Peter Nürnberg

58.8k total citations · 1 hit paper
407 papers, 17.7k citations indexed

About

Peter Nürnberg is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Peter Nürnberg has authored 407 papers receiving a total of 17.7k indexed citations (citations by other indexed papers that have themselves been cited), including 229 papers in Molecular Biology, 129 papers in Genetics and 48 papers in Cell Biology. Recurrent topics in Peter Nürnberg's work include Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (29 papers) and Genetics and Neurodevelopmental Disorders (26 papers). Peter Nürnberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (33 papers), Genomics and Rare Diseases (29 papers) and Genetics and Neurodevelopmental Disorders (26 papers). Peter Nürnberg collaborates with scholars based in Germany, United States and United Kingdom. Peter Nürnberg's 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 and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Peter Nürnberg

403 papers receiving 17.4k 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.

Incidence, Risk Factors, and Attributable Mortality of Secondary Infections in the Intensive Care Unit After Admission for Sepsis

2016 345 citations Peter Nürnberg et al. profile →

Peers

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-authorship network of co-authors of Peter Nürnberg

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Nürnberg. A scholar is included among the top collaborators of Peter Nürnberg 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 Peter Nürnberg. Peter Nürnberg 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	Polygenic risk scores for nicotine use and family history of smoking are associated with smoking behaviour 2024 ·Drug and Alcohol Dependence ·Jerome C. Foo, (unknown), Fabian Streit, Josef Frank, Norman Zacharias, Lea Zillich, Lea Sirignano, Peter Nürnberg, Thomas F. Wienker, Michael Wagner, Markus M. Nöthen, Michael Nothnagel, Henrik Walter, Bernd Lenz, Rainer Spanagel, Falk Kiefer, Georg Winterer, Marcella Rietschel, Stephanie H. Witt	0
2	Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain 2022 ·Clinical Genetics ·Luisa Averdunk, Khalid Al‐Thihli, Harald Surowy, Hermann‐Josef Lüdecke, Matthias Drechsler, Gökhan Yiğit, Lukasz Smorag, (unknown), Yun Li, Janine Altmüller, (unknown), Michael Wallot, Peter Nürnberg, Bernd Wollnik, Rami Abou Jamra, Almundher Al‐Maawali, Dagmar Wieczorek	1
3	Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability 2022 ·Genes ·Maria Asif, (unknown), (unknown), (unknown), (unknown), Christian Becker, Kerstin Becker, Holger Thiele, (unknown), (unknown), Shahid Mahmood Baig, Peter Nürnberg, Muhammad Sajid Hussain, Ghazala Kaukab Raja, Uzma Abdullah	6
4	A Homozygous AKNA Frameshift Variant Is Associated with Microcephaly in a Pakistani Family 2021 ·Genes ·(unknown), (unknown), Birgit Budde, Muhammad Tariq, (unknown), Zafar Ali, (unknown), (unknown), Naveed Altaf Malik, (unknown), Janine Altmüller, Holger Thiele, Muhammad Sajid Hussain, Sebahattin Çırak, Shahid Mahmood Baig, Peter Nürnberg	4
5	A novel remitting leukodystrophy associated with a variant in FBP2 2021 ·Brain Communications ·Agnieszka Gizak, (unknown), Steffi Dreha‐Kulaczewski, Janusz Wiśniewski, Przemysław Duda, Andreas Ohlenbusch, Brenda Huppke, Marco Henneke, Wolfgang Höhne, Janine Altmüller, Holger Thiele, Peter Nürnberg, Dariusz Rakus, Jutta Gärtner, Peter Huppke	2
6	Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism 2021 ·Genes ·Natalie Young, Maria Asif, Matthew P. Jackson, Daniel Martín Fernández‐Mayoralas, Mar Jiménez de la Peña, Beatriz Calleja‐Pérez, Sara Álvarez, (unknown), Angelika A. Noegel, Wolfgang Höhne, Peter Nürnberg, Bogusław Obara, Muhammad Sajid Hussain, Iakowos Karakesisoglou, Alberto Fernández‐Jaén	9
7	A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family 2021 ·Genes ·(unknown), Stephanie Tennstedt, Muhammad Tariq, (unknown), (unknown), Aamir Ali, Matthias Munz, Hölger Thiele, (unknown), (unknown), (unknown), Peter Nürnberg, Shahid Mahmood Baig, Jeanette Erdmann, Ilyas Ahmad	5
8	Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss 2020 ·Clinical Genetics ·Birgit Budde, (unknown), (unknown), (unknown), Janine Altmüller, Susanne Motameny, Amit Kawalia, Holger Thiele, (unknown), Christian Becker, Mohammad R. Toliat, Gudrun Nürnberg, (unknown), (unknown), Markus Pfister, Peter Nürnberg	24
9	Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database 2019 ·Nucleic Acids Research ·Eduardo Pérez‐Palma, (unknown), Peter Nürnberg, Patrick May, Dennis Lal	52
10	Assessment of genetic variant burden in epilepsy-associated brain lesions 2019 ·European Journal of Human Genetics ·Lisa‐Marie Niestroj, Patrick May, Mykyta Artomov, Katja Kobow, Roland Coras, Eduardo Pérez‐Palma, Janine Altmüller, Hölger Thiele, Peter Nürnberg, Costin Leu, Aarno Palotie, Mark J. Daly, Karl Martin Klein, Rudi Beschorner, Yvonne Weber, Ingmar Blümcke, Dennis Lal	12
11	A Novel Homozygous Nonsense Variant in BICD2 Underlies Hereditary Spastic Paraplegia Complex Type 2019 ·Pakistan Journal of Zoology ·(unknown), Saba Irshad, (unknown), (unknown), Muhammad Sajid Hussain, (unknown), Peter Nürnberg	2
12	Duplications at 19q13.33 in patients with neurodevelopmental disorders 2018 ·Neurology Genetics ·Eduardo Pérez‐Palma, Elmo Saarentaus, Marie Ravoet, G. Ferrari, Peter Nürnberg, Bertrand Isidor, Bernd A. Neubauer, Dennis Lal	2
13	Guideline‐based and bioinformatic reassessment of lesion‐associated gene and variant pathogenicity in focal human epilepsies 2018 ·Epilepsia ·Lisa‐Marie Niestroj, (unknown), Michael Nothnagel, Patrick May, Aarno Palotie, Mark J. Daly, Peter Nürnberg, Ingmar Blümcke, Dennis Lal	6
14	Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathy 2018 ·Journal of Medical Genetics ·Ilse Julia Broekaert, Kerstin Becker, Ingo Gottschalk, Friederike Körber, Jörg Dötsch, Hölger Thiele, Janine Altmüller, Peter Nürnberg, Christoph Hünseler, Sebahattin Çırak	18
15	TGFβ signaling directs serrated adenomas to the mesenchymal colorectal cancer subtype 2016 ·EMBO Molecular Medicine ·Evelyn Fessler, Jarno Drost, Sander R. van Hooff, Janneke F. Linnekamp, Xin Wang, Marnix Jansen, Felipe de Sousa e Melo, Pramudita R. Prasetyanti, Joep IJspeert, Marek Franitza, Peter Nürnberg, Carel J.M. van Noesel, Evelien Dekker, Louis Vermeulen, Hans Clevers, Jan Paul Medema	120
16	Replication of the association between CHRNA4 rs1044396 and harm avoidance in a large population-based sample 2015 ·European Neuropsychopharmacology ·Katharina Bey, Leonhard Lennertz, Sebastian Markett, Nadine Petrovsky, Jürgen Gallinat, Gerhard Gründer, Katja N. Spreckelmeyer, Thomas F. Wienker, Arian Mobascher, Norbert Dahmen, Norbert Thuerauf, Johannes Kornhuber, Falk Kiefer, Mohammad R. Toliat, Peter Nürnberg, Georg Winterer, Michael Wagner	1
17	Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency 2009 ·The Journal of Clinical Endocrinology & Metabolism ·Louise Metherell, Danielle Naville, G Halaby, Martine Bégeot, Angela Huebner, Gudrun Nürnberg, Peter Nürnberg, Jane Green, Jeremy Tomlinson, Nils Krone, Lin Lin, Michaël Racine, Daniel M. Berney, John C. Achermann, Wiebke Arlt, Adrian Clark	112
18	Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) 2009 ·Journal of Medical Genetics ·Edgar A. Otto, Kálmán Tory, Massimo Attanasio, Weibin Zhou, Moumita Chaki, (unknown), Eric L. Wise, (unknown), Boris Utsch, C. Becker, Gudrun Nürnberg, Peter Nürnberg, Ahmet Nayır, Sophie Saunier, Corinne Antignac, Friedhelm Hildebrandt	98
19	A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin. 2006 ·PubMed ·Vanita Vanita, Hans Christian Hennies, Daljit Singh, Peter Nürnberg, Karl Sperling, Jai Rup Singh	35
20	Evidence for a NOD2 -independent susceptibility locus for inflammatory bowel disease on chromosome 16p 2001 ·Proceedings of the National Academy of Sciences ·Jochen Hampe, H Frenzel, Muddassar M. Mirza, Peter J.P. Croucher, Andrew Cuthbert, Silvia Mascheretti, Klaus Huse, Matthias Platzer, Stephen Bridger, Birgit Meyer, Peter Nürnberg, Pieter Stokkers, Michael Krawczak, Christopher G. Mathew, (unknown), Stefan Schreiber	82

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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