Detlev Schindler

12.3k citations
163 papers · 6.6k · h-index 43

Impact in

  • Cancer Research top 1%
    • Carcinogens and Genotoxicity Assessment
  • Molecular Biology top 1%
    • DNA Repair Mechanisms
    • CRISPR and Genetic Engineering
    • Genomics and Chromatin Dynamics

Papers in

  • Molecular Biology 136
    • DNA Repair Mechanisms 102
    • CRISPR and Genetic Engineering 22
    • Genomics and Chromatin Dynamics 16
  • Genetics 34
    • Genomic variations and chromosomal abnormalities 14
Co-authors
Holger Hoehn (31 shared papers)Helmut Hanenberg (24 shared papers)Kornelia Neveling (16 shared papers)Reinhard Kalb (19 shared papers)Heidemarie Neitzel (13 shared papers)Manfred Kubbies (9 shared papers)Arleen D. Auerbach (10 shared papers)Peter S. Rabinovitch (8 shared papers)
Journals
Nature Genetics (7 papers)Human Genetics (6 papers)PLoS ONE (5 papers)Blood (5 papers)Cytogenetic and Genome Research (5 papers)
Partner nations
GermanyUnited StatesNetherlands

In The Last Decade

Detlev Schindler

160 papers receiving 6.5k citations

Peers

Detlev Schindler
Comparison fields: 5 of 116
  • Cancer Research 1.4k
  • Molecular Biology 5.1k
  • Genetics 1.6k
  • Cell Biology 683
  • Oncology 1.0k
Replace Quinten Waisfisz with:
Quinten Waisfisz Netherlands
Peter B. Rahl United States
Brian J. Abraham United States
Teresa Druck United States
Adrian P. Bracken Ireland
Eva Y.-H.P. Lee United States
David O. Ferguson United States
A. Malcolm R. Taylor United Kingdom
Tom Kadesch United States
James F. Amatruda United States
Detlev Schindler relative to Quinten Waisfisz Netherlands Quinten Waisfisz's profile →
Citations per field
00.5×1.5×1.8×
Quinten Waisfisz · 1×
Citations per year

Countries citing papers authored by Detlev Schindler

Since Specialization
Citations

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

Fields of papers citing papers by Detlev Schindler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 163 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
Nature Genetics ·Sarah Reid, Detlev Schindler, Helmut Hanenberg, Karen Barker, Sandra Hanks, Reinhard Kalb, Kornelia Neveling, Patrick Kelly, Sheila Seal, Marcel Freund, Melanie Wurm, Sat Dev Batish, Francis P. Lach, Sevgi Yetgin, Heidemarie Neitzel, Hany Ariffin, Marc Tischkowitz, Christopher G. Mathew, Arleen D. Auerbach, Nazneen Rahman
2006456
2
Mutation of the RAD51C gene in a Fanconi anemia–like disorder
Nature Genetics ·Fiona Vaz, Helmut Hanenberg, Beatrice Schuster, Karen Barker, Constanze Wiek, Verena Erven, Kornelia Neveling, Daniela Endt, Ian Kesterton, Flavia Autore, Franca Fraternali, Marcel Freund, Linda Hartmann, David Grimwade, Roland G. Roberts, Heiner Schaal, Shehla Mohammed, Nazneen Rahman, Detlev Schindler, Christopher G. Mathew
2010311
3
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
Nature Genetics ·Orna Levran, Claire Attwooll, Rashida Henry, Kelly Milton, Kornelia Neveling, Paula Rı́o, Sat Dev Batish, Reinhard Kalb, Eunike Velleuer, Sandra Barral, Jürg Ott, John H.J. Petrini, Detlev Schindler, Helmut Hanenberg, Arleen D. Auerbach
2005283
4
The Fanconi anaemia group G gene FANCG is identical with XRCC9
Nature Genetics ·Johan P. de Winter, Quinten Waisfisz, Martin A. Rooimans, Carola G.M. van Berkel, Lucine Bosnoyan-Collins, Noa Alon, Madeleine Carreau, Olaf Bender, Ilja Demuth, Detlev Schindler, Jan C. Pronk, Fré Arwert, Holger Hoehn, Martin Digweed, Manuel Buchwald, Hans Joenje
1998270
5
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype
Nature Genetics ·Chantal Stoepker, Karolina Hain, Beatrice Schuster, Yvonne Hilhorst‐Hofstee, Martin A. Rooimans, Jûrgen Steltenpool, Anneke B. Oostra, Katharina Eirich, Elisabeth T Korthof, Aggie Nieuwint, Nicolaas G.J. Jaspers, Thomas Bettecken, Hans Joenje, Detlev Schindler, John Rouse, Johan P. de Winter
2011233
6
Human RAD50 Deficiency in a Nijmegen Breakage Syndrome-like Disorder
The American Journal of Human Genetics ·Regina Waltes, Reinhard Kalb, Magtouf Gatei, Amanda W. Kijas, Markus Stümm, Alexandra Sobeck, Britta Wieland, Raymonda Varon, Yaniv Lerenthal, Martin F. Lavin, Detlev Schindler, Thilo Dörk
2009190
7
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Journal of Clinical Investigation ·Kerstin Knies, Shojiro Inano, Marı́a José Ramı́rez, Masamichi Ishiai, Jordi Surrallés, Minoru Takata, Detlev Schindler
2017151
8
RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous Recombination
Molecular Cell ·Shojiro Inano, Koichi Sato, Y Katsuki, Wataru Kobayashi, Hiroki Tanaka, Kazuhiro Nakajima, Shinichiro Nakada, Hiroyuki Miyoshi, Kerstin Knies, Akifumi Takaori‐Kondo, Detlev Schindler, Masamichi Ishiai, Hitoshi Kurumizaka, Minoru Takata
2017133
9
BrdU—Hoechst flow cytometry: A unique tool for quantitative cell cycle analysis
Experimental Cell Research ·Peter S. Rabinovitch, Manfred Kubbies, Y.C. Chen, Detlev Schindler, Holger Hoehn
1988132
10
Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction
Cytogenetic and Genome Research ·M Gross, Helmut Hanenberg, Stephan Lobitz, Richard Friedl, Sarah Herterich, Ralf Dietrich, Bernd Gruhn, Detlev Schindler, Holger Hoehn
2002130
11
FAAP100 is essential for activation of the Fanconi anemia‐associated DNA damage response pathway
The EMBO Journal ·(unknown), Masamichi Ishiai, Abdullah Mahmood Ali, Annette L. Medhurst, Kornelia Neveling, Reinhard Kalb, Zhijiang Yan, Yutong Xue, Anneke B. Oostra, Arleen D. Auerbach, Maureen E. Hoatlin, Detlev Schindler, Hans Joenje, Johan P. de Winter, Minoru Takata, Amom Ruhikanta Meetei, Weidong Wang
2007121
12
Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia
Cell Reports ·Kimberly A. Rickman, Francis P. Lach, Avinash Abhyankar, Frank X. Donovan, Erica Sanborn, Jennifer A. Kennedy, Carrie Sougnez, Stacey Gabriel, Olivier Elemento, Settara C. Chandrasekharappa, Detlev Schindler, Arleen D. Auerbach, Agata Smogorzewska
2015112
13
Fanconi anemia mutation causes cellular susceptibility to ambient oxygen.
PubMed ·Detlev Schindler, Holger Hoehn
1988103
14
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability
The EMBO Journal ·Massimo Bogliolo, Alex Lyakhovich, Elsa Callén, María Castellà, Enrico Cappelli, Marı́a José Ramı́rez, A. Creus, Ricard Marcos, Reinhard Kalb, Kornelia Neveling, Detlev Schindler, Jordi Surrallés
2007102
15
Overexpression of LASP-1 mediates migration and proliferation of human ovarian cancer cells and influences zyxin localisation
British Journal of Cancer ·Thomas G. P. Grünewald, Ulrike Kämmerer, C Winkler, Detlev Schindler, Albert Sickmann, A Hönig, Elke Butt
2007102
16
Identification of the Fanconi Anemia Complementation Group I Gene, FANCI
Analytical Cellular Pathology ·Josephine C. Dorsman, Marieke Levitus, Davy Rockx, Martin A. Rooimans, Anneke B. Oostra, Anneke Haitjema, Sietske T. Bakker, Jûrgen Steltenpool, Dezső Schuler, Sheila Mohan, Detlev Schindler, Fré Arwert, Gerard Pals, Christopher G. Mathew, Quinten Waisfisz, Johan P. de Winter, Hans Joenje
2007101
17
A Severe Form of Human Combined Immunodeficiency Due to Mutations in DNA Ligase IV
The Journal of Immunology ·Anselm Enders, Paul Fisch, Klaus Schwarz, Ulrich Duffner, Ulrich Pannicke, Elisabeth Nikolopoulos, Anke Peters, Marzenna Orlowska‐Volk, Detlev Schindler, Wilhelm Friedrich, Barbara Selle, Charlotte M. Niemeyer, Stephan Ehl
2006100
18
Genotype–phenotype correlations in Fanconi anemia
Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Kornelia Neveling, Daniela Endt, Holger Hoehn, Detlev Schindler
200999
19
Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition
The American Journal of Human Genetics ·Heidemarie Neitzel, Luitgard M. Neumann, Detlev Schindler, Andreas Wirges, Holger Tönnies, Marc Trimborn, Alice Krebsová, Reyk Richter, Karl Sperling
200282
20
Genetic Heterogeneity among Fanconi Anemia Heterozygotes and Risk of Cancer
Cancer Research ·Marianne Berwick, Jaya M. Satagopan, Leah Ben‐Porat, Ann D. Carlson, Katherine Mah, Rashida Henry, Raffaella Diotti, Kelly Milton, Kanan Pujara, Tom Landers, Sat Dev Batish, J. Alejandro Morales, Detlev Schindler, Helmut Hanenberg, Robert Hromas, Orna Levran, Arleen D. Auerbach
200778

About Detlev Schindler

Detlev Schindler is a scholar working on Molecular Biology, Genetics, Cancer Research, Plant Science and Cell Biology, having authored 163 papers that have together received 6.6k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (102 papers), Carcinogens and Genotoxicity Assessment (30 papers), CRISPR and Genetic Engineering (22 papers), Genomics and Chromatin Dynamics (16 papers), Chromosomal and Genetic Variations (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Microtubule and mitosis dynamics (13 papers) and Lysosomal Storage Disorders Research (13 papers). The work is most often cited by research in Cancer Research (1.4k citations), Molecular Biology (5.1k citations), Genetics (1.6k citations), Cell Biology (683 citations) and Oncology (1.0k citations). Detlev Schindler has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Holger Hoehn, Helmut Hanenberg, Kornelia Neveling, Reinhard Kalb, Heidemarie Neitzel, Manfred Kubbies, Arleen D. Auerbach, Peter S. Rabinovitch, Hans Joenje and Johan P. de Winter. Their work appears in journals such as Nature Genetics, Human Genetics, PLoS ONE, Blood and Cytogenetic and Genome Research.

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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