ER+/HER2-Breast Cancer: a comparison of Prosigna and OncotypeDX risk categories with Ki67. The Breast. 32. S105–S105. 2 indexed citations

3.

Goeppert, Benjamin, Trine Folseraas, Stéphanie Roessler, et al.. (2016). Novel Therapeutic Targets for Primary Sclerosing Cholangitis-Associated Biliary Tract Cancer Identified by Tissue Sequencing. Journal of Hepatology. 64(2). S225–S225. 1 indexed citations

4.

Quiñones‐Mateu, Miguel E. & Volker Endris. (2014). The Sequencing Continuum for Clinical Research: From Sanger to Next Gen. Science. 343(6175). 1159–1159. 1 indexed citations

5.

Endris, Volker, Karl Hackmann, Teresa Neuhann, et al.. (2010). Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia. American Journal of Medical Genetics Part A. 152A(11). 2908–2911. 43 indexed citations

6.

Berkel, Simone, Christian R. Marshall, Birgit Weiß, et al.. (2010). Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nature Genetics. 42(6). 489–491. 410 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.

Explore authors with similar magnitude of impact