Peter Nürnberg

59.5k citations
408 papers · 17.9k · 1 hit paper · h-index 71

Impact in

Papers in

  • Molecular Biology 204
    • RNA modifications and cancer 18
    • Epigenetics and DNA Methylation 17
    • Genomics and Chromatin Dynamics 16
  • Genetics 121
    • Genomic variations and chromosomal abnormalities 31
    • Genetics and Neurodevelopmental Disorders 26
    • Genomics and Rare Diseases 25
Co-authors
Gudrun Nürnberg (68 shared papers)Franz Rüschendorf (20 shared papers)Mohammad R. Toliat (57 shared papers)Janine Altmüller (96 shared papers)Hölger Thiele (65 shared papers)Christian Becker (31 shared papers)Holger Thiele (27 shared papers)Fred B. Bercovitch (11 shared papers)
Journals
The American Journal of Human Genetics (21 papers)Human Genetics (19 papers)Human Mutation (17 papers)PLoS ONE (16 papers)Nature Genetics (12 papers)
Partner nations
GermanyUnited StatesUnited Kingdom

In The Last Decade

Peter Nürnberg

404 papers receiving 17.6k citations

Peter Nürnberg's Hit Papers

Incidence, Risk Factors, and Attributable Mortality of Secondary Infections in the Intensive Care Unit After Admission for Sepsis 2016 · 353 citations
3530+3+6Years since publication100200300
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2016 JAMA

Peers

Peter Nürnberg
Comparison fields: 5 of 176
  • Developmental Biology 382
  • Sensory Systems 769
  • Genetics 4.3k
  • Molecular Biology 8.0k
  • Cell Biology 1.9k
Replace Mario R. Capecchi with:
Mario R. Capecchi United States
Han G. Brunner Netherlands
Rudi Balling Germany
Christine E. Seidman United States
Anthony P. Monaco United States
Michael J. Bamshad United States
Heiner Westphal United States
Randy L. Johnson United States
Lino Tessarollo United States
Makoto M. Taketo Japan
Peter Nürnberg relative to Mario R. Capecchi United States Mario R. Capecchi's profile →
Citations per field
00.5×1.5×2.1×
Mario R. Capecchi · 1×
Citations per year

Countries citing papers authored by Peter Nürnberg

Since Specialization
Citations

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

Fields of papers citing papers by Peter Nürnberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 408 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Incidence, Risk Factors, and Attributable Mortality of Secondary Infections in the Intensive Care Unit After Admission for Sepsis
JAMA ·Lonneke A. van Vught, Peter M. C. Klein Klouwenberg, Cristian Spitoni, Brendon P. Scicluna, Maryse A. Wiewel, Janneke Horn, Marcus J. Schultz, Peter Nürnberg, Marc J. M. Bonten, Olaf L. Cremer, Tom van der Poll
Hit paper breakdown →		2016353
2
Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
Nature Genetics ·Louise Metherell, J. Paul Chapple, Sadani N. Cooray, Alessia David, Christian Becker, Franz Rüschendorf, Danielle Naville, Martine Bégeot, Bernard Khoo, Peter Nürnberg, Angela Huebner, Michael E. Cheetham, Adrian Clark
2005324
3
G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth
Nature Genetics ·Sandra M. Pasternack, Ivar von Kügelgen, Khalid Al Aboud, Young‐Ae Lee, Franz Rüschendorf, Katrin Voß, Axel M. Hillmer, Gerhard J. Molderings, Thomas Franz, Alfredo Ramı́rez, Peter Nürnberg, Markus M. Nöthen, Regina C. Betz
2008297
4
A Genomewide Analysis Provides Evidence for Novel Linkages in Inflammatory Bowel Disease in a Large European Cohort
The American Journal of Human Genetics ·Jochen Hampe, Stefan Schreiber, Sarah H. Shaw, Kit Lau, Stephen Bridger, Andrew J. Macpherson, Lon R. Cardon, H. Sakul, Timothy Harris, Alan Buckler, Jeff Hall, Pieter Stokkers, Sander J. H. van Deventer, Peter Nürnberg, Mudassar M. Mirza, John C.W. Lee, John Edward Lennard-Jones, Christopher G. Mathew, Mark Curran
1999296
5
Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation
American Journal of Medical Genetics Part A ·Anita Rauch, Juliane Hoyer, Sabine Guth, Christiane Zweier, Cornelia Kraus, Christian Becker, Martin Zenker, Ulrike Hüffmeier, Christian T. Thiel, Franz Rüschendorf, Peter Nürnberg, André Reis, Udo Trautmann
2006290
6
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2
Nature Genetics ·(unknown), Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou, Jeroen van Reeuwijk, Bjoern Fischer, Anna Rajab, Birgit Budde, Peter Nürnberg, François Foulquier, Dirk J. Lefeber, Zsolt Urbán, S Gruenewald, Wim Annaert, Han G. Brunner, Hans van Bokhoven, Ron A. Wevers, Éva Morava, Gert Matthijs, Lionel Van Maldergem, Stefan Mundlos
2007261
7
HomozygosityMapper--an interactive approach to homozygosity mapping
Nucleic Acids Research ·Dominik Seelow, Markus Schuelke, Friedhelm Hildebrandt, Peter Nürnberg
2009257
8
Thrombocytopenia is associated with a dysregulated host response in critically ill sepsis patients
Blood ·Theodora A. M. Claushuis, Lonneke A. van Vught, Brendon P. Scicluna, Maryse A. Wiewel, Peter M. C. Klein Klouwenberg, Arie J. Hoogendijk, David S. Y. Ong, Olaf L. Cremer, Janneke Horn, Marek Franitza, Mohammad R. Toliat, Peter Nürnberg, Aeilko H. Zwinderman, Marc J. M. Bonten, Marcus J. Schultz, Tom van der Poll
2016241
9
A comprehensive linkage analysis for myocardial infarction and its related risk factors
Nature Genetics ·Ulrich Broeckel, Christian Hengstenberg, Björn Mayer, Stephan Holmer, Lisa J. Martin, Anthony G. Comuzzie, John Blangero, Peter Nürnberg, André Reis, Günter A.J. Riegger, Howard J. Jacob, Heribert Schunkert
2002234
10
Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain
The American Journal of Human Genetics ·Raimund Fahsold, Sven Hoffmeyer, Claudia Mischung, Christoph Gille, Christian Ehlers, Nazan Kücükceylan, Maher Abdel-Nour, Andreas Gewies, Hartmut Peters, Dieter Kaufmann, Annegret Buske, Sigrid Tinschert, Peter Nürnberg
2000233
11
Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness
Nature Neuroscience ·Shahid Mahmood Baig, Alexandra Koschak, Andreas Lieb, Mathias Gebhart, Claudia Dafinger, Gudrun Nürnberg, Amjad Ali, Ilyas Ahmad, Martina J. Sinnegger-Brauns, Niels Brandt, Jutta Engel, Matteo E. Mangoni, Muhammad Farooq, Habib Ullah Khan, Peter Nürnberg, Jörg Striessnig, Hanno J. Bolz
2010221
12
Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease
The American Journal of Human Genetics ·Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf, Nico Ruf, Angela M. Kaindl, Marco Henneke, Hölger Thiele, Gisela Stoltenburg‐Didinger, Fuat Aksu, Haluk Topaloğlu, Peter Nürnberg, Christoph Hübner, Bernhard Weschke, Jutta Gärtner
2004218
13
HaploPainter: a tool for drawing pedigrees with complex haplotypes
Computer applications in the biosciences ·Holger Thiele, Peter Nürnberg
2004217
14
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
Nature Genetics ·Ingo Kurth, Torsten Pamminger, J. Christopher Hennings, Désirée Soehendra, Antje K. Huebner, Annelies Rotthier, Jonathan Baets, Jan Senderek, Haluk Topaloğlu, Sandra A. Farrell, Gudrun Nürnberg, Peter Nürnberg, Peter De Jonghe, Andreas Gal, Christoph Kaether, Vincent Timmerman, Christian A. Hübner
2009187
15
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome
Journal of Clinical Investigation ·Inga Ebermann, Jennifer B. Phillips, Max C. Liebau, Robert K. Koenekoop, Bernhard Schermer, Irma López, Ellen Schäfer, Anne‐Françoise Roux, Claudia Dafinger, Antje Bernd, Eberhart Zrenner, Mireille Claustres, Bernardo Blanco, Gudrun Nürnberg, Peter Nürnberg, Rebecca Ruland, Monte Westerfield, Thomas Benzing, Hanno J. Bolz
2010182
16
Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy
Nature Genetics ·Andreas Janecke, Debra A. Thompson, Gerd Utermann, Christian Becker, Christian A. Hübner, Eduard Schmid, Christina L. McHenry, (unknown), Franz Rüschendorf, John R. Heckenlively, Bernd Wissinger, Peter Nürnberg, Andreas Gal
2004182
17
Paternal relatedness and age proximity regulate social relationships among adult female rhesus macaques
Proceedings of the National Academy of Sciences ·Anja Widdig, Peter Nürnberg, Michael Krawczak, Wolf Jürgen Streich, Fred B. Bercovitch
2001180
18
RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity
The American Journal of Human Genetics ·Dagan Jenkins, Dominik Seelow, Fernanda Sarquis Jehee, Chad A. Perlyn, Luís Garcia Alonso, Daniela Franco Bueno, Dian Donnai, Dragana Josifiova, Irene M.J. Mathijssen, Jenny E.V. Morton, Karen Helene Ørstavik, Elizabeth Sweeney, Steven A. Wall, Jeffrey L. Marsh, Peter Nürnberg, Maria Rita Passos‐Bueno, Andrew O.M. Wilkie
2007176
19
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study
The Lancet Neurology ·Hendrik Rosewich, Hölger Thiele, Andreas Ohlenbusch, Ulrike Maschke, Janine Altmüller, Peter Frommolt, Birgit Zirn, Friedrich Ebinger, H. Siemes, Peter Nürnberg, Knut Brockmann, Jutta Gärtner
2012175
20
Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis
Nature Genetics ·Massimo Attanasio, N. Henriette Uhlenhaut, Vitor H. Sousa, John F. O’Toole, Edgar A. Otto, Katrin Anlag, Claudia Klugmann, Anna-Corina Treier, Juliana Helou, John A. Sayer, Dominik Seelow, Gudrun Nürnberg, Christian Becker, Albert E. Chudley, Peter Nürnberg, Friedhelm Hildebrandt, Mathias Treier
2007174

About Peter Nürnberg

Peter Nürnberg is a scholar working on Molecular Biology, Genetics, Cell Biology, Cellular and Molecular Neuroscience and Immunology, having authored 408 papers that have together received 17.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (31 papers), Genetics and Neurodevelopmental Disorders (26 papers), Genomics and Rare Diseases (25 papers), RNA modifications and cancer (18 papers), Hearing, Cochlea, Tinnitus, Genetics (17 papers), Epigenetics and DNA Methylation (17 papers), Genomics and Chromatin Dynamics (16 papers) and Microtubule and mitosis dynamics (15 papers). The work is most often cited by research in Developmental Biology (382 citations), Sensory Systems (769 citations), Genetics (4.3k citations), Molecular Biology (8.0k citations) and Cell Biology (1.9k citations). Peter Nürnberg has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Gudrun Nürnberg, Franz Rüschendorf, Mohammad R. Toliat, Janine Altmüller, Hölger Thiele, Christian Becker, Holger Thiele, Fred B. Bercovitch, Friedhelm Hildebrandt and Michael Krawczak. Their work appears in journals such as The American Journal of Human Genetics, Human Genetics, Human Mutation, PLoS ONE and Nature Genetics.

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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